| Year |
Citation |
Score |
| 2023 |
Carlson JC, Krishnan M, Liu S, Anderson KJ, Zhang JZ, Yapp TJ, Chiyka EA, Dikec DA, Cheng H, Naseri T, Reupena MS, Viali S, Deka R, Hawley NL, McGarvey ST, et al. Improving imputation quality in Samoans through the integration of population-specific sequences into existing reference panels. Medrxiv : the Preprint Server For Health Sciences. PMID 37961708 DOI: 10.1101/2023.10.31.23297835 |
0.331 |
|
| 2023 |
Moors J, Krishnan M, Sumpter N, Takei R, Bixley M, Cadzow M, Major TJ, Phipps-Green A, Topless R, Merriman M, Rutledge M, Morgan B, Carlson JC, Zhang JZ, Russell EM, ... ... Deka R, et al. A Polynesianspecific missense CETP variant alters the lipid profile. Hgg Advances. 4: 100204. PMID 37250494 DOI: 10.1016/j.xhgg.2023.100204 |
0.349 |
|
| 2022 |
Carlson JC, Krishnan M, Rosenthal SL, Russell EM, Zhang JZ, Hawley NL, Moors J, Cheng H, Dalbeth N, de Zoysa JR, Watson H, Qasim M, Murphy R, Naseri T, Reupena MS, ... ... Deka R, et al. A stop-gain variant in is associated with atherogenic lipid profiles. Hgg Advances. 4: 100155. PMID 36340932 DOI: 10.1016/j.xhgg.2022.100155 |
0.322 |
|
| 2022 |
Taub MA, Conomos MP, Keener R, Iyer KR, Weinstock JS, Yanek LR, Lane J, Miller-Fleming TW, Brody JA, Raffield LM, McHugh CP, Jain D, Gogarten SM, Laurie CA, Keramati A, ... ... Deka R, et al. Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed. Cell Genomics. 2. PMID 35530816 DOI: 10.1016/j.xgen.2021.100084 |
0.378 |
|
| 2020 |
Carlson JC, Weeks DE, Hawley NL, Sun G, Cheng H, Naseri T, Reupena MS, Tuitele J, Deka R, McGarvey ST, Minster RL. Genome-wide association studies in Samoans give insight into the genetic architecture of fasting serum lipid levels. Journal of Human Genetics. PMID 32759990 DOI: 10.1038/S10038-020-0816-9 |
0.428 |
|
| 2020 |
Hawley NL, Pomer A, Rivara AC, Rosenthal SL, Duckham RL, Carlson JC, Naseri T, Reupena MS, Selu M, Lupematisila V, Unasa F, Vesi L, Fatu T, Unasa S, Faasalele-Savusa K, ... ... Deka R, et al. Exploring the Paradoxical Relationship of a Creb 3 Regulatory Factor Missense Variant With Body Mass Index and Diabetes Among Samoans: Protocol for the Soifua Manuia (Good Health) Observational Cohort Study. Jmir Research Protocols. 9: e17329. PMID 32706746 DOI: 10.2196/17329 |
0.346 |
|
| 2020 |
Harris DN, Kessler MD, Shetty AC, Weeks DE, Minster RL, Browning S, Cochrane EE, Deka R, Hawley NL, Reupena MS, Naseri T, McGarvey ST, O'Connor TD. Evolutionary history of modern Samoans. Proceedings of the National Academy of Sciences of the United States of America. PMID 32291332 DOI: 10.1073/Pnas.1913157117 |
0.388 |
|
| 2020 |
Carlson JC, Rosenthal SL, Russell EM, Hawley NL, Sun G, Cheng H, Naseri T, Reupena MS, Tuitele J, Deka R, McGarvey ST, Weeks DE, Minster RL. A missense variant in CREBRF is associated with taller stature in Samoans. American Journal of Human Biology : the Official Journal of the Human Biology Council. e23414. PMID 32190945 DOI: 10.1002/Ajhb.23414 |
0.364 |
|
| 2019 |
Chen A, Jandarov R, Zhou L, Calafat AM, Zhang G, Urbina EM, Sarac J, Augustin DH, Caric T, Bockor L, Petranovic MZ, Novokmet N, Missoni S, Rudan P, Deka R. Association of perfluoroalkyl substances exposure with cardiometabolic traits in an island population of the eastern Adriatic coast of Croatia. The Science of the Total Environment. 683: 29-36. PMID 31129329 DOI: 10.1016/J.Scitotenv.2019.05.250 |
0.351 |
|
| 2018 |
Krishnan M, Major TJ, Topless RK, Dewes O, Yu L, Thompson JMD, McCowan L, de Zoysa J, Stamp LK, Dalbeth N, Harré Hindmarsh J, Rapana N, Deka R, Eng WWH, Weeks DE, et al. Discordant association of the CREBRF rs373863828 A allele with increased BMI and protection from type 2 diabetes in Māori and Pacific (Polynesian) people living in Aotearoa/New Zealand. Diabetologia. PMID 29721634 DOI: 10.1007/S00125-018-4623-1 |
0.35 |
|
| 2017 |
Rej PH, Deka R, Norton HL. Understanding influences of culture and history on mtDNA variation and population structure in three populations from Assam, Northeast India. American Journal of Human Biology : the Official Journal of the Human Biology Council. PMID 28121389 DOI: 10.1002/Ajhb.22955 |
0.377 |
|
| 2016 |
Minster RL, Hawley NL, Su CT, Sun G, Kershaw EE, Cheng H, Buhule OD, Lin J, Reupena MS, Viali S, Tuitele J, Naseri T, Urban Z, Deka R, Weeks DE, et al. A thrifty variant in CREBRF strongly influences body mass index in Samoans. Nature Genetics. PMID 27455349 DOI: 10.1038/Ng.3620 |
