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Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by journal name.
Page 14: 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 |
|---|---|---|---|---|---|
| 1301 | 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 |
| 1302 | 23 | 46 | 1882 2000 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 42(11):768-774 Sheldon L; Turk J Monozygotic boys with fragile X syndrome | 1 | 2 |
| 1303 | 0 | 1 | 2013 2001 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 43(2):142-142 [Anon] Monozygotic boys with fragile X syndrome (vol 42, pg 768, 2000) | 0 | 0 |
| 1304 | 17 | 25 | 2119 2002 DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY 44(11):724-728 Berry-Kravis E Epilepsy in fragile X syndrome | 4 | 4 |
| 1305 | 16 | 86 | 2014 2001 DEVELOPMENTAL PSYCHOBIOLOGY 39(2):107-123 Roberts JE; Boccia ML; Bailey DB; Hatton DD; Skinner M Cardiovascular indices of physiological arousal in boys with fragile X syndrome | 7 | 7 |
| 1306 | 40 | 139 | 2120 2002 DEVELOPMENTAL PSYCHOBIOLOGY 40(3):323-338 Churchill JD; Grossman AW; Irwin SA; Galvez R; Klintsova AY; Weiler IJ; Greenough WT A converging-methods approach to fragile X syndrome | 2 | 7 |
| 1307 | 14 | 57 | 2121 2002 DEVELOPMENTAL PSYCHOBIOLOGY 41(2):133-146 Keysor CS; Mazzocco MMM; McLeod DR; Hoehn-Saric R Physiological arousal in females with fragile X or Turner syndrome | 1 | 1 |
| 1308 | 60 | 94 | 1472 1996 DEVELOPMENTAL PSYCHOLOGY 32(3):416-424 Hagerman RJ Biomedical advances in developmental psychology: The case of fragile X syndrome | 3 | 8 |
| 1309 | 5 | 41 | 2326 2004 DEVELOPMENTAL SCIENCE 7(1):116-130 Scerif G; Cornish K; Wilding J; Driver J; Karmiloff-Smith A Visual search in typically developing toddlers and toddlers with Fragile X or Williams syndrome | 0 | 0 |
| 1310 | 13 | 16 | 1345 1995 DIAGNOSTIC MOLECULAR PATHOLOGY 4(3):158-161 NABER SP MOLECULAR DIAGNOSIS OF FRAGILE-X SYNDROME | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1311 | 10 | 16 | 1582 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(3):161-166 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R A five-year experience with fragile X testing - Setting laboratory standards of practice and a cost-effective protocol | 1 | 2 |
| 1312 | 1 | 1 | 1583 1997 DIAGNOSTIC MOLECULAR PATHOLOGY 6(5):304-304 Marini T; Pflueger S; Jackson A; Naber S; Karpells S; Naeem R Five-year experience with Fragile X-testing - Setting laboratory standards of practice and a cost-effective protocol (vol 6, pg 161, 1997) | 0 | 0 |
| 1313 | 16 | 23 | 1781 1999 DIAGNOSTIC MOLECULAR PATHOLOGY 8(3):152-156 Tzeng CC; Cho WC; Kuo PL; Chen RM Pilot fragile X screening in normal population of Taiwan | 7 | 9 |
| 1314 | 11 | 27 | 2015 2001 DIAGNOSTIC MOLECULAR PATHOLOGY 10(1):34-40 Tzeng CC; Lin SJ; Chen YJ; Kuo PL; Jong YJ; Tsai LP; Chen RM An effective strategy of using molecular testing to screen mentally retarded individuals for fragile X syndrome | 1 | 2 |
| 1315 | 9 | 44 | 278 1985 DISEASE MARKERS 3(1):9-25 JACOBS PA; SHERMAN SL THE FRAGILE(X) - A MARKER FOR THE MARTIN-BELL SYNDROME | 6 | 8 |
