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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 6: 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 |
|---|---|---|---|---|---|
| 501 | 6 | 30 | 594 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(1):41-52 DYKENS E; LECKMAN J; PAUL R; WATSON M COGNITIVE, BEHAVIORAL, AND ADAPTIVE FUNCTIONING IN FRAGILE-X AND NON-FRAGILE-X RETARDED MEN | 32 | 38 |
| 502 | 6 | 29 | 1487 1996 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 26(3):287-301 Dykens E; Ort S; Cohen I; Finucane B; Spiridigliozzi G; Lachiewicz A; Reiss A; Freund L; Hagerman R; OConnor R Trajectories and profiles of adaptive behavior in males with fragile X syndrome: Multicenter studies | 17 | 21 |
| 503 | 4 | 17 | 421 1987 AMERICAN JOURNAL OF MENTAL DEFICIENCY 92(2):234-236 DYKENS EM; HODAPP RM; LECKMAN JF STRENGTHS AND WEAKNESSES IN THE INTELLECTUAL-FUNCTIONING OF MALES WITH FRAGILE-X SYNDROME | 24 | 44 |
| 504 | 9 | 27 | 651 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):427-430 DYKENS EM; HODAPP RM; LECKMAN JF ADAPTIVE AND MALADAPTIVE FUNCTIONING OF INSTITUTIONALIZED AND NONINSTITUTIONALIZED FRAGILE-X MALES | 16 | 27 |
| 505 | 5 | 34 | 650 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(3):422-426 DYKENS EM; HODAPP RM; ORT S; FINUCANE B; SHAPIRO LR; LECKMAN JF THE TRAJECTORY OF DEVELOPMENT IN MALES WITH FRAGILE-X SYNDROME | 31 | 50 |
| 506 | 7 | 26 | 1106 1993 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 23(1):135-145 DYKENS EM; HODAPP RM; ORT SI; LECKMAN JF TRAJECTORY OF ADAPTIVE-BEHAVIOR IN MALES WITH FRAGILE X-SYNDROME | 27 | 37 |
| 507 | 0 | 0 | 1267 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):196-196 EBERHART DE; FENG Y; WARREN ST IDENTIFICATION OF A CYTOPLASMIC ANCHOR DOMAIN RESPONSIBLE FOR THE SUBCELLULAR-LOCALIZATION OF THE FRAGILE-X MENTAL-RETARDATION PROTEIN, FMRP | 0 | 0 |
| 508 | 17 | 53 | 1485 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 | 74 | 120 |
| 509 | 0 | 0 | 1039 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):678-678 EBERHART DE; WARREN ST ABNORMAL CHROMATIN STRUCTURE ASSOCIATED WITH THE FULL FRAGILE-X MUTATION | 1 | 2 |
| 510 | 37 | 74 | 1469 1996 COLD SPRING HARBOR SYMPOSIA ON QUANTITATIVE BIOLOGY 61:679-687 Eberhart DE; Warren ST The molecular basis of fragile X syndrome | 6 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 511 | 17 | 35 | 1515 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 | 6 | 14 |
| 512 | 0 | 9 | 24 1981 LANCET 1(8219):557-557 EBERLE G; ZANKL H; ZANKL M SOURCES OF ERROR IN FRAGILE-X DETERMINATION | 4 | 8 |
| 513 | 2 | 7 | 62 1982 HUMAN GENETICS 61(2):163-164 EBERLE G; ZANKL H; ZANKL M CO-CULTIVATION STUDIES WITH CELLS OF PATIENTS BEARING FRAGILE-X CHROMOSOMES | 7 | 11 |
| 514 | 2 | 5 | 63 1982 HUMAN GENETICS 61(3):254-255 EBERLE G; ZANKL M; ZANKL H THE EXPRESSION OF FRAGILE X-CHROMOSOMES IN MEMBERS OF THE SAME FAMILY AT DIFFERENT TIMES OF EXAMINATION | 12 | 14 |
| 515 | 0 | 0 | 435 1987 CLINICAL RESEARCH 35(1):A60-A60 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 516 | 0 | 0 | 606 1988 NEUROTOXICOLOGY 9(1):139-140 EDWARDS DR; KEPPEN LD; GOLLIN SM AUTISM AND FRAGILE-X SYNDROME | 0 | 0 |
