Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Jose C. Florez"'
Autor:
Anna Köttgen, Emilie Cornec-Le Gall, Jan Halbritter, Krzysztof Kiryluk, Andrew J. Mallett, Rulan S. Parekh, Hila Milo Rasouly, Matthew G. Sampson, Adrienne Tin, Corinne Antignac, Elisabet Ars, Carsten Bergmann, Anthony J. Bleyer, Detlef Bockenhauer, Olivier Devuyst, Jose C. Florez, Kevin J. Fowler, Nora Franceschini, Masafumi Fukagawa, Daniel P. Gale, Rasheed A. Gbadegesin, David B. Goldstein, Morgan E. Grams, Anna Greka, Oliver Gross, Lisa M. Guay-Woodford, Peter C. Harris, Julia Hoefele, Adriana M. Hung, Nine V.A.M. Knoers, Jeffrey B. Kopp, Matthias Kretzler, Matthew B. Lanktree, Beata S. Lipska-Ziętkiewicz, Kathleen Nicholls, Kandai Nozu, Akinlolu Ojo, Afshin Parsa, Cristian Pattaro, York Pei, Martin R. Pollak, Eugene P. Rhee, Simone Sanna-Cherchi, Judy Savige, John A. Sayer, Francesco Scolari, John R. Sedor, Xueling Sim, Stefan Somlo, Katalin Susztak, Bamidele O. Tayo, Roser Torra, Albertien M. van Eerde, André Weinstock, Cheryl A. Winkler, Matthias Wuttke, Hong Zhang, Jennifer M. King, Michael Cheung, Michel Jadoul, Wolfgang C. Winkelmayer, Ali G. Gharavi
Publikováno v:
Kidney International, Vol. 101, no.6, p. 1126-1141 (2022)
Kidney International, 101(6), 1126-1141. ELSEVIER SCIENCE INC
Kidney Int
Kidney International, 101(6), 1126-1141. ELSEVIER SCIENCE INC
Kidney Int
Numerous genes for monogenic kidney diseases with classical patterns of inheritance, as well as genes for complex kidney diseases that manifest in combination with environmental factors, have been discovered. Genetic findings are increasingly used to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f139b55aba03fd797e4e247965ca5929
https://hdl.handle.net/2078.1/263285
https://hdl.handle.net/2078.1/263285
Autor:
Emma Ahlqvist, Catherine Godson, Rany M. Salem, Katalin Susztak, Alexander P. Maxwell, Colin N. A. Palmer, Eoin P. Brennan, Matthias Kretzler, Xin Sheng, Jose C. Florez, Robert G. Nelson, Leif Groop, Laura Smyth, Ross Doyle, Natalie R. van Zuydam, Viji Nair, Carol Forsblom, Valma Harjutsalo, Per-Henrik Groop, Gareth J. McKay, Erkka Valo, Darrell Andrews, Helen C. Looker, Mark I. McCarthy, Joel N. Hirschhorn, Niina Sandholm, Hongbo Liu, Damian Fermin, Amy Jayne McKnight, Joanne B. Cole, Emma H. Dahlström
BackgroundDiabetes is the leading cause of kidney disease, and heritability studies demonstrate a substantial, yet poorly understood, contribution of genetics to kidney complications in people with diabetes.MethodsWe performed genome-wide association
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3b7ffaf330078e25c026fe7cb4822f02
https://doi.org/10.1101/2021.08.27.21262264
https://doi.org/10.1101/2021.08.27.21262264
Autor:
