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Yuh Nung Jan grad student 1989-1995 UCSF
 (Cell-cell Signaling During Drosophila Neurogenesis and Wing Development.)
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van der Sluijs PJ, Alders M, Dingemans AJM, et al. (2021) A Case Series of Familial Variants Illustrating Variable Expression and Suggestions to Update the ACMG Criteria. Genes. 12
Tully HM, Doherty D, Wainwright M. (2021) Mortality in pediatric hydrocephalus. Developmental Medicine and Child Neurology
Miller DE, Sulovari A, Wang T, et al. (2021) Targeted long-read sequencing identifies missing disease-causing variation. American Journal of Human Genetics
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
Vegas N, Low K, Mak CCY, et al. (2020) Reply: MN1 gene loss-of-function mutation causes cleft palate in a pedigree. Brain : a Journal of Neurology
Cao J, O'Day DR, Pliner HA, et al. (2020) A human cell atlas of fetal gene expression. Science (New York, N.Y.). 370
Domcke S, Hill AJ, Daza RM, et al. (2020) A human cell atlas of fetal chromatin accessibility. Science (New York, N.Y.). 370
Epting D, Senaratne LDS, Ott E, et al. (2020) Loss of CBY1 results in a ciliopathy characterized by features of Joubert syndrome. Human Mutation
Latour BL, Van De Weghe JC, Rusterholz TD, et al. (2020) Dysfunction of the ciliary ARMC9/TOGARAM1 protein module causes Joubert syndrome. The Journal of Clinical Investigation
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