| 517 | 5 | 9 | 607 1988 NEUROTOXICOLOGY 9(3):359-365 EDWARDS DR; KEPPEN LD; RANELLS JD; GOLLIN SM AUTISM IN ASSOCIATION WITH FRAGILE X-SYNDROME IN FEMALES - IMPLICATIONS FOR DIAGNOSIS AND TREATMENT IN CHILDREN | 4 | 7 |
| 518 | 29 | 49 | 1484 1996 HUMAN MOLECULAR GENETICS 5(3):319-330 Eichler EE; Macpherson JN; Murray A; Jacobs PA; Chakravarti A; Nelson DL Haplotype and interspersion analysis of the FMR1 CGG repeat identifies two different mutational pathways for the origin of the fragile X syndrome | 22 | 46 |
| 519 | 0 | 0 | 1286 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1838-1838 EIGEL A; ZYGULSKA M; DOLSCHEID T; BOGDANOVA N; DWORNICZAK B; STEGER F; SANGUANSERMSRI T; FLATZ G; HORST J FRAGILE-X PREMUTATION FREQUENCY IN NORTHERN THAILAND | 0 | 0 |
| 520 | 10 | 18 | 910 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):56-60 EINFELD S; HALL W BEHAVIOR PHENOTYPE OF THE FRAGILE X SYNDROME | 6 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 521 | 9 | 23 | 864 1991 JOURNAL OF ABNORMAL CHILD PSYCHOLOGY 19(3):253-262 EINFELD S; HALL W; LEVY F HYPERACTIVITY AND THE FRAGILE X SYNDROME | 11 | 12 |
| 522 | 21 | 44 | 619 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 34(2):187-193 EINFELD S; MOLONY H; HALL W AUTISM IS NOT ASSOCIATED WITH THE FRAGILE-X SYNDROME | 31 | 53 |
| 523 | 3 | 6 | 1764 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 87(5):436-439 Einfeld S; Tonge B; Turner G Longitudinal course of behavioral and emotional problems in Fragile X syndrome | 5 | 5 |
| 524 | 1 | 2 | 524 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):237-238 EINFELD SL AUTISM AND THE FRAGILE-X SYNDROME | 4 | 6 |
| 525 | 0 | 0 | 1916 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:273-273 Einfeld SL; Tonge B; Turner G; Parmenter T; Smith A Longitudinal course of behavioural and emotional problems of young persons with Prader-Willi, fragile-X, Williams and Down syndromes | 0 | 0 |
| 526 | 9 | 30 | 1168 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):386-391 EINFELD SL; TONGE BJ; FLORIO T BEHAVIORAL AND EMOTIONAL DISTURBANCE IN FRAGILE-X-SYNDROME | 12 | 23 |
| 527 | 0 | 0 | 1714 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A270-A270 El-Hazmi MF Fragile X mental retardation in syndrome in Saudi Arabia. | 0 | 0 |
| 528 | 20 | 28 | 1356 1995 HUMAN GENETICS 96(5):577-584 ELALEEM AA; BOHM I; TEMTAMY S; ELAWADY M; AWADALLA M; SCHMIDTKE J; STUHRMANN M DIRECT MOLECULAR ANALYSIS OF THE FRAGILE-X SYNDROME IN A SAMPLE OF EGYPTIAN AND GERMAN PATIENTS USING NONRADIOACTIVE PCR AND SOUTHERN BLOT FOLLOWED BY CHEMILUMINESCENT DETECTION | 5 | 9 |
| 529 | 24 | 41 | 1682 1998 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 42:81-89 Elbaz A; Suedois J; Duquesnoy M; Beldjord C; Berchel C; Merault G Prevalence of fragile-X syndrome and FRAXE among children with intellectual disability in a Caribbean island, Guadeloupe, French West Indies | 5 | 8 |
| 530 | 34 | 53 | 2000 2001 BRAIN 124:1610-1618 Eliez S; Blasey CM; Freund LS; Hastie T; Reiss AL Brain anatomy, gender and IQ in children and adolescents with fragile X syndrome | 7 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 531 | 63 | 94 | 2012 2001 CURRENT OPINION IN PSYCHIATRY 14(5):443-449 Eliez S; Feinstein C The fragile X syndrome: bridging the gap from gene to behavior | 0 | 1 |
