| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2647,
Authors: 5321,
Journals: 428,
Outer References: 16458,
Words: 3536
Collection span: 1967 - 2005
View: Overview. Sorted by first author.
Page 1: 1 2 3 4 5 6 7 8 9
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 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 |
| 2 | 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 |
| 3 | 0 | 0 | 2548 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:324-324 Abbeduto L; Murphy MM Language, communication, and the behavioural phenotype of Down syndrome (DS): Insights from fragile X syndrome (FXS) and typical development | 0 | 0 |
| 4 | 15 | 39 | 2385 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; et al. Receptive language skills of adolescents and young adults with Down or fragile X syndrome | 2 | 5 |
| 5 | 0 | 0 | 2549 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:325-325 Abbeduto L; Murphy MM; Giles N; Bruno L; Richmond EK; et al. Understanding language in context: Comparisons of Down syndrome (DS) with fragile X syndrome and typical development | 0 | 0 |
| 6 | 14 | 79 | 2496 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):237-254 Abbeduto L; Seltzer MM; Shattuck P; Krauss MW; Orsmond G; et al. Psychological well-being and coping in mothers of youths with autism, Down syndrome, or fragile X syndrome | 0 | 1 |
| 7 | 0 | 0 | 1088 1993 BIOLOGICAL PSYCHIATRY 33(6A):A161-A161 ABRAMS M; FREUND L; REISS AL MOLECULAR PREDICTORS OF COGNITIVE FUNCTION IN FRAGILE X-SYNDROME | 0 | 0 |
| 8 | 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 |
| 9 | 32 | 75 | 1359 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):187-198 Abrams MT; Reiss AL Quantitative brain imaging studies of fragile X syndrome | 2 | 3 |
| 10 | 31 | 61 | 1177 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):317-327 ABRAMS MT; REISS AL; FREUND LS; BAUMGARDNER TL; CHASE GA; et al. MOLECULAR-NEUROBEHAVIORAL ASSOCIATIONS IN FEMALES WITH THE FRAGILE-X FULL MUTATION | 50 | 67 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 11 | 4 | 17 | 319 1986 AMERICAN JOURNAL OF HUMAN GENETICS 38(4):533-539 ABRUZZO MA; HUNT PA; MAYER M; JACOBS PA; WANG JCC; et al. A COMPARISON OF FRAGILE X-EXPRESSION IN LYMPHOCYTE AND LYMPHOBLASTOID CULTURES | 2 | 3 |
| 12 | 6 | 17 | 242 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(1):193-198 ABRUZZO MA; MAYER M; JACOBS PA THE EFFECT OF METHIONINE AND 5-AZACYTIDINE ON FRAGILE-X EXPRESSION | 3 | 5 |
| 13 | 3 | 15 | 389 1986 HUMAN GENETICS 73(1):20-22 ABRUZZO MA; PETTAY D; MAYER M; JACOBS PA THE EFFECT OF CAFFEINE ON FRAGILE-X EXPRESSION | 9 | 12 |
| 14 | 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 |
| 15 | 4 | 11 | 269 1985 CLINICAL GENETICS 28(2):97-99 ABUELO D; CASTREE K; PUESCHEL S; PADREMENDOZA T; ZOLNIERZ K FREQUENCY OF FRAGILE X-CHROMOSOME IN NORMAL FEMALES | 2 | 5 |
| 16 | 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 |
| 17 | 27 | 40 | 2399 2003 BIOCHEMISTRY 42(35):10437-10444 Adinolfi S; Ramos A; Martin SR; Dal Piaz F; Pucci P; et al. The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding | 6 | 7 |
| 18 | 3 | 7 | 2423 2003 GENETIC TESTING 7(4):345-346 Adir V; Shahak E; Dar H; Borochowitz ZU Detection of X chromosome aneuploidy using Southern blot analysis during routine population-based screening for Fragile X syndrome | 0 | 0 |
| 19 | 0 | 0 | 2266 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Afifi HH; Abdel-Aleem AK; Shaheen OO Fragile X syndrome: clinical and behavioral study. | 0 | 0 |
| 20 | 0 | 22 | 2345 2002 SCHIZOPHRENIA RESEARCH 58(1):37-41 Akahane A; Kunugi H; Tanaka H; Nanko S Association analysis of polymorphic CGG repeat in 5 ' UTR of the reelin and VLDLR genes with schizophrenia | 0 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 21 | 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 |
| 22 | 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 |
| 23 | 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 |
| 24 | 8 | 22 | 1173 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):294-297 ALBRIGHT SG; LACHIEWICZ AM; TARLETON JC; RAO KW; SCHWARTZ CE; et al. FRAGILE-X PHENOTYPE IN A PATIENT WITH A LARGE DE-NOVO DELETION IN XQ27-Q28 | 10 | 17 |
| 25 | 2 | 9 | 1390 1995 GENETIC COUNSELING 6(3):207-210 ALEMBIK Y; DOTT B; STOLL C RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME | 1 | 6 |
| 26 | 11 | 17 | 2181 2001 MEDICAL PRINCIPLES AND PRACTICE 10(2):73-78 Alkhalaf M; Verghese L; Mushtaq SK Cytogenetic and immunohistochemical characterization of fragile X syndrome in a Kuwaiti family: Rapid antibody test for the diagnosis of mental retardation patients | 0 | 0 |
| 27 | 0 | 0 | 2351 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Allen E; Letz R; Sherman S Association of FMR1 CGG repeat size, X-inactivation ratio and transcript level with cognitive performance among women. | 0 | 0 |
| 28 | 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 |
| 29 | 14 | 24 | 1483 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):329-333 AllinghamHawkins DJ; Brown CA; Babul R; Chitayat D; Krekewich K; et al. Tissue-specific methylation differences and cognitive function in fragile X premutation females | 8 | 13 |
| 30 | 0 | 15 | 454 1987 HUMAN GENETICS 75(1):4-6 AMAROSE AP; HUTTENLOCHER PR; SPRUDZS RM; LAITSCH TJ; PETTENATI MJ A HERITABLE FRAGILE 12Q24.13 SEGREGATING IN A FAMILY WITH THE FRAGILE X-CHROMOSOME | 2 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 31 | 12 | 18 | 2622 2005 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 132A(2):210-214 Angeli CB; Capelli LP; Auricchio MTBM; Vianna-Morgante AM; Mingroni-Netto RC; et al. AGG interspersion patterns in the CGG repeat of the FMR1 gene and linked DXS548/FRAXAC1 haplotypes in Brazilian populations | 0 | 0 |
| 32 | 12 | 37 | 2559 2004 JOURNAL OF NEUROSCIENCE 24(11):2648-2655 Antar LN; Afroz R; Dictenberg JB; Carroll RC; Bassell GJ Metabotropic glutamate receptor activation regulates Fragile X mental retardation protein and Fmr1 mRNA localization differentially in dendrites and at synapses | 10 | 15 |
| 33 | 13 | 26 | 2461 2003 NEURON 37(4):555-558 Antar LN; Bassell GJ Sunrise at the synapse: The FMRP mRNP shaping the synaptic interface | 11 | 25 |
| 34 | 14 | 20 | 1441 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(1):237-239 Antinolo G; Borrego S; Cabeza JC; Sanchez R; Sanchez J; et al. Reverse mutation in fragile X syndrome | 9 | 11 |
| 35 | 7 | 21 | 578 1988 CLINICAL GENETICS 34(4):265-271 ANVRET M; GILLBERG C; WAHLSTROM J; ALBERTSSONWIKLAND K; DAVIES K INFANTILE-AUTISM, FRAGILE (X) (Q27.3) AND RFLP ANALYSIS IN AN EXTENDED SWEDISH FAMILY | 2 | 4 |
| 36 | 13 | 31 | 2193 2001 PRENATAL DIAGNOSIS 21(6):504-511 Apessos A; Abou-Sleiman PM; Harper JC; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 1 | 16 |
| 37 | 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 |
| 38 | 2 | 7 | 619 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):978-979 ARINAMI T BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME - REPLY | 0 | 0 |
| 39 | 6 | 20 | 1112 1993 HUMAN GENETICS 92(5):431-436 ARINAMI T; ASANO M; KOBAYASHI K; YANAGI H; HAMAGUCHI H DATA ON THE CGG REPEAT AT THE FRAGILE X-SITE IN THE NONRETARDED JAPANESE POPULATION AND FAMILY SUGGEST THE PRESENCE OF A SUBGROUP OF NORMAL ALLELES PREDISPOSING TO MUTATE | 31 | 42 |
| 40 | 4 | 11 | 463 1987 HUMAN GENETICS 77(1):92-94 ARINAMI T; KONDO I; HAMAGUCHI H; TAMURA K; HIRANO T A FRAGILE-X FEMALE WITH DOWN-SYNDROME | 8 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 41 | 4 | 14 | 390 1986 HUMAN GENETICS 73(4):309-312 ARINAMI T; KONDO I; NAKAJIMA S FREQUENCY OF THE FRAGILE X-SYNDROME IN JAPANESE MENTALLY-RETARDED MALES | 25 | 30 |
| 42 | 14 | 26 | 460 1987 HUMAN GENETICS 76(4):344-347 ARINAMI T; KONDO I; NAKAJIMA S; HAMAGUCHI H FREQUENCY OF THE FRAGILE X-SYNDROME IN INSTITUTIONALIZED MENTALLY-RETARDED FEMALES IN JAPAN | 7 | 9 |
| 43 | 0 | 0 | 468 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):170-171 ARINAMI T; NAKAJIMA S; KONDO I THE FRAGILE X-SYNDROME IN A JAPANESE POPULATION OF INSTITUTIONALIZED MENTALLY-RETARDED FEMALES | 0 | 0 |
| 44 | 0 | 0 | 595 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):224-224 ARINAMI T; SATO M; KONDO I AUDITORY BRAIN-STEM RESPONSES IN THE FRAGILE-X SYNDROME | 0 | 0 |
| 45 | 10 | 24 | 501 1988 AMERICAN JOURNAL OF HUMAN GENETICS 43(1):46-51 ARINAMI T; SATO M; NAKAJIMA S; KONDO I AUDITORY BRAIN-STEM RESPONSES IN THE FRAGILE-X SYNDROME | 8 | 11 |
| 46 | 0 | 0 | 392 1986 JAPANESE JOURNAL OF HUMAN GENETICS 31(2):150-150 ARINAMI T; TAKANAWA S; KONDO I THE FRAGILE X-SYNDROME IN A JAPANESE POPULATION OF INSTITUTIONALIZED MENTALLY-RETARDED MALES | 0 | 0 |
| 47 | 0 | 0 | 470 1987 JAPANESE JOURNAL OF HUMAN GENETICS 32(2):210-211 ARINAMI T; TAMURA K; KONDO I A FRAGILE X-FEMALE WITH DOWN-SYNDROME - A CASE-REPORT | 0 | 0 |
| 48 | 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 |
| 49 | 34 | 43 | 2427 2003 HUMAN GENETICS 113(5):371-376 Arocena DG; Breece KE; Hagerman PJ Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population | 1 | 2 |
| 50 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 51 | 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 |
| 52 | 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 |
| 53 | 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 |
| 54 | 28 | 41 | 2425 2003 HEREDITY 90(3):206-211 Arrieta I; Penagarikano O; Tele M; Ortega B; Flores P; et al. The FMR1 CGG repeat and linked microsatellite markers in two Basque valleys | 0 | 0 |
| 55 | 15 | 42 | 2204 2001 REVISTA DE NEUROLOGIA 33:S41-S50 Artigas-Pallares J; Brun-Gasca C Medical treatment of fragile X syndrome | 0 | 0 |
| 56 | 2 | 7 | 2618 2004 REVISTA DE NEUROLOGIA 38(1):7-11 Artigas-Pallares J; Brun-Gasca C Can the behavioural phenotype of Fragile X syndrome be attributed to mental retardation and to attention deficit hyperactivity disorder? | 0 | 0 |
| 57 | 12 | 30 | 500 1988 AMERICAN JOURNAL OF HUMAN GENETICS 42(2):380-389 ARVEILER B; OBERLE I; VINCENT A; HOFKER MH; PEARSON PL; et al. GENETIC-MAPPING OF THE XQ27-Q28 REGION - NEW RFLP MARKERS USEFUL FOR DIAGNOSTIC APPLICATIONS IN FRAGILE-X AND HEMOPHILIA-B FAMILIES | 22 | 61 |
| 58 | 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 |
| 59 | 29 | 46 | 2646 2005 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 102(6):2180-2185 Aschrafi A; Cunningham BA; Edelman GM; Vanderklish PW The fragile X mental retardation protein and group I metabotropic glutamate receptors regulate levels of mRNA granules in brain | 0 | 0 |
| 60 | 1 | 1 | 1301 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):906-906 ASHLEY AE; MEADOWS KL; SHERMAN SL TRANSMISSION CHARACTERISTICS OF THE FMR-1 MUTATION IN THE COLLABORATIVE PROSPECTIVE-STUDY OF THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 61 | 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 |
| 62 | 27 | 42 | 1324 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1414-1425 ASHLEY AE; SHERMAN SL POPULATION-DYNAMICS OF A MEIOTIC MITOTIC EXPANSION MODEL FOR THE FRAGILE-X SYNDROME | 18 | 20 |
| 63 | 10 | 32 | 1155 1993 NATURE GENETICS 4(3):244-251 ASHLEY CT; SUTCLIFFE JS; KUNST CB; LEINER HA; EICHLER EE; et al. HUMAN AND MURINE FMR-1 - ALTERNATIVE SPLICING AND TRANSLATIONAL INITIATION DOWNSTREAM OF THE CGG-REPEAT | 74 | 120 |
| 64 | 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 |
| 65 | 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 |
| 66 | 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 |
| 67 | 5 | 25 | 213 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(2):197-204 AUGUST GJ; LOCKHART LH FAMILIAL AUTISM AND THE FRAGILE-X-CHROMOSOME | 10 | 21 |
| 68 | 20 | 46 | 2383 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 121B(1):119-127 Aziz M; Stathopulu E; Callias M; Taylor C; Turk J; et al. Clinical features of boys with fragile X premutations and intermediate alleles | 0 | 8 |
| 69 | 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 |
| 70 | 35 | 66 | 2320 2002 MONATSSCHRIFT KINDERHEILKUNDE 150(12):1486-+ Backes M; von Gontard A Behavioural phenotype of fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 71 | 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 |
| 72 | 8 | 71 | 2166 2001 JOURNAL OF BIOLOGICAL CHEMISTRY 276(21):18605-18613 Bacolla A; Pradhan S; Larson JE; Roberts RJ; Wells RD Recombinant human DNA (cytosine-5) methyltransferase - III. Allosteric control, reaction order, and influence of plasmid topology and triplet repeat length on methylation of the fragile X CGG center dot CCG sequence | 0 | 15 |
| 73 | 25 | 50 | 1125 1993 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 34(5):673-688 BAILEY A; BOLTON P; BUTLER L; LECOUTEUR A; MURPHY M; et al. PREVALENCE OF THE FRAGILE-X ANOMALY AMONGST AUTISTIC TWINS AND SINGLETONS | 11 | 50 |
| 74 | 16 | 48 | 2567 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):3-10 Bailey DB Newborn screening for fragile X syndrome | 0 | 1 |
| 75 | 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 |
| 76 | 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 |
| 77 | 16 | 33 | 2163 2001 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 31(2):165-174 Bailey DB; Hatton DD; Skinner M; Mesibov G Autistic behavior, FMR1 protein, and developmental trajectories in young males with fragile X syndrome | 16 | 22 |
