Education/CredentialsAlexander von Humboldt Fellow: Medizinischen Hochschule Hannover (Population Genetics)PhD: Dibrugarh University (Anthropology) Contact Information Email dekar@ucmail.uc.edu Peer Reviewed Publications Kaulfers, Anne-Marie; Deka, Ranjan; Dolan, Lawrence; Martin, Lisa J 2015. Association of INSIG2 Polymorphism with Overweight and LDL in Children. PloS one, 10 1, e0116340Mackey, Jason; Brown, Robert D; Sauerbeck, Laura; Hornung, Richard; Moomaw, Charles J; Koller, Daniel L; Foroud, Tatiana; Deka, Ranjan; Woo, Daniel; Kleindorfer, Dawn; Flaherty, Matthew L; Meissner, Irene; Anderson, Craig; Rouleau, Guy; Connolly, E Sander; Huston, John; Broderick, Joseph P 2015. Affected Twins in the Familial Intracranial Aneurysm Study. Cerebrovascular diseases (Basel, Switzerland), 39 2, 82-86Radmanesh, Farid; Falcone, Guido J; Anderson, Christopher D; McWilliams, David; Devan, William J; Brown, W Mark; Battey, Thomas W K; Ayres, Alison M; Raffeld, Miriam R; Schwab, Kristin; Sun, Guangyun; Deka, Ranjan; Viswanathan, Anand; Goldstein, Joshua N; Greenberg, Steven M; Tirschwell, David L; Silliman, Scott L; Selim, Magdy; Meschia, James F; Brown, Devin L; Worrall, Bradford B; Langefeld, Carl D; Woo, Daniel; Rosand, Jonathan 2015. Rare Coding Variation and Risk of Intracerebral Hemorrhage. Stroke; a journal of cerebral circulation, 46 8, 2299-301Rannikmäe, Kristiina; Davies, Gail; Thomson, Pippa A; Bevan, Steve; Devan, William J; Falcone, Guido J; Traylor, Matthew; Anderson, Christopher D; Battey, Thomas W K; Radmanesh, Farid; Deka, Ranjan; Woo, Jessica G; Martin, Lisa J; Jimenez-Conde, Jordi; Selim, Magdy; Brown, Devin L; Silliman, Scott L; Kidwell, Chelsea S; Montaner, Joan; Langefeld, Carl D; Slowik, Agnieszka; Hansen, Björn M; Lindgren, Arne G; Meschia, James F; Fornage, Myriam; Bis, Joshua C; Debette, Stéphanie; Ikram, Mohammad A; Longstreth, Will T; Schmidt, Reinhold; Zhang, Cathy R; Yang, Qiong; Sharma, Pankaj; Kittner, Steven J; Mitchell, Braxton D; Holliday, Elizabeth G; Levi, Christopher R; Attia, John; Rothwell, Peter M; Poole, Deborah L; Boncoraglio, Giorgio B; Psaty, Bruce M; Malik, Rainer; Rost, Natalia; Worrall, Bradford B; Dichgans, Martin; Van Agtmael, Tom; Woo, Daniel; Markus, Hugh S; Seshadri, Sudha; Rosand, Jonathan; Sudlow, Cathie L M 2015. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology, 84 9, 918-26Sahay, Rashmi D; Ollberding, Nicholas J; Missoni, Saša; Novokmet, Natalija; Sarac, Jelena; Sari?, Tena; Rao, Marepalli B; Rudan, Pavao; Deka, Ranjan 2015. Fish and Shellfish Intake and Diabetes in a Costal Population of the Adriatic. Collegium antropologicum, 39 2, 401-9Buhule, Olive D; Minster, Ryan L; Hawley, Nicola L; Medvedovic, Mario; Sun, Guangyun; Viali, Satupaitea; Deka, Ranjan; McGarvey, Stephen T; Weeks, Daniel E 2014. Stratified randomization controls better for batch effects in 450K methylation analysis: a cautionary tale. Frontiers in genetics, 5 , 354Falcone, Guido J; Radmanesh, Farid; Brouwers, H Bart; Battey, Thomas W K; Devan, William J; Valant, Valerie; Raffeld, Miriam R; Chitsike, Lennox P; Ayres, Alison M; Schwab, Kristin; Goldstein, Joshua N; Viswanathan, Anand; Greenberg, Steven M; Selim, Magdy; Meschia, James F; Brown, Devin L; Worrall, Bradford B; Silliman, Scott L; Tirschwell, David L; Flaherty, Matthew L; Martini, Sharyl R; Deka, Ranjan; Biffi, Alessandro; Kraft, Peter; Woo, Daniel; Rosand, Jonathan; Anderson, Christopher D 2014. APOE ? variants increase risk of warfarin-related intracerebral hemorrhage. Neurology, 83 13, 1139-46Woo, Daniel; Falcone, Guido J; Devan, William J; Brown, W Mark; Biffi, Alessandro; Howard, Timothy D; Anderson, Christopher D; Brouwers, H Bart; Valant, Valerie; Battey, Thomas W K; Radmanesh, Farid; Raffeld, Miriam R; Baedorf-Kassis, Sylvia; Deka, Ranjan; Woo, Jessica G; Martin, Lisa J; Haverbusch, Mary; Moomaw, Charles J; Sun, Guangyun; Broderick, Joseph P; Flaherty, Matthew L; Martini, Sharyl R; Kleindorfer, Dawn O; Kissela, Brett; Comeau, Mary E; Jagiella, Jeremiasz M; Schmidt, Helena; Freudenberger, Paul; Pichler, Alexander; Enzinger, Christian; Hansen, Björn M; Norrving, Bo; Jimenez-Conde, Jordi; Giralt-Steinhauer, Eva; Elosua, Roberto; Cuadrado-Godia, Elisa; Soriano, Carolina; Roquer, Jaume; Kraft, Peter; Ayres, Alison M; Schwab, Kristin; McCauley, Jacob L; Pera, Joanna; Urbanik, Andrzej; Rost, Natalia S; Goldstein, Joshua N; Viswanathan, Anand; Stögerer, Eva-Maria; Tirschwell, David L; Selim, Magdy; Brown, Devin L; Silliman, Scott L; Worrall, Bradford B; Meschia, James F; Kidwell, Chelsea S; Montaner, Joan; Fernandez-Cadenas, Israel; Delgado, Pilar; Malik, Rainer; Dichgans, Martin; Greenberg, Steven M; Rothwell, Peter M; Lindgren, Arne; Slowik, Agnieszka; Schmidt, Reinhold; Langefeld, Carl D; Rosand, Jonathan 2014. Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. American journal of human genetics, 94 4, 511-21Baylin, A; Deka, R; Tuitele, J; Viali, S; Weeks, D E; McGarvey, S T 2013. INSIG2 variants, dietary patterns and metabolic risk in Samoa. European journal of clinical nutrition, 67 1, 101-7Karns, Rebekah; Succop, Paul; Zhang, Ge; Sun, Guangyun; Indugula, Subba R; Havas-Augustin, Dubravka; Novokmet, Natalija; Durakovic, Zijad; Milanovic, Sanja Music; Missoni, Sasa; Vuletic, Silvije; Chakraborty, Ranajit; Rudan, Pavao; Deka, Ranjan 2013. Modeling metabolic syndrome through structural equations of metabolic traits, comorbid diseases, and GWAS variants. Obesity (Silver Spring, Md.), 21 12, E745-54Mackey, Jason; Brown, Robert D; Moomaw, Charles J; Hornung, Richard; Sauerbeck, Laura; Woo, Daniel; Foroud, Tatiana; Gandhi, Dheeraj; Kleindorfer, Dawn; Flaherty, Matthew L; Meissner, Irene; Anderson, Craig; Rouleau, Guy; Connolly, E Sander; Deka, Ranjan; Koller, Daniel L; Abruzzo, Todd; Huston, John; Broderick, Joseph P 2013. Familial intracranial aneurysms: is anatomic vulnerability heritable? Stroke; a journal of cerebral circulation, 44 1, 38-42Missoni, Sasa; Durakovic, Zijad; Sahay, Rashmi; Salzer, Branka; Deka, Ranjan 2013. Smoking habits according to metabolic traits in an island population of the eastern Adriatic Coast. Collegium antropologicum, 37 3, 745-53Sahay, Rashmi D; Couch, Sarah C; Missoni, Sasa; Sujoldzi?, Anita; Novokmet, Natalija; Durakovi?, Zijad; Rao, Marepalli B; Milanovi?, Sanja Musi?; Vuleti?, Silvije; Deka, Ranjan; Rudan, Pavao 2013. Dietary patterns in adults from an Adriatic Island of Croatia and their associations with metabolic syndrome and its components. Collegium antropologicum, 