| 532 | 2 | 5 | 1939 2000 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 39(2):264-266 Eliez S; Reiss AL Generics of childhood disorders: XI. Fragile X syndrome | 0 | 0 |
| 533 | 0 | 0 | 602 1988 JOURNAL OF MEDICAL GENETICS 25(2):128-128 ENGLISH C ANTHROPOMETRIC STUDIES IN THE FRAGILE X-SYNDROME | 0 | 0 |
| 534 | 0 | 0 | 2086 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):373-373 Ennis S; Brightwell G; Collins A; Jacobs P; Morton NE Phylogeny of fragile X haplotypes from an English population. | 0 | 0 |
| 535 | 0 | 0 | 2213 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):377-377 Ennis S; Collins A; Morton NE The use of SNP-based haplotypes and LD blocks to positionally clone modifying determinants of expansion of the Fragile X triplet repeat | 0 | 0 |
| 536 | 0 | 0 | 2280 2003 JOURNAL OF MEDICAL GENETICS 40:S15-S15 Ennis S; Collins A; Morton NE SNP-based haplotypes and LD blocks in the fragile X region | 0 | 0 |
| 537 | 3 | 9 | 183 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):299-301 ERBE RW FOLIC-ACID THERAPY IN THE FRAGILE-X SYNDROME | 4 | 8 |
| 538 | 0 | 0 | 94 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A131-A131 EREN M; DISTECHE C BEHAVIORAL-PHENOTYPE OF THE FRAGILE X-SYNDROME - RELATIONSHIP BETWEEN FREQUENCY OF MARKER-X, MENTAL-RETARDATION AND VERBAL DISABILITY | 3 | 5 |
| 539 | 20 | 36 | 982 1992 HUMAN GENETICS 90(1-2):55-61 ERSTER SH; BROWN WT; GOONEWARDENA P; DOBKIN CS; JENKINS EC; PERGOLIZZI RG POLYMERASE CHAIN-REACTION ANALYSIS OF FRAGILE X-MUTATIONS | 18 | 30 |
| 540 | 0 | 0 | 1977 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):585-585 Essop FB; Greenberg J; Basel D; Krause A Molecular analysis of a fragile X family with two females homozygous for a premutation. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 541 | 29 | 49 | 1629 1997 REVISTA DE NEUROLOGIA 25(143):1068-1071 EstevezGonzalez A; Roig C; Piles S; Pineda M; GarciaSanchez C Fragile-X syndrome and mental retardation | 0 | 0 |
| 542 | 0 | 0 | 1711 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A214-A214 Falik-Zaccai TC; Shachak E; Borochowitz Z; Magal N; Zatz S; Shochat M; Ziv H; Navon R; Ligum C; Shomrat R Fragile X syndrome: Population carrier screening and implication for prenatal diagnosis. | 0 | 0 |
| 543 | 0 | 0 | 1277 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1218-1218 FALIKBORENSTEIN TC; YALON M; SHACHAK L; DAR C; BOROCHOWITZ Z; NELSON DL; MACPHERSON JN; EICHLER EE LONG UNINTERRUPTED CGG REPEATS WITHIN THE FMR1 GENE - POSSIBLE MECHANISM FOR THE PREVALENCE OF THE FRAGILE-X SYNDROME AMONG TUNISIAN JEWS | 0 | 0 |
| 544 | 24 | 41 | 1526 1997 AMERICAN JOURNAL OF HUMAN GENETICS 60(1):103-112 FalikZaccai TC; Shachak E; Yalon M; Lis Z; Borochowitz Z; Macpherson JN; Nelson DL; Eichler EE Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype | 15 | 26 |
| 545 | 0 | 0 | 2218 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):585-585 Fan H; Booker JK; McCandless SE; Shashi V; Farber RA Mosaicism for FMR1 gene full mutation and deletion in a fragile X female. | 0 | 0 |
| 546 | 6 | 24 | 577 1988 CYTOGENETICS AND CELL GENETICS 48(3):142-147 FANTES J; GOSDEN J; PIPER J USE OF AN ALPHOID SATELLITE SEQUENCE TO LOCATE THE X-CHROMOSOME AUTOMATICALLY, WITH PARTICULAR REFERENCE TO IDENTIFICATION OF THE FRAGILE-X | 0 | 4 |
