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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 16: 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 |
|---|---|---|---|---|---|
| 1501 | 13 | 31 | 2032 2001 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 22(6):353-359 Myers GF; Mazzocco MMM; Maddalena A; Reiss AL No widespread psychological effect of the fragile X premutation in childhood: Evidence from a preliminary controlled study | 2 | 2 |
| 1502 | 13 | 16 | 1345 1995 DIAGNOSTIC MOLECULAR PATHOLOGY 4(3):158-161 NABER SP MOLECULAR DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| 1503 | 15 | 46 | 1361 1995 JOURNAL OF BIOLOGICAL CHEMISTRY 270(48):28970-28977 NADEL Y; WEISMANSHOMER P; FRY M THE FRAGILE-X SYNDROME SINGLE-STRAND D(CGG)(N) NUCLEOTIDE REPEATS READILY FOLD BACK TO FORM UNIMOLECULAR HAIRPIN STRUCTURES | 11 | 47 |
| 1504 | 0 | 0 | 1849 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):415-415 Najmabadi H; Taghizadeh F; Teimourian SH; Karimi-Nejad R; Shafeghati Y; Mohammady GB; Al-Madany SN; Hoseiny SS; Karimi-Nejad MH Molecular analysis of Fragile X syndrome in Iranian population. | 0 | 0 |
| 1505 | 4 | 5 | 1313 1995 BRAIN & DEVELOPMENT 17(5):322-322 NAKAHORI Y THE INCIDENCE OF THE FRAGILE-X SYNDROME IN JAPANESE - COMMENTARY ON NANBAS PAPER | 0 | 0 |
| 1506 | 10 | 20 | 890 1991 NUCLEIC ACIDS RESEARCH 19(16):4355-4359 NAKAHORI Y; KNIGHT SJL; HOLLAND J; SCHWARTZ C; ROCHE A; TARLETON J; WONG S; FLINT TJ; FROSTERISKENIUS U; BENTLEY D; DAVIES KE; HIRST MC MOLECULAR HETEROGENEITY OF THE FRAGILE-X SYNDROME | 61 | 91 |
| 1507 | 26 | 39 | 1312 1995 BRAIN & DEVELOPMENT 17(5):317-321 NANBA E; KOHNO Y; MATSUDA A; YANO M; SATO C; HASHIMOTO K; KOEDA T; YOSHINO K; KIMURA M; MAEOKA Y; YAMAMOTO T; MAEGAKI Y; EDA I; TAKESHITA K NONRADIOACTIVE DNA DIAGNOSIS FOR THE FRAGILE-X SYNDROME IN MENTALLY-RETARDED JAPANESE MALES | 5 | 15 |
| 1508 | 0 | 3 | 987 1992 JAPANESE JOURNAL OF HUMAN GENETICS 37(3):235-239 NATORI N A CASE OF ATYPICAL DUCHENNE TYPE MUSCULAR-DYSTROPHY WITH FRAGILE-X | 0 | 1 |
| 1509 | 0 | 0 | 662 1989 REVISTA BRASILEIRA DE GENETICA 12(2):391-404 NAVAJAS L; VIANNAMORGANTE AM RELATIONSHIP BETWEEN AGE AND MENTAL STATUS AND THE EXPRESSION OF THE FRAGILE(X) IN HETEROZYGOTES FOR THE MARTIN-BELL SYNDROME | 0 | 0 |
| 1510 | 3 | 45 | 1500 1996 MEDICAL ANTHROPOLOGY QUARTERLY 10(4):537-550 Nelkin D The social dynamics of genetic testing: The case of Fragile-X | 1 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1511 | 40 | 70 | 1392 1995 SEMINARS IN CELL BIOLOGY 6(1):5-11 NELSON DL THE FRAGILE-X SYNDROMES | 3 | 16 |
| 1512 | 1 | 3 | 499 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):1-17 NERI G; OPITZ JM; MIKKELSEN M; JACOBS PA; DAVIES K; TURNER G CONFERENCE REPORT - 3RD INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 6 | 15 |
| 1513 | 0 | 0 | 1971 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):372-372 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P Pharmacological reactivation of the FMR1 gene of the fragile X syndrome. | 0 | 0 |
| 1514 | 0 | 0 | 1835 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):50-50 Neri G; Pomponi MG; Pietrobono R; Chiurazzi P; Oostra BA Differential reactivation of the FMR1 gene in fragile X patients cell lines. | 0 | 0 |
| 1515 | 6 | 10 | 547 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):665-672 NERI G; SANFILIPPO S; PAVONE L; MOLLICA F; BARBERI I; GIUFFRE L; ROMANO C; MATTINA T; CAMMARATA M; RAGUSA MG; SAMMITO V; VENTIMIGLIA G; MUSUMECI SA THE FRAGILE-X IN SICILY - AN EPIDEMIOLOGICAL SURVEY | 9 | 16 |
| 1516 | 0 | 0 | 2090 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):507-507 Neri G; Tabolacci E; Pietrobono R; Pomponi MG; Chiurazzi P Histone hyperacetylation and reactivation of the fragile X syndrome gene. | 0 | 1 |
| 1517 | 11 | 14 | 1384 1995 NEW ZEALAND MEDICAL JOURNAL 108(1009):404-406 NEVILLE L; COCHRANE J; FITZGERALD P; KENNEDY M FRAGILE-X MENTAL-RETARDATION SYNDROME - DNA DIAGNOSIS AND CARRIER DETECTION IN NEW-ZEALAND FAMILIES | 0 | 0 |
| 1518 | 14 | 46 | 2111 2002 BRAIN RESEARCH 927(1):8-17 Nielsen DM; Derber WJ; McClellan DA; Crnic LS Alterations in the auditory startle response in Fmr1 targeted mutant mouse models of fragile X syndrome | 8 | 9 |
| 1519 | 8 | 17 | 149 1983 JOURNAL OF MENTAL DEFICIENCY RESEARCH 27(SEP):211-226 NIELSEN KB DIAGNOSIS OF THE FRAGILE-X SYNDROME (MARTIN-BELL SYNDROME) - CLINICAL FINDINGS IN 27 MALES WITH THE FRAGILE SITE AT XQ28 | 18 | 26 |
| 1520 | 4 | 18 | 345 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):537-544 NIELSEN KB SEX-CHROMOSOME ANEUPLOIDY IN FRAGILE-X CARRIERS | 1 | 6 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1521 | 3 | 9 | 516 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):143-147 NIELSEN KB GROWTH-PATTERN IN BOYS WITH FRAGILE-X | 3 | 3 |
| 1522 | 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 |
| 1523 | 4 | 23 | 60 1982 HUMAN GENETICS 61(2):113-117 NIELSEN KB; TOMMERUP N; DYGGVE HV; SCHOU C MACRO-ORCHIDISM AND FRAGILE-X IN MENTALLY-RETARDED MALES - CLINICAL, CYTOGENETIC, AND SOME HORMONAL INVESTIGATIONS IN MENTALLY-RETARDED MALES, INCLUDING 2 WITH THE FRAGILE SITE AT XQ28, FRA(X)(Q28) | 12 | 22 |
| 1524 | 3 | 11 | 127 1983 CLINICAL GENETICS 24(3):153-155 NIELSEN KB; TOMMERUP N; FRIIS B; HJELT K; HIPPE E FOLIC-ACID METABOLISM IN A PATIENT WITH FRAGILE-X | 0 | 9 |
| 1525 | 0 | 0 | 121 1983 CLINICAL GENETICS 23(3):241-241 NIELSEN KB; TOMMERUP N; MIKKELSEN M CLINICAL AND CYTOGENETIC FINDINGS IN 26 MENTALLY-RETARDED MALES WITH THE FRAGILE-X | 1 | 1 |
| 1526 | 6 | 26 | 136 1983 HUMAN GENETICS 64(3):240-245 NIELSEN KB; TOMMERUP N; POULSEN H; JACOBSEN P; BECK B; MIKKELSEN M CARRIER DETECTION AND X-INACTIVATION STUDIES IN THE FRAGILE-X SYNDROME - CYTOGENETIC STUDIES IN 63 OBLIGATE AND POTENTIAL CARRIERS OF THE FRAGILE-X | 23 | 35 |
| 1527 | 0 | 0 | 15 1981 CLINICAL GENETICS 19(6):493-493 NIELSEN KB; TOMMERUP N; POULSEN H; MIKKELSEN M DANISH FAMILIES WITH X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOME | 1 | 1 |
| 1528 | 3 | 8 | 159 1983 PRENATAL DIAGNOSIS 3(4):367-369 NIELSEN LB; NIELSEN KB; TOMMERUP N FRAGILE-X DEMONSTRATED RETROSPECTIVELY IN AMNIOTIC CELLS CULTURED IN LOW FOLATE MEDIUM | 2 | 4 |
| 1529 | 0 | 0 | 40 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A103-A103 NOLIN S; BROWN T; JENKINS E FRAGILE-X SYNDROME - DILEMMAS FOR GENETIC-COUNSELING | 1 | 1 |
| 1530 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1531 | 16 | 17 | 1189 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):509-512 NOLIN SL; GLICKSMAN A; HOUCK GE; BROWN WT; DOBKIN CS MOSAICISM IN FRAGILE-X AFFECTED MALES | 36 | 40 |
| 1532 | 0 | 0 | 1275 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):965-965 NOLIN SL; GLICKSMAN A; LEWIS FA; YE LL; HOUCK GE; ASHLEY AE; SHERMAN SL; BROWN WT EVIDENCE FOR A FAMILIAL FACTOR INVOLVED IN CGG REPEAT EXPANSION IN FRAGILE-X SYNDROME | 0 | 0 |
| 1533 | 22 | 52 | 1703 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(3):680-688 Nolin SL; Houck GE; Gargano AD; Blumstein H; Dobkin CS; Brown WT FMR1 CCG-repeat instability by single sperm and lymphocytes of fragile-X premutation males | 7 | 15 |
| 1534 | 0 | 0 | 1978 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):586-586 Nolin SL; Houck GE; Gargano AD; Brown WT Large fragile X premutatin alleles may often contain two AGG Interruptions. | 0 | 0 |
| 1535 | 0 | 0 | 2209 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):337-337 Nolin SL; Houck GE; Glicksman A; Gargano AD; Brown WT Large fragile X premutation alleles may often contain two AGG interruptions. | 0 | 0 |
| 1536 | 0 | 0 | 1047 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):1208-1208 NOLIN SL; HOUCK GE; LI SY; DING XH; BROWN WT; DOBKIN CS MOSAICISM IN FRAGILE-X AFFECTED MALES | 0 | 2 |
| 1537 | 1 | 7 | 535 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):443-450 NOLIN SL; JENKINS EC; BROWN WT; DOBKIN CS INSITU NICK TRANSLATION OF THE FRAGILE-X REGION | 1 | 2 |
| 1538 | 12 | 19 | 782 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):251-255 NOLIN SL; SNIDER DA; JENKINS EC; BROWN WT; KRAWCZUN M; STETKA D; HOUCK G; DOBKIN CS; STRONG G; SMITHDOBRANSKY G; VICTOR A; HUGHES K; KIMPTON D; LITTLE A; NAGARAJA U; KENEFICK B; SULLIVAN C FRAGILE-X SCREENING-PROGRAM IN NEW-YORK-STATE | 18 | 24 |
| 1539 | 4 | 6 | 944 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):328-332 NOLIN SL; SNIDER DA; JENKINS EC; DOBKIN CS; PATCHELL K; KRAWCZUN M; STRONG G; COLWELL M; VICTOR A; PAYYAPILLI T; TURCZYN M; LITTLE A; NAGARAJA U; DOYLE N; KENEFICK B; SULLIVAN C NEW-YORK-STATE SCREENING-PROGRAM FOR FRAGILE-X SYNDROME - A PROGRESS REPORT | 7 | 8 |
| 1540 | 0 | 0 | 1323 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):185-186 Nommensen D Report of the Executive Director of the National Fragile X Foundation | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1541 | 0 | 0 | 774 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):353-353 NORDSTROM AM; VONKOSKULL H LINKAGE TO DXS52 IN A FRAGILE-X NEGATIVE FAMILY | 0 | 0 |
| 1542 | 4 | 6 | 2247 2003 BIOFUTUR (229):36-37 Nourrit F Fragile X and interference. | 0 | 0 |
| 1543 | 0 | 0 | 2337 2004 JOURNAL OF INVESTIGATIVE MEDICINE 52(1):S101-S101 Nowicki ST; Jacquemont S; Li L; Nguyen DV; Gregg JP; Hagerman RJ; Hagerman PJ An approach to identify epistatic genes involved in the development of autism spectrum disorder in patients with fragile X syndrome | 0 | 0 |
