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Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by year, source, volume, issue, page.
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| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1801 | 0 | 0 | 1801 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A29-A29 Ceman S; Brown V; Warren ST Isolation of an FMRP-associated mRNP and the identification of nucleolin and the fragile X-related proteins as components of the complex. | 0 | 0 |
| 1802 | 0 | 0 | 1802 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A30-A30 Peier AM; McIlwain KL; Paylor R; Nelson DL FMR1 YAC transgenic mice: rescue of the FMRl knockout mouse and behavior of the CGG trinucleotide repeat. | 0 | 0 |
| 1803 | 0 | 0 | 1803 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A49-A49 Drasinover V; Ehrlich S; Magal N; Taub E; Libman V; et al. Increased transmission of the premutated allele compared to the normal allele in female carriers of the fragile X syndrome. | 0 | 0 |
| 1804 | 0 | 0 | 1804 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A68-A68 Fisch GS; Howard-Peebles PN; Carpenter N; Tarleton J; Simensen R; et al. Age-related features of genetic mutations producing cognitive impairment: the Fragile X mutation, NF1, and Williams Syndrome. | 0 | 0 |
| 1805 | 0 | 0 | 1805 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A103-A103 Brown WT; Rabe A; Durnas R; Haubenstock H; Dobkin C FMR1 knockout mouse shows a strain-specific severe learning impairment: A robust model for the fragile X syndrome. | 0 | 0 |
| 1806 | 0 | 0 | 1806 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A105-A105 Kenneson A; Hagedorn CH; Warren ST Quantitative studies of the fragile X mental retardation 1 (FMR1) gene product, FMRP. | 0 | 0 |
| 1807 | 0 | 0 | 1807 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A145-A145 Chernoff EJ; Nunes M; White B; McClellan J; Coll E; et al. Fragile X premutation status in a male with mental retardation. | 0 | 0 |
| 1808 | 0 | 0 | 1808 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A165-A165 Iqbal MA; Sakati N; Nester A; Ozand P Cytogenetic diagnosis of fragile X syndrome a study of 305 suspected cases in Saudi Arabia. | 0 | 0 |
| 1809 | 0 | 0 | 1809 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A214-A214 Falik-Zaccai TC; Shachak E; Borochowitz Z; Magal N; Zatz S; et al. Fragile X syndrome: Population carrier screening and implication for prenatal diagnosis. | 0 | 0 |
| 1810 | 0 | 0 | 1810 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A263-A263 Absher DM; Warren SR Functional studies of mammalian FMRP in yeast. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1811 | 0 | 0 | 1811 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A266-A266 Burman RW; Popovich BW; Yates PA; Jacky PB; Schnell JL; et al. Fully expanded fragile X CGG repeats exhibit a length-and differentiation-dependent instability in cell hybrids that is independent of DNA methylation. | 0 | 0 |
| 1812 | 0 | 0 | 1812 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A268-A268 Crawford DC; Schwartz CE; Warren ST; Sherman SL Novel repeat structures identified in African-Americans represent a new mechanism leading to fragile X CGG repeat instability. | 0 | 0 |
| 1813 | 0 | 0 | 1813 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A269-A269 DiMarco SP; Ceman S; Torre E; Warren ST FMRP is a phosphoprotein and a substrate of the Fes non-receptor tryosine kinase. | 2 | 3 |
| 1814 | 0 | 0 | 1814 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A270-A270 El-Hazmi MF Fragile X mental retardation in syndrome in Saudi Arabia. | 0 | 0 |
| 1815 | 0 | 0 | 1815 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A279-A279 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson J; et al. Haplotype and AGG-interspersion analysis of FMR1(CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 0 | 0 |
| 1816 | 0 | 0 | 1816 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A403-A403 Xu B; School JM; Buroker NE; Scott CR; Chen SH High frequency of the FMR-1 INV10+14c/t polymorphism in Asians, and its association with the Fragile X Syndrome in Caucasians. | 0 | 1 |
| 1817 | 0 | 0 | 1817 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A464-A464 Nolin SL; Houck GE; Gargano AD; Li SY; Glicksman A; et al. Instability of FMR1 alleles with 40-60 CGG repeats. | 0 | 0 |
| 1818 | 0 | 0 | 1818 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A471-A471 Ventura KA; Fraer LM; Smith EE; Merrill AE; Treat KJ; et al. Transmission on a fragile X full mutation through a normal transmitting male. | 0 | 0 |
| 1819 | 0 | 0 | 1819 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A474-A474 Lazarou LP; Warburton S; Roberts CE; Lindley VH; Bartlett S; et al. Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male. | 0 | 0 |
| 1820 | 0 | 0 | 1820 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A493-A493 Tassone F; Hagerman RJ; Taylor AK; Mills JB; Wood S; et al. FMR1 mRNA expression levels in fragile X. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1821 | 27 | 53 | 1821 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(1):25-30 Abrams MT; Kaufmann WE; Rousseau F; Oostra BA; Wolozin B; et al. FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome | 8 | 11 |
| 1822 | 5 | 20 | 1822 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(3):206-211 McConkie-Rosell A; Spiridigliozzi GA; Rounds K; Dawson DV; Sullivan JA; et al. Parental attitudes regarding carrier testing in children at risk for fragile X syndrome | 2 | 7 |
| 1823 | 0 | 5 | 1823 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(2):140-141 Hjalgrim H; Jacobsen TB; Norgaard K; Lou HC; Brondum-Nielsen K; et al. Frontal-subcortical hypofunction in the fragile X syndrome | 5 | 8 |
| 1824 | 38 | 61 | 1824 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):221-236 Holden JJA; Percy M; Allingham-Hawkins D; Brown WT; Chiurazzi P; et al. Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997 | 1 | 4 |
| 1825 | 6 | 35 | 1825 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):248-252 Weiler IJ; Greenough WT Synaptic synthesis of the Fragile X protein: Possible involvement in synapse maturation and elimination | 31 | 44 |
| 1826 | 8 | 23 | 1826 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):253-256 Fisch GS; Holden JJK; Carpenter NJ; Howard-Peebles PN; Maddalena A; et al. Age-related language characteristics of children and adolescents with fragile X syndrome | 7 | 8 |
| 1827 | 13 | 26 | 1827 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):257-263 Fisch GS; Carpenter NJ; Holden JJA; Simensen R; Howard-Peebles PN; et al. Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles | 10 | 10 |
| 1828 | 16 | 54 | 1828 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):268-279 Miller LJ; McIntosh DN; McGrath J; Shyu V; Lampe M; et al. Electrodermal responses to sensory stimuli in individuals with fragile X syndrome: A preliminary report | 32 | 41 |
| 1829 | 4 | 9 | 1829 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):281-285 Teisl JT; Reiss AL; Mazzocco MMM Maximizing the sensitivity of a screening questionnaire for determining fragile X at-risk status | 2 | 2 |
| 1830 | 28 | 47 | 1830 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):286-295 Kaufmann WE; Abrams MT; Chen WM; Reiss AL Genotype, molecular phenotype, and cognitive phenotype: Correlations in fragile X syndrome | 30 | 36 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1831 | 4 | 13 | 1831 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):296-297 Ferri R; Del Gracco S; Elia M; Musumeci SA; Pettinato S Heart rate variability and autonomic function during sleep in fragile X syndrome | 0 | 0 |
| 1832 | 4 | 28 | 1832 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):298-301 Kotilainen J; Pirinen S Dental maturity is advanced in fragile X syndrome | 2 | 2 |
| 1833 | 19 | 35 | 1833 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):302-307 Parvari R; Mumm S; Galil A; Manor E; Bar-David Y; et al. Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth | 2 | 6 |
| 1834 | 11 | 20 | 1834 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):308-312 Fisch GS; Carpenter N; Holden JJA; Howard-Peebles PN; Maddalena A; et al. Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis | 10 | 16 |
| 1835 | 13 | 41 | 1835 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):313-317 Hagerman RJ; Hills J; Scharfenaker S; Lewis H Fragile X syndrome and selective mutism | 12 | 19 |