0.456 |
|
| 2015 |
Radmanesh F, Falcone GJ, Anderson CD, McWilliams D, Devan WJ, Brown WM, Battey TW, Ayres AM, Raffeld MR, Schwab K, Sun G, Deka R, Viswanathan A, Goldstein JN, Greenberg SM, et al. Rare Coding Variation and Risk of Intracerebral Hemorrhage. Stroke; a Journal of Cerebral Circulation. PMID 26111891 DOI: 10.1161/Strokeaha.115.009838 |
0.307 |
|
| 2015 |
Rannikmäe K, Davies G, Thomson PA, Bevan S, Devan WJ, Falcone GJ, Traylor M, Anderson CD, Battey TW, Radmanesh F, Deka R, Woo JG, Martin LJ, Jimenez-Conde J, Selim M, et al. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology. 84: 918-26. PMID 25653287 DOI: 10.1212/Wnl.0000000000001309 |
0.306 |
|
| 2015 |
Kaulfers AM, Deka R, Dolan L, Martin LJ. Association of INSIG2 polymorphism with overweight and LDL in children. Plos One. 10: e0116340. PMID 25607990 DOI: 10.1371/Journal.Pone.0116340 |
0.394 |
|
| 2015 |
Mackey J, Brown RD, Sauerbeck L, Hornung R, Moomaw CJ, Koller DL, Foroud T, Deka R, Woo D, Kleindorfer D, Flaherty ML, Meissner I, Anderson C, Rouleau G, Connolly ES, et al. Affected twins in the familial intracranial aneurysm study. Cerebrovascular Diseases (Basel, Switzerland). 39: 82-6. PMID 25571891 DOI: 10.1159/000369961 |
0.311 |
|
| 2014 |
Buhule OD, Minster RL, Hawley NL, Medvedovic M, Sun G, Viali S, Deka R, McGarvey ST, Weeks DE. Stratified randomization controls better for batch effects in 450K methylation analysis: a cautionary tale. Frontiers in Genetics. 5: 354. PMID 25352862 DOI: 10.3389/Fgene.2014.00354 |
0.319 |
|
| 2014 |
Hawley NL, Minster RL, Weeks DE, Viali S, Reupena MS, Sun G, Cheng H, Deka R, Mcgarvey ST. Prevalence of adiposity and associated cardiometabolic risk factors in the Samoan genome-wide association study. American Journal of Human Biology : the Official Journal of the Human Biology Council. 26: 491-501. PMID 24799123 DOI: 10.1002/Ajhb.22553 |
0.335 |
|
| 2014 |
Woo D, Falcone GJ, Devan WJ, Brown WM, Biffi A, Howard TD, Anderson CD, Brouwers HB, Valant V, Battey TW, Radmanesh F, Raffeld MR, Baedorf-Kassis S, Deka R, Woo JG, et al. Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. American Journal of Human Genetics. 94: 511-21. PMID 24656865 DOI: 10.1016/J.Ajhg.2014.02.012 |
0.412 |
|
| 2013 |
Karns R, Succop P, Zhang G, Sun G, Indugula SR, Havas-Augustin D, Novokmet N, Durakovic Z, Milanovic SM, Missoni S, Vuletic S, Chakraborty R, Rudan P, Deka R. Modeling metabolic syndrome through structural equations of metabolic traits, comorbid diseases, and GWAS variants. Obesity (Silver Spring, Md.). 21: E745-54. PMID 23512735 DOI: 10.1002/Oby.20445 |
0.594 |
|
| 2013 |
Baylin A, Deka R, Tuitele J, Viali S, Weeks DE, Mcgarvey ST. INSIG2 variants, dietary patterns and metabolic risk in Samoa European Journal of Clinical Nutrition. 67: 101-107. PMID 22968099 DOI: 10.1038/Ejcn.2012.124 |
0.418 |
|
| 2012 |
Zhang G, Karns R, Sun G, Indugula SR, Cheng H, Havas-Augustin D, Novokmet N, Durakovic Z, Missoni S, Chakraborty R, Rudan P, Deka R. Finding missing heritability in less significant Loci and allelic heterogeneity: genetic variation in human height. Plos One. 7: e51211. PMID 23251454 DOI: 10.1371/Journal.Pone.0051211 |
0.707 |
|
| 2012 |
Martini SR, Flaherty ML, Brown WM, Haverbusch M, Comeau ME, Sauerbeck LR, Kissela BM, Deka R, Kleindorfer DO, Moomaw CJ, Broderick JP, Langefeld CD, Woo D. Risk factors for intracerebral hemorrhage differ according to hemorrhage location. Neurology. 79: 2275-82. PMID 23175721 DOI: 10.1212/Wnl.0B013E318276896F |
0.303 |
|
| 2012 |
Kansra AR, Dolan LM, Martin LJ, Deka R, Chernausek SD. IGF receptor gene variants in normal adolescents: effect on stature. European Journal of Endocrinology / European Federation of Endocrine Societies. 167: 777-81. PMID 22972910 DOI: 10.1530/Eje-12-0565 |
0.368 |
|
| 2012 |
Foroud T, Koller DL, Lai D, Sauerbeck L, Anderson C, Ko N, Deka R, Mosley TH, Fornage M, Woo D, Moomaw CJ, Hornung R, Huston J, Meissner I, Bailey-Wilson JE, et al. Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk. Stroke; a Journal of Cerebral Circulation. 43: 2846-52. PMID 22961961 DOI: 10.1161/Strokeaha.112.656397 |
0.356 |
|
| 2012 |
Woo JG, Martin LJ, Ding L, Brown WM, Howard TD, Langefeld CD, Moomaw CJ, Haverbusch M, Sun G, Indugula SR, Cheng H, Deka R, Woo D. Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis. Bmc Genetics. 13: 75. PMID 22920755 DOI: 10.1186/1471-2156-13-75 |
0.352 |
|
| 2012 |
Aslibekyan S, Jensen MK, Campos H, Linkletter CD, Loucks EB, Ordovas JM, Deka R, Rimm EB, Baylin A. Fatty Acid desaturase gene variants, cardiovascular risk factors, and myocardial infarction in the costa rica study. Frontiers in Genetics. 3: 72. PMID 22563332 DOI: 10.3389/Fgene.2012.00072 |
0.336 |
|
| 2012 |
Aslibekyan S, Jensen MK, Campos H, Linkletter CD, Loucks EB, Ordovas JM, Deka R, Rimm EB, Baylin A. Genetic variation in fatty acid elongases is not associated with intermediate cardiovascular phenotypes or myocardial infarction European Journal of Clinical Nutrition. 66: 353-359. PMID 22293571 DOI: 10.1038/Ejcn.2012.2 |
0.403 |
|
| 2012 |
Karns R, Zhang G, Sun G, Rao Indugula S, Cheng H, Havas-Augustin D, Novokmet N, Rudan D, Durakovic Z, Missoni S, Chakraborty R, Rudan P, Deka R. Genome-wide association of serum uric acid concentration: replication of sequence variants in an island population of the Adriatic coast of Croatia. Annals of Human Genetics. 76: 121-7. PMID 22229870 DOI: 10.1111/J.1469-1809.2011.00698.X |
0.679 |
|
| 2012 |
Deka R, Durakovic Z, Niu W, Zhang G, Karns R, Smolej-Narancic N, Missoni S, Caric D, Caric T, Rudan D, Salzer B, Chakraborty R, Rudan P. Prevalence of metabolic syndrome and related metabolic traits in an island population of the Adriatic Annals of Human Biology. 39: 46-53. PMID 22149059 DOI: 10.3109/03014460.2011.637512 |
0.615 |
|
| 2012 |
Karns R, Viali S, Tuitele J, Sun G, Cheng H, Weeks DE, McGarvey ST, Deka R. Common variants in FTO are not significantly associated with obesity-related phenotypes among Samoans of Polynesia. Annals of Human Genetics. 76: 17-24. PMID 22084931 DOI: 10.1111/J.1469-1809.2011.00686.X |
0.672 |
|
| 2011 |
Zhang G, Karns R, Sun G, Indugula SR, Cheng H, Havas-Augustin D, Novokmet N, Rudan D, Durakovic Z, Missoni S, Chakraborty R, Rudan P, Deka R. Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia. Plos One. 6: e29475. PMID 22216288 DOI: 10.1371/Journal.Pone.0029475 |
0.691 |
|
| 2011 |
Young KL, Sun G, Deka R, Crawford MH. Paternal genetic history of the Basque population of Spain. Human Biology. 83: 455-75. PMID 21846204 DOI: 10.3378/027.083.0402 |
0.457 |
|
| 2011 |
Young KL, Sun G, Deka R, Crawford MH. Autosomal short tandem repeat genetic variation of the Basques in Spain. Croatian Medical Journal. 52: 372-83. PMID 21674834 DOI: 10.3325/Cmj.2011.52.372 |
0.463 |
|
| 2011 |
Karns R, Zhang G, Jeran N, Havas-Augustin D, Missoni S, Niu W, Indugula SR, Sun G, Durakovic Z, Narancic NS, Rudan P, Chakraborty R, Deka R. Replication of genetic variants from genome-wide association studies with metabolic traits in an island population of the Adriatic coast of Croatia. European Journal of Human Genetics : Ejhg. 19: 341-6. PMID 21150882 DOI: 10.1038/Ejhg.2010.178 |
0.708 |
|
| 2010 |
Rubicz R, Zlojutro M, Sun G, Spitsyn V, Deka R, Young KL, Crawford MH. Genetic architecture of a small, recently aggregated Aleut population: Bering Island, Russia. Human Biology. 82: 719-36. PMID 21417891 DOI: 10.3378/027.082.0512 |
0.428 |
|
| 2010 |
Zhang G, Karns R, Narancic NS, Sun G, Cheng H, Missoni S, Durakovic Z, Rudan P, Chakraborty R, Deka R. Common SNPs in FTO gene are associated with obesity related anthropometric traits in an island population from the eastern Adriatic coast of Croatia. Plos One. 5: e10375. PMID 20442772 DOI: 10.1371/Journal.Pone.0010375 |
0.659 |
|
| 2010 |
Bollepalli S, Dolan LM, Deka R, Martin LJ. Association of FTO gene variants with adiposity in African-American adolescents. Obesity (Silver Spring, Md.). 18: 1959-63. PMID 20379142 DOI: 10.1038/Oby.2010.82 |
0.439 |
|
| 2010 |
Rubicz R, Melton PE, Spitsyn V, Sun G, Deka R, Crawford MH. Genetic structure of native circumpolar populations based on autosomal, mitochondrial, and Y chromosome DNA markers. American Journal of Physical Anthropology. 143: 62-74. PMID 20333712 DOI: 10.1002/Ajpa.21290 |
0.447 |
|
| 2010 |
Deka R, Koller DL, Lai D, Indugula SR, Sun G, Woo D, Sauerbeck L, Moomaw CJ, Hornung R, Connolly ES, Anderson C, Rouleau G, Meissner I, Bailey-Wilson JE, Huston J, et al. The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm. Stroke; a Journal of Cerebral Circulation. 41: 1132-7. PMID 20190001 DOI: 10.1161/Strokeaha.109.574640 |
0.338 |
|
| 2010 |
