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About the database ScholarIQanswers from OpenAlex & ORCID
How has Orly Elpeleg's publication output changed over time?
ScholarIQpublication output · 2001–2021
Output declined50% over the shown period — from 2 works in 2001 to 1 in 2021.
2
1
1
1
1
1
1
1
1
1
2001200420052007200820092011201220132021
What are the most-cited papers on Orly Elpeleg?
ScholarIQmost cited works
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
Ann Saada, Avraham Shaag, Hanna Mandel, Yoram Nevo, Staffan Eriksson, Orly Elpeleg
S137905309. 2001623 Citations
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA
Hanna Mandel, Raymonde Szargel, Valentina Labay, Orly Elpeleg, Ann Saada, Adel Shalata, Yefim Anbinder, Drora Berkowitz, Corina Hartman, Mila Barak, Staffan Eriksson, Nadine Cohen
S137905309. 2001586 Citations
Deleterious Mutation in the Mitochondrial Arginyl–Transfer RNA Synthetase Gene Is Associated with Pontocerebellar Hypoplasia
Simon Edvardson, Avraham Shaag, Olga A. Kolesnikova, John M. Gomori, Ivan Tarassov, Tom Einbinder, Ann Saada, Orly Elpeleg
S134425043. 2007334 CitationsOPEN ACCESS
A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism
Simon Edvardson, Yuval Cinnamon, Asaf Ta‐Shma, Avraham Shaag, Yang-In Yim, Shamir Zenvirt, Chaim Jalas, Suzanne Lesage, Alexis Brice, Albert Taraboulos, Klaus H. Kaestner, Lois E. Greene, Orly Elpeleg
PLoS ONE. 2012322 CitationsOPEN ACCESS
Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion
Orly Elpeleg, Chaya Miller, Eli Hershkovitz, Maria Bitner‐Glindzicz, Gili Bondi-Rubinstein, Shamima Rahman, Alistair T. Pagnamenta, Sharon Eshhar, Ann Saada
S134425043. 2005313 CitationsOPEN ACCESS
Related on ScholarIQ
Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy
Paper
The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA
Paper
Deleterious Mutation in the Mitochondrial Arginyl–Transfer RNA Synthetase Gene Is Associated with Pontocerebellar Hypoplasia
Paper
A Deleterious Mutation in DNAJC6 Encoding the Neuronal-Specific Clathrin-Uncoating Co-Chaperone Auxilin, Is Associated with Juvenile Parkinsonism
Paper
Deficiency of the ADP-Forming Succinyl-CoA Synthase Activity Is Associated with Encephalomyopathy and Mitochondrial DNA Depletion
Paper
A Fatal Mitochondrial Disease Is Associated with Defective NFU1 Function in the Maturation of a Subset of Mitochondrial Fe-S Proteins
Paper