| 547 | 3 | 7 | 1743 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):350-351 Faradz SMH; Buckley M; Tang LP; Leigh D; Holden JJA Molecular screening for fragile X syndrome among Indonesian children with developmental disability | 3 | 4 |
| 548 | 6 | 24 | 978 1992 GENOMICS 12(4):814-817 FAUST CJ; VERKERK AJMH; WILSON PJ; MORRIS CP; HOPWOOD JJ; OOSTRA BA; HERMAN GE GENETIC-MAPPING ON THE MOUSE X-CHROMOSOME OF HUMAN CDNA CLONES FOR THE FRAGILE-X AND HUNTER SYNDROMES | 0 | 8 |
| 549 | 1 | 6 | 1245 1994 KLINISCHE PADIATRIE 206(5):410-411 FEHLOW P; MIOSGE W; WALTHER F ASSOCIATION OF SAETHRE-CHOTZEN-SYNDROME AND FRAGILE-X-SYNDROME | 0 | 0 |
| 550 | 53 | 104 | 1672 1998 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 28(5):393-405 Feinstein C; Reiss AL Autism: The point of view from fragile X studies | 15 | 42 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 551 | 46 | 75 | 1680 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 |
| 552 | 14 | 24 | 1640 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):9-17 Felix TM; De Pina-Neto JM Fragile X syndrome - Clinical and cytogenetic studies | 0 | 0 |
| 553 | 15 | 20 | 2163 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):145-147 Feng Y Fragile X mental retardation: Misregulation of protein synthesis in the developing brain? | 1 | 2 |
| 554 | 0 | 0 | 1539 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A170-A170 Feng Y; Absher D; Brown V; Eberhart DE; Malter HE; Warren ST FMRP associates with polyribosomes as an mRNP and the I304N mutation causing severe fragile X syndrome abolishes this association. | 0 | 0 |
| 555 | 24 | 47 | 1617 1997 MOLECULAR CELL 1(1):109-118 Feng Y; Absher D; Eberhart DE; Brown V; Malter HE; Warren ST FMRP associates with polyribosomes as an mRNP, and the I304N mutation of severe fragile X syndrome abolishes this association | 65 | 114 |
| 556 | 0 | 0 | 1263 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):40-40 FENG Y; EBERHART DE; WARREN ST THE PROTEIN ABSENT IN FRAGILE-X SYNDROME (FMRP) IS A RIBOSOME-ASSOCIATED PROTEIN | 0 | 0 |
| 557 | 23 | 59 | 1613 1997 JOURNAL OF NEUROSCIENCE 17(5):1539-1547 Feng Y; Gutekunst CA; Eberhart DE; Yi H; Warren ST; Hersch SM Fragile X mental retardation protein: Nucleocytoplasmic shuttling and association with somatodendritic ribosomes | 71 | 131 |
| 558 | 7 | 10 | 1960 2000 PEDIATRIC HEMATOLOGY AND ONCOLOGY 17(7):597-600 Ferrari A; Meazza C; Casanova M Nasopharyngeal carcinoma in a boy with fragile X syndrome | 0 | 0 |
| 559 | 4 | 10 | 614 1989 AMERICAN JOURNAL OF HUMAN GENETICS 45(6):977-978 FERRI R BRAIN-STEM AUDITORY EVOKED-POTENTIALS IN THE FRAGILE-X SYNDROME | 2 | 3 |
| 560 | 0 | 0 | 461 1987 INTERNATIONAL JOURNAL OF NEUROSCIENCE 34(3-4):172-172 FERRI R; BERGONZI P; COLOGNOLA RM; MUSUMECI SA; PETRELLA MA; SANFILIPPO S; VIGLIANESI A; GIGLI GL BRAIN-STEM AUDITORY AND VISUAL EVOKED-POTENTIALS IN FRAGILE-X MENTAL-RETARDATION SYNDROME SUBJECTS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 561 | 4 | 13 | 1730 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):296-297 Ferri R; Del Gracco S; Elia M; Musumeci SA; Pettinato S Heart rate variability and autonomic function during sleep in fragile X syndrome | 0 | 0 |
