Author

Eva Albrecht

Helmholtz Munich

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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Genetic & Genomic Medicine· 1 Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:GWAS / association mapping· 3 Assay:GWAS summary statistics· 3 Organism:human· 3 Approach:statistical model· 3

Frequent Co-Authors

André Gerardus UitterlindeniD· 2 shared Christian GiegeriD· 2 shared Cornelia M. van DuijniD· 2 shared Guðmar ÞorleifssoniD· 2 shared Inês BarrosoiD· 2 shared Inga ProkopenkoiD· 2 shared Kāri StefánssoniD· 2 shared Kay‐Tee KhawiD· 2 shared

Activity by Year

2016-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

André Gerardus UitterlindenORCID

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3 papers

Recent·Most cited

Random glucose GWAS in 493,036 individuals provides insights into diabetes pathophysiology, complications and treatment stratification

Vasiliki Lagou, Longda Jiang, Anna Ulrich, Liudmila Zudina, Karla Sofia Gutiérrez González, Zhanna Balkhiyarova, Alessia Faggian, Shiqian Chen, Petar V. Todorov, Sodbo Sharapov, Alessia David, Letizia Marullo, Reedik Mägi, Roxana‐Maria Rujan, Emma Ahlqvist, , Inga Prokopenko

This study performs a GWAS on random glucose measurements in 493,036 individuals, identifying 128 loci associated with glycaemic traits and providing insights into diabetes biology and treatment.

medRxiv · Apr 17, 2021 · PreprintGenetic & Genomic Medicine

Genome-wide association study identifies 48 common genetic variants associated with handedness.

Gabriel Cuéllar-Partida, Joyce Y. Tung, Nicholas Eriksson, Eva Albrecht, Fazil Alıev, Ole A. Andreassen, Inês Barroso, Jacques Samuel Beckmann, Marco P. Boks, Dorret Irene Boomsma, Heather Allison Boyd, Monique M.B. Breteler, Harry J. Campbell, Daniel I. Chasman, Lynn F. Cherkas, , Gérard Waeber

This study identifies 48 genetic variants associated with handedness using a large GWAS, highlighting polygenic nature and genetic links to neuropsychiatric traits.

Nature Human Behaviour · Sep 28, 2020Peer-reviewedGenetics

Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

Felix R. Day, Deborah J. Thompson, Hannes Helgason, Daniel I. Chasman, Hilary Finucane, Patrick Sulem, Katherine S. Ruth, Sean Whalen, Abhishek K. Sarkar, Eva Albrecht, Elisabeth Altmaier, Marzyeh Amini, Caterina M. Barbieri, Thibaud Boutin, Archie Campbell, , John R.B Perry

This study identifies 389 genetic signals for age at menarche and finds BMI-independent causal links between puberty timing and cancer risks.

bioRxiv · Sep 23, 2016 · PreprintGenomics