| 78 | 17 | 37 | 2121 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 | 16 | 15 |
| 79 | 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 |
| 80 | 19 | 31 | 2162 2001 INFANTS AND YOUNG CHILDREN 14(1):24-33 Bailey DB; Roberts JE; Mirrett P; Hatton DD Identifying infants and toddlers with fragile X syndrome: Issues and recommendations | 6 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 81 | 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 |
| 82 | 8 | 36 | 2470 2003 PEDIATRICS 111(2):407-416 Bailey DB; Skinner D; Sparkman KL Discovering fragile X syndrome: Family experiences and perceptions | 5 | 6 |
| 83 | 0 | 0 | 315 1986 ACTA NEUROLOGICA SCANDINAVICA 73(4):447-448 BAKKE JV FRAGILE-X SYNDROME AS A CONCOMITANT TO AND PROBABLE CAUSE OF MENTAL-RETARDATION | 0 | 0 |
| 84 | 0 | 0 | 1310 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1359-1359 BAKKER C; DEGRAAFF E; ZHONG N; WILLEMSEN R; OOSTRA B INSTABILITY OF THE CGG REPEAT AND EXPRESSION OF FMR1 PROTEIN IN A MALE-PATIENT WITH A LUNG-TUMOR | 0 | 0 |
| 85 | 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 |
| 86 | 97 | 168 | 2413 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):111-123 Bakker CE; Oostra BA Understanding fragile X syndrome: insights from animal models | 4 | 5 |
| 87 | 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 |
| 88 | 23 | 52 | 1229 1994 CELL 78(1):23-33 BAKKER CE; VERHEIJ C; WILLEMSEN R; VANDERHELM R; OERLEMANS F; et al. FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION | 96 | 163 |
| 89 | 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 |
| 90 | 36 | 59 | 1423 1995 MEDICINA-BUENOS AIRES 55(5):457-466 BANARES VG UPDATING THE FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 91 | 6 | 8 | 2374 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 116A(1):99-100 Banes SL; Begleiter ML; Butler MG 45,X/46,XY mosaicism and fragile X syndrome | 0 | 0 |
| 92 | 8 | 44 | 2245 2002 AMERICAN JOURNAL OF OCCUPATIONAL THERAPY 56(5):538-546 Baranek GT; Chin YKH; Hess LMG; Yankee JG; Hatton DD; et al. Sensory processing correlates of occupational performance in children with fragile X syndrome: Preliminary findings | 1 | 1 |
| 93 | 13 | 23 | 1107 1993 GENETIKA 29(6):1026-1034 BARANOV VS; ASEEV MV; RAKISHEVA ZB; KULESHOV NP; MARINICHEVA GS; et al. MOLECULAR DIAGNOSIS OF FRAGILE X-SYNDROME (SYN MARTIN-BELL) IN THE PATIENTS OF NATIVE POPULATIONS | 0 | 2 |
| 94 | 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 |
| 95 | 7 | 13 | 251 1985 AMERICAN JOURNAL OF MEDICAL GENETICS 22(2):415-416 BARBI G; STEINBACH P FRAGILE-X AND MARTIN-BELL SYNDROME - NEW SOURCE OF INFORMATION | 1 | 3 |
| 96 | 39 | 53 | 2429 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698 Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; et al. 82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization | 8 | 8 |
| 97 | 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 |
| 98 | 60 | 93 | 2259 2002 CURRENT OPINION IN GENETICS & DEVELOPMENT 12(3):284-293 Bardoni B; Mandel JL Advances in understanding of fragile X pathogenesis and FMRP function, and in identification of X linked mental retardation genes | 31 | 39 |
| 99 | 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 |
| 100 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 101 | 45 | 85 | 2132 2001 BRAIN RESEARCH BULLETIN 56(3-4):375-382 Bardoni B; Schenck A; Mandel JL The Fragile X mental retardation protein | 6 | 9 |
| 102 | 2 | 2 | 2276 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Bardoni B; Schenck A; van de Bor V; Giangrande A; Mandel J Drosophila as a model to study the physiological pathway in which FMRP (Fragile X Mental Retardation Protein) is involved | 0 | 0 |
| 103 | 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 |
| 104 | 28 | 61 | 2420 2003 EXPERIMENTAL CELL RESEARCH 289(1):95-107 Bardoni B; Willemsen R; Weiler IJ; Schenck A; Severijnen LA; et al. NUFIP 1 (nuclear FMRP interacting protein 1) is a nucleocytoplasmic shuttling protein associated with active synaptoneurosome | 6 | 7 |
| 105 | 0 | 10 | 2338 2002 PANMINERVA MEDICA 44(1):7-10 Bargagna S; Canepa G; Tinelli F Social adjustment in children with Down mental retardation (MRD) and Fragile-X mental retardation (MRX) | 0 | 1 |
| 106 | 1 | 15 | 839 1991 ANNALES DE GENETIQUE 34(2):111-114 BARLETTA C; RAGUSA RM; GAROFALO G; SCILLATO F; RUGGERI M SEGREGATION ANALYSIS OF AUTOSOMAL FRAGILE SITES IN 3 FAMILIES WITH THE FRAGILE X-CHROMOSOME | 0 | 5 |
| 107 | 29 | 58 | 2382 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 118B(1):81-88 Barnea-Goraly N; Eliez S; Hedeus M; Menon V; White CD; et al. White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging | 0 | 6 |
| 108 | 0 | 3 | 669 1989 SCIENCE 243(4888):171-172 BARNES DM FRAGILE-X SYNDROME AND ITS PUZZLING GENETICS | 3 | 9 |
| 109 | 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 |
| 110 | 16 | 28 | 1103 1993 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 35(6):532-539 BARNICOAT AJ; DOCHERTY Z; BOBROW M WHERE HAVE ALL THE FRAGILE-X BOYS GONE | 4 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 111 | 1 | 1 | 2532 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(24):2945-2945 Barrett SK; Drazin T; Rosa D; Kupchik GS Genetic counseling for families of patients with fragile X syndrome | 0 | 0 |
| 112 | 1 | 4 | 416 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(6):601-601 BARTOLUCCI G; SZATMARI P POSSIBLE SIMILARITIES BETWEEN THE FRAGILE-X AND ASPERGERS SYNDROMES | 1 | 2 |
| 113 | 19 | 33 | 2285 2002 GENOMICS 80(2):151-157 Baskaran S; Datta S; Mandal A; Gulati N; Totey SM; et al. Instability of CGG repeats in transgenic mice | 0 | 0 |
| 114 | 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 |
| 115 | 0 | 0 | 2232 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):523-523 Bastaki LA; Al-Awadi SA; Hegazi FA; Turky NA; Mustafa MA; et al. PCR technique and significance in fragile X syndrome. | 0 | 0 |
| 116 | 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 |
| 117 | 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 |
| 118 | 30 | 52 | 1435 1995 PEDIATRICS 95(5):744-752 BAUMGARDNER TL; REISS AL; FREUND LS; ABRAMS MT SPECIFICATION OF THE NEUROBEHAVIORAL PHENOTYPE IN MALES WITH FRAGILE-X SYNDROME | 49 | 75 |
| 119 | 33 | 95 | 2619 2004 TRENDS IN NEUROSCIENCES 27(7):370-377 Bear MF; Huber KM; Warren ST The mGIuR theory of fragile X mental retardation | 8 | 10 |
