Haktan Bağış Erdem

The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance

Davut Pehli̇van, Yavuz Bayram, Nilay Güneş et al. · The American Journal of Human Genetics · 2019 · 121 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population

Tadahiro Mitani, Sedat Işıkay, Alper Gezdirici et al. · The American Journal of Human Genetics · 2021 · 102 citations · Full text

Life Sciences, Molecular Medicine, Neuroscience +15

Biallelic and monoallelic variants in PLXNA1 are implicated in a novel neurodevelopmental disorder with variable cerebral and eye anomalies

Gabriel C. Dworschak, Jaya Punetha, Jeshurun C. Kalanithy et al. · Genetics in Medicine · 2021 · 38 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

MITOCHONDRIAL DNA COPY NUMBER IS ASSOCIATED WITH ATTENTION DEFICIT HYPERACTIVITY DISORDER

Hakan Öğütlü, İbrahim Selçuk Esin, Haktan Bağış Erdem et al. · Psychiatria Danubina · 2020 · 26 citations · Full text

Medicine, Genetics, Molecular Genetics +13

Spectrum of BRCA1/BRCA2 variants in 1419 Turkish breast and ovarian cancer patients: a single center study

Taha Bahsi, Haktan Bağış Erdem · Turkish Journal of Biochemistry · 2019 · 23 citations · Full text

Life Sciences, Genetics, Oncology +17