Martin Broberg

University of Helsinki

Finland

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Articles (16)

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2025

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2025

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2024

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2020

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2020

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2020

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2020

Collaborators (29)

Hanna Ollila

University of Helsinki

FINLAND

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Emmi Helle

University of Helsinki

FINLAND

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James Doonan

Københavns Universitet

DENMARK

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Matti Pirinen

University of Helsinki

FINLAND

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Magnus Karlsson

Associate Professor

Swedish University of Agricultural Sciences

SWEDEN

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Vilma Lammi

University of Helsinki

FINLAND

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Markku Varjosalo

University of Helsinki

FINLAND

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Diego Balboa

University of Helsinki

FINLAND

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Mattia Cordioli

University of Helsinki

FINLAND

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Michael Hultström

Uppsala University

SWEDEN

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Francesca Minnai

Institute of Biotechnology

ITALY

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Vincenzo Forgetta

Chief Information and Bioinformatics Officer

5 Prime Sciences

CANADA

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Nina Mars

University of Helsinki

FINLAND

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Minttu Marttila

University of Helsinki

FINLAND

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Johanna Englund

University of Helsinki

FINLAND

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Aarno Palotie

University of Helsinki

FINLAND

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Rodrigo Lozano

Karolinska Institutet

SWEDEN

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Tiina Paunio

Research Professor

National Institute for Health and Welfare

FINLAND

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Kari Pulkki

Professor

University of Helsinki

FINLAND

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Adel Bachour

University of Helsinki

FINLAND

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Nella Junna

University of Helsinki

FINLAND

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Anniina Maria Tervi

University of Helsinki

FINLAND

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Viola Sofia Helaakoski

Institute for Molecular Medicine Finland

FINLAND

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Ole Birger Pedersen

Zealand University Hospital

DENMARK

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Teemu Palviainen

University of Helsinki

FINLAND

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Riikka Kivelä

University of Helsinki

FINLAND

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Olivia Leavy

University of Leicester

UNITED KINGDOM

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Jukka Koskela

University of Helsinki

FINLAND

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Amanda Ranta

Stanford University

UNITED STATES

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Martin Broberg

Research Interests

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Articles (16)

Genome-wide association study of long COVID

The ERBB2 c.1795C&gt;T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans

Genetic Analysis of Obstructive Sleep Apnea and Its Relationship with Severe COVID-19

Genome-wide association studies highlight novel risk loci for septal defects and left-sided congenital heart defects

Nightmares share genetic risk factors with sleep and psychiatric traits

Genetics of sleep medication purchases suggests causality from sleep problems to psychiatric traits

Large registry-based analysis of genetic predisposition to tuberculosis identifies genetic risk factors at HLA

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

Cellular shape reinforces niche to stem cell signaling in the small intestine

From Stem Cells to Populations—Using hiPSC, Next-Generation Sequencing, and GWAS to Explore the Genetic and Molecular Mechanisms of Congenital Heart Defects

Sleep apnoea is a risk factor for severe COVID-19

Mendelian randomization highlights insomnia as a risk factor for pain diagnoses

Comparative genomics highlights the importance of drug efflux transporters during evolution of mycoparasitism in Clonostachys subgenus Bionectria (Fungi, Ascomycota, Hypocreales)

Host–microbiota–insect interactions drive emergent virulence in a complex tree disease

Natural variation of root lesion nematode antagonism in the biocontrol fungus Clonostachys rosea , and identification of biocontrol factors through genome‐wide association mapping

LysM Proteins Regulate Fungal Development and Contribute to Hyphal Protection and Biocontrol Traits in Clonostachys rosea

Collaborators (29)

Hanna Ollila

Emmi Helle

James Doonan

Matti Pirinen

Magnus Karlsson

Vilma Lammi

Markku Varjosalo

Diego Balboa

Mattia Cordioli

Michael Hultström

Francesca Minnai

Vincenzo Forgetta

Nina Mars

Minttu Marttila

Johanna Englund

Aarno Palotie

Rodrigo Lozano

Tiina Paunio

Kari Pulkki

Adel Bachour

Nella Junna

Anniina Maria Tervi

Viola Sofia Helaakoski

Ole Birger Pedersen

Teemu Palviainen

Riikka Kivelä

Olivia Leavy

Jukka Koskela

Amanda Ranta

Make your next move.

The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humans