| Missing Links? Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 2369
Authors: 4634,
Journals: 373,
Outer References: 14152
Collection span: 1980 - 2004
View: Overview. Sorted by first author.
Page 10: 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 |
|---|---|---|---|---|---|
| 901 | 0 | 0 | 896 1991 SCIENCE 252(5009):1070-1070 HOFFMAN M UNRAVELING THE GENETICS OF FRAGILE X-SYNDROME | 2 | 4 |
| 902 | 15 | 21 | 1181 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 51(4):466-470 HOFSTEE Y; ARINAMI T; HAMAGUCHI H COMPARISON BETWEEN THE CYTOGENETIC TEST FOR FRAGILE-X AND THE MOLECULAR ANALYSIS OF THE FMR-1 GENE IN JAPANESE MENTALLY-RETARDED INDIVIDUALS | 12 | 18 |
| 903 | 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 |
| 904 | 0 | 0 | 103 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A174-A174 HOLDEN J; BECKETT J; MULLIGAN L; PHILLIPS A; SIMPSON N; PARTINGTON M; HAMERTON J; WANG HS; DONALD L; WHITE B A SEARCH FOR RESTRICTION FRAGMENT LENGTH POLYMORPHISMS (RFLPS) LINKED TO THE FRAGILE-X FORM OF X-LINKED MENTAL-RETARDATION | 0 | 3 |
| 905 | 5 | 9 | 1340 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):370-379 Holden JJA Workshop for family and friends .1. The fragile X gene and its mutations | 0 | 0 |
| 906 | 0 | 0 | 1036 1993 AMERICAN JOURNAL OF HUMAN GENETICS 53(3):448-448 HOLDEN JJA; CHALIFOUX M; WING M; WHITE BN; GLOVER T; STEIN C; ZEESMAN S; CHITAYAT D; TESHIMA I; BROWN C; WARREN ST THE FRAGILE-X SYNDROME AND PREMATURE MENOPAUSE | 1 | 1 |
| 907 | 0 | 5 | 273 1985 CYTOGENETICS AND CELL GENETICS 40(1-4):653-653 HOLDEN JJA; MULLIGAN LM; FORSTERGIBSON C; SIMPSON NE; WHITE BN; OBERLE I; WROGEMANN K APPLICATION OF FLANKING DNA PROBES TO CARRIER DETECTION IN THE FRAGILE-X SYNDROME | 0 | 2 |
| 908 | 36 | 61 | 1723 1999 AMERICAN JOURNAL OF MEDICAL GENETICS 83(4):221-236 Holden JJA; Percy M; Allingham-Hawkins D; Brown WT; Chiurazzi P; Fisch G; Gane L; Gunter C; Hagerman R; Jenkins EC; Kooy RF; Lubs HA; Murray A; Neri G; Schwartz C; Tranebjaerg L; Villard L; Willems PJ Eighth International Workshop on the Fragile X Syndrome and X-linked Mental Retardation, August 16-22, 1997 | 1 | 4 |
| 909 | 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 |
| 910 | 0 | 0 | 196 1984 CLINICAL RESEARCH 32(5):A885-A885 HOLMAN GH; ALLEN SM; TUCKER DA; TAWATER BA SEIZURES AND UNUSUAL VISUAL EVOKED-RESPONSES IN FRAGILE-X CARRIERS | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 911 | 8 | 12 | 548 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):673-679 HOLMGREN G; BLOMQUIST HK; DRUGGE U; GUSTAVSON KH FRAGILE-X FAMILIES IN A NORTHERN SWEDISH COUNTY - A GENEALOGICAL STUDY DEMONSTRATING APPARENT PATERNAL TRANSMISSION FROM THE 18TH-CENTURY | 10 | 10 |
| 912 | 27 | 57 | 1601 1997 JOURNAL OF INHERITED METABOLIC DISEASE 20(2):139-151 Hoogeveen AT; Oostra BA The fragile X syndrome | 6 | 10 |
| 913 | 39 | 64 | 2164 2002 MICROSCOPY RESEARCH AND TECHNIQUE 57(3):148-155 Hoogeveen AT; Willemsen R; Oostra BA Fragile X syndrome, the fragile X related proteins, and animal models | 1 | 3 |
