| Missing Links?: 1046 Citation Matrix | Graphs | Glossary HistCite Guide About |
Nodes: 9713,
Authors: 21853,
Journals: 1676,
Outer References: 261037,
Words: 13682
Collection span: 1947 - 2005
View: Overview. Sorted by journal name.
Page 51 of 98: 1 11 21 31 41 [ 51 52 53 54 55 56 57 58 59 60 ] 61 71 81 91
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
|---|---|---|---|---|---|
| 5001 | 3 | 34 | 2843 1989 HUMAN GENETICS 82 (1): 63-66 GUAZZI S; PERSICI P; GATTI R; DURAND P; OBRIEN JS; et al. HETEROGENEITY OF MESSENGER-RNA EXPRESSION IN ITALIAN FUCOSIDOSIS PATIENTS | 6 | 6 |
| 5002 | 4 | 14 | 2844 1989 HUMAN GENETICS 82 (1): 89-91 YASUDA T; IKEHARA Y; TAKAGI S; MIZUTA K; KISHI K A HEREDITARY DOUBLE DOUBLE-BANDED VARIATION IN THE VITAMIN D-BINDING PROTEIN (GC) SYSTEM ANALYZED BY IMMUNOBLOTTING - DUPLICATION OF THE 1F AND 1A2 GENES | 0 | 13 |
| 5003 | 4 | 19 | 2845 1989 HUMAN GENETICS 82 (2): 194-196 HENDRIKS RW; SANDKUYL LA; KRAAKMAN MEM; DELANGE GG; SCHUURMAN RKB POLYCLONAL HYPER-IMMUNOGLOBULIN G1(A1) SYNDROME - EVIDENCE FOR A DOMINANT IMMUNOGLOBULIN PRODUCTION REGULATOR WITHIN THE HUMAN-IMMUNOGLOBULIN HEAVY-CHAIN GENE-COMPLEX | 2 | 5 |
| 5004 | 4 | 18 | 2846 1989 HUMAN GENETICS 82 (3): 208-212 VILKKI J; SAVONTAUS ML; KALIMO H; NIKOSKELAINEN EK MITOCHONDRIAL-DNA POLYMORPHISM IN FINNISH FAMILIES WITH LEBERS HEREDITARY OPTIC NEURORETINOPATHY | 3 | 17 |
| 5005 | 1 | 21 | 2847 1989 HUMAN GENETICS 83 (1): 93-96 POLLER W; BARTH J; VOSS B DETECTION OF AN ALTERATION OF THE ALPHA-2-MACROGLOBULIN GENE IN A PATIENT WITH CHRONIC LUNG-DISEASE AND SERUM ALPHA-2-MACROGLOBULIN DEFICIENCY | 2 | 14 |
| 5006 | 8 | 32 | 2848 1989 HUMAN GENETICS 83 (2): 101-110 ZHAO T; LEE TD GM-ALLOTYPES AND KM-ALLOTYPES IN 74 CHINESE POPULATIONS - A HYPOTHESIS OF THE ORIGIN OF THE CHINESE NATION | 27 | 46 |
| 5007 | 2 | 17 | 2849 1989 HUMAN GENETICS 83 (4): 369-372 MOTTES M; CUGOLA L; PIGNATTI PF HAPLOTYPE FREQUENCIES OF THE COLLAGEN TYPE-I GENES IN THE ITALIAN POPULATION | 2 | 14 |
| 5008 | 4 | 32 | 2850 1989 HUMAN GENETICS 83 (4): 383-390 WU JS; GIUFFRA LA; GOODFELLOW PJ; MYERS S; CARSON NL; et al. THE BETA-SUBUNIT LOCUS OF THE HUMAN FIBRONECTIN RECEPTOR - DNA RESTRICTION FRAGMENT LENGTH POLYMORPHISM AND LINKAGE MAPPING STUDIES | 6 | 27 |
| 5009 | 11 | 34 | 3159 1990 HUMAN GENETICS 84 (2): 137-146 HOFFMANN R; BRAUN A; CLEVE H A MONOCLONAL-ANTIBODY AGAINST HUMAN VITAMIN-D-BINDING PROTEIN FOR THE ANALYSIS OF GENETIC-VARIATION IN THE GROUP-SPECIFIC COMPONENT SYSTEM (GC) | 1 | 3 |
| 5010 | 3 | 33 | 3160 1990 HUMAN GENETICS 84 (3): 253-257 HUFF V; COMPTON DA; STRONG LC; SAUNDERS GF A PANEL OF RESTRICTION FRAGMENT LENGTH POLYMORPHISMS FOR CHROMOSOMAL BAND-11P13 | 3 | 20 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5011 | 3 | 316 | 3161 1990 HUMAN GENETICS 84 (4): 301-336 VOGT P POTENTIAL GENETIC FUNCTIONS OF TANDEM REPEATED DNA-SEQUENCE BLOCKS IN THE HUMAN GENOME ARE BASED ON A HIGHLY CONSERVED CHROMATIN FOLDING CODE | 2 | 189 |