| 1836 | 11 | 22 | 1836 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):318-321 Linden MG; Tassone F; Gane LW; Hills JL; Hagerman RJ; et al. Compound heterozygous female with fragile X syndrome | 0 | 1 |
| 1837 | 3 | 6 | 1837 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):322-325 Allingham-Hawkins SJ; Babul-Hirji R; Chitayat D; Holden JJA; Yang KT; et al. Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data | 11 | 19 |
| 1838 | 5 | 6 | 1838 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):326-326 Vianna-Morgante AM Twinning and premature ovarian failure in premutation fragile X carriers | 10 | 11 |
| 1839 | 5 | 11 | 1839 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):327-328 Braat DDM; Smits APT; Thomas CMG Menstrual disorders and endocrine profiles in fragile X carriers prior to 40 years of age: A pilot study | 10 | 13 |
| 1840 | 3 | 9 | 1840 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):331-333 Wen GY; Jenkins EC; Goldberg EM; Genovese M; Brown WT; et al. Ultrastructure of the fragile X chromosome: New observations on the fragile site | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1841 | 6 | 11 | 1841 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):338-341 Dobkin C; Ding XH; Li SY; Houck G; Nolin SL; et al. Accelerated prenatal diagnosis of fragile X syndrome by polymerase chain reaction restriction fragment detection | 2 | 3 |
| 1842 | 8 | 14 | 1842 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):342-346 Jenkins EC; Wen GY; Kim KS; Zhong N; Sapienza VJ; et al. Prenatal fragile X detection using cytoplasmic and nuclear-specific monoclonal antibodies | 2 | 2 |
| 1843 | 11 | 14 | 1843 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):347-349 Chiurazzi P; Pomponi MG; Sharrock A; Macpherson J; Lormeau S; et al. DNA panel for interlaboratory standardization of haplotype studies on the fragile X syndrome and proposal for a new allele nomenclature | 4 | 11 |
| 1844 | 3 | 7 | 1844 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):350-351 Faradz SMH; Buckley M; Tang LP; Leigh D; Holden JJA Molecular screening for fragile X syndrome among Indonesian children with developmental disability | 3 | 5 |
| 1845 | 18 | 31 | 1845 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):179-183 Pang CP; Poon PMK; Chen QL; Lai KYC; Yin CH; et al. Trinucleotide CGG repeat in the FMR1 gene in Chinese mentally retarded patients | 8 | 11 |
| 1846 | 19 | 37 | 1846 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):184-190 Patsalis PC; Sismani C; Hettinger JA; Boumba I; Georgiou I; et al. Molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes in the Hellenic population of Greece and Cyprus: Incidence, genetic variation, and stability | 10 | 20 |
| 1847 | 20 | 34 | 1847 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):191-194 Zhong N; Ju WN; Xu WM; Ye LL; Shen Y; et al. Frequency of the fragile X syndrome in Chinese mentally retarded populations is similar to that in Caucasians | 7 | 11 |
| 1848 | 1 | 4 | 1848 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):195-197 Patsalis PC; Sismani C; Hettinger JA; Holden JJA; Lawson JS; et al. Frequencies of "grey-zone"and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada | 0 | 4 |
| 1849 | 4 | 5 | 1849 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):202-203 Tuncbilek E; Alikasifoglu M; Boduroglu K; Aktas D; Anar B Frequency of fragile X syndrome among Turkish patients with mental retardation of unknown etiology | 3 | 3 |
| 1850 | 21 | 26 | 1850 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):204-207 Mingroni-Netto RC; Costa SS; Angeli CB; Vianna-Morgante AM DXS548/FRAXAC1 haplotypes in fragile X chromosomes in the Brazilian population | 2 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1851 | 10 | 14 | 1851 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):214-216 Pekarik V; Blazkova M; Kozak L Haplotype analysis of the fragile X syndrome gene FMR1 in the Czech Republic | 2 | 5 |
| 1852 | 13 | 22 | 1852 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):217-220 Patsalis PC; Sismani C; Stylianou S; Ioannou P; Joseph G; et al. Genetic variation and intergenerational FMR1 CGG-repeat stability in 100 unrelated three-generation families from the normal population | 1 | 2 |
| 1853 | 22 | 25 | 1853 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):221-225 Schmucker B; Seidel J Mosaicism for a full mutation and a normal size allele in two fragile X males | 5 | 7 |
| 1854 | 10 | 20 | 1854 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):226-228 Glaser D; Wohrle D; Salat U; Vogel W; Steinbach P; et al. Mitotic behavior of expanded CGG repeats studied on cultured cells: Further evidence for methylation-mediated triplet repeat stability in fragile X syndrome | 5 | 8 |
| 1855 | 18 | 22 | 1855 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):229-232 Petek E; Kroisel PM; Schuster M; Zierler H; Wagner K Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene | 1 | 1 |
| 1856 | 33 | 40 | 1856 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):233-239 Taylor AK; Tassone F; Dyer PN; Hersch SM; Harris JB; et al. Tissue heterogeneity of the FMR1 mutation in a high-functioning male with fragile X syndrome | 17 | 24 |
| 1857 | 20 | 37 | 1857 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):245-249 Reyniers E; Martin JJ; Cras P; Van Marck E; Handig I; et al. Postmortem examination of two fragile X brothers with an FMR1 full mutation | 19 | 23 |
| 1858 | 46 | 64 | 1858 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):250-261 Tassone F; Hagerman RJ; Ikle DN; Dyer PN; Lampe M; et al. FMRP expression as a potential prognostic indicator in fragile X syndrome | 60 | 67 |
| 1859 | 15 | 23 | 1859 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):268-271 Zhong N; Ju W; Nelson D; Dobkin C; Brown WT Reduced mRNA for G3BP in fragile X cells: Evidence of FMR1 gene regulation | 4 | 5 |
| 1860 | 4 | 36 | 1860 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):272-276 Currie JR; Brown WT KH domain-containing proteins of yeast: Absence of a fragile X gene homologue | 0 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1861 | 11 | 27 | 1861 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):300-303 Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U; et al. Premature ovarian failure (POF) and fragile X premutation females: From POF to fragile X carrier identification, from fragile X carrier diagnosis to POF association data | 14 | 26 |
| 1862 | 4 | 11 | 1862 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):306-308 Syrrou M; Georgiou I; Patsalis PC; Bouba I; Adonakis G; et al. Fragile X premutations and (TA)n estrogen receptor polymorphism in women with ovarian dysfunction | 2 | 11 |
| 1863 | 3 | 13 | 1863 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 84(3):309-310 Zhong N; Ju WN; Brown WT; Ye LL; Jenkins EC; et al. Distribution of apolipoprotein E genotypes in fragile X syndrome and Batten disease | 0 | 0 |
| 1864 | 5 | 13 | 1864 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):197-201 Freedenberg DL; Gane LW; Richards CS; Lampe M; Hills J; et al. Fragile X syndrome and an isodicentric X chromosome in a woman with multiple anomalies, developmental delay, and normal pubertal development | 1 | 1 |
| 1865 | 10 | 14 | 1865 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 85(3):311-316 Grasso M; Faravelli F; Lo Nigro C; Chiurazzi P; Sperandeo MP; et al. Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients | 1 | 1 |
| 1866 | 7 | 12 | 1866 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 86(2):162-164 Sun YJ; Baumer A Nonrandom X inactivation and selection of fragile X full mutation in fetal fibroblasts | 1 | 3 |
| 1867 | 5 | 12 | 1867 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(4):366-368 Torrioli MG; Vernacotola S; Mariotti P; Bianchi E; Calvani M; et al. Double-blind, placebo-controlled study of L-acetylcarnitine for the treatment of hyperactive behavior in fragile X syndrome | 4 | 7 |
| 1868 | 3 | 6 | 1868 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(5):436-439 Einfeld S; Tonge B; Turner G Longitudinal course of behavioral and emotional problems in Fragile X syndrome | 6 | 6 |
| 1869 | 89 | 136 | 1869 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 88(1):11-24 Kaufmann WE; Reiss AL Molecular and cellular genetics of fragile X syndrome | 16 | 28 |