Jaakko Tuomilehto, Dolores Corella, Kathleen A. Jablonski, Jose C. Florez, Tanya Agurs-Collins, Wim H.M. Saris, Qing Pan, Torben Hansen, Malene R. Christiansen, Tuomas O. Kilpelainen, Jeanne Mccaffery, Christopher D. Gardner, Rena R. Wing, Thorkild I.A. Sørensen, Lauren M. Corso, Arne Astrup, Paul W. Franks
Publikováno v:
Diabetes. 70
Lifestyle intervention, combining calorie restriction and physical activity to induce weight loss, is the frontline treatment for overweight or obesity and well-known to reduce waist circumference (WC). Genome-wide association studies (GWAS) have ide
Autor:
Marju Orho-Melander, Humberto García-Ortiz, Xueling Sim, Amp-T D-Genes, Cheol Joo Park, Gina M. Peloso, Jason Flannick, Brian Tomlinson, Hyun Min Kang, Emilio J. Cordova, Stephen S. Rich, Richard A. Gibbs, Angélica Martínez-Hernández, Lorena Orozco, Harsha Doddapaneni, Lisa R. Yanek, Jiwon Lee, Namrata Gupta, Valeriya Lyssenko, Sohee Han, James B. Meigs, Bong-Jo Kim, Bruce M. Psaty, Leslie S. Emery, Kerrin S. Small, Pradeep Natarajan, May E. Montasser, Christian Gieger, Sharon L.R. Kardia, Sarah C. Nelson, Craig L. Hanis, Heikki A. Koistinen, María Elena González-Villalpando, Edmund Chan, Michael Y. Tsai, Benjamin Glaser, Thomas Meitinger, Matthew J. Bown, Mariaelisa Graff, John Danesh, Sekar Kathiresan, Tiinamaija Tuomi, Ramachandran S. Vasan, Gil Atzmon, Alyna T. Khan, Diego Ardissino, Yii-Der Ida Chen, David Zhang, Rob M. van Dam, Wendy S. Post, Barry I. Freedman, D. C. Rao, Michael Preuss, Donna M. Lehman, L. Adrienne Cupples, Colin N. A. Palmer, Claudia H. T. Tam, Hortensia Moreno-Macías, Markku Laakso, Peter Dornbos, Teresa Tusié-Luna, Stella Aslibekyan, Marguerite R. Irvin, Daniel J. Rader, Jee-Young Moon, Eimear E. Kenny, Lisa W. Martin, Jennifer A. Brody, Amit Khera, Erwin P. Bottinger, Sarah E. Graham, Myriam Fornage, Ruth McPherson, Nancy L. Heard-Costa, Michael Boehnke, Clicerio Gonzalez, Ryan W. Kim, Yi-Cheng Chang, Peter M. Nilsson, Yik Ying Teo, Robert Sladek, Cristen J. Willer, Fei Fei Wang, Donna K. Arnett, Mark Chaffin, Karine A. Viaud Martinez, Alanna C. Morrison, Leslie A. Lange, Ravindranath Duggirala, Donna M. Muzny, Kent D. Taylor, Niels Grarup, Soren Germer, Patricia A. Peyser, Brian E. Cade, Lewis C. Becker, Steven A. Lubitz, Nicholette D. Palmer, Susan K. Dutcher, Ronald C.W. Ma, Xuenan Mi, Xiuqing Guo, Hugh Watkins, Eric Boerwinkle, Qibin Qi, Johanna Kuusisto, Christie M. Ballantyne, Tanika N. Kelly, Rajiv Chowdhury, Elvia Mendoza-Caamal, Wing-Yee So, Tien Yin Wong, Torben Hansen, Cecilia Contreras-Cubas, Jeong-Sun Seo, Mi Yeong Hwang, Daekwan Seo, Dajiang J. Liu, Cristina Revilla-Monsalve, Paul S. de Vries, Daniel R. Witte, Yi-Jen Hung, Olle Melander, Karen L. Mohlke, Lucinda Antonacci-Fulton, Francisco Barajas-Olmos, Soo Heon Kwak, Daniel E. Weeks, Claudia Schurmann, Ginger A. Metcalf, Young-Jin Kim, Adrienne M. Stilp, Lori L. Bonnycastle, John Blangero, Ralph A. DeFronzo, Donald W. Bowden, Rasika