Author

Furkan Büyükgöl

Institutions: Broad Institute, Helmholtz Munich, Ludwig-Maximilians-Universität München

Observed institutions: Broad Institute, Helmholtz Munich, Acıbadem University, Ludwig-Maximilians-Universität München

OpenAlex ID: A5116934776

Exome sequencing reveals low-frequency and rare variant contributions to multiple sclerosis susceptibility in Turkish families

2025 · Furkan Büyükgöl, Berk Gürdamar, et al. · Scientific Reports · 6

A resource of “bottom-line” variant associations for 1,281 complex traits by integrating data across published genome-wide association studies

2026 · Trang Nguyen, Furkan Büyükgöl, et al. · Research Square · 1

Exome-sequencing of Turkish Families with Multiple Sclerosis: Low Frequency and Rare Variant Contributions into Susceptibility (P10-1.002)

2025 · Furkan Büyükgöl, Berk Gürdamar, et al. · Neurology

Works count: 3

Citation count: 7

H-index: 1

I10-index: