Concepedia

Jacqueline K. Rainger

JK

Statistics

Publications

12

Citations

2.5K

H-Index

12

Active since

2013

Affiliations

University of Edinburgh(Current)

Institute of Genetics and Cancer

Western General Hospital

University of Southampton

Oslo University Hospital

Jacqueline K. Rainger is an author at University of Edinburgh specializing in genetics, life sciences, and molecular genetics.

Publications per year

2013–2020

12

Publications

12

cGAS surveillance of micronuclei links genome instability to innate immunity

Karen J. Mackenzie, Paula Carroll, Carol-Anne Martin et al. · Nature · 2017 · 1.7K citations · Full text

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SMCHD1 mutations associated with a rare muscular dystrophy can also cause isolated arhinia and Bosma arhinia microphthalmia syndrome

Natalie D. Shaw, Harrison Brand, Zachary A Kupchinsky et al. · Nature Genetics · 2017 · 162 citations · Full text

, , +12

Heterozygous Loss-of-Function Mutations in YAP1 Cause Both Isolated and Syndromic Optic Fissure Closure Defects

Kathleen A. Williamson, Joe Rainger, James Floyd et al. · The American Journal of Human Genetics · 2014 · 109 citations · Full text

, , +9

A Restricted Repertoire of De Novo Mutations in ITPR1 Cause Gillespie Syndrome with Evidence for Dominant-Negative Effect

Meriel McEntagart, Kathleen A. Williamson, Jacqueline K. Rainger et al. · The American Journal of Human Genetics · 2016 · 104 citations · Full text

, , +17

Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center

Christina Gerth‐Kahlert, Kathleen A. Williamson, Morad Ansari et al. · Molecular Genetics & Genomic Medicine · 2013 · 93 citations · Full text

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