37 2, 335-42Woo, Daniel; Deka, Ranjan; Falcone, Guido J; Flaherty, Matthew L; Haverbusch, Mary; Martini, Sharyl R; Greenberg, Steven M; Ayres, Alison M; Sauerbeck, Laura; Kissela, Brett M; Kleindorfer, Dawn O; Moomaw, Charles J; Anderson, Christopher D; Broderick, Joseph P; Rosand, Jonathan; Langefeld, Carl D; Woo, Jessica G 2013. Apolipoprotein E, statins, and risk of intracerebral hemorrhage. Stroke; a journal of cerebral circulation, 44 11, 3013-7Aslibekyan, S; Jensen, M K; Campos, H; Linkletter, C D; Loucks, E B; Ordovas, J M; Deka, R; Rimm, E B; Baylin, A 2012. Genetic variation in fatty acid elongases is not associated with intermediate cardiovascular phenotypes or myocardial infarction. European journal of clinical nutrition, 66 3, 353-9Aslibekyan, S; Jensen, M K; Campos, H; Linkletter, C D; Loucks, E B; Ordovas, J M; Deka, R; Rimm, E B; Baylin, A 2012. Fatty Acid desaturase gene variants, cardiovascular risk factors, and myocardial infarction in the costa rica study. Frontiers in genetics, 3 , 72Biagini Myers, Jocelyn M; Khurana Hershey, Gurjit K; Deka, Ranjan; Burkle, Jeffrey W; Levin, Linda S; Bernstein, David I; Villareal, Manuel; Lockey, James E; Reponen, Tiina; Gareri, Joey; Lubetsky, Angelika; Koren, Gideon; Lemasters, Grace K 2012. Asking the right questions to ascertain early childhood secondhand smoke exposures. The Journal of pediatrics, 160 6, 1050-1Deka, 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 2012. Prevalence of metabolic syndrome and related metabolic traits in an island population of the Adriatic. Annals of human biology, 39 1, 46-53Foroud, Tatiana; Koller, Daniel L; Lai, Dongbing; Sauerbeck, Laura; Anderson, Craig; Ko, Nerissa; Deka, Ranjan; Mosley, Thomas H; Fornage, Myriam; Woo, Daniel; Moomaw, Charles J; Hornung, Richard; Huston, John; Meissner, Irene; Bailey-Wilson, Joan E; Langefeld, Carl; Rouleau, Guy; Connolly, E Sander; Worrall, Bradford B; Kleindorfer, Dawn; Flaherty, Matthew L; Martini, Sharyl; Mackey, Jason; De Los Rios La Rosa, Felipe; Brown, Robert D; Broderick, Joseph P 2012. Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk. Stroke; a journal of cerebral circulation, 43 11, 2846-52Kansra, Alvina R; Dolan, Lawrence M; Martin, Lisa J; Deka, Ranjan; Chernausek, Steven D 2012. IGF receptor gene variants in normal adolescents: effect on stature. European journal of endocrinology / European Federation of Endocrine Societies, 167 6, 777-81Karns, Rebekah; Viali, Satupaitea; Tuitele, John; Sun, Guangyun; Cheng, Hong; Weeks, Daniel E; McGarvey, Stephen T; Deka, Ranjan 2012. Common variants in FTO are not significantly associated with obesity-related phenotypes among Samoans of Polynesia. Annals of human genetics, 76 1, 17-24Karns, Rebekah; Zhang, Ge; Sun, Guangyun; Rao Indugula, Subba; Cheng, Hong; Havas-Augustin, Dubravka; Novokmet, Natalija; Rudan, Dusko; Durakovic, Zijad; Missoni, Sasa; Chakraborty, Ranajit; Rudan, Pavao; Deka, Ranjan 2012. 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 2, 121-7Martini, Sharyl R; Flaherty, Matthew L; Brown, W Mark; Haverbusch, Mary; Comeau, Mary E; Sauerbeck, Laura R; Kissela, Brett M; Deka, Ranjan; Kleindorfer, Dawn O; Moomaw, Charles J; Broderick, Joseph P; Langefeld, Carl D; Woo, Daniel 2012. Risk factors for intracerebral hemorrhage differ according to hemorrhage location. Neurology, 79 23, 2275-82Woo, Jessica G; Martin, Lisa J; Ding, Lili; Brown, W Mark; Howard, Timothy D; Langefeld, Carl D; Moomaw, Charles J; Haverbusch, Mary; Sun, Guangyun; Indugula, Subba R; Cheng, Hong; Deka, Ranjan; Woo, Daniel 2012. Quantitative criteria for improving performance of buccal DNA for high-throughput genetic analysis. BMC genetics, 13 , 75Zhang, Ge; Karns, Rebekah; Sun, Guangyun; Indugula, Subba Rao; Cheng, Hong; Havas-Augustin, Dubravka; Novokmet, Natalija; Durakovic, Zijad; Missoni, Sasa; Chakraborty, Ranajit; Rudan, Pavao; Deka, Ranjan 2012. Finding missing heritability in less significant Loci and allelic heterogeneity: genetic variation in human height. PloS one, 7 12, e51211Karns, Rebekah; Zhang, Ge; Jeran, Nina; Havas-Augustin, Dubravka; Missoni, Sasa; Niu, Wen; Indugula, Subba Rao; Sun, Guangyun; Durakovic, Zijad; Narancic, Nina Smolej; Rudan, Pavao; Chakraborty, Ranajit; Deka, Ranjan 2011. 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 3, 341-6Young, Kristin L; Sun, Guangyun; Deka, Ranjan; Crawford, Michael H 2011. Autosomal short tandem repeat genetic variation of the Basques in Spain. Croatian medical journal, 52 3, 372-83Young, Kristin L; Sun, Guangyun; Deka, Ranjan; Crawford, Michael H 2011. Paternal genetic history of the Basque population of Spain. Human biology, 83 4, 455-75Zhang, Ge; Karns, Rebekah; Sun, Guangyun; Indugula, Subba Rao; Cheng, Hong; Havas-Augustin, Dubravka; Novokmet, Natalija; Rudan, Dusko; Durakovic, Zijad; Missoni, Sasa; Chakraborty, Ranajit; Rudan, Pavao; Deka, Ranjan 2011. Extent of height variability explained by known height-associated genetic variants in an isolated population of the Adriatic coast of Croatia. PloS one, 6 12, e29475Bollepalli, Sureka; Dolan, Lawrence M; Deka, Ranjan; Martin, Lisa J 2010. Association of FTO gene variants with adiposity in African-American adolescents. Obesity (Silver Spring, Md.), 18 10, 1959-63Deka, Ranjan; Koller, Daniel L; Lai, Dongbing; Indugula, Subba Rao; Sun, Guangyun; Woo, Daniel; Sauerbeck, Laura; Moomaw, Charles J; Hornung, Richard; Connolly, E Sander; Anderson, Craig; Rouleau, Guy; Meissner, Irene; Bailey-Wilson, Joan E; Huston, John; Brown, Robert D; Kleindorfer, Dawn O; Flaherty, Matthew L; Langefeld, Carl D; Foroud, Tatiana; Broderick, Joseph P 2010. The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm. Stroke; a journal of cerebral circulation, 41 6, 1132-7Jorge-Nebert, Lucia F; Jiang, Zhengwen; Chakraborty, Ranajit; Watson, Joanna; Jin, Li; McGarvey, Stephen T; Deka, Ranjan; Nebert, Daniel W 2010. Analysis of human CYP1A1 and CYP1A2 genes and their shared bidirectional promoter in eight world populations. Human mutation, 31 1, 27-40Rubicz, Rohina; Melton, Phillip E; Spitsyn, Victor; Sun, Guangyun; Deka, Ranjan; Crawford, Michael H 2010. Genetic structure of native circumpolar populations based on autosomal, mitochondrial, and Y chromosome DNA markers. American journal of physical anthropology, 143 1, 62-74Rubicz, Rohina; Zlojutro, Mark; Sun, Guangyun; Spitsyn, Victor; Deka, Ranjan; Young, Kristin L; Crawford, Michael H 2010. Genetic architecture of a small, recently aggregated Aleut population: Bering Island, Russia. Human biology, 82 5-6, 719-36Zhang, Ge; Karns, Rebekah; Narancic, Nina Smolej; Sun, Guangyun; Cheng, Hong; Missoni, Sasa; Durakovic, Zijad; Rudan, Pavao; Chakraborty, Ranajit; Deka, Ranjan 2010. 