Concepedia

Kerry Fagan

KF

Statistics

Publications

10

Citations

439

H-Index

10

Active since

1983

Affiliations

John Hunter Hospital(Current)

Hunter Genetics

University of Newcastle Australia

Children's Hospital at Westmead

Université Paris Cité

Kerry Fagan is an author at John Hunter Hospital specializing in molecular genetics, genetics, and life sciences.

Publications per year

1983–2015

10

Publications

10

<i>FOXP1</i> mutations cause intellectual disability and a recognizable phenotype

Anna Le Fevre, Sharelle Taylor, Neva H. Malek et al. · American Journal of Medical Genetics Part A · 2013 · 102 citations

, , +17

Interstitial microduplication of Xp22.31: Causative of intellectual disability or benign copy number variant?

Feng Li, Yiping Shen, U Köhler et al. · European Journal of Medical Genetics · 2010 · 81 citations

, , +16

14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype

Carolyn Ellaway, Gladys Ho, Elisa Bettella et al. · European Journal of Human Genetics · 2012 · 76 citations · Full text

, , +10

Translocation (8;13) and T-cell lymphoma

Kerry Fagan, S Hyde, P. B. Harrison · Cancer Genetics and Cytogenetics · 1993 · 41 citations

, , +11

Refinement of genotype‐phenotype correlation in 18 patients carrying a 1q24q25 deletion

Nicolas Chatron, Véronique Haddad, Joris Andrieux et al. · American Journal of Medical Genetics Part A · 2015 · 32 citations

, , +17

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