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Science (American Association for the Advancement of Science), ISSN 0036-8075, 2011, Volume 334, Issue 6052, pp. 94 - 98
Journal Article
PloS one, ISSN 1932-6203, 2012, Volume 7, Issue 1, p. e29684
.... These genetic markers are especially useful in inferring the likely ancestral origin of an individual or estimating the apportionment of ancestry components in admixed individuals or populations... 
DETERMINING CONTINENTAL ORIGIN | MULTILOCUS GENOTYPE DATA | POLYMORPHISMS | CELL-LINE PANEL | MULTIDISCIPLINARY SCIENCES | DNA MARKERS | COPY NUMBER | POPULATION-STRUCTURE | AMERICANS | DIVERSITY | GENOME-WIDE ASSOCIATION | European Continental Ancestry Group - genetics | Gene Frequency | Humans | Asian Continental Ancestry Group - genetics | Genotype | INDEL Mutation - genetics | DNA - genetics | Genetic Variation | Electrophoresis, Capillary | Genetics, Population - methods | Indians, North American - genetics | Polymerase Chain Reaction | Polymorphism, Single Nucleotide - genetics | African Continental Ancestry Group - genetics | Genotyping Techniques - methods | Genetic markers | Analysis | Medical genetics | Genetic aspects | Native Americans | Research | Population genetics | Multiplexing | Divergence | Populations | Laboratories | Forensic engineering | Insertion | African Americans | Population studies | Genomes | Single-nucleotide polymorphism | Immunology | Population | Genetics | Deoxyribonucleic acid--DNA | Origins | Forensic science | Capillary electrophoresis | Base pairs | Markers | Principal components analysis | Clustering | Minority & ethnic groups | Studies | Pathology | Genotyping | Gene frequency | Capillary tubes | Forensic sciences | Mutation | Polymorphism | Deoxyribonucleic acid | DNA
Journal Article
by Mahajan, Anubha and Go, Min Jin and Zhang, Weihua and Below, Jennifer E and Gaulton, Kyle J and Ferreira, Teresa and Horikoshi, Momoko and Johnson, Andrew D and Ng, Maggie C Y and Prokopenko, Inga and Saleheen, Danish and Wang, Xu and Zeggini, Eleftheria and Abecasis, Goncalo R and Adair, Linda S and Almgren, Peter and Atalay, Mustafa and Aung, Tin and Baldassarre, Damiano and Balkau, Beverley and Bao, Yuqian and Barnett, Anthony H and Barroso, Ines and Basit, Abdul and Been, Latonya F and Beilby, John and Bell, Graeme I and Benediktsson, Rafn and Bergman, Richard N and Boehm, Bernhard O and Boerwinkle, Eric and Bonnycastle, Lori L and Burtt, Noël and Cai, Qiuyin and Campbell, Harry and Carey, Jason and Cauchi, Stephane and Caulfield, Mark and Chan, Juliana C N and Chang, Li-Ching and Chang, Tien-Jyun and Chang, Yi-Cheng and Charpentier, Guillaume and Chen, Chien-Hsiun and Chen, Han and Chen, Yuan-Tsong and Chia, Kee-Seng and Chidambaram, Manickam and Chines, Peter S and Cho, Nam H and Cho, Young Min and Chuang, Lee-Ming and Collins, Francis S and Cornelis, Marilyn C and Couper, David J and Crenshaw, Andrew T and van Dam, Rob M and Danesh, John and Das, Debashish and de Faire, Ulf and Dedoussis, George and Deloukas, Panos and Dimas, Antigone S and Dina, Christian and Doney, Alex S F and Donnelly, Peter J and Dorkhan, Mozhgan and van Duijn, Cornelia and Dupuis, Josée and Edkins, Sarah and Elliott, Paul and Emilsson, Valur and Erbel, Raimund and Eriksson, Johan G and Escobedo, Jorge and Esko, Tonu and Eury, Elodie and Florez, Jose C and Fontanillas, Pierre and Forouhi, Nita G and Forsen, Tom and Fox, Caroline and Fraser, Ross M and Frayling, Timothy M and Froguel, Philippe and Frossard, Philippe and Gao, Yutang and Gertow, Karl and Gieger, Christian and Gigante, Bruna and Grallert, Harald and Grant, George B and Groop, Leif C and Groves, Christopher J and Grundberg, Elin and Guiducci, Candace and Hamsten, Anders and Han, Bok-Ghee and Hara, Kazuo and Hassanali, Neelam and ... and Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi-Ethnic Samples (T2D-GENES) Consortium and South Asian Type 2 Diabetes (SAT2D) Consortium and Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium and Mexican American Type 2 Diabetes (MAT2D) Consortium and South Asian Type Diabet SAT2D Cons and DIAbet Genetics Replication & Meta and Mexican Amer Type 2 Diabet MAT2D C and Asian Genetic Epidemiology Network and Type 2 Diabet Genetic Exploration and Type 2 Diabetes Genetic Exploration by Nex-generation sequencing in muylti-Ethnic Samples (T2D-GENES) Consortium