Jorge-Nebert LF, Jiang Z, Chakraborty R, Watson J, Jin L, McGarvey ST, Deka R, Nebert DW. Analysis of human CYP1A1 and CYP1A2 genes and their shared bidirectional promoter in eight world populations. Human Mutation. 31: 27-40. PMID 19802894 DOI: 10.1002/Humu.21132 |
0.41 |
|
| 2009 |
Deka R, Xu L, Pal P, Toelupe PT, Laumoli TS, Xi H, Zhang G, Weeks DE, McGarvey ST. A tagging SNP in INSIG2 is associated with obesity-related phenotypes among Samoans. Bmc Medical Genetics. 10: 143. PMID 20028541 DOI: 10.1186/1471-2350-10-143 |
0.415 |
|
| 2009 |
Aberg K, Dai F, Viali S, Tuitele J, Sun G, Indugula SR, Deka R, Weeks DE, McGarvey ST. Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands. Bmc Medical Genetics. 10: 107. PMID 19852796 DOI: 10.1186/1471-2350-10-107 |
0.307 |
|
| 2009 |
Pal P, Mihanović M, Molnar S, Xi H, Sun G, Guha S, Jeran N, Tomljenović A, Malnar A, Missoni S, Deka R, Rudan P. Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population. Croatian Medical Journal. 50: 361-9. PMID 19673036 DOI: 10.3325/Cmj.2009.50.361 |
0.391 |
|
| 2009 |
Pal P, Xi H, Guha S, Sun G, Helfand BT, Meeks JJ, Suarez BK, Catalona WJ, Deka R. Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry. The Prostate. 69: 1548-56. PMID 19562729 DOI: 10.1002/Pros.20999 |
0.33 |
|
| 2009 |
Aberg K, Dai F, Sun G, Keighley ED, Indugula SR, Roberts ST, Zhang Q, Smelser D, Viali S, Tuitele J, Jin L, Deka R, Weeks DE, McGarvey ST. Susceptibility loci for adiposity phenotypes on 8p, 9p, and 16q in American Samoa and Samoa. Obesity (Silver Spring, Md.). 17: 518-24. PMID 19238140 DOI: 10.1038/Oby.2008.558 |
0.72 |
|
| 2009 |
Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Langefeld C, Rouleau G, Connolly ES, Lai D, et al. Genome screen in familial intracranial aneurysm. Bmc Medical Genetics. 10: 3. PMID 19144135 DOI: 10.1186/1471-2350-10-3 |
0.31 |
|
| 2008 |
Aberg K, Sun G, Smelser D, Indugula SR, Tsai HJ, Steele MS, Tuitele J, Deka R, McGarvey ST, Weeks DE. Applying novel genome-wide linkage strategies to search for loci influencing type 2 diabetes and adult height in American Samoa. Human Biology. 80: 99-123. PMID 18720898 DOI: 10.3378/1534-6617(2008)80[99:Anglst]2.0.Co;2 |
0.721 |
|
| 2008 |
Dai F, Sun G, Åberg K, Keighley ED, Indugula SR, Roberts ST, Smelser D, Viali S, Jin L, Deka R, Weeks DE, McGarvey ST. A whole genome linkage scan identifies multiple chromosomal regions influencing adiposity-related traits among Samoans. Annals of Human Genetics. 72: 780-792. PMID 18616661 DOI: 10.1111/J.1469-1809.2008.00462.X |
0.723 |
|
| 2008 |
Aberg K, Dai F, Sun G, Keighley E, Indugula SR, Bausserman L, Viali S, Tuitele J, Deka R, Weeks DE, McGarvey ST. A genome-wide linkage scan identifies multiple chromosomal regions influencing serum lipid levels in the population on the Samoan islands. Journal of Lipid Research. 49: 2169-78. PMID 18594117 DOI: 10.1194/Jlr.M800194-Jlr200 |
0.368 |
|
| 2008 |
Li H, Wen B, Chen SJ, Su B, Pramoonjago P, Liu Y, Pan S, Qin Z, Liu W, Cheng X, Yang N, Li X, Tran D, Lu D, Hsu MT, ... Deka R, et al. Paternal genetic affinity between Western Austronesians and Daic populations. Bmc Evolutionary Biology. 8: 146. PMID 18482451 DOI: 10.1186/1471-2148-8-146 |
0.377 |
|
| 2008 |
Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Rouleau G, Connolly ES, Lai D, Koller DL, et al. Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study. Stroke; a Journal of Cerebral Circulation. 39: 1434-40. PMID 18323491 DOI: 10.1161/Strokeaha.107.502930 |
0.342 |
|
| 2008 |
Xue F, Wang Y, Xu S, Zhang F, Wen B, Wu X, Lu M, Deka R, Qian J, Jin L. A spatial analysis of genetic structure of human populations in China reveals distinct difference between maternal and paternal lineages. European Journal of Human Genetics : Ejhg. 16: 705-17. PMID 18212820 DOI: 10.1038/Sj.Ejhg.5201998 |
0.414 |
|
| 2008 |
Kalra M, Pal P, Kaushal R, Amin RS, Dolan LM, Fitz K, Kumar S, Sheng X, Guha S, Mallik J, Deka R, Chakraborty R. Association of ApoE genetic variants with obstructive sleep apnea in children. Sleep Medicine. 9: 260-5. PMID 17658295 DOI: 10.1016/J.Sleep.2007.05.001 |
0.365 |
|
| 2008 |
Pal P, Xi H, Guha S, Sun G, Helfand BT, Meeks JJ, Suarez BK, Catalona WJ, Deka R. GENETIC VARIATION ON 8q24 AND SUSCEPTIBILITY TO PROSTATE CANCER IN CAUCASIAN MEN Journal of Urology. 179: 226-226. DOI: 10.1016/S0022-5347(08)60653-9 |
0.313 |
|
| 2007 |
Woo JG, Sun G, Haverbusch M, Indugula S, Martin LJ, Broderick JP, Deka R, Woo D. Quality assessment of buccal versus blood genomic DNA using the Affymetrix 500 K GeneChip. Bmc Genetics. 8: 79. PMID 17996058 DOI: 10.1186/1471-2156-8-79 |
