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Mark Seielstad, PhD

Title(s)Professor, Laboratory Medicine
SchoolSchool of Medicine
Address513 Parnassus Ave, MSB
San Francisco CA 94117
Phone415-476-0625
ORCID ORCID Icon0000-0001-5783-1401 Additional info
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    Collapse Biography 
    Collapse Education and Training
    Harvard UniversityPh.D.1998Biology
    Stanford UniversityB.S.1992Biological Sciences (w/Honors)
    Stanford UniversityA.B.1992Classical Studies
    University of California, San Francisco, CA2020Diversity, Equity, and Inclusion Champion Training
    Collapse Awards and Honors
    Fulbright Fellow2019  - 2020Senior Scholar
    American Association for the Advancement of Science (AAAS)2021Fellow (Biological Sciences)
    Sigma Xi2021Sigma Xi

    Collapse Overview 
    Collapse Overview
    Research in my lab is at the interface of genetic epidemiology and population/anthropological genetics. The main goal is to identify human genetic variation altering the risk of complex human diseases involving immunity (e.g., autoimmunity and susceptibility to infectious diseases) and metabolism (e.g., type 2 diabetes). This puts an emphasis on genomic technologies such as genome-wide SNP genotyping, and next-generation sequencing to reveal and characterize polymorphisms in whole exome and whole genome data. Much of this work is carried out in geographically diverse human populations, which are also the subject of anthropological investigations that seek to characterize the global distribution of genetic variation. A particular emphasis is placed on sequencing and coalescence analysis of the Y chromosome and mtDNA, as well as cultural practices that alter demographic and selective regimes acting on the sex-specific lineages of these two DNA molecules.

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    Collapse Publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Researchers can login to make corrections and additions, or contact us for help. to make corrections and additions.
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    Altmetrics Details PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Corrigendum to: Blood Gene Signatures of Chagas Cardiomyopathy With or Without Ventricular Dysfunction. J Infect Dis. 2020 Apr 07; 221(9):1564. Ferreira LRP, Ferreira FM, Nakaya HI, Deng X, Cândido DDS, de Oliveira LC, Billaud JN, Lanteri MC, Rigaud VO, Seielstad M, Kalil J, Fernandes F, Ribeiro ALP, Sabino EC, Cunha-Neto E. PMID: 31884515.
      View in: PubMed   Mentions:    Fields:    
    2. Methylation changes in the peripheral blood of Filipinos with type 2 diabetes suggest spurious transcription initiation at TXNIP. Hum Mol Genet. 2019 12 15; 28(24):4208-4218. Albao DS, Cutiongco-de la Paz EM, Mercado ME, Lirio A, Mariano M, Kim S, Yangco A, Melegrito J, Wad-Asen K, Gauran II, Francisco MA, Santos-Acuin C, David-Padilla C, Murphy EJ, Paz-Pacheco E, Seielstad M. PMID: 31691802.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    3. A Novel, 5-Transcript, Whole-blood Gene-expression Signature for Tuberculosis Screening Among People Living With Human Immunodeficiency Virus. Clin Infect Dis. 2019 06 18; 69(1):77-83. Rajan JV, Semitala FC, Mehta T, Seielstad M, Montalvo L, Andama A, Asege L, Nakaye M, Katende J, Mwebe S, Kamya MR, Yoon C, Cattamanchi A. PMID: 30462176.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    4. 1524-P: Discordance between A1C and Glucose for the Diagnosis of Prediabetes in a Filipino-American Population. Diabetes. 2019 Jun 1; 68(Supplement 1):1524-p. MARIA ELIZABETH P. MERCADO, SARAH KIM, MARIA C EVA, CUTIONGCO DE LA PAZ, MARK SEIELSTAD, ELIZABETH PAZ-PACHECO, ELIZABETH MURPHY. .
      View in: Publisher Site   Mentions:
    5. Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Nature. 2019 06; 570(7759):71-76. Flannick J, Mercader JM, Fuchsberger C, Udler MS, Mahajan A, Wessel J, Teslovich TM, Caulkins L, Koesterer R, Barajas-Olmos F, Blackwell TW, Boerwinkle E, Brody JA, Centeno-Cruz F, Chen L, Chen S, Contreras-Cubas C, Córdova E, Correa A, Cortes M, DeFronzo RA, Dolan L, Drews KL, Elliott A, Floyd JS, Gabriel S, Garay-Sevilla ME, García-Ortiz H, Gross M, Han S, Heard-Costa NL, Jackson AU, Jørgensen ME, Kang HM, Kelsey M, Kim BJ, Koistinen HA, Kuusisto J, Leader JB, Linneberg A, Liu CT, Liu J, Lyssenko V, Manning AK, Marcketta A, Malacara-Hernandez JM, Martínez-Hernández A, Matsuo K, Mayer-Davis E, Mendoza-Caamal E, Mohlke KL, Morrison AC, Ndungu A, Ng MCY, O'Dushlaine C, Payne AJ, Pihoker C, Post WS, Preuss M, Psaty BM, Vasan RS, Rayner NW, Reiner AP, Revilla-Monsalve C, Robertson NR, Santoro N, Schurmann C, So WY, Soberón X, Stringham HM, Strom TM, Tam CHT, Thameem F, Tomlinson B, Torres JM, Tracy RP, van Dam RM, Vujkovic M, Wang S, Welch RP, Witte DR, Wong TY, Atzmon G, Barzilai N, Blangero J, Bonnycastle LL, Bowden DW, Chambers JC, Chan E, Cheng CY, Cho YS, Collins FS, de Vries PS, Duggirala R, Glaser B, Gonzalez C, Gonzalez ME, Groop L, Kooner JS, Kwak SH, Laakso M, Lehman DM, Nilsson P, Spector TD, Tai ES, Tuomi T, Tuomilehto J, Wilson JG, Aguilar-Salinas CA, Bottinger E, Burke B, Carey DJ, Chan JCN, Dupuis J, Frossard P, Heckbert SR, Hwang MY, Kim YJ, Kirchner HL, Lee JY, Lee J, Loos RJF, Ma RCW, Morris AD, O'Donnell CJ, Palmer CNA, Pankow J, Park KS, Rasheed A, Saleheen D, Sim X, Small KS, Teo YY, Haiman C, Hanis CL, Henderson BE, Orozco L, Tusié-Luna T, Dewey FE, Baras A, Gieger C, Meitinger T, Strauch K, Lange L, Grarup N, Hansen T, Pedersen O, Zeitler P, Dabelea D, Abecasis G, Bell GI, Cox NJ, Seielstad M, Sladek R, Meigs JB, Rich SS, Rotter JI, Altshuler D, Burtt NP, Scott LJ, Morris AP, Florez JC, McCarthy MI, Boehnke M. PMID: 31118516.
      View in: PubMed   Mentions: 23     Fields:    Translation:HumansAnimals
    6. Correction: A 32 kb Critical Region Excluding Y402H in CFH Mediates Risk for Age-Related Macular Degeneration. PLoS One. 2018; 13(12):e0209943. Sivakumaran TA, Igo RP, Kidd JM, Itsara A, Kopplin LJ, Chen W, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, Chew EY, Ramprasad VL, Tay WT, Mitchell P, Seielstad M, Stambolian DE, Edwards AO, Lee KE, Leontiev DV, Jun G, Wang Y, Tian L, Qiu F, Henning AK, LaFramboise T, Sen P, Aarthi M, George R, Raman R, Das MK, Vijaya L, Kumaramanickavel G, Wong TY, Swaroop A, Abecasis GR, Klein R, Klein BEK, Nickerson DA, Eichler EE, Iyengar SK. PMID: 30571798.
