| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 9: 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 |
|---|---|---|---|---|---|
| 801 | 21 | 31 | 1011 1992 PEDIATRICS 89(3):395-400 HAGERMAN RJ; JACKSON C; AMIRI K; SILVERMAN AC; OCONNOR R; SOBESKY W GIRLS WITH FRAGILE-X SYNDROME - PHYSICAL AND NEUROCOGNITIVE STATUS AND OUTCOME | 57 | 79 |
| 802 | 0 | 0 | 2205 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):266-266 Hagerman RJ; Jacquemont S; Tassone F; Greco C; Brunberg J; Hessl D; Harris S; Zhang L; Jardini T; Ruiz L; Gane L; Hagerman PJ Fragile X-associated tremor/ataxia syndrome (FXTAS) involvement in females | 0 | 0 |
| 803 | 14 | 26 | 2312 2004 AMERICAN JOURNAL OF HUMAN GENETICS 74(5):1051-1056 Hagerman RJ; Leavitt BR; Farzin F; Jacquemont S; Greco CM; Brunberg JA; Tassone F; Hessl D; Harris SW; Zhang L; Jardini T; Gane LW; Ferranti J; Ruiz L; Leehey MA; Grigsby J; Hagerman PJ Fragile-X-associated tremor/ataxia syndrome (FXTAS) in females with the FMR1 premutation | 1 | 1 |
| 804 | 3 | 10 | 2047 2001 NEUROLOGY 57(1):127-130 Hagerman RJ; Leehey M; Heinrichs W; Tassone F; Wilson R; Hills J; Grigsby J; Gage B; Hagerman PJ Intention tremor, parkinsonism, and generalized brain atrophy in male carriers of fragile X | 29 | 45 |
| 805 | 2 | 6 | 155 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(23):1424-1424 HAGERMAN RJ; LEVITAS A DILANTIN AND THE FRAGILE X-SYNDROME | 0 | 2 |
| 806 | 13 | 68 | 141 1983 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 4(2):122-130 HAGERMAN RJ; MCBOGG P; HAGERMAN PJ THE FRAGILE-X SYNDROME - HISTORY, DIAGNOSIS, AND TREATMENT | 14 | 18 |
| 807 | 0 | 0 | 1917 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:305-305 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; Harris SW; Simon J; Church K; Bonnell J; Ognibene TC; McIntosh DN Influence of stimulants on electrodermal studies in fragile-X syndrome | 0 | 0 |
| 808 | 16 | 35 | 2167 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):168-173 Hagerman RJ; Miller LJ; McGrath-Clarke J; Riley K; Goldson E; Harris SW; Simon J; Church K; Bonnell J; Ognibene TC; McIntosh DN Influence of stimulants on electrodermal studies in fragile X syndrome | 1 | 1 |
| 809 | 12 | 44 | 529 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):377-392 HAGERMAN RJ; MURPHY MA; WITTENBERGER MD A CONTROLLED TRIAL OF STIMULANT MEDICATION IN CHILDREN WITH THE FRAGILE-X SYNDROME | 23 | 49 |
| 810 | 8 | 35 | 1336 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):336-344 Hagerman RJ; Riddle JE; Roberts LS; Breese K; Fulton M Survey of the efficacy of clonidine in fragile X syndrome | 10 | 10 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 811 | 11 | 30 | 618 1989 AMERICAN JOURNAL OF MEDICAL GENETICS 33(4):513-518 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; HABICHT K LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 34 | 46 |
| 812 | 0 | 0 | 631 1989 CLINICAL RESEARCH 37(1):A170-A170 HAGERMAN RJ; SCHREINER RA; KEMPER MB; WITTENBERGER MD; ZAHN B; HABICHT K LONGITUDINAL IQ CHANGES IN FRAGILE-X MALES | 0 | 0 |
| 813 | 30 | 58 | 621 1989 AMERICAN JOURNAL OF ORTHOPSYCHIATRY 59(1):142-152 HAGERMAN RJ; SOBESKY WE PSYCHOPATHOLOGY IN FRAGILE-X-SYNDROME | 28 | 40 |
| 814 | 24 | 29 | 1508 1996 PEDIATRICS 97(1):122-126 Hagerman RJ; Staley LW; OConner R; Lugenbeel K; Nelson D; McLean SD; Taylor A Learning-disabled males with a fragile X CGG expansion in the upper premutation size range | 25 | 35 |
| 815 | 0 | 0 | 1533 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A100-A100 Hagerman RJ; Staley-Gane L; Linden MG; Tassone F; Hills J; Taylor AK A compound heterozygous female with fragile X syndrome. | 0 | 0 |
| 816 | 1 | 12 | 171 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):123-131 HAGERMAN RJ; SYNHORST DP MITRAL-VALVE PROLAPSE AND AORTIC DILATATION IN THE FRAGILE-X SYNDROME | 9 | 17 |
| 817 | 0 | 0 | 1834 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):26-26 Hagerman RJ; Tassone F; Leehey M; Hills J; Wilson R; Landau W; Grigsby J; Gage B; Hagerman PJ Cerebellar tremor and cerebellar cortical atrophy in older males with the fragile X premutation. | 0 | 0 |
| 818 | 4 | 16 | 170 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):111-121 HAGERMAN RJ; VANHOUSEN K; SMITH ACM; MCGAVRAN L CONSIDERATION OF CONNECTIVE-TISSUE DYSFUNCTION IN THE FRAGILE-X SYNDROME | 25 | 35 |
| 819 | 27 | 37 | 1183 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):474-481 HAGERMAN RJ; WILSON P; STALEY LW; LANG KA; FAN T; UHLHORN C; JEWELLSMART S; HULL C; DRISKO J; FLOM K; TAYLOR AK EVALUATION OF SCHOOL-CHILDREN AT HIGH-RISK FOR FRAGILE-X-SYNDROME UTILIZING BUCCAL CELL FMR-1 TESTING | 17 | 36 |
| 820 | 1 | 1 | 2313 2004 AMERICAN JOURNAL OF HUMAN GENETICS 75(2):352-352 Hagerman; Hagerman The fragile-X premutation: A maturing perspective (vol 74, pg 805, 2003) | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 821 | 0 | 0 | 2355 2004 MOVEMENT DISORDERS 19:S21-S21 Hall DA; Pelak VS; Hagerman RJ; Hagerman PJ; Leehey MA Ocular motility in Fragile X premutation carriers and Fragile X associated tremor/ataxia syndrome (FXTAS) | 0 | 0 |
| 822 | 11 | 13 | 1182 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):471-473 HALLEY D; VANDENOUWELAND A; DEELEN W; VERMA I; OOSTRA B STRATEGY FOR RELIABLE PRENATAL DETECTION OF NORMAL-MALE CARRIERS OF THE FRAGILE-X-SYNDROME | 3 | 4 |
| 823 | 0 | 1 | 719 1990 JOURNAL OF THE ROYAL SOCIETY OF MEDICINE 83(6):415-415 HALSTEAD S FRAGILE X-SYNDROME | 0 | 0 |
| 824 | 0 | 0 | 1467 1996 CLINICAL CHEMISTRY 42(11):7-7 Hamdan H; Bailey A; Martinez JJ; Fenwick R; Leon JA Improved amplification and automated detection of trinucleotide repeats in the diagnosis of fragile X syndrome. | 0 | 0 |
| 825 | 7 | 20 | 1618 1997 MOLECULAR DIAGNOSIS 2(4):259-269 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in fragile X syndrome | 4 | 6 |
| 826 | 1 | 1 | 1692 1998 MOLECULAR DIAGNOSIS 3(4):249-249 Hamdan H; Tynan JA; Fenwick RA; Leon JA Automated detection of trinucleotide repeats in Fragile X syndrome (vol 2, pg 259, 1997) | 0 | 0 |
| 827 | 21 | 25 | 1557 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(4):430-434 Hammond LS; Macias MM; Tarleton JC; Pai GS Fragile X syndrome and deletions in FMR1: New case and review of the literature | 13 | 21 |
| 828 | 7 | 23 | 2302 2003 NUCLEIC ACIDS RESEARCH 31(21):6243-6248 Handa V; Saha T; Usdin K The fragile X syndrome repeats form RNA hairpins that do not activate the interferon-inducible protein kinase, PKR, but are cut by Dicer | 0 | 2 |
| 829 | 0 | 0 | 2278 2003 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 24(5):393-393 Hansen R; Goodlin-Jones B; Nowicki S; Heeren M; Herman K; Harris S; Bacalman S; Hagerman R Behavioral phenotypes in older children with autistic spectrum disorders and fragile X: Similarities and differences | 0 | 0 |
| 830 | 21 | 69 | 1624 1997 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 94(9):4587-4592 Hansen RS; Canfield TK; Fjeld AD; Mumm S; Laird CD; Gartler SM A variable domain of delayed replication in FRAXA fragile X chromosomes: X inactivation-like spread of late replication | 8 | 41 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 831 | 0 | 0 | 1028 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):31-31 HANSEN RS; CANFIELD TK; LAMB MM; GARTLER SM; LAIRD CD FRAGILE X-SYNDROME IS ASSOCIATED WITH A LARGE DOMAIN OF DELAYED REPLICATION AT THE FMR1 LOCUS | 0 | 0 |
| 832 | 18 | 52 | 1075 1993 CELL 73(7):1403-1409 HANSEN RS; CANFIELD TK; LAMB MM; GARTLER SM; LAIRD CD ASSOCIATION OF FRAGILE-X SYNDROME WITH DELAYED REPLICATION OF THE FMR1 GENE | 23 | 121 |
| 833 | 8 | 16 | 2175 2002 NATURE MEDICINE 8(11):1204-1205 Hansen RS; Laird CD A new regulatory pathway for fragile X syndrome? | 0 | 0 |
| 834 | 4 | 27 | 323 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):195-206 HANSON DM; JACKSON AW; HAGERMAN RJ SPEECH DISTURBANCES (CLUTTERING) IN MILDLY IMPAIRED MALES WITH THE MARTIN-BELL FRAGILE-X SYNDROME | 39 | 45 |
| 835 | 3 | 25 | 1135 1993 NATURE GENETICS 3(1):44-48 HANZLIK AJ; OSEMLAKHANZLIK MM; HAUSER MA; KURNIT DM A RECOMBINATION-BASED ASSAY DEMONSTRATES THAT THE FRAGILE-X SEQUENCE IS TRANSCRIBED WIDELY DURING DEVELOPMENT | 9 | 14 |
| 836 | 0 | 1 | 1462 1996 BRITISH JOURNAL OF DEVELOPMENTAL PSYCHOLOGY 14:247-248 Happe F Behavior and development in fragile X syndrome - Dykens,EM, Hodapp,RM, Leckman,JF | 0 | 0 |
| 837 | 0 | 0 | 83 1982 PEDIATRICS 69(5):670-670 HARPEY JP TREATMENT OF FRAGILE-X | 19 | 24 |
| 838 | 0 | 1 | 656 1989 NATURE 341(6243):580-580 HARRIS A; BOBROW M THE FRAGILE-X SYNDROME - DAVIES,KE | 0 | 0 |
