• Phenome-wide Association Study Relating Pretreatment Laboratory Parameters With Human Genetic Variants in AIDS Clinical Trials Group Protocols C. B. Moore, A. Verma, S. Pendergrass, S. S. Verma, D. H. Johnson, E. S. Daar, R. M. Gulick, R. Haubrich, G. K. Robbins, M. D. Ritchie, D. W. Haas, http://ofid.oxfordjournals.org/cgi/doi/10.1093/ofid/ofu113, 2, 1, ofu113-ofu113, Open Forum Infectious Diseases, 2328-8957, 2015-01-08, 10.1093/ofid/ofu113, 2015-01-19 16:18:51, CrossRef, en,

• Design and Anticipated Outcomes of the eMERGE-PGx Project: A Multicenter Pilot for Preemptive Pharmacogenomics in Electronic Health Record Systems L J Rasmussen-Torvik, S C Stallings, A S Gordon, B Almoguera, M A Basford, S J Bielinski, A Brautbar, M H Brilliant, D S Carrell, J J Connolly, D R Crosslin, K F Doheny, C J Gallego, O Gottesman, D S Kim, K A Leppig, R Li, S Lin, S Manzi, A R Mejia, J A Pacheco, V Pan, J Pathak, C L Perry, J F Peterson, C A Prows, J Ralston, L V Rasmussen, M D Ritchie, S Sadhasivam, S A Scott, M Smith, A Vega, A A Vinks, S Volpi, W A Wolf, E Bottinger, R L Chisholm, C G Chute, J L Haines, J B Harley, B Keating, I A Holm, I J Kullo, G P Jarvik, E B Larson, T Manolio, C A McCarty, D A Nickerson, S E Scherer, M S Williams, D M Roden, J C Denny, http://www.nature.com/doifinder/10.1038/clpt.2014.137, 96, 4, 482-489, Clinical Pharmacology & Therapeutics, 0009-9236, 1532-6535, 10/2014, 10.1038/clpt.2014.137, 2015-01-19 16:11:03, CrossRef, Design and Anticipated Outcomes of the eMERGE-PGx Project,

• Genetic variation in the HLA region is associated with susceptibility to herpes zoster D R Crosslin, D S Carrell, A Burt, D S Kim, J G Underwood, D S Hanna, B A Comstock, E Baldwin, M de Andrade, I J Kullo, G Tromp, H Kuivaniemi, K M Borthwick, C A McCarty, P L Peissig, K F Doheny, E Pugh, A Kho, J Pacheco, M G Hayes, M D Ritchie, S S Verma, G Armstrong, S Stallings, J C Denny, R J Carroll, D C Crawford, P K Crane, S Mukherjee, E Bottinger, R Li, B Keating, D B Mirel, C S Carlson, J B Harley, E B Larson, G P Jarvik, http://www.nature.com/doifinder/10.1038/gene.2014.51, Genes and Immunity, 1466-4879, 1476-5470, 2014-10-09, 10.1038/gene.2014.51, 2015-01-19 16:02:49, CrossRef,

• Genetic Simulation Tools for Post-Genome Wide Association Studies of Complex Diseases: Genetic Simulation Tools for Complex Diseases Huann-Sheng Chen, Carolyn M. Hutter, Leah E. Mechanic, Christopher I. Amos, Vineet Bafna, Elizabeth R. Hauser, Ryan D. Hernandez, Chun Li, David A. Liberles, Kimberly McAllister, Jason H. Moore, Dina N. Paltoo, George J. Papanicolaou, Bo P Marylyn D. Ritchie, Gabriel Rosenfeld, John S. Witte, Elizabeth M. Gillanders, Eric J. Feuer, http://doi.wiley.com/10.1002/gepi.21870, 39, 1, 11-19, Genetic Epidemiology, 07410395, 01/2015, 10.1002/gepi.21870, 2015-01-19 16:02:07, CrossRef, en, Genetic Simulation Tools for Post-Genome Wide Association Studies of Complex Diseases,

