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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 1: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1 | 42 | 92 | 1616 1997 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 3(4):313-322 Abbeduto L; Hagerman RJ Language and communication in fragile X syndrome | 10 | 14 |
| 2 | 0 | 0 | 1913 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:189-189 Abbeduto L; Kesin E; Pavetto M; Weissman M; O'Brien A; Karadottir S; Cawthon S Theory of mind deficits in mental retardation: a comparison of Down syndrome and fragile-X syndrome | 0 | 0 |
| 3 | 15 | 39 | 2233 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(3):149-160 Abbeduto L; Murphy MM; Cawthon SW; Richmond EK; Weissman MD; Karadottir S; O'Brien A Receptive language skills of adolescents and young adults with Down or fragile X syndrome | 2 | 3 |
| 4 | 14 | 79 | 2319 2004 AMERICAN JOURNAL ON MENTAL RETARDATION 109(3):237-254 Abbeduto L; Seltzer MM; Shattuck P; Krauss MW; Orsmond G; Murphy MM Psychological well-being and coping in mothers of youths with autism, Down syndrome, or fragile X syndrome | 0 | 0 |
| 5 | 0 | 0 | 1073 1993 BIOLOGICAL PSYCHIATRY 33(6A):A161-A161 ABRAMS M; FREUND L; REISS AL MOLECULAR PREDICTORS OF COGNITIVE FUNCTION IN FRAGILE X-SYNDROME | 0 | 0 |
| 6 | 27 | 53 | 1720 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 82(1):25-30 Abrams MT; Kaufmann WE; Rousseau F; Oostra BA; Wolozin B; Taylor CV; Lishaa N; Morel ML; Hoogeveen A; Reiss AL FMR1 gene expression in olfactory neuroblasts from two males with fragile X syndrome | 8 | 11 |
| 7 | 32 | 75 | 1324 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):187-198 Abrams MT; Reiss AL Quantitative brain imaging studies of fragile X syndrome | 2 | 3 |
| 8 | 31 | 61 | 1158 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):317-327 ABRAMS MT; REISS AL; FREUND LS; BAUMGARDNER TL; CHASE GA; DENCKLA MB MOLECULAR-NEUROBEHAVIORAL ASSOCIATIONS IN FEMALES WITH THE FRAGILE-X FULL MUTATION | 48 | 65 |
| 9 | 4 | 17 | 316 1986 AMERICAN JOURNAL OF HUMAN GENETICS 38(4):533-539 ABRUZZO MA; HUNT PA; MAYER M; JACOBS PA; WANG JCC; ERBE RW A COMPARISON OF FRAGILE X-EXPRESSION IN LYMPHOCYTE AND LYMPHOBLASTOID CULTURES | 2 | 3 |
| 10 | 6 | 17 | 239 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 11 | 3 | 15 | 385 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 |
| 12 | 4 | 11 | 266 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 |
| 13 | 14 | 43 | 1822 1999 RNA-A PUBLICATION OF THE RNA SOCIETY 5(9):1248-1258 Adinolfi S; Bagni C; Musco G; Gibson T; Mazzarella L; Pastore A Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains | 15 | 22 |
| 14 | 26 | 40 | 2246 2003 BIOCHEMISTRY 42(35):10437-10444 Adinolfi S; Ramos A; Martin SR; Dal Piaz F; Pucci P; Bardoni B; Mandel JL; Pastore A The N-terminus of the fragile X mental retardation protein contains a novel domain involved in dimerization and RNA binding | 2 | 3 |
| 15 | 3 | 7 | 2267 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 |
| 16 | 0 | 0 | 2125 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 |
| 17 | 5 | 19 | 1868 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 |
| 18 | 10 | 18 | 1770 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 |
| 19 | 8 | 22 | 1154 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):294-297 ALBRIGHT SG; LACHIEWICZ AM; TARLETON JC; RAO KW; SCHWARTZ CE; RICHIE R; TENNISON MB; AYLSWORTH AS FRAGILE-X PHENOTYPE IN A PATIENT WITH A LARGE DE-NOVO DELETION IN XQ27-Q28 | 10 | 17 |
| 20 | 2 | 9 | 1352 1995 GENETIC COUNSELING 6(3):207-210 ALEMBIK Y; DOTT B; STOLL C RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME | 1 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 21 | 11 | 17 | 2042 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 |