| 839 | 0 | 0 | 1839 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):135-135 Harris SW; Brown KE; Hills JL; Tassone F; Hagerman PJ; Taylor AK; Hagerman RJ Adaptive functioning and molecular relationships in individuals with fragile X syndrome. | 0 | 0 |
| 840 | 0 | 0 | 2083 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):288-288 Harris SW; Goodlin-Jones BL; Bacalman S; Jardini T; Rao S; Hagermann RJ Fragile X and autism diagnosis by two standard methodologies. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 841 | 35 | 50 | 1776 1999 CURRENT OPINION IN PSYCHIATRY 12(5):573-578 Harris SW; Hagerman RJ Fragile X syndrome: new developments | 2 | 2 |
| 842 | 0 | 0 | 2206 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):296-296 Harris SW; Tassone F; Barbato I; Hagerman RJ FMRP, FMR1-mRNA, and psychopathology correlations in women with the fragile X premutation. | 0 | 0 |
| 843 | 0 | 11 | 144 1983 JOURNAL OF MEDICAL GENETICS 20(4):280-285 HARRISON CJ; JACK EM; ALLEN TD; HARRIS R THE FRAGILE X - A SCANNING ELECTRON-MICROSCOPE STUDY | 27 | 54 |
| 844 | 0 | 0 | 1281 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):1395-1395 HART PS; OLSON SM; CRANDALL K; TARLETON J FRAGILE-X SYNDROME RESULTING FROM A 400 BASEPAIR DELETION WITHIN THE FMR1 GENE | 0 | 2 |
| 845 | 0 | 0 | 2129 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Hasanzad M; Amini SH; Taghizadeh F; Teimourian S; Karimi-Nejad R; Shafeghati Y; Karimi-Nejad M; Najmabadi H Analysis of FMR 1 methylation in Fragile X syndrome in Iranian population | 0 | 0 |
| 846 | 23 | 40 | 1107 1993 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 23(1):201-209 HASHIMOTO O; SHIMIZU Y; KAWASAKI Y LOW-FREQUENCY OF THE FRAGILE-X SYNDROME AMONG JAPANESE AUTISTIC SUBJECTS | 2 | 8 |
| 847 | 13 | 65 | 1780 1999 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 41(9):625-632 Hatton DD; Bailey DB; Hargett-Beck MQ; Skinner M; Clark RD Behavioral style of young boys with fragile X syndrome | 8 | 11 |
| 848 | 18 | 62 | 2096 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 108(2):105-116 Hatton DD; Hooper SR; Bailey DB; Skinner ML; Sullivan KM; Wheeler A Problem behavior in boys with fragile X syndrome | 4 | 5 |
| 849 | 22 | 50 | 2235 2003 AMERICAN JOURNAL ON MENTAL RETARDATION 108(6):373-390 Hatton DD; Wheeler AC; Skinner ML; Bailey DB; Sullivan KM; Roberts JE; Mirrett P; Clark RD Adaptive behavior in children with fragile X syndrome | 0 | 0 |
| 850 | 0 | 0 | 39 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A93-A93 HAVKIN S; CHAKI R; GOLDMAN B FRAGILE X-CHROMOSOME IN 2 FAMILIES WITH X-LINKED MENTAL-RETARDATION | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 851 | 14 | 36 | 1163 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):358-363 HAY DA DOES IQ DECLINE WITH AGE IN FRAGILE-X A METHODOLOGICAL CRITIQUE | 12 | 13 |
