Samer Khateb

Also affiliated with Hadassah Medical Center

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 6 papers. Top paper: “KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints—KCNV2 Study Group Report 2”.

KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints—KCNV2 Study Group Report 2

American Journal of Ophthalmology(2021)10.1016/j.ajo.2021.03.004

N/A

0DataRank · unranked

28 citations

Kaoru Fujinami, Ajoy Vincent, Fadi Nasser, Samer Khateb, Mauricio E. Vargas +32 more

KCNV2-associated retinopathy: genotype–phenotype correlations –KCNV2study group report 3

British Journal of Ophthalmology(2023)10.1136/bjo-2023-323640

N/A

0DataRank · unranked

5 citations

Michalis Georgiou, Anthony G. Robson, Kaoru Fujinami, Ajoy Vincent, Fadi Nasser +31 more

Genome-wide association study and genomic risk prediction of age-related macular degeneration in Israel

medRxiv(2023)10.1101/2023.09.06.23295126

N/A

0DataRank · unranked

0 citations

Daria Triffon, Gala Beykin, Elior Rahmani, Regev Schweiger, Liran Tiosano +10 more

Genome wide association study and genomic risk prediction of age related macular degeneration in Israel

Scientific Reports(2024)10.1038/s41598-024-63065-0

N/A

0DataRank · unranked

9 citations

Daria Triffon, Gala Beykin, Elior Rahmani, Regev Schweiger, Liran Tiosano +10 more

Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study

British Journal of Ophthalmology(2024)10.1136/bjo-2023-323747

N/A

0DataRank · unranked

7 citations

Elizabeth White, Alaa Tayyib, Lesley Everett, Ajoy Vincent, Elise Héon +52 more

Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosa

Genetics in Medicine(2025)10.1016/j.gim.2025.101427

N/A

0DataRank · unranked

3 citations

Shai Ovadia, Jaya Krishnan, Manon Bouckaert, Daan M. Panneman, Milton A. English +13 more