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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 |
|---|---|---|---|---|---|
| 1501 | 11 | 28 | 1501 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 67(1):77-80 Simon EW; Finucane BM Facial emotion identification in males with fragile X syndrome | 6 | 6 |
| 1502 | 0 | 0 | 1502 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G4-G4 Zehnbauer BA Fragile X molecular detection in clinical referrals. | 0 | 0 |
| 1503 | 0 | 0 | 1503 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G5-G5 Larsen LA; NorgaardPedersen B; Vuust J Analysis of fragile X CGG repeats in the normal range by PCR amplification and automated capillary electrophoresis. | 0 | 0 |
| 1504 | 0 | 0 | 1504 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G6-G6 Pandya A; FerreiraGonzalez A; JacksonCook C; Ware JL; Garrett CT Evaluation of fragile X CCG locus using PCR and a fluorescent automated DNA sequencer. | 0 | 0 |
| 1505 | 10 | 25 | 1505 1996 ANNALS OF CLINICAL AND LABORATORY SCIENCE 26(4):323-328 Mark HFL; Bier JAB; Scola P The frequency of chromosomal abnormalities in patients referred for fragile X analysis | 1 | 4 |
| 1506 | 20 | 37 | 1506 1996 ARCHIVES DE PEDIATRIE 3(8):814-821 Mornet E; SimonBouy B Molecular biology of fragile X syndrome: Applications to genetic counselling and molecular diagnosis | 3 | 4 |
| 1507 | 1 | 1 | 1507 1996 ARCHIVES OF DISEASE IN CHILDHOOD 74(1):88-88 Magnay D; Morritt J; Waterston T Fragile X syndrome | 0 | 0 |
| 1508 | 0 | 1 | 1508 1996 ARCHIVES OF MEDICAL RESEARCH 27(3):427-427 DiazGallardo Molecular characterization of the fragile-x syndrome in the Mexican population (vol 26, pg S77, 1995) | 0 | 0 |
| 1509 | 4 | 13 | 1509 1996 ARCHIVES OF MEDICAL RESEARCH 27(4):587-588 Rivera H Fragile X studies and authorship | 1 | 5 |
| 1510 | 13 | 24 | 1510 1996 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 225(1):27-33 Willemsen R; Bontekoe C; Tamanini F; Galjaard H; Hoogeveen A; et al. Association of FMRP with ribosomal precursor particles in the nucleolus | 25 | 30 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1511 | 12 | 81 | 1511 1996 BIOCHEMISTRY 35(15):5041-5053 Pearson CE; Sinden RR Alternative structures in duplex DNA formed within the trinucleotide repeats of the myotonic dystrophy and fragile X loci | 4 | 91 |
| 1512 | 0 | 0 | 1512 1996 BIOLOGICALS 24(3):210-210 Chehab FF; Wall J; Cai SP Lessons derived from the clinical molecular diagnosis of cystic fibrosis, thalassaemia, Fragile X and Huntington's disease | 0 | 0 |
| 1513 | 0 | 0 | 1513 1996 BIOPHYSICAL JOURNAL 70(2):SU496-SU496 Chen X; Mariappan SVS; Ratliff R; Moyzis RK; Smith SS; et al. The formation and methylation of the ''slippage structures'' in vitro: The molecular basis of the fragile-X syndrome | 0 | 0 |
| 1514 | 0 | 1 | 1514 1996 BRITISH JOURNAL OF DEVELOPMENTAL PSYCHOLOGY 14:247-248 Happe F Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 1515 | 0 | 12 | 1515 1996 BRITISH JOURNAL OF HAEMATOLOGY 93(4):841-844 Arjona SN; EloyGarcia J; Gu LH; Smetanina NS; Huisman THJ The dominant beta-thalassaemia in a Spanish family is due to a frameshift that introduces an extra CGG codon (=arginine) at the 5' end of the second exon | 0 | 5 |
| 1516 | 9 | 43 | 1516 1996 CELL 85(2):237-245 Musco G; Stier G; Joseph C; Morelli MAC; Nilges M; et al. Three-dimensional structure and stability of the KH domain: Molecular insights into the fragile X syndrome | 22 | 178 |
| 1517 | 64 | 95 | 1517 1996 CHILD AND ADOLESCENT PSYCHIATRIC CLINICS OF NORTH AMERICA 5(4):895-& Hagerman RJ Fragile X syndrome | 1 | 9 |
| 1518 | 1 | 3 | 1518 1996 CHINESE SCIENCE BULLETIN 41(5):436-437 Huang T; Shen Y; Fan Y; Wu GY Expression of two alternative splicing isoforms of fragile X gene in human placenta | 0 | 0 |
| 1519 | 0 | 0 | 1519 1996 CIRCULATION 94(8):534-534 Helbecque N; Dallongeville J; Arveiler D; Cambou JP; Evans A; et al. Relationship between VLDL receptor gene (CGG) repeat polymorphism and plasma apo E containing lipoparticles levels in a sample of European Caucasian men | 0 | 0 |
| 1520 | 0 | 0 | 1520 1996 CLINICAL CHEMISTRY 42(6):441-441 Tsongalis GJ; Hodges KA; Adkins S; Silverman LM Chemiluminescent detection of the CGG trinucleotide repeat expansion in fragile X syndrome. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1521 | 0 | 0 | 1521 1996 CLINICAL CHEMISTRY 42(11):7-7 Hamdan H; Bailey A; Martinez JJ; Fenwick R; Leon JA Improved amplification and automated detection of trinucleotide repeats in the diagnosis of fragile X syndrome. | 0 | 0 |
| 1522 | 11 | 21 | 1522 1996 CLINICAL OBSTETRICS AND GYNECOLOGY 39(4):772-782 Finucane B Should all pregnant women be offered carrier testing for fragile X syndrome? | 1 | 1 |
| 1523 | 40 | 74 | 1523 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:679-687 Eberhart DE; Warren ST The molecular basis of fragile X syndrome | 7 | 8 |
| 1524 | 13 | 56 | 1524 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:689-697 Liu Q; Siomi H; Siomi MC; Fischer U; Zhang Y; et al. Molecular characterization of the protein products of the fragile X syndrome gene and the survival of motor neurons gene | 2 | 10 |
| 1525 | 0 | 1 | 1525 1996 CONTEMPORARY PSYCHOLOGY 41(5):488-489 McGraw KO Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 1526 | 60 | 94 | 1526 1996 DEVELOPMENTAL PSYCHOLOGY 32(3):416-424 Hagerman RJ Biomedical advances in developmental psychology: The case of fragile X syndrome | 3 | 8 |
| 1527 | 16 | 39 | 1527 1996 EMBO JOURNAL 15(19):5408-5414 Fridell RA; Benson RE; Hua J; Bogerd HP; Cullen BR A nuclear role for the fragile X mental retardation protein | 35 | 67 |
| 1528 | 20 | 27 | 1528 1996 EUROPEAN JOURNAL OF HUMAN GENETICS 4(1):8-12 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; et al. Unexpected inheritance of the (CGG)(n) trinucleotide expansion in a fragile X syndrome family | 5 | 6 |
| 1529 | 21 | 44 | 1529 1996 EUROPEAN PSYCHIATRY 11(5):227-232 Barbe B; Franke P; Maier W; Leboyer M Fragile X syndrome .1. An overview on its genetic mechanism | 0 | 0 |
| 1530 | 58 | 71 | 1530 1996 EUROPEAN PSYCHIATRY 11(5):233-243 Franke P; Barbe B; Leboyer M; Maier W Fragile X syndrome .2. Cognitive and behavioral correlates of mutations of the FMR-1 gene | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1531 | 0 | 0 | 1531 1996 FASEB JOURNAL 10(6):D30-D30 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines. | 0 | 0 |
| 1532 | 0 | 4 | 1532 1996 GENETIC COUNSELING 7(3):227-230 Fryns JP; DHooghe M; Devriendt K Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 gene | 0 | 0 |
| 1533 | 7 | 14 | 1533 1996 GENETIC COUNSELING 7(4):245-247 Fryns JP Ovarian function in fragile X carriers | 0 | 0 |
| 1534 | 40 | 62 | 1534 1996 GIORNALE DI NEUROPSICHIATRIA DELL ETA EVOLUTIVA 16(2):147-154 Veneselli E; Biancheri R; Perrone MV Neuropsychiatric aspects in the fragile X syndrome | 0 | 0 |
| 1535 | 19 | 26 | 1535 1996 HUMAN GENETICS 97(4):512-515 Mornet E; Chateau C; Taillandier A; SimonBouy B; Serre JL Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome | 6 | 8 |
| 1536 | 15 | 26 | 1536 1996 HUMAN GENETICS 97(6):808-812 Haddad LA; MingroniNetto RC; ViannaMorgante AM; Pena SDJ A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males | 9 | 16 |
| 1537 | 7 | 55 | 1537 1996 HUMAN GENETICS 98(2):151-157 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines | 2 | 27 |
| 1538 | 14 | 34 | 1538 1996 HUMAN GENETICS 98(4):409-414 Schmucker B; Ballhausen WG; Pfeiffer RA Mosaicism of a microdeletion of 486 bp involving the CGG repeat of the FMR1 gene due to misalignment of GTT tandem repeats at chi-like elements flanking both breakpoints and a full mutation | 5 | 12 |
| 1539 | 8 | 13 | 1539 1996 HUMAN GENETICS 98(4):419-421 Mila M; CastellviBel S; Gine R; Vazquez C; Badenas C; et al. A female compound heterozygote (pre-and full mutation) for the CGG FMR1 expansion | 4 | 6 |