| 1870 | 17 | 24 | 1870 1999 AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY 181(4):789-792 Wenstrom KD; Descartes M; Franklin J; Cliver SP A five-year experience with fragile X screening of high-risk gravid women | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1871 | 22 | 38 | 1871 1999 ANNALES DE GENETIQUE 42(4):197-201 Arrieta I; Criado B; Martinez B; Telez M; Nunez T; et al. A survey of fragile X syndrome in a sample from Spanish Basque country | 4 | 4 |
| 1872 | 0 | 0 | 1872 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-767 Lesniak-Karpiak K; Mazzocco MM; Lanham DC; Denckla MB Behavioral assessment of social skills in children with Turner syndrome or Fragile X. | 0 | 0 |
| 1873 | 0 | 0 | 1873 1999 ARCHIVES OF CLINICAL NEUROPSYCHOLOGY 14(8):767-768 Lanham DC; Mazzocco MM; Denckla MB Depression and anxiety in girls with Fragile X or Turner Syndrome. | 1 | 1 |
| 1874 | 10 | 18 | 1874 1999 AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY 33(3):436-440 Al-Semaan Y; Malla AK; Lazosky A Schizoaffective disorder in a fragile-X carrier | 0 | 0 |
| 1875 | 20 | 36 | 1875 1999 BIOCHEMICAL JOURNAL 343:517-523 Tamanini F; van Unen L; Bakker C; Sacchi N; Galjaard H; et al. Oligomerization properties of fragile-X mental-retardation protein (FMRP) and the fragile-X-related proteins FXR1P and FXR2P | 20 | 23 |
| 1876 | 52 | 98 | 1876 1999 BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE 77(4):331-342 Khandjian EW Biology of the fragile X mental retardation protein, an RNA-binding protein | 14 | 22 |
| 1877 | 0 | 0 | 1877 1999 BLOOD 94(10):94A-94A Warren TL; Dahle CE; Buikema BS; Weiner GJ Immunotherapy of lymphoma using CgG oligodeoxynucleotides. | 0 | 0 |
| 1878 | 15 | 19 | 1878 1999 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 37(4):397-401 Houdayer C; Lemonnier A; Gerard M; Chauve C; Tredano M; et al. Improved fluorescent PCR-based assay for sizing CGG repeats at the FRAXA locus | 1 | 6 |
| 1879 | 34 | 44 | 1879 1999 CLINICAL GENETICS 55(5):346-351 Tassone F; Longshore J; Zunich J; Steinbach P; Salat U; et al. Tissue-specific methylation differences in a fragile X premutation carrier | 2 | 4 |
| 1880 | 8 | 12 | 1880 1999 CLINICAL GENETICS 56(1):98-99 Millan JM; Martinez F; Cadroy A; Gandia J; Casquero M; et al. Screening for FMR1 mutations among the mentally retarded: prevalence of the fragile X syndrome in Spain | 2 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1881 | 15 | 30 | 1881 1999 CORTEX 35(2):263-271 Cornish KM; Munir F; Cross G Spatial cognition in males with Fragile-X syndrome: Evidence for a neuropsychological phenotype | 14 | 16 |
| 1882 | 35 | 50 | 1882 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578 Harris SW; Hagerman RJ Fragile X syndrome: new developments | 2 | 2 |
| 1883 | 0 | 0 | 1883 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):137-138 Arrieta I; Criado B; Martinez B; Telez M; Fiores P; et al. Molecular and cytogenetic analysis of the fragile X syndrome in a sample from Basque Country: are the Basques a population with a low risk of developing the syndrome? | 0 | 0 |
| 1884 | 0 | 0 | 1884 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):165-165 Sofocleous C; Mavrou A; Fryssira H; Kolialexi A; Tsenghi C; et al. FMRP (Fragile X Mental Retardation Protein) studies in mentally retarded children in Greece | 0 | 0 |
| 1885 | 0 | 0 | 1885 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):167-167 Tayel SM; Al-Naggar RL; Ali FE; Al-Awadi SA Two-step fragile X screening program in mentally retarded males | 0 | 0 |
| 1886 | 13 | 65 | 1886 1999 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 41(9):625-632 Hatton DD; Bailey DB; Hargett-Beck MQ; Skinner M; Clark RD Behavioral style of young boys with fragile X syndrome | 9 | 13 |
| 1887 | 16 | 23 | 1887 1999 DIAGNOSTIC MOLECULAR PATHOLOGY 8(3):152-156 Tzeng CC; Cho WC; Kuo PL; Chen RM Pilot fragile X screening in normal population of Taiwan | 7 | 10 |
| 1888 | 22 | 54 | 1888 1999 EPILEPSIA 40(8):1092-1099 Musumeci SA; Hagerman RJ; Ferri R; Bosco P; Dalla Bernardina B; et al. Epilepsy and EEG findings in males with fragile X syndrome | 10 | 19 |
| 1889 | 14 | 23 | 1889 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(2):212-216 Ryynanen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; et al. Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies | 13 | 18 |
| 1890 | 18 | 33 | 1890 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(5):526-532 Kooy RF; Reyniers E; Verhoye M; Sijbers J; Bakker CE; et al. Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging | 9 | 21 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1891 | 21 | 34 | 1891 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(7):771-777 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Brondum-Nielsen K; et al. Analysis of FMR1 (CGG)(n) alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia | 3 | 5 |
| 1892 | 0 | 28 | 1892 1999 EXPERIMENTAL CELL RESEARCH 251(2):388-400 Yano H; Wang BE; Ahmad I; Zhang JZ; Abo T; et al. Identification of (CAG)(n) and (CGG)(n) repeat-binding proteins, CAGERs expressed in mature neurons of the mouse brain | 0 | 5 |
| 1893 | 0 | 0 | 1893 1999 FASEB JOURNAL 13(5):A703-A703 Greenough WT; Weiler IJ; Angenstein F; Klintsova A; Bauchwitz R Synthesis of the fragile X mental retardation protein at synapses: Possible role in synaptic development and plasticity | 0 | 0 |
| 1894 | 13 | 21 | 1894 1999 GENETIC TESTING 3(3):301-304 Melis MA; Addis M; Lepiani C; Congeddu E; Cossu P; et al. A strategy for fragile-X carrier screening | 0 | 2 |
| 1895 | 3 | 8 | 1895 1999 GENETICS AND MOLECULAR BIOLOGY 22(2):169-172 Pena SDJ; Sturzeneker R Diagnosis of the fragile X syndrome in males using methylation-specific PCR of the FMR1 locus | 0 | 2 |
| 1896 | 6 | 14 | 1896 1999 GENETICS AND MOLECULAR BIOLOGY 22(4):471-474 Vianna-Morgante AM; Costa SS; Pavanello RDM; Otto PA; Mingroni-Netto RC Premature ovarian failure (POF) in Brazilian fragile X carriers | 1 | 4 |
| 1897 | 6 | 10 | 1897 1999 HEREDITAS 130(2):189-190 Sucharov CC; Silva R; Rondinelli E; Moura-Neto RS Fragile X trinucleotide repeats from a normal population in Rio de Janeiro, Brazil | 0 | 1 |
| 1898 | 37 | 57 | 1898 1999 HUMAN BIOLOGY 71(1):55-68 Arrieta I; Gil A; Nunez T; Telez M; Martinez B; et al. Stability of the FMRI CGG repeat in a Basque sample | 4 | 5 |
| 1899 | 20 | 50 | 1899 1999 HUMAN MOLECULAR GENETICS 8(5):863-869 Tamanini F; Bontekoe C; Bakker CE; van Unen L; Anar B; et al. Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations | 30 | 39 |
| 1900 | 27 | 67 | 1900 1999 HUMAN MOLECULAR GENETICS 8(12):2293-2302 Burman RW; Popovich BW; Jacky PB; Turker MS Fully expanded FMR1 CGG repeats exhibit a length-and differentiation-dependent instability in cell hybrids that is independent of DNA methylation | 9 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1901 | 19 | 39 | 1901 1999 HUMAN MOLECULAR GENETICS 8(13):2557-2566 Bardoni B; Schenck A; Mandel JL A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein | 34 | 47 |
| 1902 | 16 | 32 | 1902 1999 HUMAN MUTATION 14(1):71-79 Panagopoulos I; Lassen C; Kristoffersson U; Aman P A methylation PCR approach for detection of fragile X syndrome | 3 | 4 |
| 1903 | 0 | 0 | 1903 1999 HUMAN REPRODUCTION 14:235-235 Sermon K; Seneca S; Lissens W; De Vos A; Vandervorst M; et al. Preimplantation genetic diagnosis for fragile-X syndrome | 0 | 0 |
| 1904 | 0 | 0 | 1904 1999 HUMAN REPRODUCTION 14:354-355 Gersak K; Kregar-Velikonja N; Meden-Vrtovec H; Peterlin B Fragile X premutation screening in women with premature menopause | 1 | 1 |
| 1905 | 9 | 29 | 1905 1999 INTERNATIONAL JOURNAL OF BEHAVIORAL DEVELOPMENT 23(2):519-531 Burack JA; Shulman C; Katzir E; Schaap T; Brennan JM; et al. Cognitive and behavioural development of Israeli males with fragile X and Down Syndrome | 1 | 1 |
| 1906 | 63 | 96 | 1906 1999 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 3(6):639-645 Pimentel MMG Fragile X syndrome | 0 | 5 |
| 1907 | 11 | 41 | 1907 1999 JOURNAL OF BIOLOGICAL CHEMISTRY 274(18):12797-12802 Fry M; Loeb LA Human Werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)(n) | 11 | 104 |
| 1908 | 7 | 18 | 1908 1999 JOURNAL OF CHILD NEUROLOGY 14(2):108-112 Singh R; Sutherland GR; Manson J Partial seizures with focal epileptogenic electroencephalographic patterns in three related female patients with fragile-X syndrome | 1 | 1 |