Nature genetics, ISSN 1546-1718, 2014, Volume 46, Issue 3, pp. 234 - 244
Journal Article
Journal Article
Nature (London), ISSN 1476-4687, 2013, Volume 505, Issue 7481, pp. 87 - 91
Journal Article
by Cheng, Yu-Ching and Stanne, Tara M and Giese, Anne-Katrin and Ho, Weang K and Traylor, Matthew and Amouyel, Philippe and Holliday, Elizabeth and Malik, Rainer and Xu, Huichun and Kittner, Thomas and Cole, John W and O´Connell, J.R and Danesh, John and Rasheed, Asif and Zhao, Wei and Engelter, Stefan and Grond-Ginsbach, Caspar and Kamatani, Yoichiro and Lathrop, Mark and Leys, Didier and Thijs, Vincent and Metso, Tiina M and Tatlisumak, Turgut and Pezzini, Alessano and Parati, Eugenio A and Norrving, Bo and Bevan, Steve and Rothwell, Peter and Sudlow, Cathie and Slowik, Agnieszka and Lindgren, Arne G and Walters, Matthew and Jannes, Jim and Shen, Jess and Crosslin, David and Doheny, Kimberly and Laurie, Cathy and Kanse, Sandip and Bis, Joshua and Fornage, Myriam and Mosley, Thomas H and Hopewell, J and Strauch, Konstantin and Müller-Nurasyid, Martina and Gieger, Christian and Waldenberger, Melanie and Peters, Annette and Meisinger, Christine and Ikram, Arfan and Longstreth, W.T and Meschia, James F and Seshai, Sudha and Sharma, Pankaj and Worrall, Bradford B and Jern, Christina and Levi, Christopher and Kubisch, Christian and Boncoraglio, Giorgio Battista and Markus, Hugh and Debette, Stéphanie and Rolfs, Arndt and Saleheen, D and Mitchell, Braxton and WTCCC-2 Consortium and Institutionen för biomedicin, avdelningen för patologi and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Biomedicine, Department of Pathology and Sahlgrenska Academy
Stroke (1970), ISSN 0039-2499, 02/2016, Volume 47, Issue 2, pp. 307 - 316
Journal Article
Rheumatology (Oxford, England), ISSN 1462-0324, 04/2017, Volume 56, Issue 1, pp. i67 - i77
... accumulation and outcome in SLE. Susceptibility to SLE has a strong genetic component, and trans-ancestral genetic studies have revealed a substantial commonality of shared genetic risk variants across different genetic ancestries... 
epidemiology | prevalence | systemic lupus erythematosus | ancestry | genetics | ethnicity | ethnic groups | lupus nephritis | autoantibodies | incidence | RHEUMATOID-ARTHRITIS | SUSCEPTIBILITY VARIANTS | SLE PATIENTS | MULTIETHNIC COHORT | RHEUMATOLOGY | AFRICAN-AMERICAN | COLLABORATING CLINICS | SURVEILLANCE PROGRAM | INTERNATIONAL INCEPTION COHORT | STAGE RENAL-DISEASE | GENOME-WIDE ASSOCIATION | Ethnic Groups - statistics & numerical data | European Continental Ancestry Group - genetics | Hispanic Americans - genetics | Lupus Erythematosus, Systemic - complications | Lupus Nephritis - genetics | Prevalence | Humans | Asian Continental Ancestry Group - genetics | European Continental Ancestry Group - statistics & numerical data | Hispanic Americans - statistics & numerical data | Kidney Failure, Chronic - ethnology | Socioeconomic Factors | Incidence | African Continental Ancestry Group - statistics & numerical data | Kidney Failure, Chronic - genetics | Ethnic Groups - genetics | Lupus Erythematosus, Systemic - ethnology | Lupus Erythematosus, Systemic - genetics | Lupus Nephritis - ethnology | African Continental Ancestry Group - genetics | Lupus Erythematosus, Systemic - physiopathology | Asian Continental Ancestry Group - statistics & numerical data | Kidney Failure, Chronic - etiology
Journal Article