Eric Lander, Ph.D.
Affiliations: | 1986-2004 | Whitehead Institute, Cambridge, MA, United States | |
| 2004- | Broad Institute, Cambridge, MA, United States |
Area:
Human genomeWebsite:
https://biology.mit.edu/people/eric_lander#overviewGoogle:
"Eric Lander"Bio:
Eric Steven Lander (born February 3, 1957), a mathematician and geneticist, is a Professor of Biology at the Massachusetts Institute of Technology (MIT), former member of the Whitehead Institute, and founding director of the Broad Institute of MIT and Harvard who has devoted his career to realizing the promise of the human genome for medicine. [https://en.wikipedia.org/wiki/Eric_Lander]
Cross-listing: GenetiTree
Parents
Sign in to add mentor| Peter Cameron | grad student | 1978-1980 | Oxford | |
| (Topics in algebraic coding theory) | ||||
Children
Sign in to add trainee| David Altshuler | grad student | Whitehead Institute for Biomedical Research (MIT) (Neurotree) | |
| Mark J. Daly | grad student | (Evolution Tree) | |
| Kenro Kusumi | grad student | 1990-1997 | MIT (Evolution Tree) |
| Manolis Kellis | grad student | 2000-2003 | MIT (Computational Biology Tree) |
| Bradley E. Bernstein | post-doc | MIT (Cell Biology Tree) | |
| Howard J. Jacob | post-doc | MIT (Cell Biology Tree) | |
| Leonid Kruglyak | post-doc | (FlyTree) | |
| Vamsi Mootha | post-doc | Whitehead Institute (Cell Biology Tree) | |
| Bruce Hamilton | post-doc | 1993-1998 | Whitehead Institute (Neurotree) |
Collaborators
Sign in to add collaborator| Michael S. Lawrence | collaborator | 2008- | Broad Institute (Cell Biology Tree) |
| Serge Batalov | collaborator | 2000-2004 | (GenetiTree) |
BETA: Related publications
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Publications
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| Gupta A, Martin-Rufino JD, Jones TR, et al. (2022) Inferring gene regulation from stochastic transcriptional variation across single cells at steady state. Proceedings of the National Academy of Sciences of the United States of America. 119: e2207392119 |
| Nasser J, Bergman DT, Fulco CP, et al. (2021) Genome-wide enhancer maps link risk variants to disease genes. Nature |
| Collins RL, Brand H, Karczewski KJ, et al. (2021) Author Correction: A structural variation reference for medical and population genetics. Nature |
| Sinnott-Armstrong N, Sousa IS, Laber S, et al. (2021) A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density. Cell Metabolism |
| Bick AG, Weinstock JS, Nandakumar SK, et al. (2020) Inherited causes of clonal haematopoiesis in 97,691 whole genomes. Nature |
| Collins RL, Brand H, Karczewski KJ, et al. (2020) A structural variation reference for medical and population genetics. Nature. 581: 444-451 |
| Abel HJ, Larson DE, Regier AA, et al. (2020) Mapping and characterization of structural variation in 17,795 human genomes. Nature |
| Vallabh SM, Minikel EV, Schreiber SL, et al. (2020) Towards a treatment for genetic prion disease: trials and biomarkers. The Lancet. Neurology. 19: 361-368 |
| Fulco CP, Nasser J, Jones TR, et al. (2019) Activity-by-contact model of enhancer-promoter regulation from thousands of CRISPR perturbations. Nature Genetics. 51: 1664-1669 |
| Bis JC, Jian X, Kunkle BW, et al. (2019) Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry |