Rezultati pretrage - Jeffrey Haessler

Detaljiziraj rezultate
  1. 1
    Complete remission sustained 3 years from treatment initiation is a powerful surrogate for extended survival in multiple myeloma

    Complete remission sustained 3 years from treatment initiation is a powerful surrogate for extended survival in multiple myeloma od Bart Barlogie, Elias Anaissie, Jeffrey Haessler, Fritz Van Rhee, Mauricio Pineda‐Roman, Klaus Hollmig, Yazan Alsayed, Joshua Epstein, John D. Shaughnessy, John Crowley

    Izdano 2008
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  2. 2
    Benefit of Complete Response in Multiple Myeloma Limited to High-Risk Subgroup Identified by Gene Expression Profiling

    Benefit of Complete Response in Multiple Myeloma Limited to High-Risk Subgroup Identified by Gene Expression Profiling od Jeffrey Haessler, John D. Shaughnessy, Fenghuang Zhan, John Crowley, Joshua Epstein, Frits van Rhee, Elias Anaissie, Mauricio Pineda‐Roman, Maurizio Zangari, Klaus Hollmig, Abid Mohiuddin, Yazan Alsayed, Antje Hoering, Guido Tricot, Bart Barlogie

    Izdano 2007
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  3. 3
    Incorporating bortezomib into upfront treatment for multiple myeloma: early results of total therapy 3

    Incorporating bortezomib into upfront treatment for multiple myeloma: early results of total therapy 3 od Bart Barlogie, Elias Anaissie, Frits van Rhee, Jeffrey Haessler, Klaus Hollmig, Mauricio Pineda‐Roman, Michele Cottler‐Fox, Abid Mohiuddin, Yazan Alsayed, Guido Tricot, Vanessa Bolejack, Maurizio Zangari, Joshua Epstein, Nathan Petty, Douglas Steward, Bonnie Jenkins, Jennifer Gurley, Ellen Sullivan, John Crowley, John D. Shaughnessy

    Izdano 2007
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  4. 4
    Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project

    Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project od Jill M. Johnsen, Paul L. Auer, Alanna C. Morrison, Shuo Jiao, Peng Wei, Jeffrey Haessler, Keolu Fox, Sean McGee, Joshua D. Smith, Christopher S. Carlson, Nicholas L. Smith, Eric Boerwinkle, Charles Kooperberg, Deborah A. Nickerson, Stephen S. Rich, David Green, Ulrike Peters, Mary Cushman, Alex P. Reiner

    Izdano 2013
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  5. 5
    Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies

    Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies od Quan Sun, Misa Graff, Bryce Rowland, Jia Wen, Le Huang, Tyne W. Miller‐Fleming, Jeffrey Haessler, Michael Preuß, Jin Fang Chai, Moa P. Lee, Christy L. Avery, Ching‐Yu Cheng, Nora Franceschini, Xueling Sim, Nancy J. Cox, Charles Kooperberg, Kari E. North, Yun Li, Laura M. Raffield

    Izdano 2021
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  6. 6
    Correlates and Consequences of Clonal Hematopoiesis Expansion Rate: A 16-Year Longitudinal Study of 6976 Women

    Correlates and Consequences of Clonal Hematopoiesis Expansion Rate: A 16-Year Longitudinal Study of 6976 Women od Yash Pershad, Md Mesbah Uddin, Liying Xue, Jeffrey Haessler, Jason Collins, Taralynn Mack, Elena Glick, V. M. Glaser, Kun Zhao, Siddhartha Jaiswal, JoAnn E. Manson, Urvashi Pandey, Pinkal Desai, Pradeep Natarajan, Michael C. Honigberg, Charles Kooperberg, Eric A. Whitsel, Jacob O. Kitzman, Alexander G. Bick, Alex P. Reiner

    Izdano 2025
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  7. 7
    Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array

