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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 16: 1 (A N A E-APPROCHE NEUROPSYCHOLOGIQUE DES APPRENTISSAGES CHEZ L ENFANT) 2 (AMERICAN JOURNAL OF HUMAN GENETICS) 3 (AMERICAN JOURNAL OF HUMAN GENETICS) 4 (AMERICAN JOURNAL OF HUMAN GENETICS) 5 (AMERICAN JOURNAL OF MEDICAL GENETICS) 6 (AMERICAN JOURNAL OF MEDICAL GENETICS) 7 (AMERICAN JOURNAL OF MEDICAL GENETICS) 8 (AMERICAN JOURNAL OF MEDICAL GENETICS) 9 (AMERICAN JOURNAL OF MEDICAL GENETICS) 10 (ANNALS OF NEUROLOGY) 11 (BIOPHYSICAL JOURNAL) 12 (CLINICAL GENETICS) 13 (CURRENT BIOLOGY) 14 (DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY) 15 (GENETIC TESTING) 16 (HUMAN GENETICS) 17 (JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION) 18 (JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS) 19 (JOURNAL OF MEDICAL GENETICS) 20 (JOURNAL OF NEUROSCIENCE RESEARCH) 21 (MEDICAL ANTHROPOLOGY QUARTERLY) 22 (NATURE REVIEWS NEUROSCIENCE) 23 (PEDIATRIC RESEARCH) 24 (REVISTA DE NEUROLOGIA)
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
|---|---|---|---|---|---|
| 1501 | 14 | 31 | 1093 1993 HUMAN GENETICS 91(5):469-474 LOESCH DZ; SHEFFIELD LJ; HAY DA BETWEEN-GENERATION DIFFERENCES IN ASCERTAINMENT AND PENETRANCE - RELEVANCE TO GENETIC HYPOTHESES IN FRAGILE-X | 5 | 5 |
| 1502 | 16 | 27 | 1094 1993 HUMAN GENETICS 92(3):269-272 BUYLE S; REYNIERS E; VITS L; DEBOULLE K; HANDIG I; WUYTS FLE; DEELEN W; HALLEY DJJ; OOSTRA BA; WILLEMS PJ FOUNDER EFFECT IN A BELGIAN-DUTCH FRAGILE-X POPULATION | 19 | 29 |
| 1503 | 11 | 29 | 1095 1993 HUMAN GENETICS 92(4):373-378 MORNET E; BOGYO A; DELUCHAT C; SIMONBOUY B; MATHIEU M; THEPOT F; GRISARD MC; LEGUERN E; BOUE J; BOUE A MOLECULAR ANALYSIS OF A RING CHROMOSOME-X IN A FAMILY WITH FRAGILE-X SYNDROME | 0 | 1 |
| 1504 | 6 | 20 | 1096 1993 HUMAN GENETICS 92(5):431-436 ARINAMI T; ASANO M; KOBAYASHI K; YANAGI H; HAMAGUCHI H DATA ON THE CGG REPEAT AT THE FRAGILE X-SITE IN THE NONRETARDED JAPANESE POPULATION AND FAMILY SUGGEST THE PRESENCE OF A SUBGROUP OF NORMAL ALLELES PREDISPOSING TO MUTATE | 21 | 41 |
| 1505 | 35 | 45 | 1097 1993 HUMAN GENETICS 92(5):491-498 STEINBACH P; WOHRLE D; TARIVERDIAN G; KENNERKNECHT I; BARBI G; EDLINGER H; ENDERS H; GOTZSOTHMANN M; HEILBRONNER H; HOSENFELD D; KIRCHEISEN R; MAJEWSKI F; MEINECKE P; PASSARGE E; SCHMIDT A; SEIDEL H; WOLFF G; ZANKL M MOLECULAR ANALYSIS OF MUTATIONS IN THE GENE FMR-1 SEGREGATING IN FRAGILE X-FAMILIES | 7 | 11 |
| 1506 | 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 |
| 1507 | 21 | 34 | 1216 1994 HUMAN GENETICS 94(4):395-400 MILA M; KRUYER H; GLOVER G; SANCHEZ A; CARBONELL P; CASTELLVIBEL S; VOLPINI V; ROSELL J; GABARRON J; LOPEZ I; VILLA M; BALLESTA F; ESTIVILL X MOLECULAR ANALYSIS OF THE (CGG)(N) EXPANSION IN THE FMR-1 GENE IN 59 SPANISH FRAGILE-X SYNDROME FAMILIES | 12 | 16 |
