Kathleen A. Williamson

Author

Also Known As

Alex Richter, Amanda Symmonds, Claire Cormie, Eva Serra, Hywel J. Williams, Jing, Jenny W., Joanna Warwick-Dugdale, K A Williamson, K Williamson, K. A. Williamson

Publications

10.7K

Citations

H-Index

Concepts

All Affiliations

University of Edinburgh University College London Western General Hospital Institute of Genetics and Cancer University of Oxford

About

Kathleen A. Williamson is an author at University of Edinburgh specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	18	1.7K
2	Public Health	4	4	335
3	Social Sciences	4	4	459
4	Biology	2	2	245
5	Natural Sciences	1	1	15

Kathleen A. Williamson

Publications

5.5K

Citations

H-Index

Page 1

	Year	Citations
SARS-CoV-2 Omicron is an immune escape variant with an altered cell entry pathway Brian J. Willett, Joe Grove, Oscar A. MacLean, Nature Microbiology	2022	701
Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7 Bo Meng, Steven A. Kemp, Guido Papa, Cell Reports	2021	446
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel Jie Huang, Bryan Howie, Shane McCarthy, Nature Communications	2015	374
Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations Nicola Ragge, Alison G. M. Brown, Charlotte M. Poloschek, The American Journal of Human Genetics Ocular DiseaseOphthalmologyGeneticsOcular PathologyMedicine	2005	309
The UK10K project identifies rare variants in health and disease Klaudia Walter, Josine L. Min, Jie Huang, Kölner Universitäts PublikationsServer (Universität zu Köln)	2015	299
PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humans Sanjay M. Sisodiya, S. L. Free, Kathleen A. Williamson, Nature Genetics Neurobiology Of DiseaseMolecular NeuroscienceNeurophysiologyNeuroanatomyBrain Development	2001	236
<i>SOX2</i> anophthalmia syndrome Nicola Ragge, Birgit Lorenz, Adele Schneider, American Journal of Medical Genetics Part A	2005	225
Mutations in SOX2 cause anophthalmia-esophageal-genital (AEG) syndrome Kathleen A. Williamson, Ann Hever, Joe Rainger, Human Molecular Genetics	2006	221
Detailed Ophthalmologic Evaluation of 43 Individuals with<i>PAX6</i>Mutations Melanie Hingorani, Kathleen A. Williamson, Anthony T. Moore, Investigative Ophthalmology & Visual Science	2009	189
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

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