| 562 | 7 | 41 | 1252 1994 NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY 24(6):413-426 FERRI R; MUSUMECI SA; ELIA M; DELGRACCO S; SCUDERI C; BERGONZI P BIT-MAPPED SOMATOSENSORY-EVOKED POTENTIALS IN THE FRAGILE-X SYNDROME | 7 | 15 |
| 563 | 12 | 47 | 857 1991 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 33(9):776-788 FERRIER LJ; BASHIR AS; MERYASH DL; JOHNSTON J; WOLFF P CONVERSATIONAL SKILLS OF INDIVIDUALS WITH FRAGILE-X SYNDROME - A COMPARISON WITH AUTISM AND DOWN-SYNDROME | 18 | 22 |
| 564 | 4 | 16 | 512 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):99-107 FILIPPI G; PECILE V; RINALDI A; SINISCALCO M FRAGILE-X MUTATION AND KLINEFELTER SYNDROME - A REAPPRAISAL | 9 | 13 |
| 565 | 2 | 28 | 108 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(1):113-119 FILIPPI G; RINALDI A; ARCHIDIACONO N; ROCCHI M; BALAZS I; SINISCALCO M LINKAGE BETWEEN G6PD AND FRAGILE-X SYNDROME | 19 | 43 |
| 566 | 6 | 25 | 300 1985 JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY 48(2):150-153 FINELLI PF; PUESCHEL SM; PADREMENDOZA T; OBRIEN MM NEUROLOGICAL FINDINGS IN PATIENTS WITH THE FRAGILE-X SYNDROME | 19 | 28 |
| 567 | 11 | 21 | 1468 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 |
| 568 | 0 | 1 | 736 1991 AMERICAN JOURNAL OF HUMAN GENETICS 48(4):815-815 FINUCANE B; SCOTT CI; KURTZ MB CONCURRENCE OF DOMINANT PIEBALD TRAIT AND FRAGILE X-SYNDROME | 0 | 2 |
| 569 | 8 | 14 | 904 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 42(2):184-186 FINUCANE BM; JAEGER E; DUNN E; SCOTT CI STUDY OF COLOR-VISION IN FRAGILE-X SYNDROME | 1 | 1 |
| 570 | 4 | 4 | 652 1989 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 28(6):965-966 FISCH GS FRAGILE-X AND AUTISM | 3 | 4 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 571 | 30 | 56 | 909 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):47-55 FISCH GS IS AUTISM ASSOCIATED WITH THE FRAGILE-X SYNDROME | 19 | 36 |
| 572 | 60 | 138 | 1065 1993 AMERICAN JOURNAL OF MEDICAL GENETICS 48(2):112-121 FISCH GS WHAT IS ASSOCIATED WITH THE FRAGILE-X SYNDROME | 21 | 34 |
| 573 | 51 | 134 | 1598 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 |
| 574 | 9 | 34 | 818 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):481-487 FISCH GS; ARINAMI T; FROSTERISKENIUS U; FRYNS JP; CURFS LM; BORGHGRAEF M; HOWARDPEEBLES PN; SCHWARTZ CE; SIMENSEN RJ; SHAPIRO LR RELATIONSHIP BETWEEN AGE AND IQ AMONG FRAGILE-X MALES - A MULTICENTER STUDY | 13 | 14 |
| 575 | 0 | 0 | 1817 1999 MOLECULAR PSYCHIATRY 4:S56-S56 Fisch GS; Carpenter N; Holden JA; Pandya A; Howard-Peebles PN; Tarleton J Psychopathology in genetic disorders producing cognitive deficits: Adaptive and maladative behavior in the fragile X syndrome, Williams syndrome and neurofibromatosis type 1. | 0 | 0 |
| 576 | 11 | 20 | 1733 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):308-312 Fisch GS; Carpenter N; Holden JJA; Howard-Peebles PN; Maddalena A; Borghgraef M; Steyaert J; Fryns JP Longitudinal changes in cognitive and adaptive behavior in fragile X females: A prospective multicenter analysis | 9 | 14 |