0.303 |
|
| 2007 |
Crimmins NA, Woo JG, Kaushal RD, Deka R, Dolan LM, Martin LJ. Adiponectin receptor 1 variants associated with lower insulin resistance in African Americans. Obesity (Silver Spring, Md.). 15: 1903-7. PMID 17712104 DOI: 10.1038/Oby.2007.225 |
0.35 |
|
| 2007 |
Kaushal R, Woo D, Pal P, Haverbusch M, Xi H, Moomaw C, Sekar P, Kissela B, Kleindorfer D, Flaherty M, Sauerbeck L, Chakraborty R, Broderick J, Deka R. Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes. Bmc Medical Genetics. 8: 49. PMID 17672902 DOI: 10.1186/1471-2350-8-49 |
0.445 |
|
| 2007 |
Dai F, Keighley ED, Sun G, Indugula SR, Roberts ST, Aberg K, Smelser D, Tuitele J, Jin L, Deka R, Weeks DE, McGarvey ST. Genome-wide scan for adiposity-related phenotypes in adults from American Samoa International Journal of Obesity. 31: 1832-1842. PMID 17621312 DOI: 10.1038/Sj.Ijo.0803675 |
0.703 |
|
| 2007 |
Pal P, Xi H, Sun G, Kaushal R, Meeks JJ, Thaxton CS, Guha S, Jin CH, Suarez BK, Catalona WJ, Deka R. Tagging SNPs in the kallikrein genes 3 and 2 on 19q13 and their associations with prostate cancer in men of European origin. Human Genetics. 122: 251-9. PMID 17593395 DOI: 10.1007/S00439-007-0394-3 |
0.348 |
|
| 2007 |
Bauchet M, McEvoy B, Pearson LN, Quillen EE, Sarkisian T, Hovhannesyan K, Deka R, Bradley DG, Shriver MD. Measuring European population stratification with microarray genotype data. American Journal of Human Genetics. 80: 948-56. PMID 17436249 DOI: 10.1086/513477 |
0.475 |
|
| 2007 |
Kaushal R, Pal P, Alwell K, Haverbusch M, Flaherty M, Moomaw C, Sekar P, Kissela B, Kleindorfer D, Chakraborty R, Broderick J, Deka R, Woo D. Association of ALOX5AP with ischemic stroke: a population-based case-control study. Human Genetics. 121: 601-7. PMID 17387518 DOI: 10.1007/S00439-007-0338-Y |
0.328 |
|
| 2006 |
Pal P, Xi H, Kaushal R, Sun G, Jin CH, Jin L, Suarez BK, Catalona WJ, Deka R. Variants in the HEPSIN gene are associated with prostate cancer in men of European origin. Human Genetics. 120: 187-92. PMID 16783571 DOI: 10.1007/S00439-006-0204-3 |
0.304 |
|
| 2006 |
Woo JG, Dolan LM, Deka R, Kaushal RD, Shen Y, Pal P, Daniels SR, Martin LJ. Interactions between noncontiguous haplotypes in the adiponectin gene ACDC are associated with plasma adiponectin. Diabetes. 55: 523-9. PMID 16443790 DOI: 10.2337/Diabetes.55.02.06.Db05-0446 |
0.409 |
|
| 2006 |
Woo D, Kaushal R, Kissela B, Sekar P, Wolujewicz M, Pal P, Alwell K, Haverbusch M, Ewing I, Miller R, Kleindorfer D, Flaherty M, Chakraborty R, Deka R, Broderick J. Association of Phosphodiesterase 4D with ischemic stroke: a population-based case-control study. Stroke; a Journal of Cerebral Circulation. 37: 371-6. PMID 16373644 DOI: 10.1161/01.Str.0000198843.72824.0A |
0.342 |
|
| 2006 |
Brzezinski JL, Deka R, Menon AG, Glass DN, Choi E. Variability in TRBV haplotype frequency and composition in Caucasian, African American, Western African and Chinese populations. International Journal of Immunogenetics. 32: 413-20. PMID 16313308 DOI: 10.1111/J.1744-313X.2005.00550.X |
0.417 |
|
| 2005 |
Woo D, Sekar P, Chakraborty R, Haverbusch MA, Flaherty ML, Kissela BM, Kleindorfer D, Schneider A, Khoury J, Sauerbeck LR, Deka R, Broderick JP. Genetic epidemiology of intracerebral hemorrhage. Journal of Stroke and Cerebrovascular Diseases : the Official Journal of National Stroke Association. 14: 239-43. PMID 16557295 DOI: 10.1016/J.Jstrokecerebrovasdis.2005.08.002 |
0.326 |
|
| 2005 |
Klarić IM, Pericić M, Lauc LB, Janićijević B, Kubat M, Pavicić D, Rudan I, Wang N, Jin L, Chakraborty R, Deka R, Rudan P. Genetic variation at nine short tandem repeat loci among islanders of the eastern Adriatic coast of Croatia. Human Biology. 77: 471-86. PMID 16485777 DOI: 10.1353/Hub.2005.0065 |
0.475 |
|
| 2005 |
Woo D, Kaushal R, Chakraborty R, Woo J, Haverbusch M, Sekar P, Kissela B, Pancioli A, Jauch E, Kleindorfer D, Flaherty M, Schneider A, Khatri P, Sauerbeck L, Khoury J, ... Deka R, et al. Association of apolipoprotein E4 and haplotypes of the apolipoprotein E gene with lobar intracerebral hemorrhage. Stroke; a Journal of Cerebral Circulation. 36: 1874-9. PMID 16100021 DOI: 10.1161/01.Str.0000177891.15082.B9 |
0.339 |
|
| 2005 |
Sun G, Kaushal R, Pal P, Wolujewicz M, Smelser D, Cheng H, Lu M, Chakraborty R, Jin L, Deka R. Whole-genome amplification: relative efficiencies of the current methods. Legal Medicine (Tokyo, Japan). 7: 279-86. PMID 15990351 DOI: 10.1016/J.Legalmed.2005.05.001 |