| 120 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 121 | 1 | 1 | 1636 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Beauvais P Fragile X syndrome | 0 | 0 |
| 122 | 24 | 54 | 2574 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):53-59 Beckel-Mitchener A; Greenough WT Correlates across the structural, functional, and molecular phenotypes of fragile X syndrome | 0 | 2 |
| 123 | 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 |
| 124 | 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 |
| 125 | 0 | 16 | 1105 1993 FEBS LETTERS 333(3):248-250 BEHNKRAPPA A; MOLLENHAUER J; DOERFLER W TRIPLET REPEAT SEQUENCES IN HUMAN DNA CAN BE DETECTED BY HYBRIDIZATION TO A SYNTHETIC (5'-CGG-3')(17) OLIGODEOXYRIBONUCLEOTIDE | 0 | 3 |
| 126 | 13 | 32 | 2529 2004 HUMAN MOLECULAR GENETICS 13(5):543-549 Beilina A; Tassone F; Schwartz PH; Sahota P; Hagerman PJ Redistribution of transcription start sites within the FMR1 promoter region with expansion of the downstream CGG-repeat element | 4 | 6 |
| 127 | 10 | 13 | 979 1992 COMPTES RENDUS DES SEANCES DE LA SOCIETE DE BIOLOGIE ET DE SES FILIALES 186(4):363-370 BELDJORD C; RICHARD L FRAGILE-X SYNDROME - AN HERITABLE UNSTABLE ELEMENT | 0 | 0 |
| 128 | 0 | 10 | 361 1986 ANNALES DE GENETIQUE 29(4):261-263 BELGHITI D; RAZAVIENCHA F; RAOUL O; HIRBEC G; GUILLOT F; et al. COINCIDENCE OF FAMILIAL SYSTEMIC LUPUS-ERYTHEMATOSUS AND THE FRAGILE-X SYNDROME | 0 | 3 |
| 129 | 9 | 34 | 845 1991 CELL 64(4):861-866 BELL MV; HIRST MC; NAKAHORI Y; MACKINNON RN; ROCHE A; et al. PHYSICAL MAPPING ACROSS THE FRAGILE-X - HYPERMETHYLATION AND CLINICAL EXPRESSION OF THE FRAGILE-X SYNDROME | 127 | 224 |
| 130 | 15 | 38 | 1366 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):270-279 Belser RC; Sudhalter V Arousal difficulties in males with fragile X syndrome: A preliminary report | 21 | 26 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 131 | 13 | 43 | 2122 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):28-38 Belser RC; Sudhalter V Conversational characteristics of children with fragile X syndrome: Repetitive speech | 9 | 12 |
| 132 | 26 | 47 | 2187 2001 NEUROPSYCHOLOGY 15(2):290-299 Bennetto L; Pennington BF; Porter D; Taylor AK; Hagerman RJ Profile of cognitive functioning in women with the fragile X mutation | 10 | 13 |
| 133 | 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 |
| 134 | 2 | 17 | 328 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):227-239 BERKOVITZ GD; WILSON DP; CARPENTER NJ; BROWN TR; MIGEON CJ GONADAL-FUNCTION IN MEN WITH THE MARTIN-BELL (FRAGILE-X) SYNDROME | 10 | 14 |
| 135 | 0 | 0 | 735 1990 PRACTITIONER 234(1496):946-& BERNEY T FRAGILE-X SYNDROME | 0 | 0 |
| 136 | 0 | 0 | 2126 2001 ANNALS OF NEUROLOGY 50(3):S108-S108 Berry-Kravis E Characterization of epilepsy in fragile X syndrome | 0 | 0 |
| 137 | 17 | 25 | 2261 2002 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 44(11):724-728 Berry-Kravis E Epilepsy in fragile X syndrome | 5 | 6 |
| 138 | 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 |
| 139 | 0 | 0 | 2247 2002 ANNALS OF NEUROLOGY 52(3):S86-S86 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al. Tremor and ataxia in adult fragile X premutation carriers: Blinded videotape evaluation | 0 | 0 |
| 140 | 15 | 31 | 2389 2003 ANNALS OF NEUROLOGY 53(5):616-623 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; et al. Tremor and ataxia in fragile X premutation carriers: Blinded videotape study | 11 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 141 | 0 | 0 | 2391 2003 ANNALS OF NEUROLOGY 54:S144-S144 Berry-Kravis E; Potanos K Clinical response to psychopharmacology for behavior in Fragile X syndrome | 0 | 0 |
| 142 | 0 | 0 | 2392 2003 ANNALS OF NEUROLOGY 54:S150-S150 Berry-Kravis E; Potanos K Stimulant therapy in fragile X syndrome | 0 | 0 |
| 143 | 15 | 45 | 2572 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):42-48 Berry-Kravis E; Potanos K Psychopharmacology in fragile X syndrome - Present and future | 0 | 0 |
| 144 | 16 | 20 | 2623 2005 ANNALS OF NEUROLOGY 57(1):144-147 Berry-Kravis E; Potanos K; Weinberg D; Zhou LL; Goetz CG Fragile X-associated tremor/ataxia syndrome in sisters related to X-inactivation | 0 | 1 |
| 145 | 0 | 0 | 1334 1995 ANNALS OF NEUROLOGY 38(3):499-499 BERRYKRAVIS E; CIURLIONIS R OVEREXPRESSION OF FRAGILE-X GENE (FMR-1) TRANSCRIPTS IN NEURAL CELLS RESULTS IN INCREASED LEVELS OF CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION | 0 | 0 |
| 146 | 0 | 0 | 1056 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1126-1126 BERRYKRAVIS E; HICAR M CORRELATION OF CYCLIC-AMP PRODUCTION WITH LENGTH OF FMR-1 AMPLIFICATION MUTATION IN LYMPHOBLASTOID-CELLS (LCLS) FROM PATIENTS WITH FRAGILE-X SYNDROME (FRA-X) | 0 | 0 |
| 147 | 21 | 43 | 1434 1995 PEDIATRIC RESEARCH 38(5):638-643 BERRYKRAVIS E; HICAR M; CIURLIONIS R REDUCED CYCLIC-AMP PRODUCTION IN FRAGILE-X SYNDROME - CYTOGENETIC AND MOLECULAR CORRELATIONS | 4 | 4 |
| 148 | 0 | 0 | 841 1991 ANNALS OF NEUROLOGY 30(3):450-450 BERRYKRAVIS E; HODGES C DEMONSTRATION OF ABNORMAL CYCLIC ADENOSINE-MONOPHOSPHATE PRODUCTION IN MULTIPLE TISSUES FROM INDIVIDUALS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 149 | 0 | 0 | 852 1991 CLINICAL RESEARCH 39(3):A722-A722 BERRYKRAVIS E; HODGES C DEFECTIVE CYCLIC-AMP PRODUCTION IN TISSUES FROM PATIENTS WITH FRAGILE-X SYNDROME | 0 | 0 |
| 150 | 0 | 0 | 693 1990 ANNALS OF NEUROLOGY 28(3):440-440 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE X-SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 151 | 5 | 22 | 969 1992 ANNALS OF NEUROLOGY 31(1):22-26 BERRYKRAVIS E; HUTTENLOCHER PR CYCLIC-AMP METABOLISM IN FRAGILE-X SYNDROME | 14 | 19 |
| 152 | 5 | 23 | 1074 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 45(1):81-87 BERRYKRAVIS E; SKLENA P DEMONSTRATION OF ABNORMAL CYCLIC-AMP PRODUCTION IN PLATELETS FROM PATIENTS WITH FRAGILE-X SYNDROME | 11 | 14 |
| 153 | 0 | 2 | 1019 1992 NUCLEIC ACIDS RESEARCH 20(4):928-928 BHATIA K; GUTIERREZ MI; HUPPI K; MAGRATH IT PCR DETECTION OF A NEUTRAL CGA/CGG DIMORPHISM IN EXON-6 OF THE HUMAN P53 GENE | 0 | 21 |
| 154 | 0 | 0 | 2270 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-229 Biancalana V; Beldjord C; de Martinville B; Bieth E; Blayau M; et al. 5 years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study of 22 laboratories in France. | 0 | 0 |
| 155 | 20 | 26 | 2491 2004 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 129A(3):218-224 Biancalana V; Beldjord C; Taillandier A; Szpiro-Tapia S; Cusin V; et al. Five years of molecular diagnosis of Fragile X syndrome(1997-2001): A collaborative study reporting 95% of the activity in France | 0 | 1 |