      View in: PubMed   Mentions:    Fields:    
    7. Development and evaluation of a transfusion medicine genome wide genotyping array. Transfusion. 2019 01; 59(1):101-111. Guo Y, Busch MP, Seielstad M, Endres-Dighe S, Westhoff CM, Keating B, Hoppe C, Bordbar A, Custer B, Butterworth AS, Kanias T, Mast AE, Kleinman S, Lu Y, Page GP. PMID: 30456907.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    8. Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci Data. 2018 01 23; 5:180002. Flannick J, Fuchsberger C, Mahajan A, Teslovich TM, Agarwala V, Gaulton KJ, Caulkins L, Koesterer R, Ma C, Moutsianas L, McCarthy DJ, Rivas MA, Perry JRB, Sim X, Blackwell TW, Robertson NR, Rayner NW, Cingolani P, Locke AE, Tajes JF, Highland HM, Dupuis J, Chines PS, Lindgren CM, Hartl C, Jackson AU, Chen H, Huyghe JR, van de Bunt M, Pearson RD, Kumar A, Müller-Nurasyid M, Grarup N, Stringham HM, Gamazon ER, Lee J, Chen Y, Scott RA, Below JE, Chen P, Huang J, Go MJ, Stitzel ML, Pasko D, Parker SCJ, Varga TV, Green T, Beer NL, Day-Williams AG, Ferreira T, Fingerlin T, Horikoshi M, Hu C, Huh I, Ikram MK, Kim BJ, Kim Y, Kim YJ, Kwon MS, Lee J, Lee S, Lin KH, Maxwell TJ, Nagai Y, Wang X, Welch RP, Yoon J, Zhang W, Barzilai N, Voight BF, Han BG, Jenkinson CP, Kuulasmaa T, Kuusisto J, Manning A, Ng MCY, Palmer ND, Balkau B, Stancáková A, Abboud HE, Boeing H, Giedraitis V, Prabhakaran D, Gottesman O, Scott J, Carey J, Kwan P, Grant G, Smith JD, Neale BM, Purcell S, Butterworth AS, Howson JMM, Lee HM, Lu Y, Kwak SH, Zhao W, Danesh J, Lam VKL, Park KS, Saleheen D, So WY, Tam CHT, Afzal U, Aguilar D, Arya R, Aung T, Chan E, Navarro C, Cheng CY, Palli D, Correa A, Curran JE, Rybin D, Farook VS, Fowler SP, Freedman BI, Griswold M, Hale DE, Hicks PJ, Khor CC, Kumar S, Lehne B, Thuillier D, Lim WY, Liu J, Loh M, Musani SK, Puppala S, Scott WR, Yengo L, Tan ST, Taylor HA, Thameem F, Wilson G, Wong TY, Njølstad PR, Levy JC, Mangino M, Bonnycastle LL, Schwarzmayr T, Fadista J, Surdulescu GL, Herder C, Groves CJ, Wieland T, Bork-Jensen J, Brandslund I, Christensen C, Koistinen HA, Doney ASF, Kinnunen L, Esko T, Farmer AJ, Hakaste L, Hodgkiss D, Kravic J, Lyssenko V, Hollensted M, Jørgensen ME, Jørgensen T, Ladenvall C, Justesen JM, Käräjämäki A, Kriebel J, Rathmann W, Lannfelt L, Lauritzen T, Narisu N, Linneberg A, Melander O, Milani L, Neville M, Orho-Melander M, Qi L, Qi Q, Roden M, Rolandsson O, Swift A, Rosengren AH, Stirrups K, Wood AR, Mihailov E, Blancher C, Carneiro MO, Maguire J, Poplin R, Shakir K, Fennell T, DePristo M, de Angelis MH, Deloukas P, Gjesing AP, Jun G, Nilsson P, Murphy J, Onofrio R, Thorand B, Hansen T, Meisinger C, Hu FB, Isomaa B, Karpe F, Liang L, Peters A, Huth C, O'Rahilly SP, Palmer CNA, Pedersen O, Rauramaa R, Tuomilehto J, Salomaa V, Watanabe RM, Syvänen AC, Bergman RN, Bharadwaj D, Bottinger EP, Cho YS, Chandak GR, Chan JCN, Chia KS, Daly MJ, Ebrahim SB, Langenberg C, Elliott P, Jablonski KA, Lehman DM, Jia W, Ma RCW, Pollin TI, Sandhu M, Tandon N, Froguel P, Barroso I, Teo YY, Zeggini E, Loos RJF, Small KS, Ried JS, DeFronzo RA, Grallert H, Glaser B, Metspalu A, Wareham NJ, Walker M, Banks E, Gieger C, Ingelsson E, Im HK, Illig T, Franks PW, Buck G, Trakalo J, Buck D, Prokopenko I, Mägi R, Lind L, Farjoun Y, Owen KR, Gloyn AL, Strauch K, Tuomi T, Kooner JS, Lee JY, Park T, Donnelly P, Morris AD, Hattersley AT, Bowden DW, Collins FS, Atzmon G, Chambers JC, Spector TD, Laakso M, Strom TM, Bell GI, Blangero J, Duggirala R, Tai ES, McVean G, Hanis CL, Wilson JG, Seielstad M, Frayling TM, Meigs JB, Cox NJ, Sladek R, Lander ES, Gabriel S, Mohlke KL, Meitinger T, Groop L, Abecasis G, Scott LJ, Morris AP, Kang HM, Altshuler D, Burtt NP, Florez JC, Boehnke M, McCarthy MI. PMID: 29360107.
      View in: PubMed   Mentions:    Fields:    
    9. Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proc Natl Acad Sci U S A. 2018 01 09; 115(2):379-384. PMID: 29279374.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    10. Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci Data. 2017 12 19; 4:170179. PMID: 29257133.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    11. Genomewide association study of HLA alloimmunization in previously pregnant blood donors. Transfusion. 2018 02; 58(2):402-412. Seielstad M, Page GP, Gaddis N, Lanteri M, Lee TH, Kakaiya R, Barcellos LF, Criswell LA, Triulzi D, Norris PJ, Busch MP. PMID: 29168253.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCTClinical Trials
    12. Y chromosomal evidence on the origin of northern Thai people. PLoS One. 2017; 12(7):e0181935. PMID: 28742125.
      View in: PubMed   Mentions: 1     Fields:    Translation:HumansCells
    13. A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk. Diabetes. 2017 07; 66(7):2019-2032. PMID: 28341696.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    14. Blood Gene Signatures of Chagas Cardiomyopathy With or Without Ventricular Dysfunction. J Infect Dis. 2017 02 01; 215(3):387-395. PMID: 28003350.
      View in: PubMed   Mentions: 8     Fields:    Translation:HumansCells
    15. The genetic architecture of type 2 diabetes. Nature. 2016 08 04; 536(7614):41-47. PMID: 27398621.
      View in: PubMed   Mentions: 267     Fields:    Translation:Humans
    16. Identification of genetic variants associated with susceptibility to West Nile virus neuroinvasive disease. Genes Immun. 2016 07; 17(5):298-304. PMID: 27170560.
      View in: PubMed   Mentions: 4     Fields:    Translation:Humans
    17. Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucoma. Nat Genet. 2016 May; 48(5):556-62. PMID: 27064256.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansCells
    18. Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms. Hum Mol Genet. 2016 05 15; 25(10):2070-2081. PMID: 26911676.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    19. Genome-wide meta-analysis identifies multiple novel associations and ethnic heterogeneity of psoriasis susceptibility. Nat Commun. 2015 Apr 23; 6:6916. PMID: 25903422.
      View in: PubMed   Mentions: 42     Fields:    Translation:Humans
    20. Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus. PLoS Genet. 2015 Jan; 11(1):e1004876. PMID: 25625282.
      View in: PubMed   Mentions: 43     Fields:    Translation:HumansPHPublic Health
    21. Admixed origin of the Kayah (Red Karen) in Northern Thailand revealed by biparental and paternal markers. Ann Hum Genet. 2015 Mar; 79(2):108-21. PMID: 25590861.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    22. Meta-analysis of the TNFAIP3 region in psoriasis reveals a risk haplotype that is distinct from other autoimmune diseases. Genes Immun. 2015 Mar; 16(2):120-6. PMID: 25521225.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    23. Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. Hum Mol Genet. 2015 Mar 15; 24(6):1791-800. PMID: 25429064.
      View in: PubMed   Mentions: 26     Fields:    Translation:Humans
    24. Genome-wide association meta-analysis identifies novel variants associated with fasting plasma glucose in East Asians. Diabetes. 2015 Jan; 64(1):291-8. PMID: 25187374.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    25. Whole genome sequencing to identify host genetic risk factors for severe outcomes of hepatitis a virus infection. J Med Virol. 2014 Oct; 86(10):1661-8. PMID: 24978929.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    26. Meta-analysis of genome-wide association studies in East Asian-ancestry populations identifies four new loci for body mass index. Hum Mol Genet. 2014 Oct 15; 23(20):5492-504. PMID: 24861553.