| 22 | 3 | 6 | 1736 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):322-325 Allingham-Hawkins SJ; Babul-Hirji R; Chitayat D; Holden JJA; Yang KT; Lee C; Hudson R; Gorwill H; Nolin SL; Glicksman A; Jenkins EC; Brown WT; Howard-Peebles PN; Becchi C; Cummings E; Fallon L; Seitz S; Black SH; Vianna-Morgante AM; Costa SS; Otto PA; Mingroni-Netto RC; Murray A; Webb J; MacSwinney F; Dennis N; Jacobs PA; Syrrou M; Georgiou I; Patsalis PC; Uzielli MLG; Guarducci S; Lapi E; Cecconi A; Ricci U Fragile X premutation is a significant risk factor for premature ovarian failure: The international collaborative POF in fragile X study - Preliminary data | 10 | 19 |
| 23 | 14 | 24 | 1432 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):329-333 AllinghamHawkins DJ; Brown CA; Babul R; Chitayat D; Krekewich K; Humphries T; Ray PN; Teshima IE Tissue-specific methylation differences and cognitive function in fragile X premutation females | 8 | 13 |
| 24 | 0 | 15 | 450 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 |
| 25 | 11 | 37 | 2340 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 | 0 | 0 |
| 26 | 14 | 20 | 1394 1996 AMERICAN JOURNAL OF HUMAN GENETICS 58(1):237-239 Antinolo G; Borrego S; Cabeza JC; Sanchez R; Sanchez J; Sanchez B Reverse mutation in fragile X syndrome | 7 | 11 |
| 27 | 7 | 21 | 574 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 |
| 28 | 12 | 31 | 2054 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 |
| 29 | 0 | 0 | 1898 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 |
| 30 | 2 | 7 | 615 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 31 | 6 | 20 | 1096 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 | 21 | 41 |
| 32 | 4 | 11 | 459 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 |
| 33 | 4 | 14 | 386 1986 HUMAN GENETICS 73(4):309-312 ARINAMI T; KONDO I; NAKAJIMA S FREQUENCY OF THE FRAGILE X-SYNDROME IN JAPANESE MENTALLY-RETARDED MALES | 23 | 29 |
| 34 | 14 | 26 | 456 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 |
| 35 | 0 | 0 | 464 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 |
| 36 | 0 | 0 | 591 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 |
| 37 | 10 | 24 | 497 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 |
| 38 | 0 | 0 | 388 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 |
| 39 | 0 | 0 | 466 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 |
| 40 | 26 | 43 | 2270 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 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 41 | 11 | 12 | 1892 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 |
| 42 | 0 | 0 | 1777 1999 CYTOGENETICS AND CELL GENETICS 85(1-2):137-138 Arrieta I; Criado B; Martinez B; Telez M; Fiores P; Ortega B; Penagarikano O; Lostao CM 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 |
| 43 | 21 | 38 | 1767 1999 ANNALES DE GENETIQUE 42(4):197-201 Arrieta I; Criado B; Martinez B; Telez M; Nunez T; Penagarikano O; Ortega B; Lostao CM A survey of fragile X syndrome in a sample from Spanish Basque country | 3 | 4 |
| 44 | 15 | 42 | 2065 2001 REVISTA DE NEUROLOGIA 33:S41-S50 Artigas-Pallares J; Brun-Gasca C Medical treatment of fragile X syndrome | 0 | 0 |
| 45 | 2 | 7 | 2369 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 |
| 46 | 12 | 30 | 496 1988 AMERICAN JOURNAL OF HUMAN GENETICS 42(2):380-389 ARVEILER B; OBERLE I; VINCENT A; HOFKER MH; PEARSON PL; MANDEL JL GENETIC-MAPPING OF THE XQ27-Q28 REGION - NEW RFLP MARKERS USEFUL FOR DIAGNOSTIC APPLICATIONS IN FRAGILE-X AND HEMOPHILIA-B FAMILIES | 22 | 61 |
| 47 | 11 | 14 | 1578 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 | 13 |
| 48 | 1 | 1 | 1272 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 |
| 49 | 26 | 42 | 1293 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 | 13 | 20 |
| 50 | 16 | 28 | 1511 1996 PSYCHIATRIC GENETICS 6(2):81-86 Ashworth A; Abusaad I; Walsh C; Nanko S; Murray RM; Asherson P; McGuffin P; Gill M; Owen MJ; Collier DA 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 51 | 9 | 25 | 1699 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 |
| 52 | 5 | 25 | 210 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(2):197-204 AUGUST GJ; LOCKHART LH FAMILIAL AUTISM AND THE FRAGILE-X-CHROMOSOME | 10 | 21 |
| 53 | 19 | 46 | 2231 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS 121B(1):119-127 Aziz M; Stathopulu E; Callias M; Taylor C; Turk J; Oostra B; Willemsen R; Patton M Clinical features of boys with fragile X premutations and intermediate alleles | 0 | 4 |
| 54 | 26 | 59 | 1858 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):150-156 Backes M; Genc B; Schreck J; Doerfler W; Lehmkuhl G; von Gontard A Cognitive and behavioral profile of fragile X boys: Correlations to molecular data | 7 | 10 |
| 55 | 35 | 66 | 2173 2002 MONATSSCHRIFT KINDERHEILKUNDE 150(12):1486-+ Backes M; von Gontard A Behavioural phenotype of fragile X syndrome | 0 | 0 |
| 56 | 7 | 71 | 2029 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 |
| 57 | 25 | 50 | 1108 1993 JOURNAL OF CHILD PSYCHOLOGY AND PSYCHIATRY AND ALLIED DISCIPLINES 34(5):673-688 BAILEY A; BOLTON P; BUTLER L; LECOUTEUR A; MURPHY M; SCOTT S; WEBB T; RUTTER M PREVALENCE OF THE FRAGILE-X ANOMALY AMONGST AUTISTIC TWINS AND SINGLETONS | 10 | 48 |
| 58 | 16 | 48 | 2343 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):3-10 Bailey DB Newborn screening for fragile X syndrome | 0 | 0 |
| 59 | 10 | 41 | 1904 2000 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 30(1):49-59 Bailey DB; Hatton DD; Mesibov G; Ament N; Skinner M Early development, temperament, and functional impairment in autism and fragile X syndrome | 14 | 16 |
| 60 | 13 | 23 | 1637 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 | 28 | 30 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 61 | 16 | 33 | 2027 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 | 11 | 15 |
| 62 | 17 | 37 | 1992 2001 AMERICAN JOURNAL ON MENTAL RETARDATION 106(1):16-27 Bailey DB; Hatton DD; Tassone F; Skinner M; Taylor AK Variability in FMRP and early development in males with fragile X syndrome | 13 | 12 |
| 63 | 17 | 28 | 1673 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(6):499-508 Bailey DB; Mesibov GB; Hatton DD; Clark RD; Roberts JE; Mayhew L Autistic behavior in young boys with fragile X syndrome | 29 | 36 |
| 64 | 19 | 31 | 2026 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 |
| 65 | 6 | 32 | 1911 2000 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 21(5):315-321 Bailey DB; Skinner D; Hatton D; Roberts J Family experiences and factors associated with the diagnosis of fragile X syndrome | 12 | 15 |
| 66 | 8 | 36 | 2303 2003 PEDIATRICS 111(2):407-416 Bailey DB; Skinner D; Sparkman KL Discovering fragile X syndrome: Family experiences and perceptions | 4 | 4 |
| 67 | 0 | 0 | 312 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 |
| 68 | 8 | 18 | 1956 2000 NEUROSCIENCE RESEARCH COMMUNICATIONS 26(3):265-277 Bakker CE; Kooy RF; D'Hooge R; Tamanini F; Willemsen R; Nieuwenhuizen I; De Vries BBA; Reyniers E; Hoogeveen AT; Willems PJ; De Deyn PP; Oostra BA Introduction of a FMR1 transgene in the fragile X knockout mouse. | 3 | 3 |
| 69 | 88 | 168 | 2258 2003 CYTOGENETIC AND GENOME RESEARCH 100(1-4):111-123 Bakker CE; Oostra BA Understanding fragile X syndrome: insights from animal models | 0 | 0 |
| 70 | 22 | 52 | 1208 1994 CELL 78(1):23-33 BAKKER CE; VERHEIJ C; WILLEMSEN R; VANDERHELM R; OERLEMANS F; VERMEY M; BYGRAVE A; HOOGEVEEN AT; OOSTRA BA; REYNIERS E; DEBOULLE K; DHOOGE R; CRAS P; VANVELZEN D; NAGELS G; MARTIN JJ; DEDEYN PP; DARBY JK; WILLEMS PJ FMR1 KNOCKOUT MICE - A MODEL TO STUDY FRAGILE-X MENTAL-RETARDATION | 78 | 147 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 71 | 35 | 59 | 1379 1995 MEDICINA-BUENOS AIRES 55(5):457-466 BANARES VG UPDATING THE FRAGILE-X SYNDROME | 0 | 0 |
| 72 | 6 | 8 | 2222 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 |
