Luca Lotta

12PUBLICATIONS
210CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene and molecular therapyComputational neuroscience (incl. mathematical neuroscience and theoretical neuroscience)Gene expression (incl. microarray and other genome-wide approaches)Behavioural epidemiology
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Publications (12)

|Aug 05, 2026
FNIP1 variants are associated with favourable metabolism in 1 million humans.

|Mar 14, 2026
Humans with function-disrupting variants in the myostatin gene (MSTN) have increased skeletal muscle mass and strength, and less adiposity.

Joseph L Herman, Peter Dornbos, Karl Landheer

|Feb 24, 2026
Rare coding variants in CHRNB3 associate with reduced daily cigarette smoking across ancestries.

Veera M Rajagopal, Andrey Ziyatdinov, Tyler Joseph

|Mar 06, 2025
Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases.

Carolina Roselli, Ida Surakka, Morten S Olesen

|Sep 25, 2024
Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank.

Sheila M Gaynor, Tyler Joseph, Xiaodong Bai

|Sep 13, 2024
NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke.

Juan Lorenzo Rodriguez-Flores, Shareef Khalid, Neelroop Parikshak

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Frequent Collaborators

7 joint publications

Jonathan Marchini

7 joint publications

Aris Baras

5 joint publications

Jeffrey G Reid

5 joint publications

Goncalo R Abecasis