Resultados de procura - QiPing Feng
- Mostrando 1 - 20 Resultados de 22
- Go to Next Page
-
1
-
2
PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records por Neil S. Zheng, QiPing Feng, V. Eric Kerchberger, Juan Zhao, Todd L. Edwards, Nancy J. Cox, C. Stein, Dan M. Roden, Joshua C. Denny, Wei-Qi Wei
Publicado 2020Artigo -
3
Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: Common gene sequence variation and functional characterization por Fang Li, QiPing Feng, Candace Lee, Shuzhan Wang, Linda L. Pelleymounter, Irene Moon, Bruce W. Eckloff, Eric D. Wieben, Daniel J. Schaid, Vivien C. Yee, Richard M. Weinshilboum
Publicado 2008Artigo -
4
Leveraging generative AI to prioritize drug repurposing candidates for Alzheimer’s disease with real-world clinical validation por Chao Yan, Monika E. Grabowska, Alyson L. Dickson, Bingshan Li, Zhexing Wen, Dan M. Roden, Christoph Stein, Peter J. Embí, Josh F. Peterson, QiPing Feng, Bradley Malin, Wei‐Qi Wei
Publicado 2024Artigo -
5
Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects por Dipender Gill, Marios K. Georgakis, Fotios Koskeridis, Lan Jiang, QiPing Feng, Wei‐Qi Wei, Evropi Τheodoratou, Paul Elliott, Joshua C. Denny, Rainer Malik, Εvangelos Εvangelou, Abbas Dehghan, Martin Dichgans, Ioanna Tzoulaki
Publicado 2019Artigo -
6
Association Between Low-Density Lipoprotein Cholesterol Levels and Risk for Sepsis Among Patients Admitted to the Hospital With Infection por QiPing Feng, Wei‐Qi Wei, Sandip Chaugai, Barbara Gisella Carranza Leon, Jonathan D. Mosley, Daniel A. Carranza Leon, Lan Jiang, Andrea Ihegword, Christian M. Shaffer, MacRae F. Linton, Cecilia P. Chung, C. Michael Stein
Publicado 2019Artigo -
7
The Clinical Pharmacogenomics Implementation Consortium: CPIC Guideline for SLCO1B1 and Simvastatin-Induced Myopathy por Russell A. Wilke, Laura B. Ramsey, Samuel G. Johnson, Whitney D. Maxwell, Howard L. McLeod, Deepak Voora, Ronald M. Krauss, Dan M. Roden, QiPing Feng, Rhonda M. Cooper‐DeHoff, Li Gong, Teri E. Klein, Mia Wadelius, Mikko Niemi
Publicado 2012Artigo -
8
Association of Genetic Variation With Cirrhosis: A Multi-Trait Genome-Wide Association and Gene–Environment Interaction Study por Connor A. Emdin, Mary E. Haas, Veeral Ajmera, Tracey G. Simon, Julian R. Homburger, Cynthia L. Neben, Lan Jiang, Wei‐Qi Wei, QiPing Feng, Alicia Y. Zhou, Joshua C. Denny, Kathleen E. Corey, Rohit Loomba, Sekar Kathiresan, Amit V. Khera
Publicado 2020Artigo -
9
Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms por Milton Pividori, Sumei Lu, Binglan Li, Chun Su, Matthew E. Johnson, Wei‐Qi Wei, QiPing Feng, Bahram Namjou, Krzysztof Kiryluk, Iftikhar J. Kullo, Yuan Luo, Blair D. Sullivan, Benjamin F. Voight, Carsten Skarke, Marylyn D. Ritchie, Struan F.A. Grant, Casey S. Greene
Publicado 2023Artigo -
10
The Clinical Pharmacogenetics Implementation Consortium Guideline for SLCO1B1 and Simvastatin-Induced Myopathy: 2014 Update por Laura B. Ramsey, Samuel G. Johnson, Kelly E. Caudle, Cyrine E. Haidar, Deepak Voora, Russell A. Wilke, Whitney D. Maxwell, Howard L. McLeod, Ronald M. Krauss, D M Roden, QiPing Feng, Rhonda M. Cooper‐DeHoff, Li Gong, Teri E. Klein, Mia Wadelius, Mikko Niemi
Publicado 2014Artigo -
11
Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups por Ozan Dikilitas, Daniel J. Schaid, Matthew Kosel, Robert J. Carroll, Christopher G. Chute, Joshua C. Denny, Alex Fedotov, QiPing Feng, Hákon Hákonarson, Gail P. Jarvik, Ming Ta Michael Lee, Jennifer A. Pacheco, Robb Rowley, Patrick Sleiman, Christoph Stein, Amy C. Sturm, Wei‐Qi Wei, Georgia L. Wiesner, Marc S. Williams, Yanfei Zhang, Teri A. Manolio, Iftikhar J. Kullo
Publicado 2020Artigo -
12
A statin-dependent QTL for GATM expression is associated with statin-induced myopathy por Lara M. Mangravite, Barbara E. Engelhardt, Marisa W. Medina, Joshua D. Smith, Andrew Brown, Daniel I. Chasman, Brigham H. Mecham, Bryan Howie, Heejung Shim, Devesh Naidoo, QiPing Feng, Mark J. Rieder, Yii Der I. Chen, Jerome I. Rotter, Paul M. Ridker, Jemma C. Hopewell, Sarah Parish, Jane Armitage, Rory Collins, Russell A. Wilke, Deborah A. Nickerson, Matthew Stephens, Ronald M. Krauss
Publicado 2013Artigo -
13
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns por Lisa Bastarache, Jacob Hughey, Scott J. Hebbring, Joy E. Marlo, Wanke Zhao, Wan‐Ting Ho, Sara L. Van Driest, Tracy L. McGregor, Jonathan D. Mosley, Quinn S. Wells, Michael Temple, Andrea H. Ramirez, Robert J. Carroll, Travis Osterman, Todd L. Edwards, Douglas M. Ruderfer, Digna R. Velez Edwards, Rizwan Hamid, Joy D. Cogan, Andrew M. Glazer, Wei‐Qi Wei, QiPing Feng, Murray H. Brilliant, Zhizhuang Joe Zhao, Nancy J. Cox, Dan M. Roden, Joshua C. Denny
Publicado 2018Artigo -
14
<i>LPA</i> Variants Are Associated With Residual Cardiovascular Risk in Patients Receiving Statins por Wei‐Qi Wei, Xiaohui Li, QiPing Feng, Michiaki Kubo, Iftikhar J. Kullo, Peggy Peissig, Elizabeth W. Karlson, Gail P. Jarvik, Ming Ta Michael Lee, Ning Shang, Eric Larson, Todd L. Edwards, Christian M. Shaffer, Jonathan D. Mosley, Shiro Maeda, Momoko Horikoshi, Marylyn D. Ritchie, Marc S. Williams, Eric B. Larson, David R. Crosslin, Harris T. Bland, Jennifer A. Pacheco, Laura J. Rasmussen‐Torvik, David Cronkite, George Hripcsak, Nancy J. Cox, Russell A. Wilke, Christoph Stein, Jerome I. Rotter, Yukihide Momozawa, Dan M. Roden, Ronald M. Krauss, Joshua C. Denny
Publicado 2018Revisão -
15
