Concepedia

Zeliha Görmez

ZG

Statistics

Publications

8

Citations

155

H-Index

8

Active since

2013

Affiliations

Türkiye Bilimsel ve Teknolojik Araştırma Kurumu(Current)

TUBITAK BILGEM

Istanbul University

TÜBİTAK Marmara Research Center

Acıbadem University

Zeliha Görmez is an author at Türkiye Bilimsel ve Teknolojik Araştırma Kurumu specializing in genetics, molecular genetics, and medical genetics.

ORCID

Publications per year

2013–2019

8

Publications

8

HomSI: a homozygous stretch identifier from next-generation sequencing data

Zeliha Görmez, Burcu Bakır-Güngör, Mahmut Şamil Sağıroğlu · Bioinformatics · 2013 · 45 citations · Full text

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Loss-of-Function Mutations in ELMO2 Cause Intraosseous Vascular Malformation by Impeding RAC1 Signaling

Arda Çetinkaya, Jingwei Rachel Xiong, İbrahim Vargel et al. · The American Journal of Human Genetics · 2016 · 36 citations · Full text

, , +12

Coffin-Siris syndrome with café-au-lait spots, obesity and hyperinsulinism caused by a mutation in the <i>ARID1B</i> gene

Fatma Müjgan Sönmez, Eyyüp Üçtepe, Mehmet Gündüz et al. · Intractable & Rare Diseases Research · 2016 · 16 citations · Full text

, , +17

Myophosphorylase ( PYGM ) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease

Güldal İnal Gültekin, Bahar Toptaş-Hekimoğlu, Zeliha Görmez et al. · Neuromuscular Disorders · 2017 · 14 citations · Full text

, , +10

A further family of Stromme syndrome carrying <i>CENPF</i> mutation

Ferda Özkınay, Zeliha Görmez, Mahmut Şamil Sağıroğlu et al. · American Journal of Medical Genetics Part A · 2017 · 12 citations

, , +15

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