      View in: PubMed   Mentions: 56     Fields:    Translation:Humans
    27. Joint effects of known type 2 diabetes susceptibility loci in genome-wide association study of Singapore Chinese: the Singapore Chinese health study. PLoS One. 2014; 9(2):e87762. PMID: 24520337.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    28. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. Nat Genet. 2014 Mar; 46(3):234-44. PMID: 24509480.
      View in: PubMed   Mentions: 396     Fields:    Translation:Humans
    29. Genome wide association study (GWAS) of Chagas cardiomyopathy in Trypanosoma cruzi seropositive subjects. PLoS One. 2013; 8(11):e79629. PMID: 24324551.
      View in: PubMed   Mentions: 16     Fields:    Translation:HumansAnimals
    30. Genome-wide association study of retinopathy in individuals without diabetes. PLoS One. 2013; 8(2):e54232. PMID: 23393555.
      View in: PubMed   Mentions: 5     Fields:    Translation:Humans
    31. Association of cardiovascular and metabolic disease genes with psoriasis. J Invest Dermatol. 2013 Mar; 133(3):836-839. PMID: 23190900.
      View in: PubMed   Mentions: 19     Fields:    Translation:Humans
    32. Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations. Human Molecular Genetics. 2012 Oct 1; 21(19):4365-4365. Belinda K. Cornes, Chiea Chuen Khor, Monisha E. Nongpiur, Liang Xu, Wan-Ting Tay, Yingfeng Zheng, Raghavan Lavanya, Yang Li, Renyi Wu, Xueling Sim, Ya-Xing Wang, Peng Chen, Yik Ying Teo, Kee-Seng Chia, Mark Seielstad, Jianjun Liu, Martin L. Hibberd, Ching-Yu Cheng, Seang-Mei Saw, E-Shyong Tai, Jost B. Jonas, Eranga N. Vithana, Tien Y. Wong, Tin Aung. .
      View in: Publisher Site   Mentions:
    33. Genome-wide expression profiling identifies type 1 interferon response pathways in active tuberculosis. PLoS One. 2012; 7(9):e45839. PMID: 23029268.
      View in: PubMed   Mentions: 79     Fields:    Translation:HumansAnimalsCells
    34. Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. Nat Genet. 2012 Jul 15; 44(8):904-9. PMID: 22797727.
      View in: PubMed   Mentions: 111     Fields:    Translation:Humans
    35. Genetic variants on chromosome 1q41 influence ocular axial length and high myopia. PLoS Genet. 2012; 8(6):e1002753. PMID: 22685421.
      View in: PubMed   Mentions: 35     Fields:    Translation:HumansAnimalsCells
    36. Polymorphisms in SP110 are not associated with pulmonary tuberculosis in Indonesians. Infect Genet Evol. 2012 Aug; 12(6):1319-23. PMID: 22522001.
      View in: PubMed   Mentions: 8     Fields:    Translation:Humans
    37. Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. PLoS Genet. 2012; 8(3):e1002607. PMID: 22479202.
      View in: PubMed   Mentions: 187     Fields:    Translation:Humans
    38. Meta-analysis identifies common variants associated with body mass index in east Asians. Nat Genet. 2012 Feb 19; 44(3):307-11. PMID: 22344219.
      View in: PubMed   Mentions: 155     Fields:    Translation:Humans
    39. A genome wide association study of pulmonary tuberculosis susceptibility in Indonesians. BMC Med Genet. 2012 Jan 13; 13:5. PMID: 22239941.
      View in: PubMed   Mentions: 38     Fields:    Translation:Humans
    40. Meta-analysis of genome-wide association studies identifies eight new loci for type 2 diabetes in east Asians. Nat Genet. 2011 Dec 11; 44(1):67-72. PMID: 22158537.
      View in: PubMed   Mentions: 258     Fields:    Translation:Humans
    41. Genome-wide meta-analysis of five Asian cohorts identifies PDGFRA as a susceptibility locus for corneal astigmatism. PLoS Genet. 2011 Dec; 7(12):e1002402. PMID: 22144915.
      View in: PubMed   Mentions: 17     Fields:    Translation:Humans
    42. Genetic determinants of hepatitis B vaccine response. BMC Proceedings. 2011 Dec 1; 5(Suppl 1):o3. Eileen Png, Anbupalam Thalamuthu, Rick TH Ong, Harm Snippe, Herawati Sudoyo, David H Muljono, Sangkot Marzuki, Greet J Boland, Mark Seielstad. .
      View in: Publisher Site   Mentions:
    43. A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. PLoS One. 2011; 6(10):e25598. PMID: 22022419.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansCells
    44. Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations. Hum Mol Genet. 2012 Jan 15; 21(2):437-45. Cornes BK, Khor CC, Nongpiur ME, Xu L, Tay WT, Zheng Y, Lavanya R, Li Y, Wu R, Sim X, Wang YX, Chen P, Teo YY, Chia KS, Seielstad M, Liu J, Hibberd ML, Cheng CY, Saw SM, Tai ES, Jonas JB, Vithana EN, Wong TY, Aung T. PMID: 21984434.
      View in: PubMed   Mentions: 27     Fields:    Translation:Humans
    45. SgD-CNV, a database for common and rare copy number variants in three Asian populations. Hum Mutat. 2011 Dec; 32(12):1341-9. Xu H, Poh WT, Sim X, Ong RT, Suo C, Tay WT, Khor CC, Seielstad M, Liu J, Aung T, Tai ES, Wong TY, Chia KS, Teo YY. PMID: 21882294.
      View in: PubMed   Mentions: 16     Fields:    Translation:Humans
    46. Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk. Nature. 2011 Sep 11; 478(7367):103-9. PMID: 21909115.
      View in: PubMed   Mentions: 785     Fields:    Translation:Humans
    47. Erratum: Corrigendum: Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nature Genetics. 2011 Sep 1; 43(9):919-919. Carl A Anderson, Gabrielle Boucher, Charlie W Lees, Andre Franke, Mauro D'Amato, Kent D Taylor, James C Lee, Philippe Goyette, Marcin Imielinski, Anna Latiano, Caroline Lagacé, Regan Scott, Leila Amininejad, Suzannah Bumpstead, Leonard Baidoo, Robert N Baldassano, Murray Barclay, Theodore M Bayless, Stephan Brand, Carsten Büning, Jean-Frédéric Colombel, Lee A Denson, Martine De Vos, Marla Dubinsky, Cathryn Edwards, David Ellinghaus, Rudolf S N Fehrmann, James A B Floyd, Timothy Florin, Denis Franchimont, Lude Franke, Michel Georges, Jürgen Glas, Nicole L Glazer, Stephen L Guthery, Talin Haritunians, Nicholas K Hayward, Jean-Pierre Hugot, Gilles Jobin, Debby Laukens, Ian Lawrance, Marc Lémann, Arie Levine, Cecile Libioulle, Edouard Louis, Dermot P McGovern, Monica Milla, Grant W Montgomery, Katherine I Morley, Craig Mowat, Aylwin Ng, William Newman, Roel A Ophoff, Laura Papi, Orazio Palmieri, Laurent Peyrin-Biroulet, Julián Panés, Anne Phillips, Natalie J Prescott, Deborah D Proctor, Rebecca Roberts, Richard Russell, Paul Rutgeerts, Jeremy Sanderson, Miquel Sans, Philip Schumm, Frank Seibold, Yashoda Sharma, Lisa A Simms, Mark Seielstad, A Hillary Steinhart, Stephan R Targan, Leonard H van den Berg, Morten Vatn, Hein Verspaget, Thomas Walters, Cisca Wijmenga, David C Wilson, Harm-Jan Westra, Ramnik J Xavier, Zhen Z Zhao, Cyriel Y Ponsioen, Vibeke Andersen, Leif Torkvist, Maria Gazouli, Nicholas P Anagnou, Tom H Karlsen, Limas Kupcinskas, Jurgita Sventoraityte, John C Mansfield, Subra Kugathasan, Mark S Silverberg, Jonas Halfvarson, Jerome I Rotter, Christopher G Mathew, Anne M Griffiths, Richard Gearry, Tariq Ahmad, Steven R Brant, Mathias Chamaillard, Jack Satsangi, Judy H Cho, Stefan Schreiber, Mark J Daly, Jeffrey C Barrett, Miles Parkes, Vito Annese, Hakon Hakonarson, Graham Radford-Smith, Richard H Duerr, Séverine Vermeire, Rinse K Weersma, John D Rioux. .
