Richard P. Lifton
Affiliations: | Harvard Medical School, Boston, MA, United States | ||
| 1993- | Yale University, New Haven, CT |
Area:
Genetics, Human Development, PathologyGoogle:
"Richard Lifton"Cross-listing: FlyTree
Children
Sign in to add trainee| Matthew W. State | grad student | Yale | |
| Lynn M. Boyden | grad student | 2001 | Yale |
| Keith A. Choate | grad student | 2001 | Yale |
| Karin E. Finberg | grad student | 2002 | Yale |
| Frederick H. Wilson | grad student | 2002 | Yale |
| Isabel E. Beerman | grad student | 2007 | Yale |
| Kristopher T. Kahle | grad student | 2007 | Yale |
| Catherine A. Brownstein | grad student | 2008 | Yale |
| Jia Nee Foo | grad student | 2009 | Yale |
| OrLando H. Yarborough | grad student | 2010 | Yale |
| Khalid A. Fakhro | grad student | 2011 | Yale |
| Gerald S. Goh | grad student | 2014 | Yale |
| Murim Choi | post-doc | 2007-2013 | Yale (Neurotree) |
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Publications
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| Gao E, Cheema H, Waheed N, et al. (2019) OSTα deficiency: A disorder with cholestasis, liver fibrosis and congenital diarrhea. Hepatology (Baltimore, Md.) |
| Boyden LM, Atzmony L, Hamilton C, et al. (2019) Recessive Mutations in AP1B1 Cause Ichthyosis, Deafness, and Photophobia. American Journal of Human Genetics |
| Allocco AA, Jin SC, Duy PQ, et al. (2019) Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in . Frontiers in Cellular Neuroscience. 13: 425 |
| Watanabe M, Zhang J, Mansuri MS, et al. (2019) Developmentally regulated KCC2 phosphorylation is essential for dynamic GABA-mediated inhibition and survival. Science Signaling. 12 |
| Esteghamat F, Broughton JS, Smith E, et al. (2019) CELA2A mutations predispose to early-onset atherosclerosis and metabolic syndrome and affect plasma insulin and platelet activation. Nature Genetics |
| Timberlake AT, Jin SC, Nelson-Williams C, et al. (2019) Mutations in and previously unimplicated genes of the BMP, Wnt, and Hedgehog pathways in syndromic craniosynostosis. Proceedings of the National Academy of Sciences of the United States of America |
| Ünlüsoy Aksu A, Das SK, Nelson-Williams C, et al. (2019) Recessive Mutations in Cause High Gamma-Glutamyltransferase Cholestasis. Hepatology Communications. 3: 471-477 |
| Duran D, Zeng X, Jin SC, et al. (2018) Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation. Neuron |
| Meyers N, Nelson-Williams C, Malaga-Dieguez L, et al. (2018) Hypokalemia Associated With a Claudin 10 Mutation: A Case Report. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation |
| Duchatelet S, Boyden LM, Ishida-Yamamoto A, et al. (2018) Mutations in PERP cause dominant and recessive keratoderma. The Journal of Investigative Dermatology |