0.702 |
|
| 2005 |
Jiang Z, Zhang X, Deka R, Jin L. Genome amplification of single sperm using multiple displacement amplification. Nucleic Acids Research. 33: e91. PMID 15942023 DOI: 10.1093/Nar/Gni089 |
0.35 |
|
| 2005 |
Friedlaender J, Schurr T, Gentz F, Koki G, Friedlaender F, Horvat G, Babb P, Cerchio S, Kaestle F, Schanfield M, Deka R, Yanagihara R, Merriwether DA. Expanding Southwest Pacific mitochondrial haplogroups P and Q. Molecular Biology and Evolution. 22: 1506-17. PMID 15814828 DOI: 10.1093/Molbev/Msi142 |
0.316 |
|
| 2005 |
Jiang Z, Dalton TP, Jin L, Wang B, Tsuneoka Y, Shertzer HG, Deka R, Nebert DW. Toward the evaluation of function in genetic variability: characterizing human SNP frequencies and establishing BAC-transgenic mice carrying the human CYP1A1_CYP1A2 locus. Human Mutation. 25: 196-206. PMID 15643613 DOI: 10.1002/Humu.20134 |
0.355 |
|
| 2005 |
Wen B, Li H, Gao S, Mao X, Gao Y, Li F, Zhang F, He Y, Dong Y, Zhang Y, Huang W, Jin J, Xiao C, Lu D, Chakraborty R, ... ... Deka R, et al. Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages. Molecular Biology and Evolution. 22: 725-34. PMID 15548747 DOI: 10.1093/Molbev/Msi055 |
0.362 |
|
| 2004 |
Tsai HJ, Sun G, Smelser D, Viali S, Tufa J, Jin L, Weeks DE, McGarvey ST, Deka R. Distribution of genome-wide linkage disequilibrium based on microsatellite loci in the Samoan population. Human Genomics. 1: 327-34. PMID 15588493 DOI: 10.1186/1479-7364-1-5-327 |
0.735 |
|
| 2003 |
Rudan I, Rudan D, Campbell H, Carothers A, Wright A, Smolej-Narancic N, Janicijevic B, Jin L, Chakraborty R, Deka R, Rudan P. Inbreeding and risk of late onset complex disease Journal of Medical Genetics. 40: 925-932. PMID 14684692 DOI: 10.1136/Jmg.40.12.925 |
0.333 |
|
| 2003 |
Sun G, McGarvey ST, Bayoumi R, Mulligan CJ, Barrantes R, Raskin S, Zhong Y, Akey J, Chakraborty R, Deka R. Global genetic variation at nine short tandem repeat loci and implications on forensic genetics. European Journal of Human Genetics : Ejhg. 11: 39-49. PMID 12529704 DOI: 10.1038/Sj.Ejhg.5200902 |
0.485 |
|
| 2002 |
Cerda-Flores RM, Budowle B, Jin L, Barton SA, Deka R, Chakraborty R. Maximum likelihood estimates of admixture in Northeastern Mexico using 13 short tandem repeat loci. American Journal of Human Biology : the Official Journal of the Human Biology Council. 14: 429-39. PMID 12112564 DOI: 10.1002/Ajhb.10058 |
0.42 |
|
| 2002 |
Moffett S, Martinson J, Shriver MD, Deka R, McGarvey ST, Barrantes R, Ferrell RE. Genetic diversity and evolution of the human leptin locus tetranucleotide repeat. Human Genetics. 110: 412-7. PMID 12073010 DOI: 10.1007/S00439-002-0715-5 |
0.487 |
|
| 2002 |
McGarvey S, Forrest W, Weeks D, Sun G, Smelser D, Tufa J, Viali S, Deka R. Human leptin locus (LEP) alleles and BMI in Samoans. International Journal of Obesity. 26: 783-788. PMID 12037648 DOI: 10.1038/Sj.Ijo.0801996 |
0.726 |
|
| 2002 |
Woo D, Sauerbeck LR, Kissela BM, Khoury JC, Szaflarski JP, Gebel J, Shukla R, Pancioli AM, Jauch EC, Menon AG, Deka R, Carrozzella JA, Moomaw CJ, Fontaine RN, Broderick JP. Genetic and environmental risk factors for intracerebral hemorrhage: preliminary results of a population-based study. Stroke; a Journal of Cerebral Circulation. 33: 1190-5. PMID 11988589 DOI: 10.1161/01.Str.0000014774.88027.22 |
0.373 |
|
| 2002 |
Dutta R, Reddy BM, Chattopadhyay P, Kashyap VK, Sun G, Deka R. Patterns of genetic diversity at the nine forensically approved STR loci in the Indian populations. Human Biology. 74: 33-49. PMID 11931578 DOI: 10.1353/Hub.2002.0002 |
0.443 |
|
| 2001 |
Tsai H, Sun G, Weeks DE, Kaushal R, Wolujewicz M, McGarvey ST, Tufa J, Viali S, Deka R. Type 2 Diabetes and Three Calpain-10 Gene Polymorphisms in Samoans: No Evidence of Association American Journal of Human Genetics. 69: 1236-1244. PMID 11704924 DOI: 10.1086/324646 |
0.419 |
|
| 2001 |
Reddy BM, Sun G, Luis JR, Crawford MH, Hemam NS, Deka R. Genomic Diversity at Thirteen Short Tandem Repeat Loci in a Substructured Caste Population, Golla, of Southern Andhra Pradesh, India Human Biology. 73: 175-190. PMID 11446423 DOI: 10.1353/Hub.2001.0025 |
0.38 |
|
| 2001 |
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, et al. African origin of modern humans in East Asia: A tale of 12,000 Y chromosomes Science. 292: 1151-1153. PMID 11349147 DOI: 10.1126/Science.1060011 |