| 5012 | 2 | 9 | 3162 1990 HUMAN GENETICS 84 (4): 368-370 LUCKENBACH C; KOMPF J; RITTER H GENETIC-STUDIES ON HUMAN THYROXINE-BINDING GLOBULIN (TBG) | 0 | 1 |
| 5013 | 1 | 23 | 3163 1990 HUMAN GENETICS 84 (5): 387-390 KOEBERL DD; BOTTEMA CDK; SARKAR G; KETTERLING RP; CHEN SH; et al. RECURRENT NONSENSE MUTATIONS AT ARGININE RESIDUES CAUSE SEVERE HEMOPHILIA-B IN UNRELATED HEMOPHILIACS | 3 | 28 |
| 5014 | 8 | 26 | 3164 1990 HUMAN GENETICS 85 (3): 349-354 BOWCOCK A; SARTORELLI V POLYMORPHISM AND MAPPING OF THE IGF1 GENE, AND ABSENCE OF ASSOCIATION WITH STATURE AMONG AFRICAN PYGMIES | 7 | 12 |
| 5015 | 8 | 88 | 3165 1990 HUMAN GENETICS 85 (4): 436-445 BONDUELLE M GRADIENT OF DISTRIBUTION IN EUROPE OF THE MAJOR CF MUTATION AND OF ITS ASSOCIATED HAPLOTYPE | 0 | 21 |
| 5016 | 6 | 16 | 3166 1990 HUMAN GENETICS 85 (5): 560-562 HOUWEN RHJ; SCHEFFER H; TEMEERMAN GJ; VANDERVLIES P; BUYS CHCM CLOSE LINKAGE OF THE WILSONS-DISEASE LOCUS TO D13S12 IN THE CHROMOSOMAL REGION 13Q21 AND NOT TO ESD IN 13Q14 | 10 | 10 |
| 5017 | 11 | 38 | 3167 1990 HUMAN GENETICS 85 (6): 643-647 WALTER MA; CHAMBERS CA; ZIMMERMAN B; COX DW A MULTIGENE DELETION IN THE IMMUNOGLOBULIN HEAVY-CHAIN REGION IN A HIGHLY ATOPIC INDIVIDUAL | 3 | 14 |
| 5018 | 5 | 45 | 3168 1990 HUMAN GENETICS 86 (2): 139-146 ROSENDAAL FR; BROCKERVRIENDS AHJT; VANHOUWELINGEN JC; SMIT C; VAREKAMP I; et al. SEX-RATIO OF THE MUTATION FREQUENCIES IN HEMOPHILIA-A - ESTIMATION AND METAANALYSIS | 5 | 30 |
| 5019 | 11 | 34 | 3169 1990 HUMAN GENETICS 86 (2): 191-197 BOTTARO A; CARIOTA U; DELANGE GG; DEMARCHI M; GALLINA R; et al. MULTIPLE LEVELS OF ANALYSIS OF AN IGHG4 GENE DELETION | 3 | 16 |
| 5020 | 1 | 7 | 3170 1990 HUMAN GENETICS 86 (2): 238-240 KENNERKNECHT I; SUORMALA T; BARBI G; BAUMGARTNER ER THE GENE CODING FOR THE ALPHA-CHAIN OF HUMAN PROPIONYL-COA CARBOXYLASE MAPS TO CHROMOSOME BAND-13Q32 | 3 | 6 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5021 | 1 | 17 | 3499 1991 HUMAN GENETICS 86 (4): 411-413 KALAYDJIEVA L; DWORNICZAK B; KUCINSKAS V; YURGELIAVICIUS V; KUNERT E; et al. GEOGRAPHICAL-DISTRIBUTION GRADIENTS OF THE MAJOR PKU MUTATIONS AND THE LINKED HAPLOTYPES | 3 | 24 |
| 5022 | 2 | 37 | 3500 1991 HUMAN GENETICS 87 (2): 129-133 KUMAR S; KIMBERLING WJ; GABOW PA; KENYON JB GENETIC-LINKAGE STUDIES OF AUTOSOMAL DOMINANT POLYCYSTIC KIDNEY-DISEASE - SEARCH FOR THE 2ND GENE IN A LARGE SICILIAN FAMILY | 0 | 3 |
| 5023 | 3 | 19 | 3501 1991 HUMAN GENETICS 87 (4): 465-468 CHUANG LM; TAI TY; WANG TR; CHANG YC; CHEN KH; et al. ESTERASE-D AND RETINOBLASTOMA GENE LOCI ARE TIGHTLY LINKED TO WILSONS-DISEASE IN CHINESE PEDIGREES FROM TAIWAN | 3 | 5 |
