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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by year, source, volume, issue, page.
Page 20: 1 (1) 2 (101) 3 (201) 4 (301) 5 (401) 6 (501) 7 (601) 8 (701) 9 (801) 10 (901) 11 (1001) 12 (1101) 13 (1201) 14 (1301) 15 (1401) 16 (1501) 17 (1601) 18 (1701) 19 (1801) 20 (1901) 21 (2001) 22 (2101) 23 (2201) 24 (2301)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1901 | 1 | 2 | 1901 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 |
| 1902 | 1 | 2 | 1902 2000 HUMAN REPRODUCTION 15(8):1874-1875 Marozzi A Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| 1903 | 0 | 0 | 1903 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 |
| 1904 | 10 | 41 | 1904 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 | 14 | 16 |
| 1905 | 14 | 50 | 1905 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 | 5 | 9 |
| 1906 | 20 | 59 | 1906 2000 JOURNAL OF BIOLOGICAL CHEMISTRY 275(42):33134-33141 Uliel L; Weisman-Shomer P; Oren-Jazans H; Newcomb T; Loeb LA; Fry M Human Ku antigen tightly binds and stabilizes a tetrahelical form of the fragile X syndrome d(CGG)(n) expanded sequence | 1 | 7 |
| 1907 | 0 | 0 | 1907 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 |
| 1908 | 0 | 0 | 1908 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 |
| 1909 | 0 | 0 | 1909 2000 JOURNAL OF COGNITIVE NEUROSCIENCE :146-146 Kwon H; Menon V; Eliez S; Dyer-Friedman J; Glover GH; Reiss AL Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavior and FMR-1 protein expression | 0 | 0 |
| 1910 | 13 | 39 | 1910 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(4):278-282 Wisbeck JM; Huffman LC; Freund L; Gunnar MR; Davis EP; Reiss AL Cortisol and social stressors in children with fragile X: A pilot study | 8 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1911 | 6 | 32 | 1911 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 |
| 1912 | 8 | 16 | 1912 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:81-85 Sabaratnam M Pathological and neuropathological findings in two males with fragile-X syndrome | 2 | 4 |
| 1913 | 0 | 0 | 1913 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:189-189 Abbeduto L; Kesin E; Pavetto M; Weissman M; O'Brien A; Karadottir S; Cawthon S Theory of mind deficits in mental retardation: a comparison of Down syndrome and fragile-X syndrome | 0 | 0 |
| 1914 | 0 | 0 | 1914 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:222-222 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; Li SY; Rabe A; Dumas R; Haubenstock H; Wen Y; Dobkin C; Jenkins E Progress fragile-X syndrome analysis | 0 | 0 |
| 1915 | 0 | 0 | 1915 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 |
| 1916 | 0 | 0 | 1916 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 |
| 1917 | 0 | 0 | 1917 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:305-305 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; Harris SW; Simon J; Church K; Bonnell J; Ognibene TC; McIntosh DN Influence of stimulants on electrodermal studies in fragile-X syndrome | 0 | 0 |
| 1918 | 0 | 0 | 1918 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:317-317 Karrer JH; Hagerman RJ; Karrer RS; Fitzpatrick D; Vavold J; Gora K; Chaney L Genotypic-specific event-related brain potentials among infants and toddlers with fragile-X syndrome and Down syndrome | 1 | 1 |
| 1919 | 0 | 0 | 1919 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:318-318 Hills JL; Wilson R; Sobesky W; Harris SW; Grigsby J; Butler E; Loesch D; Hagerman RJ Executive functioning deficits in adult males with the fragile-X premutation: an emerging phenotype | 0 | 0 |
| 1920 | 0 | 0 | 1920 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:374-374 Lung FW; Shu BC Fragile-X syndrome in adolescent prostitutes | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1921 | 0 | 0 | 1921 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:380-380 Manjunatha KR; Chettn GK; Arathi R; Bhaskar RG; Nandini PM; Chandra S; Bhaskaran GS; Brahmachari V Fragile-X syndrome: Cytogenetics and molecular analysis of subjects from Indian population | 0 | 0 |
| 1922 | 0 | 0 | 1922 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 |
| 1923 | 0 | 0 | 1923 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:419-419 Orsmond G; Abbeduto L; Pavetto M; O'Brien A; Kesin E; Weissman M; Karadottir S; Cawthon S Stress and coping in parents of adolescents and young adults with fragile-X syndrome or Down syndrome | 0 | 0 |
