Resultados de procura - E. Warwick Daw

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  1. 1
    Multipoint Oligogenic Analysis of Age-at-Onset Data with Applications to Alzheimer Disease Pedigrees

    Multipoint Oligogenic Analysis of Age-at-Onset Data with Applications to Alzheimer Disease Pedigrees por E. Warwick Daw, Simon Heath, Ellen M. Wijsman

    Publicado 1999
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  2. 2
    The Number of Trait Loci in Late-Onset Alzheimer Disease

    The Number of Trait Loci in Late-Onset Alzheimer Disease por E. Warwick Daw, Haydeh Payami, Ellen Nemens, David Nochlin, Thomas D. Bird, Gerard D. Schellenberg, Ellen M. Wijsman

    Publicado 2000
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  3. 3
    Genome-Wide Association Study of Personality Traits in the Long Life Family Study

    Genome-Wide Association Study of Personality Traits in the Long Life Family Study por Harold Bae, Paola Sebastiani, Jenny X. Sun, Stacy L. Andersen, E. Warwick Daw, Antonio Terracciano, Luigi Ferrucci, Thomas T. Perls

    Publicado 2013
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  4. 4
    Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy

    Genome-wide mapping of modifier chromosomal loci for human hypertrophic cardiomyopathy por E. Warwick Daw, S. N. Chen, Grazyna Czernuszewicz, Raffaella Lombardi, Yue Lu, Jianchao Ma, Robert L. Roberts, Sanjay Shete, Ali J. Marian

    Publicado 2007
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  5. 5
    Familial resemblance for ??VO2max in the sedentary state: the HERITAGE family study

    Familial resemblance for ??VO2max in the sedentary state: the HERITAGE family study por Claude Bouchard, E. Warwick Daw, Treva Rice, L. P russe, Jacques Gagnon, Michael A. Province, Arthur S. Leon, D. C. Rao, JAMES S. SKINNER, Jack H. Wilmore

    Publicado 1998
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  6. 6
    Evidence for a Novel Late-Onset Alzheimer Disease Locus on Chromosome 19p13.2

    Evidence for a Novel Late-Onset Alzheimer Disease Locus on Chromosome 19p13.2 por Ellen M. Wijsman, E. Warwick Daw, C E Yu, Haydeh Payami, Ellen J. Steinbart, David Nochlin, Erin M. Conlon, Thomas D. Bird, Gerard D. Schellenberg

    Publicado 2004
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  7. 7
    Meta-analysis of genetic variants associated with human exceptional longevity

    Meta-analysis of genetic variants associated with human exceptional longevity por Paola Sebastiani, Harold Bae, Fangui Sun, Stacy L. Andersen, E. Warwick Daw, Alberto Malovini, Toshio Kojima, Nobuyoshi Hirose, Nicole Schupf, Annibale Alessandro Puca, Thomas T. Perls

    Publicado 2013
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  8. 8
    Reproducibility of maximal exercise test data in the HERITAGE Family Study

    Reproducibility of maximal exercise test data in the HERITAGE Family Study por J. S. Skinner, K. M. Wilmore, Anna Jaskólska, Artur Jaskólski, E. Warwick Daw, Treva Rice, Jacques Gagnon, ARTHUR S. LEON, Jack H. Wilmore, D. C. Rao, Claude Bouchard

    Publicado 1999
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  9. 9
    Construction of Multi-Modal Transcriptome-Small Molecule Interaction Networks from High-Throughput Measurements to Study Human Complex Traits

    Construction of Multi-Modal Transcriptome-Small Molecule Interaction Networks from High-Throughput Measurements to Study Human Complex Traits por Vaha Akbary Moghaddam, Sandeep Acharya, Michaela Schwaiger-Haber, Shu Liao, Wooseok J. Jung, Bharat Thyagarajan, Leah P. Shriver, E. Warwick Daw, Nancy L. Saccone, Ping An, Michael R. Brent, Gary J. Patti, Michael A. Province

