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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by GCS.
Page 7: 1 (1246) 2 (77) 3 (47) 4 (34) 5 (25) 6 (19) 7 (14) 8 (11) 9 (9) 10 (7) 11 (5) 12 (4) 13 (3) 14 (2) 15 (1) 16 (1) 17 (0) 18 (0) 19 (0) 20 (0) 21 (0) 22 (0) 23 (0) 24 (0)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 601 | 0 | 4 | 76 1982 LANCET 1(8263):101-101 GARDNER AP; HOWELL RT; MCDERMOTT A FRAGILE-X CHROMOSOME - CONSISTENT DEMONSTRATION OF FRAGILE SITE IN FIBROBLAST-CULTURES | 10 | 14 |
| 602 | 6 | 36 | 188 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 |
| 603 | 0 | 4 | 218 1984 JOURNAL OF MEDICAL GENETICS 21(5):373-373 FITCHETT M; SEABRIGHT M DELETED X-CHROMOSOMES IN PATIENTS WITH THE FRAGILE X-SYNDROME | 10 | 14 |
| 604 | 3 | 11 | 227 1984 OBSTETRICS AND GYNECOLOGY 63(3):S19-S21 HOGGE WA; SCHONBERG SA; GLOVER TW; HECHT F; GOLBUS MS PRENATAL-DIAGNOSIS OF FRAGILE (X) SYNDROME | 7 | 14 |
| 605 | 6 | 18 | 263 1985 CLINICAL GENETICS 27(5):463-467 GUSTAVSON KH; DAHLBOM K; FLOOD A; HOLMGREN G; BLOMQUIST HK; SANNER G EFFECT OF FOLIC-ACID TREATMENT IN THE FRAGILE X-SYNDROME | 10 | 14 |
| 606 | 2 | 17 | 325 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 |
| 607 | 9 | 17 | 327 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):263-271 BROWN WT; COHEN IL; FISCH GS; WOLFSCHEIN EG; JENKINS VA; MALIK MN; JENKINS EC HIGH-DOSE FOLIC-ACID TREATMENT OF FRAGILE-(X) MALES | 9 | 14 |
| 608 | 21 | 26 | 331 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):313-324 TOMMERUP N; AULA P; GUSTAVII B; HEIBERG A; HOLMGREN G; VONKOSKULL H; LEISTI J; MIKKELSEN M; MITELMAN F; NIELSEN KB; STEINBACH P; STENGELRUTKOWSKI S; WAHLSTROM J; ZANG K; ZANKL M 2ND TRIMESTER PRENATAL-DIAGNOSIS OF THE FRAGILE-X | 7 | 14 |
| 609 | 9 | 31 | 359 1986 ANNALS OF HUMAN GENETICS 50:385-398 LOESCH DZ DERMATOGLYPHIC FINDINGS IN FRAGILE X-SYNDROME - A CAUSAL HYPOTHESIS POINTS TO X-Y INTERCHANGE | 9 | 14 |
| 610 | 5 | 36 | 411 1987 AMERICAN JOURNAL OF DISEASES OF CHILDREN 141(2):184-187 HAGERMAN RJ; ALTSHULSTARK D; MCBOGG P RECURRENT OTITIS-MEDIA IN THE FRAGILE X-SYNDROME | 9 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 611 | 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 |
| 612 | 11 | 14 | 525 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):337-345 PURVISSMITH SG; LAING S; SUTHERLAND GR; BAKER E PRENATAL-DIAGNOSIS OF THE FRAGILE-X - THE AUSTRALASIAN EXPERIENCE | 0 | 14 |
| 613 | 2 | 6 | 598 1988 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 18(3):458-460 LECOUTEUR A; RUTTER M; SUMMERS D; BUTLER L FRAGILE-X IN FEMALE AUTISTIC TWINS | 8 | 14 |
| 614 | 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 |
| 615 | 4 | 16 | 810 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):418-420 LEDBETTER SA; SCHWARTZ CE; DAVIES KE; LEDBETTER DH NEW SOMATIC-CELL HYBRIDS FOR PHYSICAL MAPPING IN DISTAL XQ AND THE FRAGILE-X REGION | 0 | 14 |
| 616 | 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 |
| 617 | 5 | 23 | 1059 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 |
| 618 | 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 |
