Sally Feather

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and <i>KCNJ10</i> Mutations

Detlef Böckenhauer, Sally Feather, Horia Stanescu et al. · New England Journal of Medicine · 2009 · 580 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Identification of the Gene for Oral-Facial-Digital Type I Syndrome

Maria Immacolata Ferrante, Sally Feather, Alessandro Bulfone et al. · The American Journal of Human Genetics · 2001 · 351 citations · Full text

Dentistry, Craniofacial Biology, Human Genetics +4

Genomic and clinical profiling of a national nephrotic syndrome cohort advocates a precision medicine approach to disease management

Agnieszka Bierżyńska, Hugh J. McCarthy, Katrina Soderquest et al. · Kidney International · 2017 · 288 citations · Full text

Medicine, Molecular Genetics, Nephrology +14

Mineral Metabolism and Vascular Damage in Children on Dialysis

Rukshana Shroff, Ann E. Donald, Melanie P. Hiorns et al. · Journal of the American Society of Nephrology · 2007 · 222 citations

Medicine, Nephrology, Pediatrics +14

Disruption of ROBO2 Is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux

Albertien M. van Eerde, Xueping Fan, Fabiola Quintero‐Rivera et al. · The American Journal of Human Genetics · 2007 · 214 citations · Full text

Medicine, Clinical Sciences, Urology +10