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 4, e10375Aberg, Karolina; Dai, Feng; Sun, Guangyun; Keighley, Ember D; Indugula, Subba R; Roberts, Sarah T; Zhang, Qi; Smelser, Diane; Viali, Satupaitea; Tuitele, John; Jin, Li; Deka, Ranjan; Weeks, Daniel E; McGarvey, Stephen T 2009. Susceptibility loci for adiposity phenotypes on 8p, 9p, and 16q in American Samoa and Samoa. Obesity (Silver Spring, Md.), 17 3, 518-24Aberg, Karolina; Dai, Feng; Viali, Satupaitea; Tuitele, John; Sun, Guangyun; Indugula, Subba R; Deka, Ranjan; Weeks, Daniel E; McGarvey, Stephen T 2009. Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands. BMC medical genetics, 10 , 107Deka, Ranjan; Xu, Ling; Pal, Prodipto; Toelupe, Palanitina T; Laumoli, Tuiasina S; Xi, Huifeng; Zhang, Ge; Weeks, Daniel E; McGarvey, Stephen T 2009. A tagging SNP in INSIG2 is associated with obesity-related phenotypes among Samoans. BMC medical genetics, 10 , 143Foroud, Tatiana; Sauerbeck, Laura; Brown, Robert; Anderson, Craig; Woo, Daniel; Kleindorfer, Dawn; Flaherty, Matthew L; Deka, Ranjan; Hornung, Richard; Meissner, Irene; Bailey-Wilson, Joan E; Langefeld, Carl; Rouleau, Guy; Connolly, E Sander; Lai, Dongbing; Koller, Daniel L; Huston, John; Broderick, Joseph P 2009. Genome screen in familial intracranial aneurysm. BMC medical genetics, 10 , 3Pal, Prodipto; Mihanovi?, Mate; Molnar, Sven; Xi, Huifeng; Sun, Guangyun; Guha, Saurav; Jeran, Nina; Tomljenovi?, Andrea; Malnar, Ana; Missoni, Sasa; Deka, Ranjan; Rudan, Pavao 2009. Association of tagging single nucleotide polymorphisms on 8 candidate genes in dopaminergic pathway with schizophrenia in Croatian population. Croatian medical journal, 50 4, 361-9Pal, Prodipto; Xi, Huifeng; Guha, Saurav; Sun, Guangyun; Helfand, Brian T; Meeks, Joshua J; Suarez, Brian K; Catalona, William J; Deka, Ranjan 2009. Common variants in 8q24 are associated with risk for prostate cancer and tumor aggressiveness in men of European ancestry. The Prostate, 69 14, 1548-56Woo, D; Khoury, J; Haverbusch, M M; Sekar, P; Flaherty, M L; Kleindorfer, D O; Kissela, B M; Moomaw, C J; Deka, R; Broderick, J P 2009. Smoking and family history and risk of aneurysmal subarachnoid hemorrhage. Neurology, 72 1, 69-72Zhang, Xiang; Leav, Irwin; Revelo, Monica P; Deka, Ranjan; Medvedovic, Mario; Jiang, Zhong; Ho, Shuk-Mei 2009. Deletion hotspots in AMACR promoter CpG island are cis-regulatory elements controlling the gene expression in the colon. PLoS genetics, 5 1, e1000334Aberg, Karolina; Dai, Feng; Sun, Guangyun; Keighley, Ember; Indugula, Subba Rao; Bausserman, Linda; Viali, Satupaitea; Tuitele, John; Deka, Ranjan; Weeks, Daniel E; McGarvey, Stephen T 2008. 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 10, 2169-78Aberg, Karolina; Sun, Guangyun; Smelser, Diane; Indugula, Subba Rao; Tsai, Hui-Ju; Steele, Matthew S; Tuitele, John; Deka, Ranjan; McGarvey, Stephen T; Weeks, Daniel E 2008. Applying novel genome-wide linkage strategies to search for loci influencing type 2 diabetes and adult height in American Samoa. Human biology, 80 2, 99-123Choubey, Divaker; Deka, Ranjan; Ho, Shuk-mei 2008. Interferon-inducible IFI16 protein in human cancers and autoimmune diseases. Frontiers in bioscience : a journal and virtual library, 13 , 598-608Dai, F; Sun, G; Aberg, K; Keighley, E D; Indugula, S R; Roberts, S T; Smelser, D; Viali, S; Jin, L; Deka, R; Weeks, D E; McGarvey, S T 2008. A whole genome linkage scan identifies multiple chromosomal regions influencing adiposity-related traits among Samoans. Annals of human genetics, 72 Pt 6, 780-92Deka, Ranjan; Naranci?, Nina Smolej; Xip, Huifeng; Turek, Stjepan; Cubrilo-Turek, Mirjana; Vrhovski-Hebrang, Danijela; Jani?ijevi?, Branka; Tomljenovi?, Andrea; Szirovicza, Lajos; Jin, Li; Chakraborty, Ranajit; Rudan, Pavao 2008. Metabolic syndrome in an island population of the eastern Adriatic coast of Croatia. Collegium antropologicum, 32 1, 85-91Foroud, Tatiana; Sauerbeck, Laura; Brown, Robert; Anderson, Craig; Woo, Daniel; Kleindorfer, Dawn; Flaherty, Matthew L; Deka, Ranjan; Hornung, Richard; Meissner, Irene; Bailey-Wilson, Joan E; Rouleau, Guy; Connolly, E Sander; Lai, Dongbing; Koller, Daniel L; Huston, John; Broderick, Joseph P 2008. Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study. Stroke; a journal of cerebral circulation, 39 5, 1434-40Kalra, Maninder; Pal, Prodipto; Kaushal, Ritesh; Amin, Raouf S; Dolan, Lawrence M; Fitz, Kelly; Kumar, Sunil; Sheng, Xiaohua; Guha, Saurav; Mallik, Joydeep; Deka, Ranjan; Chakraborty, Ranajit 2008. Association of ApoE genetic variants with obstructive sleep apnea in children. Sleep medicine, 9 3, 260-5Li, Hui; Wen, Bo; Chen, Shu-Juo; Su, Bing; Pramoonjago, Patcharin; Liu, Yangfan; Pan, Shangling; Qin, Zhendong; Liu, Wenhong; Cheng, Xu; Yang, Ningning; Li, Xin; Tran, Dinhbinh; Lu, Daru; Hsu, Mu-Tsu; Deka, Ranjan; Marzuki, Sangkot; Tan, Chia-Chen; Jin, Li 2008. Paternal genetic affinity between Western Austronesians and Daic populations. BMC evolutionary biology, 8 , 146Motz, Gregory T; Eppert, Bryan L; Sun, Guangyun; Wesselkamper, Scott C; Linke, Michael J; Deka, Ranjan; Borchers, Michael T 2008. Persistence of lung CD8 T cell oligoclonal expansions upon smoking cessation in a mouse model of cigarette smoke-induced emphysema. Journal of immunology (Baltimore, Md. : 1950), 181 11, 8036-43Tucak-Zori?, Sandra; Curci?, Ines Bili?; Mihalj, Hrvoje; Dumanci?, Ivana; Zeli?, Zarko; Cetina, Nada Majeti?; Smoli?, Robert; Volarevi?, Martina; Missoni, Sasa; Tomljenovi?, Andrea; Szirovicza, Lajos; Durakovi?, Zijad; Xi, Huifeng; Chakraborty, Ranajit; Deka, Ranjan; Tucak, Antun; Rudan, Pavao 2008. Prevalence of metabolic syndrome in the interior of Croatia: the Baranja region. Collegium antropologicum, 32 3, 659-65Xue, Fuzhong; Wang, Yi; Xu, Shuhua; Zhang, Feng; Wen, Bo; Wu, Xuesen; Lu, Ming; Deka, Ranjan; Qian, Ji; Jin, Li 2008. 