| 619 | 11 | 21 | 1290 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(5):991-993 SHERMAN SL THE HIGH PREVALENCE OF FRAGILE-X PREMUTATION CARRIER FEMALES - IS THIS FREQUENCY UNIQUE TO THE FRENCH-CANADIAN POPULATION | 7 | 14 |
| 620 | 16 | 33 | 1296 1995 AMERICAN JOURNAL OF MEDICAL GENETICS 58(3):249-256 LOESCH DZ; HUGGINS RM; HOANG NH GROWTH IN STATURE IN FRAGILE-X FAMILIES - A MIXED LONGITUDINAL-STUDY | 12 | 14 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 621 | 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 |
| 622 | 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 |
| 623 | 17 | 36 | 1695 1998 NEUROPSYCHOLOGIA 36(11):1239-1246 Cornish KM; Munir F; Cross G The nature of the spatial deficit in young females with Fragile-X syndrome: A neuropsychological and molecular perspective | 10 | 14 |
| 624 | 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 |
| 625 | 15 | 30 | 1775 1999 CORTEX 35(2):263-271 Cornish KM; Munir F; Cross G Spatial cognition in males with Fragile-X syndrome: Evidence for a neuropsychological phenotype | 12 | 14 |
| 626 | 8 | 46 | 67 1982 JOHNS HOPKINS MEDICAL JOURNAL 151(5):231-237 PYERITZ RE; STAMBERG J; THOMAS GH; BELL BB; ZAHKA KG; BERNHARDT BA THE MARKER XQ28 SYNDROME (FRAGILE-X SYNDROME) IN A RETARDED MAN WITH MITRAL-VALVE PROLAPSE | 8 | 13 |
| 627 | 2 | 8 | 75 1982 LANCET 1(8263):100-100 SUTHERLAND GR; JACKY PB PRENATAL-DIAGNOSIS OF FRAGILE-X CHROMOSOME | 6 | 13 |
| 628 | 3 | 20 | 180 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):259-273 HOLDEN JJA; WANG HS; WHITE BN THE FRAGILE-X SYNDROME .4. PROGRESS TOWARDS THE IDENTIFICATION OF LINKED RESTRICTION FRAGMENT LENGTH VARIANTS (RFLVS) | 4 | 13 |
| 629 | 0 | 0 | 217 1984 JOURNAL OF MEDICAL GENETICS 21(4):299-299 PEMBREY ME; WINTER RM; DAVIES KE A PERMUTATION THAT GENERATES THE DEFINITIVE MUTATION BY RECOMBINATION EXPLAINS THE INHERITANCE OF THE MARTIN-BELL SYNDROME (FRAGILE-X) | 9 | 13 |
| 630 | 11 | 29 | 241 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(3):543-552 ROSENBLATT DS; DUSCHENES EA; HELLSTROM FV; GOLICK MS; VEKEMANS MJJ; ZEESMAN SF; ANDERMANN E FOLIC-ACID BLINDED TRIAL IN IDENTICAL-TWINS WITH FRAGILE-X SYNDROME | 9 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 631 | 6 | 28 | 293 1985 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 6(2):87-90 VARLEY CK; HOLM VA; EREN MO COGNITIVE AND PSYCHIATRIC VARIABILITY IN 3 BROTHERS WITH FRAGILE X-SYNDROME | 10 | 13 |
| 632 | 43 | 97 | 361 1986 ANNALS OF THE NEW YORK ACADEMY OF SCIENCES 477:129-150 BROWN WT; JENKINS EC; KRAWCZUN MS; WISNIEWSKI K; RUDELLI R; COHEN IL; FISCH G; WOLFSCHEIN E; MIEZEJESKI C; DOBKIN C THE FRAGILE-X SYNDROME | 10 | 13 |
| 633 | 7 | 12 | 377 1986 CLINICAL GENETICS 30(4):249-254 GOONEWARDENA P; GUSTAVSON KH; HOLMGREN G; TOLUN A; CHOTAI J; JOHNSEN E; PETTERSSON U ANALYSIS OF FRAGILE X-MENTAL RETARDATION FAMILIES USING FLANKING POLYMORPHIC DNA PROBES | 7 | 13 |
| 634 | 4 | 7 | 491 1987 PRENATAL DIAGNOSIS 7(3):197-202 SUTHERLAND GR; BAKER E; PURVISSMITH S; HOCKEY A; KRUMINS E; EICHENBAUM SZ PRENATAL-DIAGNOSIS OF THE FRAGILE-X USING THYMIDINE INDUCTION | 5 | 13 |