| 1924 | 0 | 0 | 1924 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 |
| 1925 | 0 | 0 | 1925 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:483-483 Tassone F; Hagerman RJ; Loesch DZ; Lachiewicz A; Taylor AK; Hagerman PJ FMRI messenger RNA levels in male subjects with fragile-X syndrome | 0 | 0 |
| 1926 | 0 | 0 | 1926 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 |
| 1927 | 0 | 0 | 1927 2000 JOURNAL OF INVESTIGATIVE MEDICINE 48(1):11A-11A Peterson TL; Hagerman RJ; Tassone F Genotype-phenotype relationships in fragile X families. | 0 | 0 |
| 1928 | 0 | 0 | 1928 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 |
| 1929 | 0 | 0 | 1929 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 |
| 1930 | 0 | 0 | 1930 2000 JOURNAL OF MEDICAL GENETICS 37:S44-S44 James T; Trigg A; Lindley VH; Fews GA; Roberts E; McKeown C; Davison EV An unexpected finding of fragile X (FRAXA) syndrome in a fetal blood sample referred for abnormalities on ultrasound scan | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1931 | 0 | 0 | 1931 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 |
| 1932 | 0 | 0 | 1932 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 |
| 1933 | 0 | 0 | 1933 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 |
| 1934 | 21 | 36 | 1934 2000 JOURNAL OF MEDICAL GENETICS 37(1):77-79 Beresford RG; Tatlidil C; Riddell DC; Welch JP; Ludman MD; Neumann PE; Greer WL Absence of fragile X syndrome in Nova Scotia | 4 | 4 |
| 1935 | 12 | 16 | 1935 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 | 7 | 8 |
| 1936 | 36 | 66 | 1936 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? | 2 | 5 |
| 1937 | 5 | 6 | 1937 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 |
| 1938 | 4 | 15 | 1938 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 | 0 | 0 |
| 1939 | 2 | 5 | 1939 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 |
| 1940 | 1 | 5 | 1940 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(4):398-398 Levitas A Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1941 | 0 | 5 | 1941 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 |
| 1942 | 11 | 17 | 1942 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 |
| 1943 | 0 | 1 | 1943 2000 LIBRARY JOURNAL 125(11):105-105 Griffin KH Children with Fragile X Syndrome: A parents' guide. | 0 | 0 |
| 1944 | 22 | 29 | 1944 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 |
| 1945 | 57 | 117 | 1945 2000 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 6(2):96-106 Mazzocco MMM Advances in research on the fragile X syndrome | 18 | 20 |
| 1946 | 30 | 74 | 1946 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 | 33 | 42 |
| 1947 | 12 | 20 | 1947 2000 MOLECULAR AND CELLULAR PROBES 14(2):115-119 Mila M; Castellvi-Bel S; Sanchez A; Barcelo A; Badenas C; Mallolas J; Estivill X Rare variants in the promoter of the fragile X syndrome gene (FMR1) | 3 | 4 |
| 1948 | 8 | 32 | 1948 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 | 6 | 9 |
| 1949 | 20 | 37 | 1949 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 | 15 | 17 |
| 1950 | 26 | 43 | 1950 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1951 | 30 | 45 | 1951 2000 MOLECULAR MEDICINE TODAY 6(5):193-198 Kooy RF; Willemsen R; Oostra BA Fragile X syndrome at the turn of the century | 12 | 18 |
| 1952 | 4 | 13 | 1952 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 73(1):87-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation | 20 | 25 |
| 1953 | 6 | 14 | 1953 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000) | 2 | 2 |
| 1954 | 13 | 47 | 1954 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 | 13 | 15 |
| 1955 | 27 | 53 | 1955 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):255-263 de Vries BBA; Oostra BA The fragile X syndrome: A model for mental retardation | 0 | 0 |
| 1956 | 8 | 18 | 1956 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):265-277 Bakker CE; Kooy RF; D'Hooge R; Tamanini F; Willemsen R; Nieuwenhuizen I; De Vries BBA; Reyniers E; Hoogeveen AT; Willems PJ; De Deyn PP; Oostra BA Introduction of a FMR1 transgene in the fragile X knockout mouse. | 3 | 3 |
| 1957 | 26 | 45 | 1957 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 | 5 | 11 |
| 1958 | 12 | 42 | 1958 2000 NUCLEIC ACIDS RESEARCH 28(10):2141-2152 Genc B; Muller-Hartmann H; Zeschnigk M; Deissler H; Schmitz B; Majewski F; von Gontard A; Doerfler W Methylation mosaicism of 5 '-(CGG)(n)-3 ' repeats in fragile X, premutation and normal individuals | 3 | 6 |
