Ben Pode‐Shakked

Also affiliated with Sheba Medical Center, Edmond and Lily Safra Children's Hospital

Biochemistry, Genetics and Molecular BiologyMedicine

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 4 papers. Top paper: “Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations”.

Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

Genetics in Medicine(2021)10.1038/s41436-021-01232-8

N/A

0DataRank · unranked

49 citations

Rebecca C. Spillmann, Harley T. Kurata, Shawn M. Lamothe, Jasmine Maghera, Rami Abou Jamra +92 more

Biallelic DAW1 variants cause a motile ciliopathy characterized by laterality defects and subtle ciliary beating abnormalities

Genetics in Medicine(2022)10.1016/j.gim.2022.07.019

N/A

0DataRank · unranked

12 citations

Rim Hjeij, Asaf Vivante, Elizabeth A. Bearce, Laura A. Dyer, Jiaolong Wang +24 more

Oculocutaneous albinism and bleeding diathesis due to a novel deletion in the HPS3 gene

Frontiers in Genetics(2022)10.3389/fgene.2022.936064

N/A

0DataRank · unranked

3 citations

Shachar Abudi-Sinreich, Michal Macarov, Alvit Veber, Nechama Shalva, Amit M. Philosoph +4 more

Detection of the Heterozygous Recurrent MAX p.( Arg60Gln ) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly–Macrocephaly Syndrome

Clinical Genetics(2025)10.1111/cge.70101

N/A

0DataRank · unranked

0 citations

Neta Feinstein‐Goren, Lior Greenbaum, Ortal Barel, Daniel C. Koboldt, Samantha A. Brugmann +5 more