| 156 | 0 | 0 | 2300 2002 JOURNAL OF MEDICAL GENETICS 39:S73-S73 Bilgen T; Keser I; Mihci E; Tacoy S; Haspolat S; et al. Screening of the FMR1 gene (CCG)n expansion by expand long PCR in families with fragile X syndrome in antalya province. | 0 | 0 |
| 157 | 2 | 15 | 1631 1997 ANNALES MEDICO-PSYCHOLOGIQUES 155(7):457-460 BillonGalland IO The fragile X syndrome and its clinical psychotic expression | 0 | 0 |
| 158 | 7 | 10 | 2462 2003 NEURON 38(6):843-845 Billuart P; Chelly J From fragile X mental retardation protein to Rac1 GTPase: New insights from fly CYFIP | 1 | 2 |
| 159 | 46 | 131 | 1360 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):199-217 Binstock TC Fragile X and the amygdala: Cognitive, interpersonal, emotional, and neuroendocrine considerations | 4 | 4 |
| 160 | 0 | 0 | 579 1988 CLINICAL RESEARCH 36(1):A207-A207 BIXENMAN H; HECHT F; LOCKWOOD D; HECHT BK NEW COMMON FRAGILE SITE AT XQ27.3 CONFOUNDED WITH FRAGILE-X | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 161 | 0 | 0 | 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):153-153 BLACK SH; LEVINSON G; HARTON GL; PALMER FT; SISSON ME; et al. PREIMPLANTATION GENETIC TESTING (PGT) FOR FRAGILE-X (FRAX) | 2 | 3 |
| 162 | 1 | 50 | 2580 2004 MOLECULAR MICROBIOLOGY 54(3):742-754 Blaha B; Semsey S; Ferenczi S; Csiszovszki Z; Papp PP; et al. A proline tRNA(CGG) gene encompassing the attachment site of temperate phage 16-3 is functional and convertible to suppressor tRNA | 0 | 0 |
| 163 | 0 | 0 | 1082 1993 ANNALES DE PEDIATRIE 40(9):565-572 BLANC DS; DANGELO J; ETANGS NLD AUTISM AND THE FRAGILE X-SYNDROME | 1 | 1 |
| 164 | 2 | 3 | 671 1989 ZEITSCHRIFT FUR KINDER-UND JUGENDPSYCHIATRIE UND PSYCHOTHERAPIE 17(2):85-90 BLANK R MAIN SYMPTOMS - DELAYED LANGUAGE-DEVELOPMENT AND BEHAVIOR PROBLEMS - 2 CASE-REPORTS ON THE FRAGILE-X SYNDROME | 1 | 1 |
| 165 | 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 |
| 166 | 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 |
| 167 | 7 | 27 | 262 1985 CLINICAL GENETICS 27(2):113-117 BLOMQUIST HK; BOHMAN M; EDVINSSON SO; GILLBERG C; GUSTAVSON KH; et al. FREQUENCY OF THE FRAGILE X-SYNDROME IN INFANTILE-AUTISM - A SWEDISH MULTICENTER STUDY | 51 | 85 |
| 168 | 3 | 15 | 132 1983 CLINICAL GENETICS 24(6):393-398 BLOMQUIST HK; GUSTAVSON KH; HOLMGREN G; NORDENSON I; PALSSONSTRAE U FRAGILE X-SYNDROME IN MILDLY MENTALLY-RETARDED CHILDREN IN A NORTHERN SWEDISH COUNTY - A PREVALENCE STUDY | 43 | 68 |
| 169 | 0 | 0 | 673 1989 ZHURNAL NEVROPATOLOGII I PSIKHIATRII IMENI S S KORSAKOVA 89(8):101-105 BLYUMINA MG CLINICAL SIGNS OF OLIGOPHRENIA WITH FRAGILE X-CHROMOSOME IN PREPUBERTY AND POSTPUBERTY MALES | 1 | 2 |
| 170 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 171 | 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 |
| 172 | 7 | 11 | 1095 1993 CLINICAL GENETICS 44(2):109-110 BODURTHA J; JACKSONCOOK C; MADDALENA A; PISERCHIO J; WALLER R 46XY/47XYY MOSAICISM AND FRAGILE-X | 3 | 4 |
| 173 | 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 |
| 174 | 0 | 1 | 714 1990 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 31(7):1165-1166 BOLTON P THE FRAGILE X-SYNDROME - DAVIES,K | 0 | 0 |
| 175 | 27 | 59 | 1025 1992 PSYCHIATRIC GENETICS 2(4):277-300 BOLTON P; PICKLES A; BUTLER L; SUMMERS D; WEBB T; et al. FRAGILE-X IN FAMILIES MULTIPLEX FOR AUTISM AND RELATED PHENOTYPES - PREVALENCE AND CRITERIA FOR CYTOGENETIC DIAGNOSIS | 1 | 7 |
| 176 | 6 | 7 | 650 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(3):473-476 BOLTON P; RUTTER M; BUTLER L; SUMMERS D FEMALES WITH AUTISM AND THE FRAGILE-X | 7 | 11 |
| 177 | 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 |
| 178 | 29 | 45 | 2158 2001 HUMAN MOLECULAR GENETICS 10(16):1693-1699 Bontekoe CJM; Bakker CE; Nieuwenhuizen IM; van der Linde H; Lans H; et al. Instability of a (CGG)(98) repeat in the Fmr1 promoter | 12 | 15 |
| 179 | 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 |
| 180 | 2 | 3 | 1140 1993 LANCET 341(8847):769-770 BONTHRON D; STRAIN L POPULATION SCREENING FOR FRAGILE-X SYNDROME | 10 | 11 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 181 | 9 | 37 | 438 1987 CLINICAL GENETICS 32(3):179-186 BORGHGRAEF M; FRYNS JP; DIELKENS A; PYCK K; VANDENBERGHE H FRAGILE (X) SYNDROME - A STUDY OF THE PSYCHOLOGICAL PROFILE IN 23 PREPUBERTAL PATIENTS | 47 | 57 |
| 182 | 13 | 27 | 702 1990 CLINICAL GENETICS 37(5):341-346 BORGHGRAEF M; FRYNS JP; VANDENBERGHE H THE FEMALE AND THE FRAGILE X-SYNDROME - DATA ON CLINICAL AND PSYCHOLOGICAL FINDINGS IN 7 FRA(X) CARRIERS | 17 | 20 |
| 183 | 3 | 4 | 1389 1995 GENETIC COUNSELING 6(2):97-101 BORGHGRAEF M; SWILLEN A; VANDENBERGHE H; FRYNS JP FRAGILE-X BOYS - EVOLUTION OF THE MENTAL AGE IN CHILDHOOD - PRELIMINARY DATA ON 10 PREPUBERTAL BOYS | 0 | 0 |
| 184 | 2 | 9 | 856 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2054-2055 BOUVET A; BASRUR PK A MARKER FRAGILE X-CHROMOSOME ASSOCIATED WITH BALDY CALF SYNDROME | 1 | 1 |
| 185 | 1 | 4 | 316 1986 AMERICAN JOURNAL OF DISEASES OF CHILDREN 140(4):327-327 BOWERS EJ FRAGILE-X SYNDROME AND LEARNING-DISABILITIES | 1 | 2 |
| 186 | 15 | 30 | 2127 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 |
| 187 | 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 |
| 188 | 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 |
| 189 | 7 | 12 | 830 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):505-508 BRAINARD SS; SCHREINER RA; HAGERMAN RJ COGNITIVE PROFILES OF THE CARRIER FRAGILE-X WOMAN | 21 | 25 |
| 190 | 0 | 0 | 133 1983 CLINICAL RESEARCH 31(2):A290-A290 BRANDA RF; ARTHUR DC; KING RA FRAGILE X PATIENTS HAVE NORMAL FOLATE METABOLISM | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 191 | 6 | 36 | 191 1984 AMERICAN JOURNAL OF MEDICINE 77(4):602-611 BRANDA RF; ARTHUR DC; WOODS WG; DANZL TJ; KING RA FOLATE METABOLISM AND CHROMOSOMAL STABILITY IN THE FRAGILE-X SYNDROME | 5 | 14 |
| 192 | 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 |
| 193 | 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 |
| 194 | 56 | 112 | 483 1987 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 26(4):463-471 BREGMAN JD; DYKENS E; WATSON M; ORT SI; LECKMAN JF FRAGILE-X SYNDROME - VARIABILITY OF PHENOTYPIC-EXPRESSION | 24 | 41 |
| 195 | 10 | 20 | 599 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):343-354 BREGMAN JD; LECKMAN JF; ORT SI FRAGILE X-SYNDROME - GENETIC PREDISPOSITION TO PSYCHOPATHOLOGY | 44 | 72 |
| 196 | 7 | 34 | 739 1990 YALE JOURNAL OF BIOLOGY AND MEDICINE 63(4):293-299 BREGMAN JD; LECKMAN JF; ORT SI THYROID-FUNCTION IN FRAGILE-X SYNDROME MALES | 6 | 8 |
