Ayça Aykut

Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss

Hüseyin Önay, Ayça Aykut, Güney Bademci et al. · PLoS ONE · 2015 · 64 citations · Full text

Genetics, Genetic Epidemiology, Disease Gene Identification +17

A hypofunctional PAX1 mutation causes autosomal recessively inherited otofaciocervical syndrome

Esther Pohl, Ayça Aykut, Filippo Beleggia et al. · Human Genetics · 2013 · 60 citations

Mendelian Disorder, Genetic Disorder, Genetics +3

Fetal Gene Therapy Using a Single Injection of Recombinant AAV9 Rescued SMA Phenotype in Mice

Afrooz Rashnonejad, Gholamhossein Amini Chermahini, Cumhur Gündüz et al. · Molecular Therapy · 2019 · 55 citations · Full text

Targeted multi-gene panel testing for the diagnosis of Bardet Biedl syndrome: Identification of nine novel mutations across BBS1, BBS2, BBS4, BBS7, BBS9, BBS10 genes

Aslı Ece Solmaz, Hüseyin Önay, Ayça Aykut et al. · European Journal of Medical Genetics · 2015 · 45 citations

Mendelian Disorder, Genetic Disorder, Medicine +10

Melanocortin 4 receptor (MC4R) gene variants in children and adolescents having familial early-onset obesity: genetic and clinical characteristics

Ayça Aykut, Samim Özen, Damla Gökşen et al. · European Journal of Pediatrics · 2020 · 37 citations · Full text

Obesity, Metabolic Syndrome, Childhood Obesity +8