Rezultati pretrage - Hanfei Xu
- Prikaz rezultata 1 – 16 od 16
-
1
-
2
-
3
-
4
DLST-dependence dictates metabolic heterogeneity in TCA-cycle usage among triple-negative breast cancer od Ning Shen, Sovannarith Korm, Theodoros Karantanos, Dun Li, Xiaoyu Zhang, Eleni Ritou, Hanfei Xu, Andrew Lam, Justin English, Wei‐Xing Zong, Yongmei Liu, Orian S. Shirihai, Hui Feng
Izdano 2021Artigo -
5
Diabetes and Deficits in Cortical Bone Density, Microarchitecture, and Bone Size: Framingham HR-pQCT Study od Elizabeth J. Samelson, Serkalem Demissie, L. Adrienne Cupples, Xiaochun Zhang, Hanfei Xu, Yongmei Liu, Steven K. Boyd, Robert R. McLean, Kerry E Broe, Douglas P. Kiel, Mary Bouxsein
Izdano 2017Artigo -
6
The Association of Aging Biomarkers, Interstitial Lung Abnormalities, and Mortality od Jason L. Sanders, Rachel K. Putman, Josée Dupuis, Hanfei Xu, Joanne M. Murabito, Tetsuro Araki, Mizuki Nishino, Emelia J. Benjamin, Daniel Levy, Ramachandran S. Vasan, George R. Washko, Jeffrey L. Curtis, Christine M. Freeman, Russell P. Bowler, Hiroto Hatabu, George O'connor, Gary M. Hunninghake
Izdano 2020Artigo -
7
Investigating Associations of Omega-3 Fatty Acids, Lung Function Decline, and Airway Obstruction od Bonnie Patchen, Pallavi Balte, Traci M. Bartz, R. Graham Barr, Myriam Fornage, Mariaelisa Graff, David R. Jacobs, Ravi Kalhan, Rozenn N. Lemaître, George O'connor, Bruce M. Psaty, Jungkyun Seo, Michael Y. Tsai, Alexis C. Wood, Hanfei Xu, Jingwen Zhang, Sina A. Gharib, Ani Manichaikul, Kari E. North, Lyn M. Steffen, Josée Dupuis, Elizabeth C. Oelsner, Dana B. Hancock, Patricia A. Cassano
Izdano 2023Artigo -
8
Cortical and trabecular bone microarchitecture as an independent predictor of incident fracture risk in older women and men in the Bone Microarchitecture International Consortium (... od Elizabeth J. Samelson, Kerry E Broe, Hanfei Xu, Laiji Yang, Steven K. Boyd, Emmanuel Biver, Paweł Szulc, Jonathan D. Adachi, Shreyasee Amin, Elizabeth J. Atkinson, Claudie Berger, Lauren A. Burt, Roland Chapurlat, Thierry Chevalley, Serge Ferrari, David Goltzman, David A. Hanley, Marian T. Hannan, Sundeep Khosla, Yongmei Liu, Mattias Lorentzon, Dan Mellström, Blandine Merle, Maria Nethander, René Rizzoli, Elisabeth Sornay‐Rendu, Bert van Rietbergen, Daniel Sundh, Andy Kin On Wong, Claes Ohlsson, Serkalem Demissie, Douglas P. Kiel, Mary Bouxsein
Izdano 2018Artigo -
9
Overlap of Genetic Risk between Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis od Brian D. Hobbs, Rachel K. Putman, Tetsuro Araki, Mizuki Nishino, Gunnar Guðmundsson, Vilmundur Guðnason, Guðný Eiríksdóttir, Nuno R. Zilhão, Josée Dupuis, Hanfei Xu, George O'connor, Ani Manichaikul, Jennifer N. Nguyen, Anna J. Podolanczuk, Purnema Madahar, Jerome I. Rotter, David J. Lederer, R. Graham Barr, Stephen S. Rich, Elizabeth J. Ampleford, Victor E. Ortega, Stephen P. Peters, Wanda K. O’Neal, John D. Newell, Eugene R. Bleecker, Deborah A. Meyers, Richard J. Allen, Justin M. Oldham, Shwu‐Fan Ma, Imre Noth, Gisli Jenkins, Toby M. Maher, Richard Hubbard, Louise V. Wain, Tasha E. Fingerlin, David A. Schwartz, George R. Washko, Iván O. Rosas, Edwin K. Silverman, Hiroto Hatabu, Michael H. Cho, Gary M. Hunninghake
