Katherine Agre

Also affiliated with Mayo Clinic in Florida

Biochemistry, Genetics and Molecular BiologyNeuroscience

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 6 papers. Top paper: “Genetics of dilated cardiomyopathy: practical implications for heart failure management”.

Genetics of dilated cardiomyopathy: practical implications for heart failure management

Nature Reviews Cardiology(2020)10.1038/s41569-019-0284-0

N/A

0.815DataRank · unranked

228 citations

Katherine Agre, Naveen L. Pereira, Andrew Rosenbaum

Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndrome

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.002

N/A

0.568DataRank · unranked

43 citations

Gregory Costain, Laura E.R. Blok, Michael Silk, Thanh Nguyen, Xiaomin Dong +95 more

Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.06.019

N/A

0DataRank · unranked

25 citations

Philipp Kirchner, Antje Wiesener, Irma van de Beek, Quinten Waisfisz, Mieke M. van Haelst +43 more

Expanding ACTA2 genotypes with corresponding phenotypes overlapping with smooth muscle dysfunction syndrome

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.62775

N/A

0DataRank · unranked

17 citations

Kaveeta Kaw, Ellen M. Hostetler, Ana Beleza‐Meireles, Adam Smith‐Collins, Catherine Armstrong +11 more

Dominant-negative heterozygous mutations in AIRE confer diverse autoimmune phenotypes

iScience(2023)10.1016/j.isci.2023.106818

N/A

0DataRank · unranked

33 citations

Kristian Assing, Safa Barış, Stephanie L. Safgren, Işık Somuncu Johansen, Marianne Antonius Jakobsen +20 more

Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders

European Journal of Human Genetics(2024)10.1038/s41431-024-01576-0

N/A

0DataRank · unranked

5 citations

Kim Lee Ng, Filippo Pinto e Vairo, James Collins, Ronald D. Cohn, Kacie Riley +6 more