• Incorporating inter-relationships between different levels of genomic data into cancer clinical outcome prediction Dokyoon Kim, Hyunjung Shin, Kyung-Ah Sohn, Anurag Verma, Marylyn D. Ritchie, Ju Han Kim, 67, 3, 344-353, Methods (San Diego, Calif.), 1095-9130, Jun 1, 2014, PMID: 24561168,

• Admixture mapping and subsequent fine-mapping suggests a biologically relevant and novel association on chromosome 11 for type 2 diabetes in African Americans Janina M. Jeff, Loren L. Armstrong, Marylyn D. Ritchie, Joshua C. Denny, Abel N. Kho, Melissa A. Basford, Wendy A. Wolf, Jennifer A. Pacheco, Rongling Li, Rex L. Chisholm, Dan M. Roden, M. Geoffrey Hayes, Dana C. Crawford, 9, 3, e86931, PloS One, 1932-6203, 2014, PMID: 24595071 PMCID: PMC3940426,

• Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization Dan E. Arking, Sara L. Pulit, Lia Crotti, Pim van der Harst, Patricia B. Munroe, Tamara T. Koopmann, Nona Sotoodehnia, Elizabeth J. Rossin, Michael Morley, Xinchen Wang, Andrew D. Johnson, Alicia Lundby, Daníel F. Gudbjartsson, Peter A. Noseworthy, Mark Eijgelsheim, Yuki Bradford, Kirill V. Tarasov, Marcus Dörr, Martina Müller-Nurasyid, Annukka M. Lahtinen, Ilja M. Nolte, Albert Vernon Smith, Joshua C. Bis, Aaron Isaacs, Stephen J. Newhouse, Daniel S. Evans, Wendy S. Post, Daryl Waggott, Leo-Pekka Lyytikäinen, Andrew A. Hicks, Lewin Eisele, David Ellinghaus, Caroline Hayward, Pau Navarro, Sheila Ulivi, Toshiko Tanaka, David J. Tester, Stéphanie Chatel, Stefan Gustafsson, Meena Kumari, Richard W. Morris, Åsa T. Naluai, Sandosh Padmanabhan, Alexander Kluttig, Bernhard Strohmer, Andrie G. Panayiotou, Maria Torres, Michael Knoflach, Jaroslav A. Hubacek, Kamil Slowikowski, Soumya Raychaudhuri, Runjun D. Kumar, Tamara B. Harris, Lenore J. Launer, Alan R. Shuldiner, Alvaro Alonso, Joel S. Bader, Georg Ehret, Hailiang Huang, W. H. Linda Kao, James B. Strait, Peter W. Macfarlane, Morris Brown, Mark J. Caulfield, Nilesh J. Samani, Florian Kronenberg, Johann Willeit, CARe Consortium, COGENT Consortium, J. Gustav Smith, Karin H. Greiser, Henriette Meyer Zu Schwabedissen, Karl Werdan, Massimo Carella, Leopoldo Zelante, Susan R. Heckbert, Bruce M. Psaty, Jerome I. Rotter, Ivana Kolcic, Ozren Polašek, Alan F. Wright, Maura Griffin, Mark J. Daly, DCCT/EDIC, David O. Arnar, Hilma Hólm, Unnur Thorsteinsdottir, eMERGE Consortium, Joshua C. Denny, Dan M. Roden, Rebecca L. Zuvich, Valur Emilsson, Andrew S. Plump, Martin G. Larson, Christopher J. O'Donnell, Xiaoyan Yin, Marco Bobbo, Adamo P. D'Adamo, Annamaria Iorio, Gianfranco Sinagra, Angel Carracedo, Steven R. Cummings, Michael A. Nalls, Antti Jula, Kimmo K. Kontula, Annukka Marjamaa, Lasse Oikarinen, Markus Perola, Kimmo Porthan, Raimund Erbel, Per Hoffmann, Karl-Heinz Jöckel, Hagen Kälsch, Markus M. Nöthen, HRGEN Consortium, Marcel den Hoed, Ruth J. F. Loos, Dag S. Thelle, Christian Gieger, Thomas Meitinger, Siegfried Perz, Annette Peters, Hanna Prucha, Moritz F. Sinner, Melanie Waldenberger, Rudolf A. de Boer, Lude Franke, Pieter A. van der Vleuten, Britt Maria Beckmann, Eimo Martens, Abdennasser Bardai, Nynke Hofman, Arthur A. M. Wilde, Elijah R. Behr, Chrysoula Dalageorgou, John R. Giudicessi, Argelia Medeiros-Domingo, Julien Barc, Florence Kyndt, Vincent Probst, Alice Ghidoni, Roberto Insolia, Robert M. Hamilton, Stephen W. Scherer, Jeffrey Brandimarto, Kenneth Margulies, Christine E. Moravec, Fabiola del Greco M, Christian Fuchsberger, Jeffrey R. O'Connell, Wai K. Lee, Graham C. M. Watt, Harry Campbell, Sarah H. Wild, Nour E. El Mokhtari,