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 6, 705-17Bauchet, Marc; McEvoy, Brian; Pearson, Laurel N; Quillen, Ellen E; Sarkisian, Tamara; Hovhannesyan, Kristine; Deka, Ranjan; Bradley, Daniel G; Shriver, Mark D 2007. Measuring European population stratification with microarray genotype data. American journal of human genetics, 80 5, 948-56Crimmins, Nancy A; Woo, Jessica G; Kaushal, Ritesh D; Deka, Ranjan; Dolan, Lawrence M; Martin, Lisa J 2007. Adiponectin receptor 1 variants associated with lower insulin resistance in African Americans. Obesity (Silver Spring, Md.), 15 8, 1903-7Dai, F; Keighley, E D; Sun, G; Indugula, S R; Roberts, S T; Aberg, K; Smelser, D; Tuitele, J; Jin, L; Deka, R; Weeks, D E; McGarvey, S T 2007. Genome-wide scan for adiposity-related phenotypes in adults from American Samoa. International journal of obesity (2005), 31 12, 1832-42Kaushal, Ritesh; Pal, Prodipto; Alwell, Kathleen; Haverbusch, Mary; Flaherty, Matthew; Moomaw, Charles; Sekar, Padmini; Kissela, Brett; Kleindorfer, Dawn; Chakraborty, Ranajit; Broderick, Joseph; Deka, Ranjan; Woo, Daniel 2007. Association of ALOX5AP with ischemic stroke: a population-based case-control study. Human genetics, 121 5, 601-7Kaushal, Ritesh; Woo, Daniel; Pal, Prodipto; Haverbusch, Mary; Xi, Huifeng; Moomaw, Charles; Sekar, Padmini; Kissela, Brett; Kleindorfer, Dawn; Flaherty, Matthew; Sauerbeck, Laura; Chakraborty, Ranajit; Broderick, Joseph; Deka, Ranjan 2007. Subarachnoid hemorrhage: tests of association with apolipoprotein E and elastin genes. BMC medical genetics, 8 , 49Pal, Prodipto; Xi, Huifeng; Sun, Guangyun; Kaushal, Ritesh; Meeks, Joshua J; Thaxton, C Shad; Guha, Saurav; Jin, Carol H; Suarez, Brian K; Catalona, William J; Deka, Ranjan 2007. 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 3-4, 251-9Woo, Jessica G; Sun, Guangyun; Haverbusch, Mary; Indugula, Subbarao; Martin, Lisa J; Broderick, Joseph P; Deka, Ranjan; Woo, Daniel 2007. Quality assessment of buccal versus blood genomic DNA using the Affymetrix 500 K GeneChip. BMC genetics, 8 , 79Pal, Prodipto; Xi, Huifeng; Kaushal, Ritesh; Sun, Guangyun; Jin, Carol H; Jin, Li; Suarez, Brian K; Catalona, William J; Deka, Ranjan 2006. Variants in the HEPSIN gene are associated with prostate cancer in men of European origin. Human genetics, 120 2, 187-92Woo, Daniel; Kaushal, Ritesh; Kissela, Brett; Sekar, Padmini; Wolujewicz, Michael; Pal, Prodipto; Alwell, Kathleen; Haverbusch, Mary; Ewing, Irene; Miller, Rosie; Kleindorfer, Dawn; Flaherty, Matthew; Chakraborty, Ranajit; Deka, Ranjan; Broderick, Joseph 2006. Association of Phosphodiesterase 4D with ischemic stroke: a population-based case-control study. Stroke; a journal of cerebral circulation, 37 2, 371-6Woo, Jessica G; Dolan, Lawrence M; Deka, Ranjan; Kaushal, Ritesh D; Shen, Yayun; Pal, Prodipto; Daniels, Stephen R; Martin, Lisa J 2006. Interactions between noncontiguous haplotypes in the adiponectin gene ACDC are associated with plasma adiponectin. Diabetes, 55 2, 523-9Brzezinski, J L; Deka, R; Menon, A G; Glass, D N; Choi, E 2005. Variability in TRBV haplotype frequency and composition in Caucasian, African American, Western African and Chinese populations. International journal of immunogenetics, 32 6, 413-20Friedlaender, Jonathan; Schurr, Theodore; Gentz, Fred; Koki, George; Friedlaender, Françoise; Horvat, Gisele; Babb, Paul; Cerchio, Sal; Kaestle, Frederika; Schanfield, Moses; Deka, Ranjan; Yanagihara, Ric; Merriwether, D Andrew 2005. Expanding Southwest Pacific mitochondrial haplogroups P and Q. Molecular biology and evolution, 22 6, 1506-17Jiang, Zhengwen; Dalton, Timothy P; Jin, Li; Wang, Bin; Tsuneoka, Yutaka; Shertzer, Howard G; Deka, Ranjan; Nebert, Daniel W 2005. 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 2, 196-206Jiang, Zhengwen; Zhang, Xingqi; Deka, Ranjan; Jin, Li 2005. Genome amplification of single sperm using multiple displacement amplification. Nucleic acids research, 33 10, e91Klari?, Irena Martinovi?; Perici?, Marijana; Lauc, Lovorka Bara?; Jani?ijevi?, Branka; Kubat, Milovan; Pavici?, Dino; Rudan, Igor; Wang, Ning; Jin, Lin; Chakraborty, Ranajit; Deka, Ranjan; Rudan, Pavao 2005. Genetic variation at nine short tandem repeat loci among islanders of the eastern Adriatic coast of Croatia. Human biology, 77 4, 471-86Suarez, B K; Pal, P; Jin, C H; Kaushal, R; Sun, G; Jin, L; Pasche, B; Deka, R; Catalona, W J 2005. TGFBR1*6A is not associated with prostate cancer in men of European ancestry. Prostate cancer and prostatic diseases, 8 1, 50-3Sun, Guangyun; Kaushal, Ritesh; Pal, Prodipto; Wolujewicz, Michael; Smelser, Diane; Cheng, Hong; Lu, Mei; Chakraborty, Ranajit; Jin, Li; Deka, Ranjan 2005. Whole-genome amplification: relative efficiencies of the current methods. Legal medicine (Tokyo, Japan), 7 5, 279-86Wen, Bo; Li, Hui; Gao, Song; Mao, Xianyun; Gao, Yang; Li, Feng; Zhang, Feng; He, Yungang; Dong, Yongli; Zhang, Youjun; Huang, Wenju; Jin, Jianzhong; Xiao, Chunjie; Lu, Daru; Chakraborty, Ranajit; Su, Bing; Deka, Ranjan; Jin, Li 2005. Genetic structure of Hmong-Mien speaking populations in East Asia as revealed by mtDNA lineages. Molecular biology and evolution, 22 3, 725-34Woo, Daniel; Kaushal, Ritesh; Chakraborty, Ranajit; Woo, Jessica; Haverbusch, Mary; Sekar, Padmini; Kissela, Brett; Pancioli, Arthur; Jauch, Edward; Kleindorfer, Dawn; Flaherty, Matthew; Schneider, Alexander; Khatri, Pooja; Sauerbeck, Laura; Khoury, Jane; Deka, Ranjan; Broderick, Joseph 2005. Association of apolipoprotein E4 and haplotypes of the apolipoprotein E gene with lobar intracerebral hemorrhage. Stroke; a journal of cerebral circulation, 36 9, 1874-9Tsai, Hui-Ju; Sun, Guangyun; Smelser, Diane; Viali, Satupaitea; Tufa, Joseph; Jin, Li; Weeks, Daniel E; McGarvey, Stephen T; Deka, Ranjan 2004. Distribution of genome-wide linkage disequilibrium based on microsatellite loci in the Samoan population. Human genomics, 1 5, 327-34Wen, Bo; Li, Hui; Lu, Daru; Song, Xiufeng; Zhang, Feng; He, Yungang; Li, Feng; Gao, Yang; Mao, Xianyun; Zhang, Liang; Qian, Ji; Tan, Jingze; Jin, Jianzhong; Huang, Wei; Deka, Ranjan; Su, Bing; Chakraborty, Ranajit; Jin, Li 2004. Genetic evidence supports demic diffusion of Han culture. Nature, 431 7006, 302-5Rudan, I; Rudan, D; Campbell, H; Carothers, A; Wright, A; Smolej-Narancic, N; Janicijevic, B; Jin, L; Chakraborty, R; Deka, R; Rudan, P 2003. Inbreeding and risk of late onset complex disease. Journal of medical genetics, 40 12, 925-32Sun, Guangyun; McGarvey, Stephen T; Bayoumi, Riad; Mulligan, Connie J; Barrantes, Ramiro; Raskin, Salmo; Zhong, Yixi; Akey, Joshua; Chakraborty, Ranajit; Deka, Ranjan 2003. Global genetic variation at nine short tandem repeat loci and implications on forensic genetics. European journal of human genetics : EJHG, 11 1, 39-49Deka, R; Panigrahi, A; Aggarwal, S K; Guleria, S; Dash, S C; Mehta, S N; Pandey, R M; Mehra, N K 2002. Influence of pretransplant panel reactive