    Publicado 2025
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  10. 10
    Mother’s Genome or Maternally-Inherited Genes Acting in the Fetus Influence Gestational Age in Familial Preterm Birth

    Mother’s Genome or Maternally-Inherited Genes Acting in the Fetus Influence Gestational Age in Familial Preterm Birth por Jevon Plunkett, Mary F. Feitosa, Michelle Trusgnich, Michael F. Wangler, Lisanne Palomar, Zachary A.-F. Kistka, Emily DeFranco, Tammy Shen, Adrienne E.D. Stormo, Hilkka Puttonen, Mikko Hallman, Ritva Haataja, Aino Luukkonen, Vineta Fellman, Leena Peltonen, Aarno Palotie, E. Warwick Daw, Ping An, Kari Teramo, Ingrid B. Borecki, Louis J. Muglia

    Publicado 2009
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  11. 11
    New genetic loci link adipose and insulin biology to body fat distribution

    New genetic loci link adipose and insulin biology to body fat distribution por Dmitry Shungin, Thomas W. Winkler, Damien C. Croteau‐Chonka, Teresa Ferreira, Adam E. Locke, Reedik Mägi, Rona J. Strawbridge, Tune H. Pers, Krista Fischer, Anne E. Justice, Tsegaselassie Workalemahu, Joseph Wu, Martin L. Buchkovich, Nancy L. Heard‐Costa, Tamara S. Roman, Alexander Drong, Ci Song, Stefan Gustafsson, Felix R. Day, Tõnu Esko, Tove Fall, Zoltán Kutalik, Jian’an Luan, Joshua C. Randall, André Scherag, Sailaja Vedantam, Andrew R. Wood, Ming‐Huei Chen, Rudolf S.N. Fehrmann, Juha Karjalainen, Bratati Kahali, Yongmei Liu, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bragg‐Gresham, Steven Buyske, Ayşe Demirkan, Georg Ehret, Mary F. Feitosa, Anuj Goel, Anne Jackson, Toby Johnson, Marcus E. Kleber, Kati Kristiansson, Massimo Mangino, Irene Mateo Leach, Carolina Medina‐Gómez, Colin N. A. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Alena Stančáková, Yan V. Sun, Toshiko Tanaka, Alexander Teumer, Jana V. van Vliet‐Ostaptchouk, Loïc Yengo, Weihua Zhang, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Stefania Bandinelli, Amy Barrett, Claire Bellis, Amanda J. Bennett, Christian Berne, Matthias Blüher, Stefan Böhringer, Fabrice Bonnet, Yvonne Böttcher, Marcel Bruinenberg, Delia B. Carba, Ida Henriette Caspersen, Robert Clarke, E. Warwick Daw, Joris Deelen, Ewa Deelman, Graciela Delgado, Alex S. F. Doney, Niina Eklund, Michael R. Erdos, Karol Estrada, Elodie Eury, Nele Friedrich, Melissa E. Garcia, Vilmantas Giedraitis, Bruna Gigante, Alan S. Go, Alain Golay, Harald Grallert, Tanja B. Grammer, Jürgen Gräßler, Jagvir Grewal, Christopher J. Groves, Toomas Haller, Göran Hallmans

    Publicado 2015
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  12. 12
    Defining the role of common variation in the genomic and biological architecture of adult human height