      View in: Publisher Site   Mentions:
    48. Genome-wide association study in individuals of South Asian ancestry identifies six new type 2 diabetes susceptibility loci. Nat Genet. 2011 Aug 28; 43(10):984-9. Kooner JS, Saleheen D, Sim X, Sehmi J, Zhang W, Frossard P, Been LF, Chia KS, Dimas AS, Hassanali N, Jafar T, Jowett JB, Li X, Radha V, Rees SD, Takeuchi F, Young R, Aung T, Basit A, Chidambaram M, Das D, Grundberg E, Hedman AK, Hydrie ZI, Islam M, Khor CC, Kowlessur S, Kristensen MM, Liju S, Lim WY, Matthews DR, Liu J, Morris AP, Nica AC, Pinidiyapathirage JM, Prokopenko I, Rasheed A, Samuel M, Shah N, Shera AS, Small KS, Suo C, Wickremasinghe AR, Wong TY, Yang M, Zhang F, Abecasis GR, Barnett AH, Caulfield M, Deloukas P, Frayling TM, Froguel P, Kato N, Katulanda P, Kelly MA, Liang J, Mohan V, Sanghera DK, Scott J, Seielstad M, Zimmet PZ, Elliott P, Teo YY, McCarthy MI, Danesh J, Tai ES, Chambers JC. PMID: 21874001.
      View in: PubMed   Mentions: 204     Fields:    Translation:Humans
    49. A genome-wide association study of hepatitis B vaccine response in an Indonesian population reveals multiple independent risk variants in the HLA region. Hum Mol Genet. 2011 Oct 01; 20(19):3893-8. PMID: 21764829.
      View in: PubMed   Mentions: 40     Fields:    Translation:HumansCTClinical Trials
    50. Copy number polymorphisms in new HapMap III and Singapore populations. J Hum Genet. 2011 Aug; 56(8):552-60. Ku CS, Teo SM, Naidoo N, Sim X, Teo YY, Pawitan Y, Seielstad M, Chia KS, Salim A. PMID: 21677662.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    51. Genetic structure of the Mon-Khmer speaking groups and their affinity to the neighbouring Tai populations in Northern Thailand. BMC Genet. 2011 Jun 15; 12:56. PMID: 21672265.
      View in: PubMed   Mentions: 10     Fields:    Translation:HumansCells
    52. Association of variants in FRAP1 and PDGFRA with corneal curvature in Asian populations from Singapore. Hum Mol Genet. 2011 Sep 15; 20(18):3693-8. Han S, Chen P, Fan Q, Khor CC, Sim X, Tay WT, Ong RT, Suo C, Goh LK, Lavanya R, Zheng Y, Wu R, Seielstad M, Vithana E, Liu J, Chia KS, Lee JJ, Tai ES, Wong TY, Aung T, Teo YY, Saw SM. PMID: 21665993.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    53. Meta-analysis of genome-wide association studies identifies common variants associated with blood pressure variation in east Asians. Nat Genet. 2011 Jun; 43(6):531-8. PMID: 21572416.
      View in: PubMed   Mentions: 212     Fields:    Translation:Humans
    54. Transferability of type 2 diabetes implicated loci in multi-ethnic cohorts from Southeast Asia. PLoS Genet. 2011 Apr; 7(4):e1001363. Sim X, Ong RT, Suo C, Tay WT, Liu J, Ng DP, Boehnke M, Chia KS, Wong TY, Seielstad M, Teo YY, Tai ES. PMID: 21490949.
      View in: PubMed   Mentions: 68     Fields:    Translation:Humans
    55. Multi-platform segmentation for joint detection of copy number variants. Bioinformatics. 2011 Jun 01; 27(11):1555-61. Teo SM, Pawitan Y, Kumar V, Thalamuthu A, Seielstad M, Chia KS, Salim A. PMID: 21471018.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    56. Erratum: Genome-wide association identifies multiple ulcerative colitis susceptibility loci. Nature Genetics. 2011 Apr 1; 43(4):388-388. Dermot P B McGovern, Agnès Gardet, Leif Törkvist, Philippe Goyette, Jonah Essers, Kent D Taylor, Benjamin M Neale, Rick T H Ong, Caroline Lagacé, Chun Li, Todd Green, Christine R Stevens, Claudine Beauchamp, Phillip R Fleshner, Marie Carlson, Mauro D'Amato, Jonas Halfvarson, Martin L Hibberd, Mikael Lördal, Leonid Padyukov, Angelo Andriulli, Elisabetta Colombo, Anna Latiano, Orazio Palmieri, Edmond-Jean Bernard, Colette Deslandres, Daan W Hommes, Dirk J de Jong, Pieter C Stokkers, Rinse K Weersma, The NIDDK IBD Genetics Consortium, Yashoda Sharma, Mark S Silverberg, Judy H Cho, Jing Wu, Kathryn Roeder, Steven R Brant, L Phillip Schumm, Richard H Duerr, Marla C Dubinsky, Nicole L Glazer, Talin Haritunians, Andy Ippoliti, Gil Y Melmed, David S Siscovick, Eric A Vasiliauskas, Stephan R Targan, Vito Annese, Cisca Wijmenga, Sven Pettersson, Jerome I Rotter, Ramnik J Xavier, Mark J Daly, John D Rioux, Mark Seielstad. .
      View in: Publisher Site   Mentions:
    57. Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area. Hum Mol Genet. 2011 May 01; 20(9):1864-72. Khor CC, Ramdas WD, Vithana EN, Cornes BK, Sim X, Tay WT, Saw SM, Zheng Y, Lavanya R, Wu R, Wang JJ, Mitchell P, Uitterlinden AG, Rivadeneira F, Teo YY, Chia KS, Seielstad M, Hibberd M, Vingerling JR, Klaver CC, Jansonius NM, Tai ES, Wong TY, van Duijn CM, Aung T. PMID: 21307088.
      View in: PubMed   Mentions: 44     Fields:    Translation:HumansCells
    58. Meta-analysis identifies 29 additional ulcerative colitis risk loci, increasing the number of confirmed associations to 47. Nat Genet. 2011 Mar; 43(3):246-52. Anderson CA, Boucher G, Lees CW, Franke A, D'Amato M, Taylor KD, Lee JC, Goyette P, Imielinski M, Latiano A, Lagacé C, Scott R, Amininejad L, Bumpstead S, Baidoo L, Baldassano RN, Barclay M, Bayless TM, Brand S, Büning C, Colombel JF, Denson LA, De Vos M, Dubinsky M, Edwards C, Ellinghaus D, Fehrmann RS, Floyd JA, Florin T, Franchimont D, Franke L, Georges M, Glas J, Glazer NL, Guthery SL, Haritunians T, Hayward NK, Hugot JP, Jobin G, Laukens D, Lawrance I, Lémann M, Levine A, Libioulle C, Louis E, McGovern DP, Milla M, Montgomery GW, Morley KI, Mowat C, Ng A, Newman W, Ophoff RA, Papi L, Palmieri O, Peyrin-Biroulet L, Panés J, Phillips A, Prescott NJ, Proctor DD, Roberts R, Russell R, Rutgeerts P, Sanderson J, Sans M, Schumm P, Seibold F, Sharma Y, Simms LA, Seielstad M, Steinhart AH, Targan SR, van den Berg LH, Vatn M, Verspaget H, Walters T, Wijmenga C, Wilson DC, Westra HJ, Xavier RJ, Zhao ZZ, Ponsioen CY, Andersen V, Torkvist L, Gazouli M, Anagnou NP, Karlsen TH, Kupcinskas L, Sventoraityte J, Mansfield JC, Kugathasan S, Silverberg MS, Halfvarson J, Rotter JI, Mathew CG, Griffiths AM, Gearry R, Ahmad T, Brant SR, Chamaillard M, Satsangi J, Cho JH, Schreiber S, Daly MJ, Barrett JC, Parkes M, Annese V, Hakonarson H, Radford-Smith G, Duerr RH, Vermeire S, Weersma RK, Rioux JD. PMID: 21297633.