| 1508 | 13 | 19 | 1217 1994 HUMAN GENETICS 94(5):479-483 HAATAJA R; VAISANEN ML; LI MY; RYYNANEN M; LEISTI J THE FRAGILE-X SYNDROME IN FINLAND - DEMONSTRATION OF A FOUNDER EFFECT BY ANALYSIS OF MICROSATELLITE HAPLOTYPES | 11 | 19 |
| 1509 | 17 | 33 | 1355 1995 HUMAN GENETICS 96(3):323-329 DREESEN JCFM; GERAEDTS JPM; DUMOULIN JCM; EVERS JLH; PIETERS MHEC RS46(DXS548) GENOTYPING OF REPRODUCTIVE CELLS - APPROACHING PREIMPLANTATION TESTING OF THE FRAGILE-X SYNDROME | 2 | 7 |
| 1510 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1511 | 17 | 26 | 1481 1996 HUMAN GENETICS 97(4):512-515 Mornet E; Chateau C; Taillandier A; SimonBouy B; Serre JL Recurrent and unexpected segregation of the FMR1 CGG repeat in a family with fragile X syndrome | 4 | 8 |
| 1512 | 15 | 26 | 1482 1996 HUMAN GENETICS 97(6):808-812 Haddad LA; MingroniNetto RC; ViannaMorgante AM; Pena SDJ A PCR-based test suitable for screening for fragile X syndrome among mentally retarded males | 7 | 16 |
| 1513 | 5 | 55 | 1483 1996 HUMAN GENETICS 98(2):151-157 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines | 2 | 26 |
| 1514 | 11 | 15 | 1589 1997 HUMAN GENETICS 99(3):308-311 Willemsen R; Smits A; Mohkamsing S; vanBeerendonk H; deHaan A; deVries B; vandenOuweland A; Sistermans E; Galjaard H; Oostra BA Rapid antibody test for diagnosing fragile X syndrome: A validation of the technique | 34 | 41 |
| 1515 | 15 | 64 | 1590 1997 HUMAN GENETICS 100(3-4):407-414 Lavedan CN; Garrett L; Nussbaum RL Trinucleotide repeats (CGG)(22)TGG(CGG)(43)TGG(CGG)(21) from the fragile X gene remain stable in transgenic mice | 9 | 19 |
| 1516 | 14 | 19 | 1591 1997 HUMAN GENETICS 100(5-6):564-568 Larsen LA; Gronskov K; NorgaardPedersen B; BrondumNielsen K; Hasholt L; Vuust J High-throughput analysis of fragile X (CGG)(n) alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis | 5 | 23 |
| 1517 | 10 | 16 | 1592 1997 HUMAN GENETICS 101(2):186-189 Pesso R; Barkai G; Ravia Y; Gak E; Frydman M; Goldman B; Friedman E No founder effect detected in Jewish Ashkenazi patients with fragile-X syndrome | 2 | 3 |
| 1518 | 4 | 7 | 1659 1998 HUMAN GENETICS 102(1):54-56 Storm K; Handig I; Reyniers E; Oostra BA; Kooy RF; Willems PJ Incomplete EcoRI digestion may lead to false diagnosis of fragile X syndrome | 0 | 1 |
| 1519 | 21 | 41 | 1660 1998 HUMAN GENETICS 102(4):440-445 Gronskov K; Hallberg A; Brondum-Nielsen K Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations | 3 | 8 |
| 1520 | 0 | 0 | 1661 1998 HUMAN GENETICS 103(3):366-366 Gronskov K; Brondum-Nielsen K Regarding the letter from Dr. Stephen T. Warren of the Emory University School of Medicine concerning our article "Mutational analysis of the FMR1 gene in 118 mentally retarded males suspected of fragile X syndrome: absence of prevalent mutations" | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1521 | 11 | 12 | 1892 2000 HUMAN GENETICS 106(3):366-369 Arocena DG; de Diego Y; Oostra BA; Willemsen R; Rodriguez MM A fragile X case with an amplification/deletion mosaic pattern | 0 | 0 |