| 914 | 4 | 15 | 1938 2000 JOURNAL OF PSYCHOEDUCATIONAL ASSESSMENT 18(3):255-267 Hooper SR; Hatton DD; Baranek GT; Roberts JP; Bailey DB Nonverbal assessment of IQ, attention, and memory abilities in children with fragile-X syndrome using the Leiter-R | 0 | 0 |
| 915 | 5 | 24 | 290 1985 JAPANESE JOURNAL OF CANCER RESEARCH 76(10):977-983 HORI T; AYUSAWA D; GLOVER TW; SENO T EXPRESSION OF FRAGILE SITE ON THE HUMAN-X CHROMOSOME IN SOMATIC-CELL HYBRIDS BETWEEN HUMAN FRAGILE-X CELLS AND THYMIDYLATE SYNTHASE-NEGATIVE MOUSE MUTANT-CELLS | 3 | 15 |
| 916 | 0 | 0 | 207 1984 JAPANESE JOURNAL OF GENETICS 59(6):618-619 HORI T; AYUSAWA D; SENO T EXPRESSION OF THE FRAGILE X-CHROMOSOME UNDER CONDITIONS OF THYMIDYLATE STRESS | 0 | 0 |
| 917 | 0 | 0 | 462 1987 JAPANESE JOURNAL OF GENETICS 62(6):520-520 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M STRUCTURAL ALTERATION IN FRA(X)(Q27.3) ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 918 | 7 | 32 | 576 1988 CYTOGENETICS AND CELL GENETICS 47(4):177-180 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M FRAGILE-X EXPRESSION IN THYMIDINE-PROTOTROPHIC AND AUXOTROPHIC HUMAN-MOUSE SOMATIC-CELL HYBRIDS UNDER LOW AND HIGH THYMIDYLATE STRESS CONDITIONS | 1 | 3 |
| 919 | 0 | 0 | 593 1988 JAPANESE JOURNAL OF HUMAN GENETICS 33(2):245-245 HORI T; TAKAHASHI E; TSUJI H; TSUJI S; MURATA M EXPRESSION OF FRA(X)(Q27.3) ASSOCIATED WITH FRAGILE-X SYNDROME | 0 | 0 |
| 920 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 921 | 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 |
| 922 | 1 | 3 | 536 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):455-457 HOWARDPEEBLES P; FROSTERISKENIUS U FRAGILE-X TESTING IN MOTHERS OF TRANSMITTING MALES | 0 | 1 |
| 923 | 2 | 4 | 16 1981 CLINICAL GENETICS 20(1):78-78 HOWARDPEEBLES PN FRAGILE-X CHROMOSOME IN NORMAL MALES | 4 | 7 |
| 924 | 0 | 3 | 43 1982 AMERICAN JOURNAL OF HUMAN GENETICS 34(6):A129-A129 HOWARDPEEBLES PN FRAGILE X-CHROMOSOME - THE ROLE OF METHIONINE AND OTHER INVITRO MANIPULATIONS | 4 | 5 |
| 925 | 0 | 0 | 95 1983 AMERICAN JOURNAL OF HUMAN GENETICS 35(6):A135-A135 HOWARDPEEBLES PN FRAGILE X-CHROMOSOME - TECHNICAL ASPECTS FOR MAXIMIZING EXPRESSION | 0 | 0 |
| 926 | 0 | 1 | 132 1983 CLINICAL RESEARCH 31(5):A897-A897 HOWARDPEEBLES PN NORMAL-MALE TRANSMISSION OF THE FRAGILE-X - THE COUNSELING DILEMMA | 0 | 0 |
| 927 | 5 | 11 | 342 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):511-514 HOWARDPEEBLES PN METHIONINE METABOLISM AND FRAGILE-X EXPRESSION | 0 | 4 |
| 928 | 0 | 0 | 765 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):290-290 HOWARDPEEBLES PN FRAGILE-X TESTING OF FAMILY MEMBERS IN THE CLINICAL CYTOGENETICS LABORATORY - PERIMETERS AND PITFALLS | 0 | 0 |
| 929 | 2 | 4 | 814 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):445-446 HOWARDPEEBLES PN FRAGILE-X EXPRESSION - USE OF A DOUBLE INDUCTION SYSTEM | 2 | 4 |
