Muhsin Elmas

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

Comparison of clinical parameters with whole exome sequencing analysis results of autosomal recessive patients; a center experience

Muhsin Elmas, Hicran Yıldız, Müjgan Özdemir Erdoğan et al. · Molecular Biology Reports · 2018 · 27 citations

Life Sciences, Genetics, Molecular Genetics +17

Success of Face Analysis Technology in Rare Genetic Diseases Diagnosed by Whole-Exome Sequencing: A Single-Center Experience

Muhsin Elmas, Başak Göğüş · Molecular Syndromology · 2020 · 27 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Infantile Type Sandhoff Disease with Striking Brain MRI Findings and a Novel Mutation

Mehtap Beker Acay, Muhsin Elmas, Reşit Köken et al. · Polish Journal of Radiology · 2016 · 18 citations · Full text

Medicine, Neurology, Pediatrics +17