| 1959 | 32 | 54 | 1959 2000 OPTOMETRY AND VISION SCIENCE 77(11):592-599 Block SS; Brusca-Vega R; Pizzi WJ; Berry-Kravis E; Maino DM; Treitman TM Cognitive and visual processing skills and their relationship to mutation size in full and premutation female fragile X carriers | 0 | 0 |
| 1960 | 7 | 10 | 1960 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1961 | 10 | 17 | 1961 2000 PRENATAL DIAGNOSIS 20(8):611-614 Pesso R; Berkenstadt H; Cuckle H; Gak E; Peleg L; Frydman M; Barkai G Screening for fragile X syndrome in women of reproductive age | 13 | 17 |
| 1962 | 3 | 6 | 1962 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 |
| 1963 | 1 | 5 | 1963 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 |
| 1964 | 1 | 10 | 1964 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 |
| 1965 | 0 | 0 | 1965 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 |
| 1966 | 28 | 40 | 1966 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(2):351-360 Toledano-Alhadef H; Basel-Vanagaite L; Magal N; Davidov B; Ehrlich S; Drasinover V; Taub E; Halpern GJ; Ginott N; Shohat M Fragile-X carrier screening and the prevalence of premutation and full-mutation carriers in Israel | 12 | 20 |
| 1967 | 18 | 34 | 1967 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 | 7 |
| 1968 | 0 | 0 | 1968 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):177-177 Hagerman RJ; Greco C; Chudley A; Leehey M; Tassone F; Grigsby J; Hills J; Wilson R; Harris SW; Hagerman PJ Neuropathology and neurodegenerative features in some older male premutation carriers of fragile X syndrome. | 3 | 4 |
| 1969 | 0 | 0 | 1969 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 |
| 1970 | 0 | 0 | 1970 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1971 | 0 | 0 | 1971 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 |
| 1972 | 0 | 0 | 1972 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):430-430 Jakupciak JP; O'Connell CD; Atha DA; Richie KL Standardization of PCR amplification for fragile X trinucleotide repeat measurements. | 0 | 0 |
| 1973 | 0 | 0 | 1973 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):431-431 Jenkins EC; Li SY; Yao XL; Lanter S; Sudhalter V; Belser R; Ding XH; Houck GE; Glicksman A; Dobkin CS; Nolin SL; Brown WT Detecting mosaic FMR-1 (fragile X) mutations: Southern blotting versus monoclonal antibody analysis. | 0 | 0 |
| 1974 | 0 | 0 | 1974 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):436-436 Patel ZM; Menon SR; D'souza AK; Adhia RA; Sanghavi DA; Gawde HM Validity of the analysis of FMRP expression in blood smears as a screening method for the fragile X syndrome in Indian population. | 0 | 0 |
| 1975 | 0 | 0 | 1975 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):438-438 Zhou Y; Chong SS Simplified molecular diagnostic testing for fragile X syndrome using methylation-specific PCR (ms-PCR). | 0 | 0 |
| 1976 | 0 | 0 | 1976 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):554-554 Heine-Sur D; Pico G; Torres-Juan L; Bernues M; Iglesias J; Barcelo F; Rosell J A female with Fragile-X shows an affected male-like phenotype and skewed inactivation of the functional chromosome. | 0 | 0 |
| 1977 | 0 | 0 | 1977 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):585-585 Essop FB; Greenberg J; Basel D; Krause A Molecular analysis of a fragile X family with two females homozygous for a premutation. | 0 | 0 |
| 1978 | 0 | 0 | 1978 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):586-586 Nolin SL; Houck GE; Gargano AD; Brown WT Large fragile X premutatin alleles may often contain two AGG Interruptions. | 0 | 0 |
| 1979 | 0 | 0 | 1979 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):635-635 Dobkin CS; Ding X; Brown WT; El Idrissi A Reduced hippocampal GABAa receptors and increased kainic acid seizure susceptibility in the fragile X mouse. | 0 | 0 |
| 1980 | 0 | 0 | 1980 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):667-667 Brown WT; Nolin S; Houck GE; Ding XH; Glicksman A; Li SH; Brooks S; Dobkin C; Jenkins EC The Fragile X Syndrome: Screening and prenatal diagnosis. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1981 | 0 | 0 | 1981 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):669-669 Mallolas J; Badenas C; Rite M; Soler A; Borrell A; Sanchez A; Mila M Prospective study of molecular fragile X syndrome prenatal diagnosis. | 0 | 0 |
| 1982 | 6 | 26 | 1982 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(1):37-45 McConkie-Rosell A; Spiridigliozzi GA; Sullivan JA; Dawson DV; Lachiewicz AM Longitudinal study of the carrier testing process for fragile X syndrome: Perceptions and coping | 2 | 3 |
| 1983 | 14 | 42 | 1983 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(2):161-167 Irwin SA; Patel B; Idupulapati M; Harris JB; Crisostomo RA; Larsen BP; Kooy F; Willems PJ; Cras P; Kozlowski PB; Swain RA; Weiler IJ; Greenough WT Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: A quantitative examination | 37 | 64 |
| 1984 | 7 | 18 | 1984 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):110-115 Stoll C Problems in the diagnosis of fragile X syndrome in young children are still present | 3 | 3 |
| 1985 | 4 | 7 | 1985 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 100(2):156-161 Kjaer I; Hjalgrim H; Russell BG Cranial and hand skeleton in fragile X syndrome | 0 | 0 |
| 1986 | 19 | 55 | 1986 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(1):81-90 Sun HT; Cohen S; Kaufmann WE Annexin-1 is abnormally expressed in fragile X syndrome: Two-dimensional electrophoresis study in lymphocytes | 3 | 8 |
| 1987 | 15 | 32 | 1987 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(3):226-230 Schultz-Pedersen S; Hasle H; Olsen JH; Friedrich U Evidence of decreased risk of cancer in individuals with fragile X | 0 | 2 |
| 1988 | 27 | 39 | 1988 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 103(4):314-319 Johnston C; Eliez S; Dyer-Friedman J; Hessl D; Glaser B; Blasey C; Taylor A; Reiss A Neurobehavioral phenotype in carriers of the fragile X premutation | 5 | 5 |
| 1989 | 0 | 0 | 1989 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Daly E; Moore CJ; Schmitz N; Jacobs PA; Davis KE; Murphy KC; Murphy DGM Premutation expansion of CGG triplet repeats affects brain; A study of male carriers of Fragile X syndrome | 0 | 0 |
| 1990 | 1 | 1 | 1990 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 105(7):585-585 Moore CJ; Daly E; Tassone F; Jacobs PA; Davies KE; Murphy KC; Murphy KGM Neuroanatomical effect of FMR1 gene mRNA in premutation carriers of Fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1991 | 17 | 54 | 1991 2001 AMERICAN JOURNAL OF PSYCHIATRY 158(7):1040-1051 Kwon H; Menon V; Eliez S; Warsofsky IS; White CD; Dyer-Friedman J; Taylor AK; Glover GH; Reiss AL Functional neuroanatomy of visuospatial working memory in fragile X syndrome: Relation to behavioral and molecular measures | 10 | 21 |
| 1992 | 17 | 37 | 1992 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):16-27 Bailey DB; Hatton DD; Tassone F; Skinner M; Taylor AK Variability in FMRP and early development in males with fragile X syndrome | 13 | 12 |
| 1993 | 13 | 43 | 1993 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):28-38 Belser RC; Sudhalter V Conversational characteristics of children with fragile X syndrome: Repetitive speech | 8 | 9 |
| 1994 | 23 | 55 | 1994 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(3):216-230 Roberts JE; Mirrett P; Burchinal M Receptive and expressive communication development of young males with fragile X syndrome | 5 | 8 |
| 1995 | 16 | 58 | 1995 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(5):389-400 Sudhalter V; Belser RC Conversational characteristics of children with fragile x syndrome: Tangential language | 3 | 5 |
| 1996 | 26 | 32 | 1996 2001 ANNALS OF CLINICAL BIOCHEMISTRY 38:264-271 Saha S; Karmakar P; Chatterjee C; Banerjee D; Das S; Dasgupta UB Fragile X syndrome in Calcutta, India | 1 | 3 |
| 1997 | 0 | 0 | 1997 2001 ANNALS OF NEUROLOGY 50(3):S108-S108 Berry-Kravis E Characterization of epilepsy in fragile X syndrome | 0 | 0 |
| 1998 | 15 | 30 | 1998 2001 ARQUIVOS DE NEURO-PSIQUIATRIA 59(1):83-88 Boy R; Correia PS; Llerena JC; Machado-Ferreira MD; Pimentel MMG Fragile X syndrome confirmed by molecular analysis: a case-control study with pre and post-puberal patients | 0 | 0 |
| 1999 | 0 | 0 | 1999 2001 AUSTRALIAN JOURNAL OF PSYCHOLOGY 53(1):58-58 Gould E Melatonin profiles and sleep characteristics in boys with fragile X Syndrome: A preliminary study | 0 | 0 |
| 2000 | 34 | 53 | 2000 2001 BRAIN 124:1610-1618 Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome | 7 | 12 |
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