| 930 | 0 | 2 | 848 1991 CYTOGENETICS AND CELL GENETICS 56(3-4):221-221 HOWARDPEEBLES PN FRAGILE X SCREENING VS FAMILY STUDIES (ESPECIALLY IN FEMALES) - LABORATORY PROCEDURES GUIDELINES | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 931 | 2 | 5 | 924 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):161-161 HOWARDPEEBLES PN EFFECT OF DIALYZED SERA ON FRAGILE-X EXPRESSION | 0 | 0 |
| 932 | 0 | 0 | 1321 1995 CYTOGENETICS AND CELL GENETICS 69(1-2):116-116 HOWARDPEEBLES PN IT IS TIME TO ABANDON THE CYTOGENETIC FRAGILE-X TEST | 0 | 0 |
| 933 | 4 | 6 | 1441 1996 AMERICAN JOURNAL OF MEDICAL GENETICS 64(2):377-377 HowardPeebles PN Successful pregnancy in a fragile X carrier by donor egg | 2 | 3 |
| 934 | 2 | 4 | 522 1988 AMERICAN JOURNAL OF MEDICAL GENETICS 30(1-2):227-230 HOWARDPEEBLES PN; BROWN WT THE FRAGILE-X SYNDROME - VARIABILITY OF EXPRESSION IN CARRIER FEMALES | 3 | 4 |
| 935 | 1 | 2 | 181 1984 AMERICAN JOURNAL OF MEDICAL GENETICS 17(1):275-276 HOWARDPEEBLES PN; CARROLL AJ RECOMBINATION BETWEEN THE FRAGILE-X AND G6PD | 1 | 3 |
| 936 | 0 | 0 | 8 1981 AMERICAN JOURNAL OF HUMAN GENETICS 33(6):A107-A107 HOWARDPEEBLES PN; FINLEY WH TESTICULAR AND CYTOGENETIC SCREENING OF RETARDED MALES FROM THE SOUTH FOR THE FRAGILE X-LINKED MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 937 | 1 | 14 | 109 1983 AMERICAN JOURNAL OF MEDICAL GENETICS 15(4):631-635 HOWARDPEEBLES PN; FINLEY WH SCREENING OF MENTALLY-RETARDED MALES FOR MACRO-ORCHIDISM AND THE FRAGILE-X CHROMOSOME | 16 | 22 |
| 938 | 9 | 23 | 243 1985 AMERICAN JOURNAL OF HUMAN GENETICS 37(5):956-964 HOWARDPEEBLES PN; FRIEDMAN JM UNAFFECTED CARRIER MALES IN FAMILIES WITH FRAGILE-X SYNDROME | 14 | 19 |
| 939 | 6 | 12 | 925 1992 AMERICAN JOURNAL OF MEDICAL GENETICS 43(1-2):162-166 HOWARDPEEBLES PN; MADDALENA A RECENT EXPERIENCE IN PRENATAL-DIAGNOSIS OF FRAGILE-X | 3 | 3 |
| 940 | 5 | 9 | 1343 1995 DEVELOPMENTAL BRAIN DYSFUNCTION 8(4-6):408-410 HowardPeebles PN; Maddalena A; Black SH; Levinson G; Bick DP; Schulman JD Fragile X screening in pediatric and obstetrical patients | 2 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 941 | 1 | 3 | 1125 1993 LANCET 341(8847):770-770 HOWARDPEEBLES PN; MADDALENA A; BLACK SH; SCHULMAN JD POPULATION SCREENING FOR FRAGILE-X SYNDROME | 9 | 10 |
| 942 | 0 | 3 | 1196 1994 AMERICAN JOURNAL OF MEDICAL GENETICS 53(4):382-382 HOWARDPEEBLES PN; MADDALENA A; SPENCE WC; LEVINSON G; FALLON L; BICK DP; BLACK SH; SCHULMAN JD FRAGILE-X SCREENING - WHAT IS THE REAL ISSUE | 5 | 9 |
| 943 | 1 | 12 | 65 1982 HUMAN GENETICS 62(3):282-284 HOWELL RT; MCDERMOTT A REPLICATION STATUS OF THE FRAGILE X-CHROMOSOME, FRA(X) (Q27), IN 3 HETEROZYGOUS FEMALES | 21 | 30 |
| 944 | 0 | 3 | 1465 1996 CHINESE SCIENCE BULLETIN 41(5):436-437 Huang T; Shen Y; Fan Y; Wu GY Expression of two alternative splicing isoforms of fragile X gene in human placenta | 0 | 0 |
| 945 | 0 | 0 | 2285 2003 JOURNAL OF NEUROCHEMISTRY 85:1-1 Huber KM Recent progress in understanding the neural mechanisms of Fragile X Syndrome | 0 | 0 |