| 852 | 8 | 13 | 1556 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 72(2):245-246 Healey SC; Duffy DL; Martin NG; Turner G Is fragile X syndrome a risk factor for dizygotic twinning? | 2 | 4 |
| 853 | 3 | 9 | 824 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):509-509 HECHT F SEIZURE DISORDERS IN THE FRAGILE-X CHROMOSOME SYNDROME | 3 | 7 |
| 854 | 3 | 4 | 900 1991 SCIENCE 253(5027):1467-1467 HECHT F FRAGILE-X GENE | 0 | 0 |
| 855 | 2 | 7 | 374 1986 CLINICAL GENETICS 29(3):191-195 HECHT F; FRYNS JP; VLIETINCK RF; VANDENBERGHE H GENETIC-CONTROL OVER FRAGILE X-CHROMOSOME EXPRESSION | 9 | 10 |
| 856 | 2 | 6 | 154 1983 NEW ENGLAND JOURNAL OF MEDICINE 308(5):285-286 HECHT F; GLOVER TW ANTIBIOTICS CONTAINING TRIMETHOPRIM AND THE FRAGILE X-CHROMOSOME | 4 | 6 |
| 857 | 0 | 0 | 487 1987 NEW ENGLAND JOURNAL OF MEDICINE 316(8):483-483 HECHT F; HECHT BK THE FRAGILE X-CHROMOSOME | 1 | 1 |
| 858 | 0 | 0 | 47 1982 AMERICAN JOURNAL OF MEDICAL GENETICS 11(4):489-495 HECHT F; JACKY PB; SUTHERLAND GR THE FRAGILE X-CHROMOSOME - CURRENT METHODS | 16 | 35 |
| 859 | 1 | 1 | 107 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 14(4):797-797 HECHT F; JACKY PB; SUTHERLAND GR FRAGILE X-CHROMOSOME IN NORMAL MALES - REPLY | 1 | 2 |
| 860 | 0 | 0 | 4 1980 ARIZONA MEDICINE 37(11):764-766 HECHT F; KAISERMCCAW B; MOORE BC; CADIEN J; GLOVER TW THE FRAGILE X-CHROMOSOME MENTAL-RETARDATION AND LARGE TESTES | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 861 | 9 | 15 | 1577 1997 CLINICAL GENETICS 52(3):147-154 Hecimovic S; Barisic I; Muller A; Petkovic I; Baric I; Ligutic I; Pavelic K Expand long PCR for fragile X mutation detection | 8 | 23 |
| 862 | 19 | 29 | 1662 1998 HUMAN HEREDITY 48(5):256-265 Hecimovic S; Barisic I; Pavelic K DNA analysis of the fragile X syndrome in an at risk pediatric population in Croatia: Simple clinical preselection criteria can considerably improve the cost-effectiveness of fragile X screening studies | 3 | 5 |
| 863 | 16 | 28 | 2077 2002 ACTA PAEDIATRICA 91(5):535-539 Hecimovic S; Tarnik IP; Baric I; Cakarun Z; Pavelic K Screening for fragile X syndrome: results from a school for mentally retarded children | 0 | 0 |
| 864 | 8 | 22 | 539 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):543-550 HEILIG R; OBERLE I; ARVEILER B; HANAUER A; VIDAUD M; MANDEL JL IMPROVED DNA MARKERS FOR EFFICIENT ANALYSIS OF FRAGILE-X FAMILIES | 11 | 33 |
| 865 | 11 | 22 | 2229 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 122A(2):108-114 Heine-Suner D; Torres-Juan L; Morla M; Busquets X; Barcelo F; Pico G; Bonilla L; Govea N; Bernues M; Rosell J Fragile-X syndrome and skewed X-chromosome inactivation within a family: A female member with complete inactivation of the functional X chromosome | 0 | 0 |
