Ohad Wormser

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “B4GALT1‐congenital disorders of glycosylation: Expansion of the phenotypic and molecular spectrum and review of the literature”.

B4GALT1‐congenital disorders of glycosylation: Expansion of the phenotypic and molecular spectrum and review of the literature

Clinical Genetics(2020)10.1111/cge.13735

N/A

0.416DataRank · unranked

15 citations

Iris Noyman, Ohad Wormser, Abed Abu Quider, Guy Hazan, Iris Morag +6 more

SMARCA4 mutation causes human otosclerosis and a similar phenotype in mice

Journal of Medical Genetics(2023)10.1136/jmg-2023-109264

N/A

0.292DataRank · unranked

6 citations

Matan M. Jean, Yael Noy, Daniel Halpérin, Yuval Yogev, Ohad Wormser +11 more

Absence of SCAPER causes male infertility in humans and Drosophila by modulating microtubule dynamics during meiosis

Journal of Medical Genetics(2020)10.1136/jmedgenet-2020-106946

N/A

0DataRank · unranked

17 citations

Ygal Levy, Anna Bakhrat, Silvia Bonaccorsi, Lucia Graziadio, Maurizio Gatti +10 more