| 5024 | 4 | 18 | 3502 1991 HUMAN GENETICS 87 (5): 618-620 LECONIAT M; SOKOLOFF P; HILLION J; MARTRES MP; GIROS B; et al. CHROMOSOMAL LOCALIZATION OF THE HUMAN D3-DOPAMINE RECEPTOR GENE | 5 | 62 |
| 5025 | 6 | 11 | 3813 1992 HUMAN GENETICS 88 (6): 613-618 BARRAI I; BERETTA M; MAMOLINI E; SCAPOLI C; CANELLA R; et al. GENETIC STRUCTURES IN THE PO DELTA - PRINCIPAL COMPONENTS, SYSTEMIC FUNCTIONS AND THE RELATIVE AGE OF THE BETA-THALASSEMIA POLYMORPHISM | 0 | 0 |
| 5026 | 9 | 35 | 3814 1992 HUMAN GENETICS 89 (2): 199-203 CONSTANS J; RIBOUCHON MT; GOUAILLARD C; CHAVENTRE A; CLAYTON J A NEW POLYMORPHISM OF THYROXINE-BINDING GLOBULIN IN 3 AFRICAN GROUPS (MALI) WITH ENDEMIC NODULAR GOITER | 3 | 5 |
| 5027 | 6 | 19 | 3815 1992 HUMAN GENETICS 89 (3): 319-322 MONTANDON AJ; GREEN PM; BENTLEY DR; LJUNG R; KLING S; et al. DIRECT ESTIMATE OF THE HEMOPHILIA-B (FACTOR-IX DEFICIENCY) MUTATION-RATE AND OF THE RATIO OF THE SEX-SPECIFIC MUTATION-RATES IN SWEDEN | 1 | 25 |
| 5028 | 12 | 21 | 3816 1992 HUMAN GENETICS 89 (4): 401-406 BRAUN A; BICHLMAIER R; CLEVE H MOLECULAR ANALYSIS OF THE GENE FOR THE HUMAN VITAMIN-D-BINDING PROTEIN (GROUP-SPECIFIC COMPONENT) - ALLELIC DIFFERENCES OF THE COMMON GENETIC GC-TYPES | 8 | 32 |
| 5029 | 10 | 19 | 3817 1992 HUMAN GENETICS 89 (6): 607-611 SCHEFFER H; HOUWEN RHJ; TEMEERMAN GJ; LOESSNER J; BACHMANN B; et al. IDENTIFICATION OF CROSSOVERS IN WILSON DISEASE FAMILIES AS REFERENCE POINTS FOR A GENETIC LOCALIZATION OF THE GENE | 6 | 10 |
| 5030 | 10 | 45 | 4145 1993 HUMAN GENETICS 90 (5): 526-532 BRAUN A; BICHLMAIER R; MULLER B; CLEVE H MOLECULAR EVALUATION OF AN ALU REPEAT INCLUDING A POLYMORPHIC VARIABLE POLY(DA) (ALUVPA) IN THE VITAMIN-D BINDING-PROTEIN (DBP) GENE | 1 | 7 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5031 | 7 | 154 | 4146 1993 HUMAN GENETICS 91 (2): 91-117 FLINT J; HARDING RM; CLEGG JB; BOYCE AJ WHY ARE SOME GENETIC-DISEASES COMMON - DISTINGUISHING SELECTION FROM OTHER PROCESSES BY MOLECULAR ANALYSIS OF GLOBIN GENE VARIANTS | 9 | 68 |
| 5032 | 8 | 17 | 4147 1993 HUMAN GENETICS 91 (5): 504-506 KOOY RF; VANDERVEEN AY; VERLIND E; HOUWEN RHJ; SCHEFFER H; et al. PHYSICAL LOCALIZATION OF THE CHROMOSOMAL MARKER D13S31 PLACES THE WILSON DISEASE LOCUS AT THE JUNCTION OF BAND-Q14.3 AND BAND-Q21.1 OF CHROMOSOME-13 | 3 | 5 |
| 5033 | 15 | 31 | 4148 1993 HUMAN GENETICS 92 (2): 183-188 ARNAUD J; CONSTANS J AFFINITY DIFFERENCES FOR VITAMIN-D METABOLITES ASSOCIATED WITH THE GENETIC ISOFORMS OF THE HUMAN SERUM CARRIER PROTEIN (DBP) | 3 | 8 |
| 5034 | 1 | 27 | 4149 1993 HUMAN GENETICS 92 (3): 269-272 BUYLE S; REYNIERS E; VITS L; DEBOULLE K; HANDIG I; et al. FOUNDER EFFECT IN A BELGIAN-DUTCH FRAGILE-X POPULATION | 6 | 30 |
