Margaret G. Ehm

Also affiliated with Glaxosmithkline (Finland), Institut thématique Génétique, génomique et bioinformatique, Clinical Directors Network

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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 7 papers. Top paper: “The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections”.

The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

EBioMedicine(2023)10.1016/j.ebiom.2023.104630

N/A

1.0DataRank · unranked

28 citations

Fahrisa I. Maisha, Satu Strausz, Vilma Lammi, Brian E. Cade, Anniina Tervi +88 more

Risk of Midlife Stroke After Adverse Pregnancy Outcomes: The FinnGen Study

Stroke(2023)10.1161/strokeaha.123.043052

N/A

0.706DataRank · unranked

27 citations

Anni Kauko, Sarah E. Tom, Hannele Laivuori, Teemu Niiranen, Natalie A. Bello +86 more

Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata

Nature Communications(2023)10.1038/s41467-023-35974-7

N/A

0.680DataRank · unranked

22 citations

Jaakko Tyrmi, Nilüfer Rahmioğlu, Krina T. Zondervan, Christian M. Becker, FinnGen +95 more

A computational framework for defining and validating reproducible phenotyping algorithms of 313 diseases in the UK Biobank

Scientific Reports(2025)10.1038/s41598-025-05838-9

N/A

0.312DataRank · unranked

7 citations

Jonathan Davitte, Damien C. Croteau‐Chonka, C. R. Ytsma, Christopher Tomlinson, Natalie Fitzpatrick +21 more

Large-scale genome-wide analyses with proteomics integration reveal novel loci and biological insights into frailty

Nature Aging(2025)10.1038/s43587-025-00925-y

N/A

0.269DataRank · unranked

5 citations

Chenxi Qin, Moritz Krüger, Anna Kuukka, Aarno Palotie, Mark Daly +322 more

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

Publisher(2020)10.17615/tme1-9982

N/A

0DataRank · unranked

0 citations

Keolu Fox, Ping An, Li Li, Marie‐France Hivert, Laura J. Rasmussen‐Torvik +27 more

Performance of Genotype Imputation for Rare Variants Identified in Exons and Flanking Regions of Genes

UNC Libraries(2020)10.17615/4grc-0v75

N/A

0DataRank · unranked

2 citations

Li Li, Jennifer L. Aponte, John C. Whittaker, Matthew R. Nelson, Margaret G. Ehm +7 more