    Defining the role of common variation in the genomic and biological architecture of adult human height por Andrew R. Wood, Tõnu Esko, Jian Yang, Sailaja Vedantam, Tune H. Pers, Stefan Gustafsson, Audrey Y. Chu, Karol Estrada, Jian’an Luan, Zoltán Kutalik, Najaf Amin, Martin L. Buchkovich, Damien C. Croteau‐Chonka, Felix R. Day, Yanan Duan, Tove Fall, Rudolf S.N. Fehrmann, Teresa Ferreira, Anne Jackson, Juha Karjalainen, Ken Sin Lo, Adam E. Locke, Reedik Mägi, Evelin Mihailov, Eleonora Porcu, Joshua C. Randall, André Scherag, Anna A. E. Vinkhuyzen, Harm-Jan Westra, Thomas W. Winkler, Tsegaselassie Workalemahu, Wei Zhao, Devin Absher, Eva Albrecht, Denise Anderson, Jeffrey Baron, Marian Beekman, Ayşe Demirkan, Georg Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Ross M. Fraser, Anuj Goel, Jian Gong, Anne E. Justice, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Julian C. Lui, Massimo Mangino, Irene Mateo Leach, Carolina Medina‐Gómez, Michael A. Nalls, Dale R. Nyholt, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Inga Prokopenko, Janina S. Ried, Stephan Ripke, Dmitry Shungin, Alena Stančáková, Rona J. Strawbridge, Yan V. Sun, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. van Vliet‐Ostaptchouk, Thomas J. Wang, Loïc Yengo, Weihua Zhang, Uzma Afzal, Johan Ärnlöv, Gillian M. Arscott, Stefania Bandinelli, Amy Barrett, Claire Bellis, Amanda J. Bennett, Christian Berne, Matthias Blüher, Jennifer L. Bolton, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Brendan M. Buckley, Steven Buyske, Ida Henriette Caspersen, Peter S. Chines, Robert Clarke, Xueling Sim, Matthew N. Cooper, E. Warwick Daw, Pim A. de Jong, Joris Deelen, Graciela Delgado

    Publicado 2014
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  13. 13
    Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci

    Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci por Chunyu Liu, Aldi T. Kraja, Jennifer A. Smith, Jennifer A. Brody, Nora Franceschini, Joshua C. Bis, Kenneth Rice, Alanna C. Morrison, Yingchang Lu, Stefan Weiß, Xiuqing Guo, Walter Palmas, Lisa W. Martin, Yii‐Der Ida Chen, Praveen Surendran, Fotios Drenos, James P. Cook, Paul L. Auer, Audrey Y. Chu, Ayush Giri, Wei Zhao, Jóhanna Jakobsdóttir, Li‐An Lin, Jeanette M. Stafford, Najaf Amin, Hao Mei, Jie Yao, Arend Voorman, Martin G. Larson, Megan L. Grove, Albert V. Smith, Shih‐Jen Hwang, Han Chen, Tianxiao Huan, Gülüm Kosova, Nathan O. Stitziel, Sekar Kathiresan, Nilesh J. Samani, Heribert Schunkert, Panos Deloukas, Man Li, Christian Fuchsberger, Cristian Pattaro, Mathias Gorski, Charles Kooperberg, George Papanicolaou, Jacques E. Rossouw, Jessica D. Faul, Sharon L. R. Kardia, Claude Bouchard, Leslie J. Raffel, André G. Uitterlinden, Oscar H. Franco, Ramachandran S. Vasan, Christopher J. O’Donnell, Kent D. Taylor, Kiang Liu, Erwin P. Böttinger, Omri Gottesman, E. Warwick Daw, Franco Giulianini, Santhi K. Ganesh, Elias Salfati, Tamara B. Harris, Lenore J. Launer, Marcus Dörr, Stephan B. Felix, Rainer Rettig, Henry Völzke, Eric H. Kim, Wen‐Jane Lee, I‐Te Lee, Wayne H-H Sheu, Krystal S. Tsosie, Digna R. Velez Edwards, Yongmei Liu, Adolfo Correa, David R. Weir, Uwe Völker, Paul M. Ridker, Eric Boerwinkle, Vilmundur Guðnason, Alexander P. Reiner, Cornelia M. van Duijn, Ingrid B. Borecki, Todd L. Edwards, Aravinda Chakravarti, Jerome I. Rotter, Bruce M. Psaty, Ruth J. F. Loos, Myriam Fornage, Georg Ehret, Christopher Newton‐Cheh, Daniel Levy, Daniel I. Chasman