| 1544 | 2 | 14 | 692 1990 BRITISH DENTAL JOURNAL 168(4):160-162 NUNN JH; DURNING P FRAGILE-X (MARTIN BELL) SYNDROME AND DENTAL-CARE | 0 | 0 |
| 1545 | 5 | 17 | 135 1983 HUMAN GENETICS 64(2):148-150 NUSSBAUM RL; AIRHART SD; LEDBETTER DH EXPRESSION OF THE FRAGILE (X)CHROMOSOME IN AN INTERSPECIFIC SOMATIC-CELL HYBRID | 18 | 58 |
| 1546 | 38 | 118 | 362 1986 ANNUAL REVIEW OF GENETICS 20:109-145 NUSSBAUM RL; LEDBETTER DH FRAGILE-X SYNDROME - A UNIQUE MUTATION IN MAN | 63 | 112 |
| 1547 | 2 | 28 | 244 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(6):1192-1205 NUSSBAUM RL; WALMSLEY RM; LESKO JG; AIRHART SD; LEDBETTER DH THYMIDYLATE SYNTHASE-DEFICIENT CHINESE-HAMSTER CELLS - A SELECTION SYSTEM FOR HUMAN-CHROMOSOME 18 AND EXPERIMENTAL SYSTEM FOR THE STUDY OF THYMIDYLATE SYNTHASE REGULATION AND FRAGILE-X EXPRESSION | 6 | 47 |
| 1548 | 6 | 18 | 2113 2002 CLINICAL GENETICS 61(1):13-20 O'Connell CD; Atha DH; Jakupciak JP; Richie KI Standardization of PCR amplification for fragile X trinucleotide repeat measurements | 0 | 3 |
| 1549 | 0 | 0 | 2138 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 O'Connor R; Riley K; Epstein J; Wilson R; McKelvie K; Reynolds A; Hagerman R; Levine R Analysis of ADHD subtypes in Fragile X syndrome | 0 | 0 |
| 1550 | 0 | 0 | 2211 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):348-348 O'Donnell WT; Ceman S; Warren ST Phosphorylation of the fragile X mental retardation protein regulates translation of its mRNA ligands. | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1551 | 0 | 0 | 1847 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):365-365 O'Donnell WT; Warren ST Investigating the cause of macroorchidism in fragile X syndrome using oligonucleotide microarrays. | 0 | 0 |
| 1552 | 90 | 179 | 2106 2002 ANNUAL REVIEW OF NEUROSCIENCE 25:315-338 O'Donnell WT; Warren ST A decade of molecular studies of fragile X syndrome | 0 | 46 |
| 1553 | 0 | 0 | 274 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):715-715 OBERLE I; ARVEILER B; MATTEI MG; MATTEI JF; BOUE J; MANDEL JL LINKAGE ANALYSIS OF THE FRAGILE X-MENTAL RETARDATION SYNDROME WITH FLANKING POLYMORPHIC DNA MARKERS | 2 | 5 |
| 1554 | 0 | 0 | 504 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):22-23 OBERLE I; ARVEILER B; WOELFLIN A; HOFKER M; PEARSON P; MANDEL JL GENETIC AND PHYSICAL MAPPING OF THE FRAGILE-X REGION - .A. NEW POLYMORPHIC MARKERS .B. IS THE FRAGILE-X SITE A PREFERENTIAL BREAKPOINT IN CHROMOSOME REARRANGEMENTS | 0 | 0 |
| 1555 | 8 | 27 | 457 1987 HUMAN GENETICS 77(1):60-65 OBERLE I; CAMERINO G; WROGEMANN K; ARVEILER B; HANAUER A; RAIMONDI E; MANDEL JL MULTIPOINT GENETIC-MAPPING OF THE XQ26-Q28 REGION IN FAMILIES WITH FRAGILE-X MENTAL-RETARDATION AND IN NORMAL-FAMILIES REVEALS TIGHT LINKAGE OF MARKERS IN Q26-Q27 | 17 | 60 |
| 1556 | 10 | 29 | 407 1986 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 83(4):1016-1020 OBERLE I; HEILIG R; MOISAN JP; KLOEPFER C; MATTEI MG; MATTEI JF; BOUE J; FROSTERISKENIUS U; JACOBS PA; LATHROP GM; LALOUEL JM; MANDEL JL GENETIC-ANALYSIS OF THE FRAGILE-X MENTAL-RETARDATION SYNDROME WITH 2 FLANKING POLYMORPHIC DNA MARKERS | 40 | 64 |