| 946 | 13 | 40 | 2193 2002 PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA 99(11):7746-7750 Huber KM; Gallagher SM; Warren ST; Bear MF Altered synaptic plasticity in a mouse model of fragile X mental retardation | 16 | 31 |
| 947 | 0 | 0 | 1069 1993 BEHAVIOR GENETICS 23(6):555-555 HUGGINS RM THE USE OF ROBUST STATISTICAL-METHODS TO DETERMINE THE EFFECT OF GENOTYPE ON PHENOTYPE IN FRAGILE-X | 0 | 0 |
| 948 | 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 |
| 949 | 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 |
| 950 | 19 | 30 | 1638 1998 ANNALS OF HUMAN GENETICS 62:337-347 Huggins RM; Loesch DZ; Sherman SL A branching non-linear autoregressive model for the transmission of the fragile X dynamic repeat mutation | 1 | 2 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 951 | 0 | 0 | 1265 1995 AMERICAN JOURNAL OF HUMAN GENETICS 57(4):152-152 HUGHES MR; HADDAD BR; SUBRAMANIAN S; NASONKIN I; COTA J; CHONG SS SINGLE-CELL DETECTION OF THE FMR1, HD, AND SCA1 TRINUCLEOTIDE REPEATS - APPLICATION TO PREIMPLANTATION DIAGNOSIS AND INSTABILITY ANALYSIS OF FRAGILE-X SYNDROME, HUNTINGTON DISEASE, AND SPINO-CEREBELLAR ATAXIA TYPE-1 | 0 | 0 |
| 952 | 29 | 36 | 1024 1993 AMERICAN JOURNAL OF DISEASES OF CHILDREN 147(11):1236-1241 HULL C; HAGERMAN RJ A STUDY OF THE PHYSICAL, BEHAVIORAL, AND MEDICAL PHENOTYPE, INCLUDING ANTHROPOMETRIC MEASURES, OF FEMALES WITH FRAGILE-X SYNDROME | 27 | 38 |
| 953 | 0 | 0 | 1109 1993 JOURNAL OF DEVELOPMENTAL AND BEHAVIORAL PEDIATRICS 14(4):282-282 HULL CE; HAGERMAN RJ A STUDY OF THE PHENOTYPE IN HETEROZYGOUS FRAGILE-X FEMALES | 0 | 0 |
| 954 | 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 |
| 955 | 0 | 0 | 475 1987 JOURNAL OF MEDICAL GENETICS 24(10):641-641 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 1 | 1 |
| 956 | 0 | 0 | 573 1988 CLINICAL GENETICS 33(6):464-464 HULTEN M; JOHANNISSON R MEIOSIS IN THE FRAGILE-X MENTAL-RETARDATION SYNDROME | 0 | 0 |
| 957 | 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 |
| 958 | 9 | 28 | 1825 2000 AMERICAN JOURNAL OF HUMAN GENETICS 66(2):413-418 Hundscheid RDL; Sistermans EA; Thomas CMG; Braat DDM; Straatman H; Kiemeney LALM; Oostra BA; Smits APT Imprinting effect in premature ovarian failure confined to paternally inherited fragile X premutations | 14 | 29 |
| 959 | 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 |
| 960 | 5 | 14 | 2224 2003 AMERICAN JOURNAL OF MEDICAL GENETICS PART A 117A(1):6-9 Hundscheid RDL; Smits APT; Thomas CMG; Kiemeney LALM; Braat DDM Female carriers of fragile X premutations have no increased risk for additional diseases other than premature ovarian failure | 0 | 3 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 961 | 3 | 3 | 1830 2000 AMERICAN JOURNAL OF HUMAN GENETICS 67(1):256-258 Hundscheid RDL; Thomas CMG; Braat DDM; Oostra BA; Smits APT Premature ovarian failure is associated with maternally and paternally inherited premutation in Brazilian families with fragile X - Reply | 2 | 5 |