| 1540 | 30 | 49 | 1540 1996 HUMAN MOLECULAR GENETICS 5(3):319-330 Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; et al. Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome | 32 | 51 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1541 | 15 | 25 | 1541 1996 HUMAN MOLECULAR GENETICS 5(6):809-813 Tamanini F; Meijer N; Verheij C; Willems PJ; Galjaard H; et al. FMRP is associated to the ribosomes via RNA | 48 | 66 |
| 1542 | 21 | 29 | 1542 1996 HUMAN MOLECULAR GENETICS 5(6):821-825 Mornet E; Chateau C; Hirst MC; Thepot F; Taillandier A; et al. Analysis of germline variation at the FMR1 CGG repeat shows variation in the normal-premutated borderline range | 6 | 15 |
| 1543 | 18 | 53 | 1543 1996 HUMAN MOLECULAR GENETICS 5(8):1083-1091 Eberhart DE; Malter HE; Feng Y; Warren ST The fragile X mental retardation protein is a ribonucleoprotein containing both nuclear localization and nuclear export signals | 93 | 132 |
| 1544 | 2 | 4 | 1544 1996 INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS 52(2):209-210 [Anon] Fragile X syndrome | 0 | 0 |
| 1545 | 6 | 29 | 1545 1996 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 26(3):287-301 Dykens E; Ort S; Cohen I; Finucane B; Spiridigliozzi G; et al. Trajectories and profiles of adaptive behavior in males with fragile X syndrome: Multicenter studies | 19 | 23 |
| 1546 | 8 | 43 | 1546 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(8):4327-4334 Deissler H; BehnKrappa A; Doerfler W Purification of nuclear proteins from human HeLa cells that bind specifically to the unstable tandem repeat (CGG), in the human FMR1 gene | 11 | 24 |
| 1547 | 6 | 37 | 1547 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(38):22937-22940 Wang YH; Griffith J Methylation of expanded CCG triplet repeat DNA from fragile X syndrome patients enhances nucleosome exclusion | 4 | 23 |
| 1548 | 11 | 50 | 1548 1996 JOURNAL OF BIOLOGICAL CHEMISTRY 271(40):24325-24328 Godde JS; Kass SU; Hirst MC; Wolffe AP Nucleosome assembly on methylated CGG triplet repeats in the Fragile X Mental Retardation gene 1 promoter | 5 | 41 |
| 1549 | 0 | 0 | 1549 1996 JOURNAL OF INVESTIGATIVE MEDICINE 44(1):A119-A119 Merenstein SA; Sobesky WE; Taylor AK; Tran HX; Riddle JE; et al. Molecular clinical correlations in males with fragile X syndrome. | 0 | 0 |
| 1550 | 10 | 13 | 1550 1996 JOURNAL OF MEDICAL GENETICS 33(4):338-340 Mila M; CastellviBel S; Sanchez A; Lazaro C; Villa M; et al. Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene | 11 | 16 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1551 | 15 | 21 | 1551 1996 JOURNAL OF MEDICAL GENETICS 33(5):376-378 Wang ZM; Taylor AK; Bridge JA FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 17 | 22 |
| 1552 | 13 | 20 | 1552 1996 JOURNAL OF MEDICAL GENETICS 33(12):1007-1010 deVries BBA; Jansen CCAM; Duits AA; Verheij C; Willemsen R; et al. Variable FMR1 gene methylation of large expansions leads to variable phenotype in three males from one fragile X family | 31 | 38 |
| 1553 | 19 | 44 | 1553 1996 JOURNAL OF MOLECULAR BIOLOGY 258(4):614-626 Shimizu M; Gellibolian R; Oostra BA; Wells RD Cloning, characterization and properties of plasmids containing CGG triplet repeats from the FMR-1 gene | 14 | 49 |
| 1554 | 0 | 0 | 1554 1996 JOURNAL OF NEUROCHEMISTRY 67:S34-S34 Chen TA; Lu XF; Yi YH; Ho WKK Analysis of a CGG sequence at the FMR-1 locus in fragile X site by PCR-DGGE method. | 0 | 0 |
| 1555 | 0 | 0 | 1555 1996 JOURNAL OF NEUROCHEMISTRY 67:S36-S36 Chen TA; Lu XF; Ilo WKK; Yi YH; Chen SQ; et al. Variation of the CGG repeat in FMR-1 gene in non retarded Chinese population and fragile X syndrome patients | 0 | 0 |
| 1556 | 12 | 14 | 1556 1996 JOURNAL OF PEDIATRICS 129(4):611-614 Giangreco CA; Steele MW; Aston CE; Cummins JH; Wenger SL A simplified six-item checklist for screening for fragile X syndrome in the pediatric population | 11 | 22 |
| 1557 | 1 | 4 | 1557 1996 JOURNAL OF SLEEP RESEARCH 5(4):272-272 Musumeci SA; Ferri R; Elia M; DelGracco S; Scuderi C; et al. Normal respiratory pattern during sleep in young fragile X-syndrome patients | 1 | 1 |
| 1558 | 9 | 33 | 1558 1996 KOREAN JOURNAL OF GENETICS 18(3):199-210 Choi SK; Kim HY; Paik YK Cytogenetic analysis of a Korean family with fragile X syndrome | 0 | 1 |
| 1559 | 3 | 4 | 1559 1996 LANCET 348(9032):967-968 Willemsen R; Oosterwijk JC; Los FJ; Galjaard H; Oostra BA Prenatal diagnosis of fragile X syndrome | 11 | 16 |
| 1560 | 3 | 45 | 1560 1996 MEDICAL ANTHROPOLOGY QUARTERLY 10(4):537-550 Nelkin D The social dynamics of genetic testing: The case of Fragile-X | 1 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1561 | 4 | 138 | 1561 1996 MEDICAL HYPOTHESES 47(4):289-298 Fischer KM Genes for Prader Willi Syndrome Angelman syndrome and fragile X syndrome are homologous, with genetic imprinting and unstable trinucleotide repeats causing mental retardation, autism and aggression | 1 | 4 |
| 1562 | 0 | 1 | 1562 1996 MICHIGAN LAW REVIEW 94(6):1810-1838 Friedman RD Statistics and the evaluation of evidence for forensic scientists - Aitken,CGG | 0 | 3 |
| 1563 | 17 | 57 | 1563 1996 MOLECULAR AND CELLULAR BIOLOGY 16(7):3825-3832 Siomi MC; Zhang Y; Siomi H; Dreyfuss G Specific sequences in the fragile X syndrome protein FMR1 and the FXR proteins mediate their binding to 60S ribosomal subunits and the interactions among them | 58 | 109 |
| 1564 | 10 | 31 | 1564 1996 NATURE GENETICS 12(1):91-93 Khandjian EW; Corbin F; Woerly S; Rousseau F The fragile X mental retardation protein is associated with ribosomes | 70 | 101 |
| 1565 | 13 | 45 | 1565 1996 NIMHANS JOURNAL 14(3):201-207 Suresh KP; Girimaji SR; Manjunatha KR Newer genetics in mental retardation .1. Fragile X syndrome and triplet repeat mutations | 0 | 1 |
| 1566 | 5 | 27 | 1566 1996 NUCLEIC ACIDS RESEARCH 24(4):784-792 Mariappan SVS; Catasti P; Chen X; Ratliff R; Moyzis RK; et al. Solution structures of the individual single strands of the fragile X DNA triplets (GCC)(n)center dot(GGC)(n) | 12 | 49 |
| 1567 | 12 | 14 | 1567 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 1568 | 0 | 0 | 1568 1996 PEDIATRIC RESEARCH 39(2):371-371 Torrado M; Herrera J; Chertkoff L; Tenembaum S; Bin L; et al. Diagnosis value of a pediatric clinical score for the diagnosis of the Fragile X Syndrome | 0 | 0 |
| 1569 | 24 | 29 | 1569 1996 PEDIATRICS 97(1):122-126 Hagerman RJ; Staley LW; OConner R; Lugenbeel K; Nelson D; et al. Learning-disabled males with a fragile X CGG expansion in the upper premutation size range | 29 | 40 |
| 1570 | 14 | 17 | 1570 1996 PEDIATRICS 98(2):297-300 Desposito F; Cho S; Frias JL; Sherman J; Wappner RS; et al. Health supervision for children with fragile X syndrome | 3 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1571 | 35 | 63 | 1571 1996 PRENATAL DIAGNOSIS 16(13):1199-1211 Sutherland GR; Mulley JC Fragile X syndrome and Fragile XE mental retardation | 3 | 9 |
| 1572 | 16 | 28 | 1572 1996 PSYCHIATRIC GENETICS 6(2):81-86 Ashworth A; Abusaad I; Walsh C; Nanko S; Murray RM; et al. Linkage analysis of the fragile X gene FMR-1 and schizophrenia: No evidence for linkage but report of a family with schizophrenia and an unstable triplet repeat | 1 | 3 |
| 1573 | 8 | 27 | 1573 1996 PSYCHIATRY RESEARCH 64(2):97-104 Thompson NM; Rogeness GA; McClure E; Clayton R; Johnson C Influence of depression on cognitive functioning in Fragile X females | 1 | 6 |
| 1574 | 24 | 49 | 1574 1996 REVISTA MEDICA DE CHILE 124(7):865-872 Jara L; Avendano I; Aspillaga M; Blanco R Molecular and genetic features of fragile X syndrome. A review | 0 | 0 |
| 1575 | 28 | 77 | 1575 1996 SCREENING 4(4):175-192 Meadows KL; Sherman SL Fragile X syndrome: Examination of issues pertaining to population-based screening | 2 | 2 |
| 1576 | 19 | 35 | 1576 1996 SOMATIC CELL AND MOLECULAR GENETICS 22(6):435-441 Eberhart DE; Warren ST Nuclease sensitivity of permeabilized cells confirms altered chromatin formation at the fragile X locus | 7 | 15 |
| 1577 | 18 | 33 | 1577 1996 VARIATION IN THE HUMAN GENOME 197:119-126 Sutherland GR; Richards RI Unusual inheritance patterns due to dynamic mutation in fragile X syndrome | 0 | 0 |
| 1578 | 5 | 20 | 1578 1996 VARIATION IN THE HUMAN GENOME 197:126-136 Weiss KM; Sutherland GR; Harper PS; Bodmer W; Bowcock AM; et al. Unusual inheritance patterns due to dynamic mutation in fragile X syndrome - Discussion | 0 | 0 |