A. Mathias, Oluf Pedersen, Rozenn N. Lemaitre, Stephen T. McGarvey, Heribert Schunkert, Jaakko Tuomilehto, Farook Thameem, Valentin Fuster, Joshua C. Bis, George Hindy, Allan Linneberg, James G. Wilson, Kyong Soo Park, Sergio A. Islas-Andrade, Ching-Yu Cheng, Won Jung Choi, Minxian X. Wang, Xuzhi Wang, Adolfo Correa, Jai G. Broome, Gail P. Jarvik, Alexander P. Reiner, E. Shyong Tai, Juyoung Lee, Mark I. McCarthy, Nilesh J. Samani, Susan Redline, Carlos A. Aguilar-Salinas, Jerome I. Rotter, Ma. Eugenia Garay-Sevilla, Jiang He, Patrick T. Ellinor, Joseph Park, Joanne E. Curran, Nir Barzilai, Federico Centeno-Cruz, Seonwook Lee, Lawrence F. Bielak, Jianjun Liu, Charles Kooperberg, Juan M. Peralta, Jose C. Florez, Leif Groop, Noël P. Burtt, Margaret Sunitha Selvaraj, Jeffrey R. O'Connell, Ruth J. F. Loos
Large-scale gene sequencing studies for complex traits have the potential to identify causal genes with therapeutic implications. We performed gene-based association testing of blood lipid levels with rare (minor allele frequency170,000 individuals f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::08cffcbe73ed87d1953f10593c831399
https://doi.org/10.1101/2020.12.22.423783
https://doi.org/10.1101/2020.12.22.423783
Autor:
Yingchang Lu, Denis Rybin, Paul M. Ridker, Tamara B. Harris, Ruth J. F. Loos, Tuomo Rankinen, Patricia A. Peyser, Nora Franceschini, Adolfo Correa, Caroline Hayward, Jerome I. Rotter, Ayse Demirkan, Mohsen Ghanbari, Alison D. Murray, Jonathan Marten, Peitao Wu, Mike A. Nalls, Lawrence F. Bielak, Cornelia M. van Duijn, Salman M. Tajuddin, Yize Li, Michael M. Province, Jingmin Liu, Lynda M. Rose, André G. Uitterlinden, D. C. Rao, Solomon K. Musani, Vilmundur Gudnason, Albert V. Smith, Sharon L.R. Kardia, Raymond Noordam, Susan Redline, Erwin P. Bottinger, Daniel I. Chasman, Lenore J. Launer, Alan B. Zonderman, Renée de Mutsert, Mary F. Feitosa, Ching-Ti Liu, James G. Wilson, Dina Vojinovic, Charles Kooperberg, Josée Dupuis, Najaf Amin, Claude Bouchard, Jose C. Florez, Linda Kao, Dennis O. Mook-Kanamori, Karen Schwander, Blair H. Smith, Michele K. Evans, David S. Siscovick, Jason L. Vassy, James B. Meigs, Sridharan Raghavan, Donna K. Arnett, Trudy Voortman, Jun Liu
Publikováno v:
Wu, P, Rybin, D, Bielak, L F, Feitosa, M F, Franceschini, N, Li, Y, Lu, Y, Marten, J, Musani, S K, Noordam, R, Raghavan, S, Rose, L M, Schwander, K, Smith, A V, Tajuddin, S M, Vojinovic, D, Amin, N, Arnett, D K, Bottinger, E P, Demirkan, A, Florez, J C, Ghanbari, M, Harris, T B, Launer, L J, Liu, J, Liu, J, Mook-Kanamori, D O, Murray, A D, Nalls, M A, Peyser, P A, Uitterlinden, A G, Voortman, T, Bouchard, C, Chasman, D, Correa, A, de Mutsert, R, Evans, M K, Gudnason, V, Hayward, C, Kao, L, Kardia, S L R, Kooperberg, C, Loos, R J F, Province, M M, Rankinen, T, Redline, S, Ridker, P M, Rotter, J I, Siscovick, D, Smith, B H, van Duijn, C, Zonderman, A B, Rao, D C, Wilson, J G, Dupuis, J, Meigs, J B, Liu, C T & Vassy, J L 2020, ' Smoking-by-genotype interaction in type 2 diabetes risk and fasting glucose ', PLoS ONE, vol. 15, no. 5, e0230815 . https://doi.org/10.1371/journal.pone.0230815
