Paula Bray

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Andrea Cortese, Yi Zhu, Adriana Rebelo et al. · Nature Genetics · 2020 · 170 citations · Full text

Biallelic Mutations, Somatic Variant, Genetic Disorder +9

Genomic instability in the type II TGF-beta1 receptor gene in atherosclerotic and restenotic vascular cells.

T A McCaffrey, Seth Consigli, Péter M. Szabó et al. · Journal of Clinical Investigation · 1997 · 168 citations · Full text

Vascular Disease, Wound Repair, Genetics +17

Phenotypic Variability of Childhood Charcot-Marie-Tooth Disease

Kayla Cornett, Manoj P. Menezes, Paula Bray et al. · JAMA Neurology · 2016 · 95 citations · Full text

Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study

Menelaos Pipis, Shawna Feely, James M. Polke et al. · Brain · 2020 · 87 citations · Full text

p75NTR Mediates Neurotrophin-Induced Apoptosis of Vascular Smooth Muscle Cells

Shiyang Wang, Paula Bray, Timothy A. McCaffrey et al. · American Journal Of Pathology · 2000 · 81 citations · Full text

Molecular Physiology, Apoptosis, Physiology +6