      View in: PubMed   Mentions: 513     Fields:    Translation:Humans
    59. Pathway-based analysis using reduced gene subsets in genome-wide association studies. BMC Bioinformatics. 2011 Jan 12; 12:17. Zhao J, Gupta S, Seielstad M, Liu J, Thalamuthu A. PMID: 21226955.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    60. A genome-wide association study suggests contrasting associations in ACPA-positive versus ACPA-negative rheumatoid arthritis. Ann Rheum Dis. 2011 Feb; 70(2):259-65. Padyukov L, Seielstad M, Ong RT, Ding B, Rönnelid J, Seddighzadeh M, Alfredsson L, Klareskog L. PMID: 21156761.
      View in: PubMed   Mentions: 80     Fields:    Translation:Humans
    61. Genetic affinity and admixture of northern Thai people along their migration route in northern Thailand: evidence from autosomal STR loci. J Hum Genet. 2011 Feb; 56(2):130-7. PMID: 21107341.
      View in: PubMed   Mentions: 4     Fields:    Translation:HumansCells
    62. Collagen-related genes influence the glaucoma risk factor, central corneal thickness. Hum Mol Genet. 2011 Feb 15; 20(4):649-58. Vithana EN, Aung T, Khor CC, Cornes BK, Tay WT, Sim X, Lavanya R, Wu R, Zheng Y, Hibberd ML, Chia KS, Seielstad M, Goh LK, Saw SM, Tai ES, Wong TY. PMID: 21098505.
      View in: PubMed   Mentions: 77     Fields:    Translation:Humans
    63. Genome-wide association studies reveal genetic variants in CTNND2 for high myopia in Singapore Chinese. Ophthalmology. 2011 Feb; 118(2):368-75. PMID: 21095009.
      View in: PubMed   Mentions: 44     Fields:    Translation:Humans
    64. Identification of new genetic risk variants for type 2 diabetes. PLoS Genet. 2010 Sep 16; 6(9):e1001127. Shu XO, Long J, Cai Q, Qi L, Xiang YB, Cho YS, Tai ES, Li X, Lin X, Chow WH, Go MJ, Seielstad M, Bao W, Li H, Cornelis MC, Yu K, Wen W, Shi J, Han BG, Sim XL, Liu L, Qi Q, Kim HL, Ng DP, Lee JY, Kim YJ, Li C, Gao YT, Zheng W, Hu FB. PMID: 20862305.
      View in: PubMed   Mentions: 97     Fields:    Translation:HumansCells
    65. Biological, clinical and population relevance of 95 loci for blood lipids. Nature. 2010 Aug 05; 466(7307):707-13. Teslovich TM, Musunuru K, Smith AV, Edmondson AC, Stylianou IM, Koseki M, Pirruccello JP, Ripatti S, Chasman DI, Willer CJ, Johansen CT, Fouchier SW, Isaacs A, Peloso GM, Barbalic M, Ricketts SL, Bis JC, Aulchenko YS, Thorleifsson G, Feitosa MF, Chambers J, Orho-Melander M, Melander O, Johnson T, Li X, Guo X, Li M, Shin Cho Y, Jin Go M, Jin Kim Y, Lee JY, Park T, Kim K, Sim X, Twee-Hee Ong R, Croteau-Chonka DC, Lange LA, Smith JD, Song K, Hua Zhao J, Yuan X, Luan J, Lamina C, Ziegler A, Zhang W, Zee RY, Wright AF, Witteman JC, Wilson JF, Willemsen G, Wichmann HE, Whitfield JB, Waterworth DM, Wareham NJ, Waeber G, Vollenweider P, Voight BF, Vitart V, Uitterlinden AG, Uda M, Tuomilehto J, Thompson JR, Tanaka T, Surakka I, Stringham HM, Spector TD, Soranzo N, Smit JH, Sinisalo J, Silander K, Sijbrands EJ, Scuteri A, Scott J, Schlessinger D, Sanna S, Salomaa V, Saharinen J, Sabatti C, Ruokonen A, Rudan I, Rose LM, Roberts R, Rieder M, Psaty BM, Pramstaller PP, Pichler I, Perola M, Penninx BW, Pedersen NL, Pattaro C, Parker AN, Pare G, Oostra BA, O'Donnell CJ, Nieminen MS, Nickerson DA, Montgomery GW, Meitinger T, McPherson R, McCarthy MI, McArdle W, Masson D, Martin NG, Marroni F, Mangino M, Magnusson PK, Lucas G, Luben R, Loos RJ, Lokki ML, Lettre G, Langenberg C, Launer LJ, Lakatta EG, Laaksonen R, Kyvik KO, Kronenberg F, König IR, Khaw KT, Kaprio J, Kaplan LM, Johansson A, Jarvelin MR, Janssens AC, Ingelsson E, Igl W, Kees Hovingh G, Hottenga JJ, Hofman A, Hicks AA, Hengstenberg C, Heid IM, Hayward C, Havulinna AS, Hastie ND, Harris TB, Haritunians T, Hall AS, Gyllensten U, Guiducci C, Groop LC, Gonzalez E, Gieger C, Freimer NB, Ferrucci L, Erdmann J, Elliott P, Ejebe KG, Döring A, Dominiczak AF, Demissie S, Deloukas P, de Geus EJ, de Faire U, Crawford G, Collins FS, Chen YD, Caulfield MJ, Campbell H, Burtt NP, Bonnycastle LL, Boomsma DI, Boekholdt SM, Bergman RN, Barroso I, Bandinelli S, Ballantyne CM, Assimes TL, Quertermous T, Altshuler D, Seielstad M, Wong TY, Tai ES, Feranil AB, Kuzawa CW, Adair LS, Taylor HA, Borecki IB, Gabriel SB, Wilson JG, Holm H, Thorsteinsdottir U, Gudnason V, Krauss RM, Mohlke KL, Ordovas JM, Munroe PB, Kooner JS, Tall AR, Hegele RA, Kastelein JJ, Schadt EE, Rotter JI, Boerwinkle E, Strachan DP, Mooser V, Stefansson K, Reilly MP, Samani NJ, Schunkert H, Cupples LA, Sandhu MS, Ridker PM, Rader DJ, van Duijn CM, Peltonen L, Abecasis GR, Boehnke M, Kathiresan S. PMID: 20686565.
      View in: PubMed   Mentions: 1477     Fields:    Translation:HumansAnimals
    66. Support for TGFB1 as a susceptibility gene for high myopia in individuals of Chinese descent. Arch Ophthalmol. 2010 Aug; 128(8):1081-4. Khor CC, Fan Q, Goh L, Tan D, Young TL, Li YJ, Seielstad M, Goh DL, Saw SM. PMID: 20697017.
      View in: PubMed   Mentions: 9     Fields:    Translation:Humans
    67. Genomic copy number variations in three Southeast Asian populations. Hum Mutat. 2010 Jul; 31(7):851-7. Ku CS, Pawitan Y, Sim X, Ong RT, Seielstad M, Lee EJ, Teo YY, Chia KS, Salim A. PMID: 20506136.
      View in: PubMed   Mentions: 12     Fields:    Translation:Humans
    68. Analysis of 39 Crohn's disease risk loci in Swedish inflammatory bowel disease patients. Inflamm Bowel Dis. 2010 Jun; 16(6):907-9. Törkvist L, Halfvarson J, Ong RT, Lördal M, Sjöqvist U, Bresso F, Björk J, Befrits R, Löfberg R, Blom J, Carlson M, Padyukov L, D'Amato M, Seielstad M, Pettersson S. PMID: 19760754.