PLoS ONE, 15(5). PUBLIC LIBRARY SCIENCE
PLoS One (print), 15(5):e0230815. Public Library of Science
PLoS ONE
PLoS ONE, Vol 15, Iss 5, p e0230815 (2020)
PloS one, vol 15, iss 5
PLoS ONE, 15(5). PUBLIC LIBRARY SCIENCE
PLoS One (print), 15(5):e0230815. Public Library of Science
PLoS ONE
PLoS ONE, Vol 15, Iss 5, p e0230815 (2020)
PloS one, vol 15, iss 5
Publisher's version (útgefin grein)
Smoking is a potentially causal behavioral risk factor for type 2 diabetes (T2D), but not all smokers develop T2D. It is unknown whether genetic factors partially explain this variation. We performed genome-e
Smoking is a potentially causal behavioral risk factor for type 2 diabetes (T2D), but not all smokers develop T2D. It is unknown whether genetic factors partially explain this variation. We performed genome-e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f0c1eccf3ca1d1aff1e025d49a3cdcf6
https://ora.ox.ac.uk/objects/uuid:0663cf39-84eb-4f28-b151-5588f22ea9e6
https://ora.ox.ac.uk/objects/uuid:0663cf39-84eb-4f28-b151-5588f22ea9e6
Autor:
Alisa K. Manning, Joshua Chiou, Kyle J. Gaulton, Miriam S. Udler, Hyunkyung Kim, Jose C. Florez, Marcin von Grotthuss, Josep M. Mercader
Publikováno v:
Diabetes. 69
Improved understanding of disease-causing pathways for type 2 diabetes (T2D) may lead to novel therapeutic targets and individualized treatment. Rapid expansion in the number of T2D genetic loci over the past few years can be leveraged to identify pa
Publikováno v:
Diabetes Care
OBJECTIVE Type 2 diabetes (T2D) is associated with increased mortality in ethnically diverse populations, although the extent to which this association is genetically determined is unknown. We sought to determine whether T2D-related genetic variants
Autor:
Taylor J. Maxwell, Kathleen A. Jablonski, William C. Knowler, Paul W. Franks, Kieren J. Mather, Jose C. Florez, Steven E. Kahn
Publikováno v:
Diabetes. 67
The complex genetic architecture of type 2 diabetes (T2D) includes gene-by-environment (G×E) and gene-by-gene (G×G) interactions. To identify genetic markers for G×E and G×G, we screened individual markers for patterns indicative of interactions
Autor:
