Rosemary Bauer

MedicineBiochemistry, 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 6 papers. Top paper: “Distinct mechanoreceptor pezo-1 isoforms modulate food intake in the nematode Caenorhabditis elegans”.

Distinct mechanoreceptor pezo-1 isoforms modulate food intake in the nematode Caenorhabditis elegans

G3 Genes Genomes Genetics(2021)10.1093/g3journal/jkab429

N/A

0.464DataRank · unranked

21 citations

Ashka Shah, Xiaofei Bai, Jessica M. Adams, Rosemary Bauer, Janelle Jackson +10 more

Update on the Molecular Genetics of Timothy Syndrome

Frontiers in Pediatrics(2021)10.3389/fped.2021.668546

N/A

0DataRank · unranked

57 citations

Katherine W. Timothy, Andy Golden, Rosemary Bauer

Opposing effects of genetic variation in MTCH2 for obesity versus heart failure

Human Molecular Genetics(2022)10.1093/hmg/ddac176

N/A

0DataRank · unranked

9 citations

Tanner O. Monroe, Lorenzo L. Pesce, Konrad Teodor Sawicki, Mattia Quattrocelli, Rosemary Bauer +5 more

A Natural History Study of Timothy Syndrome

Orphanet Journal of Rare Diseases(2024)10.1186/s13023-024-03445-x

N/A

0DataRank · unranked

14 citations

Rosemary Bauer, Kerry Larkin, Edward P. Walsh, Dominic Abrams, M. Cecilia Gonzalez Corcia +5 more

Rare Variation in LMNA Underlies Polycystic Ovary Syndrome Pathogenesis in 2 Independent Cohorts

The Journal of Clinical Endocrinology & Metabolism(2024)10.1210/clinem/dgae761

N/A

0DataRank · unranked

6 citations

C. Richard Parker, Lidija K. Gorsic, M. Geoffrey Hayes, Allen R. Kunselman, Richard S. Legro +3 more

Pathogenic variation in insulin resistance genes is common in polycystic ovary syndrome (PCOS): a strategy for causal gene discovery using whole-exome sequencing (WES) in complex traits

medRxiv(2025)10.1101/2025.08.13.25333592

N/A

0DataRank · unranked

1 citations

C. Richard Parker, Zulma Cardona Matos, M. Geoffrey Hayes, Allen R. Kunselman, Richard S. Legro +3 more