Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases
AMERICAN JOURNAL OF HUMAN GENETICS (2016)
期刊
AMERICAN JOURNAL OF HUMAN GENETICS
卷 99, 期 1, 页码 22-39出版社
CELL PRESS
关键词
资金
- NHLBI [R21 HL121422-02, R01 HL086694]
- Canada Research Chair program
- Canadian Institute of Health Research MOP [123382]
- National Institute on Aging, NIH Intramural Research Program
- a component of the NIH Roadmap for Medical Research [UL1RR025005]
- MRC [MR/L01341X/1, MC_PC_U127561128] Funding Source: UKRI
- Medical Research Council [MC_PC_U127561128, MR/L01341X/1, MR/K026992/1] Funding Source: researchfish
- National Institute for Health Research [NF-SI-0611-10136] Funding Source: researchfish
作者
我是这篇论文的作者
推荐
A Large-Scale Exome-Wide Association Study Identifies Novel Germline Mutations in Lung Cancer
Sipeng Shen, Zaiming Li, Yunke Jiang, Weiwei Duan, Hongru Li, Sha Du, Manel Esteller, Hongbing Shen, Zhibin Hu, Yang Zhao, David C. Christiani, Feng Chen
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE (2023)
Shared components of heritability across genetically correlated traits
Jenna Lee Ballard, Luke Jen O'Connor
AMERICAN JOURNAL OF HUMAN GENETICS (2022)
Genome-wide Association Analysis of Parkinson's Disease and Schizophrenia Reveals Shared Genetic Architecture and Identifies Novel Risk Loci
Olav B. Smeland, Alexey Shadrin, Shahram Bahrami, Iris Broce, Martin Tesli, Oleksandr Frei, Katrine Wirgenes, Kevin S. O'Connell, Florian Krull, Francesco Bettella, Nils Eiel Steen, Leo Sugrue, Yunpeng Wang, Per Svenningsson, Manu Sharma, Lasse Pihlstrom, Mathias Toft, Michael O'Donovan, Srdjan Djurovic, Rahul Desikan, Anders M. Dale, Ole A. Andreassen
BIOLOGICAL PSYCHIATRY (2021)
Genome-wide association study identifies QTL for eight fruit traits in cultivated tomato (Solanum lycopersicum L.)
Minkyung Kim, Thuy Tien Phan Nguyen, Joon-Hyung Ahn, Gi-Jun Kim, Sung-Chur Sim
HORTICULTURE RESEARCH (2021)
Barcoded bulk QTL mapping reveals highly polygenic and epistatic architecture of complex traits in yeast
Alex N. Nguyen Ba, Katherine R. Lawrence, Artur Rego-Costa, Shreyas Gopalakrishnan, Daniel Temko, Franziska Michor, Michael M. Desai
ELIFE (2022)
Genome-wide association study of multiyear dynamic growth traits in hybrid Liriodendron identifies robust genetic loci associated with growth trajectories
Hui Xia, Ziyuan Hao, Yufang Shen, Zhonghua Tu, Lichun Yang, Yaxian Zong, Huogen Li
PLANT JOURNAL (2023)
Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease
Laura J. Smyth, Emma H. Dahlstrom, Anna Syreeni, Katie Kerr, Jill Kilner, Ross Doyle, Eoin Brennan, Viji Nair, Damian Fermin, Robert G. Nelson, Helen C. Looker, Christopher Wooster, Darrell Andrews, Kerry Anderson, Gareth J. McKay, Joanne B. Cole, Rany M. Salem, Peter J. Conlon, Matthias Kretzler, Joel N. Hirschhorn, Denise Sadlier, Catherine Godson, Jose C. Florez, Carol Forsblom, Alexander P. Maxwell, Per-Henrik Groop, Niina Sandholm, Amy Jayne McKnight