      View in: PubMed   Mentions: 10     Fields:    Translation:Humans
    69. Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci. Nat Genet. 2010 Jun; 42(6):508-14. Stahl EA, Raychaudhuri S, Remmers EF, Xie G, Eyre S, Thomson BP, Li Y, Kurreeman FA, Zhernakova A, Hinks A, Guiducci C, Chen R, Alfredsson L, Amos CI, Ardlie KG, Barton A, Bowes J, Brouwer E, Burtt NP, Catanese JJ, Coblyn J, Coenen MJ, Costenbader KH, Criswell LA, Crusius JB, Cui J, de Bakker PI, De Jager PL, Ding B, Emery P, Flynn E, Harrison P, Hocking LJ, Huizinga TW, Kastner DL, Ke X, Lee AT, Liu X, Martin P, Morgan AW, Padyukov L, Posthumus MD, Radstake TR, Reid DM, Seielstad M, Seldin MF, Shadick NA, Steer S, Tak PP, Thomson W, van der Helm-van Mil AH, van der Horst-Bruinsma IE, van der Schoot CE, van Riel PL, Weinblatt ME, Wilson AG, Wolbink GJ, Wordsworth BP, Wijmenga C, Karlson EW, Toes RE, de Vries N, Begovich AB, Worthington J, Siminovitch KA, Gregersen PK, Klareskog L, Plenge RM. PMID: 20453842.
      View in: PubMed   Mentions: 513     Fields:    Translation:Humans
    70. Genetic evidence supports linguistic affinity of Mlabri--a hunter-gatherer group in Thailand. BMC Genet. 2010 Mar 19; 11:18. Xu S, Kangwanpong D, Seielstad M, Srikummool M, Kampuansai J, Jin L. PMID: 20302622.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    71. New genetic associations detected in a host response study to hepatitis B vaccine. Genes Immun. 2010 Apr; 11(3):232-8. Davila S, Froeling FE, Tan A, Bonnard C, Boland GJ, Snippe H, Hibberd ML, Seielstad M. PMID: 20237496.
      View in: PubMed   Mentions: 26     Fields:    Translation:HumansPHPublic Health
    72. Genome-wide association identifies multiple ulcerative colitis susceptibility loci. Nat Genet. 2010 Apr; 42(4):332-7. McGovern DP, Gardet A, Törkvist L, Goyette P, Essers J, Taylor KD, Neale BM, Ong RT, Lagacé C, Li C, Green T, Stevens CR, Beauchamp C, Fleshner PR, Carlson M, D'Amato M, Halfvarson J, Hibberd ML, Lördal M, Padyukov L, Andriulli A, Colombo E, Latiano A, Palmieri O, Bernard EJ, Deslandres C, Hommes DW, de Jong DJ, Stokkers PC, Weersma RK, Sharma Y, Silverberg MS, Cho JH, Wu J, Roeder K, Brant SR, Schumm LP, Duerr RH, Dubinsky MC, Glazer NL, Haritunians T, Ippoliti A, Melmed GY, Siscovick DS, Vasiliauskas EA, Targan SR, Annese V, Wijmenga C, Pettersson S, Rotter JI, Xavier RJ, Daly MJ, Rioux JD, Seielstad M. PMID: 20228799.
      View in: PubMed   Mentions: 257     Fields:    Translation:Humans
    73. Comparative analyses of seven algorithms for copy number variant identification from single nucleotide polymorphism arrays. Nucleic Acids Res. 2010 May; 38(9):e105. Dellinger AE, Saw SM, Goh LK, Seielstad M, Young TL, Li YJ. PMID: 20142258.
      View in: PubMed   Mentions: 59     Fields:    Translation:Humans
    74. Hepatocyte growth factor and retinal arteriolar diameter in Singapore Chinese. Ophthalmology. 2010 May; 117(5):939-45. Khor CC, Fan Q, Goh LK, Wong TY, Li YJ, Cheung N, Seielstad M, Goh DL, Young TL, Tai ES, Saw SM. PMID: 20122738.
      View in: PubMed   Mentions: 3     Fields:    Translation:Humans
    75. Mapping human genetic diversity in Asia. Science. 2009 Dec 11; 326(5959):1541-5. Abdulla MA, Ahmed I, Assawamakin A, Bhak J, Brahmachari SK, Calacal GC, Chaurasia A, Chen CH, Chen J, Chen YT, Chu J, Cutiongco-de la Paz EM, De Ungria MC, Delfin FC, Edo J, Fuchareon S, Ghang H, Gojobori T, Han J, Ho SF, Hoh BP, Huang W, Inoko H, Jha P, Jinam TA, Jin L, Jung J, Kangwanpong D, Kampuansai J, Kennedy GC, Khurana P, Kim HL, Kim K, Kim S, Kim WY, Kimm K, Kimura R, Koike T, Kulawonganunchai S, Kumar V, Lai PS, Lee JY, Lee S, Liu ET, Majumder PP, Mandapati KK, Marzuki S, Mitchell W, Mukerji M, Naritomi K, Ngamphiw C, Niikawa N, Nishida N, Oh B, Oh S, Ohashi J, Oka A, Ong R, Padilla CD, Palittapongarnpim P, Perdigon HB, Phipps ME, Png E, Sakaki Y, Salvador JM, Sandraling Y, Scaria V, Seielstad M, Sidek MR, Sinha A, Srikummool M, Sudoyo H, Sugano S, Suryadi H, Suzuki Y, Tabbada KA, Tan A, Tokunaga K, Tongsima S, Villamor LP, Wang E, Wang Y, Wang H, Wu JY, Xiao H, Xu S, Yang JO, Shugart YY, Yoo HS, Yuan W, Zhao G, Zilfalil BA. PMID: 20007900.
      View in: PubMed   Mentions: 195     Fields:    Translation:Humans
    76. Genetic structure of the Han Chinese population revealed by genome-wide SNP variation. Am J Hum Genet. 2009 Dec; 85(6):775-85. Chen J, Zheng H, Bei JX, Sun L, Jia WH, Li T, Zhang F, Seielstad M, Zeng YX, Zhang X, Liu J. PMID: 19944401.
      View in: PubMed   Mentions: 94     Fields:    Translation:Humans
    77. Polymorphisms Identified through Genome-Wide Association Studies and Their Associations with Type 2 Diabetes in Chinese, Malays, and Asian-Indians in Singapore. Endocrinology. 2009 Dec 1; 150(12):5649-5649. Jonathan T. Tan, Daniel P. K. Ng, Siti Nurbaya, Sandra Ye, Xiu Li Lim, Helen Leong, Lin Tze Seet, Wei Fong Siew, Winston Kon, Tien Yin Wong, Seang Mei Saw, Tin Aung, Kee Seng Chia, Jeannette Lee, Suok Kai Chew, Mark Seielstad, E. Shyong Tai. .
      View in: Publisher Site   Mentions:
    78. Polymorphisms Identified through Genome-Wide Association Studies and Their Associations with Type 2 Diabetes in Chinese, Malays, and Asian-Indians in Singapore. Endocr Rev. 2009 Dec 01; 30(7):926. PMID: 28199501.
      View in: PubMed   Mentions:    Fields:    
    79. Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk. Nat Genet. 2009 Dec; 41(12):1313-8. Raychaudhuri S, Thomson BP, Remmers EF, Eyre S, Hinks A, Guiducci C, Catanese JJ, Xie G, Stahl EA, Chen R, Alfredsson L, Amos CI, Ardlie KG, Barton A, Bowes J, Burtt NP, Chang M, Coblyn J, Costenbader KH, Criswell LA, Crusius JB, Cui J, De Jager PL, Ding B, Emery P, Flynn E, Harrison P, Hocking LJ, Huizinga TW, Kastner DL, Ke X, Kurreeman FA, Lee AT, Liu X, Li Y, Martin P, Morgan AW, Padyukov L, Reid DM, Seielstad M, Seldin MF, Shadick NA, Steer S, Tak PP, Thomson W, van der Helm-van Mil AH, van der Horst-Bruinsma IE, Weinblatt ME, Wilson AG, Wolbink GJ, Wordsworth P, Altshuler D, Karlson EW, Toes RE, de Vries N, Begovich AB, Siminovitch KA, Worthington J, Klareskog L, Gregersen PK, Daly MJ, Plenge RM. PMID: 19898481.
      View in: PubMed   Mentions: 140     Fields:    Translation:Humans
    80. Polymorphisms identified through genome-wide association studies and their associations with type 2 diabetes in Chinese, Malays, and Asian-Indians in Singapore. J Clin Endocrinol Metab. 2010 Jan; 95(1):390-7. Tan JT, Ng DP, Nurbaya S, Ye S, Lim XL, Leong H, Seet LT, Siew WF, Kon W, Wong TY, Saw SM, Aung T, Chia KS, Lee J, Chew SK, Seielstad M, Tai ES. PMID: 19892838.
