Bilal K. AlWattar

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

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 3 papers. Top paper: “Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion”.

Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.18.562924

N/A

0.104DataRank · unranked

1 citations

Bilal K. AlWattar, Qifei Li, Kiran Bora, Alexandra K. Blomfield, Jasmine Lin +4 more

A Simplified Model of Activation and Deactivation of Human Rod Phototransduction—An Electroretinographic Study

Investigative Ophthalmology & Visual Science(2023)10.1167/iovs.64.12.36

N/A

0DataRank · unranked

2 citations

Annie M. Lancos, Bilal K. AlWattar, Hanna De Bruyn, Ronald M. Hansen, Anne B. Fulton +1 more

HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells

Disease Models & Mechanisms(2024)10.1242/dmm.050557

N/A

0DataRank · unranked

3 citations

Bilal K. AlWattar, Qifei Li, Kiran Bora, Alexandra K. Blomfield, Jasmine Lin +4 more