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by Willer, Cristen J and Schmidt, Ellen M and Sengupta, Sebanti and Peloso, Gina M and Gustafsson, Stefan and Kanoni, Stavroula and Ganna, Anea and Chen, Jin and Buchkovich, Martin L and Mora, Samia and Beckmann, Jacques S and Bragg-Gresham, Jennifer L and Chang, Hsing-Yi and Demirkan, Ayşe and den Hertog, Heleen M and Do, Ron and Donnelly, Louise A and Ehret, Georg B and Esko, Tõnu and Feitosa, Mary F and Ferreira, Teresa and Fischer, Krista and Fontanillas, Pierre and Fraser, Ross M and Freitag, Daniel F and Gurdasani, Deepti and Heikkilä, Kauko and Hyppönen, Elina and Isaacs, Aaron and Jackson, Anne U and Johansson, Asa and Johnson, Toby and Kaakinen, Marika and Kettunen, Johannes and Kleber, Marcus E and Li, Xiaohui and Luan, Jian'an and Lyytikäinen, Leo-Pekka and Magnusson, Patrik K. E and Mangino, Massimo and Mihailov, Evelin and Montasser, May E and Müller-Nurasyid, Martina and Nolte, Ilja M and O'Connell, Jeffrey R and Palmer, Cameron D and Perola, Markus and Petersen, Ann-Kristin and Sanna, Serena and Saxena, Richa and Service, Susan K and Shah, Sonia and Shungin, Dmitry and Sidore, Carlo and Song, Ci and Strawbridge, Rona J and Surakka, Ida and Tanaka, Toshiko and Teslovich, Tanya M and Thorleifsson, Gudmar and van den Herik, Evita G and Voight, Benjamin F and Volcik, Kelly A and Waite, Lindsay L and Wong, Anew and Wu, Ying and Zhang, Weihua and Absher, Devin and Asiki, Gershim and Barroso, Inês and Been, Latonya F and Bolton, Jennifer L and Bonnycastle, Lori L and Brambilla, Paolo and Burnett, Mary S and Cesana, Giancarlo and Dimitriou, Maria and Doney, Alex S. F and Döring, Angela and Elliott, Paul and Epstein, Stephen E and Eyjolfsson, Gudmundur Ingi and Gigante, Bruna and Goodarzi, Mark O and Grallert, Harald and Gravito, Martha L and Groves, Christopher J and Hallmans, Göran and Hartikainen, Anna-Liisa and Hayward, Caroline and Hernandez, Dena and Hicks, Anew A and Holm, Hilma and Hung, Yi-Jen and Illig, Thomas and Jones, Michelle R and Kaleebu, Pontiano and Kastelein, John J. P and Khaw, Kay-Tee and Kim, Eric and ... and Global Lipids Genetics Consortium and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Institutionen för odontologi and Näringsforskning and Umeå universitet and Medicin
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 11, pp. 1274 - 1283
Levels of low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, triglycerides and total cholesterol are heritable, modifiable... 
DENSITY-LIPOPROTEIN CHOLESTEROL | HEART-DISEASE | METAANALYSIS | GENE | GENETICS & HEREDITY | CARDIOVASCULAR-DISEASE | SUSCEPTIBILITY LOCI | RISK | IDENTIFIES 13 | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Genes | Humans | Lipids | Cholesterol, LDL | European Continental Ancestry Group | Genotype | Triglycerides | Coronary Artery Disease | Cholesterol | Studies | Asian Continental Ancestry Group | Cholesterol, HDL | African Continental Ancestry Group | Lipoproteins (low density) | Diabetes mellitus | Data processing | Risk factors | Body mass index | Lipoproteins | Genotyping | Blood pressure | Lipid metabolism | Lipoproteins (high density) | Heart diseases | European Continental Ancestry Group - genetics | Lipids - genetics | Asian Continental Ancestry Group - genetics | Cholesterol, HDL - genetics | Coronary Artery Disease - blood | Cholesterol, LDL - genetics | Lipids - blood | Coronary Artery Disease - genetics | Triglycerides - blood | Cholesterol, HDL - blood | Cholesterol, LDL - blood | African Continental Ancestry Group - genetics | Triglycerides - genetics | Quantitative trait loci | Proteolipids | Genetic aspects | Blood lipoproteins | Biological control systems | Observations | Identification and classification | Index Medicus | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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, Anew 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, Anew 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 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 South Asian Type 2 Diabetes (SAT2D) Consortium and Asian Genetic Epidemiology Network Type 2 Diabetes (AGEN-T2D) Consortium and Type 2 Diabetes Genetic Exploration by Nex-generation sequencing in muylti-Ethnic Samples (T2D-GENES) Consortium and DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium and Mexican American Type 2 Diabetes (MAT2D) Consortium and Type 2 Diabetes Genetic Exploration by Next-generation sequencing in multi-Ethnic Samples (T2D-GENES) Consortium and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Kardiovaskulär epidemiologi and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi
Nature genetics, ISSN 1061-4036, 2014, Volume 46, Issue 3, pp. 234 - 244
Journal Article
Nature, ISSN 0028-0836, 2014, Volume 505, Issue 7481, pp. 87 - 91
Journal Article
by Williams Amy, A.L and Jacobs Suzanne, S.B.R and Moreno-Macías, Hortensia and Huerta-Chagoya, Alicia and Churchhouse, Claire and Márquez-Luna, Carla and Gómez-Vázquez, María José and Burtt Noël, N.P and Aguilar-Salinas, Carlos A and González-Villalpando, Clicerio and Florez, Jose C and Orozco, Lorena and Tusié-Luna, Teresa and Altshuler, David and Ripke, Stephan and Manning, Alisa K and García-Ortíz, Humberto and Neale, Benjamin and Reich, David and Stram, Daniel O and Fernández-López, Juan Carlos and Romero-Hidalgo, Sandra and Patterson, Nick and Haiman, Christopher A and Aguilar-Delfín, Irma and Martínez-Hernández, Angélica and Centeno-Cruz, Federico and Mendoza-Caamal, Elvia and Revilla-Monsalve, Cristina and Islas-Andrade, Sergio and Córdova, Emilio and Rodríguez-Arellano, Eunice and Soberón, Xavier and Florez Jose, J.C and González-Villalpando María Elena, M.A and Henderson, Brian E and Monroe, Kristine and Wilkens, Lynne and Kolonel, Laurence N and Le Marchand, Loic and Riba, Laura and Ordóñez-Sánchez María Luisa, M.A and Rodríguez-Guillén, Rosario and Cruz-Bautista, Ivette and Rodríguez-Torres, Maribel and Muñoz-Hernández, Linda Liliana and Sáenz, Tamara and Gómez, Donají and Alvirde, Ulices and Onofrio, Robert C and Brodeur, Wendy M and Gage, Diane and Murphy, Jacquelyn and Franklin, Jennifer and Mahan, Scott and Ardlie, Kristin and Crenshaw, Andrew T and Winckler, Wendy and Prüfer, Kay and Shunkov, Michael V and Sawyer, Susanna and Stenzel, Udo and Kelso, Janet and Lek, Monkol and Sankararaman, Sriram and MacArthur, Daniel G and Derevianko, Anatoli P and Pääbo, Svante and Jacobs, Suzanne B.R and Gopal, Shuba and Grammatikos, James A and Smith, Ian C and Bullock, Kevin H and Deik, Amy A and Souza, Amanda L and Pierce, Kerry A and Clish, Clary B and Fennell, Timothy and Farjoun, Yossi and Gabriel, Stacey and Gross, Myron D and Pereira, Mark A and Seielstad, Mark and Koh, Woon-Puay and Tai, E-Shyong and Flannick, Jason and Fontanillas, Pierre and Morris, Andrew and Teslovich, Tanya M and Atzmon, Gil and Blangero, John and Bowden, Donald W and Chambers, John and Cho, Yoon Shin and Duggirala, Ravindranath and Glaser, Benjamin and Hanis, Craig and Kooner, Jaspal and Laakso, Markku and Lee, Jong-Young and ... and SIGMA Type 2 Diabet Consortium and Broad Genomics Platform and T2D-GENES Consortium and SIGMA Type 2 Diabetes Consortium and The SIGMA Type 2 Diabetes Consortium
Nature, ISSN 0028-0836, 2014, Volume 506, Issue 7486, pp. 97 - 101
Performing genetic studies in multiple human populations can identify disease risk alleles that are common in one population but rare in others(1), with the... 