| 962 | 3 | 9 | 146 1983 JOURNAL OF MEDICAL GENETICS 20(4):314-315 HUNTER AGW; MACDONALD J; EVANS JA ABSENCE OF THE FRAGILE-X IN A GROUP OF PATIENTS WITH IDIOPATHIC MENTAL-RETARDATION | 0 | 0 |
| 963 | 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 |
| 964 | 0 | 2 | 724 1990 NUCLEIC ACIDS RESEARCH 18(3):692-692 HUPKES PE; VANBENNEKOM CA; VANOOST BA; OOSTRA BA RN1, A NEW POLYMORPHIC MARKER NEAR THE FRAGILE-X LOCUS - (HGM10 ASSIGNMENT DXS-369) | 1 | 2 |
| 965 | 0 | 0 | 291 1985 JAPANESE JOURNAL OF HUMAN GENETICS 30(2):150-150 IKEDA T; MIYAGI C; HIRAYAMA K FRAGILE X-SYNDROME - REPORT OF 2 FAMILIES AND CYTOGENETIC STUDIES | 0 | 0 |
| 966 | 5 | 9 | 2110 2002 BRAIN & DEVELOPMENT 24(8):766-769 Incorpora G; Sorge G; Sorge A; Pavone L Epilepsy in fragile X syndrome | 2 | 2 |
| 967 | 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 |
| 968 | 0 | 0 | 1710 1999 AMERICAN JOURNAL OF HUMAN GENETICS 65(4):A165-A165 Iqbal MA; Sakati N; Nester A; Ozand P Cytogenetic diagnosis of fragile X syndrome a study of 305 suspected cases in Saudi Arabia. | 0 | 0 |
| 969 | 21 | 41 | 1869 2000 ANNALS OF SAUDI MEDICINE 20(3-4):214-217 Iqbal MA; Sakati N; Nester M; Ozand P Cytogenetic diagnosis of fragile X syndrome: Study of 305 suspected cases in Saudi Arabia | 0 | 0 |
| 970 | 22 | 79 | 1877 2000 CEREBRAL CORTEX 10(10):1038-1044 Irwin SA; Galvez R; Greenough WT Dendritic spine structural anomalies in fragile-X mental retardation syndrome | 27 | 45 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 971 | 12 | 28 | 2099 2002 AMERICAN JOURNAL OF MEDICAL GENETICS 111(2):140-146 Irwin SA; Idupulapati M; Gilbert ME; Harris JB; Chakravarti AB; Rogers EJ; Crisostomo RA; Larsen BP; Mehta A; Alcantara CJ; Patel B; Swain RA; Weiler IJ; Oostra BA; Greenough WT Dendritic spine and dendritic field characteristics of layer V pyramidal neurons in the visual cortex of fragile-X knockout mice | 7 | 10 |
| 972 | 14 | 42 | 1983 2001 AMERICAN JOURNAL OF MEDICAL GENETICS 98(2):161-167 Irwin SA; Patel B; Idupulapati M; Harris JB; Crisostomo RA; Larsen BP; Kooy F; Willems PJ; Cras P; Kozlowski PB; Swain RA; Weiler IJ; Greenough WT Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: A quantitative examination | 37 | 64 |
| 973 | 4 | 13 | 1952 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 73(1):87-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered Fragile-X mental retardation protein expression in response to behavioral stimulation | 20 | 25 |
| 974 | 6 | 14 | 1953 2000 NEUROBIOLOGY OF LEARNING AND MEMORY 74(1):80-93 Irwin SA; Swain RA; Christmon CA; Chakravarti A; Weiler IJ; Greenough WT Evidence for altered fragile-x mental retardation protein expression in response to behavioral stimulation (vol 73, pg 87, 2000) | 2 | 2 |
| 975 | 0 | 0 | 162 1983 TERATOLOGY 28(1):A30-A30 ISHIKIRIYAMA S; NIIKAWA N 2 JAPANESE PATIENTS WITH FRAGILE X SYNDROME | 0 | 2 |
