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Office
1959 NE Pacific St
Seattle, WA 98195Phone+1 206-598-4030Fax+1 206-616-1899
Education & Training
- University of Washington School of MedicinePost-Doctoral Fellowship, 1974 - 1977
- NIH Clinical CenterPost-Doctoral Fellowship, 1971 - 1974
- University of California (San Francisco)Residency, Internal Medicine, 1969 - 1971
- Case Western Reserve University School of MedicineClass of 1969
Certifications & Licensure
- CA State Medical License 1970 - Present
- WA State Medical License 1976 - 2025
- IL State Medical License 2003 - 2023
- OR State Medical License 2020 - 2022
- TX State Medical License 2019 - 2019
- GA State Medical License 2017 - 2018
- American Board of Internal Medicine Internal Medicine
- American Board of Medical Genetics and Genomics Clinical Genetics
Awards, Honors, & Recognition
- Regional Top Doctor Castle Connolly, 2014
- Elected Member The American Society for Clinical Investigation, 1985
- Super Doctor SuperDoctors.com
Publications & Presentations
PubMed
- 43 citationsA homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromesKelly L. Jones, Ulrike Schwarze, Margaret P Adam, Peter H. Byers, Heather C Mefford
American Journal of Medical Genetics. Part A. 2015-11-01 - 2 citationsTrue radial artery aneurysm in a patient with somatic mosaicism for a mutation in platelet-derived growth factor receptor β gene.Sherene Shalhub, Lisa Hysa, Peter H. Byers, Mark H. Meissner, Manuel Ferreira
Journal of Vascular Surgery Cases and Innovative Techniques. 2021-02-26 - 227 citationsOsteogenesis imperfecta: translation of mutation to phenotype.Peter H. Byers, G A Wallis, Marcia C. Willing
Journal of Medical Genetics. 1991-07-01
Journal Articles
- Heterozygous WNT1 Variant Causing a Variable Bone PhenotypePeter H Byers, Lynne M Bird, Brendan H Lee, American Journal of Medical Genetics Part A
Press Mentions
- New Aytu Advisory Board Working to Advance AR101 for vEDSSeptember 13th, 2021
- Aytu BioPharma Announces Formation of New Scientific Advisory Board to Support Development of AR101 for Vascular Ehlers-Danlos SyndromeSeptember 9th, 2021
Grant Support
- The Challenges Of Autosomal Recessive And Other New Forms Of OINational Institute Of Arthritis And Musculoskeletal And Skin Diseases2008
- New Research Strategies In Osteogenesis ImperfectaNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2006
- Molecular Basis Of Osteogenesis ImperfectaNational Institute Of Arthritis And Musculoskeletal And Skin Diseases1992–2005
- Mild Ol - Toward Better Understanding And TreatmentNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2004
- Gordon Research Conferences: Collagen 2003, 2005, 2007National Institute Of Arthritis And Musculoskeletal And Skin Diseases2003
- Identification And Expression Of Skin Specific GenesNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2001–2002
- Sixth International Marfan Syndrome SymposiumNational Institute Of Arthritis And Musculoskeletal And Skin Diseases2001
- Gordon Research Conferences: Collagen 2001, 2003, 2005National Institute Of Arthritis And Musculoskeletal And Skin Diseases2001
- Molecular Basis Of Ehlers-Danlos SyndromeNational Institute Of Arthritis And Musculoskeletal And Skin Diseases1996–2001
- Medical Genetics Postdoctoral FellowshipNational Institute Of General Medical Sciences1999
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