| 1316 | 16 | 24 | 974 1992 DISEASE MARKERS 10(1):1-5 KNIGHT SJL; HIRST MC; DAVIES KE MOLECULAR ANALYSIS OF THE FRAGILE X-SYNDROME | 0 | 1 |
| 1317 | 16 | 33 | 975 1992 EDUCATIONAL RESEARCH 34(3):221-228 GIBB C THE MOST COMMON-CAUSE OF LEARNING-DIFFICULTIES - A PROFILE OF FRAGILE-X SYNDROME AND ITS IMPLICATIONS FOR EDUCATION | 1 | 1 |
| 1318 | 3 | 21 | 2016 2001 ELECTROPHORESIS 22(6):1188-1193 Sung WC; Lee GB; Tzeng CC; Chen SH Plastic microchip electrophoresis for genetic screening: The analysis of polymerase chain reactions products of fragile X (CGG)n alleles | 0 | 10 |
| 1319 | 13 | 43 | 1346 1995 EMBO JOURNAL 14(11):2401-2408 SIOMI MC; SIOMI H; SAUER WH; SRINIVASAN S; NUSSBAUM RL; DREYFUSS G FXR1, AN AUTOSOMAL HOMOLOG OF THE FRAGILE-X MENTAL-RETARDATION GENE | 51 | 95 |
| 1320 | 16 | 36 | 1347 1995 EMBO JOURNAL 14(21):5358-5366 ZHANG Y; OCONNOR JP; SIOMI MC; SRINIVASAN S; DUTRA A; NUSSBAUM RL; DREYFUSS G THE FRAGILE-X MENTAL-RETARDATION SYNDROME PROTEIN INTERACTS WITH NOVEL HOMOLOGS FXR1 AND FXR2 | 63 | 111 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1321 | 15 | 39 | 1473 1996 EMBO JOURNAL 15(19):5408-5414 Fridell RA; Benson RE; Hua J; Bogerd HP; Cullen BR A nuclear role for the fragile X mental retardation protein | 32 | 65 |
| 1322 | 21 | 62 | 2017 2001 EMBO JOURNAL 20(17):4803-4813 Schaeffer C; Bardoni B; Mandel JL; Ehresmann B; Ehresmann C; Moine H The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif | 42 | 75 |
| 1323 | 0 | 0 | 199 1984 EMERGENCY MEDICINE 16(15):103-& [Anon] IN SEARCH OF THE FRAGILE-X | 0 | 0 |
| 1324 | 8 | 26 | 1649 1998 EPIGENETICS 214:280-290 Laird; Pillus; Hirst; Bestor; Jaenisch; Wilkins; Gasser; Wolffe; Francke; Bird; Riggs; Horz Rules of DNA methylation in humans inferred from the fragile X gene, FMR1 - Final general discussion | 0 | 0 |
| 1325 | 9 | 28 | 580 1988 EPILEPSIA 29(1):41-47 MUSUMECI SA; COLOGNOLA RM; FERRI R; GIGLI GL; PETRELLA MA; SANFILIPPO S; BERGONZI P; TASSINARI CA FRAGILE-X SYNDROME - A PARTICULAR EPILEPTOGENIC EEG PATTERN | 17 | 38 |
| 1326 | 0 | 0 | 1348 1995 EPILEPSIA 36:S1-S1 KLUGER G; BOHM I; LAUB MC; WALDENMEIER C; STUHRMANNSPANGENBERG M EEG IN CHILDREN WITH FRAGILE-X PREMUTATION | 0 | 0 |
| 1327 | 0 | 0 | 1349 1995 EPILEPSIA 36:S244-S244 SINGH R; SUTHERLAND G; MANSON J SEIZURES WITH EPILEPTOGENIC EEG PATTERN IN 2 SISTERS WITH FRAGILE X-SYNDROME | 0 | 0 |
| 1328 | 22 | 54 | 1782 1999 EPILEPSIA 40(8):1092-1099 Musumeci SA; Hagerman RJ; Ferri R; Bosco P; Dalla Bernardina B; Tassinari CA; De Sarro GB; Elia M Epilepsy and EEG findings in males with fragile X syndrome | 9 | 18 |
| 1329 | 18 | 32 | 1883 2000 EPILEPSIA 41(1):19-23 Musumeci SA; Bosco P; Calabrese G; Bakker C; De Sarro GB; Elia M; Ferri R; Oostra BA Audiogenic seizures susceptibility in transgenic mice with fragile X syndrome | 23 | 30 |
