David Altshuler
Affiliations: | Harvard/MIT/Broad Institute, Cambridge, MA, United States |
Area:
human genetic variation and its application to diseaseWebsite:
http://www.broad.mit.edu/about/bios/bio-altshuler.htmlGoogle:
"David Altshuler"Mean distance: 14.92 (cluster 32) | S | N | B | C | P |
Parents
Sign in to add mentor| Constance L. Cepko | grad student | Harvard | |
| Eric Lander | grad student | Whitehead Institute for Biomedical Research (MIT) (MathTree) |
Children
Sign in to add trainee| Wendy M. Winckler | grad student | 2005 | Harvard |
| Jessica S. Alston | grad student | 2012 | Harvard |
| Vineeta Agarwala | grad student | 2013 | Harvard |
| Ben Tsuda | research scientist | 2013-2016 | Broad Institute (MIT/Harvard) |
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Publications
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| Costanzo MC, von Grotthuss M, Massung J, et al. (2023) The Type 2 Diabetes Knowledge Portal: An open access genetic resource dedicated to type 2 diabetes and related traits. Cell Metabolism |
| Flannick J, Mercader JM, Fuchsberger C, et al. (2019) Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls. Nature |
| Artomov M, Joseph V, Tiao G, et al. (2019) Case-control analysis identifies shared properties of rare germline variation in cancer predisposing genes. European Journal of Human Genetics : Ejhg |
| Gusarova V, O'Dushlaine C, Teslovich TM, et al. (2018) Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes. Nature Communications. 9: 2252 |
| Flannick J, Fuchsberger C, Mahajan A, et al. (2018) Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 5: 180002 |
| Jun G, Manning A, Almeida M, et al. (2017) Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees. Proceedings of the National Academy of Sciences of the United States of America |
| Jason F, Fuchsberger C, Mahajan A, et al. (2017) Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Scientific Data. 4: 170179 |
| Mercader JM, Liao RG, Davis A, et al. (2017) A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes. Diabetes |
| Rusu V, Hoch E, Mercader JM, et al. (2017) Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms. Cell. 170: 199-212.e20 |
| Scott RA, Scott LJ, Mägi R, et al. (2017) An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans. Diabetes |