Concepedia

Burcu Türkgenç

BT

Statistics

Publications

6

Citations

175

H-Index

6

Active since

2017

Affiliations

Bursa Uludağ Üni̇versi̇tesi̇(Current)

Acıbadem University

Near East University

Başkent University

Akdeniz University

Burcu Türkgenç is an author at Bursa Uludağ Üni̇versi̇tesi̇ specializing in molecular genetics, genetics, and genetic disorders.

ORCID

Publications per year

2017–2022

6

Publications

6

Bi-allelic Mutations in M1AP Are a Frequent Cause of Meiotic Arrest and Severely Impaired Spermatogenesis Leading to Male Infertility

Margot J. Wyrwoll, Şehime Gülsün Temel, Liina Nagirnaja et al. · The American Journal of Human Genetics · 2020 · 104 citations · Full text

, , +15

A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections

Neşe Akcan, Nedime Serakıncı, Burcu Türkgenç et al. · Frontiers in Endocrinology · 2017 · 20 citations · Full text

, , +17

Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

Munis Dündar, Umut Fahrioğlu, Saliha Handan Yıldız et al. · Functional & Integrative Genomics · 2022 · 15 citations · Full text

, , +14

<i>STUB1</i>polyadenylation signal variant AACAAA does not affect polyadenylation but decreases<i>STUB1</i>translation causing SCAR16

Burcu Türkgenç, Burçin Şanlıdağ, Amber Eker et al. · Human Mutation · 2018 · 14 citations · Full text

, , +17

A novel homozygous nonsense mutation in CAST associated with PLACK syndrome

Şehime Gülsün Temel, Bahriye Karakaş, Ümmühan Şeker et al. · Cell and Tissue Research · 2019 · 11 citations · Full text

, , +15

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