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Employment (8)

Medroyal Genetic Diseases Assessment Center: Istanbul, TR

2022-05-17 to present | Head of Genetic Diseases Assessment Center (Genetic Diseases Assessment Center)
Employment
Source: Self-asserted source
Serhat Seyhan

Üsküdar University: Istanbul, TR

2022-05-12 to present | Clinical Geneticist (Clinical Genetics)
Employment
Source: Self-asserted source
Serhat Seyhan

Memorial Şişli Hastanesi: Istanbul, TR

2022-02-01 to present | Clinical Geneticist (Clinical Genetics)
Employment
Source: Self-asserted source
Serhat Seyhan

Biruni University Hospital: Istanbul, TR

2020-04-01 to 2022-02-01 | Covid-19 Diagnostic Laboratory Manager (Covid-19 Diagnostic Laboratory)
Employment
Source: Self-asserted source
Serhat Seyhan

Biruni University: Zeytinburnu, TR

2020-03-18 to 2022-02-01 | Head of Genetic Diseases Assessment Center (Genetic Diseases Assessment Center)
Employment
Source: Self-asserted source
Serhat Seyhan

Istanbul Medipol University: Istanbul, TR

2018-11-26 to 2020-03-18 | Head of Department (Clinical Genetics)
Employment
Source: Self-asserted source
Serhat Seyhan

Bakirkoy Dr Sadi Konuk Egitim ve Arastirma Hastanesi: Istanbul, TR

2016-08-02 to 2018-11-25
Employment
Source: Self-asserted source
Serhat Seyhan

University of Miami School of Medicine: Miami, FL, US

2018-08-02 to 2018-10-23 | Short term scholar (John P. Hussmann Institute for Human Genomics)
Employment
Source: Self-asserted source
Serhat Seyhan

Education and qualifications (2)

Karadeniz Teknik Üniversitesi Tıp Fakültesi: Trabzon, TR

2012-02-29 to 2016-07-30 | Residency-Clinical Geneticist (Faculty of Medicine-Clinical Genetics)
Education
Source: Self-asserted source
Serhat Seyhan

Cumhuriyet Üniversitesi: Sivas, TR

2005-09-01 to 2011-07-01 (Faculty of Medicine)
Education
Source: Self-asserted source
Serhat Seyhan

Works (13)

Featured Cover

Clinical Genetics
2025-02 | Journal article
DOI: 10.1111/cge.14700
Contributors: Mehmet Burak Mutlu; Taner Karakaya; Hamide Betül Gerik Çelebi; Fahrettin Duymuş; Serhat Seyhan; Sanem Yılmaz; Uluç Yiş; Tahir Atik; Mehmet Fatih Yetkin; Hakan Gümüş
Source: check_circle
Crossref

Utility of Optical Genome Mapping in Repeat Disorders

Clinical Genetics
2025-02 | Journal article
DOI: 10.1111/cge.14633
Contributors: Mehmet Burak Mutlu; Taner Karakaya; Hamide Betül Gerik Çelebi; Fahrettin Duymuş; Serhat Seyhan; Sanem Yılmaz; Uluç Yiş; Tahir Atik; Mehmet Fatih Yetkin; Hakan Gümüş
Source: check_circle
Crossref

The genetic causes of infertility in patients with oligozoospermia and azoospermia in Turkish population

Yeni Üroloji Dergisi
2021-06-30 | Journal article
DOI: 10.33719/yud.2021;16-2-834672
Contributors: Yavuz Onur Danacıoglu; Mustafa Gürkan Yenice; Fatih Akkas; Mustafa Soytas; Serhat Seyhan; Ali İhsan Tasci
Source: check_circle
Crossref

Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development

Journal of Clinical Investigation
2020-06-29 | Journal article
DOI: 10.1172/JCI136951
Contributors: Guney Bademci; Clemer Abad; Filiz B. Cengiz; Serhat Seyhan; Armagan Incesulu; Shengru Guo; Suat Fitoz; Emine Ikbal Atli; Nicholas C. Gosstola; Selma Demir et al.
Source: check_circle
Crossref

Molecular Heterogeneity in Cystic Fibrosis

Journal of Pediatric Genetics
2020-02-17 | Journal article
DOI: 10.1055/s-0040-1701646
Part of ISSN: 2146-4596
Part of ISSN: 2146-460X
Source: Self-asserted source
Serhat Seyhan

Optical coherence tomography and fundus autofluorescence imaging in an infant with RD3-related leber congenital amaurosis

Ophthalmic Genetics
2020-01-02 | Journal article
DOI: 10.1080/13816810.2020.1731837
ISSN: 1381-6810
ISSN: 1744-5094
Source: Self-asserted source
Serhat Seyhan

FOXF2is required for cochlear development in humans and mice

Human Molecular Genetics
2019-04-15 | Journal article
DOI: 10.1093/hmg/ddy431
ISSN: 0964-6906
ISSN: 1460-2083
Source: Self-asserted source
Serhat Seyhan

Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss

Proceedings of the National Academy of Sciences
2019-01-22 | Journal article
DOI: 10.1073/pnas.1810951116
ISSN: 0027-8424
ISSN: 1091-6490
Source: Self-asserted source
Serhat Seyhan

Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability

PLOS ONE
2018-11-30 | Journal article
DOI: 10.1371/journal.pone.0208324
Contributors: Megan McSherry; Hao Deng; Katherine E. Masih; Nursel H. Elcioglu; Pelin Celik; Ozge Balci; Filiz Basak Cengiz; Daniella Nunez; Claire J. Sineni; Serhat Seyhan et al.
Source: check_circle
Crossref

Peripheral neuropathy in Tangier disease: A literature review and assessment

Journal of the Peripheral Nervous System
2018-06 | Journal article
DOI: 10.1111/jns.12265
ISSN: 1085-9489
Source: Self-asserted source
Serhat Seyhan

22.5 MB DELETION OF 13q31.1-q34 ASSOCIATED WITH HPE, DWM, AND HSCR: A CASE REPORT AND REDEFINING THE SMALLEST DELETED REGIONS.

Genetic counseling (Geneva, Switzerland)
2016-01-01 | Journal article
PMID: 27192891
Source: Self-asserted source
Serhat Seyhan

A NEW ISOLATED 20q INTERSTITIAL DUPLICATION CASE AND ITS CLINICAL COMPARISON WITH SIMILAR ISOLATED CASES.

Genetic counseling (Geneva, Switzerland)
2016-01-01 | Journal article
PMID: 30204969
Source: Self-asserted source
Serhat Seyhan

A case of de novo mosaic 18q21.3 deletion with a mild phenotype.

Genetic counseling (Geneva, Switzerland)
2014-01-01 | Journal article
PMID: 24783659
Source: Self-asserted source
Serhat Seyhan
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