| 635 | 0 | 18 | 510 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):77-82 PHELAN MC; STEVENSON RE; COLLINS JL; TRENT HE FRAGILE-X SYNDROME AND NEOPLASIA | 7 | 13 |
| 636 | 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 |
| 637 | 21 | 61 | 527 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):355-368 MCKINLEY MJ; KEARNEY LU; NICOLAIDES KH; GOSDEN CM; WEBB TP; FRYNS JP PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME BY PLACENTAL (CHORIONIC VILLI) BIOPSY CULTURE | 8 | 13 |
| 638 | 12 | 33 | 670 1990 AMERICAN JOURNAL OF HUMAN GENETICS 46(4):738-743 ROCCHI M; ARCHIDIACONO N; RINALDI A; FILIPPI G; BARTOLUCCI G; FANCELLO GS; SINISCALCO M MENTAL-RETARDATION IN HETEROZYGOTES FOR THE FRAGILE-X MUTATION - EVIDENCE IN FAVOR OF AN X INACTIVATION-DEPENDENT EFFECT | 11 | 13 |
| 639 | 6 | 17 | 680 1990 AMERICAN JOURNAL OF MEDICAL GENETICS 37(2):265-267 MOORE PSJ; CHUDLEY AE; WINTER JSD TRUE PRECOCIOUS PUBERTY IN A GIRL WITH THE FRAGILE X-SYNDROME | 10 | 13 |
| 640 | 1 | 14 | 691 1990 BRAIN & DEVELOPMENT 12(1):128-130 WAHLSTROM J; WITTENGERSTROM I; MELLQUIST L; ANVRET M; ODEN A THE RETT SYNDROME RELATED TO FRAGILE-X(P22) IN CAFFEINE-INDUCED LYMPHOCYTE CULTURE | 0 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 641 | 18 | 36 | 707 1990 JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME 72A(6):889-896 DAVIDS JR; HAGERMAN RJ; EILERT RE ORTHOPEDIC ASPECTS OF FRAGILE-X SYNDROME | 0 | 13 |
| 642 | 18 | 35 | 858 1991 GENOMICS 10(3):576-582 SUTHERS GK; MULLEY JC; VOELCKEL MA; DAHL N; VAISANEN ML; STEINBACH P; GLASS IA; SCHWARTZ CE; VANOOST BA; THIBODEAU SN; HAITES NE; OOSTRA BA; SCHINZEL A; CARBALLO M; MORRIS CP; HOPWOOD JJ; SUTHERLAND GR LINKAGE HOMOGENEITY NEAR THE FRAGILE-X LOCUS IN NORMAL AND FRAGILE-X FAMILIES | 9 | 13 |
| 643 | 7 | 16 | 861 1991 HUMAN GENETICS 87(3):369-372 HULSEBOS TJM; OOSTRA BA; BROERSEN S; SMITS A; VANOOST BA; WESTERVELD A NEW DISTAL MARKER CLOSELY LINKED TO THE FRAGILE-X LOCUS | 4 | 13 |
| 644 | 5 | 17 | 1072 1993 BIOLOGICAL PSYCHIATRY 33(3):213-216 JEFFRIES FM; REISS AL; BROWN WT; MEYERS DA; GLICKSMAN AC; BANDYOPADHYAY S BIPOLAR SPECTRUM DISORDER AND FRAGILE-X SYNDROME - A FAMILY STUDY | 4 | 13 |
| 645 | 20 | 26 | 1077 1993 CLINICAL GENETICS 43(1):34-38 HORI T; YAMAUCHI M; SEKI N; TSUJI S; IKUKO K HERITABLE UNSTABLE DNA-SEQUENCES AND HYPERMETHYLATION ASSOCIATED WITH FRAGILE-X SYNDROME IN JAPANESE FAMILIES | 9 | 13 |
| 646 | 38 | 84 | 1090 1993 GENETIC COUNSELING 4(4):245-263 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H FRAGILE-X SYNDROME AND AUTISM - A PREVALENT ASSOCIATION OR A MISINTERPRETED CONNECTION | 6 | 13 |
| 647 | 6 | 7 | 1122 1993 LANCET 341(8841):373-374 PALOMAKI GE; HADDOW JE IS IT TIME FOR POPULATION-BASED PRENATAL SCREENING FOR FRAGILE-X | 10 | 13 |
| 648 | 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 |
| 649 | 18 | 31 | 1358 1995 HUMAN MOLECULAR GENETICS 4(9):1681-1684 QUAN F; GROMPE M; JAKOBS P; POPOVICH BW SPONTANEOUS DELETION IN THE FMR1 GENE IN A PATIENT WITH FRAGILE-X SYNDROME AND CHERUBISM | 7 | 13 |