antibodies on the posttransplant sensitization status. Transplantation proceedings, 34 8, 3082-3Dutta, Ranjan; Reddy, B Mohan; Chattopadhyay, P; Kashyap, V K; Sun, Guangyun; Deka, Ranjan 2002. Patterns of genetic diversity at the nine forensically approved STR loci in the Indian populations. Human biology, 74 1, 33-49McGarvey, S T; Forrest, W; Weeks, D E; Sun, G; Smelser, D; Tufa, J; Viali, S; Deka, R 2002. Human leptin locus (LEP) alleles and BMI in Samoans. International journal of obesity and related metabolic disorders : journal of the International Association for the Study of Obesity, 26 6, 783-8Moffett, Susan; Martinson, Jeremy; Shriver, Mark D; Deka, Ranjan; McGarvey, Stephen T; Barrantes, Ramiro; Ferrell, Robert E 2002. Genetic diversity and evolution of the human leptin locus tetranucleotide repeat. Human genetics, 110 5, 412-7Woo, Daniel; Sauerbeck, Laura R; Kissela, Brett M; Khoury, Jane C; Szaflarski, Jerzy P; Gebel, James; Shukla, Rakesh; Pancioli, Arthur M; Jauch, Edward C; Menon, Anil G; Deka, Ranjan; Carrozzella, Janice A; Moomaw, Charles J; Fontaine, Robert N; Broderick, Joseph P 2002. Genetic and environmental risk factors for intracerebral hemorrhage: preliminary results of a population-based study. Stroke; a journal of cerebral circulation, 33 5, 1190-5Ke, 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, R S; Seielstad, M; Oefner, P; Zhu, D; Jin, J; Huang, W; Chakraborty, R; Chen, Z; Jin, L 2001. African origin of modern humans in East Asia: a tale of 12,000 Y chromosomes. Science (New York, N.Y.), 292 5519, 1151-3Reddy, B H; Sun, G; Luis, J R; Crawford, M H; Hemam, N S; Deka, R 2001. Genomic diversity at thirteen short tandem repeat loci in a substructured caste population, Golla, of southern Andhra Pradesh, India. Human biology, 73 2, 175-90Reddy, B M; Sun, G; Dutta, R; Deka, R; Ranjan, D 2001. STR data for the Amp FlSTR Profiler Plus loci among Golla population of southern Andhra Pradesh, India. Journal of forensic sciences, 46 3, 734-5Tsai, H J; Sun, G; Weeks, D E; Kaushal, R; Wolujewicz, M; McGarvey, S T; Tufa, J; Viali, S; Deka, R 2001. Type 2 diabetes and three calpain-10 gene polymorphisms in Samoans: no evidence of association. American journal of human genetics, 69 6, 1236-44Su, B; Jin, L; Underhill, P; Martinson, J; Saha, N; McGarvey, S T; Shriver, M D; Chu, J; Oefner, P; Chakraborty, R; Deka, R 2000. Polynesian origins: insights from the Y chromosome. Proceedings of the National Academy of Sciences of the United States of America, 97 15, 8225-8Su, B; Sun, G; Lu, D; Xiao, J; Hu, F; Chakraborty, R; Deka, R; Jin, L 2000. Distribution of three HIV-1 resistance-conferring polymorphisms (SDF1-3'A, CCR2-641, and CCR5-delta32) in global populations. European journal of human genetics : EJHG, 8 12, 975-9Su, B; Xiao, C; Deka, R; Seielstad, M T; Kangwanpong, D; Xiao, J; Lu, D; Underhill, P; Cavalli-Sforza, L; Chakraborty, R; Jin, L 2000. Y chromosome haplotypes reveal prehistorical migrations to the Himalayas. Human genetics, 107 6, 582-90Wenger, S L; McIntire, S C; Bansal, V; Barranger, J A; Higgins, J; Balistreri, W F; Thompson, J N; Deka, R 2000. Glycogen storage disease type Ia and Sanfilippo syndrome type B in a patient with a balanced translocation. Clinical genetics, 58 5, 409-10Deka, R; Guangyun, S; Smelser, D; Zhong, Y; Kimmel, M; Chakraborty, R 1999. 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 9, 1166-77Deka, R; Guangyun, S; Wiest, J; Smelser, D; Chunhua, S; Zhong, Y; Chakraborty, R 1999. Patterns of instability of expanded CAG repeats at the ERDA1 locus in general populations. American journal of human genetics, 65 1, 192-8Parra, E; Saha, N; Soemantri, A G; McGarvey, S T; Hundrieser, J; Shriver, M D; Deka, R 1999. Genetic variation at 9 autosomal microsatellite loci in Asian and Pacific populations. Human biology, 71 5, 757-79Parra, E; Shriver, M D; Soemantri, A; McGarvey, S T; Hundrieser, J; Saha, N; Deka, R 1999. Analysis of five Y-specific microsatellite loci in Asian and Pacific populations. American journal of physical anthropology, 110 1, 1-16Su, 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; Chakraborty, R; Xiong, M; Du, R; Oefner, P; Chen, Z; Jin, L 1999. Y-Chromosome evidence for a northward migration of modern humans into Eastern Asia during the last Ice Age. American journal of human genetics, 65 6, 1718-24Parra, E J; Marcini, A; Akey, J; Martinson, J; Batzer, M A; Cooper, R; Forrester, T; Allison, D B; Deka, R; Ferrell, R E; Shriver, M D 1998. Estimating African American admixture proportions by use of population-specific alleles. American journal of human genetics, 63 6, 1839-51Pogue-Geile, M; Ferrell, R; Deka, R; Debski, T; Manuck, S 1998. Human novelty-seeking personality traits and dopamine D4 receptor polymorphisms: a twin and genetic association study. American journal of medical genetics, 81 1, 44-8Pola?ski, A; Chakraborty, R; Kimmel, M; Deka, R 1998. Dynamic balance of segregation distortion and selection maintains normal allele sizes at the myotonic dystrophy locus. Mathematical biosciences, 147 1, 93-112Chakraborty, R; Kimmel, M; Stivers, D N; Davison, L J; Deka, R 1997. Relative mutation rates at di-, tri-, and tetranucleotide microsatellite loci. Proceedings of the National Academy of Sciences of the United States of America, 94 3, 1041-6Shriver, M D; Jin, L; Ferrell, R E; Deka, R 1997. Microsatellite data support an early population expansion in Africa. Genome research, 7 6, 586-91Shriver, M D; Smith, M W; Jin, L; Marcini, A; Akey, J M; Deka, R; Ferrell, R E 1997. Ethnic-affiliation estimation by use of population-specific DNA markers. American journal of human genetics, 60 4, 957-64Chakraborty, R; Stivers, D N; Deka, R; Yu, L M; Shriver, M D; Ferrell, R E 1996. Segregation distortion of the CTG repeats at the myotonic dystrophy locus. American journal of human genetics, 59 1, 109-18Deka, R; Jin, L; Shriver, M D; Yu, L M; Saha, N; Barrantes, R; Chakraborty, R; Ferrell, R E 1996. Dispersion of human Y chromosome haplotypes based on five microsatellites in global populations. Genome research, 6 12, 1177-84Deka, R; Majumder, P P; Shriver, M D; Stivers, D N; Zhong, Y; Yu, L M; Barrantes, R; Yin, S J; Miki, T; Hundrieser, J; Bunker, C H; McGarvey, S T; Sakallah, S; Ferrell, R E; Chakraborty, R 1996. Distribution and evolution of CTG repeats at the myotonin protein kinase gene in human populations. Genome research, 6 2, 142-54Kimmel, M; Chakraborty, R; Stivers, D N; Deka, R 1996. Dynamics of repeat polymorphisms under a forward-backward mutation model: within- and between-population variability at microsatellite loci. Genetics, 143 1, 549-55Yamagata, H; Miki, T; Nakagawa, M; Johnson, K; Deka, R; Ogihara, T 1996. 