| 197 | 0 | 1 | 2541 2004 JOURNAL OF FORENSIC SCIENCES 49(1):192-193 Brenner CH; Inman K Commentary on: Thompson WC, Taroni F, Aitken CGG. How the probability of a false positive affects the value of DNA evidence. J Forensic Sci 2003;48(1): 47-54. | 0 | 0 |
| 198 | 7 | 18 | 620 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(1):92-99 BRIDGE PJ; LILLICRAP DP MOLECULAR DIAGNOSIS OF THE FRAGILE-X [FRA-(X)] SYNDROME - CALCULATION OF RISKS BASED ON FLANKING DNA MARKERS IN SMALL PHASE-UNKNOWN FAMILIES | 0 | 4 |
| 199 | 13 | 23 | 807 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):370-373 BROOKS SS; COHEN I; FERRANDO C; JENKINS EC; BROWN WT; et al. CYTOGENETICALLY NEGATIVE, LINKAGE POSITIVE FRAGILE-X SYNDROME | 0 | 1 |
| 200 | 1 | 20 | 51 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 13(2):139-148 BROOKWELL R; DANIEL A; TURNER G; FISHBURN J THE FRAGILE X(Q27) FORM OF X-LINKED MENTAL-RETARDATION - FUDR AS AN INDUCING AGENT FOR FRA(X)(Q27) EXPRESSION IN LYMPHOCYTES, FIBROBLASTS, AND AMNIOCYTES | 24 | 49 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 201 | 0 | 0 | 1320 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1947-1947 BROWN CA; BRASINGTON CK; GRASS FS PATERNAL TRANSMISSION OF A FULL MUTATION IN THE FMR1 GENE - IDENTIFICATION OF PATERNAL CGG REPEAT SHES IN MULTIPLE TISSUES | 0 | 0 |
| 202 | 0 | 0 | 1057 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1132-1132 BROWN CA; TESHIMA IE; CHITAYAT D; RAY PN IDENTIFICATION OF FULL MUTATION FRAGILE-X CARRIERS BY MULTIPLEX PCR OF THE REPEAT SEQUENCES IN THE FMR-1 AND ANDROGEN RECEPTOR GENES | 0 | 0 |
| 203 | 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 |
| 204 | 0 | 0 | 41 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A82-A82 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; et al. A CONTROLLED TRIAL OF FOLIC-ACID THERAPY IN FRAGILE-X INDIVIDUALS | 3 | 3 |
| 205 | 0 | 1 | 134 1983 CLINICAL RESEARCH 31(2):A290-A290 BROWN T; JENKINS E; FRIEDMAN E; BROOKS J; DUNCAN C; et al. FOLIC-ACID THERAPY OF FRAGILE-X SYNDROME | 0 | 0 |
| 206 | 0 | 0 | 91 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A81-A81 BROWN T; JENKINS E; SHAPIRO LR FRAGILE (X) SYNDROME PRENATAL-DIAGNOSIS REGISTRY | 0 | 0 |
| 207 | 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 |
| 208 | 25 | 47 | 2134 2001 CELL 107(4):477-487 Brown V; Jin P; Ceman S; Darnell JC; O'Donnell WT; et al. Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome | 80 | 162 |
| 209 | 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 |
| 210 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 211 | 0 | 0 | 2544 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:287-287 Brown W; Nolin S; Dobkin C; Houck G; Glicksman A; et al. Frequency of fragile X in multiplex autism: Testing the AGRE families | 0 | 0 |
| 212 | 0 | 0 | 662 1989 NEUROLOGIC CLINICS 7(1):107-121 BROWN WT THE FRAGILE-X SYNDROME | 1 | 1 |
| 213 | 18 | 37 | 678 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(2):175-180 BROWN WT INVITED EDITORIAL - THE FRAGILE-X - PROGRESS TOWARD SOLVING THE PUZZLE | 29 | 41 |
| 214 | 45 | 78 | 1355 1995 CLINICS IN LABORATORY MEDICINE 15(4):859-& Brown WT Perspectives and molecular diagnosis of the fragile X syndrome | 2 | 2 |
| 215 | 9 | 17 | 330 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):263-271 BROWN WT; COHEN IL; FISCH GS; WOLFSCHEIN EG; JENKINS VA; et al. HIGH-DOSE FOLIC-ACID TREATMENT OF FRAGILE-(X) MALES | 9 | 14 |
| 216 | 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 |
| 217 | 2 | 8 | 77 1982 LANCET 1(8263):100-100 BROWN WT; FRIEDMAN E; JENKINS EC; BROOKS J; WISNIEWSKI K; et al. ASSOCIATION OF FRAGILE-X SYNDROME WITH AUTISM | 50 | 77 |
| 218 | 0 | 0 | 759 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):211-211 BROWN WT; GOONEWARDENA P; RAY J; MIEZEJESKI C; KRAWCZUN M; et al. PRENATALLY DETECTED FRAGILE X FEMALES - COUNSELING ISSUES AND LONG-TERM FOLLOW-UPS | 0 | 0 |
| 219 | 17 | 32 | 586 1988 HUMAN GENETICS 78(3):201-205 BROWN WT; GROSS A; CHAN C; JENKINS EC; MANDEL JL; et al. MULTILOCUS ANALYSIS OF THE FRAGILE-X SYNDROME | 33 | 49 |
| 220 | 12 | 23 | 795 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):292-297 BROWN WT; GROSS A; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al. DETECTION OF FRAGILE-X NON-PENETRANT MALES BY DNA MARKER ANALYSIS | 4 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 221 | 17 | 40 | 290 1985 HUMAN GENETICS 71(1):11-18 BROWN WT; GROSS AC; CHAN CB; JENKINS EC GENETIC-LINKAGE HETEROGENEITY IN THE FRAGILE X-SYNDROME | 33 | 49 |
| 222 | 6 | 15 | 354 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):643-664 BROWN WT; GROSS AC; CHAN CB; JENKINS EC DNA LINKAGE STUDIES IN THE FRAGILE-X SYNDROME SUGGEST GENETIC-HETEROGENEITY | 36 | 49 |
| 223 | 3 | 20 | 802 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):343-346 BROWN WT; GROSS AC; GOONEWARDENA P; FERRANDO C; DOBKIN C; et al. LINKAGE IN FRAGILE-X FAMILIES OF 3 DISTAL FLANKING MARKERS - ST14, DX13, AND F8 | 1 | 2 |
| 224 | 23 | 35 | 1476 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):287-292 Brown WT; Houck GE; Ding XH; Zhong N; Nolin S; et al. Reverse mutations in the fragile X syndrome | 11 | 18 |
| 225 | 1 | 1 | 1249 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(1):28-28 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING X; et al. RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST (VOL 270, PG 1569, 1993) | 1 | 1 |
| 226 | 20 | 55 | 1122 1993 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 270(13):1569-1575 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING XH; et al. RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST | 120 | 159 |
| 227 | 12 | 39 | 787 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):158-172 BROWN WT; JENKINS E; NERI G; LUBS H; SHAPIRO LR; et al. 4TH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 1 | 7 |
| 228 | 1 | 5 | 61 1982 HOSPITAL PRACTICE 17(7):17-& BROWN WT; JENKINS EC FRAGILE X - ITS DETECTABILITY | 1 | 1 |
| 229 | 18 | 51 | 335 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):341-352 BROWN WT; JENKINS EC; COHEN IL; FISCH GS; WOLFSCHEIN EG; et al. FRAGILE-X AND AUTISM - A MULTICENTER SURVEY | 72 | 110 |
| 230 | 6 | 13 | 185 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):289-297 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; COHEN IL; et al. FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 20 | 28 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 231 | 5 | 23 | 72 1982 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 12(3):303-308 BROWN WT; JENKINS EC; FRIEDMAN E; BROOKS J; WISNIEWSKI K; et al. AUTISM IS ASSOCIATED WITH THE FRAGILE-X SYNDROME | 82 | 124 |
