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Serhat Seyhan

FOXF2 is required for cochlear development in humans and mice
2018 · Guney Bademci, Clemer Abad, et al. · Human Molecular Genetics · 33
Determining host factors contributing to disease severity in a family cluster of 29 hospitalized SARS‐CoV‐2 patients: Could genetic factors be relevant in the clinical course of COVID‐19?
2020 · Hande Ikitimur, Betul Borku Uysal, et al. · Journal of Medical Virology · 32
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Peripheral neuropathy in Tangier disease: A literature review and assessment
2018 · Metin Mercan, Vildan Yayla, et al. · Journal of the Peripheral Nervous System · 29
Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability
2018 · Megan McSherry, Katherine E. Masih, et al. · PLoS ONE · 27
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Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development
2020 · Guney Bademci, Clemer Abad, et al. · Journal of Clinical Investigation · 20
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Dysfunction of GRAP , encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss
2019 · Chong Li, Guney Bademci, et al. · Proceedings of the National Academy of Sciences · 20
Spectrum of Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
2020 · Saradadevi Thanikachalam, Elizabeth Hodapp, et al. · Genes · 18
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Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss
2023 · Memoona Ramzan, Duygu Duman, et al. · Journal of Human Genetics · 16
A genetic mimic of cerebral palsy: Homozygous NFU1 mutation with marked intrafamilial phenotypic variation
2020 · Tuğçe Aksu Uzunhan, Nafiye Emel Çakar, et al. · Brain and Development · 15
The relationship between positivity for COVID-19 RT-PCR and symptoms, clinical findings, and mortality in Turkey
2021 · Erkan Ozcan, Serap Yavuzer, et al. · Expert Review of Molecular Diagnostics · 12
Novel GPR156 variants confirm its role in moderate sensorineural hearing loss
2023 · Memoona Ramzan, Nazim Bozan, et al. · Scientific Reports · 10
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Human organoids for rapid validation of gene variants linked to cochlear malformations
2025 · Mohammad Faraz Zafeer, Memoona Ramzan, et al. · Human Genetics · 7
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22.5 MB DELETION OF 13q31.1-q34 ASSOCIATED WITH HPE, DWM, AND HSCR: A CASE REPORT AND REDEFINING THE SMALLEST DELETED REGIONS.
2016 · M Y Alp, A H Çebi, et al. · PubMed · 7
Utility of Optical Genome Mapping in Repeat Disorders
2024 · Mehmet Burak Mutlu, Taner Karakaya, et al. · Clinical Genetics · 6
Optical coherence tomography and fundus autofluorescence imaging in an infant with RD3-related leber congenital amaurosis
2020 · Funda Dikkaya, Serhat Seyhan, et al. · Ophthalmic Genetics · 3
Carboxypeptidase D deficiency causes hearing loss amenable to treatment
2025 · Memoona Ramzan, Natalie Ortiz-Vega, et al. · Journal of Clinical Investigation · 2
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The phenotyping dilemma in VRK1-related motor neuron disease: a Turkish family with young-onset amyotrophic lateral sclerosis caused by a novel mutation
2025 · Metin Mercan, Serhat Seyhan, et al. · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · 2
COVID-19 seroconversion in the aircrew from Turkey
2021 · Mehmet Sami Islamoglu, Mahir Cengiz, et al. · Travel Medicine and Infectious Disease · 2
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The genetic causes of infertility in patients with oligozoospermia and azoospermia in Turkish population
2021 · Yavuz Onur Danacıoglu, Mustafa Gürkan Yenice, et al. · Yeni Üroloji Dergisi · 2
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Molecular Heterogeneity in Cystic Fibrosis
2020 · Hasret A. Civan, Serhat Seyhan · Journal of Pediatric Genetics · 2
Genetic Variants Associated with Anterior Segment Dysgenesis in South Florida
2020 · Saradadevi Thanikachalam, Elizabeth Hodapp, et al. · 2
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Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss
2024 · Duygu Duman, Memoona Ramzan, et al. · American Journal of Medical Genetics Part A · 1
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A NEW ISOLATED 20q INTERSTITIAL DUPLICATION CASE AND ITS CLINICAL COMPARISON WITH SIMILAR ISOLATED CASES.
2016 · A H Cebi, G Karaguzel, et al. · PubMed · 1
PO103 Inherited cardiac diseases and genetic testing in clinical practice: Experience from a tertiary cardiology center
2026 · Ömer Gök, Serhat Seyhan, et al. · European Journal of Preventive Cardiology
An Overview of Drug-Resistant Epilepsies Based on Advances in Genetics: A Cohort Study
2026 · Betül Kılıç, Yasemin Topçu, et al. · Neurology India
Works count: 33
Citation count: 269
H-index: 10
I10-index: 11
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