Gökhan Yiğit

Polyhydramnios, Transient Antenatal Bartter’s Syndrome, and<i>MAGED2</i>Mutations

Kamel Laghmani, Bodo B. Beck, Sung-Sen Yang et al. · New England Journal of Medicine · 2016 · 187 citations · Full text

Medicine, Genetics, Obstetrics +16

Engineered heart muscle allografts for heart repair in primates and humans

Ahmad-Fawad Jebran, Tim Seidler, Malte Tiburcy et al. · Nature · 2025 · 118 citations · Full text

Engineering, Bioengineering, Cardiology +17

Intronic CRISPR Repair in a Preclinical Model of Noonan Syndrome–Associated Cardiomyopathy

Ulrich Hanses, Mandy Kleinsorge, Lennart Roos et al. · Circulation · 2020 · 76 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability

Nicole L. Rosin, Nursel Elçioğlu, Filippo Beleggia et al. · Human Molecular Genetics · 2015 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Human <scp><i>RAD50</i></scp> deficiency: Confirmation of a distinctive phenotype

Aviël Ragamin, Gökhan Yiğit, Kristine Bousset et al. · American Journal of Medical Genetics Part A · 2020 · 33 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17