| 5035 | 1 | 16 | 4488 1994 HUMAN GENETICS 93 (2): 162-166 KERE J; ESTIVILL X; CHILLON M; MORRAL N; NUNES V; et al. CYSTIC-FIBROSIS IN A LOW-INCIDENCE POPULATION - 2 MAJOR MUTATIONS IN FINLAND | 1 | 17 |
| 5036 | 2 | 33 | 4489 1994 HUMAN GENETICS 94 (3): 224-230 TAKESHITA H; YASUDA T; NADANO D; IIDA R; NAKANAGA M; et al. GENETICALLY POLYMORPHIC ALPHA-L-FUCOSIDASE (FUCA1) ISOZYMES DETECTED IN BLOOD-PLASMA | 0 | 3 |
| 5037 | 5 | 39 | 4490 1994 HUMAN GENETICS 94 (4): 331-338 DRECHSLER M; MEIJERSHEIJBOER EJ; SCHNEIDER S; SCHURICH B; GRONDGINSBACH C; et al. MOLECULAR ANALYSIS OF ANIRIDIA PATIENTS FOR DELETIONS INVOLVING THE WILMS-TUMOR GENE | 0 | 13 |
| 5038 | 22 | 51 | 4491 1994 HUMAN GENETICS 94 (6): 675-683 GIBSON WT; WALTER MA; AHMED AR; ALPER CA; COX DW THE IMMUNOGLOBULIN HEAVY-CHAIN AND DISEASE ASSOCIATION - APPLICATION TO PEMPHIGUS-VULGARIS | 0 | 2 |
| 5039 | 5 | 41 | 4840 1995 HUMAN GENETICS 95 (5): 495-500 WINTLE RF; COSTA T; HASLAM RHA; TESHIMA IE; COX DW MOLECULAR ANALYSIS REDEFINES 3 HUMAN-CHROMOSOME-14 DELETIONS | 1 | 15 |
| 5040 | 5 | 26 | 4841 1995 HUMAN GENETICS 96 (2): 225-228 BARRIENTOS A; CASADEMONT J; SOLANS A; MORAL P; CARDELLACH F; et al. THE 9-BP DELETION IN REGION-V OF MITOCHONDRIAL-DNA - EVIDENCE OF MUTATION RECURRENCE | 5 | 10 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5041 | 5 | 40 | 5241 1996 HUMAN GENETICS 97 (4): 476-481 Camaschella C; Roetto A; Gasparini P; Piperno A; Fortina P; et al. Allelic association of microsatellites of 6p in Italian hemochromatosis patients | 2 | 19 |
| 5042 | 4 | 31 | 5242 1996 HUMAN GENETICS 97 (5): 614-619 Erdmann J; ShimronAbarbanell D; Rietschel M; Albus M; Maier W; et al. Systematic screening for mutations in the human serotonin-2A (5-HT2A) receptor gene: Identification of two naturally occurring receptor variants and association analysis in schizophrenia | 15 | 120 |
| 5043 | 9 | 51 | 5243 1996 HUMAN GENETICS 97 (6): 759-764 Tishkoff SA; Ruano G; Kidd JR; Kidd KK Distribution and frequency of a polymorphic Alu insertion at the plasminogen activator locus in humans | 12 | 38 |
| 5044 | 16 | 74 | 5244 1996 HUMAN GENETICS 98 (1): 36-47 Dard P; SanchezMazas A; Dugoujon JM; DeLange G; Langaney A; et al. DNA analysis of the immunoglobulin IGHG loci in a Mandenka population from eastern Senegal: Correlation with Gm haplotypes and hypotheses for the evolution of the Ig CH region | 5 | 12 |
| 5045 | 3 | 28 | 5245 1996 HUMAN GENETICS 98 (1): 60-64 Brinkmann B; Meyer E; Junge A Complex mutational events at the HumD21S11 locus | 6 | 26 |
| 5046 | 13 | 55 | 5246 1996 HUMAN GENETICS 98 (1): 91-101 Chang FM; Kidd JR; Livak KJ; Pakstis AJ; Kidd KK The world-wide distribution of allele frequencies at the human dopamine D4 receptor locus | 10 | 129 |