• Pleiotropic genes for metabolic syndrome and inflammation Aldi T. Kraja, Daniel I. Chasman, Kari E. North, Alexander P. Reiner, Lisa R. Yanek, Tuomas O. Kilpeläinen, Jennifer A. Smith, Abbas Dehghan, Josée Dupuis, Andrew D. Johnson, Mary F. Feitosa, Fasil Tekola-Ayele, Audrey Y. Chu, Ilja M. Nolte, Zari Dastani, Andrew Morris, Sarah A. Pendergrass, Yan V. Sun, Marylyn D. Ritchie, Ahmad Vaez, Honghuang Lin, Symen Ligthart, Letizia Marullo, Rebecca Rohde, Yaming Shao, Mark A. Ziegler, Hae Kyung Im, Cross Consortia Pleiotropy Group, Cohorts for Heart and, Aging Research in Genetic Epidemiology, Genetic Investigation of Anthropometric Traits Consortium, Global Lipids Genetics Consortium, Meta-Analyses of Glucose, Insulin-related traits Consortium, Global BPgen Consortium, ADIPOGen Consortium, Women's Genome Health Study, Howard University Family Study, Renate B. Schnabel, Torben Jørgensen, Marit E. Jørgensen, Torben Hansen, Oluf Pedersen, Ronald P. Stolk, Harold Snieder, Albert Hofman, Andre G. Uitterlinden, Oscar H. Franco, M. Arfan Ikram, J. Brent Richards, Charles Rotimi, James G. Wilson, Leslie Lange, Santhi K. Ganesh, Mike Nalls, Laura J. Rasmussen-Torvik, James S. Pankow, Josef Coresh, Weihong Tang, W. H. Linda Kao, Eric Boerwinkle, Alanna C. Morrison, Paul M. Ridker, Diane M. Becker, Jerome I. Rotter, Sharon L. R. Kardia, Ruth J. F. Loos, Martin G. Larson, Yi-Hsiang Hsu, Michael A. Province, Russell Tracy, Benjamin F. Voight, Dhananjay Vaidya, Christopher J. O'Donnell, Emelia J. Benjamin, Behrooz Z. Alizadeh, Inga Prokopenko, James B. Meigs, Ingrid B. Borecki, 112, 4, 317-338, Molecular Genetics and Metabolism, 1096-7206, Aug 2014, PMID: 24981077 PMCID: PMC4122618,

• Knowledge boosting: a graph-based integration approach with multi-omics data and genomic knowledge for cancer clinical outcome prediction Dokyoon Kim, Je-Gun Joung, Kyung-Ah Sohn, Hyunjung Shin, Yu Rang Park, Marylyn D. Ritchie, Ju Han Kim, of the American Medical Informatics Association: JAMIA, 1527-974X, Jul 7, 2014, PMID: 25002459,

