Richard P. Lifton

Affiliations: 
Harvard Medical School, Boston, MA, United States 
 1993- Yale University, New Haven, CT 
Area:
Genetics, Human Development, Pathology
Google:
"Richard Lifton"
Cross-listing: FlyTree

Parents

Sign in to add mentor
David S. Hogness grad student 1986 Stanford (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)
BETA: Related publications

Publications

You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect.

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
See more...