    Strategies for Enriching Variant Coverage in Candidate Disease Loci on a Multiethnic Genotyping Array od Stephanie A. Bien, Genevieve L. Wojcik, Niha Zubair, Christopher R. Gignoux, Alicia R. Martin, Jonathan Kocarnik, Lisa W. Martin, Steven Buyske, Jeffrey Haessler, Ryan W. Walker, Iona Cheng, Mariaelisa Graff, Lucy Xia, Nora Franceschini, Tara C. Matise, Regina James, Lucia A. Hindorff, Loı̈c Le Marchand, Kari E. North, Christopher A. Haiman, Ulrike Peters, Ruth J. F. Loos, Charles Kooperberg, Carlos D. Bustamante, Eimear E. Kenny, Christopher S. Carlson

    Izdano 2016
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  8. 8
    A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

    A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood od Nuzulul Kurniansyah, Matthew Goodman, Tanika N. Kelly, Tali Elfassy, Kerri L. Wiggins, Joshua C. Bis, Xiuqing Guo, Walter Palmas, Kent D. Taylor, Henry J. Lin, Jeffrey Haessler, Yan Gao, Daichi Shimbo, Jennifer A. Smith, Bing Yu, Elena V. Feofanova, Roelof A.J. Smit, Zhe Wang, Shih‐Jen Hwang, Simin Liu, Sylvia Wassertheil‐Smoller, JoAnn E. Manson, Donald M. Lloyd‐Jones, Stephen S. Rich, Ruth J. F. Loos, Susan Redline, Adolfo Correa, Charles Kooperberg, Myriam Fornage, Robert C. Kaplan, Bruce M. Psaty, Jerome I. Rotter, Donna K. Arnett, Alanna C. Morrison, Nora Franceschini, Daniel Levy, Joshua C. Bis, Xiuqing Guo, Kent D. Taylor, Henry J. Lin, Jeffrey Haessler, Yan Gao, Jennifer A. Smith, Simin Liu, Sylvia Wassertheil‐Smoller, JoAnn E. Manson, Stephen S. Rich, Susan Redline, Adolfo Correa, Charles Kooperberg, Myriam Fornage, Robert C. Kaplan, Bruce M. Psaty, Jerome I. Rotter, Donna K. Arnett, Nora Franceschini, Daniel Levy, Tamar Sofer, Tamar Sofer

    Izdano 2022
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  9. 9
    Clonal Hematopoiesis Is Associated With Higher Risk of Stroke

    Clonal Hematopoiesis Is Associated With Higher Risk of Stroke od Romit Bhattacharya, Seyedeh M. Zekavat, Jeffrey Haessler, Myriam Fornage, Laura M. Raffield, Md Mesbah Uddin, Alexander G. Bick, Abhishek Niroula, Bing Yu, Christopher J. Gibson, Gabriel K. Griffin, Alanna C. Morrison, Bruce M. Psaty, W.T. Longstreth, Joshua C. Bis, Stephen S. Rich, Jerome I. Rotter, Russell P. Tracy, Adolfo Correa, Sudha Seshadri, Andrew D. Johnson, Jason Collins, Kathleen M. Hayden, Tracy E. Madsen, Christie M. Ballantyne, Siddhartha Jaiswal, Benjamin L. Ebert, Charles Kooperberg, JoAnn E. Manson, Eric A. Whitsel, Pradeep Natarajan, Alexander P. Reiner

    Izdano 2021
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  10. 10
    Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study

    Evaluation of the Metabochip Genotyping Array in African Americans and Implications for Fine Mapping of GWAS-Identified Loci: The PAGE Study od Steven Buyske, Ying Wu, Cara L. Carty, Iona Cheng, Themistocles L. Assimes, Logan Dumitrescu, Lucia A. Hindorff, Sabrina L. Mitchell, José Luis Ambite, Eric Boerwinkle, Petra Bůžková, Chris Carlson, Barbara Cochran, David Duggan, Charles B. Eaton, Megan D. Fesinmeyer, Nora Franceschini, Jeffrey Haessler, Nancy S. Jenny, Hyun Min Kang, Charles Kooperberg, Yi Lin, Loı̈c Le Marchand, Tara C. Matise, Jennifer G. Robinson, Carlos J. Rodríguez, Fredrick R. Schumacher, Benjamin F. Voight, Alicia Young, Teri A. Manolio, Karen L. Mohlke, Christopher A. Haiman, Ulrike Peters, Dana C. Crawford, Kari E. North

    Izdano 2012
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  11. 11
    Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations

    Whole-Genome Sequencing Analysis of Human Metabolome in Multi-Ethnic Populations od Elena V. Feofanova, Michael R. Brown, Taryn Alkis, Astrid M. Manuel, Xihao Li, Usman A. Tahir, Zilin Li, Kevin Mendez, Rachel S. Kelly, Qibin Qi, Han Chen, Martin G. Larson, Rozenn N. Lemaître, Alanna C. Morrison, Charles Grieser, Kari E. Wong, Robert E. Gerszten, Zhongming Zhao, Jessica Lasky‐Su, Honghuang Lin, Jeffrey Haessler, Jennifer A. Brody, Kari E. North, Kent D. Taylor, Clary B. Clish, James G. Wilson, Xihong Lin, Robert C. Kaplan, Charles Kooperberg, Bruce M. Psaty, Stephen S. Rich, Jerome I. Rotter, Ramachandran S. Vasan, Eric Boerwinkle, Bing Yu

    Izdano 2023
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  12. 12
    Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity

    Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity od Anubha Mahajan, Aylin R. Rodan, Thu H. Le, Kyle J. Gaulton, Jeffrey Haessler, Adrienne M. Stilp, Yoichiro Kamatani, Gu Zhu, Tamar Sofer, Sanjana Puri, Jeffrey N. Schellinger, Pei‐Lun Chu, Sylvia Cechova, Natalie R. van Zuydam, Johan Ärnlöv, Michael F. Flessner, Vilmantas Giedraitis, Andrew C. Heath, Michiaki Kubo, Anders Larsson, Cecilia M. Lindgren, Pamela A. F. Madden, Grant W. Montgomery, George Papanicolaou, Alex P. Reiner, Johan Sundström, Timothy A. Thornton, Lars Lind, Erik Ingelsson, Jianwen Cai, Nicholas G. Martin, Charles Kooperberg, Koichi Matsuda, John B. Whitfield, Yukinori Okada, Cathy C. Laurie, Andrew P. Morris, Nora Franceschini

    Izdano 2016
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:
  13. 13
    Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

    Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project od Yao Hu, Jeffrey Haessler, Regina Manansala, Kerri L. Wiggins, Arden Moscati, Alexa Beiser, Nancy L. Heard‐Costa, Chloé Sarnowski, Laura M. Raffield, Jaeyoon Chung, Sandro Marini, Christopher D. Anderson, Jonathan Rosand, Huichun Xu, Xiao Sun, Tanika N. Kelly, Quenna Wong, Leslie A. Lange, Jerome I. Rotter, Adolfo Correa, Ramachandran S. Vasan, Sudha Seshadri, Stephen S. Rich, Ron Do, Ruth J. F. Loos, W.T. Longstreth, Joshua C. Bis, Bruce M. Psaty, David Tirschwell, Themistocles L. Assimes, Brian Silver, Simin Liu, Rebecca D. Jackson, Sylvia Wassertheil‐Smoller, Braxton D. Mitchell, Myriam Fornage, Paul L. Auer, Alex P. Reiner, Charles Kooperberg

    Izdano 2021
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  14. 14
    Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies

    Four Susceptibility Loci for Gallstone Disease Identified in a Meta-analysis of Genome-Wide Association Studies od Amit D. Joshi, Charlotte Andersson, Stephan Buch, Stefan Stender, Raymond Noordam, Lu‐Chen Weng, Peter Weeke, Paul L. Auer, Bernhard O. Boehm, Constance Chen, Hyon K. Choi, Gary C. Curhan, Joshua C. Denny, Immaculata De Vivo, John D. Eicher, David Ellinghaus, Aaron R. Folsom, Charles S. Fuchs, Manish Gala, Jeffrey Haessler, Albert Hofman, Frank B. Hu, David J. Hunter, Harry L.A. Janssen, Jae H. Kang, Charles Kooperberg, Peter Kraft, Wolfgang Kratzer, Wolfgang Lieb, Pamela L. Lutsey, Sarwa Darwish Murad, Børge G. Nordestgaard, Louis R. Pasquale, Alex P. Reiner, Paul M. Ridker, Eric B. Rimm, Lynda M. Rose, Christian M. Shaffer, Clemens Schafmayer, Rulla M. Tamimi, André G. Uitterlinden, Uwe Völker, Henry Völzke, Yoshiyuki Wakabayashi, Janey L. Wiggs, Jun Zhu, Dan M. Roden, Bruno H. Stricker, Weihong Tang, Alexander Teumer, Jochen Hampe, Anne Tybjærg‐Hansen, Daniel I. Chasman, Andrew T. Chan, Andrew D. Johnson

    Izdano 2016
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:
  15. 15
    Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism

    Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism od Sara Lindström, Lu Wang, Erin N. Smith, William Gordon, Astrid van Hylckama Vlieg, Mariza de Andrade, Jennifer A. Brody, Jack Pattee, Jeffrey Haessler, Ben Brumpton, Daniel I. Chasman, Pierre Suchon, Ming‐Huei Chen, Constance Turman, Marine Germain, Kerri L. Wiggins, James W. MacDonald, Sigrid K. Brækkan, Sebastian M. Armasu, Nathan Pankratz, Rebecca D. Jackson, Jonas B. Nielsen, Franco Giulianini, Marja Puurunen, Manal Ibrahim, Susan R. Heckbert, Scott M. Damrauer, Pradeep Natarajan, Derek Klarin, Paul S. de Vries, Maria Sabater‐Lleal, Jennifer E. Huffman, Theo K. Bammler, Kelly A. Frazer, Bryan M. McCauley, Kent D. Taylor, James S. Pankow, Alexander P. Reiner, Maiken E. Gabrielsen, Jean‐François Deleuze, Christopher J. O’Donnell, Jihye Kim, Barbara McKnight, Peter Kraft, J.-B. Hansen, Frits R. Rosendaal, John A. Heit, Bruce M. Psaty, Weihong Tang, Charles Kooperberg, Kristian Hveem, Paul M. Ridker, Pierre‐Emmanuel Morange, Andrew D. Johnson, Christopher Kabrhel, David‐Alexandre Trégouët, Nicholas L. Smith

    Izdano 2019
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  16. 16
    Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation

    Genetic Determinants of Electrocardiographic P-Wave Duration and Relation to Atrial Fibrillation od Lu‐Chen Weng, Amelia Weber Hall, Seung Hoan Choi, Sean J. Jurgens, Jeffrey Haessler, Nathan A. Bihlmeyer, Niels Grarup, Honghuang Lin, Alexander Teumer, Ruifang Li‐Gao, Jie Yao, Xiuqing Guo, Jennifer A. Brody, Martina Müller‐Nurasyid, Katharina Schramm, Niek Verweij, Marten E. van den Berg, Jessica van Setten, Aaron Isaacs, Julia Ramírez, Helen R. Warren, Sandosh Padmanabhan, Jan A. Kors, Rudolf A. de Boer, Peter van der Meer, Moritz F. Sinner, Mélanie Waldenberger, Bruce M. Psaty, Kent D. Taylor, Uwe Völker, Jørgen K. Kanters, Man Li, Álvaro Alonso, Marco Pérez, Ilonca Vaartjes, Michiel L. Bots, Paul L. Huang, Susan R. Heckbert, Henry J. Lin, Jelena Kornej, Patricia B. Munroe, Cornelia M. van Duijn, Folkert W. Asselbergs, Bruno H. Stricker, Pim van der Harst, Stefan Kääb, Annette Peters, Nona Sotoodehnia, Jerome I. Rotter, Dennis O. Mook‐Kanamori, Marcus Dörr, Stephan B. Felix, Allan Linneberg, Torben Hansen, Dan E. Arking, Charles Kooperberg, Emelia J. Benjamin, Kathryn L. Lunetta, Patrick T. Ellinor, Steven A. Lubitz

