Mary-Claire King, PhD

Affiliations: 
1976-1995 Genetics University of California, Berkeley, Berkeley, CA, United States 
 1995- Medical genetics University of Washington, Seattle, Seattle, WA 
Area:
inherited predisposition to breast and ovarian cancer
Website:
http://depts.washington.edu/medgen/faculty/Mary-Claire_King.shtml
Google:
"Mary-Claire King"
Bio:

http://www.bcrfcure.org/qa-dr-mary-claire-king
https://en.wikipedia.org/wiki/Mary-Claire_King

Cross-listing: GenetiTree

Parents

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Allan C. Wilson grad student 1972 UC Berkeley
 (Protein polymorphisms in chimpanzee and human evolution)
Nicholas L. Petrakis post-doc 1974-1976 UCSF School of Medicine (GenetiTree)

Collaborators

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Dan J Stein collaborator (Neurotree)
BETA: Related publications

Publications

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McClellan JM, Zoghbi AW, Buxbaum JD, et al. (2023) An evolutionary perspective on complex neuropsychiatric disease. Neuron
Aburayyan A, Carlson RJ, Rabie GN, et al. (2023) Low level of GOSR2 translation from a non-AUG start codon in a family with profound hearing loss. Human Molecular Genetics
Carlson RJ, Walsh T, Mandell JB, et al. (2023) Association of Genetic Diagnoses of Childhood-Onset Hearing Loss With Cochlear Implant Outcomes. Jama Otolaryngology-- Head & Neck Surgery
Yechieli M, Gulsuner S, Ben-Pazi H, et al. (2021) Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy. Journal of Medical Genetics
Carlson RJ, Quesnel A, Wells D, et al. (2021) Genetic Heterogeneity and Core Clinical Features of NOG-Related-Symphalangism Spectrum Disorder. Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology
Baxter SK, Walsh T, Casadei S, et al. (2021) Molecular diagnosis of childhood immune dysregulation, polyendocrinopathy and enteropathy, and implications for clinical management. The Journal of Allergy and Clinical Immunology
Feurstein S, Churpek JE, Walsh T, et al. (2021) Germline variants drive myelodysplastic syndrome in young adults. Leukemia
Walsh T, Gulsuner S, Lee MK, et al. (2021) Inherited predisposition to breast cancer in the Carolina Breast Cancer Study. Npj Breast Cancer. 7: 6
Brownstein Z, Gulsuner S, Walsh T, et al. (2020) Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1. Clinical Genetics. 98: 353-364
Walsh T, Casadei S, Munson KM, et al. (2020) CRISPR-Cas9/long-read sequencing approach to identify cryptic mutations in and other tumour suppressor genes. Journal of Medical Genetics
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