173 related articles for article (PubMed ID: 19257887)
41. Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene.
Koda Y; Tachida H; Soejima M; Takenaka O; Kimura H
Ann Hum Genet; 2004 Mar; 68(Pt 2):110-9. PubMed ID: 15008790
[TBL] [Abstract][Full Text] [Related]
42. Haplotype structure and association to Crohn's disease of CARD15 mutations in two ethnically divergent populations.
Croucher PJ; Mascheretti S; Hampe J; Huse K; Frenzel H; Stoll M; Lu T; Nikolaus S; Yang SK; Krawczak M; Kim WH; Schreiber S
Eur J Hum Genet; 2003 Jan; 11(1):6-16. PubMed ID: 12529700
[TBL] [Abstract][Full Text] [Related]
43. Genetic susceptibility factors of Type 1 diabetes in Asians.
Park Y; Eisenbarth GS
Diabetes Metab Res Rev; 2001; 17(1):2-11. PubMed ID: 11241886
[TBL] [Abstract][Full Text] [Related]
44. Significant association between ERCC2 and MTHR polymorphisms and breast cancer susceptibility in Moroccan population: genotype and haplotype analysis in a case-control study.
Hardi H; Melki R; Boughaleb Z; El Harroudi T; Aissaoui S; Boukhatem N
BMC Cancer; 2018 Mar; 18(1):292. PubMed ID: 29544444
[TBL] [Abstract][Full Text] [Related]
45. Extensive linkage disequilibrium, a common 16.7-kilobase deletion, and evidence of balancing selection in the human protocadherin alpha cluster.
Noonan JP; Li J; Nguyen L; Caoile C; Dickson M; Grimwood J; Schmutz J; Feldman MW; Myers RM
Am J Hum Genet; 2003 Mar; 72(3):621-35. PubMed ID: 12577201
[TBL] [Abstract][Full Text] [Related]
46. Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin.
Pal P; Xi H; Sun G; Kaushal R; Meeks JJ; Thaxton CS; Guha S; Jin CH; Suarez BK; Catalona WJ; Deka R
Hum Genet; 2007 Nov; 122(3-4):251-9. PubMed ID: 17593395
[TBL] [Abstract][Full Text] [Related]
47. Haplotype-based association studies of IGFBP1 and IGFBP3 with prostate and breast cancer risk: the multiethnic cohort.
Cheng I; Penney KL; Stram DO; Le Marchand L; Giorgi E; Haiman CA; Kolonel LN; Pike M; Hirschhorn J; Henderson BE; Freedman ML
Cancer Epidemiol Biomarkers Prev; 2006 Oct; 15(10):1993-7. PubMed ID: 17035411
[TBL] [Abstract][Full Text] [Related]
48. Evaluation of LOXL1 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma.
Aragon-Martin JA; Ritch R; Liebmann J; O'Brien C; Blaaow K; Mercieca F; Spiteri A; Cobb CJ; Damji KF; Tarkkanen A; Rezaie T; Child AH; Sarfarazi M
Mol Vis; 2008 Mar; 14():533-41. PubMed ID: 18385788
[TBL] [Abstract][Full Text] [Related]
49. SNP haplotypes and allele frequencies show evidence for disruptive and balancing selection in the human leukocyte receptor complex.
Norman PJ; Cook MA; Carey BS; Carrington CV; Verity DH; Hameed K; Ramdath DD; Chandanayingyong D; Leppert M; Stephens HA; Vaughan RW
Immunogenetics; 2004 Jul; 56(4):225-37. PubMed ID: 15185041
[TBL] [Abstract][Full Text] [Related]
50. Haplotype patterns in cancer-related genes with long-range linkage disequilibrium: no evidence of association with breast cancer or positive selection.
Ribas G; Milne RL; Gonzalez-Neira A; Benítez J
Eur J Hum Genet; 2008 Feb; 16(2):252-60. PubMed ID: 18000525
[TBL] [Abstract][Full Text] [Related]
51. Association studies of excision repair cross-complementation group 1 (ERCC1) haplotypes with lung and head and neck cancer risk in a Caucasian population.
