Concepedia

Lionel Willatt

LW

Statistics

Publications

33

Citations

4.9K

H-Index

28

Active since

1991

Affiliations

Addenbrooke's Hospital(Current)

University of Cambridge

Wessex Regional Genetics Laboratory

Wellcome Sanger Institute

Salisbury District Hospital

Lionel Willatt is an author at Addenbrooke's Hospital specializing in life sciences, molecular genetics, and genetics.

Publications per year

1991–2011

33

Publications

33

Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes

Heather C. Mefford, Andrew J. Sharp, Carl Baker et al. · New England Journal of Medicine · 2008 · 811 citations · Full text

, , +17

Genomic and Genic Deletions of the FOX Gene Cluster on 16q24.1 and Inactivating Mutations of FOXF1 Cause Alveolar Capillary Dysplasia and Other Malformations

Paweł Stankiewicz, Partha Sen, Samarth Bhatt et al. · The American Journal of Human Genetics · 2009 · 536 citations · Full text

, , +9

Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability

Charles Shaw‐Smith, Alan Pittman, Lionel Willatt et al. · Nature Genetics · 2006 · 372 citations

, , +16

Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome

Bregje W.M. van Bon, Heather C. Mefford, Björn Menten et al. · Journal of Medical Genetics · 2009 · 370 citations · Full text

, , +15

3q29 Microdeletion Syndrome: Clinical and Molecular Characterization of a New Syndrome

Lionel Willatt, James J. Cox, John Barber et al. · The American Journal of Human Genetics · 2005 · 300 citations · Full text

, , +16

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