🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Tamar Ben‐Yosef

Technion – Israel Institute of Technology

ORCID: 0000-0003-3035-4654
Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

1in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology
Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 5 papers. Top paper: “Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: The pitfalls of homozygosity mapping”.

Genetic heterogeneity in two consanguineous families segregating early onset retinal degeneration: The pitfalls of homozygosity mapping

American Journal of Medical Genetics Part A(2009)10.1002/ajmg.a.32634
N/A
0.553DataRank · unranked
39 citations

Ronen Spiegel, Noa Auslender, Anan H Abbasi, Leah Rizel, Yasir Hujeirat +5 more

Loss-of-function variants in UBAP1L cause autosomal recessive retinal degeneration

Genetics in Medicine(2024)10.1016/j.gim.2024.101106
N/A
0.416DataRank · unranked
15 citations

Kim Rodenburg, Tamar Hayman, Giacomo Calzetti, Karolina Kamińska, Mathieu Quinodoz +20 more

De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa

Nature Genetics(2026)10.1038/s41588-025-02451-4
N/A
0.370DataRank · unranked
8 citations

Kim Rodenburg, Zuzana Cvackova, Karolina Kaminska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +212 more

Biallelic null variants in C19orf44 cause a unique late-onset retinal dystrophy phenotype characterized by patchy perifoveal chorioretinal atrophy

Genetics in Medicine(2025)10.1016/j.gim.2025.101401
N/A
0DataRank · unranked
4 citations

Maayan Avraham, Sandeep Sarma Asodu, Abigail R. Moye, Riccardo Sangermano, Leah Rizel +19 more

De novo and inherited dominant variants in U4 and U6 snRNAs cause retinitis pigmentosa

medRxiv(2025)10.1101/2025.01.06.24317169
N/A
0DataRank · unranked
15 citations

Kim Rodenburg, Zuzana Cvačková, Karolina Kamińska, Suzanne E. de Bruijn, Ana Belén Iglesias-Romero +95 more