Nedra Whitehead

Publication Activity (10 Years)

Years Active: 2019-2023
Publications (10 Years): 6

Top Topics

Muscular Dystrophy

Pulmonary Embolism

Intellectual Disability

Top Venues

Orphanet journal of rare diseases

Clinical, cosmetic and investigational dermatology

Journal of thrombosis and haemostasis : JTH

Neurology. Genetics

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

Publications

Nedra Whitehead, Stephen W Erickson, Bo Cai, Suzanne McDermott, Holly Peay, James F Howard, Lijing Ouyang, null null
Sources of variation in estimates of Duchenne and Becker muscular dystrophy prevalence in the United States. Orphanet journal of rare diseases 18 (1) (2023)
Peter B Kang, Magali Jorand-Fletcher, Wanfang Zhang, Suzanne W McDermott, Reba Berry, Chelsea Chambers, Kristen N Wong, Yara Mohamed, Shiny Thomas, Y Swamy Venkatesh, Christina Westfield, Nedra Whitehead, Nicholas E Johnson, null null
Genetic Patterns of Selected Muscular Dystrophies in the Muscular Dystrophy Surveillance, Tracking, and Research Network. Neurology. Genetics 9 (6) (2023)
Nedra Whitehead, Stephen W Erickson, Bo Cai, Suzanne McDermott, Holly Peay, James F Howard, Lijing Ouyang, null null
Sources of variation in estimates of Duchenne and Becker muscular dystrophy prevalence in the United States. Orphanet journal of rare diseases 18 (1) (2023)
Nedra Whitehead, Stephen W Erickson, Bo Cai, Suzanne McDermott, Holly Peay, James F Howard, Lijing Ouyang, null null
Sources of variation in estimates of Duchenne and Becker muscular dystrophy prevalence in the United States. Orphanet journal of rare diseases 18 (1) (2023)
Thomas L Ortel, Sreelatha Meleth, Diane Catellier, Mark Andrew Crowther, Doruk Erkan, Paul R Fortin, David Garcia, Nana Haywood, Andrzej S Kosinski, Steven R Levine, Michael J Phillips, Nedra Whitehead
Recurrent thrombosis in patients with antiphospholipid antibodies and an initial venous or arterial thromboembolic event: A systematic review and meta-analysis. Journal of thrombosis and haemostasis : JTH 18 (9) (2020)
Shaundra Eichstadt, Jean Y Tang, Daniel C Solis, Zurab Siprashvili, M Peter Marinkovich, Nedra Whitehead, Matthew Schu, Fang Fang, Stephen W Erickson, Mary E Ritchey, Max Colao, Kaye Spratt, Amir Shaygan, Mark J Ahn, Kavita Y Sarin
From Clinical Phenotype to Genotypic Modelling: Incidence and Prevalence of Recessive Dystrophic Epidermolysis Bullosa (RDEB). Clinical, cosmetic and investigational dermatology 12 (2019)