| 1557 | 0 | 0 | 880 1991 M S-MEDECINE SCIENCES 7(4):378-379 OBERLE I; MANDEL JL FRAGILE-X MENTAL-RETARDATION - VERY LOCALIZED GENOMIC IMPRINTING CLOSELY LINKED TO CLINICAL EXPRESSION | 0 | 0 |
| 1558 | 2 | 10 | 305 1985 LANCET 1(8433):871-871 OBERLE I; MANDEL JL; BOUE J; MATTEI MG; MATTEI JF POLYMORPHIC DNA MARKERS IN PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 14 | 27 |
| 1559 | 0 | 0 | 744 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):76-76 OBERLE I; ROUSSEAU F; HEITZ D; DEVYS D; ZENGERLING S; MANDEL JL MOLECULAR-BASIS OF THE FRAGILE-X SYNDROME AND DIAGNOSTIC APPLICATIONS | 0 | 0 |
| 1560 | 18 | 37 | 897 1991 SCIENCE 252(5009):1097-1102 OBERLE I; ROUSSEAU F; HEITZ D; KRETZ C; DEVYS D; HANAUER A; BOUE J; BERTHEAS MF; MANDEL JL INSTABILITY OF A 550 BASE PAIR DNA SEGMENT AND ABNORMAL METHYLATION IN FRAGILE X-SYNDROME | 394 | 835 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1561 | 0 | 0 | 99 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A146-A146 OBRIEN MM; PADREMENDOZA T; PUESCHEL SM MATERNAL NONDISJUNCTION OF FRAGILE X-CHROMOSOME RESULTING IN KLINEFELTER SYNDROME | 1 | 2 |
| 1562 | 23 | 44 | 1627 1997 PSYCHIATRIC GENETICS 7(3):115-119 ODwyer J; Holmes J; Mueller R; Taylor G The prevalence of Fragile-X syndrome in an institution for people with learning disability | 1 | 2 |
| 1563 | 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 |
| 1564 | 12 | 20 | 676 1990 AMERICAN JOURNAL OF HUMAN GENETICS 47(6):988-993 OHASHI H; KUWANO A; TSUKAHARA M; ARINAMI T; KAJII T REPLICATION PATTERNS OF THE FRAGILE-X IN HETEROZYGOUS CARRIERS - ANALYSIS BY A BRDURD ANTIBODY METHOD | 1 | 2 |
| 1565 | 13 | 54 | 2148 2002 JOURNAL OF BIOLOGICAL CHEMISTRY 277(40):37804-37810 Ohashi S; Koike K; Omori A; Ichinose S; Ohara S; Kobayashi S; Sato TA; Anzai K Identification of mRNA/protein (mRNP) complexes containing Pur alpha, mStaufen, Fragile X Protein, and myosin Va and their association with rough endoplasmic reticulum equipped with a kinesin motor | 8 | 25 |
| 1566 | 0 | 0 | 1634 1998 AMERICAN JOURNAL OF MEDICAL GENETICS 81(6):452-453 Oostra BA Fragile X syndrome is caused by a fragile gene. | 0 | 0 |
| 1567 | 13 | 15 | 2198 2002 TRENDS IN MOLECULAR MEDICINE 8(3):102-103 Oostra BA Functions of the fragile X protein | 6 | 8 |
| 1568 | 52 | 100 | 2009 2001 CLINICAL GENETICS 60(6):399-408 Oostra BA; Chiurazzi P The fragile X gene and its function | 5 | 9 |
| 1569 | 68 | 117 | 1386 1995 PEDIATRIC RESEARCH 38(5):629-637 OOSTRA BA; HALLEY DJJ COMPLEX BEHAVIOR OF SIMPLE REPEATS - THE FRAGILE-X SYNDROME | 7 | 11 |
| 1570 | 24 | 43 | 1565 1997 ANNALS OF MEDICINE 29(6):563-567 Oostra BA; Hoogeveen AT Animal model for fragile X syndrome | 2 | 8 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1571 | 22 | 25 | 1116 1993 JOURNAL OF MEDICAL GENETICS 30(5):410-413 OOSTRA BA; JACKY PB; BROWN WT; ROUSSEAU F GUIDELINES FOR THE DIAGNOSIS OF FRAGILE-X SYNDROME | 45 | 60 |
| 1572 | 2 | 3 | 729 1990 PRENATAL DIAGNOSIS 10(8):545-546 OOSTRA BA; SANDKUYL LA; HALLEY DJJ RISK CALCULATION OF MISSED PRENATAL-DIAGNOSIS OF FRAGILE-X SYNDROME | 1 | 1 |