| 577 | 10 | 14 | 1437 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):362-364 Fisch GS; Carpenter N; HowardPeebles PN; Maddalena A; Simensen R; Tarleton J; JulienInalsingh C; Chalifoux M; Holden JJA Lack of association between mutation size and cognitive/behavior deficits in fragile X males: A brief report | 1 | 3 |
| 578 | 4 | 9 | 1430 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):319-322 Fisch GS; Carpenter N; Maddalena A; Tarleton J; JulienInalsingh C; Holden JJA Rater reliability of fragile X mutation size estimates: A multilaboratory analysis | 5 | 5 |
| 579 | 13 | 26 | 1726 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):257-263 Fisch GS; Carpenter NJ; Holden JJA; Simensen R; Howard-Peebles PN; Maddalena A; Pandya A; Nance W Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: Growth, development, and profiles | 7 | 7 |
| 580 | 16 | 23 | 530 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):393-399 FISCH GS; COHEN IL; GROSS AC; JENKINS V; JENKINS EC; BROWN WT FOLIC-ACID TREATMENT OF FRAGILE-X MALES - A FURTHER STUDY | 4 | 9 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 581 | 32 | 50 | 546 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):655-663 FISCH GS; COHEN IL; JENKINS EC; BROWN WT SCREENING DEVELOPMENTALLY DISABLED MALE POPULATIONS FOR FRAGILE-X - THE EFFECT OF SAMPLE-SIZE | 17 | 21 |
| 582 | 12 | 24 | 357 1986 AMERICAN JOURNAL OF PSYCHIATRY 143(1):71-73 FISCH GS; COHEN IL; WOLF EG; BROWN WT; JENKINS EC; GROSS A AUTISM AND THE FRAGILE X-SYNDROME | 19 | 28 |
| 583 | 11 | 21 | 922 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):142-148 FISCH GS; FRYNS JP FACTORS WHICH CONTRIBUTE TO CYTOGENETIC FREQUENCY OF EXPRESSION IN FAMILIES OF FRAGILE-X FEMALES | 1 | 1 |
| 584 | 0 | 0 | 1528 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A6-A6 Fisch GS; Holden JJA; Chalifoux M; Carpenter NJ; Howard-Peebles PN; Maddalena A; Simensen R; Tarleton J; Borghgraef M; Steyaert J; Fryns JP Natural history of cognitive and adaptive behavior in young fragile X males and females: A 6-year prospective multicenter study. | 0 | 0 |
| 585 | 16 | 34 | 1161 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):346-352 FISCH GS; HOLDEN JJA; SIMENSEN R; CARPENTER N; HOWARDPEEBLES PN; MADDALENA A; SANDGRUND A; JACQUES JR; MCGANN B FRAGILE-X-SYNDROME A PERVASIVE DEVELOPMENTAL DISABILITY - COGNITIVE-ABILITY AND ADAPTIVE-BEHAVIOR IN MATES WITH THE FULL MUTATION | 10 | 12 |
| 586 | 0 | 0 | 1034 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):432-432 FISCH GS; HOLDEN JJA; SIMENSEN R; CARPENTER NJ; HOWARDPEEBLES PN; MADDALENA A; SANDGRUND A; JACQUES JR; MCGANN B IS FRAGILE X-SYNDROME A PERVASIVE DEVELOPMENTAL DISABILITY - COGNITIVE AND ADAPTIVE ABILITIES IN MALES WITH THE FULL MUTATION | 0 | 0 |
| 587 | 8 | 23 | 1725 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):253-256 Fisch GS; Holden JJK; Carpenter NJ; Howard-Peebles PN; Maddalena A; Pandya A; Nance W Age-related language characteristics of children and adolescents with fragile X syndrome | 7 | 8 |
| 588 | 0 | 0 | 1706 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A68-A68 Fisch GS; Howard-Peebles PN; Carpenter N; Tarleton J; Simensen R; Holden JJA Age-related features of genetic mutations producing cognitive impairment: the Fragile X mutation, NF1, and Williams Syndrome. | 0 | 0 |
