Výsledky vyhledávání - Miao Ling Chee

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    Analysis of clinically relevant variants from ancestrally diverse Asian genomes Autor Sock Hoai Chan, Yasmin Bylstra, Jing Xian Teo, Jyn Ling Kuan, Nicolas Bertin, Mar González-Porta, Maxime Hebrard, Roberto Tirado-Magallanes, Joanna Tan, Justin Jeyakani, Zhihui Li, Jin Fang Chai, Yap Seng Chong, Sonia Dávila, Liuh Ling Goh, Eng Sing Lee, Eleanor Wong, Tien Yin Wong, Tin Aung, Kenneth Ban, Claire Bellis, Miao Li Chee, Miao Ling Chee, Wen Jie Chew, Calvin Chin, Stuart A. Cook, Rinkoo Dalan, Rajkumar Dorajoo, Chester L. Drum, Paul Elliott, Johan G. Eriksson, Roger Foo, Daphne Gardner, Peter D. Gluckman, Denise Li Meng Goh, Kanika Jain, Sylvia Kam, Irfahan Kassam, Lakshmi Narayanan Lakshmanan, Caroline Lee, Jimmy Lee, Soo Chin Lee, Yung Seng Lee, Hengtong Li, Chia Wei Lim, Tock Han Lim, Marie Loh, Sebastian Maurer‐Stroh, Theresia Mina, Shi Qi Mok, Hong Kiat Ng, Chee Jian Pua, Elio Ríboli, Tyler Hyungtaek Rim, Charumathi Sabanayagam, Wey Cheng Sim, Tavintharan Subramaniam, Ee Shien Tan, Eng King Tan, Erwin Tantoso, Darwin Tay, Yik Ying Teo, Yih‐Chung Tham, Li-xian Grace Toh, Pi Kuang Tsai, Rob M. van Dam, Lavanya Veeravalli, Gervais Wansaicheong Khin-lin, Andreas Wilm, Chengxi Yang, Fabian Yap, Yik Weng Yew, Shyam Prabhakar, Jianjun Liu, Ching‐Yu Cheng, Birgit Eisenhaber, Neerja Karnani, Khai Pang Leong, Xueling Sim, Khung Keong Yeo, John C. Chambers, E Shyong Tai, Patrick Tan, Saumya Shekhar Jamuar, Joanne Ngeow, Weng Khong Lim

    Vydáno 2022
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    A catalog of genetic loci associated with kidney function from analyses of a million individuals Autor 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

    Vydáno 2019
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    Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies Autor Mathias Gorski, Humaira Rasheed, Alexander Teumer, Laurent F. Thomas, Sarah E. Graham, Garðar Sveinbjörnsson, Thomas W. Winkler, Felix Günther, Klaus Stark, Jin Fang Chai, Bamidele O. Tayo, Matthias Wuttke, Yong Li, Adrienne Tin, Tarunveer S. Ahluwalia, Johan Ärnlöv, Bjørn Olav Åsvold, Stephan J. L. Bakker, Bernhard Banas, Nisha Bansal, Mary L. Biggs, Ginevra Biino, Michael Böhnke, Eric Boerwinkle, Erwin P. Böttinger, Hermann Brenner, Ben Brumpton, Robert J. Carroll, Layal Chaker, John Chalmers, Miao-Li Chee, Miao-Ling Chee, Ching‐Yu Cheng, Audrey Y. Chu, Marina Ciullo, Massimiliano Cocca, James P. Cook, Josef Coresh, Daniele Cusi, Martin H. de Borst, Frauke Degenhardt, Kai‐Uwe Eckardt, Karlhans Endlich, Michele K. Evans, Mary F. Feitosa, André Franke, Sandra Freitag‐Wolf, Christian Fuchsberger, Piyush Gampawar, Ron T. Gansevoort, Mohsen Ghanbari, Sahar Ghasemi, Vilmantas Giedraitis, Christian Gieger, Daníel F. Guðbjartsson, Stein Hallan, Pavel Hamet, Asahi Hishida, Kevin Ho, Edith Hofer, Bernd Holleczek, Hilma Hólm, Anselm Hoppmann, Katrin Horn, Nina Hutri‐Kähönen, Kristian Hveem, Shih‐Jen Hwang, M. Arfan Ikram, Navya Shilpa Josyula, Bettina Jung, Mika Kähönen, Irma Karabegović, Chiea Chuen Khor, Wolfgang Köenig, Holly Kramer, Bernhard K. Krämer, Brigitte Kühnel, Johanna Kuusisto, Markku Laakso, Leslie A. Lange, Terho Lehtimäki, Man Li, Wolfgang Lieb, Lars Lind, Cecilia M. Lindgren, Ruth J. F. Loos, Mary Ann Lukas, Leo‐Pekka Lyytikäinen, Anubha Mahajan, Pamela R. Matías‐García, Christa Meisinger, Thomas Meitinger, Olle Melander, Yuri Milaneschi, Pashupati P. Mishra, Nina Mononen, Andrew P. Morris, Josyf C. Mychaleckyj, Girish N. Nadkarni, Mariko Naito