0.319 |
|
| 2001 |
Reddy B, Sun G, Ranjan D, Deka R. STR data for the Amp FlSTR Profiler Plus loci among Golla population of southern Andhra Pradesh, India. Journal of Forensic Sciences. 46: 734-735. DOI: 10.1520/Jfs15034J |
0.392 |
|
| 2000 |
Su B, Xiao C, Deka R, Seielstad MT, Kangwanpong D, Xiao J, Lu D, Underhill P, Cavalli-Sforza L, Chakraborty R, Jin L. Y chromosome haplotypes reveal prehistorical migrations to the Himalayas. Human Genetics. 107: 582-590. PMID 11153912 DOI: 10.1007/S004390000406 |
0.431 |
|
| 2000 |
Su B, Jin L, Underbill P, Martinson J, Saha N, McGarvey ST, Shriver MD, Chu J, Oefner P, Chakraborty R, Deka R. Polynesian origins: Insights from the Y chromosome Proceedings of the National Academy of Sciences of the United States of America. 97: 8225-8228. PMID 10899994 DOI: 10.1073/Pnas.97.15.8225 |
0.415 |
|
| 1999 |
Su B, Xiao J, Underhill P, Deka R, Zhang W, Akey J, Huang W, Shen D, Lu D, Luo J, Chu J, Tan J, Shen P, Davis R, Cavalli-Sforza L, et al. Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age. American Journal of Human Genetics. 65: 1718-24. PMID 10577926 DOI: 10.1086/302680 |
0.339 |
|
| 1999 |
Deka R, Guangyun S, Smelser D, Zhong Y, Kimmel M, Chakraborty R. Rate and directionality of mutations and effects of allele size constraints at anonymous, gene-associated, and disease-causing trinucleotide loci. Molecular Biology and Evolution. 16: 1166-77. PMID 10486972 DOI: 10.1093/Oxfordjournals.Molbev.A026207 |
0.746 |
|
| 1999 |
Deka R, Guangyun S, Wiest J, Smelser D, Chunhua S, Zhong Y, Chakraborty R. Patterns of Instability of Expanded CAG Repeats at the ERDA1 Locus in General Populations American Journal of Human Genetics. 65: 192-198. PMID 10364532 DOI: 10.1086/302453 |
0.726 |
|
| 1999 |
Deka R, Shriver MD, Yu LM, Heidreich EM, Jin L, Zhong Y, McGarvey ST, Agarwal SS, Bunker CH, Miki T, Hundrieser J, Yin SJ, Raskin S, Barrantes R, Ferrell RE, et al. Genetic variation at twentythree microsatellite loci in sixteen human populations Journal of Genetics. 78: 99-121. DOI: 10.1007/Bf02924561 |
0.456 |
|
| 1998 |
Parra EJ, Marcini A, Akey J, Martinson J, Batzer MA, Cooper R, Forrester T, Allison DB, Deka R, Ferrell RE, Shriver MD. Estimating African American admixture proportions by use of population-specific alleles. American Journal of Human Genetics. 63: 1839-51. PMID 9837836 DOI: 10.1086/302148 |
0.453 |
|
| 1998 |
Pogue-Geile M, Ferrell R, Deka R, Debski T, Manuck S. Human novelty-seeking personality traits and dopamine D4 receptor polymorphisms: a twin and genetic association study. American Journal of Medical Genetics. 81: 44-8. PMID 9514587 DOI: 10.1002/(Sici)1096-8628(19980207)81:1<44::Aid-Ajmg9>3.0.Co;2-N |
0.405 |
|
| 1998 |
Polański A, Chakraborty R, Kimmel M, Deka R. Dynamic balance of segregation distortion and selection maintains normal allele sizes at the myotonic dystrophy locus. Mathematical Biosciences. 147: 93-112. PMID 9401353 DOI: 10.1016/S0025-5564(97)00082-5 |
0.4 |
|
| 1997 |
Shriver MD, Jin L, Ferrell RE, Deka R. Microsatellite data support an early population expansion in Africa Genome Research. 7: 586-591. PMID 9199931 DOI: 10.1101/Gr.7.6.586 |
0.385 |
|
| 1997 |
Chakraborty R, Kimmel M, Stivers DN, Davison LJ, Deka R. Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci. Proceedings of the National Academy of Sciences of the United States of America. 94: 1041-6. PMID 9023379 DOI: 10.1073/Pnas.94.3.1041 |
0.306 |
|
| 1996 |
Deka R, Jin L, Shriver MD, Yu LM, Saha N, Barrantes R, Chakraborty R, Ferrell RE. Dispersion of human Y chromosome haplotypes based on five microsatellites in global populations. Genome Research. 6: 1177-84. PMID 8973912 DOI: 10.1101/Gr.6.12.1177 |
0.461 |
|
| 1996 |
Deka R, Majumder PP, Shriver MD, Stivers DN, Zhong Y, Yu LM, Barrantes R, Yin SJ, Miki T, Hundrieser J, Bunker CH, McGarvey ST, Sakallah S, Ferrell RE, Chakraborty R. Distribution and evolution of CTG repeats at the myotonin protein kinase gene in human populations. Genome Research. 6: 142-54. PMID 8919693 DOI: 10.1101/Gr.6.2.142 |
0.478 |
|
| 1996 |
Yamagata H, Miki T, Nakagawa M, Johnson K, Deka R, Ogihara T. Association of CTG repeats and the 1-kb Alu insertion/deletion polymorphism at the myotonin protein kinase gene in the Japanese population suggests a common Eurasian origin of the myotonic dystrophy mutation. Human Genetics. 97: 145-147. PMID 8566943 DOI: 10.1007/Bf02265255 |
