Author

Micha Gawlik

Universitätsklinikum WürzburgORCID 0000-0002-2166-3992Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Celso ArangoiD· 2 shared Aaron J. GorelikiD· 1 shared Akitoyo HishimotoiD· 1 shared Alexander L. RichardsiD· 1 shared Alexander S Hatoum· 1 shared Alexis C. EdwardsiD· 1 shared Alice BrauniD· 1 shared Anders D Børglum· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Celso ArangoORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintOct 22, 2025

Genome-wide association studies identify 77 loci for suicidality and provide novel biological insights

Sarah M. C. Colbert, Maria Koromina, Alexander S Hatoum…·Bharath Holla

This study identifies 77 genetic loci associated with suicidality through genome-wide association analyses across multiple cohorts and provides biological insights into its genetic architecture.

4 citations

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsbioRxivPreprintApr 18, 2019

Analyses of rare and common alleles in parent-proband trios implicate rare missense variants in SLC6A1 in schizophrenia and confirm the involvement of loss of function intolerant and neurodevelopmental disorder genes.

Elliott Rees, Jun Han, Joanne Morgan…·Michael John Owen

The paper analyzes rare and common alleles in schizophrenia trios, identifying rare missense variants in SLC6A1 and confirming the role of neurodevelopmental disorder genes.

3 citations

humanwhole-exome sequencing

𝕏 PostBluesky