| 976 | 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 |
| 977 | 2 | 6 | 211 1984 JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS 14(4):451-452 JACKSON A; HOGERMAN R; LEVITAS A SEROTONIN LEVELS IN FRAGILE-X AUTISTIC PATIENTS | 1 | 3 |
| 978 | 1 | 45 | 1799 1999 JOURNAL OF EARLY INTERVENTION 22(2):137-151 Jackson SC; Roberts JE Family and professional congruence in communication assessments of preschool boys with fragile X syndrome | 0 | 0 |
| 979 | 0 | 0 | 756 1991 AMERICAN JOURNAL OF HUMAN GENETICS 49(4):257-257 JACKSONCOOK J; PISERCHIO C; VIRGINIA J MOSAIC XY/XYY AND FRAGILE-X IN A 4-YEAR-OLD MALE BODURTHA | 0 | 0 |
| 980 | 0 | 1 | 1 1980 AMERICAN JOURNAL OF HUMAN GENETICS 32(6):A73-A73 JACKY PB EXPRESSION IN FIBROBLAST-CULTURE OF THE FRAGILE X-CHROMOSOME ASSOCIATED WITH FAMILIAL SEX-LINKED MENTAL-RETARDATION - FACTORS INFLUENCING A RELIABLE DETERMINATION OF THE FREQUENCY OF EXPRESSION | 0 | 0 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 981 | 4 | 23 | 806 1991 AMERICAN JOURNAL OF MEDICAL GENETICS 38(2-3):400-403 JACKY PB; AHUJA YR; ANYANEYEBOA K; BREG WR; CARPENTER NJ; FROSTERISKENIUS UG; FRYNS JP; GLOVER TW; GUSTAVSON KH; HOEGERMAN SF; HOLMGREN G; HOWARDPEEBLES PN; JENKINS EC; KRAWCZUN MS; NERI G; PETTIGREW A; SCHAAP T; SCHONBERG SA; SHAPIRO LR; SPINNER N; STEINBACH P; VIANNAMORGANTE AM; WATSON MS; WILMOT PL GUIDELINES FOR THE PREPARATION AND ANALYSIS OF THE FRAGILE-X CHROMOSOME IN LYMPHOCYTES | 31 | 44 |
| 982 | 0 | 0 | 1086 1993 CYTOGENETICS AND CELL GENETICS 63(4):256-256 JACKY PB; BERRY TL; LAMB OA; LANGLOIS MI; OLSON CL; REISS JA; WEEKS FF; YOSHITOMI MJ ARE FRAGILE-X CHROMOSOME-STUDIES DEAD | 0 | 0 |
| 983 | 2 | 15 | 112 1983 ANNALES DE GENETIQUE 26(3):171-173 JACKY PB; DILL FJ FRAGILE-X CHROMOSOME AND CHROMOSOME CONDENSATION | 1 | 4 |
| 984 | 0 | 0 | 972 1992 CYTOGENETICS AND CELL GENETICS 60(3-4):266-266 JACKY PB; JENKINS EC FRAGILE-X CYTOGENETIC GUIDELINES REVIEWED - RELEVANCE TO FRA(X) MOLECULAR GENETIC-STUDIES AND TO APPROPRIATENESS OF CHROMOSOME-STUDIES IN ALL CASES OF DEVELOPMENTAL DELAY - A DISCUSSION | 0 | 0 |
| 985 | 0 | 0 | 156 1983 PATHOLOGY 15(1):105-106 JACKY PB; SUTHERLAND GR FRAGILE-X EXPRESSION IN FIBROBLASTS | 0 | 0 |
| 986 | 0 | 0 | 868 1991 JOURNAL OF MEDICAL GENETICS 28(12):809-810 JACOBS PA THE FRAGILE-X SYNDROME | 6 | 10 |
| 987 | 7 | 12 | 1117 1993 JOURNAL OF MEDICAL GENETICS 30(6):454-459 JACOBS PA; BULLMAN H; MACPHERSON J; YOUINGS S; ROONEY V; WATSON A; DENNIS NR POPULATION STUDIES OF THE FRAGILE-X - A MOLECULAR APPROACH | 46 | 79 |
| 988 | 1 | 3 | 347 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):567-572 JACOBS PA; MAYER M; ABRUZZO MA STUDIES OF THE FRAGILE (X) SYNDROME IN POPULATIONS OF MENTALLY-RETARDED INDIVIDUALS IN HAWAII | 13 | 16 |
| 989 | 2 | 6 | 350 1986 AMERICAN JOURNAL OF MEDICAL GENETICS 23(1-2):611-617 JACOBS PA; SHERMAN S; TURNER G; WEBB T THE FRAGILE(X) SYNDROME - THE MUTATION PROBLEM | 14 | 19 |