    Vydáno 2022
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    X-chromosome and kidney function: evidence from a multi-trait genetic analysis of 908,697 individuals reveals sex-specific and sex-differential findings in genes regulated by andro... Autor Markus Scholz, Katrin Horn, Janne Pott, Matthias Wuttke, Andreas Kühnapfel, M. Kamal Nasr, Holger Kirsten, Yong Li, Anselm Hoppmann, Mathias Gorski, Sahar Ghasemi, Man Li, Adrienne Tin, Jin Fang Chai, Massimiliano Cocca, Luyu Wang, Teresa Nutile, Masato Akiyama, Bjørn Olav Åsvold, Nisha Bansal, Mary L. Biggs, Thibaud Boutin, Hermann Brenner, Ben Brumpton, Ralph Burkhardt, Jianwen Cai, Archie Campbell, Harry Campbell, John Chalmers, Daniel I. Chasman, Miao Ling Chee, Miao Li Chee, Xu Chen, Ching‐Yu Cheng, Renata Cífková, Martha L. Daviglus, Graciela Delgado, Katalin Dittrich, Todd L. Edwards, Karlhans Endlich, J. Michael Gaziano, Ayush Giri, Franco Giulianini, Scott D. Gordon, Daníel F. Guðbjartsson, Stein Hallan, Pavel Hamet, Catharina A. Hartman, Caroline Hayward, Iris M. Heid, Jacklyn N. Hellwege, Bernd Holleczek, Hilma Hólm, Nina Hutri‐Kähönen, Kristian Hveem, Berend Isermann, Jost B. Jonas, Peter K. Joshi, Yoichiro Kamatani, Masahiro Kanai, Mika Kastarinen, Chiea Chuen Khor, Wieland Kieß, Marcus E. Kleber, Antje Körner, Péter Kovács, Alena Krajčoviechová, Holly Kramer, Bernhard K. Krämer, Mikko Kuokkanen, Mika Kähönen, Leslie A. Lange, James P. Lash, Terho Lehtimäki, Hengtong Li, Bridget M. Lin, Jianjun Liu, Markus Loeffler, Leo‐Pekka Lyytikäinen, Patrik K. E. Magnusson, Nicholas G. Martin, Koichi Matsuda, Yuri Milaneschi, Pashupati P. Mishra, Nina Mononen, Grant W. Montgomery, Dennis O. Mook‐Kanamori, Josyf C. Mychaleckyj, Winfried März, Matthias Nauck, Kjell Nikus, Ilja M. Nolte, Raymond Noordam, Yukinori Okada, Ísleifur Ólafsson, Albertine J. Oldehinkel, Brenda W.J.H. Penninx, Markus Perola, Nicola Pirastu, Ozren Polašek