Arnita F. Norwood, Thomas J. Wang, Stephen B. Kritchevsky, Joan M. Lappe, Katherine L. Tucker, James G. Wilson, Carl D. Langefeld, Yingchang Lu, Andrew Bjonnes, Pamela L. Lutsey, Jaeyoung Hong, James S. Pankow, James B. Meigs, Joshua C. Bis, Jose M. Ordovas, Jeffery D. Roizen, Tamara B. Harris, Nicholette D. Palmer, Chao-Qiang Lai, Erwin P. Bottinger, Hakon Hakanarson, Jasmin Divers, Lingyi Lu, Kathryn E. Hatchell, Saonli Basu, Bryan Kestenbaum, Yongmei Liu, Heidi J. Kalkwarf, Cassianne Robinson-Cohen, Bishwa Raj Sapkota, John A. Shepherd, Sharon E. Oberfield, Lynne E. Wagenknecht, Donald W. Bowden, Eric Boerwinkle, Andrea Kelly, Ian H. de Boer, Josée Dupuis, Alessandra Chesi, Bruce M. Psaty, Babette S. Zemel, Vicente Gilsanz, Ching-Ti Liu, Richa Saxena, Struan F.A. Grant, Dan E. Arking, Jonathan P. Bradfield, Corinne D. Engelman, Solomon K. Musani, Denise K. Houston, Barry I. Freedman, Mike A. Nalls, Dharambir K. Sanghera, Julie T. Ziegler, Jill M. Norris, Jerome I. Rotter, Jose C. Florez, Ruth J. F. Loos, Erin D. Michos, Liana K. Billings
Context Vitamin D inadequacy is common in the adult population of the United States. Although the genetic determinants underlying vitamin D inadequacy have been studied in people of European ancestry, less is known about populations with Hispanic or
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b3a6dc352025736028f313db8e5c2e3
https://europepmc.org/articles/PMC6276579/
https://europepmc.org/articles/PMC6276579/
Autor:
Tazeen H. Jafar, Lars Lind, Peter Almgren, Wendy Winckler, Eitaro Nakashima, Young Min Cho, Annette Peters, Rona J. Strawbridge, Ananda R. Wickremasinghe, Katharine R. Owen, Lee-Ming Chuang, Tien-Jyun Chang, Graeme I. Bell, James B. Meigs, Bill Musk, Timo A. Lakka, Elin Grundberg, Wei Lu, Sarah Edkins, George Dedoussis, Weiping Jia, Danish Saleheen, Suthesh Sivapalaratnam, Maria Samuel, Tien Yin Wong, Lu Qi, Pierre Fontanillas, Momoko Horikoshi, Jirong Long, Abdul Basit, Anubha Mahajan, Andrew T. Hattersley, Markus M. Nöthen, Denis Rybin, Inger Njølstad, S. Krithika, Miguel Cruz, Delilah Zabaneh, Leena Peltonen, Jasmina Kravic, Sangsoo Kim, David Couper, Lori L. Bonnycastle, Heather M. Stringham, Yi-Cheng Chang, Paul Elliott, Eric J.G. Sijbrands, Nita G. Forouhi, Alena Stančáková, Ghazala Mirza, Robert W. Lawrence, Ruth J. F. Loos, Norman Klopp, Shiro Maeda, Martina Müller-Nurasyid, Jer-Yuarn Wu, Jianjun Liu, Kee Seng Chia, Elodie Eury, Loukianos S. Rallidis, Timothy M. Frayling, Ken Yamamoto, David Altshuler, Gunnar Sigurosson, Harald Grallert, Jackie F. Price, Barbara Thorand, Jouko Saramies, Malene M. Kristensen, Sonali Pechlivanis, Inês Barroso, Jong-Young Lee, Melissa Parkin, Josée Dupuis, Stéphane Lobbens, Jesús Kumate, Elena Tremoli, Sudhir Kowlessur, Xueling Sim, Norihiro Kato, Philippe Froguel, Kathleen Stirrups, Eero Lindholm, Alex S. F. Doney, Andres Metspalu, Yu-Tang Gao, Roman Wennauer, Xiao-Ou Shu, Marilyn C. Cornelis, Veikko Salomaa, Nanette R. Lee, Johanna Kuusisto, Caroline S. Fox, Man Li, James Scott, Wing-Yee So, Andrew R. Wood, Inga Prokopenko, Oddgeir L. Holmen, Tin Aung, Ryoichi Takayanagi, Chen Suo, Hara Kazuo, Carl G. P. Platou, Ann M. Kelly, Teresa Ferreira, Karl-Heinz Jöckel, Wei-Yen Lim, James F. Wilson, Tom