NATURE COMMUNICATIONS (2022)
Identification of novel genome-wide pleiotropic associations with oral inflammatory traits
Yanjiao Jin, Jie Yang, Shuyue Zhang, Xuefeng Shi, Jin Li, Songlin Wang
MOLECULAR GENETICS AND GENOMICS (2022)
Genome-wide association study identifies risk loci for progressive chronic lymphocytic leukemia
Wei-Yu Lin, Sarah E. Fordham, Nicola Sunter, Claire Elstob, Thahira Rahman, Elaine Willmore, Colin Shepherd, Gordon Strathdee, Tryfonia Mainou-Fowler, Rachel Piddock, Hannah Mearns, Timothy Barrow, Richard S. Houlston, Helen Marr, Jonathan Wallis, Geoffrey Summerfield, Scott Marshall, Andrew Pettitt, Christopher Pepper, Christopher Fegan, Francesco Forconi, Martin J. S. Dyer, Sandrine Jayne, April Sellors, Anna Schuh, Pauline Robbe, David Oscier, James Bailey, Syed Rais, Alison Bentley, Lynn Cawkwell, Paul Evans, Peter Hillmen, Guy Pratt, David J. Allsup, James M. Allan
NATURE COMMUNICATIONS (2021)
Genome-wide association study identifies Sjogren's risk loci with functional implications in immune and glandular cells
Bhuwan Khatri, Kandice L. Tessneer, Astrid Rasmussen, Farhang Aghakhanian, Tove Ragna Reksten, Adam Adler, Ilias Alevizos, Juan-Manuel Anaya, Lara A. Aqrawi, Eva Baecklund, Johan G. Brun, Sara Magnusson Bucher, Maija-Leena Eloranta, Fiona Engelke, Helena Forsblad-d'Elia, Stuart B. Glenn, Daniel Hammenfors, Juliana Imgenberg-Kreuz, Janicke Liaaen Jensen, Svein Joar Auglaend Johnsen, Malin Jonsson, Marika Kvarnstrom, Jennifer A. Kelly, He Li, Thomas Mandl, Javier Martin, Gaetane Nocturne, Katrine Braekke Norheim, Oyvind Palm, Kathrine Skarstein, Anna M. Stolarczyk, Kimberly E. Taylor, Maria Teruel, Elke Theander, Swamy Venuturupalli, Daniel J. Wallace, Kiely M. Grundahl, Kimberly S. Hefner, Lida Radfar, David M. Lewis, Donald U. Stone, C. Erick Kaufman, Michael T. Brennan, Joel M. Guthridge, Judith A. James, R. Hal Scofield, Patrick M. Gaffney, Lindsey A. Criswell, Roland Jonsson, Per Eriksson, Simon J. Bowman, Roald Omdal, Lars Ronnblom, Blake Warner, Maureen Rischmueller, Torsten Witte, A. Darise Farris, Xavier Mariette, Marta E. Alarcon-Riquelme, Caroline H. Shiboski, Marie Wahren-Herlenius, Wan-Fai Ng, Kathy L. Sivils, Indra Adrianto, Gunnel Nordmark, Christopher J. Lessard
NATURE COMMUNICATIONS (2022)
A gene-level methylome-wide association analysis identifies novel Alzheimer's disease genes
Chong Wu, Jonathan Bradley, Yanming Li, Lang Wu, Hong-Wen Deng
BIOINFORMATICS (2021)
A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts
Yogasudha Veturi, Anastasia Lucas, Yuki Bradford, Daniel Hui, Scott Dudek, Elizabeth Theusch, Anurag Verma, Jason E. Miller, Iftikhar Kullo, Hakon Hakonarson, Patrick Sleiman, Daniel Schaid, Charles M. Stein, Digna R. Velez Edwards, QiPing Feng, Wei-Qi Wei, Marisa W. Medina, Ronald M. Krauss, Thomas J. Hoffmann, Neil Risch, Benjamin F. Voight, Daniel J. Rader, Marylyn D. Ritchie
