Metin Eser profile image
Metin Eser Specialist UNIVERSITY OF HEALTH SCIENCES, İSTANBUL ÜMRANİYE HEALTH RESEARCH CENTER, DEPARTMENT OF INTERNAL MEDICINE, DEPARTMENT OF MEDICAL GENETICS
Publication 5 Review 0 CrossRef Cited 1
5 Publication
0 Review
1 CrossRef Cited
0000-0001-7118-7958

Research Fields

Developmental Genetics

Institution

UNIVERSITY OF HEALTH SCIENCES, İSTANBUL ÜMRANİYE HEALTH RESEARCH CENTER, DEPARTMENT OF INTERNAL MEDICINE, DEPARTMENT OF MEDICAL GENETICS

Publications

Genetic Complexity of SLE: A Retrospective Analysis of Gene Mutations and Clinical Correlations
Authors: Metin Eser , Gulam Hekimoğlu , Özgür Kasapçopur , Sezgin Şahin , Nergis Akay , Betül Sözeri
Published: 2026 , Medical Records
DOI: -
FAVORITE 0 TOTAL DOWNLOAD COUNT 52

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52

Poly (ADP-ribose) Polymerase Inhibitor Responses in High-Grade Serous Ovarian Cancer: Insights from BRCA Germline-Negative and Somatic Mutation-Positive Cases
Authors: Metin Eser , Gulam Hekimoğlu , Murat Hakkı Yarar , Fatma Gülçiçek Ayrancı , Esra Keles Peker , Murat Api , Melike Özçelik
Published: 2025 , Black Sea Journal of Health Science
DOI: 10.19127/bshealthscience.1793827
FAVORITE 0 TOTAL DOWNLOAD COUNT 228

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228

Myotonia may be a sign that prompts genetic testing for myotonic dystrophy type 1
Authors: Metin Eser , Gulam Hekimoğlu , Büşra Kutlubay
Published: 2025 , The European Research Journal
DOI: 10.18621/eurj.1553885
FAVORITE 0 TOTAL DOWNLOAD COUNT 420

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420

X-Linked Intellectual Disability with NEXMIF Gene Mutation and Developmental Delay with GNAO1 Gene Mutation: Case Report
Authors: Tayfun Aygün , Sevim Yener , Nurullah Yücel , Gulam Hekimoğlu , Metin Eser , Zekeriya İlce
Published: 2024 , Medical Research Reports
DOI: 10.55517/mrr.1439712
FAVORITE 0 TOTAL DOWNLOAD COUNT 489

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489

Epidemiological Evaluation of Next-Generation Sequencing and MLPA Results in Patients with a Presumptive Cystic Fibrosis Diagnosis
Authors: Sezin Canbek , Murat Hakkı Yarar , Metin Eser , Hakan Yazan
Published: 2024 , Osmangazi Tıp Dergisi
DOI: 10.20515/otd.1482361
FAVORITE 0 TOTAL DOWNLOAD COUNT 1223

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1223

Articles published in
Black Sea Journal of Health Science
Black Sea Journal of Health Science
Medical Records
Medical Records
Medical Research Reports
Medical Research Reports
Osmangazi Tıp Dergisi
Osmangazi Tıp Dergisi
The European Research Journal
The European Research Journal
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Publications

X-Linked Intellectual Disability with NEXMIF Gene Mutation and Developmental Delay with GNAO1 Gene Mutation: Case Report
Authors: Tayfun Aygün , Sevim Yener , Nurullah Yücel , Gulam Hekimoğlu , Metin Eser , Zekeriya İlce
Published: 2024 , Medical Research Reports
DOI: 10.55517/mrr.1439712
CITED 1 FAVORITE 0 TOTAL DOWNLOAD COUNT 489

1

0

489

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