| 1330 | 14 | 24 | 2264 2003 EUROPEAN CHILD & ADOLESCENT PSYCHIATRY 12(4):172-177 Sabaratnam M; Murthy NV; Wijeratne A; Buckingham A; Payne S Autistic-like behaviour profile and psychiatric morbidity in Fragile X Syndrome - A prospective ten-year follow-up study | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1331 | 57 | 91 | 1212 1994 EUROPEAN JOURNAL OF CLINICAL INVESTIGATION 24(1):1-10 ROUSSEAU F THE FRAGILE-X SYNDROME - IMPLICATIONS OF MOLECULAR-GENETICS FOR THE CLINICAL SYNDROME | 7 | 10 |
| 1332 | 9 | 31 | 1089 1993 EUROPEAN JOURNAL OF HUMAN GENETICS 1(1):72-79 DEVRIES BBA; WIEGERS AM; DEGRAAFF E; VERKERK AJMH; VANHEMEL JO; HALLEY DJJ; FRYNS JP; CURFS LMG; NIERMEIJER MF; OOSTRA BA MENTAL STATUS AND FRAGILE-X EXPRESSION IN RELATION TO FMR-1 GENE MUTATION | 36 | 48 |
| 1333 | 19 | 27 | 1474 1996 EUROPEAN JOURNAL OF HUMAN GENETICS 4(1):8-12 Malzac P; Biancalana V; Voelckel MA; Moncla A; Pellissier MC; Boccaccio I; Mattei JF Unexpected inheritance of the (CGG)(n) trinucleotide expansion in a fragile X syndrome family | 4 | 6 |
| 1334 | 10 | 28 | 1584 1997 EUROPEAN JOURNAL OF HUMAN GENETICS 5(2):89-93 FulchignoniLataud MC; Olchwang S; Serre JL The fragile X CGG repeat shows a marked level of instability in hereditary non-polyposis colorectal cancer patients | 1 | 6 |
| 1335 | 0 | 0 | 1650 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:44-44 Tamanini F; van Unen L; Bontekoe C; Bakker; Willemsen R; Oostra BA; Hoogeveen AT Oligomerization and intracellular transport of the Fragile X Mental Retardation Protein | 0 | 0 |
| 1336 | 0 | 0 | 1651 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:63-63 Weinhausel A; Skarits C; Wolschek M; Haas OA Diagnostic evaluation of the fragile X syndrome with methylation-sensitive PCR (MS-PCR) | 0 | 0 |
| 1337 | 0 | 0 | 1652 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:107-107 Peixoto A; Santos R; Seruca R; Amorim A; Castedo S Haplotype analysis in fragile X and normal Portuguese populations | 0 | 0 |
| 1338 | 0 | 0 | 1653 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:116-116 Duran M; Valverde L; Molina M; Onaindia ML; Tejada MI Carrier screening for fragile X by PCR in females: comparison with obligated carriers | 0 | 0 |
| 1339 | 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 |
| 1340 | 0 | 0 | 1655 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6:159-159 Strelnikov V; Nemstova M; Demina N; Galkina V; Kuleshov N; Zaletayev D DNA testing for fragile X syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1341 | 23 | 30 | 1656 1998 EUROPEAN JOURNAL OF HUMAN GENETICS 6(5):518-522 Peixoto A; dos Santos MR; Seruca R; Amorim A; Castedo S Analysis of FMR1 and flanking microsatellite markers in normal and fragile X chromosomes in Portugal: evidence for a "protector" haplotype | 1 | 1 |
| 1342 | 14 | 23 | 1783 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(2):212-216 Ryynanen M; Heinonen S; Makkonen M; Kajanoja E; Mannermaa A; Pertti K Feasibility and acceptance of screening for fragile X mutations in low-risk pregnancies | 12 | 16 |
| 1343 | 18 | 33 | 1784 1999 EUROPEAN JOURNAL OF HUMAN GENETICS 7(5):526-532 Kooy RF; Reyniers E; Verhoye M; Sijbers J; Bakker CE; Oostra BA; Willems PJ; Van der Linden A Neuroanatomy of the fragile X knockout mouse brain studied using in vivo high resolution magnetic resonance imaging | 7 | 20 |