NATURE GENETICS (2021)
Exome-Wide Association Study Identified Clusters of Pleiotropic Genetic Associations with Alzheimer's Disease and Thirteen Cardiovascular Traits
Yury Loika, Elena Loiko, Irina Culminskaya, Alexander M. Kulminski
GENES (2023)
Genome-wide association study identifies five risk loci for pernicious anemia
Triin Laisk, Maarja Lepamets, Mariann Koel, Erik Abner, Andres Metspalu, Reedik Maegi
NATURE COMMUNICATIONS (2021)
Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome
Ruikun Cai, Yichao Dong, Mingxia Fang, Yuxuan Fan, Zian Cheng, Yue Zhou, Jianen Gao, Feifei Han, Changlong Guo, Xu Ma
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY (2021)
FinnGen provides genetic insights from a well-phenotyped isolated population
Mitja Kurki, Juha Karjalainen, Priit Palta, Timo P. Sipila, Kati Kristiansson, Kati M. Donner, Mary P. Reeve, Hannele Laivuori, Mervi Aavikko, Mari A. Kaunisto, Anu Loukola, Elisa Lahtela, Hannele Mattsson, Paivi Laiho, Pietro Della Briotta Parolo, Arto A. Lehisto, Masahiro Kanai, Nina Mars, Joel Ramo, Tuomo Kiiskinen, Henrike O. Heyne, Kumar Veerapen, Sina Rueger, Susanna Lemmela, Wei Zhou, Sanni Ruotsalainen, Kalle Parn, Tero Hiekkalinna, Sami Koskelainen, Teemu Paajanen, Vincent Llorens, Javier Gracia-Tabuenca, Harri Siirtola, Kadri Reis, Abdelrahman G. Elnahas, Benjamin Sun, Christopher N. Foley, Katriina Aalto-Setala, Kaur Alasoo, Mikko Arvas, Kirsi Auro, Shameek Biswas, Argyro Bizaki-Vallaskangas, Olli Carpen, Chia-Yen Chen, Oluwaseun A. Dada, Zhihao Ding, Margaret G. Ehm, Kari Eklund, Martti Farkkila, Hilary Finucane, Andrea Ganna, Awaisa Ghazal, Robert R. Graham, Eric M. Green, Antti Hakanen, Marco Hautalahti, Asa K. Hedman, Mikko Hiltunen, Reetta Hinttala, Iiris Hovatta, Xinli Hu, Adriana Huertas-Vazquez, Laura Huilaja, Julie Hunkapiller, Howard Jacob, Jan-Nygaard Jensen, Heikki Joensuu, Sally John, Valtteri Julkunen, Marc Jung, Juhani Junttila, Kai Kaarniranta, Mika Kahonen, Risto Kajanne, Lila Kallio, Reetta Kalviainen, Jaakko Kaprio, Nurlan Kerimov, Johannes Kettunen, Elina Kilpelainen, Terhi Kilpi, Katherine Klinger, Veli-Matti Kosma, Teijo Kuopio, Venla Kurra, Triin Laisk, Jari Laukkanen, Nathan Lawless, Aoxing Liu, Simonne Longerich, Reedik Magi, Johanna Makela, Antti Makitie, Anders Malarstig, Arto Mannermaa, Joseph Maranville, Athena Matakidou, Tuomo Meretoja, Sahar Mozaffari, Mari E. K. Niemi, Marianna Niemi, Teemu Niiranen, George Okafo, Hanna M. Ollila, Antti Palomaki, Tuula Palotie, Jukka Partanen, Dirk S. Paul, Margit Pelkonen, Rion K. Pendergrass, Slave Petrovski, Anne Pitkaranta, Adam Platt, David Pulford, Eero Punkka, Pirkko Pussinen, Neha Raghavan, Fedik Rahimov, Deepak Rajpal, Nicole