| 1573 | 33 | 48 | 967 1992 CHROMOSOMA 101(7):381-387 OOSTRA BA; VERKERK AJMH THE FRAGILE X-SYNDROME - ISOLATION OF THE FMR-1 GENE AND CHARACTERIZATION OF THE FRAGILE-X MUTATION | 11 | 26 |
| 1574 | 59 | 84 | 2118 2002 CYTOGENETIC AND GENOME RESEARCH 99(1-4):257-264 Oostra BA; Willemsen R The X chromosome and fragile X mental retardation | 0 | 1 |
| 1575 | 0 | 0 | 1404 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(1):17-17 Oostra BA; Willemsen R; Mandel JL; DeVries B; Devys D Rapid screening test for fragile X syndrome. | 0 | 0 |
| 1576 | 103 | 406 | 169 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):5-94 OPITZ JM; SUTHERLAND GR CONFERENCE REPORT - INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION | 50 | 115 |
| 1577 | 0 | 0 | 1923 2000 JOURNAL OF INTELLECTUAL DISABILITY RESEARCH 44:419-419 Orsmond G; Abbeduto L; Pavetto M; O'Brien A; Kesin E; Weissman M; Karadottir S; Cawthon S Stress and coping in parents of adolescents and young adults with fragile-X syndrome or Down syndrome | 0 | 0 |
| 1578 | 0 | 0 | 1537 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Osthus RC; DiMaio MS; Mahoney MJ; Bale AE Significance of borderline fragile X premutations. | 0 | 0 |
| 1579 | 0 | 0 | 1085 1993 CYTOGENETICS AND CELL GENETICS 63(4):254-254 OSTROWSKI RS; GRASS FS; LOVETTJELLEMA J AN INVESTIGATION OF THE FRAGILE-X SITE AS IT RELATES TO CHROMOSOME OVERLAP IN CULTURED HUMAN WHITE BLOOD-CELLS | 0 | 0 |
| 1580 | 15 | 43 | 2170 2002 MOLECULAR AND CELLULAR BIOLOGY 22(23):8332-8341 Otero YD; Severijnen LA; van Cappellen G; Schrier M; Oostra B; Willemsen R Transport of fragile X mental retardation protein via granules in neurites of PC12 cells | 6 | 15 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1581 | 13 | 23 | 1025 1993 AMERICAN JOURNAL OF HUMAN GENETICS 52(2):297-304 OUDET C; MORNET E; SERRE JL; THOMAS F; LENTESZENGERLING S; KRETZ C; DELUCHAT C; TEJADA I; BOUE J; BOUE A; MANDEL JL LINKAGE DISEQUILIBRIUM BETWEEN THE FRAGILE-X MUTATION AND 2 CLOSELY LINKED CA REPEATS SUGGESTS THAT FRAGILE-X CHROMOSOMES ARE DERIVED FROM A SMALL NUMBER OF FOUNDER CHROMOSOMES | 49 | 111 |
| 1582 | 0 | 0 | 758 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):269-269 PAJARES IL; DELICADO A; DETORRES ML; MARTIN VL; CASTROVIEJO IP; SOLERA J FRAGILE-X SYNDROME WITH EXTRAMICROCHROMOSOME | 0 | 0 |
| 1583 | 0 | 0 | 120 1983 CLINICAL GENETICS 23(3):236-236 PAJARES IL; DELICADO A; GALLEGO A; CASTROVIEJO IP FAMILIAL X-LINKED MENTAL-RETARDATION AND FRAGILE X-CHROMOSOMES IN 6 SPANISH FAMILIES | 1 | 1 |
| 1584 | 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 |
| 1585 | 16 | 32 | 1792 1999 HUMAN MUTATION 14(1):71-79 Panagopoulos I; Lassen C; Kristoffersson U; Aman P A methylation PCR approach for detection of fragile X syndrome | 3 | 4 |
| 1586 | 0 | 0 | 1453 1996 AMERICAN JOURNAL OF PATHOLOGY 149(5):G6-G6 Pandya A; FerreiraGonzalez A; JacksonCook C; Ware JL; Garrett CT Evaluation of fragile X CCG locus using PCR and a fluorescent automated DNA sequencer. | 0 | 0 |