| 1909 | 1 | 45 | 1909 1999 JOURNAL OF EARLY INTERVENTION 22(2):137-151 Jackson SC; Roberts JE Family and professional congruence in communication assessments of preschool boys with fragile X syndrome | 0 | 0 |
| 1910 | 8 | 10 | 1910 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:47-53 Carmichael B; Pembrey M; Turner G; Barnicoat A Diagnosis of fragile-X syndrome: the experiences of parents | 9 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1911 | 19 | 34 | 1911 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:314-324 York A; von Fraunhofer N; Turk J; Sedgwick P Fragile-X syndrome, Down's syndrome and autism: awareness and knowledge amongst special educators | 2 | 4 |
| 1912 | 11 | 42 | 1912 1999 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 43:466-474 Garner C; Callias M; Turk J Executive function and theory of mind performance of boys with fragile-X syndrome | 3 | 4 |
| 1913 | 0 | 0 | 1913 1999 JOURNAL OF MEDICAL GENETICS 36:S64-S64 Lazarau L; Warburton SA; Roberts CE; Hughes HE; Bartlett S; et al. Fragile X syndrome carrier females with full mutations inherited from a normal transmitting male | 0 | 0 |
| 1914 | 0 | 0 | 1914 1999 JOURNAL OF MEDICAL GENETICS 36:S65-S65 Chotai K; Payne SJ A fragile-X male mosaic for normal, premutation and full mutation FMR-1 alleles | 0 | 0 |
| 1915 | 10 | 21 | 1915 1999 JOURNAL OF MEDICAL GENETICS 36(2):167-170 de Vries BBA; van den Boer-van den Berg HMA; Niermeijer MF; Tibben A Dilemmas in Counselling females with the fragile X syndrome | 0 | 1 |
| 1916 | 2 | 5 | 1916 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-171 Macpherson J; Murray A; Webb J; Jacobs P Fragile X syndrome: of POF and premutations | 1 | 2 |
| 1917 | 0 | 0 | 1917 1999 JOURNAL OF MEDICAL GENETICS 36(2):171-172 De Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF Fragile X syndrome: of POF and premutations | 0 | 0 |
| 1918 | 12 | 18 | 1918 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; et al. Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 9 |
| 1919 | 16 | 22 | 1919 1999 JOURNAL OF MEDICAL GENETICS 36(6):467-470 de Vries BBA; Mohkamsing S; van den Ouweland AMW; Mol E; Gelsema K; et al. Screening for the fragile X syndrome among the mentally retarded: a clinical study | 4 | 12 |
| 1920 | 5 | 6 | 1920 1999 JOURNAL OF MEDICAL GENETICS 36(7):565-566 Moore SJ; Strain L; Cole GF; Miedzybrodzka Z; Kelly KF; et al. Fragile X syndrome with FMR1 and FMR2 deletion | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1921 | 18 | 28 | 1921 1999 JOURNAL OF MEDICAL SCREENING 6(2):70-76 Wildhagen MF; van Os TAM; Polder JJ; ten Kate LP; Habbema JDF Efficacy of cascade testing for fragile X syndrome | 3 | 5 |
| 1922 | 20 | 43 | 1922 1999 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 38(10):1294-1301 Murphy DGM; Mentis MJ; Pietrini P; Grady CL; Moore CJ; et al. Premutation female carriers of fragile X syndrome: A pilot study on brain anatomy and metabolism | 8 | 9 |
| 1923 | 4 | 4 | 1923 1999 LANCET 353(9159):1153-1154 Hong CJ; Song HL; Lai HC; Tsai SJ; Hsiao KJ Methanol/acetone treatment helps the amplification of FMR1 CGG repeat fragment in dried blood spots from Guthrie cards | 1 | 5 |
| 1924 | 4 | 5 | 1924 1999 MEDICAL JOURNAL OF AUSTRALIA 170(12):624-624 Cohen J; Loesch DZ Fragile X syndrome: do professionals know about it? | 0 | 0 |
| 1925 | 7 | 113 | 1925 1999 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 5(4):305-313 Hagerman RJ Psychopharmacological interventions in fragile X syndrome, fetal alcohol syndrome, Prader-Willi syndrome, Angelman syndrome, Smith-Magenis syndrome, and velocardiofacial syndrome | 0 | 2 |
| 1926 | 24 | 74 | 1926 1999 MOLECULAR AND CELLULAR BIOLOGY 19(8):5675-5684 White PJ; Borts RH; Hirst MC Stability of the human fragile X (CGG)(n) triplet repeat array in Saccharomyces cerevisiae deficient in aspects of DNA metabolism | 12 | 45 |
| 1927 | 17 | 46 | 1927 1999 MOLECULAR AND CELLULAR BIOLOGY 19(12):7925-7932 Ceman S; Brown V; Warren ST Isolation of an FMRP-associated messenger ribonucleoprotein particle and identification of nucleolin and the fragile X-related proteins as components of the complex | 50 | 76 |
| 1928 | 0 | 0 | 1928 1999 MOLECULAR PSYCHIATRY 4:S56-S56 Fisch GS; Carpenter N; Holden JA; Pandya A; Howard-Peebles PN; et al. Psychopathology in genetic disorders producing cognitive deficits: Adaptive and maladative behavior in the fragile X syndrome, Williams syndrome and neurofibromatosis type 1. | 0 | 0 |
| 1929 | 6 | 30 | 1929 1999 NATURE GENETICS 22(1):98-101 Coffee B; Zhang FP; Warren ST; Reines D Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells | 27 | 102 |
| 1930 | 1 | 1 | 1930 1999 NATURE GENETICS 22(2):209-209 Coffee B Acetylated histones are associated with FMR1 in normal but not fragile X-syndrome cells (vol 22, pg 98, 1999) | 2 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1931 | 19 | 53 | 1931 1999 NEUROSCIENCE 94(1):185-192 Paradee W; Melikian HE; Rasmussen DL; Kenneson A; Conn PJ; et al. Fragile X mouse: Strain effects of knockout phenotype and evidence suggesting deficient amygdala function | 23 | 42 |
| 1932 | 14 | 23 | 1932 1999 PRENATAL DIAGNOSIS 19(13):1223-1230 Sermon K; Seneca S; Vanderfaeillie A; Lissens W; Joris H; et al. Preimplantation diagnosis for fragile X syndrome based on the detection of the non-expanded paternal and maternal CGG | 2 | 26 |
| 1933 | 15 | 43 | 1933 1999 RNA-A PUBLICATION OF THE RNA SOCIETY 5(9):1248-1258 Adinolfi S; Bagni C; Musco G; Gibson T; Mazzarella L; et al. Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains | 22 | 29 |
| 1934 | 10 | 20 | 1934 1999 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 27(3):175-181 Sarimski K Play and communicative behaviour in young boys with fragile-X syndrome. | 0 | 1 |
| 1935 | 22 | 40 | 1935 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(1):6-15 Tassone F; Hagerman RJ; Taylor AK; Gane LW; Godfrey TE; et al. Elevated levels of FMR1 mRNA in carrier males: A new mechanism of involvement in the fragile-X syndrome | 62 | 96 |
| 1936 | 9 | 28 | 1936 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):413-418 Hundscheid RDL; Sistermans EA; Thomas CMG; Braat DDM; Straatman H; et al. Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations | 15 | 31 |
| 1937 | 32 | 52 | 1937 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):480-493 Crawford DC; Schwartz CE; Meadows KL; Newman JL; Taft LF; et al. Survey of the fragile X syndrome CGG repeat and the short-tendem-repeat and single-nucleotide-polymorphism haplotypes in an African American population | 9 | 18 |
| 1938 | 8 | 8 | 1938 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):11-13 Sherman SL Premature ovarian failure among fragile X premutation carriers: Parent-of-origin effect? | 4 | 8 |
| 1939 | 2 | 4 | 1939 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):253-254 Murray A; Ennis S; Morton N No evidence for parent of origin influencing premature ovarian failure in fragile X premutation carriers | 9 | 17 |
| 1940 | 6 | 8 | 1940 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):254-255 Vianna-Morgante AM; Costa SS Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X | 8 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1941 | 3 | 3 | 1941 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):256-258 Hundscheid RDL; Thomas CMG; Braat DDM; Oostra BA; Smits APT Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X - Reply | 2 | 5 |
| 1942 | 0 | 0 | 1942 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Jin P; Feng Y; Brown V; Warren ST Identification of polyribosomes-associated mRNAs regulated by fragile X mental retardation protein (FMRP) using oligonucleotide microarrays. | 1 | 2 |
| 1943 | 0 | 0 | 1943 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):18-18 Brown V; Ceman S; Jin P; Jin C; Wilkinson KD; et al. Messenger RNAs associated with the fragile X mental retardation protein in mouse brain. | 1 | 1 |
| 1944 | 0 | 0 | 1944 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):25-25 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool-PCR. | 0 | 0 |
| 1945 | 0 | 0 | 1945 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):26-26 Hagerman RJ; Tassone F; Leehey M; Hills J; Wilson R; et al. Cerebellar tremor and cerebellar cortical atrophy in older males with the fragile X premutation. | 0 | 0 |
| 1946 | 0 | 0 | 1946 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P; Oostra BA Differential reactivation of the FMR1 gene in fragile X patients cell lines. | 0 | 0 |
