Author

Michael H. Hühn

AstraZeneca (Sweden)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genomics· 2 Molecular Biology· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:variant effect prediction· 2 Assay:whole-exome sequencing· 2 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Organism:mouse· 1 Research Focus:spatial domain detection· 1

Frequent Co-Authors

Adam PlattiD· 2 shared Alex Mackay· 2 shared Daniel MuthasiD· 2 shared Graham Belfield· 2 shared Henric OlssoniD· 2 shared Julia LindgreniD· 2 shared Quanli WangiD· 2 shared Slavé PetrovskiiD· 2 shared

Activity by Year

2020-2024 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersGenomics

Adam PlattORCID

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Author profile →

3 papers

Recent·Most cited

Translational mapping of spatially resolved transcriptomes in human and mouse pulmonary fibrosis

Lovisa Franzén, Martina Olsson Lindvall, Michael H. Hühn, Victoria Ptasinski, Laura C. Setyo, Benjamin P. Keith, Astrid Collin, Steven Oag, Thomas Volckaert, Annika Borde, Joakim Lundeberg, Julia Lindgren, Graham Belfield, Sonya G. Jackson, Anna Ollerstam, , Jorrit J. Hornberg

This study maps spatial transcriptomes of human and mouse pulmonary fibrosis to identify fibrotic niches and differences in alveolar regeneration.

Nature Genetics · Jul 1, 2024Peer-reviewedMolecular Biology

Surveying the contribution of rare variants to the genetic architecture of human disease through exome sequencing of 177,882 UK Biobank participants

Quanli Wang, Ryan S. Dhindsa, Keren Carss, Andrew Robert Harper, Abhishek Nag, Ioanna Tachmazidou, Dimitrios Vitsios, Sri V. V. Deevi, Alex Mackay, Daniel Muthas, Michael H. Hühn, Susan J. Monkley, Henric Olsson, Sebastian Wasilewski, Katherine R. Smith, , AstraZeneca Genomics Initiative

This study uses exome sequencing of 177,882 UK Biobank participants to assess the role of rare variants in 10,533 phenotypes, identifying 911 significant gene-phenotype relationships.

bioRxiv · Dec 13, 2020 · PreprintGenomics

A broad exome study of the genetic architecture of asthma reveals novel patient subgroups

Sophia Cameron‐Christie, Alex Mackay, Quanli Wang, Henric Olsson, B. Angermann, Glenda Lassi, Julia Lindgren, Michael H. Hühn, Yoichiro Ohne, Monica L. Gavala, Jingya Wang, Gundula Povysil, Sri V. V. Deevi, Graham Belfield, Inken Dillmann, , Slavé Petrovski

This study uses exome data from 24,576 asthma cases and 120,530 controls to identify rare variants associated with asthma risk, revealing novel subgroups and gene effects.

bioRxiv · Dec 10, 2020 · PreprintGenomics