| 1522 | 3 | 6 | 1893 2000 HUMAN GENETICS 107(2):195-196 Castellvi-Bel S; Fernandez-Burriel M; Rife M; Jimenez D; Mallolas J; Sanchez A; Ramos F; Mila M Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles | 1 | 2 |
| 1523 | 34 | 47 | 2022 2001 HUMAN GENETICS 108(6):450-458 Weinhausel A; Haas OA Evaluation of the fragile X (FRAXA) syndrome with methylation-sensitive PCR | 2 | 6 |
| 1524 | 1 | 4 | 2269 2003 HUMAN GENETICS 112(5-6):619-620 Macpherson J; Waghorn A; Hammans S; Jacobs P Observation of an excess of fragile-X premutations in a population of males referred with spinocerebellar ataxia | 5 | 6 |
| 1525 | 26 | 43 | 2270 2003 HUMAN GENETICS 113(5):371-376 Arocena DG; Breece KE; Hagerman PJ Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population | 1 | 1 |
| 1526 | 4 | 22 | 1593 1997 HUMAN HEREDITY 47(5):254-262 Gurling HMD; Bolton PF; Vincent J; Melmer G; Rutter M Molecular and cytogenetic investigations of the fragile X region including the Frax A and Frax E CGG trinucleotide repeat sequences in families multiplex for autism and related phenotypes | 0 | 7 |
| 1527 | 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 |
| 1528 | 8 | 24 | 1098 1993 HUMAN MOLECULAR GENETICS 2(4):399-404 VERKERK AJMH; DEGRAAFF E; DEBOULLE K; EICHLER EE; KONECKI DS; REYNIERS E; MANCA A; POUSTKA A; WILLEMS PJ; NELSON DL; OOSTRA BA ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 | 0 | 75 |
| 1529 | 0 | 1 | 1099 1993 HUMAN MOLECULAR GENETICS 2(8):1348-1348 VERKERK AJMH; DEGRAAFF E; DEBOULLE K; EICHLER EE; KONECKI DS; REYNIERS E; MANCA A; POUSTKA A; WILLEMS PJ; NELSON DL; OOSTRA BA ALTERNATIVE SPLICING IN THE FRAGILE X-GENE FMR1 (VOL 2, PG 399, 1993) | 3 | 6 |
| 1530 | 10 | 29 | 1100 1993 HUMAN MOLECULAR GENETICS 2(9):1429-1435 RICHARDS RI; HOLMAN K; YU S; SUTHERLAND GR FRAGILE-X SYNDROME UNSTABLE ELEMENT, P(CCG)N, AND OTHER SIMPLE TANDEM REPEAT SEQUENCES ARE BINDING-SITES FOR SPECIFIC NUCLEAR PROTEINS | 11 | 80 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1531 | 12 | 46 | 1101 1993 HUMAN MOLECULAR GENETICS 2(10):1659-1665 HORNSTRA IK; NELSON DL; WARREN ST; YANG TP HIGH-RESOLUTION METHYLATION ANALYSIS OF THE FMR1 GENE TRINUCLEOTIDE REPEAT REGION IN FRAGILE X-SYNDROME | 34 | 77 |
| 1532 | 11 | 16 | 1102 1993 HUMAN MOLECULAR GENETICS 2(11):1973-1974 TARLETON J; RICHIE R; SCHWARTZ C; RAO K; AYLSWORTH AS; LACHIEWICZ A AN EXTENSIVE DE-NOVO DELETION REMOVING FMR1 IN A PATIENT WITH MENTAL-RETARDATION AND THE FRAGILE X-SYNDROME PHENOTYPE | 29 | 50 |
| 1533 | 23 | 31 | 1218 1994 HUMAN MOLECULAR GENETICS 3(3):393-398 REISS AL; KAZAZIAN HH; KREBS CM; MCAUGHAN A; BOEHM CD; ABRAMS MT; NELSON DL FREQUENCY AND STABILITY OF THE FRAGILE-X PREMUTATION | 29 | 61 |