| 1947 | 0 | 0 | 1947 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Kenneson A; Zhang F; Warren ST Fragile X premutation alleles are associated with reduced FMRP levels due to a reduction of message translatability. | 0 | 0 |
| 1948 | 0 | 0 | 1948 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):57-57 Li MM; Nelson L; Bamshad M; Ward K Fragile X mosaics in a family with multiple mildly affected individuals. | 0 | 0 |
| 1949 | 0 | 0 | 1949 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):130-130 Khalifa M; Struthers J High frequency of Klinefelter syndrome among a large population of patients referred for Fragile X syndrome testing due to undiagnosed mental retardation. | 0 | 0 |
| 1950 | 0 | 0 | 1950 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):135-135 Harris SW; Brown KE; Hills JL; Tassone F; Hagerman PJ; et al. Adaptive functioning and molecular relationships in individuals with fragile X syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1951 | 0 | 0 | 1951 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):184-184 Tassone F; Hagerman RJ; Taylor AK; Hagerman PJ Clinical and molecular correlations in individuals with a fragile X full mutation. | 0 | 0 |
| 1952 | 0 | 0 | 1952 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):200-200 Ceman SS; Kenneson A; Nelson R; Jin C; Lakkis L; et al. Development and characterization of a unique set of anti-FMRP antibodies using a novel strategy. | 0 | 0 |
| 1953 | 0 | 0 | 1953 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):236-236 Mathews DJ; Hudson R; Eichier E; Chakravarti A Sequence variation and linkage disequilibrium at the fragile X syndrome locus. | 0 | 0 |
| 1954 | 0 | 0 | 1954 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):238-238 Sullivan AK; Crawford DC; Meadows KL; Wilson B; Sherman SL Parent-child transmission of intermediate FMR1 CGG repeat alleles: Examination of factors associated with repeat instability. | 0 | 0 |
| 1955 | 0 | 0 | 1955 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):247-247 Brown NM; Friez MJ; Longshore JW; Stenzel TT Evaluation of an automated commercially available PCR kit for determination of Fragile X (FRAXA) normal, gray-zone and premutation allele sizes. | 0 | 0 |
| 1956 | 0 | 0 | 1956 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):248-248 Murphy KM; Nunes ME Comparison of child-only versus mother/child sample collection in Fragile X testing. | 0 | 0 |
| 1957 | 0 | 0 | 1957 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):254-254 Weinhaeusel A; Skarits C; Haas OA Methylation-sensitive PCR (MS-PCR) analysis of the fragile X (FRAXA) syndrome. | 0 | 0 |
| 1958 | 0 | 0 | 1958 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):348-348 Dyack S; Steele L; Koultchitski G; Yang Y; Weksberg R; et al. AGG interruptions in the CGG trinucleotide repeat tract of the FMR1 gene may contribute to stability of Fragile X premutations. | 0 | 0 |
| 1959 | 0 | 0 | 1959 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):360-360 Ramos FJ; Mila M; Ortilles M; Rife M; Tazon B; et al. Validity of the analysis of the FMRP expression in bloodsmears as a screening method for the Fragile X Syndrome. | 1 | 1 |
| 1960 | 0 | 0 | 1960 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):364-364 Chen SH; Xu B; Shoof JM; Buroker NE; Scott CR Evidence for a stepwise expansion of the CGG repeats within the FMR1 gene. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1961 | 0 | 0 | 1961 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 Nolin SL; Rousseau F; Houck GE; Gargano AD; Biancalana V; et al. FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? | 0 | 0 |
| 1962 | 0 | 0 | 1962 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 O'Donnell WT; Warren ST Investigating the cause of macroorchidism in fragile X syndrome using oligonucleotide microarrays. | 0 | 0 |
| 1963 | 0 | 0 | 1963 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Raca G; Siyanova E; Mirkin S Janus effects of premutation size CGG repeats on gene expression. | 1 | 1 |
| 1964 | 0 | 0 | 1964 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Parades WJ; Warren ST Meiotic stability of a fragile X premutation CGG trinucleotide repeat in a mouse model. | 0 | 0 |
| 1965 | 0 | 0 | 1965 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):415-415 Najmabadi H; Taghizadeh F; Teimourian SH; Karimi-Nejad R; Shafeghati Y; et al. Molecular analysis of Fragile X syndrome in Iranian population. | 0 | 0 |
| 1966 | 0 | 0 | 1966 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):428-428 Brown WT; Ding X; Idrissi AE; Scalia J; Glicksman A; et al. Fragile X transgene and embryonic lethality in mice. | 0 | 0 |
| 1967 | 27 | 42 | 1967 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(4):229-236 Lachiewicz AM; Dawson DV; Spiridigliozzi GA Physical characteristics of young boys with fragile X syndrome: Reasons for difficulties in making a diagnosis in young males | 12 | 13 |
| 1968 | 8 | 22 | 1968 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 92(5):336-342 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Carrier testing in fragile X syndrome: Effect on self-concept | 2 | 4 |
| 1969 | 24 | 33 | 1969 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 93(2):99-106 Larsen LA; Armstrong JSM; Gronskov K; Hjalgrim H; Macpherson JN; et al. Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: Implications for multiple mutational pathways towards fragile X alleles | 4 | 6 |
| 1970 | 27 | 35 | 1970 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(3):232-236 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; et al. Fragile X males with unmethylated, full mutation trinucleotide repeat expansions have elevated levels of FMR1 messenger RNA | 20 | 26 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1971 | 3 | 24 | 1971 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 94(5):345-360 Fryns JP; Borghgraef M; Brown TW; Chelly J; Fisch GS; et al. 9th international workshop on fragile X syndrome and X-linked mental retardation | 0 | 3 |
| 1972 | 10 | 14 | 1972 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):105-107 Tuncbilek E; Alikasifoglu M; Aktas D; Duman F; Yanik H; et al. Screening for the fragile X syndrome among mentally retarded males by hair root analysis | 6 | 6 |
| 1973 | 16 | 33 | 1973 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):123-129 Hjalgrim H; Hansen BF; Brondum-Nielsen K; Nolting D; Kjaer I Aspects of skeletal development in fragile X syndrome fetuses | 2 | 4 |
| 1974 | 30 | 59 | 1974 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):150-156 Backes M; Genc B; Schreck J; Doerfler W; Lehmkuhl G; et al. Cognitive and behavioral profile of fragile X boys: Correlations to molecular data | 8 | 12 |
| 1975 | 12 | 46 | 1975 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):307-315 Gould EL; Loesch DZ; Martin MJ; Hagerman RJ; Armstrong SM; et al. Melatonin profiles and sleep characteristics in boys with fragile X syndrome: A preliminary study | 13 | 19 |
| 1976 | 3 | 11 | 1976 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(4):358-360 Missirian C; Moncla A; Voelckel MA; Ravix V; Philip N Fragile X syndrome and 22q11.2 microdeletion in the same sibship | 0 | 0 |
| 1977 | 4 | 9 | 1977 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(5):516-517 Limprasert P; Jaruratanasirikul S; Vasiknanonte P Unilateral macroorchidism in fragile X syndrome | 2 | 2 |
| 1978 | 76 | 116 | 1978 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(2):153-163 Bardoni B; Mandel JL; Fisch GS FMR1 gene and fragile X syndrome | 12 | 21 |
| 1979 | 33 | 48 | 1979 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):183-188 Willemsen R; Oostra BA FMRP detection assay for the diagnosis of the fragile X syndrome | 2 | 4 |
| 1980 | 22 | 33 | 1980 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):189-194 Sherman SL Premature ovarian failure in the fragile X syndrome | 15 | 30 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1981 | 28 | 40 | 1981 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(3):195-203 Tassone F; Hagerman RJ; Chamberlain WD; Hagerman PJ Transcription of the FMR1 gene in individuals with fragile X syndrome | 29 | 34 |
| 1982 | 14 | 37 | 1982 2000 AMERICAN JOURNAL ON MENTAL RETARDATION 105(4):286-299 Kau ASM; Reider EE; Payne L; Meyer WA; Freund L Early behavior signs of psychiatric phenotypes in fragile X syndrome | 2 | 4 |
