Sally Feather - Concepedia

Author

Sally Feather

University College London

Also Known As

S A Feather, S Feather, S. A. Feather, S. Feather, Sally A. Feather, Sally FEATHER, Sally Feather, Sally A. Feather

Publications

3.3K

Citations

H-Index

Concepts

All Affiliations

University College London St James's University Hospital Great Ormond Street Hospital Institute of Child Health Leeds Teaching Hospitals NHS Trust

About

Sally Feather is an author at University College London specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	17	2K
2	Public Health	2	2	291
3	Engineering	1	1	61
4	Health Sciences	1	1	221
5	Social Sciences	1	1	80

Sally Feather

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, and <i>KCNJ10</i> Mutations Detlef Böckenhauer, Sally Feather, Horia Stanescu, New England Journal of Medicine	2009	568
Identification of the Gene for Oral-Facial-Digital Type I Syndrome Maria Immacolata Ferrante, Sally Feather, Alessandro Bulfone, The American Journal of Human Genetics Genetic DisorderOral CavityGeneticsPathogenesisGenetic Epidemiology	2001	348
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, Kidney International GlomerulonephritisUrologyRenal DiseasePrecision Medicine ApproachKidney Research	2017	274
Mineral Metabolism and Vascular Damage in Children on Dialysis Rukshana Shroff, Ann E. Donald, Melanie P. Hiorns, Journal of the American Society of Nephrology NutritionHypertensionDialysisIntact Parathyroid HormoneDialysis Therapy	2007	221
Disruption of ROBO2 Is Associated with Urinary Tract Anomalies and Confers Risk of Vesicoureteral Reflux Albertien M. van Eerde, Xueping Fan, Fabiola Quintero‐Rivera, The American Journal of Human Genetics Urinary Tract AnomaliesUrological ResearchUrologyVoiding DysfunctionMedicine	2007	213
OFD1 Is a Centrosomal/Basal Body Protein Expressed during Mesenchymal-Epithelial Transition in Human Nephrogenesis Leila Romio, Andrew M. Fry, Paul J.D. Winyard, Journal of the American Society of Nephrology Ofd1 LocalizationCytoskeletonCell CycleMesenchymal-epithelial TransitionCellular Physiology	2004	178
Simultaneous Sequencing of 24 Genes Associated with Steroid-Resistant Nephrotic Syndrome Hugh J. McCarthy, Agnieszka Bierżyńska, M. Wherlock, Clinical Journal of the American Society of Nephrology	2013	172
Primary, Nonsyndromic Vesicoureteric Reflux and Its Nephropathy Is Genetically Heterogeneous, with a Locus on Chromosome 1 Sally Feather, Sue Malcolm, Adrian S. Woolf, The American Journal of Human Genetics UrologyGenetic DisorderGeneticsRenal PathologyPathology	2000	132
De Novo Uroplakin IIIa Heterozygous Mutations Cause Human Renal Adysplasia Leading to Severe Kidney Failure Dagan Jenkins, Maria Bitner‐Glindzicz, Sue Malcolm, Journal of the American Society of Nephrology UrologyRenal FunctionMendelian DisorderGenetic DisorderMedicine	2005	125
The oral-facial-digital syndrome type 1 (OFD1), a cause of polycystic kidney disease and associated malformations, maps to Xp22.2-Xp22.3 Sally Feather Human Molecular Genetics	1997	104

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