| 866 | 0 | 0 | 1976 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):554-554 Heine-Sur D; Pico G; Torres-Juan L; Bernues M; Iglesias J; Barcelo F; Rosell J A female with Fragile-X shows an affected male-like phenotype and skewed inactivation of the functional chromosome. | 0 | 0 |
| 867 | 23 | 34 | 994 1992 JOURNAL OF MEDICAL GENETICS 29(11):794-801 HEITZ D; DEVYS D; IMBERT G; KRETZ C; MANDEL JL INHERITANCE OF THE FRAGILE-X SYNDROME - SIZE OF THE FRAGILE-X PREMUTATION IS A MAJOR DETERMINANT OF THE TRANSITION TO FULL MUTATION | 72 | 108 |
| 868 | 9 | 33 | 895 1991 SCIENCE 251(4998):1236-1239 HEITZ D; ROUSSEAU F; DEVYS D; SACCONE S; ABDERRAHIM H; LEPASLIER D; COHEN D; VINCENT A; TONIOLO D; DELLAVALLE G; JOHNSON S; SCHLESSINGER D; OBERLE I; MANDEL JL ISOLATION OF SEQUENCES THAT SPAN THE FRAGILE-X AND IDENTIFICATION OF A FRAGILE-X RELATED CPG ISLAND | 86 | 139 |
| 869 | 12 | 18 | 1808 1999 JOURNAL OF MEDICAL GENETICS 36(3):253-257 Helderman-van den Enden ATJM; Maaswinkel-Mooij PD; Hoogendoorn E; Willemsen R; Maat-Kievit JA; Losekoot M; Oostra BA Monozygotic twin brothers with the fragile X syndrome: different CGG repeats and different mental capacities | 3 | 8 |
| 870 | 0 | 0 | 17 1981 CLINICAL RESEARCH 29(1):A134-A134 HERBST DS; GERRARD JW; DUNN HG; DILL FJ; KALOUSEK DK; KRYWANIUK LW; KNOLL J; CHUDLEY AE NONSPECIFIC X-LINKED MENTAL-RETARDATION, MACRO-ORCHIDISM AND THE FRAGILE X-CHROMOSOME MARKER | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 871 | 0 | 0 | 2208 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):330-330 Herman K; Nowicki S; Tassone F; Koldewyn K; Bacalman S; Jacquemont S; Barboto I; Levine R; Hagerman P; Hagerman R Correlations between DNA, FMRP, and mRNA levels and ADOS-G and ADI-R scores in patients with Fragile X Syndrome. | 0 | 0 |
| 872 | 25 | 40 | 2053 2001 PEDIATRICS 108(5):art. no.-e88 Hessl D; Dyer-Friedman J; Glaser B; Wisbeck J; Barajas RG; Taylor A; Reiss AL The influence of environmental and genetic factors on behavior problems and autistic symptoms in boys and girls with fragile X syndrome | 0 | 7 |
| 873 | 19 | 43 | 2195 2002 PSYCHONEUROENDOCRINOLOGY 27(7):855-872 Hessl D; Glaser B; Dyer-Friedman J; Blasey C; Hastie T; Gunnar M; Reiss AL Cortisol and behavior in fragile X syndrome | 5 | 7 |
| 874 | 39 | 74 | 2345 2004 MENTAL RETARDATION AND DEVELOPMENTAL DISABILITIES RESEARCH REVIEWS 10(1):17-24 Hessl D; Rivera SM; Reiss AL The neuroanatomy and neuroendocrinotogy of fragile X syndrome | 0 | 0 |
| 875 | 0 | 0 | 1919 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:318-318 Hills JL; Wilson R; Sobesky W; Harris SW; Grigsby J; Butler E; Loesch D; Hagerman RJ Executive functioning deficits in adult males with the fragile-X premutation: an emerging phenotype | 0 | 0 |
| 876 | 9 | 18 | 877 1991 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 30(5):831-834 HILTON DK; MARTIN CA; HEFFRON WM; HALL BD; JOHNSON GL IMIPRAMINE TREATMENT OF ADHD IN A FRAGILE-X CHILD | 4 | 9 |
