
Eimear E Kenny, PhD
About Me
Dr. Eimear Kenny, PhD, is a Professor of Medicine and Genetics, and the Founding Director of the Institute for Genomic Health. She leads research at the interface of genomics, medicine, and computer science. She uses data science and massive-scale databases of genomic information to improve human health. Her research spans several different areas, including population and statistical genetics; machine-learning approaches for genomic discovery for rare and common diseases; genomic risk prediction for preventive health; clinical trials in genomic medicine; and digital app development for precision medicine. Her goal is to lead a new paradigm for genomic research embedded in health systems and to enable genomic medicine on a global scale. She is a scientific advisor to many initiatives in government, non-profit and industry arenas.
Language
English
Position
DIRECTOR, INSTITUTE FOR GENOMIC HEALTH, PROFESSOR | Medicine, General Internal Medicine, PROFESSOR | Genetics and Genomic Sciences
Research Topics
Genetics, Genomics
Multi-Disciplinary Training Areas
Disease Mechanisms and Therapeutics (DMT), Neuroscience [NEU]
Video
Education
BSc, Trinity College Dublin
MSc, University of Leeds
PhD, Rockefeller University
Post-doc, Stanford University
Publications
Selected Publications
- Healthcare professionals’ experiences returning monogenic, polygenic, and integrated risk results in the eMERGE study. Sabrina A. Suckiel, Laura Golfinopoulos, Courtney L. Scherr, Brenna M. Boyd, Wendy K. Chung, Hakon Hakonarson, Ingrid A. Holm, Iftikhar J. Kullo, Nita A. Limdi, Michael F. Murray, Melanie F. Myers, Cynthia A. Prows, Maya Sabatello, Georgia L. Wiesner, Eimear E. Kenny, Noura S. Abul-Husn. Human Genetics and Genomics Advances
- Prediction and characterization of genetically regulated expression of asthma tissues from African-ancestry populations. Sarah D. Slack, Erika Esquinca, Christopher H. Arehart, Meher Preethi Boorgula, Brooke Szczesny, Alex Romero, Monica Campbell, Sameer Chavan, Nicholas Rafaels, Harold Watson, R. Clive Landis, Nadia N. Hansel, Charles N. Rotimi, Christopher O. Olopade, Camila A. Figueiredo, Carole Ober, Andrew H. Liu, Eimear E. Kenny, Kai Kammers, Ingo Ruczinski, Margaret A. Taub, Michelle Daya, Christopher R. Gignoux, Katerina Kechris, Kathleen C. Barnes, Rasika A. Mathias, Randi K. Johnson. Journal of Allergy and Clinical Immunology
- cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions. Eric Van Buren, Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou, Nicholette D. Palmer, Donna K. Arnett, John Blangero, Eric Boerwinkle, Brian E. Cade, Jenna C. Carlson, April P. Carson, Yii Der Ida Chen, Joanne Curran, Ravindranath Duggirala, Myriam Fornage, Nora Franceschini, Misa Graff, Charles Gu, Xiuqing Guo, Jiang He, Nancy Heard-Cosa, Lifang Hou, Yi Jen Hung, Rita R. Kalyani, Sharon L.R. Kardia, Eimear Kenny, Charles Kooperberg, Brian G. Kral, Leslie Lange, Dan Levy, Changwei Li, Simin Liu, Donald Lloyd-Jones, Ruth J.F. Loos, Ani W. Manichaikul, Lisa Warsinger Martin, Rasika Mathias, Ryan L. Minster, Braxton D. Mitchell, Josyf C. Mychaleckyj, Take Naseri, Kari North, Jeff O’Connell, James A. Perry, Patricia A. Peyser, Michael Preuss, Girish Nadkarni, Bruce Gelb. Nature Methods