| 1983 | 22 | 37 | 1983 2000 ANNALES DE GENETIQUE 43(1):29-34 Gonzalez-del Angel A; Vidal S; Saldana Y; del Castillo V; Alcantara MA; et al. Molecular diagnosis of the fragile X and FRAXE syndromes in patients with mental retardation of unknown cause in Mexico | 2 | 4 |
| 1984 | 5 | 19 | 1984 2000 ANNALS OF SAUDI MEDICINE 20(1):16-19 Al Husain M; Salih MAM; Zaki OK; Al Othman L; Al Nasser MN A clinical study of mentally retarded children with fragile X syndrome in Saudi Arabia | 0 | 0 |
| 1985 | 21 | 41 | 1985 2000 ANNALS OF SAUDI MEDICINE 20(3-4):214-217 Iqbal MA; Sakati N; Nester M; Ozand P Cytogenetic diagnosis of fragile X syndrome: Study of 305 suspected cases in Saudi Arabia | 0 | 0 |
| 1986 | 5 | 8 | 1986 2000 AUSTRALIAN AND NEW ZEALAND JOURNAL OF MEDICINE 30(1):86-88 Driscoll G; Clark J; Elakis G; Turner G Early menopause in a family carrying a fragile X premutation | 1 | 3 |
| 1987 | 2 | 29 | 1987 2000 BEHAVIOR RESEARCH METHODS INSTRUMENTS & COMPUTERS 32(1):5-10 Boccia ML; Roberts JE Behavior and autonomic nervous system function assessed via heart period measures: The case of hyperarousal in boys with fragile X syndrome | 8 | 11 |
| 1988 | 9 | 19 | 1988 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(2):608-610 Beaulieu MA A distinct FMRP polysomal population at an advanced stage of mammalian erythropoiesis | 2 | 2 |
| 1989 | 11 | 33 | 1989 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 275(3):973-980 Sung YJ; Conti J; Currie JR; Brown WT; Denman RB RNAs that interact with the Fragile X syndrome RNA binding protein FMRP | 27 | 35 |
| 1990 | 4 | 46 | 1990 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 278(3):833-838 Patel PK; Bhavesh NS; Hosur RV Cation-dependent conformational switches in d-TGGCGGC containing two triplet repeats of Fragile X Syndrome: NMR observations | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1991 | 11 | 38 | 1991 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 279(3):904-908 Ceman S; Nelson R; Warren ST Identification of mouse YB1/p50 as a component of the FMRP-associated mRNP particle | 21 | 29 |
| 1992 | 11 | 52 | 1992 2000 BRAIN AND COGNITION 44(3):387-401 Munir F; Cornish KM; Wilding J Nature of the working memory deficit in Fragile-X syndrome | 8 | 9 |
| 1993 | 11 | 14 | 1993 2000 BRITISH JOURNAL OF OBSTETRICS AND GYNAECOLOGY 107(8):969-972 Kallinen J; Korhonen K; Kortelainen S; Heinonen S; Ryynanen M Pregnancy outcome in carriers of fragile X | 0 | 0 |
| 1994 | 11 | 59 | 1994 2000 CELL 100(3):323-332 Lewis HA; Musunuru K; Jensen KB; Edo C; Chen H; et al. Sequence-specific RNA binding by a Nova KH domain: Implications for paraneoplastic disease and the fragile X syndrome | 9 | 97 |
| 1995 | 24 | 79 | 1995 2000 CEREBRAL CORTEX 10(10):1038-1044 Irwin SA; Galvez R; Greenough WT Dendritic spine structural anomalies in fragile-X mental retardation syndrome | 35 | 55 |
| 1996 | 23 | 38 | 1996 2000 CEREBRAL CORTEX 10(10):1045-1052 Braun K; Segal M FMRP involvement in formation of synapses among cultured hippocampal neurons | 21 | 23 |
| 1997 | 4 | 18 | 1997 2000 CHINESE SCIENCE BULLETIN 45(6):516-520 Chen YT; Bardoni B; Yu M; Zhu N; Wu GY; et al. Fragile X mental retardation protein interacts with TDG | 0 | 0 |
| 1998 | 0 | 0 | 1998 2000 CLINICAL CHEMISTRY 46(6):A206-A206 Boday A; Prusa R; Matoska V Radioactive PCR for the screening and diagnostics of fragile X chromosome syndrome - FRAXA. | 0 | 0 |
| 1999 | 7 | 12 | 1999 2000 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 38(9):935-938 Poon PMK; Zhao Z; Wu XQ; Ni YX; Pang CP Rapid analysis of CGG repeat length in the FMR1 gene | 0 | 0 |
| 2000 | 6 | 13 | 2000 2000 CLINICAL GENETICS 57(6):456-458 Lisik M The comparison of anthropometric variables in mentally retarded boys with and without fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2001 | 24 | 33 | 2001 2000 CLINICAL GENETICS 58(2):111-115 Kallinen J; Heinonen S; Mannermaa A; Ryynanen M Prenatal diagnosis of fragile X syndrome and the risk of expansion of a premutation | 3 | 5 |
| 2002 | 3 | 13 | 2002 2000 CLINICAL RHEUMATOLOGY 19(4):262-264 Granel B; Ravix V; Pedeillier K; Serratrice J; Disdier P; et al. A first molecular approach towards CGG repeat expansion in FMR1 gene in systemic lupus erythematosus and in Sjogren's syndrome: A preliminary report | 0 | 0 |
| 2003 | 1 | 6 | 2003 2000 CYTOGENETICS AND CELL GENETICS 89(1-2):11-13 Bardoni B; Giglio S; Schenck A; Rocchi M; Mandel JL Assignment of NUFIP1 (Nuclear FMRP Interacting Protein 1) gene to chromosome 13q14 and assignment of a pseudogene to chromosome 6q12 | 2 | 2 |
| 2004 | 23 | 46 | 2004 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome | 1 | 2 |
| 2005 | 0 | 43 | 2005 2000 EMBO JOURNAL 19(17):4745-4758 Yaremchuk A; Cusack S; Tukalo M Crystal structure of a eukaryote/archaeon-like prolyl-tRNA synthetase and its complex with tRNA(Pro)(CGG) | 0 | 31 |
| 2006 | 20 | 32 | 2006 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; et al. Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 26 | 35 |
| 2007 | 9 | 21 | 2007 2000 EUROPEAN JOURNAL OF HUMAN GENETICS 8(4):247-252 Murray A; Ennis S; MacSwiney F; Webb J; Morton NE Reproductive and menstrual history of females with fragile X expansions | 11 | 15 |
| 2008 | 0 | 0 | 2008 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:104-104 Braun K; Segal M FMRP involvement in the formation of functional synaptic connections among cultured hippocampal neurons | 0 | 0 |
| 2009 | 0 | 0 | 2009 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:305-305 Beckel-Mitchener AC; Weiler IJ; Klintsova AY; Harms L; Belt B; et al. Analysis of protein synthesis in Fragile X knockout mice | 0 | 0 |
| 2010 | 0 | 18 | 2010 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12(1):381-384 Miller WJ; Skinner JA; Foss GS; Davies KE Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain | 0 | 7 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2011 | 24 | 40 | 2011 2000 EXPERIMENTAL CELL RESEARCH 258(1):162-170 Bakker CE; Otero YD; Bontekoe C; Raghoe P; Luteijn T; et al. Immunocytochemical and biochemical characterization of FMRP, FXR1P, and FXR2P in the mouse | 22 | 31 |
| 2012 | 0 | 0 | 2012 2000 GENETIC COUNSELING 11(3):281-311 [Anon] ACTS: Of the 9th International Workshop on Fragile X Syndrome and X Linked Mental Retardation August 23-25, 1999, Le Bischenberg, Strasbourg, France - Abstracts | 0 | 0 |
| 2013 | 11 | 16 | 2013 2000 GENETIC TESTING 4(3):235-239 Tzountzouris J; Kennedy D; Skuterud M; Connolly-Wilson M; Holden JJA; et al. Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome | 0 | 1 |
| 2014 | 6 | 10 | 2014 2000 GENETIC TESTING 4(3):241-242 Brown WT; Nolin SL Apparent FMR1 allele instability in non-Fragile X males - Invited commentary | 0 | 1 |
| 2015 | 17 | 20 | 2015 2000 GENETIC TESTING 4(3):289-292 Geva E; Yaron Y; Shomrat R; Ben-Yehuda A; Zabari S; et al. The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families | 3 | 4 |
| 2016 | 31 | 44 | 2016 2000 GENETICS IN MEDICINE 2(4):242-248 Burman RW; Anoe KS; Popovich BW Fragile X full mutations ave more similar in siblings than in unrelated patients: further evidence for a familial factor in CGG repeat dynamics | 1 | 2 |
| 2017 | 11 | 12 | 2017 2000 HUMAN GENETICS 106(3):366-369 Arocena DG; de Diego Y; Oostra BA; Willemsen R; Rodriguez MM A fragile X case with an amplification/deletion mosaic pattern | 0 | 0 |
| 2018 | 3 | 6 | 2018 2000 HUMAN GENETICS 107(2):195-196 Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; et al. Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles | 1 | 3 |
| 2019 | 14 | 62 | 2019 2000 HUMAN MOLECULAR GENETICS 9(1):93-100 Balakumaran BS; Freudenreich CH; Zakian VA CGG/CCG repeats exhibit orientation-dependent instability and orientation-independent fragility in Saccharomyces cerevisiae | 0 | 20 |
| 2020 | 53 | 82 | 2020 2000 HUMAN MOLECULAR GENETICS 9(6):901-908 Jin P; Warren ST Understanding the molecular basis of fragile X syndrome | 44 | 82 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2021 | 26 | 55 | 2021 2000 HUMAN MOLECULAR GENETICS 9(10):1487-1493 Tamanini F; Kirkpatrick LL; Schonkeren J; van Unen L; Bontekoe C; et al. The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins | 9 | 14 |
| 2022 | 42 | 62 | 2022 2000 HUMAN MOLECULAR GENETICS 9(12):1759-1769 Crawford DC; Zhang FP; Wilson B; Warren ST; Sherman SL Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability | 7 | 11 |