| 1579 | 0 | 1 | 1579 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):191-192 Fombonne E The fragile X syndrome | 0 | 0 |
| 1580 | 14 | 25 | 1580 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):195-201 Mandel JL The fragile X mental retardation syndrome: the FMR1 gene and its mutations | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1581 | 13 | 24 | 1581 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):202-208 Hagerman RJ Fragile X syndrome: meeting the challenges of diagnosis and care | 0 | 0 |
| 1582 | 12 | 16 | 1582 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):209-212 Fombonne E Epidemiological studies of fragile X syndrome | 0 | 0 |
| 1583 | 8 | 9 | 1583 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):221-223 Ponsot G Fragile X syndrome. Early recognition. | 0 | 0 |
| 1584 | 6 | 9 | 1584 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):224-226 Gerard CL; Guillotte E; Servel F; Barbeau M Assessment and remediation of communication disorders in children with fragile X syndrome | 0 | 0 |
| 1585 | 3 | 10 | 1585 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):227-231 Roge B Fragile X syndrome. Special education: the French context | 0 | 0 |
| 1586 | 13 | 27 | 1586 1997 A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT 9(5):232-238 Turk J Treatments and services for individuals with fragile X syndrome and their families | 0 | 0 |
| 1587 | 26 | 41 | 1587 1997 AMERICAN JOURNAL OF HUMAN GENETICS 60(1):103-112 FalikZaccai TC; Shachak E; Yalon M; Lis Z; Borochowitz Z; et al. Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype | 17 | 27 |
| 1588 | 22 | 35 | 1588 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(3):660-667 deVries BBA; vandenOuweland AMW; Mohkamsing S; Duivenvoorden HJ; Mol E; et al. Screening and diagnosis for the fragile X syndrome among the mentally retarded: An epidemiological and psychological survey | 44 | 80 |
| 1589 | 0 | 0 | 1589 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Fisch GS; Holden JJA; Chalifoux M; Carpenter NJ; Howard-Peebles PN; et al. Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study. | 0 | 0 |
| 1590 | 0 | 0 | 1590 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Kenneson A; Cramer DW; Warren ST The fragile X premutation is not a major risk for early menopause. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1591 | 0 | 0 | 1591 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A8-A8 Toth-Fejel S; Gunter K; McMilin K; Reifsteck C; Chen XN; et al. High rate of chromosome 11 structural mosaicism in chromosome 11 terminal deletions: fragile site expression and CGG repeat expansion at FRA11B as a genetic mechanism. | 0 | 0 |
| 1592 | 0 | 0 | 1592 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Brown VL; Small K; Lakkis L; Wilkinson KD; Warren ST Purification and characterization of the fragile X mental retardation protein. | 0 | 0 |
| 1593 | 0 | 0 | 1593 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A26-A26 Corbin F; Bouillon M; Rousseau F; Khandjian EW The fragile-X mental retardation protein is a mRNA chaperone associated with translating complexes. | 0 | 0 |
| 1594 | 0 | 0 | 1594 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A30-A30 Gunter C; Paradee W; Newman J; Sherman SL; Warren ST A novel biallelic polymorphism in the FMR1 gene shows strong linkage disequilibrium With CGG repeats and flanking microsatellite markers. | 1 | 1 |
| 1595 | 0 | 0 | 1595 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A33-A33 Ju W; Xu WM; Hwang YW; Brown WT; Zhong N Molecular pathogenetic studies of the fragile X syndrome: Double knockouts of FMR1 and FXR1 affect early development of Xenopus oocytes. | 0 | 0 |
| 1596 | 0 | 0 | 1596 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A100-A100 Hagerman RJ; Staley-Gane L; Linden MG; Tassone F; Hills J; et al. A compound heterozygous female with fragile X syndrome. | 0 | 0 |
| 1597 | 0 | 0 | 1597 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A109-A109 Perroni L; Grasso M; Garavelli L; Argusti A; Cavani S; et al. Three cases of high functioning fragile X males | 0 | 0 |
| 1598 | 0 | 0 | 1598 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A110-A110 Rhee LE; Hatcher SL; Robb KM; Towner DR Fragile X syndrome associated with birth defects. | 0 | 0 |
| 1599 | 0 | 0 | 1599 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A128-A128 Jenkins EC; Wen GY; Goldberg EM; Genovese M; Brown WT; et al. Fragile X chromosome longitudinal sections studied by transmission electron microscopy. | 0 | 0 |
| 1600 | 0 | 0 | 1600 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Paradee W; Rasmussen D; Melikian H; Conn PJ; Warren ST Hippocampus-independent deficits in the Fragile X mouse. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1601 | 0 | 0 | 1601 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Osthus RC; DiMaio MS; Mahoney MJ; Bale AE Significance of borderline fragile X premutations. | 0 | 0 |
| 1602 | 0 | 0 | 1602 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A170-A170 Feng Y; Absher D; Brown V; Eberhart DE; Malter HE; et al. FMRP associates with polyribosomes as an mRNP and the I304N mutation causing severe fragile X syndrome abolishes this association. | 0 | 0 |
| 1603 | 0 | 0 | 1603 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A175-A175 Kaufmann WE; Abrams MT; Chen W; Reiss AL Genotype and molecular phenotype in fragile X syndrome. | 0 | 0 |
| 1604 | 0 | 0 | 1604 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A177-A177 Mangel L; Ternes T; Schmitz B; Doerfler W Characterization of new 5 '-(CGG)(n)-3 ' trinucleotide repeat-containing loci in the human genome. | 0 | 0 |
| 1605 | 0 | 0 | 1605 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A182-A182 Sandberg G; Schalling M Detection of methylated CpG sequences in the FMR-1 promoter using the sodium bisulfite method and expression studies after in vitro methylation and CGG repeat insert. | 0 | 0 |
| 1606 | 0 | 0 | 1606 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A192-A192 Staley-Gane L; Holloway SL; Flynn L; Logan L; Hageman RJ Assessment of patient agenda prior to genetic counseling for fragile X syndrome. | 0 | 0 |
| 1607 | 0 | 0 | 1607 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A219-A219 de Vries BBA; van den Ouweland AMW; Mohkamsing S; Duivenvoorden HJ; Halley DJJ; et al. A fragile X screening program in The Netherlands: prevalence of fragile X syndrome lower than previously considered, but the disorder is still underdiagnosed. | 0 | 0 |
| 1608 | 0 | 0 | 1608 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A303-A303 Ashley AE; Robinson H; Glicksman AE; Nolin SL; Schwartz C; et al. Identification of risk factors associated with instability of the FMR1 CGG repeat. | 0 | 0 |
| 1609 | 0 | 0 | 1609 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A304-A304 Bat O; Kimmel M; Axelrod DE; Chakraborty R Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease. | 0 | 0 |
| 1610 | 0 | 0 | 1610 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A306-A306 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the fragile X syndrome gene. | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1611 | 0 | 0 | 1611 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A313-A313 Layman LC; Moffitt DV; McDonough PG; Song M; Shamoun D; et al. Correlation and vertical transmission of fragile X syndrome and ovarian failure within a single family. | 0 | 0 |
| 1612 | 0 | 0 | 1612 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A316-A316 Nolin SL; Houck GE; Blumstein H; Ye LL; Dobkin CS; et al. Single cell analysis shows different FMR1 CGG repeat stability in sperm and lymphocytes of premutation males. | 1 | 2 |
| 1613 | 0 | 0 | 1613 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A321-A321 Tassone F; Hagerman RJ; Ikle D; Dyer PN; Lampe M; et al. FMRP expression as a potential prognostic indicator in fragile X syndrome. | 1 | 1 |