| 1534 | 20 | 28 | 1219 1994 HUMAN MOLECULAR GENETICS 3(3):399-405 MACPHERSON JN; BULLMAN H; YOUINGS SA; JACOBS PA INSERT SIZE AND FLANKING HAPLOTYPE IN FRAGILE-X AND NORMAL-POPULATIONS - POSSIBLE MULTIPLE ORIGINS FOR THE FRAGILE-X MUTATION | 28 | 57 |
| 1535 | 21 | 33 | 1220 1994 HUMAN MOLECULAR GENETICS 3(4):615-620 MEIJER H; DEGRAAFF E; MERCKX DML; JONGBLOED RJE; DEDIESMULDERS CEM; ENGELEN JJM; FRYNS JP; CURFS PMG; OOSTRA BA A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1 GENE CAUSES THE CLINICAL PHENOTYPE OF THE FRAGILE X SYNDROME | 46 | 78 |
| 1536 | 17 | 29 | 1221 1994 HUMAN MOLECULAR GENETICS 3(9):1543-1551 SNOW K; TESTER DJ; KRUCKEBERG KE; SCHAID DJ; THIBODEAU SN SEQUENCE-ANALYSIS OF THE FRAGILE-X TRINUCLEOTIDE REPEAT - IMPLICATIONS FOR THE ORIGIN OF THE FRAGILE-X MUTATION | 47 | 115 |
| 1537 | 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 |
| 1538 | 25 | 49 | 1357 1995 HUMAN MOLECULAR GENETICS 4(1):45-49 DEGRAAFF E; ROUILLARD P; WILLEMS PJ; SMITS APT; ROUSSEAU F; OOSTRA BA HOTSPOT FOR DELETIONS IN THE CGG REPEAT REGION OF FMR1 IN FRAGILE-X PATIENTS | 27 | 46 |
| 1539 | 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 |
| 1540 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1541 | 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 |
| 1542 | 21 | 35 | 1594 1997 HUMAN MOLECULAR GENETICS 6(7):971-979 Moutou C; Vincent MC; Biancalana V; Mandel JL Transition from premutation to full mutation in fragile X syndrome is likely to be prezygotic | 18 | 33 |
| 1543 | 12 | 38 | 1595 1997 HUMAN MOLECULAR GENETICS 6(9):1465-1472 Corbin F; Bouillon M; Fortin A; Morin S; Rousseau F; Khandjian EW The fragile X mental retardation protein is associated with poly(A)(+) mRNA in actively translating polyribosomes | 55 | 85 |
| 1544 | 18 | 64 | 1596 1997 HUMAN MOLECULAR GENETICS 6(11):1791-1801 Stoger R; Kajimura TM; Brown WT; Laird CD Epigenetic variation illustrated by DNA methylation patterns of the fragile-X gene FMR1 | 12 | 36 |
| 1545 | 13 | 28 | 1663 1998 HUMAN MOLECULAR GENETICS 7(1):109-113 Chiurazzi P; Pomponi MG; Willemsen R; Oostra BA; Neri G In vitro reactivation of the FMR1 gene involved in fragile X syndrome | 21 | 47 |
| 1546 | 13 | 29 | 1664 1998 HUMAN MOLECULAR GENETICS 7(13):2121-2128 Khandjian EW; Bardoni B; Corbin F; Sittler A; Giroux S; Heitz D; Tremblay S; Pinset C; Montarras D; Rousseau F; Mandel JL Novel isoforms of the fragile X related protein FXR1P are expressed during myogenesis | 17 | 27 |
| 1547 | 17 | 50 | 1790 1999 HUMAN MOLECULAR GENETICS 8(5):863-869 Tamanini F; Bontekoe C; Bakker CE; van Unen L; Anar B; Willemsen R; Yoshida M; Galjaard H; Oostra BA; Hoogeveen AT Different targets for the fragile X-related proteins revealed by their distinct nuclear localizations | 26 | 36 |