| 5047 | 12 | 38 | 5247 1996 HUMAN GENETICS 98 (2): 145-150 Bertorelle G; Calafell F; Francalacci P; Bertranpetit J; Barbujani G Geographic homogeneity and non-equilibrium patterns of mtDNA sequences in Tuscany, Italy | 0 | 1 |
| 5048 | 11 | 21 | 5631 1997 HUMAN GENETICS 99 (1): 1-7 PerezLezaun A; Calafell F; Mateu E; Comas D; RuizPacheco R; et al. Microsatellite variation and the differentiation of modern humans | 61 | 85 |
| 5049 | 23 | 55 | 5632 1997 HUMAN GENETICS 99 (4): 443-449 Comas D; Calafell F; Mateu E; PerezLezaun A; Bosch E; et al. Mitochondrial DNA variation and the origin of the Europeans | 29 | 41 |
| 5050 | 11 | 43 | 5633 1997 HUMAN GENETICS 99 (4): 513-520 Angelicheva D; Calafell F; Savov A; Jordanova A; Kufardjieva A; et al. Cystic fibrosis mutations and associated haplotypes in Bulgaria - A comparative population genetic study | 1 | 9 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5051 | 6 | 57 | 5634 1997 HUMAN GENETICS 99 (5): 565-572 Macek M; Macek M; Krebsova A; Nash E; Hamosh A; et al. Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survival | 1 | 6 |
| 5052 | 3 | 18 | 5635 1997 HUMAN GENETICS 99 (5): 573-577 Li JP; Iwamoto S; Sugimoto N; Okuda H; Kajii E Dinucleotide repeat in the 3' flanking region provides a clue to the molecular evolution of the Duffy gene | 0 | 3 |
| 5053 | 2 | 32 | 5636 1997 HUMAN GENETICS 100 (1): 80-83 Lauteala T; HorelliKuitunen N; Closs E; Savontaus ML; Lukkarinen M; et al. Human cationic amino acid transporter gene hCAT-2 is assigned to 8p22 but is not the causative gene in lysinuric protein intolerance | 1 | 5 |
| 5054 | 3 | 27 | 5637 1997 HUMAN GENETICS 100 (1): 138-144 Mefford H; vandenEngh G; Friedman C; Trask BJ Analysis of the variation in chromosome size among diverse human populations by bivariate flow karyotyping | 0 | 8 |
| 5055 | 6 | 52 | 5638 1997 HUMAN GENETICS 100 (2): 189-194 Zschocke J; Mallory JP; Eiken HG; Nevin NC Phenylketonuria and the peoples of Northern Ireland | 4 | 18 |
| 5056 | 4 | 36 | 5639 1997 HUMAN GENETICS 100 (2): 224-229 Klauck SM; Munstermann E; BieberMartig B; Ruhl D; Lisch S; et al. Molecular genetic analysis of the FMR-1 gene in a large collection of autistic patients | 12 | 27 |
| 5057 | 7 | 41 | 5640 1997 HUMAN GENETICS 100 (3-4): 350-355 Cali F; Dianzani I; Desviat LR; Perez B; Ugarte M; et al. The STR252-IVS10nt546-VNTR7 phenylalanine hydroxylase minihaplotype in five Mediterranean samples | 2 | 5 |
| 5058 | 25 | 53 | 5641 1997 HUMAN GENETICS 100 (5-6): 536-543 Lell JT; Brown MD; Schurr TG; Sukernik RI; Starikovskaya YB; et al. Y chromosome polymorphisms in Native American and Siberian populations: identification of Native American Y chromosome haplotypes | 34 | 44 |