Izdano 2019Artigo -
10
Genome-Wide Association Study of Susceptibility to Idiopathic Pulmonary Fibrosis od Richard J. Allen, Beatriz Guillén‐Guío, Justin M. Oldham, Shwu‐Fan Ma, Amy Dressen, Megan L. Paynton, Luke M. Kraven, Ma’en Obeidat, Xuan Li, Michael Ng, Rebecca Braybrooke, María Molina‐Molina, Brian D. Hobbs, Rachel K. Putman, Phuwanat Sakornsakolpat, Helen Booth, William A. Fahy, Simon P. Hart, Mike Hill, Nik Hirani, Richard Hubbard, Robin J. McAnulty, Ann Millar, Vidya Navaratnam, Eunice Oballa, Helen Parfrey, Gauri Saini, Moira K. B. Whyte, Yingze Zhang, Naftali Kaminski, Ayodeji Adegunsoye, Mary E. Strek, Margaret Neighbors, Xuting R. Sheng, Gunnar Guðmundsson, Vilmundur Guðnason, Hiroto Hatabu, David J. Lederer, Ani Manichaikul, John D. Newell, George O'connor, Victor E. Ortega, Hanfei Xu, Tasha E. Fingerlin, Yohan Bossé, Ke Hao, Philippe Joubert, David C. Nickle, Don D. Sin, Wim Timens, Dominic Furniss, Andrew P. Morris, Krina T. Zondervan, Ian P. Hall, Ian Sayers, Martin D. Tobin, Toby M. Maher, Michael H. Cho, Gary M. Hunninghake, David A. Schwartz, Brian L. Yaspan, Philip L. Molyneaux, Carlos Flores, Imre Noth, Gisli Jenkins, Louise V. Wain
Izdano 2019Artigo -
11
Pulmonary Function and Blood DNA Methylation: A Multiancestry Epigenome-Wide Association Meta-analysis od Mi Kyeong Lee, Tianxiao Huan, Daniel L. McCartney, Geetha Chittoor, Maaike de Vries, Lies Lahousse, Jennifer N. Nguyen, Jennifer A. Brody, Juan Castillo‐Fernandez, Natalie Terzikhan, Cancan Qi, Roby Joehanes, Josine L. Min, Gordon Smilnak, Jessica Shaw, Chen Xi Yang, Elena Colicino, Thanh T. Hoang, Mairead L. Bermingham, Hanfei Xu, Anne E. Justice, Cheng‐Jian Xu, Stephen S. Rich, Simon R. Cox, Judith M. Vonk, Ivana Nedeljković, Nona Sotoodehnia, Pei-Chien Tsai, Joel Schwartz, Janice M. Leung, Sinjini Sikdar, Rosie M. Walker, Sarah E. Harris, Diana A. van der Plaat, David Van Den Berg, Traci M. Bartz, Tim D. Spector, Pantel Vokonas, Riccardo E. Marioni, Adele M. Taylor, Yongmei Liu, R. Graham Barr, Leslie A. Lange, Andrea Baccarelli, Ma’en Obeidat, Myriam Fornage, Tianyuan Wang, James M. Ward, Alison A. Motsinger‐Reif, Gibran Hemani, Gerard H. Koppelman, Jordana T. Bell, Sina A. Gharib, Guy Brusselle, H. Marike Boezen, Kari E. North, Daniel Levy, Kathryn L. Evans, Josée Dupuis, Charles E. Breeze, Ani Manichaikul, Stephanie J. London
Izdano 2022Revisão -
12
Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk od Nick Shrine, Abril G. Izquierdo, Jing Chen, Richard Packer, Robert J. Hall, Anna L. Guyatt, Chiara Batini, Rebecca Thompson, Chandan Pavuluri, Vidhi Malik, Brian D. Hobbs, Matthew Moll, Wonji Kim, Ruth Tal‐Singer, Per Bakke, Katherine A. Fawcett, Catherine John, Kayesha Coley, Noemi Nicole Piga, Alfred Pozarickij, Kuang Lin, Iona Y. Millwood, Zhengming Chen, Liming Li, Sara Wijnant, Lies Lahousse, Guy Brusselle, André G. Uitterlinden, Ani Manichaikul, Elizabeth C. Oelsner, Stephen S. Rich, R. Graham Barr, Shona M. Kerr, Véronique Vitart, Michael R. Brown, Matthias Wielscher, Medea Imboden, Ayoung Jeong, Traci M. Bartz, Sina A. Gharib, Claudia Flexeder, Stefan Karrasch, Christian Gieger, Annette Peters, Beate Stubbe, Xiaowei Hu, Victor E. Ortega, Deborah A. Meyers, Eugene R. Bleecker, Stacey Gabriel, Namrata Gupta, Albert V. Smith, Jian’an Luan, Jinghua Zhao, Ailin Falkmo Hansen, Arnulf Langhammer, Cristen J. Willer, Laxmi Bhatta, David J. Porteous, Blair H. Smith, Archie Campbell, Tamar Sofer, Jiwon Lee, Martha L. Daviglus, Bing Yu, Elise Lim, Hanfei Xu, George O'connor, Gaurav Thareja, Omar Albagha, Said I. Ismail, Wadha Al‐Muftah, Radja Badji, Hamdi Mbarek, Dima Darwish, Tasnim Fadl, Heba Yasin, Maryem Ennaifar, Rania G. Abdel‐latif, Fatima Alkuwari, Muhammad Arshad Alvi, Yasser Al‐Sarraj, Chadi Saad, Asmaa Althani, Eleni Fethnou, Fatima Qafoud, Eiman Alkhayat, Nahla Afifi, Sara Tomei, Wei Liu, Stephan Lorenz, Najeeb Syed, Hakeem Almabrazi, Fazulur Rehaman Vempalli, Ramzi Temanni, Tariq Abu Saqri, Mohammedhusen Khatib, Mehshad Hamza, Tariq Abu Zaid, Ahmed El Khouly
Izdano 2023Revisão -
13
Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure od Heming Wang, Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee, Yan V. Sun, Amy R. Bentley, Alisa K. Manning, Hugues Aschard, Tuomas O. Kilpeläinen, Marjan Ilkov, Michael R. Brown, A.R.V.R. Horimoto, Melissa A. Richard, Traci M. Bartz, Dina Vojinović, Elise Lim, Jovia L. Nierenberg, Yongmei Liu, Kumaraswamy Naidu Chitrala, Tuomo Rankinen, Solomon K. Musani, Nora Franceschini, Rainer Rauramaa, Maris Alver, Phyllis C. Zee, Sarah E. Harris, Peter J. van der Most, Ilja M. Nolte, Patricia B. Munroe, Colin N. A. Palmer, Brigitte Kühnel, Stefan Weiß, Wanqing Wen, Kelly Hall, Leo‐Pekka Lyytikäinen, Jeff O’Connell, Guðný Eiríksdóttir, Lenore J. Launer, Paul S. de Vries, Dan E. Arking, Han Chen, Eric Boerwinkle, José Eduardo Krieger, Pamela J. Schreiner, Stephen Sidney, James M. Shikany, Kenneth Rice, Yii‐Der Ida Chen, Sina A. Gharib, Joshua C. Bis, Annemarie I. Luik, M. Arfan Ikram, André G. Uitterlinden, Najaf Amin, Hanfei Xu, Daniel Levy, Jiang He, Kurt K. Lohman, Alan B. Zonderman, Treva Rice, Mario Sims, Gregory Wilson, Tamar Sofer, Stephen S. Rich, Walter Palmas, Jie Yao, Xiuqing Guo, Jerome I. Rotter, Nienke R. Biermasz, Dennis O. Mook‐Kanamori, Lisa W. Martin, Ana Barac, Robert B. Wallace, Daniel J. Gottlieb, Pirjo Komulainen, Sami Heikkinen, Reedik Mägi, Lili Milani, Andres Metspalu, John M. Starr, Yuri Milaneschi, RJ Waken, Chuan Gao, Mélanie Waldenberger, Annette Peters, Konstantin Strauch, Thomas Meitinger, Till Roenneberg, Uwe Völker, Marcus Dörr, Xiao‐Ou Shu, Sutapa Mukherjee, David R. Hillman, Mika Kähönen, Lynne E. Wagenknecht, Christian Gieger, Hans J. Grabe, Wei Zheng