Jones NR; Spratt TE; Berg AS; Muscat JE; Lazarus P; Gallagher CJ
Cancer Epidemiol; 2011 Apr; 35(2):175-81. PubMed ID: 20863778
[TBL] [Abstract][Full Text] [Related]
52. SNP identification, linkage disequilibrium, and haplotype analysis for a 200-kb genomic region in a Korean population.
Kim KJ; Lee HJ; Park MH; Cha SH; Kim KS; Kim HT; Kimm K; Oh B; Lee JY
Genomics; 2006 Nov; 88(5):535-40. PubMed ID: 16919420
[TBL] [Abstract][Full Text] [Related]
53. Usefulness of COMT gene polymorphisms in North African populations.
Boussetta S; Cherni L; Pakstis AJ; Ben Salem N; Elkamel S; Khodjet-El-Khil H; Kidd KK; Elgaaied ABA
Gene; 2019 May; 696():186-196. PubMed ID: 30790653
[TBL] [Abstract][Full Text] [Related]
54. Genetic and environmental risk factors for rheumatoid arthritis in a UK African ancestry population: the GENRA case-control study.
Traylor M; Curtis C; Patel H; Breen G; Hyuck Lee S; Xu X; Newhouse S; Dobson R; Steer S; Cope AP; Markus HS; Lewis CM; Scott IC
Rheumatology (Oxford); 2017 Aug; 56(8):1282-1292. PubMed ID: 28407095
[TBL] [Abstract][Full Text] [Related]
55. Contribution of Asian Haplotype of KCNJ18 to Susceptibility to and Ethnic Differences in Thyrotoxic Periodic Paralysis.
Noso S; Babaya N; Hiromine Y; Ito H; Taketomo Y; Yoshida S; Niwano F; Monobe K; Minohara T; Okada T; Tsugawa M; Kawabata Y; Ikegami H
J Clin Endocrinol Metab; 2019 Dec; 104(12):6338-6344. PubMed ID: 31361309
[TBL] [Abstract][Full Text] [Related]
56. Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias.
Bush WS; Crawford DC; Alexander C; George AL; Roden DM; Ritchie MD
Pharmacogenomics; 2009 Jun; 10(6):1043-53. PubMed ID: 19530973
[TBL] [Abstract][Full Text] [Related]
57. High-density SNP mapping of the HLA region identifies multiple independent susceptibility loci associated with selective IgA deficiency.
Ferreira RC; Pan-Hammarström Q; Graham RR; Fontán G; Lee AT; Ortmann W; Wang N; Urcelay E; Fernández-Arquero M; Núñez C; Jorgensen G; Ludviksson BR; Koskinen S; Haimila K; Padyukov L; Gregersen PK; Hammarström L; Behrens TW
PLoS Genet; 2012 Jan; 8(1):e1002476. PubMed ID: 22291608
[TBL] [Abstract][Full Text] [Related]
58. Latest HapMap update aims to direct researchers to genetic basis of disease.
Schmidt C
J Natl Cancer Inst; 2005 Nov; 97(22):1638-40. PubMed ID: 16288113
[No Abstract] [Full Text] [Related]
59. Lactase haplotype diversity in the Old World.
Hollox EJ; Poulter M; Zvarik M; Ferak V; Krause A; Jenkins T; Saha N; Kozlov AI; Swallow DM
Am J Hum Genet; 2001 Jan; 68(1):160-172. PubMed ID: 11095994
[TBL] [Abstract][Full Text] [Related]
60. Type 2 Diabetes Risk Allele Loci in the Qatari Population.
O'Beirne SL; Salit J; Rodriguez-Flores JL; Staudt MR; Abi Khalil C; Fakhro KA; Robay A; Ramstetter MD; Al-Azwani IK; Malek JA; Zirie M; Jayyousi A; Badii R; Al-Nabet Al-Marri A; Chiuchiolo MJ; Al-Shakaki A; Chidiac O; Gharbiah M; Bener A; Stadler D; Hackett NR; Mezey JG; Crystal RG
PLoS One; 2016; 11(7):e0156834. PubMed ID: 27383215
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]