| 877 | 20 | 33 | 1134 1993 NATURE GENETICS 3(1):36-43 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; HOUSMAN DE; SCHALLING M TISSUE SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE-X SYNDROME | 91 | 154 |
| 878 | 1 | 1 | 1140 1993 NATURE GENETICS 5(3):312-312 HINDS HL; ASHLEY CT; SUTCLIFFE JS; NELSON DL; WARREN ST; HOUSMAN DE; SCHALLING M TISSUE-SPECIFIC EXPRESSION OF FMR-1 PROVIDES EVIDENCE FOR A FUNCTIONAL-ROLE IN FRAGILE X-SYNDROME (VOL 3, PG 36, 1993) | 6 | 7 |
| 879 | 10 | 39 | 831 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 41(3):289-294 HINTON VJ; BROWN WT; WISNIEWSKI K; RUDELLI RD ANALYSIS OF NEOCORTEX IN 3 MALES WITH THE FRAGILE-X SYNDROME | 76 | 117 |
| 880 | 0 | 0 | 1035 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):446-446 HINTON VJ; DOBKIN CS; BROWN WT; JENKINS EC; GOONEWARDENA P; MIEZEJESKI CM VARIABILITY OF VISUAL-SPATIAL DEFICITS OBSERVED IN FRAGILE X-FEMALES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 881 | 15 | 23 | 915 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):87-95 HINTON VJ; DOBKIN CS; HALPERIN JM; JENKINS EC; BROWN WT; DING XH; COHEN IL; ROUSSEAU F; MIEZEJESKI CM MODE OF INHERITANCE INFLUENCES BEHAVIORAL EXPRESSION AND MOLECULAR CONTROL OF COGNITIVE DEFICITS IN FEMALE CARRIERS OF THE FRAGILE-X SYNDROME | 5 | 8 |
| 882 | 22 | 37 | 1364 1995 JOURNAL OF CLINICAL AND EXPERIMENTAL NEUROPSYCHOLOGY 17(4):518-528 HINTON VJ; HALPERIN JM; DOBKIN CS; DING XH; BROWN WT; MIEZEJESKI CM COGNITIVE AND MOLECULAR ASPECTS OF FRAGILE-X | 5 | 7 |
| 883 | 5 | 9 | 878 1991 LANCET 338(8772):956-957 HIRST M; KNIGHT S; DAVIES K; CROSS G; OCRAFT K; RAEBURN S; HEEGER S; EUNPU D; JENKINS EC; LINDENBAUM R PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 29 | 35 |
| 884 | 2 | 5 | 853 1991 CYTOGENETICS AND CELL GENETICS 58(3-4):2067-2067 HIRST M; NAKAHORI Y; KNIGHT S; ROCHE A; RAUT C; RACK K; FLYNN G; BUCKLE V; BELL M; CLAUSSEN U; LUDECKE H; SENGER G; HORSTHEMKE B; HOLLAND J; BENTLEY D; SUPER M; DAVIES K A YAC CONTIG ACROSS THE FRAGILE-X REGION DERIVED FROM CHROMOSOME MICRODISSECTION MARKERS | 0 | 0 |
| 885 | 27 | 46 | 1222 1994 HUMAN MOLECULAR GENETICS 3(9):1553-1560 HIRST MC; GREWAL PK; DAVIES KE PRECURSOR ARRAYS FOR TRIPLET REPEAT EXPANSION AT THE FRAGILE-X LOCUS | 37 | 108 |
| 886 | 38 | 77 | 969 1992 CLINICAL SCIENCE 83(3):255-264 HIRST MC; KNIGHT SJL; BELL MV; SUPER M; DAVIES KE THE FRAGILE-X SYNDROME | 2 | 3 |
| 887 | 15 | 29 | 1118 1993 JOURNAL OF MEDICAL GENETICS 30(8):647-650 HIRST MC; KNIGHT SJL; CHRISTODOULOU Z; GREWAL PK; FRYNS JP; DAVIES KE ORIGINS OF THE FRAGILE-X SYNDROME MUTATION | 16 | 32 |
| 888 | 16 | 34 | 989 1992 JOURNAL OF INHERITED METABOLIC DISEASE 15(4):532-538 HIRST MC; KNIGHT SM; NAKAHORI Y; ROCHE A; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 0 |
| 889 | 11 | 17 | 872 1991 JOURNAL OF MEDICAL GENETICS 28(12):824-829 HIRST MC; NAKAHORI Y; KNIGHT SJL; SCHWARTZ C; THIBODEAU SN; ROCHE A; FLINT TJ; CONNOR JM; FRYNS JP; DAVIES KE GENOTYPE PREDICTION IN THE FRAGILE-X SYNDROME | 27 | 36 |
| 890 | 9 | 25 | 889 1991 NUCLEIC ACIDS RESEARCH 19(12):3283-3288 HIRST MC; RACK K; NAKAHORI Y; ROCHE A; BELL MV; FLYNN G; CHRISTADOULOU Z; MACKINNON RN; FRANCIS M; LITTLER AJ; ANAND R; POUSTKA AM; LEHRACH H; SCHLESSINGER D; DURSO M; BUCKLE VJ; DAVIES KE A YAC CONTIG ACROSS THE FRAGILE X SITE DEFINES THE REGION OF FRAGILITY | 16 | 42 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 891 | 2 | 8 | 260 1985 CLINICAL GENETICS 27(2):118-121 HIRTH L; SINGH S; SCHILLING S; MULLER E; GOEDDE HW DERMATOGLYPHIC FINDINGS IN PATIENTS WITH FRAGILE X-CHROMOSOME | 2 | 6 |
| 892 | 16 | 33 | 1857 2000 AMERICAN JOURNAL OF MEDICAL GENETICS 95(2):123-129 Hjalgrim H; Hansen BF; Brondum-Nielsen K; Nolting D; Kjaer I Aspects of skeletal development in fragile X syndrome fetuses | 2 | 3 |
| 893 | 0 | 5 | 1722 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(2):140-141 Hjalgrim H; Jacobsen TB; Norgaard K; Lou HC; Brondum-Nielsen K; Jonassen O Frontal-subcortical hypofunction in the fragile X syndrome | 5 | 6 |
| 894 | 4 | 13 | 843 1991 CLINICAL PEDIATRICS 30(5):318-321 HO HH; EAVES LC; PAYNE E VARIABILITY OF DEVELOPMENT IN 3 SIBLINGS WITH FRAGILE-X SYNDROME | 0 | 1 |
| 895 | 9 | 19 | 644 1989 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 19(2):343-347 HO HH; KALOUSEK DK BRIEF REPORT - FRAGILE X-SYNDROME IN AUTISTIC BOYS | 10 | 14 |
| 896 | 20 | 37 | 578 1988 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 30(2):257-261 HO HZ; GLAHN TJ; HO JC THE FRAGILE-X SYNDROME | 2 | 3 |
| 897 | 6 | 24 | 715 1990 JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY 29(2):214-219 HODAPP RM; DYKENS EM; HAGERMAN RJ; SCHREINER R; LACHIEWICZ AM; LECKMAN JF DEVELOPMENTAL IMPLICATIONS OF CHANGING TRAJECTORIES OF IQ IN MALES WITH FRAGILE-X SYNDROME | 31 | 44 |
| 898 | 6 | 28 | 865 1991 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 21(4):503-516 HODAPP RM; DYKENS EM; ORT SI; ZELINSKY DG; LECKMAN JF CHANGING PATTERNS OF INTELLECTUAL STRENGTHS AND WEAKNESSES IN MALES WITH FRAGILE-X SYNDROME | 5 | 15 |
| 899 | 1 | 22 | 958 1992 AMERICAN JOURNAL ON MENTAL RETARDATION 97(1):39-46 HODAPP RM; LECKMAN JF; DYKENS EM; SPARROW SS; ZELINSKY DG; ORT SI K-ABC PROFILES IN CHILDREN WITH FRAGILE-X SYNDROME, DOWN-SYNDROME, AND NONSPECIFIC MENTAL-RETARDATION | 15 | 37 |
| 900 | 3 | 23 | 352 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):685-699 HOEGERMAN SF; RARY JM SPECULATION ON THE ROLE OF TRANSPOSABLE ELEMENTS IN HUMAN GENETIC-DISEASE WITH PARTICULAR ATTENTION TO ACHONDROPLASIA AND THE FRAGILE-X SYNDROME | 10 | 19 |
Page 9: 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)
Generated by: HistCite(Vlad).
Version: 2004.08.24