| 1614 | 0 | 0 | 1614 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A324-A324 Zhong N; Ju W; Xu WM; Liu B; Dobkin C; et al. Molecular pathogenetic studies of the fragile X syndrome: A candidate transcript targeted by the fragile X protein FMRP. | 0 | 0 |
| 1615 | 0 | 0 | 1615 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A330-A330 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; et al. Methylation analysis of the fragile X syndrome by PCR. | 0 | 0 |
| 1616 | 0 | 0 | 1616 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A389-A389 Ye LL; Ju W; Xu WM; Schupf N; Jenkins EC; et al. Distribution of apolipoprotein E genotypes in the fragile X syndrome, Batten disease, and Down syndrome populations. | 0 | 0 |
| 1617 | 0 | 0 | 1617 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Sucharov CC; Varandas FR; Rondinelli E; Carakushansky G; Moura-Neto RS Establishment of a differential diagnostic of patients with Mental Retardation based on Southern-blot and PCR considering the frequency of Fragile X trinucleotide repeats from normal population in Rio de Janeiro, Brazil. | 0 | 0 |
| 1618 | 0 | 0 | 1618 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A407-A407 Taylor AK; Tassone F; Staley-Gane L; Hagerman RJ Identical premutation size in multiple tissues of a male fragile X carrier. | 0 | 0 |
| 1619 | 28 | 44 | 1619 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):961-967 Gronskov K; Hjalgrim H; Bjerager MO; BrondumNielsen K Deletion of all CGG repeats plus flanking sequences in FMR1 does not abolish gene expression | 5 | 6 |
| 1620 | 30 | 43 | 1620 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(6):1362-1369 Kenneson A; Cramer DW; Warren ST Fragile X premutations are not a major cause of early menopause | 13 | 22 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1621 | 8 | 29 | 1621 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(1):62-69 McConkieRosell A; Spiridigliozzi GA; Iafolla T; Tarleton J; Lachiewicz AM Carrier testing in the fragile X syndrome: Attitudes and opinions of obligate carriers | 7 | 13 |
| 1622 | 3 | 14 | 1622 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(4):445-449 Wen GY; Jenkins EC; Yao XL; Yoon D; Brown WT; et al. Transmission electron microscopy of chromosomes by longitudinal section preparation: Application to fragile X chromosome analysis | 3 | 5 |
| 1623 | 3 | 11 | 1623 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 69(1):114-116 Martin NG; Healey SC; Pangan TS; Heath AC; Turner G Do mothers of dizygotic twins have earlier menopause? A role for fragile X? | 5 | 12 |
| 1624 | 8 | 13 | 1624 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(2):245-246 Healey SC; Duffy DL; Martin NG; Turner G Is fragile X syndrome a risk factor for dizygotic twinning? | 2 | 4 |
| 1625 | 22 | 25 | 1625 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(4):430-434 Hammond LS; Macias MM; Tarleton JC; Pai GS Fragile X syndrome and deletions in FMR1: New case and review of the literature | 15 | 22 |
| 1626 | 13 | 51 | 1626 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 73(4):463-469 Ritchie RJ; Chakrabarti L; Knight SJL; Harding RM; Davies KE Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28 | 2 | 6 |
| 1627 | 12 | 39 | 1627 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(2):167-171 Miezejeski CM; Heaney G; Belser R; Brown WT; Jenkins EC; et al. Longer brainstem auditory evoked response latencies of individuals with fragile X syndrome related to sedation | 0 | 0 |
| 1628 | 0 | 0 | 1628 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 74(6):568-568 Bleiweiss H; Pollini A; Goldemberg A; Schuarzberg C; Staszauer M; et al. Treatment of patients with fragile X syndrome and psychiatric abnormalities. | 0 | 0 |
| 1629 | 0 | 0 | 1629 1997 AMERICAN JOURNAL OF PATHOLOGY 151(5):G3-G3 Shrimpton AE; Hicks K; Lamberson CM Fragile X syndrome molecular detection. | 0 | 0 |
| 1630 | 22 | 32 | 1630 1997 ANNALES DE GENETIQUE 40(3):139-144 Gerard B; LeHeuzey MF; Brunie G; Lewine P; Saiag MC; et al. Systematic screening for fragile X syndrome in a cohort of 574 mentally retarded children | 4 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1631 | 2 | 15 | 1631 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):457-460 BillonGalland IO The fragile X syndrome and its clinical psychotic expression | 0 | 0 |
| 1632 | 0 | 0 | 1632 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):460-460 Koupernik; Doutheau; Rapporteur The fragile X syndrome and its clinical psychotic expression - Discussion | 0 | 0 |
| 1633 | 6 | 10 | 1633 1997 ANNALS OF CLINICAL BIOCHEMISTRY 34:517-520 Chen TA; Lu XF; Che PK; Ho WKK Variation of the CGG repeat in FMR-1 gene in normal and fragile X Chinese subjects | 6 | 7 |
| 1634 | 28 | 43 | 1634 1997 ANNALS OF MEDICINE 29(6):563-567 Oostra BA; Hoogeveen AT Animal model for fragile X syndrome | 3 | 8 |
| 1635 | 0 | 0 | 1635 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Mornet E Fragile X syndrome - Response | 0 | 0 |
| 1636 | 1 | 1 | 1636 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Beauvais P Fragile X syndrome | 0 | 0 |
| 1637 | 17 | 20 | 1637 1997 ARCHIVES DE PEDIATRIE 4(3):227-236 Cossee M; Moutou C; Biancalana V; Bouix JC; Plessis G; et al. The fragile X syndrome is still underdiagnosed: Efficacy of molecular testing in mentally retarded probands | 3 | 3 |
| 1638 | 2 | 23 | 1638 1997 ARCHIVES OF DISEASE IN CHILDHOOD 76(3):264-267 Corrigan N; Stewart M; Scott M; Fee F Fragile X, iron, and neurodevelopmental screening in 8 year old children with mild to moderate learning difficulties | 0 | 4 |
| 1639 | 1 | 1 | 1639 1997 ARCHIVES OF MEDICAL RESEARCH 28(1):149-149 Rivera H Fragile X studies and authorship (vol 27, pg 587, 1996) | 0 | 0 |
| 1640 | 27 | 35 | 1640 1997 BRAZILIAN JOURNAL OF GENETICS 20(4):731-739 Mingroni-Netto RC; Pavanello RCM; Otto PA; Vianna-Morgante AM Experience with molecular and cytogenetic diagnosis of fragile X syndrome in Brazilian families | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1641 | 0 | 0 | 1641 1997 BRITISH MEDICAL JOURNAL 315(7102):208-208 White C Screening for fragile X is cost effective and accurate | 0 | 0 |
| 1642 | 4 | 11 | 1642 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175 Barnicoat A Screening for fragile X syndrome: a model for genetic disorders? | 1 | 4 |
| 1643 | 8 | 10 | 1643 1997 BRITISH MEDICAL JOURNAL 315(7117):1223-1226 Turner G; Robinson H; Wake S; Laing S; Partington M Case finding for the fragile X syndrome and its consequences | 5 | 9 |
| 1644 | 18 | 26 | 1644 1997 CLINICAL GENETICS 51(1):1-6 Loesch DZ; Petrovic V; Francis DI; Oertel R; Slater H ''Reduction'' of CGG trinucleotide expansion from mother to offspring in seven fragile-X families | 4 | 7 |
| 1645 | 1 | 9 | 1645 1997 CLINICAL GENETICS 51(1):71-74 Behjati F; Mullarkey M; Bergbaum A; Berry AC; Docherty Z Chromosome deletion 17p11.2 (Smith-Magenis syndrome) in seven new patients, four of whom had been referred for fragile-X investigation | 0 | 6 |
| 1646 | 9 | 15 | 1646 1997 CLINICAL GENETICS 52(3):147-154 Hecimovic S; Barisic I; Muller A; Petkovic I; Baric I; et al. Expand long PCR for fragile X mutation detection | 8 | 23 |
| 1647 | 11 | 14 | 1647 1997 CLINICAL GENETICS 52(4):211-215 Arvio M; Peippo M; Simola KOJ Applicability of a checklist for clinical screening of the fragile X syndrome | 10 | 15 |
| 1648 | 42 | 64 | 1648 1997 CURRENT OPINION IN NEUROLOGY 10(2):142-147 Chakrabarti L; Davies KE Fragile X syndrome | 2 | 4 |
| 1649 | 0 | 0 | 1649 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P250-P250 Malarchuk S; Li S; Wertelecki W; Bychkova A; Livshits L Analysis of patients with fragile X syndrome in Ukraine. | 0 | 0 |
| 1650 | 0 | 0 | 1650 1997 CYTOGENETICS AND CELL GENETICS 77(1-2):P287-P287 Tengstrom C; Ikonen A; Kaski M; Autio S High resolution banding and fragile X - screening in persons with mild mental retardation. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1651 | 10 | 16 | 1651 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; et al. A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol | 1 | 2 |
