Professor of Pathology, University Wash
Medical Genetics
Dr. Peter H. Byers, MD
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Peter Byers practices Medical Genetics. He researched medicine at Case Western Reserve University School of Medicine. He received 3 awards: "Regional Top Doctor", "Elected Member" and "Super Doctor". Peter H. Byers is a published doctor. He published 41 publications, including: 'A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromes.' Peter H. Byers is registered with Medicare.
Publications
- A homozygous B3GAT3 mutation causes a severe syndrome with multiple fractures, expanding the phenotype of linkeropathy syndromes.
- Vascular Ehlers-Danlos Syndrome in siblings with biallelic COL3A1 sequence variants and marked clinical variability in the extended family.
- Survival is affected by mutation type and molecular mechanism in vascular Ehlers-Danlos syndrome (EDS type IV).
- Pregnancy-related deaths and complications in women with vascular Ehlers-Danlos syndrome.
- 0041 Cross-sectional Multicenter Study of Osteogenesis Imperfecta in North America - Results from the Linked Clinical Research Centers.
- FKBP14-related Ehlers-Danlos syndrome: Expansion of the phenotype to include vascular complications.
- Allelic background of LEPRE1 mutations that cause recessive forms of osteogenesis imperfecta in different populations.
- Actionable, Pathogenic Incidental Findings in 1,000 Participants' Exomes.
- Ehlers-Danlos syndrome: A showcase of conditions that lead to understanding matrix biology.
- WNT1 Mutations in Families Affected by Moderately Severe and Progressive Recessive Osteogenesis Imperfecta.
- Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen.
- Heritable collagen disorders: the paradigm of the ehlers-danlos syndrome.
- Characterization of Tissue-Specific and Developmentally Regulated Alternative Splicing of Exon 64 in the COL5A1 Gene.
- EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta.
- COL3A1 haploinsufficiency results in a variety of Ehlers-Danlos syndrome type IV with delayed onset of complications and longer life expectancy.
- Recurrence of perinatal lethal osteogenesis imperfecta in sibships: parsing the risk between parental mosaicism for dominant mutations and autosomal recessive inherita...
- Mutations in the Gene Encoding the RER Protein FKBP65 Cause Autosomal-Recessive Osteogenesis Imperfecta.
- Homozygosity for a missense mutation in SERPINH1, which encodes the collagen chaperone protein HSP47, results in severe recessive osteogenesis imperfecta.
- Generalized connective tissue disease in Crtap-/- mouse.
- Molecular mechanisms of classical Ehlers-Danlos syndrome (EDS).
- The bicuspid aortic valve: an integrated phenotypic classification of leaflet morphology and aortic root shape.
- CRTAP and LEPRE1 mutations in recessive osteogenesis imperfecta.
- Defective C-propeptides of the proalpha2(I) chain of type I procollagen impede molecular assembly and result in osteogenesis imperfecta.
- Natural variation in four human collagen genes across an ethnically diverse population.
- Gene targeting of mutant COL1A2 alleles in mesenchymal stem cells from individuals with osteogenesis imperfecta.
- Type XXVII collagen at the transition of cartilage to bone during skeletogenesis.
- Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integ...
- Usefulness of bicuspid aortic valve phenotype to predict elastic properties of the ascending aorta.
- CRTAP is required for prolyl 3- hydroxylation and mutations cause recessive osteogenesis imperfecta.
- Aneurysm syndromes caused by mutations in the TGF-beta receptor.
- 2005 ASHG Presidential Address. If only we spoke the same language--we would have so much to discuss.
- 2005 ASHG Award for Excellence in Human Genetics Education. Introductory speech of Joseph D. McInerney.
- Bovine model of Marfan syndrome results from an amino acid change (c.3598G > A, p.E1200K) in a calcium-binding epidermal growth factor-like domain of fibrillin-1.
- Stability related bias in residues replacing glycines within the collagen triple helix (Gly-Xaa-Yaa) in inherited connective tissue disorders.
- Determination of the molecular basis of Marfan syndrome: a growth industry.
- Rare autosomal recessive cardiac valvular form of Ehlers-Danlos syndrome results from mutations in the COL1A2 gene that activate the nonsense-mediated RNA decay pathway.
- Gene targeting in stem cells from individuals with osteogenesis imperfecta.
- Order of intron removal influences multiple splice outcomes, including a two-exon skip, in a COL5A1 acceptor-site mutation that results in abnormal pro-alpha1(V) N-pro...
- Spontaneous direct carotid-cavernous fistula in Ehlers-Danlos syndrome type IV: two case reports and a review of the literature.
- Killing the messenger: new insights into nonsense-mediated mRNA decay.
Schools
Case Western Reserve University School of Medicine
University of Washington
Doctors Specialties
- Clinical Genetics
- Internal Medicine
- Medical Genetics
Accepted Insurances
- Blue Card PPO
- Cigna HMO
- Cigna PPO
- Great West Healthcare-Cigna PPO
- Open Access Plus
- Commercial Insurance Company
- First Choice Health PPO
- Group Health Cooperative
- Connect
- Medicaid
- Medicare MCR
- ODS Health Plan
- Heritage Plus
- Heritage Signature
- Providence Health Plans
- Preferred Provider Network PPN
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
Awards
- Regional Top Doctor
- Elected Member
- Super Doctor
Education
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UCSF -
Case Western Reserve University School of Medicine
Hospital
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Seattle Children's Hospital -
University of Washington Medical Center
Drug Facts
| NPI NUMBER | 1477796936 | |
| NPPES Provider LastName | BYERS | |
| NPPES Provider FirstName | PETER | |
| NPPES Provider ZIPCode | 235071999 | |
| NPPES Provider State | VA | |
| Specialty Description | Emergency Medicine | |
| Total Claim Count | 194.0 | |
| Distinct Opioid Count | 2.0 | |
| Opioid Claim Count | 56.0 | |
| Percent Opioid Claims | 28.87 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1477796936 |
| Last Name Of The Provider | BYERS |
| First Name Of The Provider | PETER |
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