    Vydáno 2024
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    Genome-wide association meta-analyses and fine-mapping elucidate pathways influencing albuminuria Autor Alexander Teumer, Yong Li, Sahar Ghasemi, Bram P. Prins, Matthias Wuttke, Tobias Hermle, Ayush Giri, Karsten B. Sieber, Chengxiang Qiu, Holger Kirsten, Adrienne Tin, Audrey Y. Chu, Nisha Bansal, Mary F. Feitosa, Lihua Wang, Jin Fang Chai, Massimiliano Cocca, Christian Fuchsberger, Mathias Gorski, Anselm Hoppmann, Katrin Horn, Man Li, Jonathan Marten, Damia Noce, Teresa Nutile, Sanaz Sedaghat, Garðar Sveinbjörnsson, Bamidele O. Tayo, Peter J. van der Most, Yizhe Xu, Zhi Yu, Lea Gerstner, Johan Ärnlöv, Stephan J. L. Bakker, Daniela Baptista, Mary L. Biggs, Eric Boerwinkle, Hermann Brenner, Ralph Burkhardt, Robert J. Carroll, Miao-Li Chee, Miao-Ling Chee, Mengmeng Chen, Ching‐Yu Cheng, James P. Cook, Josef Coresh, Tanguy Corre, John Danesh, Martin H. de Borst, Alessandro De Grandi, Renée de Mutsert, Aiko P. J. de Vries, Frauke Degenhardt, Katalin Dittrich, Jasmin Divers, Kai‐Uwe Eckardt, Georg Ehret, Karlhans Endlich, Janine F. Felix, Oscar H. Franco, André Franke, Barry I. Freedman, Sandra Freitag‐Wolf, Ron T. Gansevoort, Vilmantas Giedraitis, Martin Gögele, Franziska Grundner-Culemann, Daníel F. Guðbjartsson, Vilmundur Guðnason, Pavel Hamet, Tamara B. Harris, Andrew A. Hicks, Hilma Hólm, Valencia Hui Xian Foo, Shih‐Jen Hwang, M. Arfan Ikram, Erik Ingelsson, Vincent W. V. Jaddoe, Jóhanna Jakobsdóttir, Navya Shilpa Josyula, Bettina Jung, Mika Kähönen, Chiea Chuen Khor, Wieland Kieß, Wolfgang Köenig, Antje Körner, Péter Kovács, Holly Kramer, Bernhard K. Krämer, Florian Kronenberg, Leslie A. Lange, Carl D. Langefeld, Jeannette Jen-Mai Lee, Terho Lehtimäki, Wolfgang Lieb, S. M. L. Lim, Lars Lind, Cecilia M. Lindgren, Jianjun Liu, Markus Loeffler

    Vydáno 2019
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    Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline Autor Mathias Gorski, Bettina Jung, Yong Li, Pamela R. Matías‐García, Matthias Wuttke, Stefan Coassin, Chris H. L. Thio, Marcus E. Kleber, Thomas W. Winkler, Veronika Wanner, Jin Fang Chai, Audrey Y. Chu, Massimiliano Cocca, Mary F. Feitosa, Sahar Ghasemi, Anselm Hoppmann, Katrin Horn, Man Li, Teresa Nutile, Markus Scholz, Karsten B. Sieber, Alexander Teumer, Adrienne Tin, Judy Wang, Bamidele O. Tayo, Tarunveer S. Ahluwalia, Peter Almgren, Stephan J. L. Bakker, Bernhard Banas, Nisha Bansal, Mary L. Biggs, Eric Boerwinkle, Erwin P. Böttinger, Hermann Brenner, Robert J. Carroll, John Chalmers, Miao-Li Chee, Miao-Ling Chee, Ching‐Yu Cheng, Josef Coresh, Martin H. de Borst, Frauke Degenhardt, Kai‐Uwe Eckardt, Karlhans Endlich, André Franke, Sandra Freitag‐Wolf, Piyush Gampawar, Ron T. Gansevoort, Mohsen Ghanbari, Christian Gieger, Pavel Hamet, Kevin Ho, Edith Hofer, Bernd Holleczek, Valencia Hui Xian Foo, Nina Hutri‐Kähönen, Shih‐Jen Hwang, M. Arfan Ikram, Navya Shilpa Josyula, Mika Kähönen, Chiea Chuen Khor, Wolfgang Köenig, Holly Kramer, Bernhard K. Krämer, Brigitte Kühnel, Leslie A. Lange, Terho Lehtimäki, Wolfgang Lieb, Ruth J. F. Loos, Mary Ann Lukas, Leo‐Pekka Lyytikäinen, Christa Meisinger, Thomas Meitinger, Olle Melander, Yuri Milaneschi, Pashupati P. Mishra, Nina Mononen, Josyf C. Mychaleckyj, Girish N. Nadkarni, Matthias Nauck, Kjell Nikus, Boting Ning, Ilja M. Nolte, Michelle L. O’Donoghue, Marju Orho‐Melander, Sarah A. Pendergrass, Brenda W.J.H. Penninx, Michael Preuß, Bruce M. Psaty, Laura M. Raffield, Olli T. Raitakari, Rainer Rettig, Myriam Rheinberger, Kenneth Rice, Alexander R. Rosenkranz, Peter Rossing, Jerome I. Rotter, Charumathi Sabanayagam, Helena Schmidt, Reinhold Schmidt