| 1587 | 17 | 53 | 1820 1999 NEUROSCIENCE 94(1):185-192 Paradee W; Melikian HE; Rasmussen DL; Kenneson A; Conn PJ; Warren ST Fragile X mouse: Strain effects of knockout phenotype and evidence suggesting deficient amygdala function | 19 | 37 |
| 1588 | 0 | 0 | 1538 1997 AMERICAN JOURNAL OF HUMAN GENETICS 61(4):A160-A160 Paradee W; Rasmussen D; Melikian H; Conn PJ; Warren ST Hippocampus-independent deficits in the Fragile X mouse. | 0 | 0 |
| 1589 | 0 | 0 | 1848 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(4):366-366 Parades WJ; Warren ST Meiotic stability of a fragile X premutation CGG trinucleotide repeat in a mouse model. | 0 | 0 |
| 1590 | 1 | 2 | 1195 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):380-381 PARK V; HOWARDPEEBLES P; SHERMAN S; TAYLOR A; WULFSBERG E POLICY STATEMENT - AMERICAN-COLLEGE-OF-MEDICAL-GENETICS - FRAGILE-X-SYNDROME - DIAGNOSTIC AND CARRIER TESTING | 16 | 27 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1591 | 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 |
| 1592 | 4 | 29 | 173 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):175-194 PARTINGTON MW THE FRAGILE-X SYNDROME .2. PRELIMINARY DATA ON GROWTH AND DEVELOPMENT IN MALES | 51 | 65 |
| 1593 | 8 | 18 | 318 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):111-126 PARTINGTON MW FEMALE RELATIVES IN FAMILIES WITH THE FRAGILE X-SYNDROME | 4 | 7 |
| 1594 | 3 | 7 | 1439 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):370-372 Partington MW; Moore DY; Turner GM Confirmation of early menopause in fragile X carriers | 23 | 42 |
| 1595 | 6 | 10 | 919 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):120-123 PARTINGTON MW; ROBINSON H; LAING S; TURNER G MORTALITY IN THE FRAGILE-X SYNDROME - PRELIMINARY DATA | 2 | 3 |
| 1596 | 19 | 35 | 1732 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):302-307 Parvari R; Mumm S; Galil A; Manor E; Bar-David Y; Carmi R Deletion of 8.5 Mb, including the FMR1 gene, in a male with the fragile X syndrome phenotype and overgrowth | 2 | 6 |
| 1597 | 14 | 28 | 1203 1994 BRITISH JOURNAL OF CLINICAL PRACTICE 48(1):42-44 PATEL BD THE FRAGILE-X SYNDROME | 1 | 1 |
| 1598 | 3 | 46 | 1873 2000 BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS 278(3):833-838 Patel PK; Bhavesh NS; Hosur RV Cation-dependent conformational switches in d-TGGCGGC containing two triplet repeats of Fragile X Syndrome: NMR observations | 4 | 9 |
| 1599 | 0 | 0 | 1974 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):436-436 Patel ZM; Menon SR; D'souza AK; Adhia RA; Sanghavi DA; Gawde HM Validity of the analysis of FMRP expression in blood smears as a screening method for the fragile X syndrome in Indian population. | 0 | 0 |
| 1600 | 0 | 0 | 1654 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:144-144 Patsalis P; Sismani C; Hettinger JA; Boumba I; Georgiou I; Stylianidou G; Anastasiadou V; Koukoulli R; Pagoulatos G; Syrrou M Population-based molecular screening of fragile X (FRAXA) and FRAXE mental retardation syndromes: incidence, genetic variation and stability | 0 | 0 |
Page 16: 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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