| 1652 | 1 | 1 | 1652 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(5):304-304 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; et al. Five-year experience with Fragile X-testing - Setting laboratory standards of practice and a cost-effective protocol (vol 6, pg 161, 1997) | 0 | 0 |
| 1653 | 13 | 28 | 1653 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(2):89-93 FulchignoniLataud MC; Olchwang S; Serre JL The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients | 1 | 6 |
| 1654 | 21 | 33 | 1654 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(5):293-298 Bontekoe CJM; deGraaff E; Nieuwenhuizen IM; Willemsen R; Oostra BA FMR1 premutation allele (CGG)(81) is stable in mice | 16 | 18 |
| 1655 | 27 | 48 | 1655 1997 FOLIA HISTOCHEMICA ET CYTOBIOLOGICA 35(3):135-141 Szot M The fragile X syndrome | 0 | 0 |
| 1656 | 6 | 15 | 1656 1997 GENETIC COUNSELING 8(1):1-6 Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; et al. Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology | 1 | 3 |
| 1657 | 11 | 19 | 1657 1997 GENETIC TESTING 1(3):151-155 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; et al. Methylation analysis of the fragile X syndrome by PCR | 2 | 3 |
| 1658 | 5 | 8 | 1658 1997 HOSPITAL PRACTICE 32(4):73-& Warren ST Trinucleotide repetition and fragile X syndrome | 3 | 5 |
| 1659 | 11 | 15 | 1659 1997 HUMAN GENETICS 99(3):308-311 Willemsen R; Smits A; Mohkamsing S; vanBeerendonk H; deHaan A; et al. Rapid antibody test for diagnosing fragile X syndrome: A validation of the technique | 39 | 45 |
| 1660 | 8 | 11 | 1660 1997 HUMAN GENETICS 99(6):793-795 Chen SH; Schoof JM; Buroker NE; Scott CR The identification of a (CGG)(6)AGG insertion within the CGG repeat of the FMR1 gene in Asians | 5 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1661 | 17 | 64 | 1661 1997 HUMAN GENETICS 100(3-4):407-414 Lavedan CN; Garrett L; Nussbaum RL Trinucleotide repeats (CGG)(22)TGG(CGG)(43)TGG(CGG)(21) from the fragile X gene remain stable in transgenic mice | 14 | 19 |
| 1662 | 15 | 19 | 1662 1997 HUMAN GENETICS 100(5-6):564-568 Larsen LA; Gronskov K; NorgaardPedersen B; BrondumNielsen K; Hasholt L; et al. High-throughput analysis of fragile X (CGG)(n) alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis | 8 | 24 |
| 1663 | 10 | 16 | 1663 1997 HUMAN GENETICS 101(2):186-189 Pesso R; Barkai G; Ravia Y; Gak E; Frydman M; et al. No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome | 2 | 4 |
| 1664 | 16 | 23 | 1664 1997 HUMAN GENETICS 101(2):214-218 Hirst MC; Arinami T; Laird CD Sequence analysis of long FMR1 arrays in the Japanese population: insights into the generation of long (CGG)(n) tracts | 4 | 9 |
| 1665 | 4 | 22 | 1665 1997 HUMAN HEREDITY 47(5):254-262 Gurling HMD; Bolton PF; Vincent J; Melmer G; Rutter M Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes | 0 | 8 |
| 1666 | 22 | 35 | 1666 1997 HUMAN MOLECULAR GENETICS 6(7):971-979 Moutou C; Vincent MC; Biancalana V; Mandel JL Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic | 23 | 34 |
| 1667 | 13 | 38 | 1667 1997 HUMAN MOLECULAR GENETICS 6(9):1465-1472 Corbin F; Bouillon M; Fortin A; Morin S; Rousseau F; et al. The fragile X mental retardation protein is associated with poly(A)(+) mRNA in actively translating polyribosomes | 70 | 93 |
| 1668 | 18 | 64 | 1668 1997 HUMAN MOLECULAR GENETICS 6(11):1791-1801 Stoger R; Kajimura TM; Brown WT; Laird CD Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1 | 12 | 38 |
| 1669 | 26 | 38 | 1669 1997 HUMAN MUTATION 10(5):393-399 Wang YC; Lin ML; Lin SJ; Li YC; Li SY Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome | 7 | 10 |
| 1670 | 51 | 134 | 1670 1997 INTERNATIONAL REVIEW OF RESEARCH IN MENTAL RETARDATION, VOL 21 21:221-247 Fisch GS Longitudinal assessment of cognitive-behavioral deficits produced by the fragile-X mutation | 0 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1671 | 24 | 61 | 1671 1997 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 27(4):415-435 Mazzocco MMM; Kates WR; Baumgardner TL; Freund LS; Reiss AL Autistic behaviors among girls with fragile X syndrome | 20 | 25 |
| 1672 | 15 | 47 | 1672 1997 JOURNAL OF BIOLOGICAL CHEMISTRY 272(27):16761-16768 Deissler H; Wilm M; Genc B; Schmitz B; Ternes T; et al. Rapid protein sequencing by tandem mass spectrometry and cDNA cloning of p20-CGGBP - A novel protein that binds to the unstable triplet repeat 5'-d(CGG)(n)-3' in the human FMR1 gene | 5 | 17 |
| 1673 | 4 | 60 | 1673 1997 JOURNAL OF BIOLOGICAL CHEMISTRY 272(27):16783-16792 Bacolla A; Gellibolian R; Shimizu M; Amirhaeri S; Kang S; et al. Flexible DNA: Genetically unstable CTG center dot CAG and CGG center dot CCG from human hereditary neuromuscular disease genes | 3 | 57 |
| 1674 | 21 | 51 | 1674 1997 JOURNAL OF CLINICAL INVESTIGATION 100(2):331-338 Jakala P; Hanninen T; Ryynanen M; Laakso M; Partanen K; et al. Fragile-X: Neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes | 13 | 21 |
| 1675 | 32 | 57 | 1675 1997 JOURNAL OF INHERITED METABOLIC DISEASE 20(2):139-151 Hoogeveen AT; Oostra BA The fragile X syndrome | 6 | 10 |
| 1676 | 0 | 0 | 1676 1997 JOURNAL OF MEDICAL GENETICS 34:SP69-SP69 Webb J; Murray A; Conway G; Jacobs P Premature ovarian failure and fragile X | 0 | 0 |
| 1677 | 0 | 0 | 1677 1997 JOURNAL OF MEDICAL GENETICS 34:505-505 Brady AF; Suri M; Emerson J; Bell J; Chotai K; et al. Unusual X chromosome inactivation resulting in fragile X phenotype in a girl with a deletion on (X)(q26q27) | 0 | 0 |
| 1678 | 0 | 0 | 1678 1997 JOURNAL OF MEDICAL GENETICS 34:531-531 Cottrell S; Redmond E; McMahon C; Genet S; Barnicoat A Two deletions causing reversal to normal phenotype in fragile X syndrome. | 0 | 0 |
| 1679 | 0 | 0 | 1679 1997 JOURNAL OF MEDICAL GENETICS 34:539-539 Buckingham A; Bell JA; Payne SJ; Masters K; Emmerson J; et al. Recurrence of Turner's syndrome in a fragile-X family | 0 | 0 |
| 1680 | 0 | 0 | 1680 1997 JOURNAL OF MEDICAL GENETICS 34:541-541 Moore S; Dean JCS; Cole GF; Hamilton L; Kelly KF; et al. Fragile X Syndrome resulting from a deletion of the FMR1 gene | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1681 | 17 | 29 | 1681 1997 JOURNAL OF MEDICAL GENETICS 34(1):1-5 Morton JE; Bundey S; Webb TP; MacDonald F; Rindl PM; et al. Fragile X syndrome is less common than previously estimated | 28 | 47 |
| 1682 | 7 | 10 | 1682 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; et al. Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 1683 | 1 | 2 | 1683 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350 Loesch DZ FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male | 1 | 1 |
| 1684 | 0 | 1 | 1684 1997 JOURNAL OF MEDICAL GENETICS 34(4):350-350 Taylor AK FMR1 fully expanded mutation with minimal methylation in a high functioning fragile X male - Reply | 0 | 0 |
| 1685 | 21 | 32 | 1685 1997 JOURNAL OF MEDICAL GENETICS 34(8):627-631 Kunst CB; Leeflang EP; Iber JC; Arnheim N; Warren ST The effect of FMR1 CGG repeat interruptions on mutation frequency as measured by sperm typing | 3 | 16 |
| 1686 | 12 | 38 | 1686 1997 JOURNAL OF MEDICAL GENETICS 34(11):907-911 vanRijn MA; deVries BBA; Tibben A; vandenOuweland AMW; Halley DJJ; et al. DNA testing for fragile X syndrome: implications for parents and family | 3 | 4 |
| 1687 | 11 | 15 | 1687 1997 JOURNAL OF MEDICAL GENETICS 34(11):924-926 Losekoot M; Hoogendoorn E; Olmer R; Jansen CCAM; Oosterwijk JC; et al. Prenatal diagnosis of the fragile X syndrome: loss of mutation owing to a double recombinant or gene conversion event at the FMR1 locus | 1 | 7 |
| 1688 | 0 | 28 | 1688 1997 JOURNAL OF MOLECULAR BIOLOGY 267(5):1171-1185 Tippin DB; Sundaralingam M Nine polymorphic crystal structures of d(CCGGGCCCGG), d(CCGGGCCm(5)CGG), d(Cm(5)CGGGCCm(5)CGG) and d(CCGGGCC(Br)(5)CGG) in three different conformations: Effects of spermine binding and methylation on the bending and condensation of A-DNA | 0 | 19 |
| 1689 | 23 | 59 | 1689 1997 JOURNAL OF NEUROSCIENCE 17(5):1539-1547 Feng Y; Gutekunst CA; Eberhart DE; Yi H; Warren ST; et al. Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes | 85 | 145 |