Izdano 2020Pré-impressão -
14
Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure od Heming Wang, Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee, Yan V. Sun, Amy R. Bentley, Alisa K. Manning, Hugues Aschard, Tuomas O. Kilpeläinen, Marjan Ilkov, Michael R. Brown, A.R.V.R. Horimoto, Melissa A. Richard, Traci M. Bartz, Dina Vojinović, Elise Lim, Jovia L. Nierenberg, Yongmei Liu, Kumaraswamy Naidu Chitrala, Tuomo Rankinen, Solomon K. Musani, Nora Franceschini, Rainer Rauramaa, Maris Alver, Phyllis C. Zee, Sarah E. Harris, Peter J. van der Most, Ilja M. Nolte, Patricia B. Munroe, Colin N. A. Palmer, Brigitte Kühnel, Stefan Weiß, Wanqing Wen, Kelly Hall, Leo‐Pekka Lyytikäinen, Jeff O’Connell, Guðný Eiríksdóttir, Lenore J. Launer, Paul S. de Vries, Dan E. Arking, Han Chen, Eric Boerwinkle, José Eduardo Krieger, Pamela J. Schreiner, Stephen Sidney, James M. Shikany, Kenneth Rice, Yii‐Der Ida Chen, Sina A. Gharib, Joshua C. Bis, Annemarie I. Luik, M. Arfan Ikram, André G. Uitterlinden, Najaf Amin, Hanfei Xu, Daniel Levy, Jiang He, Kurt K. Lohman, Alan B. Zonderman, Treva Rice, Mario Sims, Gregory Wilson, Tamar Sofer, Stephen S. Rich, Walter Palmas, Jie Yao, Xiuqing Guo, Jerome I. Rotter, Nienke R. Biermasz, Dennis O. Mook‐Kanamori, Lisa W. Martin, Ana Barac, Robert B. Wallace, Daniel J. Gottlieb, Pirjo Komulainen, Sami Heikkinen, Reedik Mägi, Lili Milani, Andres Metspalu, John M. Starr, Yuri Milaneschi, RJ Waken, Chuan Gao, Mélanie Waldenberger, Annette Peters, Konstantin Strauch, Thomas Meitinger, Till Roenneberg, Uwe Völker, Marcus Dörr, Xiao‐Ou Shu, Sutapa Mukherjee, David R. Hillman, Mika Kähönen, Lynne E. Wagenknecht, Christian Gieger, Hans J. Grabe, Wei Zheng
Izdano 2021Artigo -
15
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data od Pierrick Wainschtein, Deepti Jain, Zhili Zheng, Stella Aslibekyan, Diane M. Becker, Wenjian Bi, Jennifer A. Brody, Jenna C. Carlson, Adolfo Correa, Margaret Mengmeng Du, Lindsay Fernández‐Rhodes, Kendra Ferrier, Misa Graff, Xiuqing Guo, Jiang He, Nancy L. Heard‐Costa, Heather M. Highland, Joel N. Hirschhorn, Candace M Howard-Claudio, Carmen R. Isasi, Rebecca D. Jackson, Jicai Jiang, Roby Joehanes, Anne E. Justice, Rita R. Kalyani, Sharon L. R. Kardia, Ethan M. Lange, Meryl S. LeBoff, Seunggeun Lee, Xihao Li, Zilin Li, Elise Lim, D. Y. Lin, Xihong Lin, Simin Liu, Yingchang Lu, JoAnn E. Manson, Lisa W. Martin, Caitlin McHugh, Julie