• Genetic determinants of age-related macular degeneration in diverse populations from the PAGE study Nicole A. Restrepo, Kylee L. Spencer, Robert Goodloe, Tiana A. Garrett, Gerardo Heiss, Petra Bůžková, Neal Jorgensen, Richard A. Jensen, Tara C. Matise, Lucia A. Hindorff, Barbara E. K. Klein, Ronald Klein, Tien Y. Wong, Ching-Yu Ch Belinda K. Cornes, E.-Shyong Tai, Marylyn D. Ritchie, Jonathan L. Haines, Dana C. Crawford, 55, 10, 6839-6850, Investigative Ophthalmology & Visual Science, 1552-5783, Oct 2014, PMID: 25205864 PMCID: PMC4214207,

• Defining the role of common variation in the genomic and biological architecture of adult human height Andrew R. Wood, Tonu Esko, Jian Yang, Sailaja Vedantam, Tune H. Pers, Stefan Gustafsson, Audrey Y. Chu, Karol Estrada, Jian'an Luan, Zoltán Kutalik, Najaf Amin, Martin L. Buchkovich, Damien C. Croteau-Chonka, Felix R. Day, Yanan Duan, Tove Fall, Rudolf Fehrmann, Teresa Ferreira, Anne U. Jackson, Juha Karjalainen, Ken Sin Lo, Adam E. Locke, Reedik Mägi, Evelin Mihailov, Eleonora Porcu, Joshua C. Randall, André Scherag, Anna A. E. Vinkhuyzen, Harm-Jan Westra, Thomas W. Winkler, Tsegaselassie Workalemahu, Jing Hua Zhao, Devin Absher, Eva Albrecht, Denise Anderson, Jeffrey Baron, Marian Beekman, Ayse Demirkan, Georg B. Ehret, Bjarke Feenstra, Mary F. Feitosa, Krista Fischer, Ross M. Fraser, Anuj Goel, Jian Gong, Anne E. Justice, Stavroula Kanoni, Marcus E. Kleber, Kati Kristiansson, Unhee Lim, Vaneet Lotay, Julian C. Lui, Massimo Mangino, Irene Mateo Leach, Carolina Medina-Gomez, Michael A. Nalls, Dale R. Nyholt, Cameron D. Palmer, Dorota Pasko, Sonali Pechlivanis, Inga Prokopenko, Janina S. Ried, Stephan Ripke, Dmitry Shungin, Alena Stancáková, Rona J. Strawbridge, Yun Ju Sung, Toshiko Tanaka, Alexander Teumer, Stella Trompet, Sander W. van der Laan, Jessica van Setten, Jana V. Van Vliet-Ostaptchouk, Zhaoming Wang, Loïc Yengo, Weihua Zhang, Uzma Afzal, Johan Arnlöv, Gillian M. Arscott, Stefania Bandinelli, Amy Barrett, Claire Bellis, Amanda J. Bennett, Christian Berne, Matthias Blüher, Jennifer L. Bolton, Yvonne Böttcher, Heather A. Boyd, Marcel Bruinenberg, Brendan M. Buckley, Steven Buyske, Ida H. Caspersen, Peter S. Chines, Robert Clarke, Simone Claudi-Boehm, Matthew Cooper, E. Warwick Daw, Pim A. De Jong, Joris Deelen, Graciela Delgado, Josh C. Denny, Rosalie Dhonukshe-Rutten, Maria Dimitriou, Alex S. F. Doney, Marcus Dörr, Niina Eklund, Elodie Eury, Lasse Folkersen, Melissa E. Garcia, Frank Geller, Vilmantas Giedraitis, Alan S. Go, Harald Grallert, Tanja B. Grammer, Jürgen Gräßler, Henrik Grönberg, Lisette C. P. G. M. de Groot, Christopher J. Groves, Jeffrey Haessler, Per Hall, Toomas Haller, Goran Hallmans, Anke Hannemann, Catharina A. Hartman, Maija Hassinen, Caroline Hayward, Nancy L. Heard-Costa, Quinta Helmer, Gibran Hemani, Anjali K. Henders, Hans L. Hillege, Mark A. Hlatky, Wolfgang Hoffmann, Per Hoffmann, Oddgeir Holmen, Jeanine J. Houwing-Duistermaat, Thomas Illig, Aaron Isaacs, Alan L. James, Janina Jeff, Berit Johansen, Åsa Johansson, Jennifer Jolley, Thorhildur Juliusdottir, Juhani Junttila, Abel N. Kho, Leena Kinnunen, Norman Klopp, Thomas Kocher, Wolfgang Kratzer, Peter Lichtner, Lars Lind, Jaana Lindström, Stéphane Lobbens, Mattias Lorentzon, Yingchang Lu, Valeriya Lyssenko,

• Regulatory Polymorphisms in Human DBH Affect Peripheral Gene Expression and Sympathetic Activity Elizabeth S. Barrie, David Weinshenker, Anurag Verma, Sarah A. Pendergrass, Leslie A. Lange, Marylyn D. Ritchie, James G. Wilson, Helena Kuivaniemi, Gerard Tromp, David J. Carey, Glenn S. Gerhard, Murray H. Brilliant, Scott J. Hebbring, Joseph F. Cubells, Julia K. Pinsonneault, Greg J. Norman, Wolfgang Sadee, 115, 12, 1017-1025, Circulation Research, 1524-4571, Dec 5, 2014, PMID: 25326128 PMCID: PMC4258174,

• Controlling for population structure and genotyping platform bias in the eMERGE multi-institutional biobank linked to electronic health records David R. Crosslin, Gerard Tromp, Amber Burt, Daniel S. Kim, Shefali S. Verma, Anastasia M. Lucas, Yuki Bradford, Dana C. Crawford, Sebastian M. Armasu, John A. Heit, M. Geoffrey Hayes, Helena Kuivaniemi, Marylyn D. Ritchie, Gail P. Jarvik, Mariza de Andrade, electronic Medical Records and Genomics (eMERGE) Network, 5, 352, Frontiers in Genetics, 1664-8021, 2014, PMID: 25414722 PMCID: PMC4220165,

• Genetic Variants Associated with Serum Thyroid Stimulating Hormone (TSH) Levels in European Americans and African Americans from the eMERGE Network Jennifer R. Malinowski, Joshua C. Denny, Suzette J. Bielinski, Melissa A. Basford, Yuki Bradford, Peggy L. Peissig, David Carrell, David R. Crosslin, Jyotishman Pathak, Luke Rasmussen, Jennifer Pacheco, Abel Kho, Katherine M. Newton, Rongling Li, Iftikhar J. Kullo, Christopher G. Chute, Rex L. Chisholm, Gail P. Jarvik, Eric B. Larson, Catherine A. McCarty, Daniel R. Masys, Dan M. Roden, Mariza de Andrade, Marylyn D. Ritchie, Dana C. Crawford, 9, 12, e111301, PloS One, 1932-6203, 2014, PMID: 25436638 PMCID: PMC4249871,

• Detection of Pleiotropy through a Phenome-Wide Association Study (PheWAS) of Epidemiologic Data as Part of the Environmental Architecture for Genes Linked to Environment (EAGLE) Study Molly A. Hall, Anurag Verma, Kristin D. Brown-Gentry, Robert Goodloe, Jonathan Boston, Sarah Wilson, Bob McClellan, Cara Sutcliffe, Holly H. Dilks, Nila B. Gillani, Hailing Jin, Ping Mayo, Melissa Allen, Nathalie Schnetz-Boutaud, Dana C. Crawford, Marylyn D. Ritchie, Sarah A. Pendergrass, 10, 12, e1004678, PLoS genetics, 1553-7404, Dec 2014, PMID: 25474351 PMCID: PMC4256091,