Forsén, Qi Sun, Valur Emilsson, Gonçalo R. Abecasis, Fan Zhang, Timo Saaristo, Harry Campbell, Ying Wu, Mark Seielstad, Wei Zheng, Han Chen, Stavroula Kanoni, Yuqian Bao, Jose C. Florez, Wan Ting Tay, Ronald C. WMa, Gerald Steinbach, Min Jin Go, Rong Zhang, Junbin Liang, Vasiliki Lagou, Leif Groop, Emil Rehnberg, Nabi Shah, Weihua Zhang, Yun Li, Bengt Sennblad, Olle Melander, Nancy L. Pedersen, Muhammed Islam, Jaakko Tuomilehto, Young Jin Kim, Richard N. Bergman, Juliana C.N. Chan, Eleftheria Zeggini, Andrew D. Johnson, Kees Hovingh, Joban Sehmi, Rainer Rauramaa, Satu Männistö, Reedik Mägi, Samuel Liju, Mingyu Yang, Ayellet V. Segrè, Noël P. Burtt, Mozhgan Dorkhan, Beverley Balkau, Neelam Hassanali, Hyun Min Kang, Fabrizio Veglia, Eeva Korpi-Hyövälti, Loic Yengo, Elizabeth J. Rossin, Angela Silveira, Maggie C.Y. Ng, Yuan-Tsong Chen, Anders Hamsten, David R. Matthews, Mark J. Caulfield, Emmi Tikkanen, Tanya M. Teslovich, John R. B. Perry, Karen L. Mohlke, Sarah E. Hunt, Soo Heon Kwak, Jorge Escobedo, Christopher J. Groves, Ulf de Faire, Jeremy B M Jowett, Gudmar Thorleifsson, Michael Roden, Evelin Mihailov, Viswanathan Mohan, Craig L. Hanis, Thomas WMühleisen, Congrong Wang, Sonia Shah, Kyle J. Gaulton, Jaspal S. Kooner, Jiro Nakamura, Mustafa Atalay, Linda S. Adair, S Wiltshire, Tõnu Esko, Anna Jonsson, Antigone S. Dimas, Karin Leander, Li Ching Chang, George B. Grant, Bo Isomaa, Anne U. Jackson, Claudia Langenberg, Kristian Hveem, Yoon Shin Cho, Astradur B. Hreidarsson, Xu Wang, Keizo Ohnaka, Alexandra C. Nica, Simon D. Rees, Pau Navarro, Sekar Kathiresan, Rob M. van Dam, Zafar I. Hydrie, Bok Ghee Han, Francis S. Collins, Fuu Jen Tsai, Unnur Thorsteinsdottir, Ross M. Fraser, Caroline Hayward, Cornelia M. van Duijn, Samuli Ripatti, Mieke D. Trip, Hyung Lae Kim, Rafn Benediktsson, Candace Guiducci, Bruna Gigante, Kyong Soo Park, Wen Hong L. Kao, Tom Wilsgaard, Leena Kinnunen, John Danesh, Alan James, Alan R. Shuldiner, Mitsuhiro Yokota, Jen Mai Lee, Kari Stefansson, Erik Ingelsson, Colin N. A. Palmer, David J. Hunter, Paul Zimmet, Manickam Chidambaram, Sirkka Keinänen-Kiukaanniemi, Laura J. Scott, Susanne Moebus, Benjamin F. Voight, Wolfgang Rathmann, Hassan Khan, Thomas Illig, Prasad Katulanda, Christian Gieger, Andrew D. Morris, Yik Ying Teo, Andrew P. Morris, Venkatesan Radha, N. William Rayner, Johan G. Eriksson, Christian Dina, Igor Rudan, Sailaja Vedantam, Cheng Hu, James S. Pankow, Ann-Christine Syvänen, Karl Gertow, Valeriya Lyssenko, Guillaume Charpentier, Albert Hofman, Chiea Chuen Khor, Joseph Trakalo, Peter Kraft, Takashi Kadowaki, Qiuyin Cai, John C. Chambers, André G. Uitterlinden, Simon C. Potter, Nicholas J. Wareham, Soumya Raychaudhuri, Jian'an Luan, Tiinamaija Tuomi, Anthony H. Barnett, Juha Saltevo, Robert A. Scott, Valgerdur Steinthorsdottir, Peng Keat Ng, Mark