| 990 | 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 |
| # | LCR | NCR | Nodes / Date / Journal / Authors | LCS | GCS |
| 991 | 0 | 0 | 2079 2002 AMERICAN JOURNAL OF HUMAN GENETICS 71(4):185-185 Jacquemont S; Hagerman RJ; Leehey M; Greco C; Brunberg J; Tassone F; Gane LW; Jardini T; Harris SW; Zhang L; Grigsby J; Des Portes V; Berry-Kravis E; Brown WT; Hagerman PJ Characterization of a progressive neurological condition in older adult male carriers of the fragile X premutation. | 2 | 2 |
| 992 | 18 | 36 | 2200 2003 AMERICAN JOURNAL OF HUMAN GENETICS 72(4):869-878 Jacquemont S; Hagerman RJ; Leehey M; Grigsby J; Zhang L; Brunberg JA; Greco C; Des Portes V; Jardini T; Levine R; Berry-Kravis E; Brown WT; Schaeffer S; Kissel J; Tassone F; Hagerman PJ Fragile X premutation tremor/ataxia syndrome: Molecular, clinical, and neuroimaging correlates | 10 | 19 |
| 993 | 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 |
| 994 | 0 | 0 | 2203 2003 AMERICAN JOURNAL OF HUMAN GENETICS 73(5):163-163 Jacquemont S; Hagerman RJ; Leehey MA; Hall DA; Levine RA; Brunberg JA; Zhang L; Jardini T; Harris SW; Herman K; Berry-Kravis E; Tassone F; Hagerman PJ Penetrance of the fragile X-associated tremor/ataxia syndrome (FXTAS) in a premutation carrier population: Initial results from a California family-based study. | 0 | 0 |
| 995 | 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 |
| 996 | 21 | 51 | 1600 1997 JOURNAL OF CLINICAL INVESTIGATION 100(2):331-338 Jakala P; Hanninen T; Ryynanen M; Laakso M; Partanen K; Mannermaa A; Soininen H Fragile-X: Neuropsychological test performance, CGG triplet repeat lengths, and hippocampal volumes | 12 | 19 |
| 997 | 0 | 0 | 1972 2001 AMERICAN JOURNAL OF HUMAN GENETICS 69(4):430-430 Jakupciak JP; O'Connell CD; Atha DA; Richie KL Standardization of PCR amplification for fragile X trinucleotide repeat measurements. | 0 | 0 |
| 998 | 3 | 10 | 140 1983 JOURNAL DE GENETIQUE HUMAINE 31(2):133-139 JALBERT H; BAETEMAN MA; TROCHETROYER C; MATTEI MG; MATTEI JF; LEROUX D; JALBERT P MENTAL-RETARDATION WITH FRAGILE-X - NEITHER INACTIVATION NOR DELETION OF THE SEGMENT Q28-]Q TER ENZYMATIC AND MORPHOMETRIC DATA | 0 | 0 |
| 999 | 0 | 0 | 157 1983 PEDIATRIE 38(3):191-198 JALBERT P FRAGILE X-LINKED MENTAL-RETARDATION - MORE QUESTIONS | 1 | 3 |
| 1000 | 0 | 0 | 1930 2000 JOURNAL OF MEDICAL GENETICS 37:S44-S44 James T; Trigg A; Lindley VH; Fews GA; Roberts E; McKeown C; Davison EV An unexpected finding of fragile X (FRAXA) syndrome in a fetal blood sample referred for abnormalities on ultrasound scan | 0 | 0 |
Page 10: 1 (Abbeduto L) 2 (BELGHITI D) 3 (Brown WT) 4 (Chen X) 5 (DAKER MG) 6 (DYKENS E) 7 (FITCHETT M) 8 (GLOVER TW) 9 (HAGERMAN RJ) 10 (HOFFMAN M) 11 (JANCAR J) 12 (KIMCHISARFATY C) 13 (LEE JT) 14 (MAES B) 15 (MIGEON BR) 16 (Myers GF) 17 (Patsalis PC) 18 (REISS AL) 19 (Schenck A) 20 (SMITS APT) 21 (SZABO P) 22 (TURNER G) 23 (Wang YC) 24 (WOHRLE D)
Generated by: HistCite(Vlad).
Version: 2004.08.24