• Phenome-wide association study (PheWAS) in EMR-linked pediatric cohorts, genetically links PLCL1 to speech language development and IL5-IL13 to Eosinophilic Esophagitis Bahram Namjou, Keith Marsolo, Robert J. Caroll, Joshua C. Denny, Marylyn D. Ritchie, Shefali S. Verma, Todd Lingren, Aleksey Porollo, Beth L. Cobb, Cassandra Perry, Leah C. Kottyan, Marc E. Rothenberg, Susan D. Thompson, Ingrid A. Holm, Isaac S. Kohane, John B. Harley, 5, 401, Frontiers in Genetics, 1664-8021, 2014, PMID: 25477900 PMCID: PMC4235428,

• Genomic architecture of pharmacological efficacy and adverse events Aparna Chhibber, Deanna L. Kroetz, Kelan G. Tantisira, Michael McGeachie, Cheng Ch Robert Plenge, Eli Stahl, Wolfgang Sadee, Marylyn D. Ritchie, Sarah A. Pendergrass, 15, 16, 2025-2048, Pharmacogenomics, 1744-8042, Dec 2014, PMID: 25521360,

• Imputation and quality control steps for combining multiple genome-wide datasets Shefali S. Verma, Mariza de Andrade, Gerard Tromp, Helena Kuivaniemi, Elizabeth Pugh, Bahram Namjou-Khales, Shubhabrata Mukherjee, Gail P. Jarvik, Leah C. Kottyan, Amber Burt, Yuki Bradford, Gretta D. Armstrong, Kimberly Derr, Dana C. Crawford, Jonathan L. Haines, Rongling Li, David Crosslin, Marylyn D. Ritchie, http://journal.frontiersin.org/journal/10.3389/fgene.2014.00370/abstract, 5, Frontiers in Genetics, 1664-8021, 2014-12-11, 10.3389/fgene.2014.00370, 2015-01-15 20:45:07, CrossRef,

• eMERGEing progress in genomics-the first seven years Dana C. Crawford, David R. Crosslin, Gerard Tromp, Iftikhar J. Kullo, Helena Kuivaniemi, M. Geoffrey Hayes, Joshua C. Denny, William S. Bush, Jonathan L. Haines, Dan M. Roden, Catherine A. McCarty, Gail P. Jarvik, Marylyn D. Ritchie, 5, 184, Frontiers in Genetics, 1664-8021, 2014, PMID: 24987407 PMCID: PMC4060012,

• Diverse convergent evidence in the genetic analysis of complex disease: coordinating omic, informatic, and experimental evidence to better identify and validate risk factors Timothy H. Ciesielski, Sarah A. Pendergrass, Marquitta J. White, Nuri Kodaman, Rafal S. Sobota, Minjun Huang, Jacquelaine Bartlett, Jing Li, Qinxin Pan, Jiang Gui, Scott B. Selleck, Christopher I. Amos, Marylyn D. Ritchie, Jason H. Moore, Scott M. Williams, 7, 10, BioData Mining, 1756-0381, 2014, PMID: 25071867 PMCID: PMC4112852,

• Phenome-wide association studies demonstrating pleiotropy of genetic variants within FTO with and without adjustment for body mass index Robert M. Cronin, Julie R. Field, Yuki Bradford, Christian M. Shaffer, Robert J. Carroll, Jonathan D. Mosley, Lisa Bastarache, Todd L. Edwards, Scott J. Hebbring, Simon Lin, Lucia A. Hindorff, Paul K. Crane, Sarah A. Pendergrass, Marylyn D. Ritchie, Dana C. Crawford, Jyotishman Pathak, Suzette J. Bielinski, David S. Carrell, David R. Crosslin, David H. Ledbetter, David J. Carey, Gerard Tromp, Marc S. Williams, Eric B. Larson, Gail P. Jarvik, Peggy L. Peissig, Murray H. Brilliant, Catherine A. McCarty, Christopher G. Chute, Iftikhar J. Kullo, Erwin Bottinger, Rex Chisholm, Maureen E. Smith, Dan M. Roden, Joshua C. Denny, 5, 250, Frontiers in Genetics, 1664-8021, 2014, PMID: 25177340 PMCID: PMC4134007,

• Knowledge-driven genomic interactions: an application in ovarian cancer Dokyoon Kim, Ruowang Li, Scott M. Dudek, Alex T. Frase, Sarah A. Pendergrass, Marylyn D. Ritchie, 7, 20, BioData Mining, 1756-0381, 2014, PMID: 25214892 PMCID: PMC4161273,

• Electronic medical records and genomics (eMERGE) network exploration in cataract: Several new potential susceptibility loci Web Page, Marylyn D. Ritchie, Shefali S. Verma, Molly A. Hall, Robert J. Goodloe, Richard L. Berg, Dave S. Carrell, Christopher S. Carlson, Lin Chen, David R. Crosslin, Joshua C. Denny, Gail Jarvik, Rongling Li, James G. Linneman, Jyoti Pathak, Peggy Peissig, Luke V. Rasmussen, Andrea H. Ramirez, Xiaoming Wang, Russell A. Wilke, Wendy A. Wolf, Eric S. Torstenson, Stephen D. Turner, Catherine A. McCarty, http://www.molvis.org/molvis/v20/1281/, Phase 1, 2014-09-19, NT025, Electronic medical records and genomics (eMERGE) network exploration in cataract,

• Analysis pipeline for the epistasis search - statistical versus biological filtering Xiangqing Sun, Qing Lu, Shubhabrata Mukheerjee, Paul K. Crane, Robert Elston, Marylyn D. Ritchie, 5, 106, Frontiers in Genetics, 1664-8021, 2014, PMID: 24817878 PMCID: PMC4012196,

• Validation of PhenX measures in the personalized medicine research project for use in gene/environment studies. Catherine A. McCarty, Richard Berg, Carla M. Rottscheit, Carol J. Waudby, Terrie Kitchner, Murray Brilliant, Marylyn D. Ritchie, 7, 1, BMC medical genomics, 2014, PMID: 24423110 PMCID: PMC3896802,

• Environment-wide association study (EWAS) for type 2 diabetes in the Marshfield Personalized Medicine Research Project Biobank. Molly A. Hall, Scott M. Dudek, Robert Goodloe, Dana C. Crawford, Sarah A. Pendergrass, Peggy Peissig, Murray Brilliant, Catherine A. McCarty, Marylyn D. Ritchie, 200-211, Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing, 2014, PMID: 24297547,

• Genomewide association study of atazanavir pharmacokinetics and hyperbilirubinemia in AIDS Clinical Trials Group protocol A5202. Daniel H. Johnson, Charles Venuto, Marylyn D. Ritchie, Gene D. Morse, Eric S. Daar, Paul J. McLaren, David W. Haas, Pharmacogenetics and genomics, 2014 Feb 19, PMID: 24557078,

• A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects. Khader Shameer, Joshua C. Denny, Keyue Ding, Hayan Jouni, David R. Crosslin, Mariza de Andrade, Christopher G. Chute, Peggy Peissig, Jennifer A. Pacheco, Rongling Li, Lisa Bastarache, Abel N. Kho, Marylyn D. Ritchie, Daniel R. Masys, Rex L. Chisholm, Eric B. Larson, Catherine A. McCarty, Dan M. Roden, Gail P. Jarvik, Iftikhar J. Kullo, 133, 1, Human genetics, 2014 Jan, PMID: 24026423 PMCID: PMC3880605,

• Polygenic inheritance of paclitaxel-induced sensory peripheral neuropathy driven by axon outgrowth gene sets in CALGB 40101 (Alliance). A. Chhibber, J. Mefford, E. A. Stahl, S. A. Pendergrass, R. M. Baldwin, K. Owzar, M. Li, E. P. Winer, C. A. Hudis, H. Zembutsu, M. Kubo, Y. Nakamura, H. L. McLeod, M. J. Ratain, L. N. Shulman, M. D. Ritchie, R. M. Plenge, J. S. Witte, D. L. Kroetz, The pharmacogenomics journal, 2014 Feb 11, PMID: 24513692,