| Year |
Citation |
Score |
| 2018 |
Ligthart S, Vaez A, Võsa U, Stathopoulou MG, de Vries PS, Prins BP, Van der Most PJ, Tanaka T, Naderi E, Rose LM, Wu Y, Karlsson R, Barbalic M, Lin H, Pool R, ... ... Suktitipat B, et al. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. American Journal of Human Genetics. 103: 691-706. PMID 30388399 DOI: 10.1016/J.Ajhg.2018.09.009 |
0.471 |
|
| 2018 |
Lert-Itthiporn W, Suktitipat B, Grove H, Sakuntabhai A, Malasit P, Tangthawornchaikul N, Matsuda F, Suriyaphol P. Validation of genotype imputation in Southeast Asian populations and the effect of single nucleotide polymorphism annotation on imputation outcome. Bmc Medical Genetics. 19: 23. PMID 29439659 DOI: 10.1186/S12881-018-0534-8 |
0.346 |
|
| 2015 |
Qayyum R, Becker LC, Becker DM, Faraday N, Yanek LR, Leal SM, Shaw C, Mathias R, Suktitipat B, Bray PF. Genome-wide association study of platelet aggregation in African Americans. Bmc Genetics. 16: 58. PMID 26024889 DOI: 10.1186/S12863-015-0217-9 |
0.338 |
|
| 2015 |
Pithukpakorn M, Roothumnong E, Angkasekwinai N, Suktitipat B, Assawamakin A, Luangwedchakarn V, Umrod P, Thongnoppakhun W, Foongladda S, Suputtamongkol Y. HLA-DRB1 and HLA-DQB1 Are Associated with Adult-Onset Immunodeficiency with Acquired Anti-Interferon-Gamma Autoantibodies. Plos One. 10: e0128481. PMID 26011559 DOI: 10.1371/Journal.Pone.0128481 |
0.334 |
|
| 2014 |
Tresukosol D, Suktitipat B, Hunnangkul S, Kamkaew R, Poldee S, Tassaneetrithep B, Likidlilid A. Effects of cytochrome P450 2C19 and paraoxonase 1 polymorphisms on antiplatelet response to clopidogrel therapy in patients with coronary artery disease. Plos One. 9: e110188. PMID 25329996 DOI: 10.1371/Journal.Pone.0110188 |
0.337 |
|
| 2014 |
Suktitipat B, Naktang C, Mhuantong W, Tularak T, Artiwet P, Pasomsap E, Jongjaroenprasert W, Fuchareon S, Mahasirimongkol S, Chantratita W, Yimwadsana B, Charoensawan V, Jinawath N. Copy number variation in Thai population. Plos One. 9: e104355. PMID 25118596 DOI: 10.1371/Journal.Pone.0104355 |
0.346 |
|
| 2013 |
Kim Y, Suktitipat B, Yanek LR, Faraday N, Wilson AF, Becker DM, Becker LC, Mathias RA. Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation. Plos One. 8: e64179. PMID 23704978 DOI: 10.1371/Journal.Pone.0064179 |
0.381 |
|
| 2012 |
Suktitipat B, Mathias RA, Vaidya D, Yanek LR, Young JH, Becker LC, Becker DM, Wilson AF, Fallin MD. The robustness of generalized estimating equations for association tests in extended family data. Human Heredity. 74: 17-26. PMID 23038411 DOI: 10.1159/000341636 |
0.458 |
|
| 2011 |
N'Diaye A, Chen GK, Palmer CD, Ge B, Tayo B, Mathias RA, Ding J, Nalls MA, Adeyemo A, Adoue V, Ambrosone CB, Atwood L, Bandera EV, Becker LC, Berndt SI, ... ... Suktitipat B, et al. Identification, replication, and fine-mapping of Loci associated with adult height in individuals of african ancestry. Plos Genetics. 7: e1002298. PMID 21998595 DOI: 10.1371/Journal.Pgen.1002298 |
0.389 |
|
| 2011 |
Faraday N, Yanek LR, Yang XP, Mathias R, Herrera-Galeano JE, Suktitipat B, Qayyum R, Johnson AD, Chen MH, Tofler GH, Ruczinski I, Friedman AD, Gylfason A, Thorsteinsdottir U, Bray PF, et al. Identification of a specific intronic PEAR1 gene variant associated with greater platelet aggregability and protein expression. Blood. 118: 3367-75. PMID 21791418 DOI: 10.1182/Blood-2010-11-320788 |
0.375 |
|
| 2011 |
Mathias RA, Sergeant S, Ruczinski I, Torgerson DG, Hugenschmidt CE, Kubala M, Vaidya D, Suktitipat B, Ziegler JT, Ivester P, Case D, Yanek LR, Freedman BI, Rudock ME, Barnes KC, et al. The impact of FADS genetic variants on ω6 polyunsaturated fatty acid metabolism in African Americans. Bmc Genetics. 12: 50. PMID 21599946 DOI: 10.1186/1471-2156-12-50 |
0.348 |
|
| 2011 |
Kaewsutthi S, Phasukkijwatana N, Joyjinda Y, Chuenkongkaew W, Kunhapan B, Tun AW, Suktitipat B, Lertrit P. Mitochondrial haplogroup background may influence Southeast Asian G11778A Leber hereditary optic neuropathy. Investigative Ophthalmology & Visual Science. 52: 4742-8. PMID 21398275 DOI: 10.1167/Iovs.10-5816 |
0.329 |
|
| 2011 |
Kral BG, Mathias RA, Suktitipat B, Ruczinski I, Vaidya D, Yanek LR, Quyyumi AA, Patel RS, Zafari AM, Vaccarino V, Hauser ER, Kraus WE, Becker LC, Becker DM. A common variant in the CDKN2B gene on chromosome 9p21 protects against coronary artery disease in Americans of African ancestry. Journal of Human Genetics. 56: 224-9. PMID 21270820 DOI: 10.1038/Jhg.2010.171 |
0.405 |
|
| 2010 |
Assimes TL, Hólm H, Kathiresan S, Reilly MP, Thorleifsson G, Voight BF, Erdmann J, Willenborg C, Vaidya D, Xie C, Patterson CC, Morgan TM, Burnett MS, Li M, Hlatky MA, ... ... Suktitipat B, et al. Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. Journal of the American College of Cardiology. 56: 1552-63. PMID 20933357 DOI: 10.1016/J.Jacc.2010.06.022 |
0.348 |
|
| 2006 |
Tharaphan P, Chuenkongkaew WL, Luangtrakool K, Sanpachudayan T, Suktitipat B, Suphavilai R, Srisawat C, Sura T, Lertrit P. Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy. Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society. 26: 264-7. PMID 17204919 DOI: 10.1097/01.Wno.0000249318.88991.C4 |
0.31 |
|
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