      View in: PubMed   Mentions: 39     Fields:    Translation:Humans
    81. Differential association of cataract sub-types with obesity and FTO polymorphisms. Acta Ophthalmologica. 2009 Sep 1; 87:0-0. L LIM, E TAI, T AUNG, W TAY, SM SAW, M SEIELSTAD, TY WONG. .
      View in: Publisher Site   Mentions:
    82. Singapore Genome Variation Project: a haplotype map of three Southeast Asian populations. Genome Res. 2009 Nov; 19(11):2154-62. Teo YY, Sim X, Ong RT, Tan AK, Chen J, Tantoso E, Small KS, Ku CS, Lee EJ, Seielstad M, Chia KS. PMID: 19700652.
      View in: PubMed   Mentions: 64     Fields:    Translation:Humans
    83. The PRL -1149 G/T polymorphism and rheumatoid arthritis susceptibility. Arthritis Rheum. 2009 May; 60(5):1250-4. Lee YC, Raychaudhuri S, Cui J, De Vivo I, Ding B, Alfredsson L, Padyukov L, Costenbader KH, Seielstad M, Graham RR, Klareskog L, Gregersen PK, Plenge RM, Karlson EW. PMID: 19404952.
      View in: PubMed   Mentions: 7     Fields:    Translation:Humans
    84. Relation of age-related cataract with obesity and obesity genes in an Asian population. Am J Epidemiol. 2009 May 15; 169(10):1267-74. Lim LS, Tai ES, Aung T, Tay WT, Saw SM, Seielstad M, Wong TY. PMID: 19329528.
      View in: PubMed   Mentions: 11     Fields:    Translation:Humans
    85. Different patterns of associations with anti-citrullinated protein antibody-positive and anti-citrullinated protein antibody-negative rheumatoid arthritis in the extended major histocompatibility complex region. Arthritis Rheum. 2009 Jan; 60(1):30-8. Ding B, Padyukov L, Lundström E, Seielstad M, Plenge RM, Oksenberg JR, Gregersen PK, Alfredsson L, Klareskog L. PMID: 19116921.
      View in: PubMed   Mentions: 52     Fields:    Translation:Humans
    86. Identification of tuberculosis susceptibility genes with human macrophage gene expression profiles. PLoS Pathog. 2008 Dec; 4(12):e1000229. Thuong NT, Dunstan SJ, Chau TT, Thorsson V, Simmons CP, Quyen NT, Thwaites GE, Thi Ngoc Lan N, Hibberd M, Teo YY, Seielstad M, Aderem A, Farrar JJ, Hawn TR. PMID: 19057661.
      View in: PubMed   Mentions: 56     Fields:    Translation:HumansCells
    87. Polymorphisms at newly identified lipid-associated loci are associated with blood lipids and cardiovascular disease in an Asian Malay population. J Lipid Res. 2009 Mar; 50(3):514-20. Tai ES, Sim XL, Ong TH, Wong TY, Saw SM, Aung T, Kathiresan S, Orho-Melander M, Ordovas JM, Tan JT, Seielstad M. PMID: 18987386.
      View in: PubMed   Mentions: 23     Fields:    Translation:Humans
    88. Genetic association and expression studies indicate a role of toll-like receptor 8 in pulmonary tuberculosis. PLoS Genet. 2008 Oct; 4(10):e1000218. Davila S, Hibberd ML, Hari Dass R, Wong HE, Sahiratmadja E, Bonnard C, Alisjahbana B, Szeszko JS, Balabanova Y, Drobniewski F, van Crevel R, van de Vosse E, Nejentsev S, Ottenhoff TH, Seielstad M. PMID: 18927625.
      View in: PubMed   Mentions: 89     Fields:    Translation:HumansCells
    89. Common variants at CD40 and other loci confer risk of rheumatoid arthritis. Nat Genet. 2008 Oct; 40(10):1216-23. Raychaudhuri S, Remmers EF, Lee AT, Hackett R, Guiducci C, Burtt NP, Gianniny L, Korman BD, Padyukov L, Kurreeman FA, Chang M, Catanese JJ, Ding B, Wong S, van der Helm-van Mil AH, Neale BM, Coblyn J, Cui J, Tak PP, Wolbink GJ, Crusius JB, van der Horst-Bruinsma IE, Criswell LA, Amos CI, Seldin MF, Kastner DL, Ardlie KG, Alfredsson L, Costenbader KH, Altshuler D, Huizinga TW, Shadick NA, Weinblatt ME, de Vries N, Worthington J, Seielstad M, Toes RE, Karlson EW, Begovich AB, Klareskog L, Gregersen PK, Daly MJ, Plenge RM. PMID: 18794853.
      View in: PubMed   Mentions: 228     Fields:    Translation:HumansCells
    90. Association of skin barrier genes within the PSORS4 locus is enriched in Singaporean Chinese with early-onset psoriasis. J Invest Dermatol. 2009 Mar; 129(3):606-14. Chen H, Toh TK, Szeverenyi I, Ong RT, Theng CT, McLean WH, Seielstad M, Lane EB. PMID: 18787534.
      View in: PubMed   Mentions: 11     Fields:    Translation:HumansCells
    91. FTO variants are associated with obesity in the Chinese and Malay populations in Singapore. Diabetes. 2008 Oct; 57(10):2851-7. Tan JT, Dorajoo R, Seielstad M, Sim XL, Ong RT, Chia KS, Wong TY, Saw SM, Chew SK, Aung T, Tai ES. PMID: 18599522.
      View in: PubMed   Mentions: 68     Fields:    Translation:Humans
    92. The Singapore Genome Variation Project. European Journal of Cancer Supplements. 2008 Jul 1; 6(9):200. Y.Y. Teo, X.L. Sim, C.S. Ku, R.T.H. Ong, A. Tan, E. Tantoso, Y. Pawitan, M. Seielstad, E.J.D. Lee, K.S. Chia. .
      View in: Publisher Site   Mentions:
    93. Whole genome-amplified DNA: insights and imputation. Nat Methods. 2008 Apr; 5(4):279-80. Teo YY, Inouye M, Small KS, Fry AE, Potter SC, Dunstan SJ, Seielstad M, Barroso I, Wareham NJ, Rockett KA, Kwiatkowski DP, Deloukas P. PMID: 18376389.
      View in: PubMed   Mentions: 6     Fields:    Translation:Humans
    94. Analysis of association of the TIRAP (MAL) S180L variant and tuberculosis in three populations. Nat Genet. 2008 Mar; 40(3):261-2; author reply 262-3. Nejentsev S, Thye T, Szeszko JS, Stevens H, Balabanova Y, Chinbuah AM, Hibberd M, van de Vosse E, Alisjahbana B, van Crevel R, Ottenhoff TH, Png E, Drobniewski F, Todd JA, Seielstad M, Horstmann RD. PMID: 18305471.
      View in: PubMed   Mentions: 15     Fields:    Translation:Humans
    95. OR.103. Combined Analysis of Three Genome-wide Scans Reveals Additional Loci Associated with Rheumatoid Arthritis. Clinical Immunology. 2008 Jan 1; 127:s41. Mark Seielstad, Leonid Padyukov, Xiayi Ke, Bo Ding, Erwin Tantoso, Twee Hee Rick Ong, Lars Alfredsson, Robert Plenge, Peter Gregersen, Jane Worthington, Lars Klareskog. .
      View in: Publisher Site   Mentions:
    96. TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study. N Engl J Med. 2007 Sep 20; 357(12):1199-209. Plenge RM, Seielstad M, Padyukov L, Lee AT, Remmers EF, Ding B, Liew A, Khalili H, Chandrasekaran A, Davies LR, Li W, Tan AK, Bonnard C, Ong RT, Thalamuthu A, Pettersson S, Liu C, Tian C, Chen WV, Carulli JP, Beckman EM, Altshuler D, Alfredsson L, Criswell LA, Amos CI, Seldin MF, Kastner DL, Klareskog L, Gregersen PK. PMID: 17804836.