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 2, 145-7Deka, R; Jin, L; Shriver, M D; Yu, L M; DeCroo, S; Hundrieser, J; Bunker, C H; Ferrell, R E; Chakraborty, R 1995. Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations. American journal of human genetics, 56 2, 461-74Deka, R; Miki, T; Yin, S J; McGarvey, S T; Shriver, M D; Bunker, C H; Raskin, S; Hundrieser, J; Ferrell, R E; Chakraborty, R 1995. Normal CAG repeat variation at the DRPLA locus in world populations. American journal of human genetics, 57 2, 508-11Deka, R; Shriver, M D; Yu, L M; Ferrell, R E; Chakraborty, R 1995. Intra- and inter-population diversity at short tandem repeat loci in diverse populations of the world. Electrophoresis, 16 9, 1659-64Shriver, M D; Jin, L; Boerwinkle, E; Deka, R; Ferrell, R E; Chakraborty, R 1995. A novel measure of genetic distance for highly polymorphic tandem repeat loci. Molecular biology and evolution, 12 5, 914-20Vanyukov, M M; Moss, H B; Yu, L M; Deka, R 1995. A dinucleotide repeat polymorphism at the gene for monoamine oxidase A and measures of aggressiveness. Psychiatry research, 59 1-2, 35-41Vanyukov, M M; Moss, H B; Yu, L M; Tarter, R E; Deka, R 1995. 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 2, 122-6Deka, R; DeCroo, S; Jin, L; McGarvey, S T; Rothhammer, F; Ferrell, R E; Chakraborty, R 1994. Population genetic characteristics of the D1S80 locus in seven human populations. Human genetics, 94 3, 252-8Deka, R; Mc Garvey, S T; Ferrell, R E; Kamboh, M I; Yu, L M; Aston, C E; Jin, L; Chakraborty, R 1994. Genetic characterization of American and Western Samoans. Human biology, 66 5, 805-22Deka, R; Shriver, M D; Yu, L M; Jin, L; Aston, C E; Chakraborty, R; Ferrell, R E 1994. Conservation of human chromosome 13 polymorphic microsatellite (CA)n repeats in chimpanzees. Genomics, 22 1, 226-30Finegold, D N; Armitage, M M; Galiani, M; Matise, T C; Pandian, M R; Perry, Y M; Deka, R; Ferrell, R E 1994. Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13. Pediatric research, 36 3, 414-7Hoffner, L; Deka, R; Chakravarti, A; Surti, U 1994. Cytogenetics and origins of pediatric germ cell tumors. Cancer genetics and cytogenetics, 74 1, 54-8Deka, R; Chakraborty, R; DeCroo, S; Rothhammer, F; Barton, S A; Ferrell, R E 1992. Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations. American journal of human genetics, 51 6, 1325-33Ely, J; Deka, R; Chakraborty, R; Ferrell, R E 1992. Comparison of five tandem repeat loci between humans and chimpanzees. Genomics, 14 3, 692-8Hoffner, L; Shen-Schwarz, S; Deka, R; Chakravarti, A; Surti, U 1992. Genetics and biology of human ovarian teratomas. III. Cytogenetics and origins of malignant ovarian germ cell tumors. Cancer genetics and cytogenetics, 62 1, 58-65Steele, M W; Wenger, S L; Deka, R; Mulvihill, J J; Sukarachana, K 1992. Genetic analyses on a set of parasitic conjoined twins. American journal of medical genetics, 42 6, 856Deka, R; Chakroborty, R; Ferrell, R E 1991. A population genetic study of six VNTR loci in three ethnically defined populations. Genomics, 11 1, 83-92Deka, R; Chakravarti, A; Surti, U; Hauselman, E; Reefer, J; Majumder, P P; Ferrell, R E 1990. Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers. American journal of human genetics, 47 4, 644-55Laig, M; Pape, M; Hundrieser, J; Flatz, G; Sanguansermsri, T; Das, B M; Deka, R; Yongvanit, P; Mularlee, N 1990. The distribution of the Hb constant spring gene in Southeast Asian populations. Human genetics, 84 2, 188-90Chakravarti, A; Majumder, P P; Slaugenhaupt, S A; Deka, R; Warren, A C; Surti, U; Ferrell, R E; Antonarakis, S E 1989. Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas. Progress in clinical and biological research, 311 , 45-79Heo, D S; Snyderman, C; Gollin, S M; Pan, S; Walker, E; Deka, R; Barnes, E L; Johnson, J T; Herberman, R B; Whiteside, T L 1989. Biology, cytogenetics, and sensitivity to immunological effector cells of new head and neck squamous cell carcinoma lines. Cancer research, 49 18, 5167-75Deka, R; Reddy, A P; Mukherjee, B N; Das, B M; Banerjee, S; Roy, M; Dey, B; Malhotra, K C; Walter, H 1988. Hemoglobin E distribution in ten endogamous population groups of Assam, India. Human heredity, 38 5, 261-6Hundrieser, J; Deka, R; Gogoi, B C; Papp, T; Flatz, G 1988. DNA haplotypes and frameworks associated with the beta-globin gene in the Kachari population of Assam (India). Human heredity, 38 4, 240-5Hundrieser, J; Deka, R; Gogoi, B C 1987. Alpha-thalassemia in the Kachari population of Assam (India). Hemoglobin, 11 5, 517-9Walter, H; Mukherjee, B N; Gilbert, K; Lindenberg, P; Dannewitz, A; Malhotra, K C; Das, B M; Deka, R 1986. Investigations on the variability of haptoglobin, transferrin and Gc polymorphisms in Assam, India. Human heredity, 36 6, 388-96Das, B M; Deka, R 1985. Population study in Assam: ABO blood groups, haemoglobin E and G-6-PD deficiency. Anthropologischer Anzeiger; Bericht über die biologisch-anthropologische Literatur, 43 1, 81-6Deka, R 1984. A genetic survey in four Mongoloid populations of the Garo Hills, India. Anthropologischer Anzeiger; Bericht über die biologisch-anthropologische Literatur, 42 1, 41-5Deka, R 1981. Fertility and haemoglobin genotypes: a population study in Upper Assam (India). Human genetics, 59 2, 172-4Deka, R 1976. Age at menarche and haemoglobin E among the Kachari women of Upper Assam. Man in India, 56 4, 349-54Das, B M; Deka, R 1975. Predominance of the haemoglobin E gene in a Mongoloid population in Assam (India). Humangenetik, 30 2, 187-91Cerda-Flores, Ricardo M; Budowle, Bruce; Jin, Li; Barton, Sara Ann; Deka, Ranjan; Chakraborty, Ranajit . 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 4, 429-39Deka, R; De Croo, S; Yu, L M; Ferrell, R E . Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations. Human genetics, 90 1-2, 86-90Hawley, Nicola L; Minster, Ryan L; Weeks, Daniel E; Viali, Satupaitea; Reupena, Muagututia Sefuiva; Sun, Guangyun; Cheng, Hong; Deka, Ranjan; Mcgarvey, Stephen T . 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 4, 491-501Woo, Daniel; Sekar, Padmini; Chakraborty, Ranajit; Haverbusch, Mary A; Flaherty, Matthew L; Kissela, Brett M; Kleindorfer, Dawn; Schneider, Alexander; Khoury, Jane; Sauerbeck, Laura R; Deka, Ranjan; Broderick, Joseph P . Genetic epidemiology of intracerebral hemorrhage. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 14 6, 239-43