    Publicado 2016
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  14. 14
    A catalog of genetic loci associated with kidney function from analyses of a million individuals

    A catalog of genetic loci associated with kidney function from analyses of a million individuals por Matthias Wuttke, Yong Li, Man Li, Karsten B. Sieber, Mary F. Feitosa, Mathias Gorski, Adrienne Tin, Lihua Wang, Audrey Y. Chu, Anselm Hoppmann, Holger Kirsten, Ayush Giri, Jin Fang Chai, Garðar Sveinbjörnsson, Bamidele O. Tayo, Teresa Nutile, Christian Fuchsberger, Jonathan Marten, Massimiliano Cocca, Sahar Ghasemi, Yizhe Xu, Katrin Horn, Damia Noce, Peter J. van der Most, Sanaz Sedaghat, Zhi Yu, Masato Akiyama, Saima Afaq, Tarunveer S. Ahluwalia, Peter Almgren, Najaf Amin, Johan Ärnlöv, Stephan J. L. Bakker, Nisha Bansal, Daniela Baptista, Sven Bergmann, Mary L. Biggs, Ginevra Biino, Michael Boehnke, Eric Boerwinkle, Mathilde Boissel, Erwin P. Böttinger, Thibaud Boutin, Hermann Brenner, Marco Brumat, Ralph Burkhardt, Adam S. Butterworth, Eric Campana, Archie Campbell, Harry Campbell, Mickaël Canouil, Robert J. Carroll, Eulalia Catamo, John C. Chambers, Miao-Ling Chee, Miao-Li Chee, Xu Chen, Ching‐Yu Cheng, Yurong Cheng, Kaare Christensen, Renata Cífková, Marina Ciullo, Maria Pina Concas, James P. Cook, Josef Coresh, Tanguy Corre, Cinzia Sala, Daniele Cusi, John Danesh, E. Warwick Daw, Martin H. de Borst, Alessandro De Grandi, Renée de Mutsert, Aiko P. J. de Vries, Frauke Degenhardt, Graciela Delgado, Ayşe Demirkan, Emanuele Di Angelantonio, Katalin Dittrich, Jasmin Divers, Rajkumar Dorajoo, Kai‐Uwe Eckardt, Georg Ehret, Paul Elliott, Karlhans Endlich, Michele K. Evans, Janine F. Felix, Valencia Hui Xian Foo, Oscar H. Franco, André Franke, Barry I. Freedman, Sandra Freitag‐Wolf, Yechiel Friedlander, Philippe Froguel, Ron T. Gansevoort, He Gao, Paolo Gasparini, J. Michael Gaziano, Vilmantas Giedraitis, Christian Gieger

    Publicado 2019
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  15. 15
    Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

    Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals por Praveen Surendran, Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook, Lingyan Chen, Borbála Mifsud, Chen Yao, Aldi T. Kraja, James Cartwright, Jacklyn N. Hellwege, Ayush Giri, Vinicius Tragante, Guðmar Þorleifsson, Dajiang J. Liu, Bram P. Prins, Isobel D. Stewart, Claudia P. Cabrera, James Eales, Artur Akbarov, Paul L. Auer, Lawrence F. Bielak, Joshua C. Bis, Vickie Braithwaite, Jennifer A. Brody, E. Warwick Daw, Helen R. Warren, Fotios Drenos, Yan V. Sun, Jessica D. Faul, Eric B. Fauman, Cristiano Fava, Teresa Ferreira, Christopher N. Foley, Nora Franceschini, He Gao, Olga Giannakopoulou, Franco Giulianini, Daníel F. Guðbjartsson, Xiuqing Guo, Sarah E. Harris, Aki S. Havulinna, Anna Helgadóttir, Jennifer E. Huffman, Shih‐Jen Hwang, Stavroula Kanoni, Jukka Kontto, Martin G. Larson, Ruifang Li‐Gao, Jaana Lindström, Luca A. Lotta, Yingchang Lu, Jian’an Luan, Anubha Mahajan, Giovanni Malerba, Nicholas G. D. Masca, Hao Mei, Cristina Menni, Dennis O. Mook‐Kanamori, David Mosén-Ansorena, Martina Müller‐Nurasyid, Guillaume Paré, Dirk S. Paul, Markus Perola, Alaitz Poveda, Rainer Rauramaa, Melissa A. Richard, Tom G. Richardson, Nuno Sepúlveda, Xueling Sim, Albert V. Smith, Jennifer A. Smith, James R Staley, Alena Stanáková, Patrick Sulem, Sébastien Thériault, Unnur Þorsteinsdóttir, Stella Trompet, Tibor V. Varga, Digna R. Velez Edwards, Giovanni Veronesi, Stefan Weiß, Sara M. Willems, Jie Yao, Robin Young, Bing Yu, Weihua Zhang, Jinghua Zhao, Wei Zhao, Wei Zhao, Εvangelos Εvangelou, Stefanie Aeschbacher, Eralda Asllanaj, Stefan Blankenberg, Lori L. Bonnycastle, Jette Bork‐Jensen, Ivan Brandslund, Peter S. Braund, Stephen Burgess

    Publicado 2020
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  16. 16
    A saturated map of common genetic variants associated with human height

    A saturated map of common genetic variants associated with human height por Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Julia Sidorenko, Eric Bartell, Saori Sakaue, Marielisa Graff, Anders Eliasen, Yunxuan Jiang, Sridharan Raghavan, Jenkai Miao, Joshua Arias, Sarah E. Graham, Ronen E. Mukamel, Cassandra N. Spracklen, Xianyong Yin, Shyh‐Huei Chen, Teresa Ferreira, Heather H Highland, Yingjie Ji, Tugce Karaderi, Kuang Lin, Kreete Lüll, Deborah E. Malden, Carolina Medina‐Gómez, Moara Machado, Amy Moore, Sina Rüeger, Xueling Sim, Scott Vrieze, Tarunveer S. Ahluwalia, Masato Akiyama, Matthew Allison, Marcus Alvarez, Mette K. Andersen, Alireza Ani, Vivek Appadurai, Liubov Arbeeva, Seema Bhaskar, Lawrence F. Bielak, Sailalitha Bollepalli, Lori L. Bonnycastle, Jette Bork‐Jensen, Jonathan P. Bradfield, Yuki Bradford, Peter S. Braund, Jennifer A. Brody, Kristoffer Sølvsten Burgdorf, Brian E. Cade, Hui Cai, Qiuyin Cai, Archie Campbell, Marisa Cañadas‐Garre, Eulalia Catamo, Jin Fang Chai, Xiaoran Chai, Li-Ching Chang, Yi‐Cheng Chang, Chien-Hsiun Chen, Alessandra Chesi, Seung Hoan Choi, Ren‐Hua Chung, Massimiliano Cocca, Maria Pina Concas, Christian Couture, Gabriel Cuéllar-Partida, Rebecca Danning, E. Warwick Daw, Frauke Degenhard, Graciela E. Delgado, Alessandro Delitala, Ayşe Demirkan, Xuan Deng, Poornima Devineni, Alexander Dietl, Maria Dimitriou, Latchezar Dimitrov, Rajkumar Dorajoo, Arif B. Ekici, Jorgen Engmann, Zammy Fairhurst-Hunter, Aliki‐Eleni Farmaki, Jessica D. Faul, Juan-Carlos Fernandez-Lopez, Lukas Forer, Margherita Francescatto, Sandra Freitag‐Wolf, Christian Fuchsberger, Tessel E. Galesloot, Yan Gao, Zishan Gao, Frank Geller, Olga Giannakopoulou, Franco Giulianini, Anette P. Gjesing, Anuj Goel, Scott D. Gordon, Mathias Gorski, Jakob Grove, Xiuqing Guo

