Serpil Eraslan - Bogazici University

基本信息

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职业迁徙

个人简介

Serpil Eraslan currently works at Diagnosis Centre for Genetic Disorders, Koc University Hospital. Serpil does research in Genetics.

研究兴趣

论文共 82 篇作者统计合作学者相似作者

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Clinical and Molecular Characteristics of Patients with Fascio-scapulo-humeral Dystrophy 1 (FSHD 1): the First Cohort Investigating the Genotype-phenotype Characteristics of FSHD 1 Patients in Turkey (P3-11.019)

Gulshan Yunisova,Serpil Eraslan,Sahin Avci,İlker Eren,Mehmet Demirhan,Hulya Kayserili,Piraye Oflazer

Neurology（2024）

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Prenatal Diagnosis of Crossed Pulmonary Arteries with a Postnatal Diagnosis of CHARGE Syndrome

Funda Oztunc,Riza Madazli,Hakan Erenel,Didem Kaymak,Serpil Eraslan,Hulya Kayserili

FETAL AND PEDIATRIC PATHOLOGYno. 3 (2024): 246-250

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Identification of Germline Variants in 546 Breast/ Ovarian Cancer Families: Complementary Testing with Multigene NGS and MLPA Panels

Hilal Piril Saracoglu, Esra Borklu, Umut Altunoglu,Fatih Selcukbiricik,Kayhan Erturk,Dogan Vatansever,Levent Celik, Sahin Lacin, Didem Tunali,Sahin Avci,Orhan Agcaoglu,Hasan Karanlik, Can Atalay, Kerim Kaban,Ece Dilege,Cagatay Taskiran, Abdullah Igci,Nil Molinas Mandel,Serpil Eraslan, Hulya Kayserili

EUROPEAN JOURNAL OF HUMAN GENETICS (2024): 590-590

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Nance-Horan Syndrome: Characterization of dental, clinical and molecular features in three new families

Yeliz Guven,Hilal Piril Saracoglu,Sermin Dicle Aksakal,Tugba Kalaycı,Umut Altunoglu,Zehra Oya Uyguner,Serpil Eraslan,Esra Borklu,Hülya Kayserili

Research Square (Research Square) (2023)

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Revisiting TOP2B-related phenotypes: Three new cases and literature review

Ece Çepni,Esra Börklü,Şahin Avcı,Tuğba Kalaycı,Serpil Eraslan,Hülya Kayserili

Clinical geneticsno. 2 (2023): 251-258

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A Retrospective Cross-Sectional Analysis of Familial Adenomatous Polyposis Coli Cases

Elanur Yilmaz,Esra Yucel,Hilal-Piril Saracoglu,Emre Balik,Sahin Avci,Serpil Eraslan,Dursun Bugra,Hulya Kayserili

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 566-566

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The clinical and genetic characteristics of 17 cases with Congenital Myasthenic Syndrome: Data from a single center

Gulshan Yunisova,Ayfer Arduc Akcay,Sahin Avci,Serpil Eraslan,Hulya Kayserili,Piraye Oflazer

NEUROLOGY（2023）

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Nance-Horan Syndrome: Characterization of Dental, Clinical and Molecular Features in Three New Families

Yeliz Guven,Hilal Piril Saracoglu,Sermin Dicle Aksakal,Tugba Kalayci,Umut Altunoglu,Zehra Oya Uyguner,Serpil Eraslan,Esra Borklu,Hulya Kayserili

BMC oral health（2023）

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The Clinical and Genetic Characteristics of 17 Cases with Congenital Myasthenic Syndrome: Data from a Single Center (P2-8.002)

Gulshan Yunisova,Ayfer Arduç Akçay,Şahin Avcı,Serpil Eraslan,Hülya Kayserili,Piraye Oflazer

Neurologyno. 17_supplement_2 (2023)

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A New Family with a Novel OTUD6B Mutation: Practicing Whole Exome Sequencing for Antenatal Diagnosis of Tetralogy of Fallot

Esra Borklu,Umut Altunoglu,Serpil Eraslan,Hulya Kayserili

Molecular syndromology（2022）

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