I. McCarthy, Åsa K. Hedman, Kerrin S. Small, Julia Meyer, Frank B. Hu, Cecilia M. Lindgren, Jennifer E. Below, Nancy J. Cox, Jennie Hui, Andrew Crenshaw, Latonya F. Been, Nam H. Cho, Janani Pinidiyapathirage, A. Samad Shera, Bernhard OBoehm, Jason Carey, Augustine Kong, Twee Hee Ong, Philippe M. Frossard, Donald W. Bowden, Toshimasa Yamauchi, Steve E. Humphries, Cordelia Langford, Xinzhong Li, Hiroshi Ikegami, Stéphane Cauchi, Ching-Ti Liu, Michael Boehnke, Peter M. Nilsson, Debashish Das, John Beilby, Robin Young, Christian Herder, Asif Rasheed, Neil Robertson, Raimund Erbel, Fumihiko Takeuchi, Markku Laakso, Esteban J. Parra, Panos Deloukas, Eric Boerwinkle, Adan Valladares-Salgado, Chien-Hsiun Chen, Kay-Tee Khaw, Damiano Baldassarre, Ashok Kumar, E. Shyong Tai, Peter S. Chines, Dharambir KSanghera, Peter Donnelly
Publikováno v:
Nature Genetics, 46(3), 234-+. Nature Publishing Group
Nature genetics
Nature Genetics; Vol 46
Mahajan, A, Go, M J, Zhang, W, Below, J E, Gaulton, K J, Ferreira, T, Horikoshi, M, Johnson, A D, Ng, M C Y, Prokopenko, I, Saleheen, D, Wang, X, Zeggini, E, Abecasis, G R, Adair, L S, Almgren, P, Atalay, M, Aung, T, Baldassarre, D, Balkau, B, Bao, Y, Barnett, A H, Barroso, I, Basit, A, Been, L F, Beilby, J, Bell, G I, Benediktsson, R, Bergman, R N, Boehm, B O, Boerwinkle, E, Bonnycastle, L L, Burtt, N, Cai, Q, Campbell, H, Carey, J, Cauchi, S, Caulfield, M, Chan, J C N, Chang, L-C, Chang, T-J, Chang, Y-C, Fraser, R M, Hayward, C & Morris, A & Navarro, P & Price, J F & Rudan, I & Wilson, J F & Zhang, R 2014, ' Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility ', Nature Genetics, vol. 46, no. 3, pp. 234-244 . https://doi.org/10.1038/ng.2897
Nature Genetics
Nature genetics, 46(3), 234-244. Nature Publishing Group
Nature genetics
Nature Genetics; Vol 46
Mahajan, A, Go, M J, Zhang, W, Below, J E, Gaulton, K J, Ferreira, T, Horikoshi, M, Johnson, A D, Ng, M C Y, Prokopenko, I, Saleheen, D, Wang, X, Zeggini, E, Abecasis, G R, Adair, L S, Almgren, P, Atalay, M, Aung, T, Baldassarre, D, Balkau, B, Bao, Y, Barnett, A H, Barroso, I, Basit, A, Been, L F, Beilby, J, Bell, G I, Benediktsson, R, Bergman, R N, Boehm, B O, Boerwinkle, E, Bonnycastle, L L, Burtt, N, Cai, Q, Campbell, H, Carey, J, Cauchi, S, Caulfield, M, Chan, J C N, Chang, L-C, Chang, T-J, Chang, Y-C, Fraser, R M, Hayward, C & Morris, A & Navarro, P & Price, J F & Rudan, I & Wilson, J F & Zhang, R 2014, ' Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility ', Nature Genetics, vol. 46, no. 3, pp. 234-244 . https://doi.org/10.1038/ng.2897
Nature Genetics
Nature genetics, 46(3), 234-244. Nature Publishing Group
To access publisher's full text version of this article click on the hyperlink at the bottom of the page To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated published meta-analyses of genome-wide assoc