Peer Reviewed Publications Kaulfers, Anne-Marie; Deka, Ranjan; Dolan, Lawrence; Martin, Lisa J 2015. Association of INSIG2 Polymorphism with Overweight and LDL in Children. PloS one, 10 1, e0116340Mackey, Jason; Brown, Robert D; Sauerbeck, Laura; Hornung, Richard; Moomaw, Charles J; Koller, Daniel L; Foroud, Tatiana; Deka, Ranjan; Woo, Daniel; Kleindorfer, Dawn; Flaherty, Matthew L; Meissner, Irene; Anderson, Craig; Rouleau, Guy; Connolly, E Sander; Huston, John; Broderick, Joseph P 2015. Affected Twins in the Familial Intracranial Aneurysm Study. Cerebrovascular diseases (Basel, Switzerland), 39 2, 82-86Radmanesh, Farid; Falcone, Guido J; Anderson, Christopher D; McWilliams, David; Devan, William J; Brown, W Mark; Battey, Thomas W K; Ayres, Alison M; Raffeld, Miriam R; Schwab, Kristin; Sun, Guangyun; Deka, Ranjan; Viswanathan, Anand; Goldstein, Joshua N; Greenberg, Steven M; Tirschwell, David L; Silliman, Scott L; Selim, Magdy; Meschia, James F; Brown, Devin L; Worrall, Bradford B; Langefeld, Carl D; Woo, Daniel; Rosand, Jonathan 2015. Rare Coding Variation and Risk of Intracerebral Hemorrhage. Stroke; a journal of cerebral circulation, 46 8, 2299-301Rannikmäe, Kristiina; Davies, Gail; Thomson, Pippa A; Bevan, Steve; Devan, William J; Falcone, Guido J; Traylor, Matthew; Anderson, Christopher D; Battey, Thomas W K; Radmanesh, Farid; Deka, Ranjan; Woo, Jessica G; Martin, Lisa J; Jimenez-Conde, Jordi; Selim, Magdy; Brown, Devin L; Silliman, Scott L; Kidwell, Chelsea S; Montaner, Joan; Langefeld, Carl D; Slowik, Agnieszka; Hansen, Björn M; Lindgren, Arne G; Meschia, James F; Fornage, Myriam; Bis, Joshua C; Debette, Stéphanie; Ikram, Mohammad A; Longstreth, Will T; Schmidt, Reinhold; Zhang, Cathy R; Yang, Qiong; Sharma, Pankaj; Kittner, Steven J; Mitchell, Braxton D; Holliday, Elizabeth G; Levi, Christopher R; Attia, John; Rothwell, Peter M; Poole, Deborah L; Boncoraglio, Giorgio B; Psaty, Bruce M; Malik, Rainer; Rost, Natalia; Worrall, Bradford B; Dichgans, Martin; Van Agtmael, Tom; Woo, Daniel; Markus, Hugh S; Seshadri, Sudha; Rosand, Jonathan; Sudlow, Cathie L M 2015. Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease. Neurology, 84 9, 918-26Sahay, Rashmi D; Ollberding, Nicholas J; Missoni, Saša; Novokmet, Natalija; Sarac, Jelena; Sari?, Tena; Rao, Marepalli B; Rudan, Pavao; Deka, Ranjan 2015. Fish and Shellfish Intake and Diabetes in a Costal Population of the Adriatic. Collegium antropologicum, 39 2, 401-9Buhule, Olive D; Minster, Ryan L; Hawley, Nicola L; Medvedovic, Mario; Sun, Guangyun; Viali, Satupaitea; Deka, Ranjan; McGarvey, Stephen T; Weeks, Daniel E 2014. Stratified randomization controls better for batch effects in 450K methylation analysis: a cautionary tale. Frontiers in genetics, 5 , 354Falcone, Guido J; Radmanesh, Farid; Brouwers, H Bart; Battey, Thomas W K; Devan, William J; Valant, Valerie; Raffeld, Miriam R; Chitsike, Lennox P; Ayres, Alison M; Schwab, Kristin; Goldstein, Joshua N; Viswanathan, Anand; Greenberg, Steven M; Selim, Magdy; Meschia, James F; Brown, Devin L; Worrall, Bradford B; Silliman, Scott L; Tirschwell, David L; Flaherty, Matthew L; Martini, Sharyl R; Deka, Ranjan; Biffi, Alessandro; Kraft, Peter; Woo, Daniel; Rosand, Jonathan; Anderson, Christopher D 2014. APOE ? variants increase risk of warfarin-related intracerebral hemorrhage. Neurology, 83 13, 1139-46Woo, Daniel; Falcone, Guido J; Devan, William J; Brown, W Mark; Biffi, Alessandro; Howard, Timothy D; Anderson, Christopher D; Brouwers, H Bart; Valant, Valerie; Battey, Thomas W K; Radmanesh, Farid; Raffeld, Miriam R; Baedorf-Kassis, Sylvia; Deka, Ranjan; Woo, Jessica G; Martin, Lisa J; Haverbusch, Mary; Moomaw, Charles J; Sun, Guangyun; Broderick, Joseph P; Flaherty, Matthew L; Martini, Sharyl R; Kleindorfer, Dawn O; Kissela, Brett; Comeau, Mary E; Jagiella, Jeremiasz M; Schmidt, Helena; Freudenberger, Paul; Pichler, Alexander; Enzinger, Christian; Hansen, Björn M; Norrving, Bo; Jimenez-Conde, Jordi; Giralt-Steinhauer, Eva; Elosua, Roberto; Cuadrado-Godia, Elisa; Soriano, Carolina; Roquer, Jaume; Kraft, Peter; Ayres, Alison M; Schwab, Kristin; McCauley, Jacob L; Pera, Joanna; Urbanik, Andrzej; Rost, Natalia S; Goldstein, Joshua N; Viswanathan, Anand; Stögerer, Eva-Maria; Tirschwell, David L; Selim, Magdy; Brown, Devin L; Silliman, Scott L; Worrall, Bradford B; Meschia, James F; Kidwell, Chelsea S; Montaner, Joan; Fernandez-Cadenas, Israel; Delgado, Pilar; Malik, Rainer; Dichgans, Martin; Greenberg, Steven M; Rothwell, Peter M; Lindgren, Arne; Slowik, Agnieszka; Schmidt, Reinhold; Langefeld, Carl D; Rosand, Jonathan 2014. Meta-analysis of genome-wide association studies identifies 1q22 as a susceptibility locus for intracerebral hemorrhage. American journal of human genetics, 94 4, 511-21Baylin, A; Deka, R; Tuitele, J; Viali, S; Weeks, D E; McGarvey, S T 2013. INSIG2 variants, dietary patterns and metabolic risk in Samoa. European journal of clinical nutrition, 67 1, 101-7Karns, Rebekah; Succop, Paul; Zhang, Ge; Sun, Guangyun; Indugula, Subba R; Havas-Augustin, Dubravka; Novokmet, Natalija; Durakovic, Zijad; Milanovic, Sanja Music; Missoni, Sasa; Vuletic, Silvije; Chakraborty, Ranajit; Rudan, Pavao; Deka, Ranjan 2013. Modeling metabolic syndrome through structural equations of metabolic traits, comorbid diseases, and GWAS variants. Obesity (Silver Spring, Md.), 21 12, E745-54Mackey, Jason; Brown, Robert D; Moomaw, Charles J; Hornung, Richard; Sauerbeck, Laura; Woo, Daniel; Foroud, Tatiana; Gandhi, Dheeraj; Kleindorfer, Dawn; Flaherty, Matthew L; Meissner, Irene; Anderson, Craig; Rouleau, Guy; Connolly, E Sander; Deka, Ranjan; Koller, Daniel L; Abruzzo, Todd; Huston, John; Broderick, Joseph P 2013. Familial intracranial aneurysms: is anatomic vulnerability heritable? Stroke; a journal of cerebral circulation, 44 1, 38-42Missoni, Sasa; Durakovic, Zijad; Sahay, Rashmi; Salzer, Branka; Deka, Ranjan 2013. Smoking habits according to metabolic traits in an island population of the eastern Adriatic Coast. Collegium antropologicum, 37 3, 745-53Sahay, Rashmi D; Couch, Sarah C; Missoni, Sasa; Sujoldzi?, Anita; Novokmet, Natalija; Durakovi?, Zijad; Rao, Marepalli B; Milanovi?, Sanja Musi?; Vuleti?, Silvije; Deka, Ranjan; Rudan, Pavao 2013. 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Genetics, 143 1, 549-55Yamagata, H; Miki, T; Nakagawa, M; Johnson, K; Deka, R; Ogihara, T 1996. 