TRANSPORTER | INSULIN-RESISTANCE | KCNQ1 | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY | LINKS | POPULATIONS | MELLITUS | ASSOCIATION | ANCESTRY | GENOME | Haplotypes | Humans | Liver | Male | Genomes | Endoplasmic Reticulum | Confidence intervals | Body mass index | Ratios | Monocarboxylic Acid Transporters | Metabolites | Population | Female | Diabetes Mellitus, Type 2 | Age | Genetic Predisposition to Disease | Genome-Wide Association Study | Genealogy | European Continental Ancestry Group | Lipid Metabolism | Triglycerides | Gene expression | Studies | SLC16A11 protein, human | Asian Continental Ancestry Group | Animals | Alleles | Mexico | Neanderthals | Polymorphism, Single Nucleotide | Diabetes | HeLa Cells | Indians, North American | African Continental Ancestry Group | RNA, Messenger | Methods | Cohort Studies | Diabetes Mellitus, Type 2 - genetics | Asian Continental Ancestry Group - genetics | RNA, Messenger - metabolism | Haplotypes - genetics | Lipid Metabolism - genetics | African Continental Ancestry Group - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Endoplasmic Reticulum - genetics | Liver - metabolism | RNA, Messenger - genetics | Neanderthals - genetics | Triglycerides - metabolism | Indians, North American - genetics | Polymorphism, Single Nucleotide - genetics | Liver - cytology | Monocarboxylic Acid Transporters - genetics | Index Medicus
Journal Article
Science, ISSN 0036-8075, 10/2011, Volume 334, Issue 6052, pp. 94 - 98
We present an Aboriginal Australian genomic sequence obtained from a 100-year-old lock of hair donated by an Aboriginal man from southern Western Australia in... 
Gene flow | Highlands | Aboriginal Australians | Genomics | REPORTS | Alleles | Admixtures | Genomes | Modeling | We they distinction | Asians | Y-CHROMOSOME | NEW-GUINEA | HUMAN-EVOLUTION | MULTIDISCIPLINARY SCIENCES | SEQUENCE | SETTLEMENT | DIVERSITY | MODEL | ESKIMO | HISTORY | Dispersal | Contamination | Mobility | Native peoples | Australia | Haplotypes | Western Australia | Humans | Asian Continental Ancestry Group - genetics | Male | Phylogeny | Hominidae - genetics | DNA, Mitochondrial - genetics | Ethnic Groups - genetics | Computer Simulation | Far East | Oceanic Ancestry Group - genetics | European Continental Ancestry Group - genetics | Gene Flow | Gene Frequency | Sequence Analysis, DNA | Linkage Disequilibrium | Animals | Genetics, Population - methods | Asia | Polymorphism, Single Nucleotide | Genome, Mitochondrial | African Continental Ancestry Group | Genome, Human | Emigration and Immigration | Physiological aspects | Australian aborigines | Genetic aspects | Research | Nucleotide sequencing | Population genetics | Human genetics | DNA sequencing | Index Medicus | Populations and Evolution | DNA, Mitochondrial | Humanities and Social Sciences | Life Sciences | Ethnic Groups | Biological anthropology | Genetics | Hominidae | Oceanic Ancestry Group | Genetics, Population | European Continental Ancestry Group | Asian Continental Ancestry Group
Journal Article
Nature Genetics, ISSN 1061-4036, 12/2014, Volume 46, Issue 12, pp. 1267 - 1273
Journal Article