    Vydáno 2020
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    Large-Scale Whole-Genome Sequencing of Three Diverse Asian Populations in Singapore Autor Degang Wu, Jinzhuang Dou, Xiaoran Chai, Claire Bellis, Andreas Wilm, Chih Chuan Shih, Wendy Wei Jia Soon, Nicolas Bertin, Clarabelle Bitong Lin, Chiea Chuen Khor, Michael DeGiorgio, Shanshan Cheng, Li Bao, Neerja Karnani, William Ying Khee Hwang, Sonia Dávila, Patrick Tan, Asim Shabbir, Angela Moh, Eng‐King Tan, Jia Nee Foo, Liuh Ling Goh, Khai Pang Leong, Roger Foo, Carolyn S.P. Lam, Mark Richards, Ching‐Yu Cheng, Tin Aung, Tien Yin Wong, Huck‐Hui Ng, Jianjun Liu, Chaolong Wang, Matthew Ackers‐Johnson, Edita Aliwarga, Kenneth Ban, Denis Bertrand, John C. Chambers, Dana Leng Hui Chan, Cheryl Xue Li Chan, Miao Li Chee, Miao Ling Chee, Pauline Chen, Yunxin Chen, Elaine Guo Yan Chew, Wen Jie Chew, Lynn Hui Yun Chiam, Jenny Pek Ching Chong, I-Ly Joanna Chua, Stuart A. Cook, Wei Dai, Rajkumar Dorajoo, Chuan-Sheng Foo, Rick Siow Mong Goh, Axel M. Hillmer, Ishak D. Irwan, Fazlur Jaufeerally, Asif Javed, Justin Jeyakani, John Tat Hung Koh, Jia Yu Koh, Pavitra Krishnaswamy, Jyn Ling Kuan, Kumari Neelam, Ai Shan Lee, Seow Eng Lee, Lee Sheldon, Yen Ling Lee, See Ting Leong, Zheng Li, Peter Yiqing Li, Jun Xian Liew, Oi Wah Liew, Su Chi Lim, Weng Khong Lim, Chia Wei Lim, Tingsen Benson Lim, Choon Kiat Lim, Seet Yoong Loh, Au Wing Lok, Calvin Chin, Shivani Majithia, Sebastian Maurer‐Stroh, Wee Yang Meah, Shi Qi Mok, Niranjan Nargarajan, Pauline C. Ng, Sarah B. Ng, Zhenyuan Ng, Jessica Yan Xia Ng, Ebonne Ng, Shi Ling Ng, Simon Nusinovici, Chin Thing Ong, Bangfen Pan, Vincent Pedergnana, Stanley Poh, Shyam Prabhakar, Kumar M. Prakash, Ivy Quek, Charumathi Sabanayagam

    Vydáno 2019
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