0.457 |
|
| 1995 |
Vanyukov MM, Moss HB, Yu LM, Deka R. A dinucleotide repeat polymorphism at the gene for monoamine oxidase A and measures of aggressiveness. Psychiatry Research. 59: 35-41. PMID 8771218 DOI: 10.1016/0165-1781(95)02719-X |
0.352 |
|
| 1995 |
Deka R, Shriver MD, Yu LM, Ferrell RE, Chakraborty R. Intra- and inter-population diversity at short tandem repeat loci in diverse populations of the world. Electrophoresis. 16: 1659-64. PMID 8582352 DOI: 10.1002/Elps.11501601275 |
0.418 |
|
| 1995 |
Vanyukov MM, Moss HB, Yu LM, Tarter RE, Deka R. Preliminary evidence for an association of a dinucleotide repeat polymorphism at the MAOA gene with early onset alcoholism/substance abuse. American Journal of Medical Genetics. 60: 122-6. PMID 7485245 DOI: 10.1002/Ajmg.1320600207 |
0.323 |
|
| 1995 |
Shriver MD, Jin L, Boerwinkle E, Deka R, Ferrell RE, Chakraborty R. A novel measure of genetic distance for highly polymorphic tandem repeat loci. Molecular Biology and Evolution. 12: 914-20. PMID 7476137 DOI: 10.1093/Oxfordjournals.Molbev.A040268 |
0.438 |
|
| 1994 |
Deka R, DeCroo S, Jin L, McGarvey ST, Rothhammer F, Ferrell RE, Chakraborty R. Population Genetic Characteristics of the D1S80 locus in seven human populations Human Genetics. 94: 252-258. PMID 8076940 DOI: 10.1007/Bf00208279 |
0.478 |
|
| 1994 |
Deka R, Shriver MD, Yu LM, Jin L, Aston CE, Chakraborty R, Ferrell RE. Conservation of human chromosome 13 polymorphic microsatellite (CA)n repeats in chimpanzees. Genomics. 22: 226-30. PMID 7959776 DOI: 10.1006/Geno.1994.1369 |
0.398 |
|
| 1994 |
Finegold DN, Armitage MM, Galiani M, Matise TC, Pandian MR, Perry YM, Deka R, Ferrell RE. Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13. Pediatric Research. 36: 414-7. PMID 7808841 DOI: 10.1203/00006450-199409000-00024 |
0.345 |
|
| 1992 |
Chakraborty R, Deka R, Jin L, Ferrell RE. Allele sharing at six VNTR loci and genetic distances among three ethnically defined human populations. American Journal of Human Biology : the Official Journal of the Human Biology Council. 4: 387-397. PMID 28524310 DOI: 10.1002/Ajhb.1310040315 |
0.479 |
|
| 1992 |
Deka R, Chakroborty R, Ferrell RE. A population genetic study of six VNTR loci in three ethnically defined populations. Genomics. 11: 83-92. PMID 1765387 DOI: 10.1016/0888-7543(91)90104-M |
0.485 |
|
| 1992 |
Steele MW, Wenger SL, Deka R, Mulvihill JJ, Sukarachana K. Genetic analyses on a set of parasitic conjoined twins. American Journal of Medical Genetics. 42: 856. PMID 1554027 DOI: 10.1002/Ajmg.1320420626 |
0.307 |
|
| 1992 |
Ely J, Deka R, Chakraborty R, Ferrell RE. Comparison of five tandem repeat loci between humans and chimpanzees. Genomics. 14: 692-8. PMID 1427897 DOI: 10.1016/S0888-7543(05)80170-3 |
0.424 |
|
| 1992 |
Deka R, De Croo S, Yu LM, Ferrell RE. Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations. Human Genetics. 90: 86-90. PMID 1427793 DOI: 10.1007/Bf00210749 |
0.448 |
|
| 1990 |
Laig M, Pape M, Hundrieser J, Flatz G, Sanguansermsri T, Das BM, Deka R, Yongvanit P, Mularlee N. The distribution of the Hb constant spring gene in Southeast Asian populations. Human Genetics. 84: 188-90. PMID 2298455 DOI: 10.1007/Bf00208939 |
0.346 |
|
| 1988 |
Deka R, Reddy AP, Mukherjee BN, Das BM, Banerjee S, Roy M, Dey B, Malhotra KC, Walter H. Hemoglobin E distribution in ten endogamous population groups of Assam, India. Human Heredity. 38: 261-6. PMID 3235091 DOI: 10.1159/000153796 |
0.339 |
|
| 1988 |
Hundrieser J, Deka R, Gogoi BC, Papp T, Flatz G. DNA haplotypes and frameworks associated with the beta-globin gene in the Kachari population of Assam (India). Human Heredity. 38: 240-245. PMID 3169799 DOI: 10.1159/000153791 |
0.324 |
|
| 1986 |
Walter H, Mukherjee BN, Gilbert K, Lindenberg P, Dannewitz A, Malhotra KC, Das BM, Deka R. Investigations on the variability of haptoglobin, transferrin and Gc polymorphisms in Assam, India. Human Heredity. 36: 388-96. PMID 3793118 DOI: 10.1159/000153663 |
0.444 |
|
| 1981 |
Deka R. Fertility and haemoglobin genotypes: A population study in upper Assam (India) Human Genetics. 59: 172-174. PMID 7199022 DOI: 10.1007/Bf00293071 |
0.37 |
|
| 1975 |
Das BM, Deka R. Predominance of the haemoglobin E gene in a Mongoloid population in Assam (India). Humangenetik. 30: 187-91. PMID 1193605 DOI: 10.1007/Bf00291953 |
0.329 |
|
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