| 1548 | 17 | 39 | 1791 1999 HUMAN MOLECULAR GENETICS 8(13):2557-2566 Bardoni B; Schenck A; Mandel JL A novel RNA-binding nuclear protein that interacts with the fragile X mental retardation (FMR1) protein | 26 | 44 |
| 1549 | 46 | 82 | 1894 2000 HUMAN MOLECULAR GENETICS 9(6):901-908 Jin P; Warren ST Understanding the molecular basis of fragile X syndrome | 36 | 73 |
| 1550 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1551 | 31 | 62 | 1896 2000 HUMAN MOLECULAR GENETICS 9(12):1759-1769 Crawford DC; Zhang FP; Wilson B; Warren ST; Sherman SL Fragile X CGG repeat structures among African-Americans: identification of a novel factor responsible for repeat instability | 5 | 10 |
| 1552 | 25 | 55 | 1897 2000 HUMAN MOLECULAR GENETICS 9(19):2909-2918 Crawford DC; Wilson B; Sherman SL Factors involved in the initial mutation of the fragile X CGG repeat as determined by sperm small pool PCR | 3 | 9 |
| 1553 | 19 | 31 | 2023 2001 HUMAN MOLECULAR GENETICS 10(4):329-338 Laggerbauer B; Ostareck D; Keidel EM; Ostareck-Lederer A; Fischer U Evidence that fragile X mental retardation protein is a negative regulator of translation | 55 | 80 |
| 1554 | 22 | 64 | 2024 2001 HUMAN MOLECULAR GENETICS 10(24):2803-2811 Huot ME; Mazroui R; Leclerc P; Khandjian EW Developmental expression of the fragile X-related 1 proteins in mouse testis: association with microtubule elements | 3 | 3 |
| 1555 | 25 | 40 | 2144 2002 HUMAN MOLECULAR GENETICS 11(4):371-378 Dombrowski C; Levesque S; Morel ML; Rouillard P; Morgan K; Rousseau F Premutation and intermediate-size FMR1 alleles in 10,572 males from the general population: Loss of an AGG interruption is a late event in the generation of fragile X syndrome alleles | 15 | 22 |
| 1556 | 26 | 57 | 2145 2002 HUMAN MOLECULAR GENETICS 11(24):3007-3017 Mazroui R; Huot ME; Tremblay S; Filion C; Labelle Y; Khandjian EW Trapping of messenger RNA by Fragile X Mental Retardation protein into cytoplasmic granules induces translation repression | 10 | 18 |
| 1557 | 36 | 53 | 2271 2003 HUMAN MOLECULAR GENETICS 12(14):1689-1698 Bardoni B; Castets M; Huot ME; Schenck A; Adinolfi S; Corbin F; Pastore A; Khandjian EW; Mandel JL 82-FIP, a novel FMRP (Fragile X Mental Retardation Protein) interacting protein, shows a cell cycle-dependent intracellular localization | 3 | 3 |
| 1558 | 38 | 52 | 2272 2003 HUMAN MOLECULAR GENETICS 12(23):3087-3096 Mazroui R; Huot ME; Tremblay S; Boilard N; Labelle Y; Khandjian EW Fragile X Mental Retardation protein determinants required for its association with polyribosomal mRNPs | 2 | 2 |
| 1559 | 26 | 38 | 1597 1997 HUMAN MUTATION 10(5):393-399 Wang YC; Lin ML; Lin SJ; Li YC; Li SY Novel point mutation within intron 10 of FMR-1 gene causing fragile X syndrome | 6 | 9 |