| 650 | 29 | 43 | 1428 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):302-308 deGraaff E; deVries BBA; Willemsen R; vanHemel JO; Mohkamsing S; Oostra BA; vandenOuweland AMW The fragile X phenotype in a mosaic male with a deletion showing expression of the FMR1 protein in 28% of the cells | 11 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 651 | 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 |
| 652 | 22 | 31 | 1435 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):350-355 WrightTalamante C; Cheema A; Riddle JE; Luckey DW; Taylor AK; Hagerman RJ A controlled study of longitudinal IQ changes in females and males with fragile X syndrome | 11 | 13 |
| 653 | 8 | 29 | 1553 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 68(1):62-69 McConkieRosell A; Spiridigliozzi GA; Iafolla T; Tarleton J; Lachiewicz AM Carrier testing in the fragile X syndrome: Attitudes and opinions of obligate carriers | 7 | 13 |
| 654 | 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 |
| 655 | 12 | 30 | 1641 1998 ARQUIVOS DE NEURO-PSIQUIATRIA 56(1):18-23 Guerreiro MM; Camargo EE; Kato M; Marques-De-Faria AP; Ciasca SM; Guerreiro CAM; Netto JRM; Moura-Ribeiro MVL Fragile X syndrome - Clinical, electroencephalographic and neuroimaging characteristics | 7 | 13 |
| 656 | 3 | 66 | 1677 1998 JOURNAL OF BIOLOGICAL CHEMISTRY 273(41):26998-27008 Parsons MA; Sinden RR; Izban MG Transcriptional properties of RNA polymerase II within triplet repeat-containing DNA from the human myotonic dystrophy and fragile X loci | 0 | 13 |
| 657 | 9 | 21 | 1884 2000 EUROPEAN JOURNAL OF HUMAN GENETICS 8(4):247-252 Murray A; Ennis S; MacSwiney F; Webb J; Morton NE Reproductive and menstrual history of females with fragile X expansions | 10 | 13 |
| 658 | 16 | 17 | 2006 2001 CELL 107(5):555-557 Kaytor MD; Orr HT RNA targets of the fragile X protein | 5 | 13 |
| 659 | 5 | 37 | 2114 2002 CURRENT BIOLOGY 12(15):1331-1335 Inoue SB; Shimoda M; Nishinokubi I; Siomi MC; Okamura M; Nakamura A; Kobayashi S; Ishida N; Siomi H A role for the Drosophila fragile X-related gene in circadian output | 9 | 13 |
| 660 | 15 | 44 | 2143 2002 HUMAN BRAIN MAPPING 16(4):206-218 Rivera SM; Menon V; White CD; Glaser B; Reiss AL Functional brain activation during arithmetic processing in females with fragile X Syndrome is related to FMRI protein expression | 7 | 13 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 661 | 22 | 75 | 2172 2002 MOLECULAR AND CELLULAR NEUROSCIENCE 19(2):138-151 Li JX; Pelletier MR; Velazquez JLP; Carlen PL Reduced cortical synaptic plasticity and GluR1 expression associated with fragile X mental retardation protein deficiency | 9 | 13 |
| 662 | 13 | 30 | 2242 2003 ARCHIVES OF NEUROLOGY 60(1):117-121 Leehey MA; Munhoz RP; Lang AE; Brunberg JA; Grigsby J; Greco C; Jacquemont S; Tassone F; Lozano AM; Hagerman PJ; Hagerman RJ The fragile X premutation presenting as essential tremor | 6 | 13 |
| 663 | 1 | 7 | 30 1981 NEW ENGLAND JOURNAL OF MEDICINE 305(22):1348-1348 NIELSEN KB; TOMMERUP N; DYGGVE H; SCHOU C MACROORCHIDISM, MENTAL-RETARDATION, AND THE FRAGILE-X | 8 | 12 |
| 664 | 1 | 7 | 81 1982 PEDIATRICS 69(5):668-669 RHOADS FA X-LINKED MENTAL-RETARDATION AND FRAGILE-X OR MARKER-X SYNDROME | 11 | 12 |
