Katrina Prescott - Concepedia

Author

Katrina Prescott

Also Known As

Abhijit Dixit, Alison Kraus, I. Karen Temple, K E Prescott, K Prescott, K. Prescott, Katrina E. Prescott, Katrina Prescott, Nathalie Boddaert, Nicola Ragge

Publications

5.5K

Citations

H-Index

Concepts

All Affiliations

Chapel Allerton Hospital University College London Leeds Teaching Hospitals NHS Trust Wellcome Sanger Institute University of Liverpool

About

Katrina Prescott is an author at Chapel Allerton Hospital specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	17	1K
2	Public Health	3	3	240
3	Social Sciences	2	2	154
4	Anatomy	2	2	180
5	Biostatistics	1	1	159

Katrina Prescott

Publications

2.9K

Citations

H-Index

Page 1

	Year	Citations
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study Jenny Lord, Dominic McMullan, Ruth Y. Eberhardt, The Lancet	2019	694
<i>DICER1</i> syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome I. Slade, Chiara Bacchelli, H. Davies, Journal of Medical Genetics	2011	361
Genetic heterogeneity in Cornelia de Lange syndrome (CdLS) and CdLS-like phenotypes with observed and predicted levels of mosaicism Morad Ansari, Gemma Poke, Quentin R. V. Ferry, Journal of Medical Genetics	2014	165
Discriminating Power of Localized Three-Dimensional Facial Morphology Peter Hammond, Tim J. Hutton, Judith Allanson, The American Journal of Human Genetics Geometric ModelingFacial Recognition SystemFacial AnimationBiometricsMorphology	2005	159
Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study Lord J, McMullan DJ, Eberhardt RY, Yearbook of pediatric endocrinology GeneticsGenetic EpidemiologyDiagnosisGynecologyFetal Medicine	2019	155
Great vessel development requires biallelic expression of Chd7 and Tbx1 in pharyngeal ectoderm in mice Victoria Randall, Karen McCue, Catherine Roberts, Journal of Clinical Investigation	2009	149
Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness Isabelle Audo, Kinga M. Bujakowska, Elise Orhan, The American Journal of Human Genetics Ocular DiseaseDevelopmental BiologyMendelian DisorderOphthalmologyGenetic Disorder	2012	132
Identification of the First ATRIP–Deficient Patient and Novel Mutations in ATR Define a Clinical Spectrum for ATR–ATRIP Seckel Syndrome Tomoo Ogi, Sarah Walker, Tom Stiff, PLoS Genetics	2012	112
Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy Anne O’Donnell‐Luria, Lynn Pais, Víctor Faúndes, The American Journal of Human Genetics Neurodevelopmental DisordersDevelopmental BiologyHeterozygous VariantsKmt2e CauseGenetics	2019	97
Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome Josephina Meester, Laura Southgate, Anna-Barbara Stittrich, The American Journal of Human Genetics Developmental AnomalyMendelian DisorderGenetic DisorderGeneticsPathogenesis	2015	89

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