| 232 | 0 | 0 | 56 1982 CLINICAL RESEARCH 30(2):A291-A291 BROWN WT; JENKINS EC; FRIEDMAN E; WISNIEWSKI K; FRENCH JH THE FRAGILE X-SYNDROME - A GENETIC CAUSE OF AUTISM | 0 | 0 |
| 233 | 5 | 11 | 924 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):96-102 BROWN WT; JENKINS EC; GOONEWARDENA P; MIEZEJESKI C; ATKIN J; et al. PRENATALLY DETECTED FRAGILE-X FEMALES - LONG-TERM FOLLOW-UP-STUDIES SHOW HIGH-RISK OF MENTAL IMPAIRMENT | 4 | 4 |
| 234 | 23 | 47 | 457 1987 HUMAN GENETICS 75(4):311-321 BROWN WT; JENKINS EC; GROSS AC; CHAN CB; KRAWCZUN MS; et al. FURTHER EVIDENCE FOR GENETIC-HETEROGENEITY IN THE FRAGILE-X SYNDROME | 33 | 54 |
| 235 | 43 | 97 | 364 1986 ANNALS OF THE NEW YORK ACADEMY OF SCIENCES 477:129-150 BROWN WT; JENKINS EC; KRAWCZUN MS; WISNIEWSKI K; RUDELLI R; et al. THE FRAGILE-X SYNDROME | 10 | 13 |
| 236 | 0 | 4 | 29 1981 LANCET 2(8254):1055-1055 BROWN WT; MEZZACAPPA PM; JENKINS EC SCREENING FOR FRAGILE X SYNDROME BY TESTICULAR SIZE MEASUREMENT | 16 | 23 |
| 237 | 0 | 0 | 2545 2004 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 48:288-288 Brown WT; Nolin S; Houck G; Ding X; Glicksman A; et al. The fragile X syndrome (FXS): Screening and prenatal diagnosis | 0 | 0 |
| 238 | 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 |
| 239 | 16 | 24 | 1460 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):191-195 Brown WT; Nolin S; Houck G; Ding XH; Glicksman A; et al. Prenatal diagnosis and carrier screening for fragile X by PCR | 20 | 28 |
| 240 | 0 | 0 | 2109 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):667-667 Brown WT; Nolin S; Houck GE; Ding XH; Glicksman A; et al. The Fragile X Syndrome: Screening and prenatal diagnosis. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 241 | 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 |
| 242 | 0 | 0 | 2225 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):347-347 Brown WT; Nolin SL; Dobkin CS; Houck GS; Glicksman A; et al. Frequency of fragile X in multiplex autism: Testing the AGRE families. | 0 | 0 |
| 243 | 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 |
| 244 | 1 | 3 | 524 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):201-205 BROWN WT; RUDELLI RD; WISNIEWSKI HM FRAGILE-X SYNDROME - NEUROPATHOLOGY CENTER | 1 | 1 |
| 245 | 8 | 14 | 456 1987 HUMAN GENETICS 75(3):294-295 BROWN WT; SHERMAN SL; DOBKIN CS HYPOTHESIS REGARDING THE NATURE OF THE FRAGILE-X MUTATION - A REPLY | 3 | 5 |
| 246 | 6 | 10 | 486 1987 LANCET 1(8527):280-280 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; et al. RFLP FOR LINKAGE ANALYSIS OF FRAGILE-X SYNDROME | 21 | 35 |
| 247 | 0 | 0 | 444 1987 CYTOGENETICS AND CELL GENETICS 46(1-4):587-587 BROWN WT; WU Y; GROSS AC; CHAN CB; DOBKIN CS; et al. LINKAGE OF FLANKING PROBES IN 40 FRAGILE X-FAMILIES | 1 | 7 |
| 248 | 12 | 22 | 544 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):551-566 BROWN WT; YE W; GROSS AC; CHAN CB; DOBKIN CS; et al. MULTIPOINT LINKAGE OF 9 ANONYMOUS PROBES TO HPRT, FACTOR-IX, AND FRAGILE-X | 8 | 25 |
| 249 | 6 | 13 | 1442 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(3):641-643 Brown WT; Zhong N; Dobkin C Positive fragile X microsatellite associations point to a common mechanism of dynamic mutation evolution | 7 | 12 |
| 250 | 0 | 0 | 1302 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):913-913 BROWN WT; ZHONG N; KAJANOJA E; SMITS B; CURLEY D; et al. FRAGILE-X FOUNDER CHROMOSOME EFFECTS AND NEW MUTATIONS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 251 | 0 | 0 | 1053 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):781-781 BROWN WT; ZHONG N; YE L; DOBKIN C FOUNDER FRAGILE-X CHROMOSOMES | 0 | 0 |
| 252 | 27 | 36 | 1363 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):230-241 Brun C; Obiols JE; Cheema A; OConnor R; Riddle J; et al. Longitudinal IQ changes in fragile X females | 1 | 1 |
| 253 | 9 | 15 | 2201 2001 REVISTA DE NEUROLOGIA 33:S29-S32 Brun-Gasca C; Artigas-Pallares J Psycholinguistic aspects of fragile X chromosome syndrome | 0 | 1 |
| 254 | 14 | 47 | 2244 2002 AMERICAN JOURNAL OF NEURORADIOLOGY 23(10):1757-1766 Brunberg JA; Jacquemont S; Hagerman RJ; Berry-Kravis EM; Grigsby J; et al. Fragile X premutation carriers: Characteristic MR imaging findings of adult male patients with progressive cerebellar and cognitive dysfunction | 17 | 27 |
| 255 | 0 | 0 | 96 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A127-A127 BRYANT EM; GLADSTONE P; MARTIN GM EXPRESSION OF THE FRAGILE-X IN MOUSE-X HUMAN SOMATIC-CELL HYBRIDS | 2 | 2 |
| 256 | 0 | 0 | 9 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A99-A99 BRYANT EM; HOEHN H; MARTIN GM EXPRESSION OF THE FRAGILE X IN EUPLOID SOMATIC-CELL HYBRIDS | 3 | 3 |
| 257 | 1 | 10 | 136 1983 CYTOGENETICS AND CELL GENETICS 35(3):223-225 BRYANT EM; MARTIN GM; HOEHN H FRAGILE-X EXPRESSION STUDIED BY CLONAL ANALYSIS AND SOMATIC-CELL HYBRIDIZATION | 9 | 12 |
| 258 | 16 | 30 | 459 1987 HUMAN GENETICS 76(2):165-172 BUCHANAN JA; BUCKTON KE; GOSDEN CM; NEWTON MS; CLAYTON JF; et al. 10 FAMILIES WITH FRAGILE-X SYNDROME - LINKAGE RELATIONSHIPS WITH 4 DNA PROBES FROM DISTAL-XQ | 9 | 16 |
| 259 | 0 | 0 | 1313 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1603-1603 BUCHANAN JA; KLOCK RJ; DORAN K; KENNEDY D; WYATT P PRENATAL TEST FOR FRAGILE-X SYNDROME REVEALS APPARENT FMR1 GENE CONTRACTION | 0 | 0 |
| 260 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 261 | 0 | 0 | 771 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):289-289 BUCKLEY D; JALAL S; DEWALD G FRAGILE-X STUDIES - WHAT IS PRACTICAL | 0 | 0 |
| 262 | 0 | 0 | 1414 1995 JOURNAL OF MEDICAL GENETICS 32(2):154-154 BULLOCK S; FELIX CA; BUTTERWORTH MA; STEVENSON K; WILLIAMS D THE USE OF MOLECULAR DNA TESTING TO DISTINGUISH BETWEEN MUTATIONS AT THE FRAGILE-X A-SITES AND E-SITES | 0 | 0 |
| 263 | 0 | 0 | 1261 1994 JOURNAL OF MEDICAL GENETICS 31(2):173-173 BULLOCK S; LINDLEY V COMPLEMENTARY CYTOGENETIC AND MOLECULAR ANALYSIS OF A REFERRAL FOR FRAGILE-X TESTING | 0 | 0 |
| 264 | 0 | 0 | 1413 1995 JOURNAL OF MEDICAL GENETICS 32(2):153-153 BULLOCK S; LINDLEY VH; STEVENSON K; COLE T MOLECULAR DNA TESTING OF A FAMILY MANIFESTING FRAGILE-X SYNDROME IN BOTH THE FRAX-A FULL MUTATION AND MOSAIC FORMS | 0 | 0 |
| 265 | 0 | 0 | 494 1987 PRACTITIONER 231(1431):910-& BUNDEY S THE FRAGILE X-SYNDROME | 1 | 1 |
| 266 | 6 | 13 | 699 1990 BRITISH JOURNAL OF HOSPITAL MEDICINE 43(1):17-17 BUNDEY S FRAGILE-X SYNDROME | 1 | 1 |
| 267 | 3 | 4 | 1142 1993 LANCET 341(8847):770-770 BUNDEY S; NORMAN E POPULATION SCREENING FOR FRAGILE-X SYNDROME | 8 | 8 |
