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

Priyanka Ahimaz

New York Genome Center

ORCID: 0000-0001-5112-1599

Also affiliated with Columbia University

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 5 papers. Top paper: “Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis”.

Bi-allelic missense disease-causing variants in RPL3L associate neonatal dilated cardiomyopathy with muscle-specific ribosome biogenesis

Human Genetics(2020)10.1007/s00439-020-02188-6
N/A
2.1DataRank · unranked
32 citations

Loukas Argyriou, Francisco Martínez‐Azorín, Susanne Morlot, Gökhan Yiğit, Teresa M. Lee +19 more

Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays

European Journal of Human Genetics(2023)10.1038/s41431-023-01434-5
N/A
0.494DataRank · unranked
26 citations

Leticia S. Matsuoka, Michael March, Dong Li, Elly Brokamp, Sara Benito‐Sanz +32 more

Phenotype driven molecular genetic test recommendation for diagnosing pediatric rare disorders

npj Digital Medicine(2024)10.1038/s41746-024-01331-1
N/A
0.373DataRank · unranked
11 citations

Priyanka Ahimaz, Quan M. Nguyen, Rachel Lewis, Wendy K. Chung, Casey Ta +7 more

Phenotype-Driven Molecular Genetic Test Recommendation for Diagnosing Pediatric Rare Disorders

Research Square(2023)10.21203/rs.3.rs-3593490/v1
N/A
0.208DataRank · unranked
3 citations

Fangyi Chen, Priyanka Ahimaz, Kai Wang, Wendy K. Chung, Casey Ta +2 more

Identification and validation of candidate risk genes in endocytic vesicular trafficking associated with esophageal atresia and tracheoesophageal fistulas

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100107
N/A
0DataRank · unranked
11 citations

Priyanka Ahimaz, Nicole A. Edwards, Jacob Hagen, Christophe Fauré, Lu Qiao +13 more