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Works (11)

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

PLOS Genetics
2021-07-29 | Journal article
Contributors: Enrique Audain; Anthony B. Firulli; Anna Wilsdon; Jeroen Breckpot; Jose M. G. Izarzugaza; Tomas W. Fitzgerald; Anne-Karin Kahlert; Alejandro Sifrim; Florian Wünnemann; Yasset Perez-Riverol et al.
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Crossref

CRISPR perturbations at many coronary artery disease loci impair vascular endothelial cell functions

2021-02-11 | Preprint
Contributors: Florian Wünnemann; Thierry Fotsing Tadjo; Melissa Beaudoin; Simon Lalonde; Ken Sin Lo; Guillaume Lettre
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Crossref

Loss of ADAMTS19 causes progressive non-syndromic heart valve disease

Nature Genetics
2020-01 | Journal article
Contributors: Florian Wünnemann; Asaf Ta-Shma; Christoph Preuss; Severine Leclerc; Patrick Piet van Vliet; Andrea Oneglia; Maryse Thibeault; Emily Nordquist; Joy Lincoln; Franka Scharfenberg et al.
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Crossref

Validation of Genome-Wide Polygenic Risk Scores for Coronary Artery Disease in French Canadians.

Circulation. Genomic and precision medicine
2019-06-11 | Journal article
Source: Self-asserted source
Florian Wünnemann

Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene.

European journal of human genetics : EJHG
2019-02-28 | Journal article
Source: Self-asserted source
Florian Wünnemann

ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm

Nature Genetics
2019-01-19 | Journal article
Contributors: Russell A. Gould; Hamza Aziz; Courtney E. Woods; Manuel Alejandro Seman-Senderos; Elizabeth Sparks; Christoph Preuss; Florian Wünnemann; Djahida Bedja; Cassandra R. Moats; Sarah A. McClymont et al.
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Crossref

Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor.

Frontiers in Physiology
2017-06-13 | Journal article
Source: Self-asserted source
Florian Wünnemann

At the Heart of a Complex Disease ‘Molecular Genetics of Congenital Heart Disease’

eLS
2017-02 | Other
Part of ISBN: 9780470015902
Contributors: Christoph Preuss; Florian Wünnemann; Gregor Andelfinger
Source: Self-asserted source
Florian Wünnemann via Crossref Metadata Search

Molecular Pathways and Animal Models of Hypoplastic Left Heart Syndrome

Congenital Heart Diseases: The Broken Heart
2016 | Other
Part of ISBN: 9783709118825
Contributors: Florian Wünnemann; Gregor U. Andelfinger
Source: Self-asserted source
Florian Wünnemann via Crossref Metadata Search

Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease

PLOS Genetics
2016-10 | Journal article
Part of ISSN: 1553-7404
Contributors: Christoph Preuss; Melanie Capredon; Florian Wünnemann; Philippe Chetaille; Andrea Prince; Beatrice Godard; Severine Leclerc; Nara Sobreira; Hua Ling; Philip Awadalla et al.
Source: Self-asserted source
Florian Wünnemann via Crossref Metadata Search

Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome.

The Canadian journal of cardiology
2015-04-13 | Journal article
Source: Self-asserted source
Florian Wünnemann