    Izdano 2020
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:
  17. 17
    Genetic Landscape of the ACE2 Coronavirus Receptor

    Genetic Landscape of the ACE2 Coronavirus Receptor od Zhijian Yang, Erin Macdonald-Dunlop, Jiantao Chen, Ranran Zhai, Ting Li, Anne Richmond, Lucija Klarić, Nicola Pirastu, Ning Zheng, Chenqing Zheng, Yipeng Wang, Tingting Huang, Yazhou He, Huiming Guo, Kejun Ying, Stefan Gustafsson, Bram P. Prins, Anna Ramisch, Emmanouil T. Dermitzakis, Grace Png, Niclas Eriksson, Jeffrey Haessler, Xiaowei Hu, Daniela Zanetti, Thibaud Boutin, Shih‐Jen Hwang, Eleanor Wheeler, Maik Pietzner, Laura M. Raffield, Anette Kalnapenkis, James E. Peters, Ana Viñuela, Arthur Gilly, Sölve Elmståhl, George Dedoussis, John R. Petrie, Ozren Polašek, Lasse Folkersen, Yan Chen, Chen Yao, Urmo Võsa, Erola Pairo‐Castineira, Sara Clohisey, Andrew D. Bretherick, Konrad Rawlik, Tõnu Esko, Stefan Enroth, Åsa Johansson, Ulf Gyllensten, Claudia Langenberg, Daniel Levy, Caroline Hayward, Themistocles L. Assimes, Charles Kooperberg, Ani Manichaikul, Agneta Siegbahn, Lars Wallentin, Lars Lind, Eleftheria Zeggini, Jochen M. Schwenk, Adam S. Butterworth, Karl Michaëlsson, Yudi Pawitan, Peter K. Joshi, J. Kenneth Baillie, Anders Mälarstig, Alexander P. Reiner, James F. Wilson, Xia Shen

    Izdano 2022
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:
  18. 18
    Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism

    Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous throm... od Marcus Tan, Chelsea A. Isom, Yangzi Liu, David‐Alexandre Trégouët, Sara Lindström, Lu Wang, Erin N. Smith, William Gordon, Astrid van Hylckama Vlieg, Mariza De Andrade, Jennifer A. Brody, Jack Pattee, Jeffrey Haessler, Ben Brumpton, Daniel I. Chasman, Pierre Suchon, Ming‐Huei Chen, Constance Turman, Marine Germain, Kerri L. Wiggins, James MacDonald, Sigrid K. Brækkan, Sebastian M. Armasu, Nathan Pankratz, Rabecca D Jackson, Jonas B. Nielsen, Franco Giulianini, Marja Puurunen, Manal Ibrahim, Susan R. Heckbert, Theo K. Bammler, Kelly A. Frazer, Bryan M. McCauley, Kent D. Taylor, James S. Pankow, Alexander P. Reiner, Maiken E. Gabrielsen, Jean‐François Deleuze, Christopher J. O’Donnell, Jihye Kim, Barbara McKnight, Peter Kraft, J.-B. Hansen, Frits R. Rosendaal, John A. Heit, Bruce M. Psaty, Weihong Tang, Charles Kooperberg, Kristian Hveem, Paul M. Ridker, Pierre‐Emmanuel Morange, Andrew M. Johnson, Christopher Kabrhel, David‐Alexandre Trégouët, Nicholas H. Smith, Lang Wu, Dan Zhou, Eric R. Gamazon