A. Renaud, Bridget Riley-Gillis, Rodosthenis Rodosthenous, Elmo Saarentaus, Aino Salminen, Eveliina Salminen, Veikko Salomaa, Johanna Schleutker, Raisa Serpi, Huei-yi Shen, Richard Siegel, Kaisa Silander, Sanna Siltanen, Sirpa Soini, Hilkka Soininen, Jae Hoon Sul, Ioanna Tachmazidou, Kaisa Tasanen, Pentti Tienari, Sanna Toppila-Salmi, Taru Tukiainen, Tiinamaija Tuomi, Joni A. Turunen, Jacob C. Ulirsch, Felix Vaura, Petri Virolainen, Jeffrey Waring, Dawn Waterworth, Robert Yang, Mari Nelis, Anu Reigo, Andres Metspalu, Lili Milani, Tonu Esko, Caroline Fox, Aki S. Havulinna, Markus Perola, Samuli Ripatti, Anu Jalanko, Tarja Laitinen, Tomi P. Makela, Robert Plenge, Mark McCarthy, Heiko Runz, Mark J. Daly, Aarno Palotie
NATURE (2023)
The Associations of Childhood Psychosocial Factors With Cognitive Function in Midlife-The Young Finns Study
Amanda Nurmi, Laura Pulkki-Raback, Pia Salo, Katja Pahkala, Markus Juonala, Nina Hutri-Kahonen, Mika Kahonen, Terho Lehtimaki, Eero Jokinen, Liisa Keltikangas-Jarvinen, Tomi P. Laitinen, Paivi Tossavainen, Leena Taittonen, Jorma S. A. Viikari, Olli T. Raitakari, Suvi P. Rovio
NEUROPSYCHOLOGY (2023)
Dissecting the polygenic basis of atherosclerosis via disease-associated cell state signatures
Tiit Ord, Tapio Lonnberg, Valtteri Nurminen, Aarthi Ravindran, Henri Niskanen, Miika Kiema, Kadri Ounap, Maleeha Maria, Pierre R. Moreau, Pashupati P. Mishra, Senthil Palani, Jenni Virta, Heidi Liljenback, Einari Aavik, Anne Roivainen, Seppo Yla-Herttuala, Johanna P. Laakkonen, Terho Lehtimaki, Minna U. Kaikkonen
AMERICAN JOURNAL OF HUMAN GENETICS (2023)
The characteristics of elevated blood pressure in abdominal obesity correspond to primary hypertension: a cross-sectional study
Jyrki Taurio, Elina J. Hautaniemi, Jenni K. Koskela, Arttu Eraranta, Mari Hamalainen, Antti Tikkakoski, Jarkko A. Kettunen, Mika Kahonen, Onni Niemela, Eeva Moilanen, Jukka Mustonen, Ilkka Porsti
BMC CARDIOVASCULAR DISORDERS (2023)
Polygenic Scores Help Reduce Racial Disparities in Predictive Accuracy of Automated Type 1 Diabetes Classification Algorithms
Aaron J. Deutsch, Lauren Stalbow, Timothy D. Majarian, Josep M. Mercader, Alisa K. Manning, Jose C. Florez, Ruth J. F. Loos, Miriam S. Udler
DIABETES CARE (2023)
The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes
Alicia Huerta-Chagoya, Philip Schroeder, Ravi J. Mandla, Aaron Deutsch, Wanying Zhu, Lauren Petty, Xiaoyan Yi, Joanne B. Cole, Miriam S. Udler, Peter Dornbos, Bianca Porneala, Daniel DiCorpo, Ching-Ti H. Liu, Josephine Li, Lukasz Szczerbinski, Varinderpal Kaur, Joohyun Kim, Yingchang Lu, Alicia Martin, Decio L. Eizirik, Piero Marchetti, Lorella Marselli, Ling Chen, Shylaja Srinivasan, Jennifer Todd, Jason Flannick, Rose Gubitosi-Klug, Lynne Levitsky, Rachana Shah, Megan Kelsey, Brian Burke, Dana M. Dabelea, Jasmin Divers, Santica Marcovina, Lauren Stalbow, Ruth J. F. Loos, Burcu F. Darst, Charles Kooperberg, Laura M. Raffield, Christopher Haiman, Quan Sun, Joseph B. McCormick, Susan P. Fisher-Hoch, Maria L. Ordonez, James J. Meigs, Leslie Baier, Clicerio Gonzalez-Villalpando, Maria Elena Gonzalez-Villalpando, Lorena Orozco, Lourdes Garcia-Garcia, Andres A. Moreno-Estrada, Carlos Aguilar-Salinas, Teresa Tusie, Josee Dupuis, Maggie C. Y. Ng, Alisa M. Manning, Heather Highland, Miriam Cnop, Robert Hanson, Jennifer Below, Jose C. Florez, Aaron M. Leong, Josep Mercader
DIABETOLOGIA (2023)
Association of Mitochondrial DNA Copy Number With Brain MRI Markers and Cognitive Function A Meta-analysis of Community-Based Cohorts
Yuankai Zhang, Xue Liu, Kerri L. Wiggins, Nuzulul L. Kurniansyah, Xiuqing Guo, Amanda L. Rodrigue, Wei Zhao, Lisa R. Yanek, Scott M. Ratliff, Achilleas Pitsillides, Juan Sebastian Aguirre Patino, Tamar Sofer, Dan E. Arking, Thomas R. Austin, Alexa S. Beiser, John Blangero, Eric E. Boerwinkle, Jan Bressler, Joanne E. Curran, Lifang Hou, Timothy J. Hughes, Sharon L. R. Kardia, Lenore J. Launer, Daniel Levy, Thomas H. Mosley, Ilya M. Nasrallah, Stephen S. Rich, Jerome Rotter, Sudha Seshadri, Wassim Tarraf, Kevin A. Gonzalez, Vasan Ramachandran, Kristine Yaffe, Paul A. Nyquist, Bruce M. Psaty, Charles C. DeCarli, Jennifer M. Smith, David C. Glahn, Hector M. Gonzalez, Joshua R. Bis, Myriam L. Fornage, Susan Heckbert, Annette L. Fitzpatrick, Chunyu Liu, Claudia L. Satizabal
NEUROLOGY (2023)
Advanced Glycation End Products (AGEs) in Diet and Skin in Relation to Stool Microbiota: The Rotterdam Study
Jinluan Chen, Djawad Radjabzadeh, Carolina Medina-Gomez, Trudy Voortman, Joyce B. J. van Meurs, M. Arfan Ikram, Andre G. Uitterlinden, Robert Kraaij, M. Carola Zillikens
NUTRIENTS (2023)
Sexual dimorphisms in serum calcium and phosphate concentrations in the Rotterdam Study
Ariadne Bosman, W. Nadia H. Koek, Natalia Campos-Obando, Bram C. J. van der Eerden, M. A. Ikram, Andre G. Uitterlinden, Johannes P. T. M. van Leeuwen, M. C. Zillikens
SCIENTIFIC REPORTS (2023)
Oligogenic Architecture of Rare Noncoding Variants Distinguishes 4 Congenital Heart Disease Phenotypes
Mengyao Yu, Matthew Aguirre, Meiwen Jia, Ketrin Gjoni, Aldo Cordova-Palomera, Chad Munger, Dulguun Amgalan, X. Rosa Ma, Alexandre Pereira, Catherine Tcheandjieu, Christine Seidman, Jonathan Seidman, Martin Tristani-Firouzi, Wendy Chung, Elizabeth Goldmuntz, Deepak Srivastava, Ruth J. F. Loos, Nathalie Chami, Heather Cordell, Martina Dressen, Bertram Mueller-Myhsok, Harald Lahm, Markus Krane, Katherine S. Pollard, Jesse M. Engreitz, Sarah Gagliano A. Taliun, Bruce D. Gelb, James R. Priest
CIRCULATION-GENOMIC AND PRECISION MEDICINE (2023)
Genetic insights into resting heart rate and its role in cardiovascular disease
Yordi van de Vegte, Ruben P. Eppinga, M. Yldau van der Ende, Yanick Hagemeijer, Yuvaraj V. Mahendran, Elias Y. Salfati, Albert E. Smith, Vanessa Tan, Dan V. Arking, Ioanna Ntalla, Emil A. Appel, Claudia Schurmann, Jennifer Brody, Rico Rueedi, Ozren Polasek, Gardar Sveinbjornsson, Cecile Lecoeur, Claes Ladenvall, Jing Hua Zhao, Aaron Isaacs, Lihua Wang, Jian'an Luan, Shih-Jen Hwang, Nina U. Mononen, Kirsi F. Auro, Anne Jackson, Lawrence Bielak, Linyao Zeng, Nabi Shah, Maria Nethander, Archie Campbell, Tuomo Rankinen, Sonali Pechlivanis, Lu Qi, Wei Zhao, Federica Rizzi, Toshiko Tanaka, Antonietta Robino, Massimiliano Cocca, Leslie Lange, Martina Mueller-Nurasyid, Carolina E. Roselli, Weihua Zhang, Marcus J. Kleber, Xiuqing Guo, Henry E. Lin, Francesca Pavani, Tessel Galesloot, Raymond E. Noordam, Yuri Milaneschi, Katharina Schraut, Marcel den Hoed, Frauke E. Degenhardt, Stella Trompet, Marten van den Berg, Giorgio Pistis, Yih-Chung S. Tham, Stefan L. Weiss, Xueling J. Sim, Hengtong M. Li, Peter van der Most, Ilja Nolte, Leo-Pekka R. Lyytikaeinen, M. Abdullah Said, Daniel Witte, Carlos M. Iribarren, Lenore S. Launer, Susan Ring, Paul de Vries, Peter P. Sever, Allan Linneberg, Erwin M. Bottinger, Sandosh Padmanabhan, Bruce Psaty, Nona Sotoodehnia, Ivana Kolcic, Delnaz D. Roshandel, Andrew O. Paterson, David F. Arnar, Daniel Gudbjartsson, Hilma Holm, Beverley T. Balkau, Claudia H. Silva, Christopher Newton-Cheh, Kjell Nikus, Perttu L. Salo, Karen A. Mohlke, Patricia Peyser, Heribert Schunkert, Mattias Lorentzon, Jari C. Lahti, Dabeeru C. Rao, Marilyn D. Cornelis, Jessica A. Faul, Jennifer Smith, Katarzyna Stolarz-Skrzypek, Stefania Bandinelli, Maria Pina Concas, Gianfranco Sinagra, Thomas Meitinger, Melanie F. Waldenberger, Moritz Sinner, Konstantin E. Strauch, Graciela D. Delgado, Kent Taylor, Jie Yao, Luisa Foco, Olle Melander, Jacqueline de Graaf, Renee de Mutsert, Eco J. C. de Geus, Asa K. Johansson, Peter K. Joshi, Lars Lind, Andre W. Franke, Peter V. Macfarlane, Kirill Tarasov, Nicholas B. Tan, Stephan Felix, E-Shyong Q. Tai, Debra Quek, Harold Snieder, Johan Ormel, Martin Ingelsson, Cecilia P. Lindgren, Andrew T. Morris, Olli Raitakari, Torben Hansen, Themistocles Assimes, Vilmundur J. Gudnason, Nicholas C. Timpson, Alanna B. Morrison, Patricia P. Munroe, David Strachan, Niels Grarup, Ruth J. F. R. Loos, Susan Heckbert, Peter Vollenweider, Caroline Hayward, Kari Stefansson, Philippe Froguel, Leif J. Groop, Nicholas M. Wareham, Cornelia F. van Duijn, Mary J. Feitosa, Christopher O'Donnell, Mika Kaehoenen, Markus Perola, Michael Boehnke, Sharon L. R. Kardia, Jeanette Erdmann, Colin N. A. Palmer, Claes J. Ohlsson, David G. Porteous, Johan Eriksson, Claude Bouchard, Susanne Moebus, Peter R. Kraft, David Weir, Daniele Cusi, Luigi Ferrucci, Sheila Ulivi, Giorgia Girotto, Adolfo Correa, Stefan Kaeaeb, Annette C. Peters, John S. Chambers, Jaspal Kooner, Winfried I. Maerz, Jerome A. Rotter, Andrew Hicks, J. Gustav Smith, Lambertus A. L. M. O. Kiemeney, Dennis Mook-Kanamori, Brenda W. J. H. Penninx, Ulf F. Gyllensten, James Wilson, Stephen Burgess, Johan Sundstroem, Wolfgang Lieb, J. Wouter Jukema, Mark Eijgelsheim, Edward L. M. Lakatta, Ching-Yu Cheng, Marcus Doerr, Tien-Yin Wong, Charumathi J. Sabanayagam, Albertine Oldehinkel, Harriette Riese, Terho Lehtimaeki, Niek Verweij, Pim van der Harst
NATURE COMMUNICATIONS (2023)
Ancestral diversity in lipoprotein(a) studies helps address evidence gaps
Moa P. Lee, Sofia F. Dimos, Laura M. Raffield, Zhe Wang, Anna F. Ballou, Carolina G. Downie, Christopher H. Arehart, Adolfo Correa, Paul S. de Vries, Zhaohui Du, Christopher R. Gignoux, Penny Gordon-Larsen, Xiuqing Guo, Jeffrey Haessler, Annie Green Howard, Yao Hu, Helina Kassahun, Shia T. Kent, J. Antonio G. Lopez, Keri L. Monda, Kari E. North, Ulrike Peters, Michael H. Preuss, Stephen S. Rich, Shannon L. Rhodes, Jie Yao, Rina Yarosh, Michael Y. Tsai, Jerome Rotter, Charles L. Kooperberg, Ruth J. F. Loos, Christie Ballantyne, Christy L. Avery, Mariaelisa Graff
OPEN HEART (2023)
Exposure factors associated with dementia among older adults in Iceland: the AGES-Reykjavik study
Vaka Valsdottir, Brynja Bjork Magnusdottir, Haukur Freyr Gylfason, Milan Chang, Thor Aspelund, Vilmundur Gudnason, Lenore J. Launer, Maria K. Jonsdottir
GEROSCIENCE (2023)
Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants
Kristin L. Young, Virginia Fisher, Xuan Deng, Jennifer A. Brody, Misa Graff, Elise Lim, Bridget M. Lin, Hanfei Xu, Najaf Amin, Ping An, Stella Aslibekyan, Alison E. Fohner, Bertha Hidalgo, Petra Lenzini, Robert Kraaij, Carolina Medina-Gomez, Ivana Prokic, Fernando Rivadeneira, Colleen Sitlani, Ran Tao, Jeroen van Rooij, Di Zhang, Jai G. Broome, Erin J. Buth, Benjamin D. Heavner, Deepti Jain, Albert Smith, Kathleen Barnes, Meher Preethi Boorgula, Sameer Chavan, Dawood Darbar, Mariza De Andrade, Xiuqing Guo, Jeffrey Haessler, Marguerite R. Irvin, Rita R. Kalyani, Sharon L. R. Kardia, Charles Kooperberg, Wonji Kim, Rasika A. Mathias, Merry-Lynn McDonald, Braxton D. Mitchell, Patricia A. Peyser, Elizabeth A. Regan, Susan Redline, Alexander P. Reiner, Stephen S. Rich, Jerome I. Rotter, Jennifer A. Smith, Scott Weiss, Kerri L. Wiggins, Lisa R. Yanek, Donna Arnett, Nancy L. Heard-Costa, Suzanne Leal, Danyu Lin, Barbara McKnight, Michael Province, Cornelia M. van Duijn, Kari E. North, L. Adrienne Cupples, Ching-Ti Liu
HUMAN GENETICS AND GENOMICS ADVANCES (2023)
The role of admixture in the rare variant contribution to inflammatory bowel disease
Courtney Astore, Shivam Sharma, Sini Nagpal, David J. Cutler, John D. Rioux, Judy H. Cho, Dermot P. B. Mcgovern, Steven R. Brant, Subra Kugathasan, I. King Jordan, Greg Gibson
GENOME MEDICINE (2023)