| 268 | 5 | 29 | 300 1985 JOURNAL OF MEDICAL GENETICS 22(4):258-266 BUNDEY S; WEBB TP; THAKE A; TODD J A COMMUNITY STUDY OF SEVERE MENTAL-RETARDATION IN THE WEST MIDLANDS AND THE IMPORTANCE OF THE FRAGILE X-CHROMOSOME IN ITS ETIOLOGY | 16 | 32 |
| 269 | 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 |
| 270 | 4 | 4 | 491 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 BURD L THE FRAGILE X-CHROMOSOME | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 271 | 16 | 37 | 374 1986 CHILD STUDY JOURNAL 16(4):285-296 BURD L; KERBESHIAN J FRAGILE X-SYNDROME - DEVELOPMENTAL ASPECTS | 0 | 1 |
| 272 | 2 | 2 | 1491 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):376-376 Burgess B; Partington M; Turner G; Robinson H Normal age of menarche in fragile X syndrome | 3 | 3 |
| 273 | 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 |
| 274 | 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 |
| 275 | 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 |
| 276 | 27 | 41 | 970 1992 ARCHIVES FRANCAISES DE PEDIATRIE 49(2):99-103 BURSZTEJN C; ALEMBIK Y; STOLL C; POUPIER G; FELLER L; et al. FRAGILE-X SYNDROME ASSOCIATED WITH INFANTILE-AUTISM AND PSYCHOTIC DISORDERS | 0 | 2 |
| 277 | 11 | 19 | 2515 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191 Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; et al. Premature ovarian failure and fragile X premutation: a study on 45 women | 0 | 0 |
| 278 | 6 | 12 | 706 1990 HUMAN GENETICS 84(2):216-217 BUTLER MG NO SIGNIFICANT RELATIONSHIP BETWEEN AGE AND FREQUENCY OF CHROMOSOME LESIONS IN MENTALLY-RETARDED INDIVIDUALS WITH OR WITHOUT THE FRAGILE X-SYNDROME | 1 | 4 |
| 279 | 7 | 32 | 791 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):260-268 BUTLER MG; ALLEN GA; HAYNES JL; SINGH DN; WATSON MS; et al. ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT THE FRAGILE-X SYNDROME | 16 | 22 |
| 280 | 3 | 4 | 521 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):165-168 BUTLER MG; ALLEN GA; SINGH DN; CARPENTER NJ; HALL BD PHOTOANTHROPOMETRIC ANALYSIS OF INDIVIDUALS WITH THE FRAGILE-X SYNDROME | 6 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 281 | 10 | 23 | 1022 1992 PEDIATRICS 89(6):1059-1062 BUTLER MG; BRUNSCHWIG A; MILLER LK; HAGERMAN RJ STANDARDS FOR SELECTED ANTHROPOMETRIC MEASUREMENTS IN MALES WITH THE FRAGILE X-SYNDROME | 25 | 29 |
| 282 | 5 | 12 | 561 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):775-778 BUTLER MG; DEV VG; SHAH D; ULM JE; WILMOT PL; et al. THE USE OF EARLY SIMULTANEOUS PERCUTANEOUS UMBILICAL BLOOD-SAMPLING (PUBS) AND AMNIOCENTESIS FOR PRENATAL FRAGILE-X CHROMOSOME DIAGNOSIS | 0 | 0 |
| 283 | 2 | 15 | 560 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):767-773 BUTLER MG; FLETCHER M; GALE DD; MEANEY FJ; MCLEOD DR; et al. METACARPOPHALANGEAL PATTERN PROFILE ANALYSIS IN FRAGILE-X SYNDROME | 4 | 8 |
| 284 | 0 | 0 | 626 1989 AMERICAN JOURNAL OF PHYSICAL ANTHROPOLOGY 78(2):200-200 BUTLER MG; HAYNES JL; ALLEN GA; SINGH DN ANTHROPOMETRIC COMPARISON OF MENTALLY-RETARDED MALES WITH AND WITHOUT FRAGILE X-SYNDROME | 0 | 0 |
| 285 | 3 | 5 | 588 1988 HUMAN GENETICS 78(4):383-383 BUTLER MG; JOSEPH GM; RAMES LJ; CACHEIRO N; LOZZIO CB CHROMOSOME BREAKAGE IN CONTROL AND FRAGILE-X SUBJECTS USING FOLATE-DEFICIENT CULTURE CONDITIONS | 2 | 2 |
| 286 | 5 | 10 | 849 1991 CLINICAL GENETICS 39(5):347-354 BUTLER MG; MANGRUM T; GUPTA R; SINGH DN A 15-ITEM CHECKLIST FOR SCREENING MENTALLY-RETARDED MALES FOR THE FRAGILE X-SYNDROME | 28 | 32 |
| 287 | 2 | 10 | 562 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 31(4):779-781 BUTLER MG; NAJJAR JL DO SOME PATIENTS WITH FRAGILE-X SYNDROME HAVE PRECOCIOUS PUBERTY | 13 | 15 |
| 288 | 8 | 9 | 1176 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):315-316 BUTLER MG; PRATESI R; VNENCAKJONES CL MOLECULAR-GENETIC SCREENING IN CYTOGENETICALLY NORMAL MENTALLY-RETARDED MALES WITH MANIFESTATIONS OF FRAGILE-X-SYNDROME | 3 | 3 |
| 289 | 15 | 26 | 1410 1995 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 39:544-553 Butler MG; Pratesi R; VnencakJones CL Molecular genetic analysis of mentally retarded males with features of the fragile-X syndrome | 0 | 1 |
| 290 | 18 | 37 | 1096 1993 CLINICAL GENETICS 44(3):129-138 BUTLER MG; PRATESI R; WATSON MS; BREG WR; SINGH DN ANTHROPOMETRIC AND CRANIOFACIAL PATTERNS IN MENTALLY-RETARDED MALES WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 291 | 7 | 23 | 1129 1993 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 37:131-142 BUTLER MG; SINGH DN CLINICAL AND CYTOGENETIC SURVEY OF INSTITUTIONALIZED MENTALLY-RETARDED PATIENTS WITH EMPHASIS ON THE FRAGILE-X SYNDROME | 4 | 9 |
| 292 | 16 | 27 | 1110 1993 HUMAN GENETICS 92(3):269-272 BUYLE S; REYNIERS E; VITS L; DEBOULLE K; HANDIG I; et al. FOUNDER EFFECT IN A BELGIAN-DUTCH FRAGILE-X POPULATION | 23 | 30 |
| 293 | 2 | 4 | 114 1983 ANNALES DE GENETIQUE 26(3):147-149 CALVAMERCADO MP; MAUNOURY C; RETHORE MO; LEJEUNE J FRAGILE-X AND INHIBITION OF DIHYDROFOLATE-REDUCTASE - COMPARED EFFECTS OF 2 ANTIBIOTICS - TRIMETHOPRIME AND PYRIMETHAMINE | 6 | 13 |
| 294 | 3 | 52 | 2207 2001 REVISTA DE NEUROLOGIA 33:S65-S70 Calvani M; D'Iddio S; de Gaetano A; Mariotti P; Mosconi L; et al. L-acetylcarnityne treatment on fragile X patients hyperactive behaviour | 0 | 0 |
| 295 | 8 | 33 | 156 1983 NATURE 306(5944):701-704 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE OF FRAGILE X MENTAL-RETARDATION SYNDROME TO HEMOPHILIA-B AND TRANSMISSION THROUGH A NORMAL-MALE | 78 | 171 |
| 296 | 0 | 0 | 200 1984 CYTOGENETICS AND CELL GENETICS 37(1-4):432-432 CAMERINO G; MATTEI MG; MATTEI JF; JAYE M; MANDEL JL CLOSE LINKAGE BETWEEN THE LOCI FOR THE FRAGILE X MENTAL-RETARDATION AND HEMOPHILIA-B | 0 | 0 |
| 297 | 2 | 13 | 583 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(5):646-649 CAMMARATA S; ARCHIDIACONO N; ROMEO G; BENASSI G; GUARINO M; et al. PREVALENCE OF MENTAL-RETARDATION RELATED TO FRAGILE X SYNDROME AND OTHER CHROMOSOMAL-ABNORMALITIES IN THE REPUBLIC OF SAN MARINO | 0 | 2 |
| 298 | 3 | 24 | 206 1984 HUMAN GENETICS 67(1):99-102 CANTU ES; JACOBS PA FRAGILE (X) EXPRESSION - RELATIONSHIP TO THE CELL-CYCLE | 4 | 7 |
| 299 | 4 | 18 | 245 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):947-955 CANTU ES; NUSSBAUM RL; AIRHART SD; LEDBETTER DH FRAGILE (X) EXPRESSION INDUCED BY FUDR IS TRANSIENT AND INVERSELY RELATED TO LEVELS OF THYMIDYLATE SYNTHASE ACTIVITY | 3 | 5 |
| 300 | 9 | 32 | 691 1990 AMERICAN JOURNAL ON MENTAL RETARDATION 94(4):442-447 CANTU ES; STONE JW; WING AA; LANGEE HR; WILLIAMS CA CYTOGENETIC SURVEY FOR AUTISTIC FRAGILE-X CARRIERS IN A MENTAL-RETARDATION CENTER | 5 | 16 |