Søgeresultater - Sahar V. Mozaffari

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  1. 1
    Heritability estimation and differential analysis of count data with generalized linear mixed models in genomic sequencing studies

    Heritability estimation and differential analysis of count data with generalized linear mixed models in genomic sequencing studies af Shiquan Sun, Jiaqiang Zhu, Sahar V. Mozaffari, Carole Ober, Mengjie Chen, Xiang Zhou

    Udgivet 2018
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  2. 2
    A gene-based association method for mapping traits using reference transcriptome data

    A gene-based association method for mapping traits using reference transcriptome data af Eric R. Gamazon, Heather E. Wheeler, Kaanan P. Shah, Sahar V. Mozaffari, Keston Aquino-Michaels, Robert J. Carroll, Anne E. Eyler, Joshua C. Denny, Dan L. Nicolae, Nancy J. Cox, Hae Kyung Im

    Udgivet 2015
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  3. 3
    Genome‐wide association and multi‐omics studies identify <i>MGMT</i> as a novel risk gene for Alzheimer's disease among women

    Genome‐wide association and multi‐omics studies identify <i>MGMT</i> as a novel risk gene for Alzheimer's disease among women af Jaeyoon Chung, Anjali Das, Xinyu Sun, Débora R. Sobreira, Yuk Yee Leung, Catherine Igartua, Sahar V. Mozaffari, Yi‐Fan Chou, Sam Thiagalingam, Jesse Mez, Xiaoling Zhang, Gyungah Jun, Thor D. Stein, Brian W. Kunkle, Eden R. Martin, Margaret A. Pericak‐Vance, Richard Mayeux, Jonathan L. Haines, Gerard D. Schellenberg, Marcelo A. Nóbrega, Kathryn L. Lunetta, Jayant M. Pinto, Weixin Wang, Carole Ober, Lindsay A. Farrer

    Udgivet 2022
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  4. 4
    Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits

    Coupling metabolomics and exome sequencing reveals graded effects of rare damaging heterozygous variants on gene function and human traits af Nora Scherer, Daniel Fässler, Oleg Borisov, Yurong Cheng, Pascal Schlosser, Matthias Wuttke, Stefan Haug, Yong Li, Fabian Telkämper, Suraj Patil, Heike Meiselbach, Christina S.F. Wong, Urs Berger, Peggy Sekula, Anselm Hoppmann, Ulla T. Schultheiß, Sahar V. Mozaffari, Yannan Xi, Robert Graham, Miriam Schmidts, Michael Köttgen, Peter J. Oefner, Felix Knauf, Kai‐Uwe Eckardt, Sarah C. Grünert, Karol Estrada, Ines Thiele, Johannes Hertel, Anna Köttgen

    Udgivet 2025
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  5. 5
    Genetic Inhibition of APOL1 Pore-Forming Function Prevents APOL1-Mediated Kidney Disease

    Genetic Inhibition of APOL1 Pore-Forming Function Prevents APOL1-Mediated Kidney Disease af Adriana M. Hung, Victoria A. Assimon, Hua‐Chang Chen, Zhihong Yu, Caitlyn Vlasschaert, Jefferson L. Triozzi, Helen Lai Wah Chan, Lee Wheless, Otis D. Wilson, Shailja C. Shah, Taralynn Mack, Trevor Thompson, Michael E. Matheny, Saranya Chandrasekar, Sahar V. Mozaffari, Cecilia P. Chung, Philip S. Tsao, Katalin Suszták, Edward D. Siew, Karol Estrada, J. Michael Gaziano, Robert Graham, Ran Tao, Maarten Hoek, Cassianne Robinson‐Cohen, Eric M. Green, Alexander G. Bick

    Udgivet 2023
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  6. 6
    Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure

    Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure af Marios Arvanitis, Emmanouil Tampakakis, Yanxiao Zhang, Wei Wang, Adam Auton, Michelle Agee, Stella Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare, Diptavo Dutta, Stephanie Glavaris, Ali R. Keramati, Nilanjan Chatterjee, C. Neil, Bing Ren, Wendy S. Post, Alexis Battle

    Udgivet 2020
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  7. 7
    Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways

    Genome-wide meta-analysis of insomnia prioritizes genes associated with metabolic and psychiatric pathways af Kyoko Watanabe, Philip R. Jansen, Jeanne E. Savage, Priyanka Nandakumar, Xin Wang, Michelle Agee, Stella Aslibekyan, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Janie F. Shelton, Jing Shi, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Wei Wang, David A. Hinds, Joel Gelernter, Daniel F. Levey, Renato Polimanti, Murray B. Stein, Eus J.W. Van Someren, August B. Smit, Daniëlle Posthuma

    Udgivet 2022
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  8. 8
    Genetic determinants of daytime napping and effects on cardiometabolic health

    Genetic determinants of daytime napping and effects on cardiometabolic health af Hassan S. Dashti, Iyas Daghlas, Jacqueline M. Lane, Yunru Huang, Miriam S. Udler, Heming Wang, Hanna M. Ollila, Samuel E. Jones, Jaegil Kim, Andrew R. Wood, Michelle Agee, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Marie K. Luff, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare, Michael N. Weedon, Stella Aslibekyan, Marta Garaulet, Richa Saxena

    Udgivet 2021
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  9. 9
    Genome-wide association study of musical beat synchronization demonstrates high polygenicity

    Genome-wide association study of musical beat synchronization demonstrates high polygenicity af Maria Niarchou, Daniel E. Gustavson, J. Fah Sathirapongsasuti, Manuel Anglada-Tort, Else Eising, Eamonn Bell, Evonne McArthur, Péter Straub, Stella Aslibekyan, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Jey C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Steven J. Pitts, G. David Poznik, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, J. Devin McAuley, John A. Capra, Fredrik Ullén, Nicole Creanza, Miriam A. Mosing, David A. Hinds, Lea K. Davis, Nori Jacoby, Reyna L. Gordon

    Udgivet 2022
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  10. 10
    Genome evolution in the allotetraploid frog Xenopus laevis

    Genome evolution in the allotetraploid frog Xenopus laevis af Adam M. Session, Yoshinobu Uno, Taejoon Kwon, Jarrod Chapman, Atsushi Toyoda, Shuji Takahashi, Akimasa Fukui, Akira Hikosaka, Atsushi Suzuki, Mariko Kondo, Simon J. van Heeringen, Ian K. Quigley, Sven Heinz, Hajime Ogino, Haruki Ochi, Uffe Hellsten, Jessica B. Lyons, Oleg Simakov, Nicholas H. Putnam, Jonathan C. Stites, Yoko Kuroki, Toshiaki Tanaka, Tatsuo Michiue, Minoru Watanabe, Ozren Bogdanović, Ryan Lister, Γεώργιος Γεωργίου, Sarita Paranjpe, Ila van Kruijsbergen, Shengqiang Shu, Joseph W. Carlson, Tsutomu Kinoshita, Yuko Ohta, Shuuji Mawaribuchi, Jerry Jenkins, Jane Grimwood, Jeremy Schmutz, Therese Mitros, Sahar V. Mozaffari, Yutaka Suzuki, Yoshikazu Haramoto, Takamasa Yamamoto, Chiyo Takagi, Rebecca Heald, Kelly E. Miller, Christian Haudenschild, Jacob O. Kitzman, Takuya Nakayama, Yumi Izutsu, Jacques Robert, Joshua D. Fortriede, Kevin A. Burns, Vaneet Lotay, Kamran Karimi, Y. Yasuoka, Darwin S. Dichmann, Martin F. Flajnik, Douglas W. Houston, Jay Shendure, Louis DuPasquier, Peter D. Vize, Aaron M. Zorn, Michihiko Ito, Edward M. Marcotte, John B. Wallingford, Yuzuru Ito, Makoto Asashima, Naoto Ueno, Yoichi Matsuda, Gert Jan C. Veenstra, Asao Fujiyama, Richard M. Harland, Masanori Taira, Daniel S. Rokhsar

    Udgivet 2016
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  11. 11
    Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy

    Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy af Kristi Krebs, Jonas Bovijn, Neil S. Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson, Dage Särg, Erik Abner, Triin Laisk, Yang Luo, Line Skotte, Frank Geller, Bjarke Feenstra, Wei Wang, Adam Auton, Soumya Raychaudhuri, Tõnu Esko, Andres Metspalu, Sven Laur, Dan M. Roden, Wei‐Qi Wei, Michael V. Holmes, Cecilia M. Lindgren, Elizabeth J. Phillips, Reedik Mägi, Lili Milani, João Fadista, Michelle Agee, Stella Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah K. Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Marie K. Luff, Jennifer C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare

    Udgivet 2020
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  12. 12
    Genetic analyses identify widespread sex-differential participation bias

    Genetic analyses identify widespread sex-differential participation bias af Nicola Pirastu, Mattia Cordioli, Priyanka Nandakumar, Gianmarco Mignogna, Abdel Abdellaoui, Benjamin Hollis, Masahiro Kanai, Veera M. Rajagopal, Pietro Della Briotta Parolo, Nikolas Baya, Caitlin E. Carey, Juha Karjalainen, Thomas D. Als, Matthijs D. van der Zee, Felix R. Day, Ken K. Ong, Michelle Agee, Stella Aslibekyan, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Marie K. Luff, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Janie F. Shelton, Suyash Shringarpure, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir Zare, Preben Bo Mortensen, Ole Mors, Thomas Werge, Merete Nordentoft, David M. Hougaard, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Takayuki Morisaki, Eco J. C. de Geus, Rino Bellocco, Yukinori Okada, Anders D. Børglum, Peter K. Joshi, Adam Auton, David A. Hinds, Benjamin M. Neale, Raymond K. Walters, Michel G. Nivard, John R. B. Perry, Andrea Ganna

    Udgivet 2021
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  13. 13
    Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes

    Integration of questionnaire-based risk factors improves polygenic risk scores for human coronary heart disease and type 2 diabetes af Max Tamlander, Nina Mars, Matti Pirinen, Aarno Palotie, Mark J. Daly, Bridget Riley-Gills, Howard J. Jacob, Dirk S. Paul, Heiko Runz, Sally John, Robert M. Plenge, Joseph Maranville, George Okafo, Nathan Lawless, Heli Salminen‐Mankonen, Mark I. McCarthy, Julie Hunkapiller, Meg Ehm, Kirsi Auro, Simonne Longerich, Caroline S. Fox, Anders Mälarstig, Katherine Klinger, Deepak Raipal, Eric Green, Robert Graham, Robert Yang, Chris O’Donnell, Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Antti Hakanen, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Juhani Junttila, Raisa Serpi, Tarja Laitinen, Veli‐Matti Kosma, Arto Mannermaa, Jari Laukkanen, Marco Hautalahti, Outi Tuovila, Raimo Pakkanen, Jeffrey Waring, Ioanna Tachmazidou, Chia-Yen Chen, Shameek Biswas, Zhihao Ding, Marc Jung, Rion Pendergrass, David Pulford, Neha Raghavan, Adriana Huertas‐Vázquez, Jae-Hoon Sul, Xinli Hu, Sahar V. Mozaffari, Dawn Waterworth, Nicole Renaud, Ma ́en Obeidat, Samuli Ripatti, Johanna Schleutker, Mikko Arvas, Olli Carpén, Reetta Hinttala, Johannes Kettunen, Katriina Aalto‐Setälä, Mika Kähönen, Johanna Mäkelä, Reetta Kälviäinen, Valtteri Julkunen, Hilkka Soininen, Anne M. Remes, Mikko Hiltunen, Jukka Peltola, Pentti J. Tienari, Juha O. Rinne, Roosa Kallionpää, Ali Abbasi, Adam Ziemann, Sahar Esmaeeli, Nizar Smaoui, Anne Lehtonen, Susan Eaton, Sanni Lahdenperä, Janet van Adelsberg, Natalie Bowers, Edmond Teng, Sarah A. Pendergrass, Onuralp Söylemez, Kari Linden, Fanli Xu, Laura Addis, John D. Eicher, Minna Raivio, Beryl B. Cummings, Juulia Partanen, Martti Färkkilâ, Jukka Koskela

    Udgivet 2022
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  14. 14
    FinnGen: Unique genetic insights from combining isolated population and national health register data

    FinnGen: Unique genetic insights from combining isolated population and national health register data af Mitja Kurki, Juha Karjalainen, Priit Palta, Timo P. Sipilä, Kati Kristiansson, Kati Donner, Mary Pat Reeve, Hannele Laivuori, Mervi Aavikko, Mari Kaunisto, Anu Loukola, Elisa Lahtela, Hannele Mattsson, Päivi Laiho, Pietro Della Briotta Parolo, Arto Lehistö, Masahiro Kanai, Nina Mars, Joel Rämö, Tuomo Kiiskinen, Henrike Heyne, Kumar Veerapen, Sina Rüeger, Susanna Lemmelä, Wei Zhou, Sanni Ruotsalainen, Kalle Pärn, Tero Hiekkalinna, Sami Koskelainen, Teemu Paajanen, Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard J. Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja, Sahar V. Mozaffari, Mari Niemi, Marianna Niemi

    Udgivet 2022
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  15. 15
    FinnGen provides genetic insights from a well-phenotyped isolated population

    FinnGen provides genetic insights from a well-phenotyped isolated population af Mitja Kurki, Juha Karjalainen, Priit Palta, Timo P. Sipilä, Kati Kristiansson, Kati Donner, Mary Pat Reeve, Hannele Laivuori, Mervi Aavikko, Mari Kaunisto, Anu Loukola, Elisa Lahtela, Hannele Mattsson, Päivi Laiho, Pietro Della Briotta Parolo, Arto Lehistö, Masahiro Kanai, Nina Mars, Joel Rämö, Tuomo Kiiskinen, Henrike Heyne, Kumar Veerapen, Sina Rüeger, Susanna Lemmelä, Wei Zhou, Sanni Ruotsalainen, Kalle Pärn, Tero Hiekkalinna, Sami Koskelainen, Teemu Paajanen, Vincent Llorens, Javier Gracia‐Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Benjamin B. Sun, Christopher N. Foley, Katriina Aalto‐Setälä, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpén, Chia‐Yen Chen, Oluwaseun Alexander Dada, Zhihao Ding, Margaret G. Ehm, Kari K. Eklund, Martti Färkkilâ, Hilary K. Finucane, Andrea Ganna, Awaisa Ghazal, Robert Graham, Eric M. Green, Antti Hakanen, Marco Hautalahti, Åsa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas‐Vázquez, Laura Huilaja, Julie Hunkapiller, Howard Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kähönen, Risto Kajanne, Lila Kallio, Reetta Kälviäinen, Jaakko Kaprio, Nurlan Kerimov, Johannes Kettunen, Elina Kilpeläinen, Terhi Kilpi, K. Klinger, Veli‐Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari A. Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Mägi, Johanna Mäkelä, Antti Mäkitie, Anders Mälarstig, Graham J. Mann, Joseph Maranville, Athena Matakidou, Tuomo J Meretoja, Sahar V. Mozaffari

    Udgivet 2023
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  16. 16
    Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy

    Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy af Jaakko Tyrmi, Tea Kaartokallio, A. Inkeri Lokki, Tiina Jääskeläinen, Eija Kortelainen, Sanni Ruotsalainen, Juha Karjalainen, Samuli Ripatti, Anna Kivioja, Triin Laisk, Johannes Kettunen, Anneli Pouta, Katja Kivinen, Eero Kajantie, Seppo Heinonen, Juha Kere, Hannele Laivuori, Eeva Ekholm, Reija Hietala-Koivu, Leea Keski‐Nisula, Kaarin Mäkikallio, Jukka Uotila, Susanna Sainio, Terhi Saisto, Marja Vääräsmäki, Tia Aalto-Viljakainen, Leena Georgiadis, Jenni Heikkinen‐Eloranta, Miira M. Klemetti, Sanna Suomalainen‐König, Satu Wedenoja, Satu Leminen, Aija Lähdesmäki, Susanna Mehtälä, Christina Salmén, Aarno Palotie, Mark J. Daly, Bridget Riley-Gills, Howard J. Jacob, Dirk S. Paul, Athena Matakidou, Adam Platt, Heiko Runz, Sally John, George Okafo, Nathan Lawless, Robert M. Plenge, Joseph Maranville, Mark I. McCarthy, Julie Hunkapiller, Margaret G. Ehm, Kirsi Auro, Simonne Longerich, Caroline S. Fox, Anders Mälarstig, K. Klinger, Deepak Raipal, Eric Green, Robert Graham, Robert Yang, Chris O ́Donnell, Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Antti Hakanen, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Juhani Junttila, Raisa Serpi, Tarja Laitinen, Veli‐Matti Kosma, Jari A. Laukkanen, Marco Hautalahti, Outi Tuovila, Raimo Pakkanen, Jeffrey F. Waring, Bridget Riley‐Gillis, Fedik Rahimov, Ioanna Tachmazidou, Chia‐Yen Chen, Zhihao Ding, Marc Jung, Shameek Biswas, Rion Pendergrass, David Pulford, Neha Raghavan, Adriana Huertas‐Vázquez, Jae-Hoon Sul, Xinli Hu, Sahar V. Mozaffari, Dawn Waterworth, Nicole Renaud, Ma ́en Obeidat, Johanna Schleutker, Mikko Arvas, Olli Carpén, Reetta Hinttala, Graham J. Mann

    Udgivet 2023
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  17. 17
    Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women

    Comprehensive Inherited Risk Estimation for Risk-Based Breast Cancer Screening in Women af Nina Mars, Sini Kerminen, Max Tamlander, Matti Pirinen, Eveliina Jakkula, Kirsimari Aaltonen, Tuomo J Meretoja, Sirpa Heinävaara, Elisabeth Widén, Samuli Ripatti, Aarno Palotie, Mark J. Daly, Bridget Riley-Gills, Howard Jacob, Dirk S. Paul, Athena Matakidou, Adam Platt, Heiko Runz, Sally John, George Okafo, Nathan Lawless, Robert M. Plenge, Joseph Maranville, Mark I. McCarthy, Julie Hunkapiller, Margaret G. Ehm, Kirsi Auro, Simonne Longerich, Caroline S. Fox, Anders Mälarstig, K. Klinger, Deepak Raipal, Eric Green, Robert Graham, Robert Yang, Chris O’Donnell, Tomi P. Mäkelä, Jaakko Kaprio, Petri Virolainen, Antti Hakanen, Terhi Kilpi, Markus Perola, Jukka Partanen, Anne Pitkäranta, Juhani Junttila, Raisa Serpi, Tarja Laitinen, Veli‐Matti Kosma, Jari A. Laukkanen, Marco Hautalahti, Outi Tuovila, Raimo Pakkanen, Jeffrey F. Waring, Bridget Riley‐Gillis, Fedik Rahimov, Ioanna Tachmazidou, Chia‐Yen Chen, Heiko Runz, Zhihao Ding, Marc Jung, Shameek Biswas, Rion Pendergrass, Julie Hunkapiller, Margaret G. Ehm, David Pulford, Neha Raghavan, Adriana Huertas‐Vázquez, Jae-Hoon Sul, Anders Mälarstig, Xinli Hu, K. Klinger, Robert Graham, Eric Green, Sahar V. Mozaffari, Dawn Waterworth, Nicole Renaud, Ma’en Obeidat, Samuli Ripatti, Johanna Schleutker, Markus Perola, Mikko Arvas, Olli Carpén, Reetta Hinttala, Johannes Kettunen, Graham J. Mann, Katriina Aalto‐Setälä, Mika Kähönen, Jari A. Laukkanen, Johanna Mäkelä, Reetta Kälviäinen, Valtteri Julkunen, Hilkka Soininen, Anne M. Remes, Mikko Hiltunen, Jukka Peltola, Minna Raivio, Pentti Tienari, Juha O. Rinne, Roosa Kallionpää, Juulia Partanen

    Udgivet 2024
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  18. 18
    A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease

    A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease af Douglas P. Wightman, Iris E. Jansen, Jeanne E. Savage, Alexey Shadrin, Shahram Bahrami, Dominic Holland, Arvid Rongve, Sigrid Børte, Bendik S. Winsvold, Ole Kristian Drange, Amy E. Martinsen, Anne Heidi Skogholt, Cristen J. Willer, Geir Bråthen, Ingunn Bosnes, Jonas B. Nielsen, Lars G. Fritsche, Laurent F. Thomas, Linda M. Pedersen, Maiken E. Gabrielsen, Marianne Bakke Johnsen, Tore Wergeland Meisingset, Wei Zhou, Petroula Proitsi, Angela Hodges, Richard Dobson, Latha Velayudhan, Karl Heilbron, Adam Auton, Michelle Agee, Stella Aslibekyan, Elizabeth Babalola, Robert K. Bell, Jessica Bielenberg, Katarzyna Bryc, Emily Bullis, Briana Cameron, Daniella Coker, Gabriel Cuéllar-Partida, Devika Dhamija, Sayantan Das, Sarah L. Elson, Teresa Filshtein, Kipper Fletez‐Brant, Pierre Fontanillas, Will Freyman, Pooja Gandhi, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Katelyn Kukar, Vanessa Lane, Keng‐Han Lin, Maya Lowe, Marie K. Luff, Jey C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Steven J. Micheletti, Meghan E. Moreno, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Jared O’Connell, Aaron A. Petrakovitz, G. David Poznik, Morgan Schumacher, Anjali J. Shastri, Janie F. Shelton, Jingchunzi Shi, Suyash Shringarpure, Chao Tian, Vinh Tran, Joyce Y. Tung, Xin Wang, Wei Wang, Catherine H. Weldon, Peter Wilton, Julia Sealock, Lea K. Davis, Nancy L. Pedersen, Chandra A. Reynolds, Ida Karlsson, Sigurður H. Magnússon, Hreinn Stefánsson, Steinunn Þórðardóttir, Pálmi V. Jónsson, Jón Snædal, Anna Zettergren, Ingmar Skoog, Silke Kern, Margda Wærn, Henrik Zetterberg, Kaj Blennow, Eystein Stordal, Kristian Hveem

    Udgivet 2021
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    Artigo
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  19. 19
    Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders

    Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders af Chris Eijsbouts, Tenghao Zheng, Nicholas A. Kennedy, Ferdinando Bonfiglio, Carl A. Anderson, Loukas Moutsianas, Jo Holliday, Jingchunzi Shi, Suyash Shringarpure, Michelle Agee, Stella Aslibekyan, Adam Auton, Robert K. Bell, Katarzyna Bryc, Sarah Clark, Sarah L. Elson, Kipper Fletez‐Brant, Pierre Fontanillas, Nicholas A. Furlotte, Pooja Gandhi, Karl Heilbron, Barry Hicks, David A. Hinds, Karen E. Huber, Ethan M. Jewett, Yunxuan Jiang, Aaron Kleinman, Keng‐Han Lin, Nadia K. Litterman, Marie K. Luff, Jey C. McCreight, Matthew H. McIntyre, Kimberly F. McManus, Joanna L. Mountain, Sahar V. Mozaffari, Priyanka Nandakumar, Elizabeth S. Noblin, Carrie A. M. Northover, Jared O’Connell, Aaron A. Petrakovitz, Steven J. Pitts, G. David Poznik, J. Fah Sathirapongsasuti, Anjali J. Shastri, Janie F. Shelton, Chao Tian, Joyce Y. Tung, Robert J. Tunney, Vladimir Vacic, Xin Wang, Amir S. Zare, Alexandru-Ioan Voda, Purna Kashyap, Lin Chang, Emeran A. Mayer, Margaret Heitkemper, Gregory S. Sayuk, Tamar Ringel‐Kulka, Yehuda Ringel, William D. Chey, Shanti Eswaran, Juanita L. Merchant, Robert J. Shulman, Luís Bujanda, Koldo García‐Etxebarria, Aldona Dlugosz, Greger Lindberg, Peter T. Schmidt, Pontus Karling, Bodil Ohlsson, Susanna Walter, Åshild Faresjö, Magnus Simrén, Jonas Halfvarson, Piero Portincasa, Giovanni Barbara, Paolo Usai‐Satta, Matteo Neri, Gerardo Nardone, Rosario Cuomo, Francesca Galeazzi, Massimo Bellini, Anna Latiano, Lesley A. Houghton, Daisy Jonkers, Alexander Kurilshikov, Rinse K. Weersma, Mihai G. Netea, Jonas Tesarz, Annika Gauss, Miriam Goebel‐Stengel, Viola Andresen, Thomas Frieling, Christian Pehl, Rainer Schaefert, Beate Niesler, Wolfgang Lieb, Kurt Hanevik, Nina Langeland, Knut‐Arne Wensaas

    Udgivet 2021
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