    Publicado 2022
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  17. 17
    Genetic studies of body mass index yield new insights for obesity biology

    Genetic studies of body mass index yield new insights for obesity biology por Adam E. Locke, Bratati Kahali, Sonja I. Berndt, Anne E. Justice, Tune H. Pers, Felix R. Day, C. E. Powell, Sailaja Vedantam, Martin L. Buchkovich, Jian Yang, Damien C. Croteau‐Chonka, Tõnu Esko, Tove Fall, Teresa Ferreira, Stefan Gustafsson, Zoltán Kutalik, Jian’an Luan, Reedik Mägi, Joshua C. Randall, Thomas W. Winkler, Andrew R. Wood, Tsegaselassie Workalemahu, Jessica D. Faul, Jennifer A. Smith, Wei Zhao, Wei Zhao, Ming‐Huei Chen, Rudolf S.N. Fehrmann, Åsa K. Hedman, Juha Karjalainen, Ellen M. Schmidt, Devin Absher, Najaf Amin, Denise Anderson, Marian Beekman, Jennifer L. Bolton, Jennifer L. Bragg‐Gresham, Steven Buyske, Ayşe Demirkan, Guohong Deng, Georg Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Anuj Goel, Jian Gong, Anne Jackson, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Massimo Mangino, Irene Mateo Leach, Carolina Medina‐Gómez, Sarah E. Medland, Michael A. Nalls, Lyle J. Palmer, Dorota Pasko, Sonali Pechlivanis, Marjolein J. Peters, Inga Prokopenko, Dmitry Shungin, Alena Stančáková, Rona J. Strawbridge, Yan V. Sun, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. van Vliet‐Ostaptchouk, Thomas J. Wang, Loïc Yengo, Weihua Zhang, Aaron Isaacs, Eva Albrecht, Johan Ärnlöv, Gillian M. Arscott, Antony Attwood, Stefania Bandinelli, Amy Barrett, Isabelita Bas, Claire Bellis, Amanda J. Bennett, Christian Berne, Roza Blagieva, Matthias Blüher, Stefan Böhringer, Lori L. Bonnycastle, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Ida Henriette Caspersen, Yii‐Der Ida Chen, Robert Clarke, E. Warwick Daw, Anton J. M. de Craen, Graciela Delgado, Maria Dimitriou

    Publicado 2015
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  18. 18
    Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

    Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits por Aldi T. Kraja, Chunyu Liu, Jessica L. Fetterman, Mariaelisa Graff, Henri Theil, C. Charles Gu, Lisa R. Yanek, Mary F. Feitosa, Dan E. Arking, Daniel I. Chasman, Kristin L. Young, Symen Ligthart, W. David Hill, Stefan Weiß, Jian’an Luan, Franco Giulianini, Ruifang Li‐Gao, Fernando Pires Hartwig, Shiow J. Lin, Lihua Wang, Tom G. Richardson, Jie Yao, Eliana Portilla-Fernández, Mohsen Ghanbari, Mary K. Wojczynski, Wen‐Jane Lee, Maria Argos, Sebastian M. Armasu, Ruteja A. Barve, Kathleen A. Ryan, Ping An, Thomas Baranski, Suzette J. Bielinski, Donald W. Bowden, Ulrich Broeckel, Kaare Christensen, Audrey Y. Chu, Janie Corley, Simon R. Cox, André G. Uitterlinden, Fernando Rivadeneira, Cheryl D. Cropp, E. Warwick Daw, Alan B. Zonderman, Lisa de las Fuentes, He Gao, Ioanna Tzoulaki, Tarunveer S. Ahluwalia, Renée de Mutsert, Leslie Emery, A. Mesut Erzurumluoglu, James A. Perry, Mao Fu, Nita G. Forouhi, Zhenglong Gu, Yang Hai, Sarah E. Harris, Gibran Hemani, Steven C. Hunt, Marguerite R. Irvin, Anna Jonsson, Anne E. Justice, Nicola D. Kerrison, Nicholas B. Larson, Keng-Hung Lin, Latisha Love‐Gregory, Rasika A. Mathias, Joseph H. Lee, Matthias Nauck, Raymond Noordam, Ken K. Ong, James S. Pankow, Amit Patki, Alison Pattie, Astrid Petersmann, Qibin Qi, Rasmus Ribel‐Madsen, Rebecca Rohde, Kevin Sandow, Theresia M. Schnurr, Tamar Sofer, John M. Starr, Adele M. Taylor, Alexander Teumer, Nicholas J. Timpson, Hugoline G. de Haan, Yujie Wang, Peter Weeke, Christine A. Williams, Hongsheng Wu, Wei Yang, Donglin Zeng, Daniel R. Witte, Bruce S. Weir, Nicholas J. Wareham, Henrik Vestergaard, Stephen T. Turner, Christian Torp‐Pedersen, Evie Stergiakouli, Wayne Huey‐Herng Sheu