| 1690 | 5 | 12 | 1690 1997 JOURNAL OF SPECIAL EDUCATION 31(3):362-376 Powell L; Houghton S; Douglas G Comparison of etiology-specific cognitive functioning profiles for individuals with fragile X and individuals with Down syndrome | 2 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1691 | 8 | 35 | 1691 1997 JOURNAL OF THEORETICAL BIOLOGY 188(1):53-67 Bat O; Kimmel M; Axelrod DE Computer simulation of expansions of DNA triplet repeats in the fragile X syndrome and Huntington's disease | 2 | 4 |
| 1692 | 42 | 92 | 1692 1997 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 3(4):313-322 Abbeduto L; Hagerman RJ Language and communication in fragile X syndrome | 10 | 17 |
| 1693 | 26 | 47 | 1693 1997 MOLECULAR CELL 1(1):109-118 Feng Y; Absher D; Eberhart DE; Brown V; Malter HE; et al. FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association | 89 | 134 |
| 1694 | 7 | 20 | 1694 1997 MOLECULAR DIAGNOSIS 2(4):259-269 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in fragile X syndrome | 4 | 6 |
| 1695 | 22 | 42 | 1695 1997 NATURE GENETICS 15(2):165-169 Malter HE; Iber JC; Willemsen R; deGraaff E; Tarleton JC; et al. Characterization of the full fragile X syndrome mutation in fetal gametes | 58 | 89 |
| 1696 | 7 | 34 | 1696 1997 NATURE STRUCTURAL BIOLOGY 4(9):712-716 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; et al. The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome | 7 | 46 |
| 1697 | 1 | 1 | 1697 1997 NATURE STRUCTURAL BIOLOGY 4(10):840-840 Musco G; Kharrat A; Stier G; Fraternali F; Gibson TJ; et al. The solution structure of the first KH domain of FMR1, the protein responsible for the fragile X syndrome (vol 4, pg 712, 1997) | 1 | 2 |
| 1698 | 15 | 33 | 1698 1997 NEUROBIOLOGY OF DISEASE 4(5):329-336 Bardoni B; Sittler A; Shen Y; Mandel JL Analysis of domains affecting intracellular localization of the FMRP protein | 22 | 28 |
| 1699 | 0 | 0 | 1699 1997 NEUROLOGY 48(3):5062-5062 Mostofsky SH; Mazzocco MM; Aakalu G; Warsofsky IS; Denckla MB; et al. Aberrant posterior vermis size in fragile X syndrome: Correlation with neurocognitive performance | 0 | 0 |
| 1700 | 17 | 31 | 1700 1997 NUCLEIC ACIDS RESEARCH 25(14):2883-2887 Sandberg G; Schalling M Effect of in vitro promoter methylation and CGG repeat expansion on FMR-1 expression | 10 | 24 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1701 | 0 | 35 | 1701 1997 NUCLEIC ACIDS RESEARCH 25(15):3042-3050 Vuidepot AL; Bontems F; Gervais M; Guiard B; Shechter E; et al. NMR analysis of CYP1(HAP1) DNA binding domain - CYC1 upstream activation sequence interactions: recognition of a CGG trinucleotide and of an additional thymine 5 bp downstream by the zinc cluster and the N-terminal extremity of the protein | 0 | 4 |
| 1702 | 3 | 10 | 1702 1997 PEDIATRICS 99(5):753-753 Hagerman R Fragile X: Treatment of hyperactivity | 0 | 1 |
| 1703 | 24 | 69 | 1703 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(9):4587-4592 Hansen RS; Canfield TK; Fjeld AD; Mumm S; Laird CD; et al. A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication | 8 | 41 |
| 1704 | 18 | 58 | 1704 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5395-5400 Weiler IJ; Irwin SA; Klintsova AY; Spencer CM; Brazelton AD; et al. Fragile X mental retardation protein is translated near synapses in response to neurotransmitter activation | 102 | 192 |
| 1705 | 10 | 29 | 1705 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(10):5401-5404 Comery TA; Harris JB; Willems PJ; Oostra BA; Irwin SA; et al. Abnormal dendritic spines in fragile X knockout mice: Maturation and pruning deficits | 125 | 220 |
| 1706 | 23 | 44 | 1706 1997 PSYCHIATRIC GENETICS 7(3):115-119 ODwyer J; Holmes J; Mueller R; Taylor G The prevalence of Fragile-X syndrome in an institution for people with learning disability | 1 | 3 |
| 1707 | 2 | 54 | 1707 1997 PSYCHIATRY RESEARCH-NEUROIMAGING 75(1):31-48 Kates WR; Abrams MT; Kaufmann WE; Breiter SN; Reiss AL Reliability and validity of MRI measurement of the amygdala and hippocampus in children with fragile X syndrome | 20 | 63 |
| 1708 | 31 | 49 | 1708 1997 REVISTA DE NEUROLOGIA 25(143):1068-1071 EstevezGonzalez A; Roig C; Piles S; Pineda M; GarciaSanchez C Fragile-X syndrome and mental retardation | 1 | 1 |
| 1709 | 4 | 10 | 1709 1997 SOUTH AFRICAN MEDICAL JOURNAL 87(4):418-420 Goldman A; Krause A; Jenkins T Fragile X syndrome occurs in the South African black population | 2 | 4 |
| 1710 | 76 | 123 | 1710 1997 WESTERN JOURNAL OF MEDICINE 166(2):129-137 Hagerman RJ Fragile X syndrome - Molecular and clinical insights and treatment issues | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1711 | 8 | 22 | 1711 1997 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 97(8):33-37 Gorbachevskaya NL; Denisova LV Bioelectric brain activity in patients with syndrome of fragile X-chromosome and in their mothers | 0 | 1 |
| 1712 | 28 | 42 | 1712 1998 AMERICAN JOURNAL OF HUMAN GENETICS 63(3):776-785 Ashley-Koch AE; Robinson H; Glicksman AE; Nolin SL; Schwartz CE; et al. Examination of factors associated with instability of the FMR1 CGG repeat | 15 | 22 |
| 1713 | 24 | 39 | 1713 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 75(3):277-282 Jara L; Aspillaga M; Avendano I; Obreque V; Blanco R; et al. Distribution of (CGG)n and FMR-1 associated microsatellite alleles in a normal Chilean population | 6 | 7 |
| 1714 | 1 | 1 | 1714 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 78(4):397-399 Ritchie RJ; Chakrabarti L; Knight SJL; Harding RM; Davies KE Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28. (vol 73, pg 463, 1997) | 0 | 0 |
| 1715 | 22 | 33 | 1715 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 79(3):200-204 Bonaventure G; Torrado M; Barreiro C; Chertkoff L Fragile X founder effects in Argentina | 0 | 4 |
| 1716 | 0 | 0 | 1716 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 81(6):452-453 Oostra BA Fragile X syndrome is caused by a fragile gene. | 0 | 0 |
| 1717 | 0 | 0 | 1717 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 81(6):552-552 von Gontard A; Backes M; Schreck J; Genc B; Doerfler W Behavioural phenotype of the fragile-X-syndrome. | 0 | 0 |
| 1718 | 0 | 0 | 1718 1998 AMERICAN JOURNAL OF PATHOLOGY 153(5):1651-1651 Wages J; Bloch W; Burman R; Popovich B; Kruckeberg KE; et al. Size accuracy in a fragile X size-polymorphism assay | 0 | 0 |
| 1719 | 13 | 23 | 1719 1998 AMERICAN JOURNAL ON MENTAL RETARDATION 103(1):29-39 Bailey DB; Hatton DD; Skinner M Early developmental trajectories of males with fragile X syndrome | 30 | 32 |
| 1720 | 20 | 30 | 1720 1998 ANNALS OF HUMAN GENETICS 62:337-347 Huggins RM; Loesch DZ; Sherman SL A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1721 | 2 | 5 | 1721 1998 ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE 152(1):89-90 Tsuchiya KD; Forsythe M; Robin NH; Tunnessen WW Picture of the month - Fragile X syndrome | 0 | 0 |
| 1722 | 14 | 24 | 1722 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):9-17 Felix TM; De Pina-Neto JM Fragile X syndrome - Clinical and cytogenetic studies | 0 | 0 |
| 1723 | 12 | 30 | 1723 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):18-23 Guerreiro MM; Camargo EE; Kato M; Marques-De-Faria AP; Ciasca SM; et al. Fragile X syndrome - Clinical, electroencephalographic and neuroimaging characteristics | 8 | 14 |
| 1724 | 0 | 0 | 1724 1998 BIOPHYSICAL JOURNAL 74(2):A333-A333 Sinden RR; Pearson CE; Chastain PD; Potaman VN; Levene SD Unusual helical properties and alternative structures of CTG and CGG repeats. | 0 | 0 |
| 1725 | 15 | 21 | 1725 1998 CLINICAL CHEMISTRY AND LABORATORY MEDICINE 36(8):649-653 Poon PMK; Chen QL; Lai KYC; Wong CK; Pang CP CGG repeat interruptions in the FMR1 gene in patients with infantile autism | 0 | 2 |
| 1726 | 12 | 28 | 1726 1998 CLINICAL GENETICS 53(3):179-183 Chan SY; Wong V DNA diagnosis of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders and fragile X syndrome | 2 | 5 |
| 1727 | 8 | 10 | 1727 1998 CLINICAL GENETICS 53(3):200-201 Mornet E; Chateau C; Simon-Bouy B; Serre JL The intermediate alleles of the fragile X CGG repeat in patients with mental retardation | 3 | 7 |
| 1728 | 19 | 30 | 1728 1998 CLINICAL GENETICS 54(4):309-314 Russo S; Briscioli V; Cogliati F; Macchi M; Lalatta F; et al. An unusual fragile X sibship: female compound heterozygote and male with a partially methylated full mutation | 0 | 1 |
| 1729 | 0 | 2 | 1729 1998 CLINICAL GENETICS 54(4):365-365 Toro-Sola MA Fragile X and Rett syndromes in Puerto Rico | 0 | 0 |
| 1730 | 7 | 12 | 1730 1998 CLINICAL GENETICS 54(4):366-367 Vatta S; Cigui I; Demori E; Morgutti M; Pecile V; et al. Fragile X syndrome, mental retardation and macroorchidism | 3 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1731 | 31 | 107 | 1731 1998 CURRENT OPINION IN GENETICS & DEVELOPMENT 8(2):245-253 Tapscott SJ; Klesert TR; Widrow RJ; Stoger R; Laird CD Fragile-X syndrome and myotonic dystrophy: parallels and paradoxes | 1 | 10 |
| 1732 | 12 | 14 | 1732 1998 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 40(1):62-64 Gringras P; Barnicoat A Retesting for fragile X syndrome in cytogenetically normal males | 1 | 3 |
| 1733 | 8 | 26 | 1733 1998 EPIGENETICS 214:280-290 Laird; Pillus; Hirst; Bestor; Jaenisch; et al. Rules of DNA methylation in humans inferred from the fragile X gene, FMR1 - Final general discussion | 0 | 0 |
| 1734 | 0 | 0 | 1734 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:44-44 Tamanini F; van Unen L; Bontekoe C; Bakker; Willemsen R; et al. Oligomerization and intracellular transport of the Fragile X Mental Retardation Protein | 0 | 0 |
| 1735 | 0 | 0 | 1735 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:63-63 Weinhausel A; Skarits C; Wolschek M; Haas OA Diagnostic evaluation of the fragile X syndrome with methylation-sensitive PCR (MS-PCR) | 0 | 0 |
| 1736 | 0 | 0 | 1736 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:103-103 Syrrou M; Yapijakis C; Bouba I; Georgiou I; Patsalis PC; et al. Intra-population variation of CAG and CGG trinucleotide repeats in X-linked androgen receptor and FMR-1 genes in the Hellenic population | 0 | 0 |
| 1737 | 0 | 0 | 1737 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:107-107 Peixoto A; Santos R; Seruca R; Amorim A; Castedo S Haplotype analysis in fragile X and normal Portuguese populations | 0 | 0 |
| 1738 | 0 | 0 | 1738 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:116-116 Duran M; Valverde L; Molina M; Onaindia ML; Tejada MI Carrier screening for fragile X by PCR in females: comparison with obligated carriers | 0 | 0 |
| 1739 | 0 | 0 | 1739 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:144-144 Patsalis P; Sismani C; Hettinger JA; Boumba I; Georgiou I; et al. Population-based molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes: incidence, genetic variation and stability | 0 | 0 |
| 1740 | 0 | 0 | 1740 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:159-159 Strelnikov V; Nemstova M; Demina N; Galkina V; Kuleshov N; et al. DNA testing for fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1741 | 23 | 30 | 1741 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6(5):518-522 Peixoto A; dos Santos MR; Seruca R; Amorim A; Castedo S Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype | 2 | 2 |
| 1742 | 0 | 0 | 1742 1998 EUROPEAN JOURNAL OF NEUROSCIENCE 10:429-429 Castren M; Haapasalo AK; Oostra BE; Castren E Subcellular localization of FMRP and its mutated form I304N in PC12 cells and rat hippocampal neurons | 0 | 0 |
| 1743 | 0 | 0 | 1743 1998 FASEB JOURNAL 12(8):A1322-A1322 Warren ST The molecular basis of Fragile X syndrome | 0 | 0 |
| 1744 | 0 | 10 | 1744 1998 GENERAL HOSPITAL PSYCHIATRY 20(2):126-127 Silva JA; Ferrari MM; Leong GB Erotomania in a case of fragile-X syndrome | 0 | 1 |
| 1745 | 0 | 28 | 1745 1998 GENOMICS 47(3):414-418 Albanese V; Holbert S; Saada C; Meier-Ewert S; Lebre AS; et al. CAG/CTG and CGG/GCC repeats in human brain reference cDNAs: Outcome in searching for new dynamic mutations | 0 | 7 |
| 1746 | 23 | 62 | 1746 1998 GENOMICS 50(2):229-240 Lavedan C; Grabczyk E; Usdin K; Nussbaum RL Long uninterrupted CGG repeats within the first exon of the human FMR1 gene are not intrinsically unstable in transgenic mice | 17 | 21 |
| 1747 | 4 | 7 | 1747 1998 HUMAN GENETICS 102(1):54-56 Storm K; Handig I; Reyniers E; Oostra BA; Kooy RF; et al. Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome | 1 | 1 |
| 1748 | 23 | 41 | 1748 1998 HUMAN GENETICS 102(4):440-445 Gronskov K; Hallberg A; Brondum-Nielsen K Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations | 4 | 8 |
| 1749 | 0 | 0 | 1749 1998 HUMAN GENETICS 103(3):366-366 Gronskov K; Brondum-Nielsen K Regarding the letter from Dr. Stephen T. Warren of the Emory University School of Medicine concerning our article "Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations" | 0 | 0 |
| 1750 | 21 | 29 | 1750 1998 HUMAN HEREDITY 48(5):256-265 Hecimovic S; Barisic I; Pavelic K DNA analysis of the fragile X syndrome in an at risk pediatric population in Croatia: Simple clinical preselection criteria can considerably improve the cost-effectiveness of fragile X screening studies | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1751 | 14 | 28 | 1751 1998 HUMAN MOLECULAR GENETICS 7(1):109-113 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the FMR1 gene involved in fragile X syndrome | 23 | 50 |
| 1752 | 20 | 35 | 1752 1998 HUMAN MOLECULAR GENETICS 7(12):1935-1946 Gunter C; Paradee W; Crawford DC; Meadows KA; Newman J; et al. Re-examination of factors associated with expansion of CGG repeats using a single nucleotide polymorphism in FMR1 | 14 | 26 |
| 1753 | 14 | 29 | 1753 1998 HUMAN MOLECULAR GENETICS 7(13):2121-2128 Khandjian EW; Bardoni B; Corbin F; Sittler A; Giroux S; et al. Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis | 24 | 33 |
| 1754 | 2 | 4 | 1754 1998 HUMAN MUTATION 12(6):431-431 Vincent JB; Gurling HMD Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome | 3 | 5 |
| 1755 | 0 | 0 | 1755 1998 HUMAN MUTATION 12(6):432-432 Wang YC; Li SY Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome - Response | 0 | 1 |
| 1756 | 19 | 36 | 1756 1998 HUMAN REPRODUCTION 13(5):1184-1187 Conway GS; Payne NN; Webb J; Murray A; Jacobs PA Fragile X premutation screening in women with premature ovarian failure | 9 | 33 |
| 1757 | 14 | 22 | 1757 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 107:29-36 Baskaran S; Naseerullah MK; Manjunatha KR; Chetan GK; Arthi R; et al. Triplet repeat polymorphism & fragile X syndrome in the Indian context | 3 | 6 |
| 1758 | 14 | 26 | 1758 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 108:12-16 Jain U; Verma IC; Kapoor AK Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India | 3 | 4 |
| 1759 | 13 | 42 | 1759 1998 JOURNAL OF APPLIED RESEARCH IN INTELLECTUAL DISABILITIES 11(3):175-191 Turk J Fragile X syndrome and attentional deficits | 12 | 17 |
| 1760 | 10 | 39 | 1760 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(4):321-328 Mazzocco MMM; Pulsifer M; Fiumara A; Cocuzza M; Nigro F; et al. Brief report: Autistic behaviors among children with fragile X or Rett syndrome: Implications for the classification of pervasive developmental disorder | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1761 | 53 | 104 | 1761 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(5):393-405 Feinstein C; Reiss AL Autism: The point of view from fragile X studies | 18 | 45 |
| 1762 | 17 | 28 | 1762 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):499-508 Bailey DB; Mesibov GB; Hatton DD; Clark RD; Roberts JE; et al. Autistic behavior in young boys with fragile X syndrome | 31 | 40 |
| 1763 | 12 | 36 | 1763 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):509-517 Mazzocco MMM; Baumgardner T; Freund LS; Reiss AL Social functioning among girls with fragile X or Turner syndrome and their sisters | 11 | 15 |
| 1764 | 12 | 37 | 1764 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(25):15521-15527 Brown V; Small K; Lakkis L; Feng Y; Gunter C; et al. Purified recombinant Fmrp exhibits selective RNA binding as an intrinsic property of the fragile X mental retardation protein | 45 | 69 |
| 1765 | 6 | 30 | 1765 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(27):17122-17127 Bolivar J; Guelman S; Iglesias C; Ortiz M; Valdivia MM The fragile-X-related gene FXR1 is a human autoantigen processed during apoptosis | 3 | 7 |
| 1766 | 4 | 66 | 1766 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(41):26998-27008 Parsons MA; Sinden RR; Izban MG Transcriptional properties of RNA polymerase II within triplet repeat-containing DNA from the human myotonic dystrophy and fragile X loci | 0 | 14 |
| 1767 | 1 | 38 | 1767 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(46):30466-30471 Mangel L; Ternes T; Schmitz B; Doerfler W New 5 '-(CGG)(n)-3 ' repeats in the human genome | 3 | 5 |
| 1768 | 11 | 33 | 1768 1998 JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS 15(4):745-756 Chen X; Mariappan SVS; Moyzis RK; Bradbury EM; Gupta G Hairpin induced slippage and hyper-methylation of the fragile X DNA triplets | 4 | 16 |
| 1769 | 7 | 40 | 1769 1998 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 39(5):699-710 van Lieshout CFM; De Meyer RE; Curfs LMG; Fryns JP Family contexts, parental behaviour, and personality profiles of children and adolescents with Prader-Willi, fragile-X, or Williams syndrome | 4 | 16 |
| 1770 | 50 | 75 | 1770 1998 JOURNAL OF CLINICAL LIGAND ASSAY 21(4):424-431 Feldman GL; Monaghan KG Fragile X syndrome: A review of the molecular and clinical features | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1771 | 0 | 0 | 1771 1998 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 19(5):381-381 Taylor RJ; Scharfenaker S; O'Connor R; Lampe M; Kovach T; et al. Severe language impairment in fragile X syndrome: Clinical correlates and treatment approaches | 0 | 0 |
| 1772 | 0 | 29 | 1772 1998 JOURNAL OF EXPERIMENTAL MEDICINE 188(12):2335-2342 Sun SQ; Zhang XH; Tough DF; Sprent J Type I interferon-mediated stimulation of T cells by CgG DNA | 0 | 135 |
| 1773 | 24 | 41 | 1773 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:81-89 Elbaz A; Suedois J; Duquesnoy M; Beldjord C; Berchel C; et al. Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies | 6 | 8 |
| 1774 | 17 | 41 | 1774 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:490-499 Turk J; Cornish K Face recognition and emotion perception in boys with fragile-X syndrome | 12 | 18 |
| 1775 | 3 | 35 | 1775 1998 JOURNAL OF INTERFERON AND CYTOKINE RESEARCH 18(8):609-616 Xu Z; Williams BRG Genomic features of human PKR: Alternative splicing and a polymorphic CGG repeat in the 5 '-untranslated region | 0 | 5 |
| 1776 | 0 | 0 | 1776 1998 JOURNAL OF INVESTIGATIVE MEDICINE 46(1):87A-87A Miller LJ; McIntosh D; McGrath J; Shyu V; Lampe M; et al. Electrodermal responses to sensory stimuli in individuals with fragile X sydrome. | 0 | 0 |
| 1777 | 0 | 33 | 1777 1998 JOURNAL OF LUMINESCENCE 79(1):1-8 Padlyak BV; Koepke C; Wisniewski K; Grinberg M; Gutsze A; et al. Spectroscopic evaluation of the CGG (CaO-Ga2O3-GeO2) glass doped with chromium | 0 | 3 |
| 1778 | 27 | 51 | 1778 1998 JOURNAL OF MEDICAL GENETICS 35(2):103-111 Wohrle D; Salat U; Glaser D; Mucke J; Meisel-Stosiek M; et al. Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats | 19 | 32 |
| 1779 | 140 | 197 | 1779 1998 JOURNAL OF MEDICAL GENETICS 35(7):579-589 de Vries BBA; Halley DJJ; Oostra BA; Niermeijer MF The fragile X syndrome | 32 | 52 |
| 1780 | 5 | 8 | 1780 1998 JOURNAL OF MEDICAL GENETICS 35(10):878-878 Jenkins T; Krause A Molecular evidence that fragile X syndrome occurs in the South African black population | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1781 | 10 | 40 | 1781 1998 JOURNAL OF MOLECULAR BIOLOGY 275(1):3-16 Darlow JM; Leach DRF Secondary structures in d(CGG) and d(CCG) repeat tracts | 8 | 44 |
| 1782 | 7 | 29 | 1782 1998 JOURNAL OF MOLECULAR BIOLOGY 275(1):17-23 Darlow JM; Leach DRF Evidence for two preferred hairpin folding patterns in d(CGG).d(CCG) repeat tracts in vivo | 3 | 21 |
| 1783 | 8 | 39 | 1783 1998 JOURNAL OF MOLECULAR BIOLOGY 283(1):111-120 Mariappan SVS; Silks LA; Bradbury EM; Gupta G Fragile X DNA triplet repeats, (GCC)(n), form hairpins with single hydrogen-bonded cytosine center dot cytosine mispairs at the CpG sites: Isotope-edited nuclear magnetic resonance spectroscopy on (GCC)(n) with selective (15)N4-labeled cytosine bases | 4 | 18 |
| 1784 | 17 | 40 | 1784 1998 JOURNAL OF NEUROSCIENCE RESEARCH 51(1):41-48 Berry-Kravis E; Ciurlionis R Overexpression of fragile X gene (FMR-1) transcripts increases cAMP production in neural cells | 1 | 1 |
| 1785 | 20 | 36 | 1785 1998 JOURNAL OF PEDIATRICS 133(3):363-365 Meyer GA; Blum NJ; Hitchcock W; Fortina P Absence of the fragile X CGG trinucleotide repeat expansion in girls diagnosed with a pervasive developmental disorder | 0 | 3 |
| 1786 | 2 | 88 | 1786 1998 MEDICAL HYPOTHESES 51(3):223-233 Fischer KM Expanded (CAG)(n), (CGG)(n) and (GAA)(n) trinucleotide repeat microsatellites, and mutant purine synthesis and pigmentation genes cause schizophrenia and autism | 0 | 2 |
| 1787 | 0 | 0 | 1787 1998 MOLECULAR BIOLOGY OF THE CELL 9:185A-185A Lichtenstein H; Tartakoff A Nuclear export of the Fragile X gene product, FMRP | 0 | 0 |
| 1788 | 1 | 1 | 1788 1998 MOLECULAR DIAGNOSIS 3(4):249-249 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in Fragile X syndrome (vol 2, pg 259, 1997) | 0 | 0 |
| 1789 | 18 | 63 | 1789 1998 NEUROLOGY 50(1):121-130 Mostofsky SH; Mazzocco MMM; Aakalu G; Warsofsky IS; Denckla MB; et al. Decreased cerebellar posterior vermis size in fragile X syndrome - Correlation with neurocognitive performance | 21 | 48 |
| 1790 | 0 | 0 | 1790 1998 NEUROLOGY 50(4):A86-A86 Mostofsky SH; Reiss AL; Freund L Examination of posterior vermis size in young males with fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1791 | 17 | 36 | 1791 1998 NEUROPSYCHOLOGIA 36(11):1239-1246 Cornish KM; Munir F; Cross G The nature of the spatial deficit in young females with Fragile-X syndrome: A neuropsychological and molecular perspective | 12 | 16 |
| 1792 | 6 | 11 | 1792 1998 NEUROREPORT 9(3):477-481 Steward O; Bakker CE; Willems PJ; Oostra BA No evidence for disruption of normal patterns of mRNA localization in dendrites or dendritic transport of recently synthesized mRNA in FMR1 knockout mice, a model for human fragile-X mental retardation syndrome | 12 | 18 |
| 1793 | 0 | 26 | 1793 1998 NUCLEIC ACIDS RESEARCH 26(12):3001-3005 Dutta R; Gao YG; Priebe W; Wang AHJ Binding of the modified daunorubicin WP401 adjacent to a T-G base pair induces the reverse Watson-Crick conformation: crystal structures of the WP401-TGGCCG and WP401-CGG[br(5)C]CG complexes | 0 | 5 |
| 1794 | 19 | 33 | 1794 1998 OPTOMETRY AND VISION SCIENCE 75(12):856-859 Kranjc BS; Brezigar A; Peterlin B Bilateral macular dysplasia in fragile X syndrome | 0 | 0 |
| 1795 | 30 | 41 | 1795 1998 REVISTA MEDICA DE CHILE 126(8):911-918 Jara L; Lopez M; Mellado C; Aspillaga M; Avendano I; et al. Clinical and metabolic screening for fragile X syndrome in 300 patients with unspecific mental retardation | 1 | 1 |
| 1796 | 10 | 25 | 1796 1998 REVISTA MEDICA DE CHILE 126(12):1447-1454 Aspillaga M; Jara L; Avendano I; Lopez M Fragile X syndrome. Clinical analysis of 300 Chilean patients with unspecific mental retardation | 1 | 1 |
| 1797 | 2 | 13 | 1797 1998 STEROIDS 63(1):2-4 Joseph DR The rat androgen-binding protein (ABP/SHBG) gene contains triplet repeats similar to unstable triplets: Evidence that the ABP/SHBG and the fragile X-related 2 genes overlap | 0 | 9 |
| 1798 | 71 | 143 | 1798 1998 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 98(9):54-63 Vorsanova SG; Vekhova NV; Demidova IA; Yurov YB Syndrome of mental retardation, linked with fragile X-chromosome: problems of diagnostics and inheritance | 0 | 0 |
| 1799 | 15 | 24 | 1799 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(1):98-103 Willemsen R; Anar B; Otero YD; de Vries BBA; Hilhorst-Hofstee Y; et al. Noninvasive test for fragile X syndrome, using hair root analysis | 22 | 24 |
| 1800 | 27 | 52 | 1800 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(3):680-688 Nolin SL; Houck GE; Gargano AD; Blumstein H; Dobkin CS; et al. FMR1 CCG-repeat instability by single sperm and lymphocytes of fragile-X premutation males | 8 | 15 |