| 1560 | 2 | 4 | 1665 1998 HUMAN MUTATION 12(6):431-431 Vincent JB; Gurling HMD Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome | 3 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1561 | 0 | 0 | 1666 1998 HUMAN MUTATION 12(6):432-432 Wang YC; Li SY Point mutation in intron 10 of FMR1 is unlikely to be a cause of fragile X syndrome - Response | 0 | 1 |
| 1562 | 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 |
| 1563 | 18 | 36 | 1667 1998 HUMAN REPRODUCTION 13(5):1184-1187 Conway GS; Payne NN; Webb J; Murray A; Jacobs PA Fragile X premutation screening in women with premature ovarian failure | 8 | 31 |
| 1564 | 0 | 0 | 1793 1999 HUMAN REPRODUCTION 14:235-235 Sermon K; Seneca S; Lissens W; De Vos A; Vandervorst M; Vanderfaellie A; Bonnefont JP; Van Steirteghem A; Liebaers I Preimplantation genetic diagnosis for fragile-X syndrome | 0 | 0 |
| 1565 | 0 | 0 | 1794 1999 HUMAN REPRODUCTION 14:354-355 Gersak K; Kregar-Velikonja N; Meden-Vrtovec H; Peterlin B Fragile X premutation screening in women with premature menopause | 1 | 1 |
| 1566 | 0 | 0 | 1898 2000 HUMAN REPRODUCTION 15:12-12 Apessos A; Harper J; Delhanty JDA Preimplantation genetic diagnosis of the fragile X syndrome by use of linked polymorphic markers | 0 | 0 |
| 1567 | 0 | 0 | 1899 2000 HUMAN REPRODUCTION 15:47-48 Hundscheid RDL; Sistermans EA; Thomas CMG; Straatman H; Kiemeney LALM; Oostra BA; Smits APT; Braat DDM Shorter reproductive life and a high risk for premature ovarian failure (POF) in women who have inherited fragile X premutations from their fathers | 0 | 0 |
| 1568 | 16 | 41 | 1900 2000 HUMAN REPRODUCTION 15(1):197-202 Marozzi A; Vegetti W; Manfredini E; Tibiletti MG; Testa G; Crosignani PG; Ginelli E; Meneveri R; Dalpra L Association between idiopathic premature ovarian failure and fragile X premutation | 10 | 29 |
| 1569 | 1 | 2 | 1901 2000 HUMAN REPRODUCTION 15(8):1874-1874 Rychlik DF Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| 1570 | 1 | 2 | 1902 2000 HUMAN REPRODUCTION 15(8):1874-1875 Marozzi A Regarding recall bias in the association between idiopathic premature ovarian failure and fragile X premutation | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1571 | 7 | 25 | 2025 2001 HUMAN REPRODUCTION 16(3):457-462 Hundscheid RDL; Braat DDM; Kiemeney LALM; Smits APT; Thomas CMG Increased serum FSH in female fragile X premutation carriers with either regular menstrual cycles or on oral contraceptives | 6 | 10 |
| 1572 | 20 | 29 | 2273 2003 HUMAN REPRODUCTION 18(8):1637-1640 Gersak K; Meden-Vrtovec H; Peterlin B Fragile X premutation in women with sporadic premature ovarian failure in Slovenia | 0 | 0 |
| 1573 | 14 | 22 | 1668 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 107:29-36 Baskaran S; Naseerullah MK; Manjunatha KR; Chetan GK; Arthi R; Rao GVB; Girimaji SR; Srinath S; Sheshadri S; Devi RR; Brahmachari V Triplet repeat polymorphism & fragile X syndrome in the Indian context | 2 | 6 |