| 5059 | 4 | 31 | 5642 1997 HUMAN GENETICS 100 (5-6): 657-665 Bassett JHD; Pannett AAJ; Forbes SA; Thakker RV; McCarthy M; et al. The European Consortium on MEN1 - Linkage disequilibrium studies in multiple endocrine neoplasia type 1 (MEN1) | 0 | 9 |
| 5060 | 6 | 36 | 5643 1997 HUMAN GENETICS 101 (2): 135-140 Ott R; Waye JS; Chang PL Evolutionary origins of two tightly linked mutations in arylsulfatase-A pseudodeficiency | 0 | 7 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5061 | 3 | 23 | 5644 1997 HUMAN GENETICS 101 (2): 214-218 Hirst MC; Arinami T; Laird CD Sequence analysis of long FMR1 arrays in the Japanese population: insights into the generation of long (CGG)(n) tracts | 1 | 10 |
| 5062 | 4 | 39 | 6052 1998 HUMAN GENETICS 102 (2): 231-235 Sturzeneker R; Haddad LA; Bevilacqua RAU; Simpson AJG; Pena SDJ Polarity of mutations in tumor-associated microsatellite instability | 3 | 8 |
| 5063 | 9 | 39 | 6053 1998 HUMAN GENETICS 102 (6): 647-652 Rolf B; Horst B; Eigel A; Sanguansermsri T; Brinkmann B; et al. Microsatellite profiles reveal an unexpected genetic relationship between Asian populations | 2 | 6 |
| 5064 | 24 | 61 | 6054 1998 HUMAN GENETICS 103 (2): 211-227 Kidd KK; Morar B; Castiglione CM; Zhao HY; Pakstis AJ; et al. A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus | 35 | 95 |
| 5065 | 3 | 31 | 6492 1999 HUMAN GENETICS 104 (1): 43-48 Thomas NS; Sharp AJ; Browne CE; Skuse D; Hardie C; et al. Xp deletions associated with autism in three females | 17 | 29 |
| 5066 | 23 | 66 | 6493 1999 HUMAN GENETICS 104 (2): 149-157 Destro-Bisol G; Maviglia R; Caglia A; Boschi I; Spedini G; et al. Estimating European admixture in African Americans by using microsatellites and a microsatellite haplotype (CD4/Alu) | 9 | 23 |
| 5067 | 7 | 28 | 6494 1999 HUMAN GENETICS 104 (4): 333-340 Wei CC; Chiang FT; Lin KS; Lin LI The spectrum of microsatellite loci on chromosomes 7 and 8 in Taiwan aboriginal populations: a comparative population genetic study | 0 | 3 |
| 5068 | 4 | 25 | 6495 1999 HUMAN GENETICS 104 (6): 486-491 Humphries A; Ationu A; Lalloz MRA; Layton DM Ancestral origin of variation in the triosephosphate isomerase gene promoter | 0 | 2 |
| 5069 | 4 | 25 | 6496 1999 HUMAN GENETICS 105 (1-2): 72-78 Gross E; Arnold N; Goette J; Schwarz-Boeger U; Kiechle M A comparison of BRCA1 mutation analysis by direct sequencing, SSCP and DHPLC | 27 | 95 |
| 5070 | 20 | 47 | 6497 1999 HUMAN GENETICS 105 (6): 567-576 Flint J; Bond J; Rees DC; Boyce AJ; Roberts-Thomson JM; et al. Minisatellite mutational processes reduce F-st estimates | 11 | 16 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5071 | 10 | 16 | 6498 1999 HUMAN GENETICS 105 (6): 577-581 Thomas MG; Bradman N; Flinn HM High throughput analysis of 10 microsatellite and 11 diallelic polymorphisms on the human Y-chromosome | 32 | 40 |