| 665 | 5 | 26 | 87 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(5):869-878 POPOVICH BW; ROSENBLATT DS; COOPER BA; VEKEMANS M INTRACELLULAR FOLATE DISTRIBUTION IN CULTURED FIBROBLASTS FROM PATIENTS WITH THE FRAGILE-X SYNDROME | 8 | 12 |
| 666 | 2 | 4 | 111 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 | 12 |
| 667 | 1 | 10 | 133 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 |
| 668 | 4 | 11 | 189 1984 ANNALES DE GENETIQUE 27(4):230-232 LEJEUNE J; RETHORE MO; DEBLOIS MC; RAVEL A ASSAY OF FOLIC-ACID TREATMENT IN FRAGILE-X SYNDROME | 7 | 12 |
| 669 | 14 | 34 | 251 1985 AMERICAN JOURNAL OF MENTAL DEFICIENCY 90(2):119-123 DELACRUZ FF FRAGILE-X SYNDROME | 9 | 12 |
| 670 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 671 | 14 | 52 | 398 1986 JOURNAL OF PEDIATRIC PSYCHOLOGY 11(1):91-102 MADISON LS; MOSHER GA; GEORGE CH FRAGILE-X SYNDROME - DIAGNOSIS AND RESEARCH | 0 | 12 |
| 672 | 4 | 7 | 451 1987 HUMAN GENETICS 75(3):269-271 WINTER RM POPULATION-GENETICS IMPLICATIONS OF THE PREMUTATION HYPOTHESIS FOR THE GENERATION OF THE FRAGILE X-MENTAL RETARDATION GENE | 11 | 12 |
| 673 | 16 | 41 | 468 1987 JOURNAL OF MEDICAL GENETICS 24(1):14-22 CONNOR JM; PIRRIT LA; YATES JRW; CROSSLEY JA; IMRIE SJ; COLGAN JM LINKAGE ANALYSIS USING MULTIPLE XQ DNA POLYMORPHISMS IN NORMAL-FAMILIES, FAMILIES WITH THE FRAGILE X-SYNDROME, AND OTHER FAMILIES WITH X-LINKED CONDITIONS | 7 | 12 |
| 674 | 4 | 18 | 542 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):613-623 WARREN ST; ZHANG F; SUTCLIFFE JS; PETERS JF STRATEGY FOR MOLECULAR-CLONING OF THE FRAGILE-X SITE DNA | 7 | 12 |
| 675 | 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 |
| 676 | 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 |
| 677 | 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 |
| 678 | 25 | 46 | 940 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):299-306 CLARKE A; BRADLEY D; GILLESPIE K; REES D; HOLLAND A; THOMAS NST FRAGILE-X MENTAL-RETARDATION AND THE IDURONATE SULFATASE LOCUS - TESTING LAIRD MODEL OF FRA(X) INHERITANCE | 7 | 12 |
| 679 | 5 | 25 | 953 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 44(5):543-550 LOESCH DZ; HAY DA; SHEFFIELD LJ FRAGILE-X FAMILY WITH UNUSUAL DIGITAL AND FACIAL ABNORMALITIES, CLEFT-LIP AND PALATE, AND EPILEPSY | 8 | 12 |
| 680 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 681 | 17 | 18 | 1186 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):490-496 MADDALENA A; HICKS BD; SPENCE WC; LEVINSON G; HOWARDPEEBLES PN PRENATAL-DIAGNOSIS IN KNOWN FRAGILE-X CARRIERS | 7 | 12 |
| 682 | 1 | 16 | 1205 1994 CANCER RESEARCH 54(19):5212-5216 LEE ST; MCGLENNEN RC; LITZ CE CLONAL DETERMINATION BY THE FRAGILE-X (FMR1) AND PHOSPHOGLYCERATE KINASE (PGK) GENES IN HEMATOLOGICAL MALIGNANCIES | 1 | 12 |
| 683 | 19 | 28 | 1215 1994 HUMAN GENETICS 93(2):143-147 VAISANEN ML; KAHKONEN M; LEISTI J DIAGNOSIS OF FRAGILE-X SYNDROME BY DIRECT MUTATION ANALYSIS | 9 | 12 |
| 684 | 10 | 23 | 1230 1994 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 24(4):473-485 MAZZOCCO MMM; PENNINGTON BF; HAGERMAN RJ SOCIAL COGNITION SKILLS AMONG FEMALES WITH FRAGILE-X | 9 | 12 |