| 73 | 8 | 44 | 2103 2002 AMERICAN JOURNAL OF OCCUPATIONAL THERAPY 56(5):538-546 Baranek GT; Chin YKH; Hess LMG; Yankee JG; Hatton DD; Hooper SR Sensory processing correlates of occupational performance in children with fragile X syndrome: Preliminary findings | 1 | 1 |
| 74 | 13 | 23 | 1091 1993 GENETIKA 29(6):1026-1034 BARANOV VS; ASEEV MV; RAKISHEVA ZB; KULESHOV NP; MARINICHEVA GS; BYCHKOVA AM; ZUKIN VD; LEDASCHEVA EA; AMOASHYI DS; KUZNETZOVA TV; VAHARLOVSKY VG MOLECULAR DIAGNOSIS OF FRAGILE X-SYNDROME (SYN MARTIN-BELL) IN THE PATIENTS OF NATIVE POPULATIONS | 0 | 2 |
| 75 | 21 | 44 | 1475 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 |
| 76 | 7 | 13 | 248 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 |
| 77 | 36 | 53 | 2271 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698 Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; Corbin F; Pastore A; Khandjian EW; Mandel JL 82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization | 3 | 3 |
| 78 | 55 | 93 | 2117 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 | 18 | 30 |
| 79 | 68 | 116 | 1862 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 97(2):153-163 Bardoni B; Mandel JL; Fisch GS FMR1 gene and fragile X syndrome | 10 | 20 |
| 80 | 17 | 39 | 1791 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 | 26 | 44 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 81 | 42 | 85 | 2002 2001 BRAIN RESEARCH BULLETIN 56(3-4):375-382 Bardoni B; Schenck A; Mandel JL The Fragile X mental retardation protein | 4 | 6 |
| 82 | 2 | 2 | 2132 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 |
| 83 | 0 | 10 | 2190 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 |
| 84 | 1 | 15 | 832 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 |
| 85 | 28 | 58 | 2230 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; Moseley M; Reiss AL White matter tract alterations in fragile X syndrome: Preliminary evidence from diffusion tensor imaging | 0 | 4 |
| 86 | 0 | 3 | 663 1989 SCIENCE 243(4888):171-172 BARNES DM FRAGILE-X SYNDROME AND ITS PUZZLING GENETICS | 3 | 9 |
| 87 | 4 | 11 | 1573 1997 BRITISH MEDICAL JOURNAL 315(7117):1174-1175 Barnicoat A Screening for fragile X syndrome: a model for genetic disorders? | 1 | 4 |
| 88 | 16 | 28 | 1088 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 |
| 89 | 1 | 1 | 2333 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 |
| 90 | 1 | 4 | 412 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 91 | 14 | 22 | 1668 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 107:29-36 Baskaran S; Naseerullah MK; Manjunatha KR; Chetan GK; Arthi R; Rao GVB; Girimaji SR; Srinath S; Sheshadri S; Devi RR; Brahmachari V Triplet repeat polymorphism & fragile X syndrome in the Indian context | 2 | 6 |
| 92 | 0 | 0 | 2092 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):523-523 Bastaki LA; Al-Awadi SA; Hegazi FA; Turky NA; Mustafa MA; Naguib KA PCR technique and significance in fragile X syndrome. | 0 | 0 |
| 93 | 7 | 35 | 1615 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 | 1 | 4 |
| 94 | 0 | 0 | 1543 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 |
| 95 | 30 | 52 | 1388 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 | 46 | 71 |
| 96 | 1 | 1 | 1567 1997 ARCHIVES DE PEDIATRIE 4(2):195-195 Beauvais P Fragile X syndrome | 0 | 0 |
| 97 | 23 | 54 | 2350 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 | 0 |
| 98 | 0 | 0 | 1885 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:305-305 Beckel-Mitchener AC; Weiler IJ; Klintsova AY; Harms L; Belt B; Spangler CC; Greenough WT Analysis of protein synthesis in Fragile X knockout mice | 0 | 0 |
| 99 | 1 | 9 | 1576 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 | 5 |
| 100 | 10 | 13 | 970 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 |
Page 1: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
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