Frederik H. Lassen

Oxford, ENG, United Kingdom

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 19 publications

The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.

The Biobank Rare Variant consortium powers the discovery of rare genetic associations through global collaboration.

Journal: medRxiv : the preprint server for health sciences

Published: June 04, 2026

Molecular dynamics of Brodmann Area 22 in development and autism.

Molecular dynamics of Brodmann Area 22 in development and autism.

Journal: bioRxiv : the preprint server for biology

Published: April 10, 2026

The epidemiology of cubital tunnel syndrome: a UK Biobank case-control study.

The epidemiology of cubital tunnel syndrome: a UK Biobank case-control study.

Journal: The Journal of hand surgery, European volume

Published: March 11, 2026

Individuals whose phenotype deviates from genetic expectation defined by common variation are enriched for rare damaging variants in genes that cause rare disease.

Individuals whose phenotype deviates from genetic expectation defined by common variation are enriched for rare damaging variants in genes that cause rare disease.

Journal: medRxiv : the preprint server for health sciences

Published: January 08, 2026

Individuals who deviate from polygenic expectation are enriched for damaging variants in genes linked to rare disease.

Individuals who deviate from polygenic expectation are enriched for damaging variants in genes linked to rare disease.

Journal: American journal of human genetics

Published: January 07, 2026

Disruption of Cell-Type-Specific Molecular Programs of Medium Spiny Neurons in Autism.

Disruption of Cell-Type-Specific Molecular Programs of Medium Spiny Neurons in Autism.

Journal: bioRxiv : the preprint server for biology

Published: November 24, 2025

Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseases.

Meta-analysis across six global biobanks identifies recessive coding associations with complex traits and diseases.

Journal: American journal of human genetics

Published: September 15, 2025

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Exome sequencing and analysis of 44,028 British South Asians enriched for high autozygosity.

Journal: Nature genetics

Published: June 08, 2025

Combining evidence from human genetic and functional screens to identify pathways altering obesity and fat distribution.

Combining evidence from human genetic and functional screens to identify pathways altering obesity and fat distribution.

Journal: American journal of human genetics

Published: May 09, 2025

Combining evidence from human genetic and functional screens to identify pathways altering obesity and fat distribution.

Combining evidence from human genetic and functional screens to identify pathways altering obesity and fat distribution.

Journal: medRxiv : the preprint server for health sciences

Published: October 07, 2024

Protocol to profile spatially resolved NLRP3 inflammasome complexes using APEX2-based proximity labeling.

Protocol to profile spatially resolved NLRP3 inflammasome complexes using APEX2-based proximity labeling.

Journal: STAR protocols

Published: August 02, 2024

Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum.

Genome-wide analyses identify 21 infertility loci and over 400 reproductive hormone loci across the allele frequency spectrum.

Journal: medRxiv : the preprint server for health sciences

Published: April 02, 2024

Showing 1-12 of 19

Last Updated: 09/26/2026