| 1344 | 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 |
| 1345 | 0 | 0 | 2122 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:55-56 Carmichael B Fragile X Syndrome - its impact on families | 0 | 0 |
| 1346 | 0 | 0 | 2123 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:63-63 Hagerman PJ; Greco CM; Tassone F; Chudley A; Del Bigio MR; Jacquemont S; Leehey M; Hagerman RJ Neuronal intranuclear inclusions in a new cerebellar tremor/ataxia syndrome among fragile X carriers | 0 | 0 |
| 1347 | 0 | 0 | 2124 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Loesch DZ Effect of prennutation in the FMR1 gene on cognitive and physical phenotype in fragile X assessed by pedigree analysis. | 0 | 0 |
| 1348 | 0 | 0 | 2125 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:220-220 Afifi HH; Abdel-Aleem AK; Shaheen OO Fragile X syndrome: clinical and behavioral study. | 0 | 0 |
| 1349 | 0 | 0 | 2126 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:227-227 Steinbach P; Jakubiczka S; Bettecken T X inactivation and fragile X methylation in human placentas | 0 | 0 |
| 1350 | 0 | 0 | 2127 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-228 Tzeng C; Chen W; Huang K Prevalence of fragile-X female carrier in Taiwan is lower than expected | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1351 | 0 | 0 | 2128 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:228-229 Biancalana V; Beldjord C; de Martinville B; Bieth E; Blayau M; Bonnefont J; Creveaux I; Cusin V; Doco-Fenzy M; Fellmann F; Gerson F; Guiochon-Mantel A; Houdayer C; Kottler M; Lesca G; Philippe C; Prieur F; Puissant H; Raynaud M; Saugier-Veber P; Taillandier A; Taine L; Voelckel M 5 years of molecular diagnosis of Fragile X syndrome (1997-2001): a collaborative study of 22 laboratories in France. | 0 | 0 |
| 1352 | 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 |
| 1353 | 0 | 0 | 2130 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Gryschenko NV; Malarchuk SG; Livshits LA CGG-repeat expansion and metilation status of the promotor region of FMR1 gene analysis in the Fragile-X sindrome patients from Ukraine | 0 | 0 |
| 1354 | 0 | 0 | 2131 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:229-229 Deelen WH; Jansen C; Ramlakhan SR; Labrijn-Marks I; Olmer R; Dooijes D; vanden Ouweland AMW; Halley DJJ Five years experience with DIG labeled probes on Southern blots applied in Fragile X diagnostics | 0 | 0 |
| 1355 | 2 | 2 | 2132 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Bardoni B; Schenck A; van de Bor V; Giangrande A; Mandel J Drosophila as a model to study the physiological pathway in which FMRP (Fragile X Mental Retardation Protein) is involved | 0 | 0 |
| 1356 | 0 | 0 | 2133 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Zalfa F; Primerano B; Lauro C; Giorgi M; Moro A; Spinelli G; Tongiorgi E; Costra B; Amaldi F; Bagni C Towards an understanding of the Fragile X syndrome: FMRP is translated at the synapses where it acts as a translational regulator | 0 | 0 |