| 1574 | 14 | 26 | 1669 1998 INDIAN JOURNAL OF MEDICAL RESEARCH 108:12-16 Jain U; Verma IC; Kapoor AK Prevalence of fragile X(A) syndrome in mentally retarded children at a genetics referral centre in Delhi, India | 2 | 3 |
| 1575 | 0 | 0 | 1903 2000 INFANT MENTAL HEALTH JOURNAL 21(4-5):330-330 Ghuman JK; Tierney E; Kau A; Reider E Social interaction problems in infants and preschool children with fragile-X syndrome, Smith-Lemli-Opitz syndrome and other developmental disorders | 0 | 0 |
| 1576 | 19 | 31 | 2026 2001 INFANTS AND YOUNG CHILDREN 14(1):24-33 Bailey DB; Roberts JE; Mirrett P; Hatton DD Identifying infants and toddlers with fragile X syndrome: Issues and recommendations | 6 | 6 |
| 1577 | 7 | 18 | 1223 1994 INTELLIGENCE 19(1):45-50 DANIELS JK; OWEN MJ; MCGUFFIN P; THOMPSON L; DETTERMAN DK; CHORNEY M; CHORNEY K; SMITH D; SKUDER P; VIGNETTI S; MCCLEARN GE; PLOMIN R IQ AND VARIATION IN THE NUMBER OF FRAGILE-X CGG REPEATS - NO ASSOCIATION IN A NORMAL SAMPLE | 2 | 9 |
| 1578 | 9 | 29 | 1795 1999 INTERNATIONAL JOURNAL OF BEHAVIORAL DEVELOPMENT 23(2):519-531 Burack JA; Shulman C; Katzir E; Schaap T; Brennan JM; Iarocci G; Wilansky P; Amir N Cognitive and behavioural development of Israeli males with fragile X and Down Syndrome | 1 | 1 |
| 1579 | 2 | 4 | 1486 1996 INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS 52(2):209-210 [Anon] Fragile X syndrome | 0 | 0 |
| 1580 | 59 | 96 | 1796 1999 INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE 3(6):639-645 Pimentel MMG Fragile X syndrome | 0 | 5 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1581 | 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 |
| 1582 | 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 |
| 1583 | 0 | 0 | 984 1992 INTERNATIONAL JOURNAL OF PSYCHOLOGY 27(3-4):395-395 SIMENSEN RJ; SAUL RA; TARLETON JD; PHELAN MC NEUROPSYCHOLOGICAL FUNCTIONING IN FRAGILE X-SYNDROME AND MONOSOMY-X MOSAICISM - A CASE PRESENTATION | 0 | 0 |
| 1584 | 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 |
| 1585 | 24 | 128 | 138 1983 INTERNATIONAL REVIEW OF CYTOLOGY-A SURVEY OF CELL BIOLOGY 81:107-143 SUTHERLAND GR THE FRAGILE X-CHROMOSOME | 39 | 131 |
| 1586 | 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 |
| 1587 | 45 | 118 | 2274 2003 INTERNATIONAL REVIEW OF RESEARCH IN MENTAL RETARDATION, VOL 27 27:83-119 Murphy MM; Abbeduto L Language and communication in fragile X syndrome | 0 | 0 |
| 1588 | 8 | 28 | 139 1983 IRISH JOURNAL OF MEDICAL SCIENCE 152(12):440-445 DEARCE MA; LAW E; MASTERSON JG NON-SPECIFIC X-LINKED MENTAL-RETARDATION WITH FRAGILE-X CHROMOSOME - SOMATIC FEATURES, CYTOGENETIC DIAGNOSIS AND ELEMENTS FOR GENETIC-COUNSELING | 1 | 3 |