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 2, 145-7Deka, R; Jin, L; Shriver, M D; Yu, L M; DeCroo, S; Hundrieser, J; Bunker, C H; Ferrell, R E; Chakraborty, R 1995. Population genetics of dinucleotide (dC-dA)n.(dG-dT)n polymorphisms in world populations. American journal of human genetics, 56 2, 461-74Deka, R; Miki, T; Yin, S J; McGarvey, S T; Shriver, M D; Bunker, C H; Raskin, S; Hundrieser, J; Ferrell, R E; Chakraborty, R 1995. Normal CAG repeat variation at the DRPLA locus in world populations. American journal of human genetics, 57 2, 508-11Deka, R; Shriver, M D; Yu, L M; Ferrell, R E; Chakraborty, R 1995. Intra- and inter-population diversity at short tandem repeat loci in diverse populations of the world. Electrophoresis, 16 9, 1659-64Shriver, M D; Jin, L; Boerwinkle, E; Deka, R; Ferrell, R E; Chakraborty, R 1995. A novel measure of genetic distance for highly polymorphic tandem repeat loci. Molecular biology and evolution, 12 5, 914-20Vanyukov, M M; Moss, H B; Yu, L M; Deka, R 1995. A dinucleotide repeat polymorphism at the gene for monoamine oxidase A and measures of aggressiveness. Psychiatry research, 59 1-2, 35-41Vanyukov, M M; Moss, H B; Yu, L M; Tarter, R E; Deka, R 1995. 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 2, 122-6Deka, R; DeCroo, S; Jin, L; McGarvey, S T; Rothhammer, F; Ferrell, R E; Chakraborty, R 1994. Population genetic characteristics of the D1S80 locus in seven human populations. Human genetics, 94 3, 252-8Deka, R; Mc Garvey, S T; Ferrell, R E; Kamboh, M I; Yu, L M; Aston, C E; Jin, L; Chakraborty, R 1994. Genetic characterization of American and Western Samoans. Human biology, 66 5, 805-22Deka, R; Shriver, M D; Yu, L M; Jin, L; Aston, C E; Chakraborty, R; Ferrell, R E 1994. Conservation of human chromosome 13 polymorphic microsatellite (CA)n repeats in chimpanzees. Genomics, 22 1, 226-30Finegold, D N; Armitage, M M; Galiani, M; Matise, T C; Pandian, M R; Perry, Y M; Deka, R; Ferrell, R E 1994. Preliminary localization of a gene for autosomal dominant hypoparathyroidism to chromosome 3q13. Pediatric research, 36 3, 414-7Hoffner, L; Deka, R; Chakravarti, A; Surti, U 1994. Cytogenetics and origins of pediatric germ cell tumors. Cancer genetics and cytogenetics, 74 1, 54-8Deka, R; Chakraborty, R; DeCroo, S; Rothhammer, F; Barton, S A; Ferrell, R E 1992. Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populations. American journal of human genetics, 51 6, 1325-33Ely, J; Deka, R; Chakraborty, R; Ferrell, R E 1992. Comparison of five tandem repeat loci between humans and chimpanzees. Genomics, 14 3, 692-8Hoffner, L; Shen-Schwarz, S; Deka, R; Chakravarti, A; Surti, U 1992. Genetics and biology of human ovarian teratomas. III. Cytogenetics and origins of malignant ovarian germ cell tumors. Cancer genetics and cytogenetics, 62 1, 58-65Steele, M W; Wenger, S L; Deka, R; Mulvihill, J J; Sukarachana, K 1992. Genetic analyses on a set of parasitic conjoined twins. American journal of medical genetics, 42 6, 856Deka, R; Chakroborty, R; Ferrell, R E 1991. A population genetic study of six VNTR loci in three ethnically defined populations. Genomics, 11 1, 83-92Deka, R; Chakravarti, A; Surti, U; Hauselman, E; Reefer, J; Majumder, P P; Ferrell, R E 1990. Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers. American journal of human genetics, 47 4, 644-55Laig, M; Pape, M; Hundrieser, J; Flatz, G; Sanguansermsri, T; Das, B M; Deka, R; Yongvanit, P; Mularlee, N 1990. The distribution of the Hb constant spring gene in Southeast Asian populations. Human genetics, 84 2, 188-90Chakravarti, A; Majumder, P P; Slaugenhaupt, S A; Deka, R; Warren, A C; Surti, U; Ferrell, R E; Antonarakis, S E 1989. Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas. Progress in clinical and biological research, 311 , 45-79Heo, D S; Snyderman, C; Gollin, S M; Pan, S; Walker, E; Deka, R; Barnes, E L; Johnson, J T; Herberman, R B; Whiteside, T L 1989. Biology, cytogenetics, and sensitivity to immunological effector cells of new head and neck squamous cell carcinoma lines. Cancer research, 49 18, 5167-75Deka, R; Reddy, A P; Mukherjee, B N; Das, B M; Banerjee, S; Roy, M; Dey, B; Malhotra, K C; Walter, H 1988. Hemoglobin E distribution in ten endogamous population groups of Assam, India. Human heredity, 38 5, 261-6Hundrieser, J; Deka, R; Gogoi, B C; Papp, T; Flatz, G 1988. DNA haplotypes and frameworks associated with the beta-globin gene in the Kachari population of Assam (India). Human heredity, 38 4, 240-5Hundrieser, J; Deka, R; Gogoi, B C 1987. Alpha-thalassemia in the Kachari population of Assam (India). Hemoglobin, 11 5, 517-9Walter, H; Mukherjee, B N; Gilbert, K; Lindenberg, P; Dannewitz, A; Malhotra, K C; Das, B M; Deka, R 1986. Investigations on the variability of haptoglobin, transferrin and Gc polymorphisms in Assam, India. Human heredity, 36 6, 388-96Das, B M; Deka, R 1985. Population study in Assam: ABO blood groups, haemoglobin E and G-6-PD deficiency. Anthropologischer Anzeiger; Bericht über die biologisch-anthropologische Literatur, 43 1, 81-6Deka, R 1984. A genetic survey in four Mongoloid populations of the Garo Hills, India. Anthropologischer Anzeiger; Bericht über die biologisch-anthropologische Literatur, 42 1, 41-5Deka, R 1981. Fertility and haemoglobin genotypes: a population study in Upper Assam (India). Human genetics, 59 2, 172-4Deka, R 1976. Age at menarche and haemoglobin E among the Kachari women of Upper Assam. Man in India, 56 4, 349-54Das, B M; Deka, R 1975. Predominance of the haemoglobin E gene in a Mongoloid population in Assam (India). Humangenetik, 30 2, 187-91Cerda-Flores, Ricardo M; Budowle, Bruce; Jin, Li; Barton, Sara Ann; Deka, Ranjan; Chakraborty, Ranajit . 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 4, 429-39Deka, R; De Croo, S; Yu, L M; Ferrell, R E . Variable number of tandem repeat (VNTR) polymorphism at locus D17S5 (YNZ22) in four ethnically defined human populations. Human genetics, 90 1-2, 86-90Hawley, Nicola L; Minster, Ryan L; Weeks, Daniel E; Viali, Satupaitea; Reupena, Muagututia Sefuiva; Sun, Guangyun; Cheng, Hong; Deka, Ranjan; Mcgarvey, Stephen T . 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 4, 491-501Woo, Daniel; Sekar, Padmini; Chakraborty, Ranajit; Haverbusch, Mary A; Flaherty, Matthew L; Kissela, Brett M; Kleindorfer, Dawn; Schneider, Alexander; Khoury, Jane; Sauerbeck, Laura R; Deka, Ranjan; Broderick, Joseph P . Genetic epidemiology of intracerebral hemorrhage. Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 14 6, 239-43