☰

Dan Doherty, MD PhD

Affiliations: 
University of Washington, Seattle Childrens Research Institute 
Website:
https://www.seattlechildrens.org/directory/daniel-a-doherty/
Google:
"Dan Doherty"
Bio:

http://physio.ucsf.edu/Jan/Symposium2016.html
https://books.google.com/books?id=QlTw46sdK9UC

Mean distance: 14.75 (cluster 23)
 		SNBCP
Tree Publications Grants Similar researchers Related pubs Distance to... Nearest Nobel PubMed Report error

Parents

Sign in to add mentor
Yuh Nung Jan grad student 1989-1995 UCSF
 (Cell-cell Signaling During Drosophila Neurogenesis and Wing Development.)

Children

Sign in to add trainee

Collaborators

Sign in to add collaborator
Kathleen Millen collaborator University of Chicago, University of Washington, Seattle Children's Research Institute
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.

Alghadeer A, Hanson-Drury S, Patni AP, et al. (2023) Single-cell census of human tooth development enables generation of human enamel. Developmental Cell
Serpieri V, Mortarini G, Loucks H, et al. (2023) Recurrent, founder and hypomorphic variants contribute to the genetic landscape of Joubert syndrome. Journal of Medical Genetics
Penon-Portmann M, Eldomery MK, Potocki L, et al. (2022) De novo heterozygous variants in SLC30A7 are a candidate cause for Joubert syndrome. American Journal of Medical Genetics. Part A
Van De Weghe JC, Gomez A, Doherty D. (2022) The Joubert-Meckel-Nephronophthisis Spectrum of Ciliopathies. Annual Review of Genomics and Human Genetics
van der Sluijs PJ, Joosten M, Alby C, et al. (2022) Discovering a new part of the phenotypic spectrum of Coffin-Siris syndrome in a fetal cohort. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Serpieri V, D'Abrusco F, Dempsey JC, et al. (2021) haploinsufficiency causes a recognisable neurodevelopmental phenotype at the mild end of the Joubert syndrome spectrum. Journal of Medical Genetics
Inskeep KA, Zarate YA, Monteil D, et al. (2021) Genetic and phenotypic heterogeneity in KIAA0753-related ciliopathies. American Journal of Medical Genetics. Part A
Aldinger KA, Thomson Z, Phelps IG, et al. (2021) Spatial and cell type transcriptional landscape of human cerebellar development. Nature Neuroscience
Van De Weghe JC, Giordano JL, Mathijssen IB, et al. (2021) TMEM218 dysfunction causes ciliopathies, including Joubert and Meckel syndromes. Hgg Advances. 2
Epting D, Senaratne LDS, Ott E, et al. (2020) Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome. Human Mutation
See more...