| 5072 | 7 | 10 | 6935 2000 HUMAN GENETICS 106 (1): 130-132 Destro-Bisol G; Spedini G; Pascali VL Application of different genetic distance methods to microsatellite data | 8 | 9 |
| 5073 | 3 | 6 | 6936 2000 HUMAN GENETICS 106 (4): 453-454 Qian YP; Qian BZ; Su B; Yu JK; Ke YH; et al. Multiple origins of Tibetan Y chromosomes | 15 | 16 |
| 5074 | 1 | 46 | 6937 2000 HUMAN GENETICS 106 (5): 546-552 Mattevi VS; Coimbra CEA; Santos RV; Salzano FM; Hutz MH Association of the low-density lipoprotein receptor gene with obesity in Native American populations | 2 | 10 |
| 5075 | 2 | 30 | 6938 2000 HUMAN GENETICS 106 (6): 663-668 Jones AC; Sampson JR; Hoogendoorn B; Cohen D; Cheadle JP Application and evaluation of denaturing HPLC for molecular genetic analysis in tuberous sclerosis | 5 | 30 |
| 5076 | 16 | 34 | 6939 2000 HUMAN GENETICS 107 (4): 312-319 Comas D; Calafell F; Benchemsi N; Helal A; Lefranc G; et al. Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits | 16 | 31 |
| 5077 | 9 | 20 | 6940 2000 HUMAN GENETICS 107 (5): 483-487 Wolford JK; Blunt D; Ballecer C; Prochazka M High-throughput SNP detection by using DNA pooling and denaturing high performance liquid chromatography (DHPLC) | 5 | 47 |
| 5078 | 14 | 40 | 6941 2000 HUMAN GENETICS 107 (5): 504-512 Yao YG; Watkins WS; Zhang YP Evolutionary history of the mtDNA 9-bp deletion in Chinese populations and its relevance to the peopling of east and southeast Asia | 8 | 22 |
| 5079 | 14 | 28 | 6942 2000 HUMAN GENETICS 107 (6): 582-590 Su B; Xiao CJ; Deka R; Seielstad MT; Kangwanpong D; et al. Y chromosome haplotypes reveal prehistorical migrations to the Himalayas | 29 | 29 |
| 5080 | 27 | 56 | 6943 2000 HUMAN GENETICS 107 (6): 630-641 Nebel A; Filon D; Weiss DA; Weale M; Faerman M; et al. High-resolution Y chromosome haplotypes of Israeli and Palestinian Arabs reveal geographic substructure and substantial overlap with haplotypes of Jews | 15 | 20 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5081 | 17 | 49 | 7443 2001 HUMAN GENETICS 108 (1): 20-30 Seixas S; Garcia O; Trovoada MJ; Santos MT; Amorim A; et al. Patterns of haplotype diversity within the serpin gene cluster at 14q32.1: insights into the natural history of the alpha 1-antitrypsin polymorphism | 0 | 9 |
| 5082 | 8 | 19 | 7444 2001 HUMAN GENETICS 108 (1): 55-58 Quintana-Murci L; Krausz C; Heyer E; Gromoll J; Seifer I; et al. The relationship between Y chromosome DNA haplotypes and Y chromosome deletions leading to male infertility | 6 | 12 |
| 5083 | 8 | 44 | 7445 2001 HUMAN GENETICS 108 (4): 290-298 Le Marechal C; Audrezet MP; Quere I; Raguenes O; Langonne S; et al. Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): major implications for genetic counselling | 5 | 30 |
| 5084 | 26 | 54 | 7446 2001 HUMAN GENETICS 109 (2): 224-233 de Pancorbo MM; Lopez-Martinez M; Martinez-Bouzas C; Castro A; Fernandez-Fernandez I; et al. The Basques according to polymorphic Alu insertions | 4 | 12 |
| 5085 | 26 | 54 | 7447 2001 HUMAN GENETICS 109 (3): 339-350 Roychoudhury S; Roy S; Basu A; Banerjee R; Vishwanathan H; et al. Genomic structures and population histories of linguistically distinct tribal groups of India | 14 | 18 |
| 5086 | 26 | 48 | 7448 2001 HUMAN GENETICS 109 (6): 659-674 Weale ME; Yepisko; posyan L; Jager RF; Hovhannisyan N; et al. Armenian Y chromosome haplotypes reveal strong regional structure within a single ethno-national group | 15 | 16 |
| 5087 | 39 | 65 | 7981 2002 HUMAN GENETICS 110 (1): 80-88 Tajima A; Pan IH; Fucharoen G; Fucharoen S; Matsuo M; et al. Three major lineages of Asian Y chromosomes: implications for the peopling of east and southeast Asia | 9 | 9 |
| 5088 | 10 | 23 | 7982 2002 HUMAN GENETICS 110 (6): 592-600 Ploski R; Wozniak M; Pawlowski R; Monies DM; Branicki W; et al. Homogeneity and distinctiveness of Polish paternal lineages revealed by Y chromosome microsatellite haplotype analysis | 4 | 12 |
| 5089 | 3 | 30 | 7983 2002 HUMAN GENETICS 111 (3): 255-262 Moulard B; Genton P; Grid D; Jeanpierre M; Ouazzani R; et al. Haplotype study of West European and North African Unverricht-Lundborg chromosomes: evidence for a few founder mutations | 0 | 3 |
| 5090 | 10 | 24 | 8553 2003 HUMAN GENETICS 112 (3): 255-261 Nasidze I; Sarkisian T; Kerimov A; Stoneking M Testing hypotheses of language replacement in the Caucasus: evidence from the Y-chromosome | 6 | 6 |
| # | LCR | NCR | Node / Date / Journal / Author | LCS | GCS |
| 5091 | 22 | 40 | 8554 2003 HUMAN GENETICS 112 (4): 353-363 Bosch E; Calafell F; Rosser ZH; Norby S; Lynnerup N; et al. High level of male-biased Scandinavian admixture in Greenlandic Inuit shown by Y-chromosomal analysis | 7 | 8 |
| 5092 | 26 | 83 | 8555 2003 HUMAN GENETICS 112 (5-6): 457-469 Norio R Finnish Disease Heritage II: population prehistory and genetic roots of Finns | 1 | 8 |
| 5093 | 20 | 38 | 8556 2003 HUMAN GENETICS 112 (5-6): 534-541 Carvajal-Carmona LG; Ophoff R; Service S; Hartiala J; Molina J; et al. Genetic demography of Antioquia (Colombia) and the Central Valley of Costa Rica | 4 | 9 |
| 5094 | 11 | 30 | 8557 2003 HUMAN GENETICS 113 (3): 211-219 Collins-Schramm HE; Chima B; Operario DJ; Criswell LA; Seldin MF Markers informative for ancestry demonstrate consistent megabase-length linkage disequilibrium in the African American population | 0 | 3 |
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