    Publicado 2018
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  19. 19
    Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

    Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals por Thomas W. Winkler, Humaira Rasheed, Alexander Teumer, Mathias Gorski, Bryce Rowan, Kira J. Stanzick, Laurent F. Thomas, Adrienne Tin, Anselm Hoppmann, Audrey Y. Chu, Bamidele O. Tayo, Chris H. L. Thio, Daniele Cusi, Jin Fang Chai, Karsten B. Sieber, Katrin Horn, Man Li, Markus Scholz, Massimiliano Cocca, Matthias Wuttke, Peter J. van der Most, Qiong Yang, Sahar Ghasemi, Teresa Nutile, Yong Li, Giulia Pontali, Felix Günther, Abbas Dehghan, Adolfo Correa, Afshin Parsa, Agnese Feresin, Aiko P. J. de Vries, Alan B. Zonderman, Albert V. Smith, Albertine J. Oldehinkel, Alessandro De Grandi, Alexander R. Rosenkranz, André Franke, Andrej Teren, Andres Metspalu, Andrew A. Hicks, Andrew P. Morris, Anke Tönjes, Anna Morgan, Anna Podgornaia, Annette Peters, Antje Körner, Anubha Mahajan, Archie Campbell, Barry I. Freedman, Beatrice Spedicati, Belén Ponte, Ben Schöttker, Ben Brumpton, Bernhard Banas, Bernhard K. Krämer, Bettina Jung, Bjørn Olav Åsvold, Blair H. Smith, Boting Ning, Brenda W.J.H. Penninx, Brett Vanderwerff, Bruce M. Psaty, Candace M. Kammerer, Carl D. Langefeld, Caroline Hayward, Cassandra N. Spracklen, Cassianne Robinson‐Cohen, Catharina A. Hartman, Cecilia M. Lindgren, Chaolong Wang, Charumathi Sabanayagam, Chew‐Kiat Heng, Chiara Lanzani, Chiea Chuen Khor, Ching‐Yu Cheng, Christian Fuchsberger, Christian Gieger, Christian M. Shaffer, Christina‐Alexandra Schulz, Cristen J. Willer, Daniel I. Chasman, Daníel F. Guðbjartsson, Daniela Ruggiero, Daniela Toniolo, Darina Czamara, David J. Porteous, Dawn Waterworth, Deborah Mascalzoni, Dennis O. Mook‐Kanamori, Dermot F. Reilly, E. Warwick Daw, Edith Hofer, Eric Boerwinkle, Erika Salvi, Erwin P. Böttinger, E Shyong Tai, Eulalia Catamo, Federica Rizzi, Feng Guo

    Publicado 2022
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