| 2023 | 35 | 55 | 2023 2000 HUMAN MOLECULAR GENETICS 9(19):2909-2918 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR | 3 | 11 |
| 2024 | 0 | 0 | 2024 2000 HUMAN REPRODUCTION 15:12-12 Apessos A; Harper J; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 0 | 0 |
| 2025 | 0 | 0 | 2025 2000 HUMAN REPRODUCTION 15:47-48 Hundscheid RDL; Sistermans EA; Thomas CMG; Straatman H; Kiemeney LALM; et al. Shorter reproductive life and a high risk for premature ovarian failure (POF) in women who have inherited fragile X premutations from their fathers | 0 | 0 |
| 2026 | 17 | 41 | 2026 2000 HUMAN REPRODUCTION 15(1):197-202 Marozzi A; Vegetti W; Manfredini E; Tibiletti MG; Testa G; et al. Association between idiopathic premature ovarian failure and fragile X premutation | 10 | 30 |
| 2027 | 1 | 2 | 2027 2000 HUMAN REPRODUCTION 15(8):1874-1874 Rychlik DF Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| 2028 | 1 | 2 | 2028 2000 HUMAN REPRODUCTION 15(8):1874-1875 Marozzi A Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 1 | 1 |
| 2029 | 0 | 0 | 2029 2000 INFANT MENTAL HEALTH JOURNAL 21(4-5):243-243 Lis A; Zennaro A; Pinto M; Peroni S; Snaidero R Paternal styles identified with the self reflective scale and the CGG | 0 | 0 |
| 2030 | 0 | 0 | 2030 2000 INFANT MENTAL HEALTH JOURNAL 21(4-5):330-330 Ghuman JK; Tierney E; Kau A; Reider E Social interaction problems in infants and preschool children with fragile-X syndrome, Smith-Lemli-Opitz syndrome and other developmental disorders | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2031 | 10 | 41 | 2031 2000 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 30(1):49-59 Bailey DB; Hatton DD; Mesibov G; Ament N; Skinner M Early development, temperament, and functional impairment in autism and fragile X syndrome | 16 | 19 |
| 2032 | 20 | 50 | 2032 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(3):2231-2238 Weisman-Shomer P; Naot Y; Fry M Tetrahelical forms of the fragile X syndrome expanded sequence d(CGG)(n) are destabilized by two heterogeneous nuclear ribonucleoprotein-related telomeric DNA-binding proteins | 7 | 10 |
| 2033 | 9 | 29 | 2033 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(9):6447-6452 Muller-Hartmann H; Deissler H; Naumann F; Schmitz B; Schroer J; et al. The human 20-kDa 5 '-(CGG)(n)-3 '-binding protein is targeted to the nucleus and affects the activity of the FMR1 promoter | 11 | 16 |
| 2034 | 27 | 59 | 2034 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(42):33134-33141 Uliel L; Weisman-Shomer P; Oren-Jazans H; Newcomb T; Loeb LA; et al. Human Ku antigen tightly binds and stabilizes a tetrahelical form of the fragile X syndrome d(CGG)(n) expanded sequence | 1 | 7 |
| 2035 | 0 | 0 | 2035 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :57-57 Merin NM; Menon V; White CD; Glover GH; Reiss AL Gaze processing deficits in fragile X syndrome investigated using fMRI | 0 | 0 |
| 2036 | 0 | 0 | 2036 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :98-98 White CD; Menon V; Eliez S; Reiss AL An fMRI study of brain activation in Fragile X Syndrome during a go-nogo task | 0 | 0 |
| 2037 | 0 | 0 | 2037 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :146-146 Kwon H; Menon V; Eliez S; Dyer-Friedman J; Glover GH; et al. Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavior and FMR-1 protein expression | 0 | 0 |
| 2038 | 13 | 39 | 2038 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(4):278-282 Wisbeck JM; Huffman LC; Freund L; Gunnar MR; Davis EP; et al. Cortisol and social stressors in children with fragile X: A pilot study | 9 | 11 |
| 2039 | 6 | 32 | 2039 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(5):315-321 Bailey DB; Skinner D; Hatton D; Roberts J Family experiences and factors associated with the diagnosis of fragile X syndrome | 12 | 15 |
| 2040 | 8 | 16 | 2040 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85 Sabaratnam M Pathological and neuropathological findings in two males with fragile-X syndrome | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2041 | 0 | 0 | 2041 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:189-189 Abbeduto L; Kesin E; Pavetto M; Weissman M; O'Brien A; et al. Theory of mind deficits in mental retardation: a comparison of Down syndrome and fragile-X syndrome | 0 | 0 |
| 2042 | 0 | 0 | 2042 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:222-222 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al. Progress fragile-X syndrome analysis | 0 | 0 |
| 2043 | 0 | 0 | 2043 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:247-247 Cornish KM; Munir F Profile of memory and attention problems in adults with fragile-X syndrome: Clinical and educational implications | 0 | 0 |
| 2044 | 0 | 0 | 2044 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:273-273 Einfeld SL; Tonge B; Turner G; Parmenter T; Smith A Longitudinal course of behavioural and emotional problems of young persons with Prader-Willi, fragile-X, Williams and Down syndromes | 0 | 0 |
| 2045 | 0 | 0 | 2045 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:305-305 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; et al. Influence of stimulants on electrodermal studies in fragile-X syndrome | 0 | 0 |
| 2046 | 0 | 0 | 2046 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:317-317 Karrer JH; Hagerman RJ; Karrer RS; Fitzpatrick D; Vavold J; et al. Genotypic-specific event-related brain potentials among infants and toddlers with fragile-X syndrome and Down syndrome | 1 | 1 |
| 2047 | 0 | 0 | 2047 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:318-318 Hills JL; Wilson R; Sobesky W; Harris SW; Grigsby J; et al. Executive functioning deficits in adult males with the fragile-X premutation: an emerging phenotype | 0 | 0 |
| 2048 | 0 | 0 | 2048 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:374-374 Lung FW; Shu BC Fragile-X syndrome in adolescent prostitutes | 0 | 0 |
| 2049 | 0 | 0 | 2049 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:380-380 Manjunatha KR; Chettn GK; Arathi R; Bhaskar RG; Nandini PM; et al. Fragile-X syndrome: Cytogenetics and molecular analysis of subjects from Indian population | 0 | 0 |
| 2050 | 0 | 0 | 2050 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:405-405 Munir F; Comish KM; Wilding J A neuropsychological profile of attention and hyperactivity in boys with fragile-X syndrome: Implications for clinical intervention | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2051 | 0 | 0 | 2051 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:419-419 Orsmond G; Abbeduto L; Pavetto M; O'Brien A; Kesin E; et al. Stress and coping in parents of adolescents and young adults with fragile-X syndrome or Down syndrome | 0 | 0 |
| 2052 | 0 | 0 | 2052 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:449-449 Sabaratnam M; Murthy V; Wijeratne A Fragile-X syndrome: A 10-year follow-up | 0 | 0 |
| 2053 | 0 | 0 | 2053 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:483-483 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; et al. FMRI messenger RNA levels in male subjects with fragile-X syndrome | 0 | 0 |
| 2054 | 0 | 0 | 2054 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:496-497 Tzeng CC; Lin SJ; Chen YY; Chen RM An effective strategy of using a molecular test to screen individuals with mental retardation for fragile-X syndrome | 0 | 0 |
| 2055 | 0 | 0 | 2055 2000 JOURNAL OF INVESTIGATIVE MEDICINE 48(1):11A-11A Peterson TL; Hagerman RJ; Tassone F Genotype-phenotype relationships in fragile X families. | 0 | 0 |
| 2056 | 0 | 0 | 2056 2000 JOURNAL OF MEDICAL GENETICS 37:S18-S18 Mandel JL The fragile X syndrome: from families to CGG expansions and FMR1 gene function | 0 | 0 |
| 2057 | 0 | 0 | 2057 2000 JOURNAL OF MEDICAL GENETICS 37:S20-S20 Fisher A; Macpherson JN; Dennis NR; Barber JCK Targeted testing for fragile X: an audit of the first year. | 0 | 0 |
| 2058 | 0 | 0 | 2058 2000 JOURNAL OF MEDICAL GENETICS 37:S44-S44 James T; Trigg A; Lindley VH; Fews GA; Roberts E; et al. An unexpected finding of fragile X (FRAXA) syndrome in a fetal blood sample referred for abnormalities on ultrasound scan | 0 | 0 |
| 2059 | 0 | 0 | 2059 2000 JOURNAL OF MEDICAL GENETICS 37:S66-S66 Lazarou LP; Myring J; Knight SJL; Gardner AP; Clarke A Fragile X (E) syndrome. How common is it? | 0 | 0 |
