Concepedia

Adel Shalata

AS

Statistics

Publications

32

Citations

2K

H-Index

19

Active since

1998

Affiliations

Technion – Israel Institute of Technology(Current)

Bnai Zion Medical Center

Tel Aviv University

Western Galilee Hospital

Rambam Health Care Campus

Adel Shalata is an author at Technion – Israel Institute of Technology specializing in genetics, life sciences, and molecular genetics.

ORCID

Publications per year

1998–2024

32

Publications

32

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

Hanna Mandel, Raymonde Szargel, Valentina Labay et al. · Nature Genetics · 2001 · 585 citations

, , +11

Mutations in SLC19A2 cause thiamine-responsive megaloblastic anaemia associated with diabetes mellitus and deafness

Valentina Labay, Tal Raz, Dana Baron et al. · Nature Genetics · 1999 · 275 citations

, , +10

Hypotrichosis with juvenile macular dystrophy is caused by a mutation in CDH3, encoding P-cadherin

Eli Sprecher, Gabriele Richard, Raziel Lurie et al. · Nature Genetics · 2001 · 188 citations

, , +12

Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p

Meral Gunay‐Aygun, Yifat Zivony-Elboum, Fatma Gümrük et al. · Blood · 2010 · 156 citations · Full text

, , +13

A Focal Epilepsy and Intellectual Disability Syndrome Is Due to a Mutation in TBC1D24

Mark Corbett, Melanie Bahlo, Lachlan A. Jolly et al. · The American Journal of Human Genetics · 2010 · 118 citations · Full text

, , +14

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