Výsledky vyhledávání - Marie Verbanck

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  1. 1
    HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases

    HOPS: a quantitative score reveals pervasive horizontal pleiotropy in human genetic variation is driven by extreme polygenicity of human traits and diseases Autor Daniel M. Jordan, Marie Verbanck, Ron Do

    Vydáno 2019
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  2. 2
    Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases

    Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases Autor Marie Verbanck, Chia‐Yen Chen, Benjamin M. Neale, Ron Do

    Vydáno 2018
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  3. 3
    Publisher Correction: Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases

    Publisher Correction: Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases Autor Marie Verbanck, Chia‐Yen Chen, Benjamin M. Neale, Ron Do

    Vydáno 2018
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  4. 4
    No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study

    No causal effects of serum urate levels on the risk of chronic kidney disease: A Mendelian randomization study Autor Daniel M. Jordan, Hyon K. Choi, Marie Verbanck, Ruth Topless, Hong‐Hee Won, Girish N. Nadkarni, Tony R. Merriman, Ron Do

    Vydáno 2019
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  5. 5
    Tissue-specific genetic features inform prediction of drug side effects in clinical trials

    Tissue-specific genetic features inform prediction of drug side effects in clinical trials Autor Áine Duffy, Marie Verbanck, Amanda Dobbyn, Hong‐Hee Won, Joshua L. Rein, Iain S. Forrest, Girish N. Nadkarni, Ghislain Rocheleau, Ron Do

    Vydáno 2020
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  6. 6
    DNA Damage and the Activation of the p53 Pathway Mediate Alterations in Metabolic and Secretory Functions of Adipocytes

    DNA Damage and the Activation of the p53 Pathway Mediate Alterations in Metabolic and Secretory Functions of Adipocytes Autor Bastien Vergoni, Pierre-Jean Cornejo, Jérôme Gilleron, Mansour Djedaini, Franck Ceppo, Arnaud Jacquel, Gwennaëlle Bouget, Clémence Ginet, Teresa Gonzalez, Julie O’Sullivan Maillet, Véronique Dhennin, Marie Verbanck, Patrick Auberger, Philippe Froguel, Jean‐François Tanti, Mireille Cormont

    Vydáno 2016
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  7. 7
    The expression of genes in top obesity-associated loci is enriched in insula and substantia nigra brain regions involved in addiction and reward

    The expression of genes in top obesity-associated loci is enriched in insula and substantia nigra brain regions involved in addiction and reward Autor Fatou Kiné Ndiaye, Marlène Huyvaert, Ana Ortalli, Mickaël Canouil, Cécile Lecœur, Marie Verbanck, Stéphane Lobbens, Amna Khamis, Lorella Marselli, Piero Marchetti, J. Kerr–Conte, François Pattou, Michel Marre, Ronan Roussel, Beverley Balkau, Philippe Froguel, Amélie Bonnefond

    Vydáno 2019
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  8. 8
    The kynurenine pathway is activated in human obesity and shifted toward kynurenine monooxygenase activation

    The kynurenine pathway is activated in human obesity and shifted toward kynurenine monooxygenase activation Autor Marie Favennec, Benjamin Hennart, Robert Caïazzo, Audrey Leloire, Loïc Yengo, Marie Verbanck, Abdelilah Arredouani, Michel Marre, Marie Pigeyre, Alban Bessede, Gilles J. Guillemin, Giulia Chinetti, Bart Staels, François Pattou, Beverley Balkau, Delphine Allorge, Philippe Froguel, Odile Poulain‐Godefroy

    Vydáno 2015
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  9. 9
    Expression and functional assessment of candidate type 2 diabetes susceptibility genes identify four new genes contributing to human insulin secretion

    Expression and functional assessment of candidate type 2 diabetes susceptibility genes identify four new genes contributing to human insulin secretion Autor Fatou Kiné Ndiaye, Ana Ortalli, Mickaël Canouil, Marlène Huyvaert, Clara Salazar-Cardozo, Cécile Lecœur, Marie Verbanck, Valérie Pawlowski, Raphaël Boutry, Emmanuelle Durand, Iandry Rabearivelo, Olivier Sand, Lorella Marselli, Julie Kerr‐Conte, Vikash Chandra, Raphaël Scharfmann, Odile Poulain‐Godefroy, Piero Marchetti, François Pattou, Amar Abderrahmani, Philippe Froguel, Amélie Bonnefond

    Vydáno 2017
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  10. 10
    Exploiting the GTEx resources to decipher the mechanisms at GWAS loci

    Exploiting the GTEx resources to decipher the mechanisms at GWAS loci Autor Alvaro Barbeira, Rodrigo Bonazzola, Eric R. Gamazon, Yanyu Liang, YoSon Park, Sarah Kim-Hellmuth, Gao Wang, Zhuoxun Jiang, Dan Zhou, Farhad Hormozdiari, Boxiang Liu, Abhiram Rao, Andrew R. Hamel, Milton Pividori, François Aguet, Lisa Bastarache, Daniel M. Jordan, Marie Verbanck, Ron Do, Matthew Stephens, Kristin Ardlie, Mark McCarthy, Stephen B. Montgomery, Ayellet V. Segrè, Christopher D. Brown, Tuuli Lappalainen, Xiaoquan Wen, Hae Kyung Im

    Vydáno 2019
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  11. 11
    Exploiting the GTEx resources to decipher the mechanisms at GWAS loci

    Exploiting the GTEx resources to decipher the mechanisms at GWAS loci Autor Alvaro Barbeira, Rodrigo Bonazzola, Eric R. Gamazon, Yanyu Liang, YoSon Park, Sarah Kim-Hellmuth, Gao Wang, Zhuoxun Jiang, Dan Zhou, Farhad Hormozdiari, Boxiang Liu, Abhiram Rao, Andrew R. Hamel, Milton Pividori, François Aguet, Lisa Bastarache, Daniel M. Jordan, Marie Verbanck, Ron Do, Matthew Stephens, Kristin Ardlie, Mark McCarthy, Stephen B. Montgomery, Ayellet V. Segrè, Christopher D. Brown, Tuuli Lappalainen, Xiaoquan Wen, Hae Kyung Im

    Vydáno 2021
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  12. 12
    Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

    Large-scale genome-wide association study of coronary artery disease in genetically diverse populations Autor Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni, Shining Ma, Kyung Min Lee, Huaying Fang, Fei Chen, Yingchang Lu, Noah L. Tsao, Sridharan Raghavan, Satoshi Koyama, Bryan R. Gorman, Marijana Vujković, Derek Klarin, Michael G. Levin, Nasa Sinnott-Armstrong, Genevieve L. Wojcik, Mary E. Plomondon, Thomas M. Maddox, Stephen W. Waldo, Alexander G. Bick, Saiju Pyarajan, Jie Huang, Rebecca J. Song, Yuk‐Lam Ho, Steven Buyske, Charles Kooperberg, Jeffrey Haessler, Ruth J. F. Loos, Ron Do, Marie Verbanck, Kumardeep Chaudhary, Kari E. North, Christy L. Avery, Mariaelisa Graff, Christopher A. Haiman, Loı̈c Le Marchand, Lynne R. Wilkens, Joshua C. Bis, Hampton L. Leonard, Botong Shen, Leslie A. Lange, Ayush Giri, Ozan Dikilitas, Iftikhar J. Kullo, Ian B. Stanaway, Gail P. Jarvik, Allan Gordon, Scott J. Hebbring, Bahram Namjou, Kenneth M. Kaufman, Kaoru Ito, Kazuyoshi Ishigaki, Yoichiro Kamatani, Shefali S. Verma, Marylyn D. Ritchie, Rachel L. Kember, Aris Baras, Luca A. Lotta, Sekar Kathiresan, Elizabeth R. Hauser, Donald R. Miller, Jennifer S. Lee, Danish Saleheen, Peter D. Reaven, Kelly Cho, J. Michael Gaziano, Pradeep Natarajan, Jennifer E. Huffman, Benjamin F. Voight, Daniel J. Rader, Kyong–Mi Chang, Julie A. Lynch, Scott M. Damrauer, Peter W.F. Wilson, Hua Tang, Yan V. Sun, Philip S. Tsao, Christopher J. O’Donnell, Themistocles L. Assimes

    Vydáno 2022
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  13. 13
    Genetic analyses of diverse populations improves discovery for complex traits