| 2060 | 0 | 0 | 2060 2000 JOURNAL OF MEDICAL GENETICS 37:S75-S75 Fratter C; Morsman A; Seller A Genetic analysis for Fragile X syndrome by fluorescent PCR | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2061 | 0 | 0 | 2061 2000 JOURNAL OF MEDICAL GENETICS 37:S78-S78 Chotai K; Buckingham AE; Bentley CM; Wycherley RJ; Payne SJ Fragile-X intermediate alleles - A clinical dilemma | 0 | 0 |
| 2062 | 21 | 36 | 2062 2000 JOURNAL OF MEDICAL GENETICS 37(1):77-79 Beresford RG; Tatlidil C; Riddell DC; Welch JP; Ludman MD; et al. Absence of fragile X syndrome in Nova Scotia | 4 | 5 |
| 2063 | 12 | 16 | 2063 2000 JOURNAL OF MEDICAL GENETICS 37(8):603-604 Willemsen R; Olmer R; Otero YD; Oostra BA Twin sisters, monozygotic with the fragile X mutation, but with a different phenotype | 8 | 8 |
| 2064 | 39 | 66 | 2064 2000 JOURNAL OF MEDICAL GENETICS 37(11):842-850 Salat U; Bardoni B; Wohrle D; Steinbach P Increase of FMRP expression, raised levels of FMR1 mRNA, and clonal selection in proliferating cells with unmethylated fragile X repeat expansions: a clue to the sex bias in the transmission of full mutations? | 4 | 6 |
| 2065 | 5 | 6 | 2065 2000 JOURNAL OF MOLECULAR DIAGNOSTICS 2(3):128-131 Daly TM; Rafii A; Martin RA; Zehnbauer BA Novel polymorphism in the FMR1 gene resulting in a "pseudodeletion" of FMR1 in a commonly used fragile X assay | 0 | 0 |
| 2066 | 4 | 15 | 2066 2000 JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT 18(3):255-267 Hooper SR; Hatton DD; Baranek GT; Roberts JP; Bailey DB Nonverbal assessment of IQ, attention, and memory abilities in children with fragile-X syndrome using the Leiter-R | 1 | 1 |
| 2067 | 3 | 5 | 2067 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(2):264-266 Eliez S; Reiss AL Generics of childhood disorders: XI. Fragile X syndrome | 0 | 0 |
| 2068 | 1 | 5 | 2068 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-398 Levitas A Fragile X syndrome | 0 | 0 |
| 2069 | 0 | 5 | 2069 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-399 Lombroso PJ Fragile X syndrome - Dr. Lombroso replies | 0 | 0 |
| 2070 | 11 | 17 | 2070 2000 JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION 99(5):402-407 Wang YC; Li C; Lin ML; Lin WH; Li SY Molecular diagnosis of fragile X syndrome and distribution of CGG repeats in the FMR-1 gene in Taiwanese | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2071 | 0 | 1 | 2071 2000 LIBRARY JOURNAL 125(11):105-105 Griffin KH Children with Fragile X Syndrome: A parents' guide. | 0 | 0 |
| 2072 | 22 | 29 | 2072 2000 MENTAL RETARDATION 38(3):207-215 Maes B; Fryns JP; Ghesquiere P; Borghgraef M Phenotypic checklist to screen for fragile X syndrome in people with mental retardation | 2 | 5 |
| 2073 | 60 | 117 | 2073 2000 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 6(2):96-106 Mazzocco MMM Advances in research on the fragile X syndrome | 20 | 24 |
| 2074 | 31 | 74 | 2074 2000 MOLECULAR AND CELLULAR BIOLOGY 20(22):8536-8547 Wan LL; Dockendorff TC; Jongens TA; Dreyfuss G Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein | 44 | 57 |
| 2075 | 12 | 20 | 2075 2000 MOLECULAR AND CELLULAR PROBES 14(2):115-119 Mila M; Castellvi-Bel S; Sanchez A; Barcelo A; Badenas C; et al. Rare variants in the promoter of the fragile X syndrome gene (FMR1) | 5 | 5 |
| 2076 | 8 | 32 | 2076 2000 MOLECULAR BRAIN RESEARCH 75(2):337-341 Valentine G; Chakravarty S; Sarvey J; Bramham C; Herkenham M Fragile X (fmr1) mRNA expression is differentially regulated in two adult models of activity-dependent gene expression | 7 | 9 |
| 2077 | 21 | 37 | 2077 2000 MOLECULAR BRAIN RESEARCH 80(1):17-25 Todd PK; Mack KJ Sensory stimulation increases cortical expression of the fragile X mental retardation protein in vivo | 17 | 17 |
| 2078 | 28 | 43 | 2078 2000 MOLECULAR DIAGNOSIS 5(3):169-178 Gold B; Radu D; Balanko A; Chiang CS Diagnosis of Fragile X syndrome by Southern blot hybridization using a chemiluminescent probe: A laboratory protocol | 0 | 1 |
| 2079 | 32 | 45 | 2079 2000 MOLECULAR MEDICINE TODAY 6(5):193-198 Kooy RF; Willemsen R; Oostra BA Fragile X syndrome at the turn of the century | 15 | 21 |
| 2080 | 4 | 13 | 2080 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 73(1):87-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; et al. Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation | 23 | 27 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2081 | 6 | 14 | 2081 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; et al. Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000) | 2 | 2 |
| 2082 | 13 | 47 | 2082 2000 NEUROPSYCHOLOGIA 38(9):1261-1270 Munir F; Cornish KM; Wilding J A neuropsychological profile of attention deficits in young males with fragile X syndrome | 17 | 21 |
| 2083 | 28 | 53 | 2083 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):255-263 de Vries BBA; Oostra BA The fragile X syndrome: A model for mental retardation | 0 | 0 |
| 2084 | 8 | 18 | 2084 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):265-277 Bakker CE; Kooy RF; D'Hooge R; Tamanini F; Willemsen R; et al. Introduction of a FMR1 transgene in the fragile X knockout mouse. | 3 | 3 |
| 2085 | 32 | 45 | 2085 2000 NUCLEIC ACIDS RESEARCH 28(7):1535-1541 Weisman-Shomer P; Cohen E; Fry M Interruption of the fragile X syndrome expanded sequence d(CGG)(n) by interspersed d(AGG) trinucleotides diminishes the formation and stability of d(CGG)(n) tetrahelical structures | 6 | 11 |
| 2086 | 14 | 42 | 2086 2000 NUCLEIC ACIDS RESEARCH 28(10):2141-2152 Genc B; Muller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; et al. Methylation mosaicism of 5 '-(CGG)(n)-3 ' repeats in fragile X, premutation and normal individuals | 3 | 6 |
| 2087 | 33 | 54 | 2087 2000 OPTOMETRY AND VISION SCIENCE 77(11):592-599 Block SS; Brusca-Vega R; Pizzi WJ; Berry-Kravis E; Maino DM; et al. Cognitive and visual processing skills and their relationship to mutation size in full and premutation female fragile X carriers | 0 | 0 |
| 2088 | 7 | 10 | 2088 2000 PEDIATRIC HEMATOLOGY AND ONCOLOGY 17(7):597-600 Ferrari A; Meazza C; Casanova M Nasopharyngeal carcinoma in a boy with fragile X syndrome | 0 | 0 |
| 2089 | 10 | 17 | 2089 2000 PRENATAL DIAGNOSIS 20(8):611-614 Pesso R; Berkenstadt H; Cuckle H; Gak E; Peleg L; et al. Screening for fragile X syndrome in women of reproductive age | 13 | 17 |
| 2090 | 3 | 6 | 2090 2000 PRENATAL DIAGNOSIS 20(10):854-855 Wilkin H; Tuohy J; Theewis W Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 2091 | 1 | 5 | 2091 2000 REVISTA DE NEUROLOGIA 30(10):996-997 Serrano-Castro PJ; Serrano-Castillo P A historical description of the association of macro-orchidea, mental retardation and cranial dysmorphia in males (fragile X chromosome syndrome) by A.B Richerand | 0 | 0 |
| 2092 | 1 | 10 | 2092 2000 VETERINARNI MEDICINA 45(10-11):308-310 Slota E; Danielak-Czech B; Pietraszewska J; Kozubska-Sobocinska A Preliminary identification of the fragile X in two crossbred cows | 0 | 1 |
| 2093 | 0 | 0 | 2093 2001 ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY 221:U3-U3 Rodesittisuk P; Romero RM; Haworth IS Conformation of fragile X-associated triplet repeat DNA containing C-C mismatch pairs. | 0 | 0 |
| 2094 | 29 | 40 | 2094 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(2):351-360 Toledano-Alhadef H; Basel-Vanagaite L; Magal N; Davidov B; Ehrlich S; et al. Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel | 13 | 22 |
| 2095 | 21 | 34 | 2095 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(3):504-515 Wohrle D; Salat U; Hameister H; Vogel W; Steinbach P Demethylation, reactivation, and destabilization of human fragile X full-mutation alleles in mouse embryocarcinoma cells | 4 | 10 |
| 2096 | 0 | 0 | 2096 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; et al. Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| 2097 | 0 | 0 | 2097 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):291-291 Thiele H; Peters H; Bahrke D; Hansmann I Homozygosity for a premutation of the FMR1 gene and normal phenotype in two sisters from a family with fragile X syndrome. | 0 | 0 |
| 2098 | 0 | 0 | 2098 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):352-352 Gantois I; Reyniers E; Kooy RF Identification of genes differentially expressed in the fragile X syndrome. | 0 | 0 |
| 2099 | 0 | 0 | 2099 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Naumann F; Muller-Hartmann H; Deissler H; Doerfler W Functional studies on the human 5 '-CGG-3 '-binding protein CGGBP1 (p20). | 0 | 0 |
| 2100 | 0 | 0 | 2100 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P Pharmacological reactivation of the FMR1 gene of the fragile X syndrome. | 0 | 0 |