| 589 | 7 | 13 | 1160 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):339-345 FISCH GS; NELSON DL; SNOW K; THIBODEAU SN; CHALIFOUX M; HOLDEN JJA RELIABILITY OF DIAGNOSTIC-ASSESSMENT OF NORMAL AND PREMUTATION STATUS IN THE FRAGILE-X-SYNDROME USING DNA TESTING | 8 | 11 |
| 590 | 0 | 0 | 778 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):469-469 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; BORGHGRAEF M; CURFS LM; HOWARDPEEBLES PN; ARINAMI T; MAVROU A DIFFERENCES IN DECLINE IN IQ AMONG FRAGILE-X MALES - EVIDENCE FOR GENETIC-HETEROGENEITY | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 591 | 9 | 27 | 907 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):28-34 FISCH GS; SHAPIRO LR; SIMENSEN R; SCHWARTZ CE; FRYNS JP; BORGHGRAEF M; CURFS LM; HOWARDPEEBLES PN; ARINAMI T; MAVROU A LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X MALES - CLINICAL-EVIDENCE OF MORE THAN ONE MUTATION | 12 | 12 |
| 592 | 0 | 0 | 985 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):397-398 FISCH GS; SHAPIRO LR; SIMENSEN RJ; FRYNS JP; BORGHGRAEF M; CURFS LK; HOWARDPEEBLES PN; ARINAMI T; MAVROU A LONGITUDINAL CHANGES IN IQ AMONG FRAGILE(X) MALES - CLINICAL-EVIDENCE FOR MORE THAN ONE MUTATION | 0 | 0 |
| 593 | 0 | 0 | 983 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):327-327 FISCH GS; SHAPIRO LR; SIMENSEN RJ; FRYNS JP; BORGHGRAEF M; CURFS LM; HOWARDPEEBLES PN; ARINAMI T; MAVROU A LONGITUDINAL CHANGES IN IQ AMONG FRAGILE(X) MALES - CLINICAL-EVIDENCE FOR MORE THAN ONE MUTATION | 0 | 0 |
| 594 | 7 | 16 | 807 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):404-407 FISCH GS; SILVERMAN W; JENKINS EC GENETIC AND OTHER FACTORS THAT CONTRIBUTE TO VARIABILITY IN CYTOGENETIC EXPRESSION IN FRAGILE-X MALES | 4 | 7 |
| 595 | 9 | 16 | 1162 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):353-357 FISCH GS; SIMENSEN R; ARINAMI T; BORGHGRAEF M; FRYNS JP LONGITUDINAL CHANGES IN IQ AMONG FRAGILE-X FEMALES - A PRELIMINARY MULTICENTER ANALYSIS | 9 | 10 |
| 596 | 15 | 41 | 1436 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):356-361 Fisch GS; Simensen R; Tarleton J; Chalifoux M; Holden JJ; Carpenter N; HowardPeebles PN; Maddalena A Longitudinal study of cognitive abilities and adaptive behavior levels in fragile X males: A prospective multicenter analysis | 24 | 31 |
| 597 | 17 | 39 | 2147 2002 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 32(2):107-114 Fisch GS; Simensen RJ; Schroer RJ Longitudinal changes in cognitive and adaptive Behavior scores in children and adolescents with the fragile X mutation or autism | 2 | 2 |
| 598 | 18 | 65 | 1260 1995 AMERICAN JOURNAL OF HUMAN GENETICS 56(5):1147-1155 FISCH GS; SNOW K; THIBODEAU SN; CHALIFAUX M; HOLDEN JJA; NELSON DL; HOWARDPEEBLES PN; MADDALENA A THE FRAGILE-X PREMUTATION IN CARRIERS AND ITS EFFECT ON MUTATION SIZE IN OFFSPRING | 24 | 34 |
| 599 | 4 | 138 | 1501 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 | 0 | 4 |
| 600 | 0 | 0 | 1929 2000 JOURNAL OF MEDICAL GENETICS 37:S20-S20 Fisher A; Macpherson JN; Dennis NR; Barber JCK Targeted testing for fragile X: an audit of the first year. | 0 | 0 |
Page 6: 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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