    Izdano 2024
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  19. 19
    Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

    Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk od Marios K. Georgakis, Rainer Malik, Omar El Bounkari, Natalie R. Hasbani, Jiang Li, Jennifer E. Huffman, Gabrielle Shakt, Reinier Tack, Tamara N. Kimball, Yaw Asare, Alanna C. Morrison, Noah L. Tsao, Renae Judy, Braxton D. Mitchell, Huichun Xu, May E. Montasser, Ron Do, Eimear E. Kenny, Ruth J. F. Loos, James G. Terry, J. Jeffrey Carr, Joshua C. Bis, Bruce M. Psaty, W. T. Longstreth, Kendra A. Young, Sharon M. Lutz, Michael Cho, Jai Broome, Alyna Khan, Fei Fei Wang, Nancy L. Heard‐Costa, Sudha Seshadri, Ramachandran S. Vasan, Nicholette D. Allred, B. I. Freedman, Donald W. Bowden, Lisa R. Yanek, Brian G. Kral, Lewis C. Becker, Patricia A. Peyser, Lawrence F. Bielak, Farah Ammous, April P. Carson, Michael E. Hall, Laura M. Raffield, Stephen S. Rich, Wendy S. Post, Russell P. Tracy, Kent D. Taylor, Xiuqing Guo, Michael C. Mahaney, Joanne E. Curran, John Blangero, Shoa L. Clarke, Jeffrey Haessler, Yao Hu, Themistocles L. Assimes, Charles Kooperberg, Jürgen Bernhagen, Christopher D. Anderson, Scott M. Damrauer, Ramin Zand, Laura M. Raffield, Paul S. de Vries, Martin Dichgans

    Izdano 2025
    Preuzmi cijeli tekst
    Artigo
    Spremi u popis
    Spremljeno u:
  20. 20
    Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies

    Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies od Andrew P. Morris, Thu H Le, Hao Wu, Artur Akbarov, Peter J. van der Most, Gibran Hemani, George Davey Smith, Anubha Mahajan, Kyle J. Gaulton, Girish N. Nadkarni, Adán Valladares‐Salgado, Niels H. Wacher, Josyf C. Mychaleckyj, Nicole Dueker, Xiuqing Guo, Yang Hai, Jeffrey Haessler, Yoichiro Kamatani, Adrienne M. Stilp, Gu Zhu, James P. Cook, Johan Ärnlöv, Susan H. Blanton, Martin H. de Borst, Erwin P. Böttinger, Thomas A. Buchanan, Sylvia Cechova, Fadi J. Charchar, Pei-Lun Chu, Jeffrey Damman, James Eales, Ali G. Gharavi, Vilmantas Giedraitis, Andrew C. Heath, Eli Ipp, Krzysztof Kiryluk, Holly Kramer, Michiaki Kubo, Anders Larsson, Cecilia M. Lindgren, Yingchang Lu, Pamela A. F. Madden, Grant W. Montgomery, George Papanicolaou, Leslie J. Raffel, Ralph L. Sacco, Elena Sánchez, Holger Stark, Johan Sundström, Kent D. Taylor, Anny H. Xiang, Aleksandra Živković, Lars Lind, Erik Ingelsson, Nicholas G. Martin, John B. Whitfield, Jianwen Cai, Cathy C. Laurie, Yukinori Okada, Koichi Matsuda, Charles Kooperberg, Yii-Der Ida Chen, Tatjana Rundek, Stephen S. Rich, Ruth J. F. Loos, Esteban J. Parra, Miguel Cruz, Jerome I. Rotter, Harold Snieder, Maciej Tomaszewski, Benjamin D. Humphreys, Nora Franceschini

    Izdano 2018
    Preuzmi cijeli tekst Preuzmi cijeli tekst
    Revisão
    Spremi u popis
    Spremljeno u:

Alati za pretragu: