Imke Christiaans

Also affiliated with University of Groningen

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: “Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect”.

Shared genetic pathways contribute to risk of hypertrophic and dilated cardiomyopathies with opposite directions of effect

Nature Genetics(2021)10.1038/s41588-020-00762-2

N/A

7.0DataRank · unranked

297 citations

Catherine Francis, Xiao Yun Xu, Alexa M.C. Vermeer, Andrew R. Harper, Roy Huurman +65 more

Large scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

medRxiv(2023)10.1101/2023.01.28.23285147

N/A

0.436DataRank · unranked

12 citations

Sean Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Sean J. Jurgens +57 more

Lymphedema as first clinical presentation of Cantu Syndrome: reversed phenotyping after identification of gain-of-function variant in ABCC9

European Journal of Human Genetics(2022)10.1038/s41431-022-01210-x

N/A

0DataRank · unranked

6 citations

Conor McClenaghan, Imke Christiaans, Mariëlle Alders, Kirsten van Duinen, Mieke M. van Haelst +3 more

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy

medRxiv(2024)10.1101/2024.07.04.24309755

N/A

0DataRank · unranked

0 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +65 more

Large-scale genome-wide association analyses identify novel genetic loci and mechanisms in hypertrophic cardiomyopathy

Nature Genetics(2025)10.1038/s41588-025-02087-4

N/A

0DataRank · unranked

55 citations

Sean L. Zheng, Christopher Grace, Paloma Jordà, Catherine Francis, Dominique M West +95 more

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.016

N/A

0DataRank · unranked

2 citations

Alexa M.C. Vermeer, Pieter G. Postema, Rafik Tadros, Forrest Z. Bowling, Hildur M. Aegisdottir +66 more