| 685 | 20 | 27 | 1292 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(6):1408-1413 LOESCH DZ; HUGGINS R; PETROVIC V; SLATER H EXPANSION OF THE CGG REPEAT IN FRAGILE-X IN THE FMR1 GENE DEPENDS ON THE SEX OF THE OFFSPRING | 5 | 12 |
| 686 | 40 | 75 | 1330 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):252-269 Cohen IL Behavioral profiles of autistic and nonautistic fragile X males | 11 | 12 |
| 687 | 13 | 35 | 1375 1995 JOURNAL OF MEDICAL GENETICS 32(12):925-929 KIRCHGESSNER CU; WARREN ST; WILLARD HF X INACTIVATION OF THE FMR1 FRAGILE-X MENTAL-RETARDATION GENE | 5 | 12 |
| 688 | 6 | 13 | 1395 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 | 6 | 12 |
| 689 | 12 | 14 | 1506 1996 PEDIATRIC NEUROLOGY 15(4):358-360 Kluger G; Bohm I; Laub MC; Waldenmaier C Epilepsy and fragile X gene mutations | 6 | 12 |
| 690 | 3 | 11 | 1555 1997 AMERICAN JOURNAL OF MEDICAL GENETICS 69(1):114-116 Martin NG; Healey SC; Pangan TS; Heath AC; Turner G Do mothers of dizygotic twins have earlier menopause? A role for fragile X? | 5 | 12 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 691 | 7 | 10 | 1608 1997 JOURNAL OF MEDICAL GENETICS 34(3):250-251 Willemsen R; Los F; Mohkamsing S; vandenOuweland A; Deelen W; Galjaard H; Oostra B Rapid antibody test for prenatal diagnosis of fragile X syndrome on amniotic fluid cells: A new appraisal | 10 | 12 |
| 692 | 23 | 55 | 1895 2000 HUMAN MOLECULAR GENETICS 9(10):1487-1493 Tamanini F; Kirkpatrick LL; Schonkeren J; van Unen L; Bontekoe C; Bakker C; Nelson DL; Galjaard H; Oostra BA; Hoogeveen AT The fragile X-related proteins FXR1P and FXR2P contain a functional nucleolar-targeting signal equivalent to the HIV-1 regulatory proteins | 7 | 12 |
| 693 | 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 |
| 694 | 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 |
| 695 | 28 | 39 | 2199 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(2):454-464 Nolin SL; Brown WT; Glicksman A; Houck GE; Gargano AD; Sullivan A; Biancalana V; Brondum-Nielsen K; Hjalgrim H; Holinski-Feder E; Kooy F; Longshore J; Macpherson J; Mandel JL; Matthijs G; Rousseau F; Steinbach P; Vaisanen ML; von Koskull H; Sherman SL Expansion of the fragile X CGG repeat in females with premutation or intermediate alleles | 8 | 12 |
| 696 | 15 | 31 | 2237 2003 ANNALS OF NEUROLOGY 53(5):616-623 Berry-Kravis E; Lewin F; Wuu J; Leehey M; Hagerman R; Hagerman P; Goetz CG Tremor and ataxia in fragile X premutation carriers: Blinded videotape study | 8 | 12 |
| 697 | 1 | 15 | 34 1981 PEDIATRICS 68(4):594-595 GERALD PS X-LINKED MENTAL-RETARDATION AND THE FRAGILE-X SYNDROME | 5 | 11 |
| 698 | 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 |
| 699 | 8 | 23 | 126 1983 CLINICAL GENETICS 23(6):436-440 SILVERMAN W; LUBIN R; JENKINS EC; BROWN WT THE STRENGTH OF ASSOCIATION BETWEEN FRAGILE(X) CHROMOSOME PRESENCE AND MENTAL-RETARDATION | 8 | 11 |
| 700 | 0 | 18 | 372 1986 CLINICAL ENDOCRINOLOGY 24(3):327-333 OHARE JP; OBRIEN IAD; ARENDT J; ASTLEY P; RATCLIFFE W; ANDREWS H; WALTERS R; CORRALL RJM DOES MELATONIN DEFICIENCY CAUSE THE ENLARGED GENITALIA OF THE FRAGILE-X SYNDROME | 9 | 11 |
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