Tamieka Whyte

Publications by Year

Research Areas

Muscle Physiology and Disorders, Cellular transport and secretion, Neurogenetic and Muscular Disorders Research, Genetic Associations and Epidemiology, Mitochondrial Function and Pathology

Most-Cited Works

• → Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signaling(2013)367 cited
• → SGK196 Is a Glycosylation-Specific O -Mannose Kinase Required for Dystroglycan Function(2013)216 cited
• → Mutations in INPP5K , Encoding a Phosphoinositide 5-Phosphatase, Cause Congenital Muscular Dystrophy with Cataracts and Mild Cognitive Impairment(2017)73 cited
• → Bi-allelic mutations in MYL1 cause a severe congenital myopathy(2018)48 cited
• → ECEL1 gene related contractural syndrome: Long-term follow-up and update on clinical and pathological aspects(2018)14 cited
• → G.P.154(2014)2 cited
• → A.P.11(2014)1 cited
• → P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling(2014)
• → P75 Exome sequencing identifies EPG5 mutations in two siblings with a childhood onset vacuolar myopathy(2014)