Peter H Byers (P H Byers, Peter Byers)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2023
Publications (10 Years): 6

Top Topics

Intellectual Disability

Dna Methylation

Top Venues

American journal of medical genetics. Part A

Genetics in medicine : official journal of the American College of Medical Genetics

Journal of the American Heart Association

This page only lists publications with an associated author ORCID identifier.

Publications

Sara B Stephens, Sherene Shalhub, Nicholas Dodd, Jesse Li, Michael Huang, Seitaro Oda, Kalyan Kancherla, Tam T Doan, Siddharth K Prakash, Justin D Weigand, Federico M Asch, Taylor Beecroft, Alana C Cecchi, Teniola Shittu, Liliana Preiss, Scott A LeMaire, Richard B Devereux, Reed E Pyeritz, Kathryn W Holmes, Mary J Roman, Ronald V Lacro, Ralph V Shohet, Rajesh Krishnamurthy, Kim Eagle, Peter H Byers, Dianna M Milewicz, Shaine Alaine Morris
Vertebral Tortuosity Is Associated With Increased Rate of Cardiovascular Events in Vascular Ehlers-Danlos Syndrome. Journal of the American Heart Association (2023)
Johannes Zschocke, Peter H Byers, Andrew O M Wilkie
Mendelian inheritance revisited: dominance and recessiveness in medical genetics. Nature reviews. Genetics (2023)
Majd Marrache, Peter H Byers, Paul D Sponseller
Orthopaedic Conditions Associated with Aneurysms. JBJS reviews 8 (6) (2021)
Keren Machol, Trevor D Hadley, Jake Schmidt, David Cuthbertson, Henri Traboulsi, Rodrigo C Silva, Chloe Citron, Sobiah Khan, Kate Citron, Erin Carter, Kenneth Brookler, Jay R Shapiro, Robert D Steiner, Peter H Byers, Francis H Glorieux, Michaela Durigova, Peter Smith, Michael B Bober, Vernon R Sutton, Brendan H Lee, null null, Sandesh C S Nagamani, Cathleen Raggio
Hearing loss in individuals with osteogenesis imperfecta in North America: Results from a multicenter study. American journal of medical genetics. Part A 182 (4) (2019)
Ulrike Schwarze, Tim Cundy, Yajuan J Liu, Paul L Hofman, Peter H Byers
Compound heterozygosity for a frameshift mutation and an upstream deletion that reduces expression of SERPINH1 in siblings with a moderate form of osteogenesis imperfecta. American journal of medical genetics. Part A 179 (8) (2019)
Peter H Byers, John Belmont, James Black, Julie De Backer, Michael Frank, Xavier Jeunemaitre, Diana Johnson, Melanie Pepin, Leema Robert, Lynn Sanders, Nigel Wheeldon
Diagnosis, natural history, and management in vascular Ehlers-Danlos syndrome. American journal of medical genetics. Part C, Seminars in medical genetics 175 (1) (2017)
S Bellur, M Jain, D Cuthbertson, D Krakow, J R Shapiro, Robert D Steiner, P A Smith, Michael B Bober, T Hart, J Krischer, M Mullins, Peter H Byers, Melanie G Pepin, M Durigova, F H Glorieux, F Rauch, V R Sutton, B Lee, null null, S C Nagamani
Cesarean delivery is not associated with decreased at-birth fracture rates in osteogenesis imperfecta. Genetics in medicine : official journal of the American College of Medical Genetics 18 (6) (2015)
Melanie G Pepin, Mitzi L Murray, Samuel Bailey, Dru Leistritz-Kessler, Ulrike Schwarze, Peter H Byers
The challenge of comprehensive and consistent sequence variant interpretation between clinical laboratories. Genetics in medicine : official journal of the American College of Medical Genetics 18 (1) (2015)