Parents
Sign in to add mentor| Marcus W. Feldman | grad student | 1994 | Stanford (Evolution Tree) |
| Andy Clark | post-doc | Penn State |
Children
Sign in to add trainee| Jim Wilson | grad student | (GenetiTree) | |
| David Emile Reich | grad student | 1999 | St. Catherine's College, Oxford University |
| Elizabeth T. Cirulli | grad student | 2010 | Duke |
| Kimberly E. Pelak | grad student | 2012 | Duke |
| Elizabeth T. Cirulli | post-doc | Duke University School of Medicine | |
| Xinchen Wang | post-doc | (Computational Biology Tree) |
Collaborators
Sign in to add collaborator| Stephen F. Traynelis | collaborator | Institute for Genomic Medicine, Columbia University (Neurotree) |
BETA: Related publications
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Publications
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| Butler-Laporte G, Povysil G, Kosmicki JA, et al. (2022) Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. Plos Genetics. 18: e1010367 |
| Zoghbi AW, Dhindsa RS, Goldberg TE, et al. (2021) High-impact rare genetic variants in severe schizophrenia. Proceedings of the National Academy of Sciences of the United States of America. 118 |
| Nickols NG, Goetz MB, Graber CJ, et al. (2021) Hormonal intervention for the treatment of veterans with COVID-19 requiring hospitalization (HITCH): a multicenter, phase 2 randomized controlled trial of best supportive care vs best supportive care plus degarelix: study protocol for a randomized controlled trial. Trials. 22: 431 |
| Kosmicki JA, Horowitz JE, Banerjee N, et al. (2021) Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. American Journal of Human Genetics |
| Amador A, Bostick CD, Olson H, et al. (2020) Modelling and treating GRIN2A developmental and epileptic encephalopathy in mice. Brain : a Journal of Neurology |
| Desch K, Ozel AB, Halvorsen M, et al. (2020) Whole exome sequencing identifies rare variants in STAB2 associated with venous thromboembolic disease. Blood |
| McNamara MG, Lopes A, Wasan H, et al. (2020) Landmark survival analysis and impact of anatomic origin in prospective clinical trials of biliary tract cancer. Journal of Hepatology |
| Kokkinos J, Ignacio RMC, Sharbeen G, et al. (2020) Targeting the undruggable in pancreatic cancer using nano-based gene silencing drugs. Biomaterials. 240: 119742 |
| Wang X, Goldstein DB. (2020) Enhancer Domains Predict Gene Pathogenicity and Inform Gene Discovery in Complex Disease. American Journal of Human Genetics. 106: 215-233 |
| Gelfman S, Dugger SA, Araujo Martins Moreno C, et al. (2019) A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS. Genome Research |