Holly K. Tabor, Ph.D.

Affiliations: 
Stanford University, Palo Alto, CA 
Google:
"Holly Tabor"
Mean distance: 16440.9
 

Parents

Sign in to add mentor
Richard Morris Myers grad student 2002 Stanford
 (Candidate gene approaches for studying the genetics of complex traits.)
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.

Green RC, Goddard KA, Jarvik GP, et al. (2016) Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. American Journal of Human Genetics. 99: 246
Green RC, Goddard KA, Jarvik GP, et al. (2016) Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. American Journal of Human Genetics
Nelson SC, Crouch JM, Bamshad MJ, et al. (2016) Use of metaphors about exome and whole genome sequencing. American Journal of Medical Genetics. Part A
Brothers KB, Holm IA, Childerhose JE, et al. (2015) When Participants in Genomic Research Grow Up: Contact and Consent at the Age of Majority. The Journal of Pediatrics
Emond MJ, Louie T, Emerson J, et al. (2015) Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis. Plos Genetics. 11: e1005273
Chong JX, Burrage LC, Beck AE, et al. (2015) Autosomal-Dominant Multiple Pterygium Syndrome Is Caused by Mutations in MYH3. American Journal of Human Genetics. 96: 841-9
Chong JX, McMillin MJ, Shively KM, et al. (2015) De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay. American Journal of Human Genetics. 96: 462-73
Amendola LM, Dorschner MO, Robertson PD, et al. (2015) Actionable exomic incidental findings in 6503 participants: challenges of variant classification. Genome Research. 25: 305-15
Delgado F, Tabor HK, Chow PM, et al. (2015) Single-nucleotide polymorphism arrays and unexpected consanguinity: considerations for clinicians when returning results to families. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 400-4
Crouch J, Yu JH, Shankar AG, et al. (2015) "We don't know her history, her background": adoptive parents' perspectives on whole genome sequencing results. Journal of Genetic Counseling. 24: 67-77
See more...