Sarah Bowdin

Also affiliated with Hospital for Sick Children, Cambridge University Hospitals NHS Foundation Trust

Biochemistry, Genetics and Molecular Biology

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 2 papers. Top paper: “Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays”.

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

Advancing diagnosis and research for rare genetic diseases in Indigenous peoples

Nature Genetics(2024)10.1038/s41588-023-01642-1

N/A

0DataRank · unranked

14 citations

Daria Julkowska, Sarah Bowdin, Azure Hermes, Christopher R. McMaster, Elissa Prichep +20 more