    Genetic analyses of diverse populations improves discovery for complex traits Autor Genevieve L. Wojcik, Mariaelisa Graff, Katherine K. Nishimura, Ran Tao, Jeffrey Haessler, Christopher R. Gignoux, Heather M. Highland, Yesha Patel, Elena P. Sorokin, Christy L. Avery, Gillian M. Belbin, Stephanie A. Bien, Iona Cheng, Sinéad Cullina, Chani J. Hodonsky, Yao Hu, Laura M. Huckins, Janina M. Jeff, Anne E. Justice, Jonathan Kocarnik, Unhee Lim, Bridget M. Lin, Yingchang Lu, Sarah C. Nelson, Sung-Shim L. Park, Hannah Poisner, Michael Preuß, Melissa A. Richard, Claudia Schurmann, Veronica Wendy Setiawan, Alexandra Sockell, Karan Vahi, Marie Verbanck, Abhishek Vishnu, Ryan W. Walker, Kristin L. Young, Niha Zubair, Victor Acuña-Alonso, José Luis Ambite, Kathleen C. Barnes, Eric Boerwinkle, Erwin P. Böttinger, Carlos D. Bustamante, Christian Caberto, Samuel Canizales‐Quinteros, Matthew P. Conomos, Ewa Deelman, Ron Do, Kimberly F. Doheny, Lindsay Fernández‐Rhodes, Myriam Fornage, Benyam Hailu, Gerardo Heiss, Brenna M. Henn, Lucia A. Hindorff, Rebecca D. Jackson, Cecelia Laurie, Cathy C. Laurie, Yuqing Li, Dan-Yu Lin, Andrés Moreno‐Estrada, Girish N. Nadkarni, Paul J. Norman, Loreall Pooler, Alexander P. Reiner, Jane Romm, Chiara Sabatti, Karla Sandoval, Xin Sheng, Eli A. Stahl, Daniel O. Stram, Timothy A. Thornton, Christina L. Wassel, Lynne R. Wilkens, Cheryl A. Winkler, Sachi Yoneyama, Steven Buyske, Christopher A. Haiman, Charles Kooperberg, Loı̈c Le Marchand, Ruth J. F. Loos, Tara C. Matise, Kari E. North, Ulrike Peters, Eimear E. Kenny, Christopher S. Carlson

    Vydáno 2019
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  14. 14
    Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders

    Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders Autor Symen Ligthart, Ahmad Vaez, Urmo Võsa, Maria G. Stathopoulou, Paul S. de Vries, Bram P. Prins, Peter J. van der Most, Toshiko Tanaka, Elnaz Naderi, Lynda M. Rose, Ying Wu, Robert Karlsson, Maja Barbalić, Honghuang Lin, René Pool, Gu Zhu, Aurélien Mace, Carlo Sidore, Stella Trompet, Massimo Mangino, Maria Sabater‐Lleal, John P. Kemp, Ali Abbasi, Tim Kacprowski, Niek Verweij, Albert V. Smith, Tao Huang, Carola Marzi, Mary F. Feitosa, Kurt K. Lohman, Marcus E. Kleber, Yuri Milaneschi, Christian Mueller, Mahmudul Huq, Efthymia Vlachopoulou, Leo-Pekka Lyytikäinen, Christopher Oldmeadow, Joris Deelen, Markus Perola, Jing Hua Zhao, Bjarke Feenstra, Marzyeh Amini, Jari Lahti, Katharina E. Schraut, Myriam Fornage, Bhoom Suktitipat, Wei-Min Chen, Xiaohui Li, Teresa Nutile, Giovanni Malerba, Jian’an Luan, Tom Bak, Nicholas J. Schork, Fabiola Del Greco M, Elisabeth Thiering, Anubha Mahajan, Riccardo E. Marioni, Evelin Mihailov, Joel Eriksson, Ayse Bilge Ozel, Weihua Zhang, Maria Nethander, Yu-Ching Cheng, Stella Aslibekyan, Wei Ang, Ilaria Gandin, Loïc Yengo, Laura Portas, Charles Kooperberg, Edith Hofer, Kumar B. Rajan, Claudia Schurmann, Wouter den Hollander, Tarunveer S. Ahluwalia, Jing Zhao, Harmen H. M. Draisma, Ian Ford, Nicholas J. Timpson, Alexander Teumer, Hongyan Huang, Simone Wahl, Yongmei Liu, Jie Huang, Hae‐Won Uh, Frank Geller, Peter K. Joshi, Lisa R. Yanek, Elisabetta Trabetti, Benjamin Lehne, Diego Vozzi, Marie Verbanck, Ginevra Biino, Yasaman Saba, Ingrid Meulenbelt, Jeff R. O’Connell, Markku Laakso, Franco Giulianini, Patrik K. E. Magnusson, Christie M. Ballantyne, J. J. Hottenga

    Vydáno 2018
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