Mikulla, Solomon K. Musani, Maggie Ng, Deborah A. Nickerson, Colin N. A. Palmer, James A. Perry, Ulrike Peters, Michael Preuß, Qibin Qi, Laura M. Raffield, Laura J. Rasmussen‐Torvik, Alex P. Reiner, Emily M. Russell, Colleen M. Sitlani, Jennifer A. Smith, Cassandra N. Spracklen, Tao Wang, Zhe Wang, Jennifer Wessel, Hanfei Xu, Mohammad Yaser, Sachiko Yoneyama, Kendra A. Young, Jingwen Zhang, Xinruo Zhang, Hufeng Zhou, Xiaofeng Zhu, Sebastian Zoellner, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Allison E. Ashley‐Koch, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis, Thomas W. Blackwell
Izdano 2022Artigo -
16
Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele od Xinruo Zhang, Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu, Zhe Wang, Kendra Ferrier, Geetha Chittoor, Navya Shilpa Josyula, Mariah Meyer, Shreyash Gupta, Xihao Li, Zilin Li, Matthew Allison, Diane M. Becker, Lawrence F. Bielak, Joshua C. Bis, Meher Preethi Boorgula, Donald W. Bowden, Jai Broome, Erin Buth, Christopher S. Carlson, Kyong–Mi Chang, Sameer Chavan, Yen‐Feng Chiu, Lee‐Ming Chuang, Matthew P. Conomos, Dawn L. DeMeo, Mengmeng Du, Ravindranath Duggirala, Celeste Eng, Alison E. Fohner, Barry I. Freedman, Melanie E. Garrett, Xiuqing Guo, Chris Haiman, Ben Heavner, Bertha Hidalgo, James E. Hixson, Yuk‐Lam Ho, Brian D. Hobbs, Donglei Hu, Qin Hui, Chii‐Min Hwu, Rebecca D. Jackson, Deepti Jain, Rita R. Kalyani, Sharon L.R. Kardia, Tanika N. Kelly, Ethan M. Lange, Michael A. LeNoir, Changwei Li, Loı̈c Le Marchand, Merry‐Lynn McDonald, Caitlin McHugh, Alanna C. Morrison, Take Naseri, Jeffrey R. O’Connell, Christopher J O'Donnell, Nicholette D. Allred, James S. Pankow, James A. Perry, Ulrike Peters, Michael Preuß, D. C. Rao, Elizabeth A. Regan, Sefuiva M Reupena, Dan M. Roden, José Rodríguez‐Santana, Colleen M. Sitlani, Jennifer A. Smith, Hemant K. Tiwari, Ramachandran S. Vasan, Zeyuan Wang, Daniel E. Weeks, Jennifer Wessel, Kerri L. Wiggins, Lynne R. Wilkens, Peter W.F. Wilson, Lisa R. Yanek, Zachary T. Yoneda, Wei Zhao, Sebastian Zöllner, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes, John Blangero, Eric Boerwinkle, Esteban G. Burchard, April P. Carson, Daniel I. Chasman, Yii‐Der Ida Chen, Joanne E. Curran, Myriam Fornage, Victor R. Gordeuk, Jiang He, Susan R. Heckbert, Lifang Hou, Marguerite R. Irvin
Izdano 2025Artigo
Alati za pretragu:
Povezani predmeti
Medicine
Internal medicine
Biology
Gene
Genetics
Genotype
Genome-wide association study
Single-nucleotide polymorphism
Disease
Endocrinology
Lung
Genetic association
Pathology
Bioinformatics
Computational biology
Computer science
Framingham Risk Score
Genome
Osteoporosis
Association (psychology)
Bone density
Bone mineral
COPD
Diabetes mellitus
Femoral neck
Framingham Heart Study
Idiopathic pulmonary fibrosis
Lung function
Obesity
Operating system