      View in: PubMed   Mentions: 352     Fields:    Translation:HumansCells
    97. Genetic variation in Northern Thailand Hill Tribes: origins and relationships with social structure and linguistic differences. BMC Evol Biol. 2007 Aug 16; 7 Suppl 2:S12. Besaggio D, Fuselli S, Srikummool M, Kampuansai J, Castrì L, Tyler-Smith C, Seielstad M, Kangwanpong D, Bertorelle G. PMID: 17767728.
      View in: PubMed   Mentions: 14     Fields:    Translation:Humans
    98. On the usage of HWE for identifying genotyping errors. Ann Hum Genet. 2007 Sep; 71(Pt 5):701-3; author reply 704. Teo YY, Fry AE, Clark TG, Tai ES, Seielstad M. PMID: 17388941.
      View in: PubMed   Mentions: 20     Fields:    Translation:Humans
    99. A whole genome long-range haplotype (WGLRH) test for detecting imprints of positive selection in human populations. Bioinformatics. 2006 Sep 01; 22(17):2122-8. Zhang C, Bailey DK, Awad T, Liu G, Xing G, Cao M, Valmeekam V, Retief J, Matsuzaki H, Taub M, Seielstad M, Kennedy GC. PMID: 16845142.
      View in: PubMed   Mentions: 28     Fields:    Translation:HumansAnimals
    100. Twin births in Singapore: a population-based study using the National Birth Registry. Ann Acad Med Singap. 2004 Mar; 33(2):195-9. Chia KS, Lee JJ, Cheung P, Cheung KH, Seielstad M, Wilcox MM, Liu E. PMID: 15098633.
      View in: PubMed   Mentions:
    101. A novel Y-chromosome variant puts an upper limit on the timing of first entry into the Americas. Am J Hum Genet. 2003 Sep; 73(3):700-5. Seielstad M, Yuldasheva N, Singh N, Underhill P, Oefner P, Shen P, Wells RS. PMID: 12929085.
      View in: PubMed   Mentions: 18     Fields:    Translation:HumansCells
    102. Allele frequency and genotype distribution of polymorphisms within disease-related genes is influenced by ethnic population sub-structuring in Sudan. Genetica. 2003 Sep; 119(1):57-63. Bereir RE, Mohamed HS, Seielstad M, El Hassani AM, Khalil EA, Peacock CS, Blackwell JM, Ibrahim ME. PMID: 12903747.
      View in: PubMed   Mentions: 6     Fields:    Translation:HumansCells
    103. Testing for population subdivision and association in four case-control studies. Am J Hum Genet. 2002 Aug; 71(2):304-11. Ardlie KG, Lunetta KL, Seielstad M. PMID: 12096349.
      View in: PubMed   Mentions: 51     Fields:    Translation:Humans
    104. Patterns of linkage disequilibrium in the human genome. Nat Rev Genet. 2002 Apr; 3(4):299-309. Ardlie KG, Kruglyak L, Seielstad M. PMID: 11967554.
      View in: PubMed   Mentions: 288     Fields:    Translation:HumansAnimals
    105. Detection of novel ALAD gene polymorphisms using denaturing high-performance liquid chromatography. Hum Biol. 2001 Jun; 73(3):429-42. Niu T, Seielstad M, Zeng X, Apffel A, Li G, Hahnenberger K, Xu X. PMID: 11459423.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    106. African origin of modern humans in East Asia: a tale of 12,000 Y chromosomes. Science. 2001 May 11; 292(5519):1151-3. Ke Y, Su B, Song X, Lu D, Chen L, Li H, Qi C, Marzuki S, Deka R, Underhill P, Xiao C, Shriver M, Lell J, Wallace D, Wells RS, Seielstad M, Oefner P, Zhu D, Jin J, Huang W, Chakraborty R, Chen Z, Jin L. PMID: 11349147.
      View in: PubMed   Mentions: 30     Fields:    Translation:HumansCells
    107. Y chromosome haplotypes reveal prehistorical migrations to the Himalayas. Hum Genet. 2000 Dec; 107(6):582-90. Su B, Xiao C, Deka R, Seielstad MT, Kangwanpong D, Xiao J, Lu D, Underhill P, Cavalli-Sforza L, Chakraborty R, Jin L. PMID: 11153912.
      View in: PubMed   Mentions: 56     Fields:    Translation:HumansCells
    108. Y chromosome sequence variation and the history of human populations. Nat Genet. 2000 Nov; 26(3):358-61. Underhill PA, Shen P, Lin AA, Jin L, Passarino G, Yang WH, Kauffman E, Bonné-Tamir B, Bertranpetit J, Francalacci P, Ibrahim M, Jenkins T, Kidd JR, Mehdi SQ, Seielstad MT, Wells RS, Piazza A, Davis RW, Feldman MW, Cavalli-Sforza LL, Oefner PJ. PMID: 11062480.
      View in: PubMed   Mentions: 224     Fields:    Translation:HumansAnimalsCells
    109. Asymmetries in the maternal and paternal genetic histories of Colombian populations. Am J Hum Genet. 2000 Nov; 67(5):1062-6. Seielstad M. PMID: 11023812.
      View in: PubMed   Mentions: 3     Fields:    Translation:HumansCells
    110. Whiffs of selection. Nat Genet. 2000 Oct; 26(2):131-2. Seielstad M. PMID: 11017059.
      View in: PubMed   Mentions: 1     Fields:    Translation:Humans
    111. The distribution of human genetic diversity: a comparison of mitochondrial, autosomal, and Y-chromosome data. Am J Hum Genet. 2000 Mar; 66(3):979-88. Jorde LB, Watkins WS, Bamshad MJ, Dixon ME, Ricker CE, Seielstad MT, Batzer MA. PMID: 10712212.
      View in: PubMed   Mentions: 94     Fields:    Translation:HumansCells
    112. Population growth of human Y chromosomes: a study of Y chromosome microsatellites. Mol Biol Evol. 1999 Dec; 16(12):1791-8. Pritchard JK, Seielstad MT, Perez-Lezaun A, Feldman MW. PMID: 10605120.
      View in: PubMed   Mentions: 181     Fields:    Translation:HumansCells
    113. A view of modern human origins from Y chromosome microsatellite variation. Genome Res. 1999 Jun; 9(6):558-67. Seielstad M, Bekele E, Ibrahim M, Touré A, Traoré M. PMID: 10400923.
      View in: PubMed   Mentions: 24     Fields:    Translation:HumansAnimalsCells
    114. Genetic evidence for a higher female migration rate in humans. Nat Genet. 1998 Nov; 20(3):278-80. Seielstad MT, Minch E, Cavalli-Sforza LL. PMID: 9806547.
      View in: PubMed   Mentions: 134     Fields:    Translation:HumansCells
    115. Population genetics of Y-chromosome short tandem repeats in humans. J Mol Evol. 1997 Sep; 45(3):265-70. Pérez-Lezaun A, Calafell F, Seielstad M, Mateu E, Comas D, Bosch E, Bertranpetit J. PMID: 9302320.
      View in: PubMed   Mentions: 17     Fields:    Translation:HumansAnimalsCells
    116. Cw*1701 defines a divergent african HLA-C allelic lineage. Immunogenetics. 1997; 46(3):173-80. Wells RS, Seielstad MT, Bunce M, Tyan DB, Bekele E, Parham P. PMID: 9211742.
      View in: PubMed   Mentions:    Fields:    Translation:HumansCells
    117. Geographic clustering of human Y-chromosome haplotypes. Ann Hum Genet. 1996 09; 60(5):401-8. Ruiz Linares A, Nayar K, Goldstein DB, Hebert JM, Seielstad MT, Underhill PA, Lin AA, Feldman MW, Cavalli Sforza LL. PMID: 8912793.
      View in: PubMed   Mentions: 12     Fields:    Translation:HumansCells
    118. Construction of human Y-chromosomal haplotypes using a new polymorphic A to G transition. Hum Mol Genet. 1994 Dec; 3(12):2159-61. Seielstad MT, Hebert JM, Lin AA, Underhill PA, Ibrahim M, Vollrath D, Cavalli-Sforza LL. PMID: 7881413.
      View in: PubMed   Mentions: 33     Fields:    Translation:HumansAnimalsCells