| 1357 | 0 | 0 | 2134 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-231 Gantois I; Reyniers E; Kooy F Differential gene expression in the fragile X mouse model | 0 | 0 |
| 1358 | 0 | 0 | 2135 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:231-232 Pietrobono R; Pomponi MG; Tabolacci E; Oostra B; Chiurazzi P; Neri G Quantitative analysis of DNA demethylation and trascriptional reactivation of the FMR1 gene in fragile X cells treated with 5-azadeoxycytidine | 0 | 0 |
| 1359 | 0 | 0 | 2136 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:232-232 McKelvie KB; Reynolds A; Tassone F; Taylor AK; Hagerman RJ Evidence for skewed X chromosome inactivation in females with the fragile X full mutation | 0 | 0 |
| 1360 | 0 | 0 | 2137 2002 EUROPEAN JOURNAL OF HUMAN GENETICS 10:323-323 Wilson R; Epstein JH; McKelvie K; Grisgby J; Nagamoto H; Harris S; Reynolds A; Hagerman R Psychological and neuropsychological findings in adults with the premutation and full mutation for Fragile X Syndrome | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1361 | 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 |
| 1362 | 0 | 0 | 1885 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12:305-305 Beckel-Mitchener AC; Weiler IJ; Klintsova AY; Harms L; Belt B; Spangler CC; Greenough WT Analysis of protein synthesis in Fragile X knockout mice | 0 | 0 |
| 1363 | 0 | 18 | 1886 2000 EUROPEAN JOURNAL OF NEUROSCIENCE 12(1):381-384 Miller WJ; Skinner JA; Foss GS; Davies KE Localization of the fragile X mental retardation 2 (FMR2) protein in mammalian brain | 0 | 7 |
| 1364 | 11 | 19 | 2327 2004 EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY 112(2):189-191 Bussani C; Papi L; Sestini R; Baldinotti F; Bucciantini S; Bruni V; Scarselli G Premature ovarian failure and fragile X premutation: a study on 45 women | 0 | 0 |
| 1365 | 0 | 0 | 200 1984 EUROPEAN JOURNAL OF PEDIATRICS 141(4):265-265 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN BOYS WITH THE FRAGILE-X SYNDROME | 1 | 4 |
| 1366 | 9 | 34 | 279 1985 EUROPEAN JOURNAL OF PEDIATRICS 143(4):269-275 LARGO RH; SCHINZEL A DEVELOPMENTAL AND BEHAVIORAL DISTURBANCES IN 13 BOYS WITH FRAGILE X-SYNDROME | 26 | 37 |
| 1367 | 1 | 1 | 976 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(6):469-470 MUNDLOS S FRAGILE-X SOLVED | 0 | 0 |
| 1368 | 1 | 1 | 977 1992 EUROPEAN JOURNAL OF PEDIATRICS 151(8):617-617 MUNDLOS S GIRLS WITH THE FRAGILE-X SYNDROME | 0 | 0 |
| 1369 | 10 | 27 | 699 1990 EUROPEAN NEUROLOGY 30(1):32-37 RAIMONDI E; LENTI C; ROMAGNONI M; NEGRI R; GAMBINI E; MUSETTI L; DECARLI L FRAGILE-X MENTAL-RETARDATION IN A LARGE 5-GENERATION FAMILY - A CLINICAL AND CYTOGENETIC STUDY | 0 | 0 |
| 1370 | 21 | 44 | 1475 1996 EUROPEAN PSYCHIATRY 11(5):227-232 Barbe B; Franke P; Maier W; Leboyer M Fragile X syndrome .1. An overview on its genetic mechanism | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1371 | 58 | 71 | 1476 1996 EUROPEAN PSYCHIATRY 11(5):233-243 Franke P; Barbe B; Leboyer M; Maier W Fragile X syndrome .2. Cognitive and behavioral correlates of mutations of the FMR-1 gene | 4 | 5 |
| 1372 | 14 | 23 | 383 1986 EXPERIMENTAL CELL BIOLOGY 54(1):40-48 JENKINS EC; BROWN WT; BROOKS J; DUNCAN CJ; SANZ MM; SILVERMAN WP; LELE KP; MASIA A; KATZ E; LUBIN RA; NOLIN SL LOW-FREQUENCIES OF APPARENTLY FRAGILE X-CHROMOSOMES IN NORMAL CONTROL CULTURES - A POSSIBLE EXPLANATION | 16 | 20 |
| 1373 | 0 | 0 | 1350 1995 FASEB JOURNAL 9(6):A1324-A1324 SMITH SS; LAAYOUN A; BAKER DJ; KHO MR RECOGNITION OF TELOMERE-LIKE STRUCTURES FROM THE HUMAN C-HA-RAS GENE AND THE TRINUCLEOTIDE REPEAT OF THE FMR-1 GENE OF FRAGILE-X BY HUMAN DNA METHYLTRANSFERASE | 0 | 0 |
| 1374 | 0 | 0 | 1477 1996 FASEB JOURNAL 10(6):D30-D30 Kramer PR; Pearson CE; Sinden RR Stability of triplet repeats of myotonic dystrophy and fragile X loci in human mutator mismatch repair cell lines. | 0 | 0 |
| 1375 | 0 | 0 | 1657 1998 FASEB JOURNAL 12(8):A1322-A1322 Warren ST The molecular basis of Fragile X syndrome | 0 | 0 |
| 1376 | 0 | 0 | 1785 1999 FASEB JOURNAL 13(5):A703-A703 Greenough WT; Weiler IJ; Angenstein F; Klintsova A; Bauchwitz R Synthesis of the fragile X mental retardation protein at synapses: Possible role in synaptic development and plasticity | 0 | 0 |
| 1377 | 0 | 1 | 384 1986 FEDERATION PROCEEDINGS 45(3):702-702 MIXON JC; DEV VG DIMETHYLSULFOXIDE (DMSO) INCREASES FRAGILE X EXPRESSION IN THE PRESENCE OF 5-FLUORO-2'-DEOXYURIDINE (FUDR) | 0 | 0 |
| 1378 | 26 | 48 | 1585 1997 FOLIA HISTOCHEMICA ET CYTOBIOLOGICA 35(3):135-141 Szot M The fragile X syndrome | 0 | 0 |
| 1379 | 0 | 10 | 1658 1998 GENERAL HOSPITAL PSYCHIATRY 20(2):126-127 Silva JA; Ferrari MM; Leong GB Erotomania in a case of fragile-X syndrome | 0 | 1 |
| 1380 | 9 | 43 | 2139 2002 GENES & DEVELOPMENT 16(19):2491-2496 Caudy AA; Myers M; Hannon GJ; Hammond SM Fragile X-related protein and VIG associate with the RNA interference machinery | 14 | 66 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1381 | 15 | 79 | 2140 2002 GENES & DEVELOPMENT 16(19):2497-2508 Ishizuka A; Siomi MC; Siomi H A Drosophila fragile X protein interacts with components of RNAi and ribosomal proteins | 15 | 52 |
| 1382 | 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 |
| 1383 | 5 | 30 | 1213 1994 GENETIC COUNSELING 5(2):129-139 MAES B; FRYNS JP; VANWALLEGHEM M; VANDENBERGHE H PERSONAL INDEPENDENCE OF ADULT MENTALLY-RETARDED MEN WITH FRAGILE-X SYNDROME | 0 | 0 |
| 1384 | 4 | 6 | 1214 1994 GENETIC COUNSELING 5(4):377-380 WIEGERS AM; CURFS LMG; MEIJER H; OOSTRA B; FRYNS JP A DELETION OF 1.6 KB PROXIMAL TO THE CGG REPEAT OF THE FMR1-GENE CAUSES FRAGILE X-LIKE PSYCHOLOGICAL FEATURES | 0 | 0 |
| 1385 | 3 | 4 | 1351 1995 GENETIC COUNSELING 6(2):97-101 BORGHGRAEF M; SWILLEN A; VANDENBERGHE H; FRYNS JP FRAGILE-X BOYS - EVOLUTION OF THE MENTAL AGE IN CHILDHOOD - PRELIMINARY DATA ON 10 PREPUBERTAL BOYS | 0 | 0 |
| 1386 | 2 | 9 | 1352 1995 GENETIC COUNSELING 6(3):207-210 ALEMBIK Y; DOTT B; STOLL C RETT-LIKE SYNDROME IN FRAGILE-X SYNDROME | 1 | 6 |
| 1387 | 1 | 4 | 1353 1995 GENETIC COUNSELING 6(4):293-296 FRYNS JP SCREENING FOR THE FRAGILE-X SYNDROME - THE NECESSITY OF INTERNATIONAL GUIDELINES FOR MOLECULAR-GENETICS PREDICTIVE TESTING IN GENERAL | 2 | 3 |
| 1388 | 0 | 4 | 1478 1996 GENETIC COUNSELING 7(3):227-230 Fryns JP; DHooghe M; Devriendt K Macrocephaly, hypospadias grade III-IV, and fragile X-like behavior in identical twins without involvement of the FMR-1 gene | 0 | 0 |
| 1389 | 7 | 14 | 1479 1996 GENETIC COUNSELING 7(4):245-247 Fryns JP Ovarian function in fragile X carriers | 0 | 0 |
| 1390 | 6 | 15 | 1586 1997 GENETIC COUNSELING 8(1):1-6 Patsalis PC; Sismani C; Hadjimarcou MI; Rose N; Stylianidou G; Koukoulli R; Anastasiadou V; Deltas CC; Middleton L Cytogenetic and fragile X molecular testing of individuals with mental retardation of unknown etiology | 1 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 1391 | 0 | 0 | 1887 2000 GENETIC COUNSELING 11(3):281-311 [Anon] ACTS: Of the 9th International Workshop on Fragile X Syndrome and X Linked Mental Retardation August 23-25, 1999, Le Bischenberg, Strasbourg, France - Abstracts | 0 | 0 |
| 1392 | 0 | 0 | 2141 2002 GENETIC COUNSELING 13(2):207-261 [Anon] Abstracts of the 10th International Workshop on Fragile X and X-Linked Mental Retardation - 19-22 September 2001, Frascati, Italy | 0 | 0 |
| 1393 | 0 | 0 | 2328 2004 GENETIC COUNSELING 15(2):239-286 [Anon] Abstracts of the 11(th) International Workshop on Fragile X and X-Linked Mental Retardation - 27-30 August 2003, Pafos, Cyprus | 0 | 0 |
| 1394 | 12 | 26 | 1354 1995 GENETIC EPIDEMIOLOGY 12(3):279-290 HUGGINS RM; LOESCH DZ USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF FRAGILE-X ON MEANS AND VARIANCE-COMPONENTS OF A QUANTITATIVE TRAIT | 1 | 2 |
| 1395 | 22 | 42 | 2329 2004 GENETIC EPIDEMIOLOGY 26(4):294-304 Huggins RM; Loesch DZ; Qian GQ; Bui QM; Mitchell RJ; Dobson M; Taylor AK Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X | 0 | 0 |
| 1396 | 11 | 19 | 1587 1997 GENETIC TESTING 1(3):151-155 Das S; Kubota T; Song M; Daniel R; Berry-Kravis EM; Prior TW; Popovich B; Rosser L; Arinami T; Ledbetter DH Methylation analysis of the fragile X syndrome by PCR | 2 | 3 |
| 1397 | 13 | 21 | 1786 1999 GENETIC TESTING 3(3):301-304 Melis MA; Addis M; Lepiani C; Congeddu E; Cossu P; Cao A A strategy for fragile-X carrier screening | 0 | 2 |
| 1398 | 9 | 16 | 1888 2000 GENETIC TESTING 4(3):235-239 Tzountzouris J; Kennedy D; Skuterud M; Connolly-Wilson M; Holden JJA; Lin CC; Mak-Tam E; Somerville MJ; Summers AM; Allingham-Hawkins DJ Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: Implications for molecular diagnosis of the Fragile X syndrome | 0 | 1 |
| 1399 | 5 | 10 | 1889 2000 GENETIC TESTING 4(3):241-242 Brown WT; Nolin SL Apparent FMR1 allele instability in non-Fragile X males - Invited commentary | 0 | 1 |
| 1400 | 16 | 20 | 1890 2000 GENETIC TESTING 4(3):289-292 Geva E; Yaron Y; Shomrat R; Ben-Yehuda A; Zabari S; Peretz H; Naiman T; Yeger H; Orr-Urtreger A The risk of Fragile X premutation expansion is lower in carriers detected by general prenatal screening than in carriers from known Fragile X families | 3 | 4 |
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