A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease por Connor A. Emdin, Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin, George Hindy, Lan Jiang, Wei‐Qi Wei, QiPing Feng, Juha Karjalainen, Aki S. Havulinna, Tuomo Kiiskinen, Alexander G. Bick, Diego Ardissino, James G. Wilson, Heribert Schunkert, Ruth McPherson, Hugh Watkins, Roberto Elosúa, Matthew J. Bown, Nilesh J. Samani, Usman Baber, Jeanette Erdmann, Namrata Gupta, John Danesh, Danish Saleheen, Kyong–Mi Chang, Marijana Vujković, Benjamin F. Voight, Scott M. Damrauer, Julie A. Lynch, David E. Kaplan, Marina Serper, Philip S. Tsao, Josep M. Mercader, Craig L. Hanis, Mark J. Daly, Joshua C. Denny, Stacey Gabriel, Sekar Kathiresan
Publicado 2020Artigo -
16
Strong protective effect of the<i>APOL1</i>p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease por Yask Gupta, David J. Friedman, Michelle Mcnulty, Atlas Khan, Brandon M. Lane, Chen Wang, Juntao Ke, Gina Jin, Benjamin Wooden, Andrea L. Knob, Tze Y. Lim, Gerald B. Appel, Kinsie Huggins, Lili Liu, Adele Mitrotti, Megan C. Stangl, Andrew S. Bomback, Rik Westland, Monica Bodria, Maddalena Marasà, Ning Shang, David Cohen, Russell J. Crew, William Morello, Pietro A. Canetta, Jai Radhakrishnan, Jeremiah Martino, Qingxue Liu, Wendy K. Chung, Angelica Espinoza, Yuan Luo, Wei‐Qi Wei, QiPing Feng, Chunhua Weng, Yilu Fang, Iftikhar J. Kullo, Mohammadreza Naderian, Nita A. Limdi, Marguerite R. Irvin, Hemant K. Tiwari, Sumit Mohan, Maya K. Rao, Geoffrey K. Dube, Ninad S. Chaudhary, Orlando M. Gutiérrez, Suzanne E. Judd, Mary Cushman, Leslie A. Lange, Ethan M. Lange, Daniel L. Bivona, Miguel Verbitsky, Cheryl A. Winkler, Jeffrey B. Kopp, Dominick Santoriello, Ibrahim Batal, Sérgio Veloso Brant Pinheiro, Eduardo Oliveira, Ana Cristina Simões e Silva, Isabella Pisani, Enrico Fiaccadori, Fangming Lin, Loreto Gesualdo, Antonio Amoroso, Gian Marco Ghiggeri, Vivette D. D’Agati, Riccardo Magistroni, Eimear E. Kenny, Ruth J. F. Loos, Giovanni Montini, Friedhelm Hildebrandt, Dirk S. Paul, Slavé Petrovski, David B. Goldstein, Matthias Kretzler, Rasheed Gbadegesin, Ali G. Gharavi, Krzysztof Kiryluk, Matthew G. Sampson, Martin R. Pollak, Simone Sanna‐Cherchi
Publicado 2023Pré-impressão -
17
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease por Yask Gupta, David J. Friedman, Michelle Mcnulty, Atlas Khan, Brandon M. Lane, Chen Wang, Juntao Ke, Gina Jin, Benjamin Wooden, Andrea L. Knob, Tze Y. Lim, Gerald B. Appel, Kinsie Huggins, Lili Liu, Adele Mitrotti, Megan C. Stangl, Andrew S. Bomback, Rik Westland, Monica Bodria, Maddalena Marasà, Ning Shang, David J. Cohen, Russell J. Crew, William Morello, Pietro A. Canetta, Jai Radhakrishnan, Jeremiah Martino, Qingxue Liu, Wendy K. Chung, Angelica Espinoza, Yuan Luo, Wei‐Qi Wei, QiPing Feng, Chunhua Weng, Yilu Fang, Iftikhar J. Kullo, Mohammadreza Naderian, Nita A. Limdi, Marguerite R. Irvin, Hemant K. Tiwari, Sumit Mohan, Maya K. Rao, Geoffrey K. Dube, Ninad S. Chaudhary, Orlando M. Gutiérrez, Suzanne E. Judd, Mary Cushman, Leslie A. Lange, Ethan M. Lange, Daniel L. Bivona, Miguel Verbitsky, Cheryl A. Winkler, Jeffrey B. Kopp, Dominick Santoriello, Ibrahim Batal, Sérgio Veloso Brant Pinheiro, Eduardo A. Oliveira, Ana Cristina Simões e Silva, Isabella Pisani, Enrico Fiaccadori, Fangming Lin, Loreto Gesualdo, Antonio Amoroso, Gian Marco Ghiggeri, Vivette D. D’Agati, Riccardo Magistroni, Eimear E. Kenny, Ruth J. F. Loos, Giovanni Montini, Friedhelm Hildebrandt, Dirk S. Paul, Slavé Petrovski, David B. Goldstein, Matthias Kretzler, Rasheed Gbadegesin, Ali G. Gharavi, Krzysztof Kiryluk, Matthew G. Sampson, Martin R. Pollak, Simone Sanna‐Cherchi
Publicado 2023Artigo -
18
Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations por Niall J. Lennon, Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin, Jennifer E. Below, Sonja I. Berndt, Wendy K. Chung, James J. Cimino, Ellen Wright Clayton, John J. Connolly, David R. Crosslin, Ozan Dikilitas, Digna R. Velez Edwards, QiPing Feng, Marissa Fisher, Robert R. Freimuth, Tian Ge, Sonja Berndt, Joel N. Hirschhorn, Ruth J. F. Loos, Joseph Glessner, Allan Gordon, Candace Patterson, Hákon Hákonarson, Maegan Harden, Margaret Harr, Joel N. Hirschhorn, Clive Hoggart, Li Hsu, Marguerite R. Irvin, Gail P. Jarvik, Elizabeth W. Karlson, Atlas Khan, Amit V. Khera, Krzysztof Kiryluk, Iftikhar J. Kullo, Katie Larkin, Nita A. Limdi, Jodell E. Linder, Ruth J. F. Loos, Yuan Luo, Edyta Małolepsza, Teri A. Manolio, Lisa J. Martin, L.R. McCarthy, Elizabeth M. McNally, James B. Meigs, Tesfaye B. Mersha, Jonathan D. Mosley, Anjene Musick, Bahram Namjou, Nihal Pai, Lorenzo L. Pesce, Ulrike Peters, Josh F. Peterson, Cynthia A. Prows, Megan J. Puckelwartz, Heidi L. Rehm, Dan M. Roden, Elisabeth A. Rosenthal, Robb Rowley, Konrad Teodor Sawicki, Daniel J. Schaid, Roelof A. J. Smit, Johanna L. Smith, Jordan W. Smoller, Minta Thomas, Hemant K. Tiwari, Diana M. Toledo, Nataraja Sarma Vaitinadin, David L. Veenstra, Theresa L. Walunas, Zhe Wang, Wei‐Qi Wei, Chunhua Weng, Georgia L. Wiesner, Xianyong Yin, Eimear E. Kenny
Publicado 2024Artigo -
19
The power of genetic diversity in genome-wide association studies of lipids por Sarah E. Graham, Shoa L. Clarke, Kuan-Han Wu, Stavroula Kanoni, Greg J. M. Zajac, Shweta Ramdas, Ida Surakka, Ioanna Ntalla, Sailaja Vedantam, Thomas W. Winkler, Adam E. Locke, Eirini Marouli, Mi Yeong Hwang, Sohee Han, Akira Narita, Ananyo Choudhury, Amy R. Bentley, Kenneth Ekoru, Anurag Verma, Bhavi Trivedi, Hilary C. Martin, Karen A. Hunt, Qin Hui, Derek Klarin, Xiang Zhu, Gudmar Thorleifsson, Anna Helgadóttir, Daníel F. Guðbjartsson, Hilma Hólm, Isleifur Olafsson, Masato Akiyama, Saori Sakaue, Chikashi Terao, Masahiro Kanai, Wei Zhou, Ben Brumpton, Humaira Rasheed, Sanni Ruotsalainen, Aki S. Havulinna, Yogasudha Veturi, QiPing Feng, Elisabeth A. Rosenthal, Todd Lingren, Jennifer A. Pacheco, Sarah A. Pendergrass, Jeffrey Haessler, Franco Giulianini, Yuki Bradford, Jason E. Miller, Archie Campbell, Kuang Lin, Iona Y. Millwood, George Hindy, Asif Rasheed, Jessica D. Faul, Wei Zhao, David R. Weir, Constance Turman, Hongyan Huang, Mariaelisa Graff, Anubha Mahajan, Michael R. Brown, Weihua Zhang, Ketian Yu, Ellen M. Schmidt, Anita Pandit, Stefan Gustafsson, Xianyong Yin, Jian’an Luan, Jing-Hua Zhao, Fumihiko Matsuda, Hye-Mi Jang, Kyungheon Yoon, Carolina Medina‐Gómez, Achilleas Pitsillides, Jouke‐Jan Hottenga, Gonneke Willemsen, Andrew R. Wood, Yingji Ji, Zishan Gao, Simon Haworth, Ruth E. Mitchell, Jin Fang Chai, Mette Aadahl, Jie Yao, Ani Manichaikul, Helen R. Warren, Julia Ramírez, Jette Bork‐Jensen, Line Lund Kårhus, Anuj Goel, Maria Sabater‐Lleal, Raymond Noordam, Carlo Sidore, Edoardo Fiorillo, Aaron F. McDaid, Pedro Marques‐Vidal, Matthias Wielscher, Stella Trompet, Naveed Sattar
Publicado 2021Revisão -
20
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids por Shweta Ramdas, Jonathan Judd, Sarah E. Graham, Stavroula Kanoni, Yuxuan Wang, Ida Surakka, Brandon M. Wenz, Shoa L. Clarke, Alessandra Chesi, Andrew D. Wells, Konain Fatima Bhatti, Sailaja Vedantam, Thomas W. Winkler, Adam E. Locke, Eirini Marouli, Greg J.M. Zajac, Kuan-Han Wu, Ιωάννα Ντάλλα, Qin Hui, Derek Klarin, Austin T. Hilliard, Zeyuan Wang, Chao Xue, Guðmar Þorleifsson, Anna Helgadóttir, Daníel F. Guðbjartsson, Hilma Hólm, Ísleifur Ólafsson, Mi Yeong Hwang, Sohee Han, Masato Akiyama, Saori Sakaue, Chikashi Terao, Masahiro Kanai, Wei Zhou, Ben Brumpton, Humaira Rasheed, Aki S. Havulinna, Yogasudha Veturi, Jennifer A. Pacheco, Elisabeth A. Rosenthal, Todd Lingren, QiPing Feng, Iftikhar J. Kullo, Akira Narita, Jun Takayama, Hilary C. Martin, Karen A. Hunt, Bhavi Trivedi, Jeffrey Haessler, Franco Giulianini, Yuki Bradford, Jason E. Miller, Archie Campbell, Kuang Lin, Iona Y. Millwood, Asif Rasheed, George Hindy, Jessica D. Faul, Wei Zhao, David R. Weir, Constance Turman, Hongyan Huang, Mariaelisa Graff, Ananyo Choudhury, Dhriti Sengupta, Anubha Mahajan, Michael R. Brown, Weihua Zhang, Ketian Yu, Ellen M. Schmidt, Anita Pandit, Stefan Gustafsson, Xianyong Yin, Jian’an Luan, Jinghua Zhao, Fumihiko Matsuda, Hye-Mi Jang, Kyungheon Yoon, Carolina Medina‐Gómez, Achilleas Pitsillides, Jouke‐Jan Hottenga, Andrew R. Wood, Yingji Ji, Zishan Gao, Simon Haworth, Ruth E. Mitchell, Jin Fang Chai, Mette Aadahl, Anne A. Bjerregaard, Jie Yao, Ani Manichaikul, Wen‐Jane Lee, Chao A. Hsiung, Helen R. Warren, Julia Ramírez, Jette Bork‐Jensen, Line Lund Kårhus, Anuj Goel, Maria Sabater‐Lleal
Publicado 2022Artigo
Ferramentas de procura:
Materias Relacionadas
Medicine
Biology
Gene
Genetics
Internal medicine
Genotype
Single-nucleotide polymorphism
Bioinformatics
Disease
Computational biology
Genome-wide association study
Pharmacology
Statin
Computer science
Genetic association
Pathology
Phenotype
Myopathy
Endocrinology
Engineering
Hydroxymethylglutaryl-CoA Reductase Inhibitors
Law
Odds ratio
Pharmacogenetics
Political science
Programming language
Quantitative trait locus
Biochemistry
Cardiology
Cirrhosis