| 1589 | 0 | 0 | 206 1984 IRISH JOURNAL OF MEDICAL SCIENCE 153(1):29-30 DEARCE MA; LAW E A SIMPLE STATISTICAL APPROACH TO AVOID FALSE POSITIVES IN THE CYTOGENETIC DIAGNOSIS OF FRAGILE X-CHROMOSOMES | 0 | 0 |
| 1590 | 0 | 0 | 1103 1993 IRISH MEDICAL JOURNAL 86(3):92-& KEENAN E; KEANE V; RAMSEY L FRAGILE-X SYNDROME - A REVIEW | 1 | 1 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1591 | 0 | 0 | 1104 1993 IRISH MEDICAL JOURNAL 86(5):172-172 LYNCH SA FRAGILE-X SYNDROME | 0 | 0 |
| 1592 | 8 | 11 | 1359 1995 ISRAEL JOURNAL OF MEDICAL SCIENCES 31(5):323-325 DAR H; SCHAAP T; BAITOR H; BOROCHOWITZ Z; GELMANKOHAN Z; CHEMKE T; CHAKI R; COHEN H; FALIKBORENSTEIN Z; CHEMKE J ETHNIC DISTRIBUTION OF THE FRAGILE-X SYNDROME IN ISRAEL - EVIDENCE OF FOUNDER CHROMOSOMES() | 1 | 1 |
| 1593 | 1 | 5 | 2331 2004 ISRAEL JOURNAL OF PSYCHIATRY AND RELATED SCIENCES 41(1):70-70 Kandil ST; Bilici M; Aksu HB; Celep F; Karaguzel A Early infantile autism and fragile X anomaly | 0 | 0 |
| 1594 | 1 | 5 | 1224 1994 ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES 15(7):365-368 MUSUMECI SA; ELIA M; FERRI R; SCUDERI C; DELGRACCO S EVOKED SPIKES AND GIANT SOMATOSENSORY-EVOKED POTENTIALS IN A PATIENT WITH FRAGILE-X SYNDROME | 3 | 8 |
| 1595 | 20 | 55 | 1105 1993 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 270(13):1569-1575 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING XH; DOBKIN C; ZHONG N; HENDERSON J; BROOKS SS; JENKINS EC RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST | 103 | 154 |
| 1596 | 1 | 1 | 1225 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(1):28-28 BROWN WT; HOUCK GE; JEZIOROWSKA A; LEVINSON FN; DING X; DOBKIN C; ZHONG N; HENDERSON J; BROOKS SS; JENKINS EC RAPID FRAGILE-X CARRIER SCREENING AND PRENATAL-DIAGNOSIS USING A NONRADIOACTIVE PCR TEST (VOL 270, PG 1569, 1993) | 1 | 1 |
| 1597 | 30 | 48 | 1226 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):507-514 TAYLOR AK; SAFANDA JF; FALL MZ; QUINCE C; LANG KA; HULL CE; CARPENTER I; STALEY LW; HAGERMAN RJ MOLECULAR PREDICTORS OF COGNITIVE INVOLVEMENT IN FEMALE CARRIERS OF FRAGILE-X SYNDROME | 76 | 89 |
| 1598 | 41 | 81 | 1227 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):536-542 WARREN ST; NELSON DL ADVANCES IN MOLECULAR ANALYSIS OF FRAGILE-X SYNDROME | 59 | 125 |
| 1599 | 13 | 16 | 1228 1994 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 271(7):552-553 CASKEY CT FRAGILE-X SYNDROME - IMPROVING UNDERSTANDING AND DIAGNOSIS | 2 | 2 |
| 1600 | 21 | 55 | 2332 2004 JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION 291(4):460-469 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; Brunberg JA; Zhang L; Jardini T; Gane LW; Harris SW; Herman K; Grigsby J; Greco CM; Berry-Kravis E; Tassone F; Hagerman PJ Penetrance of the fragile X - Associated tremor/ataxia syndrome in a premutation carrier population | 3 | 3 |
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