Claire J. Sineni

<i>FOXF2</i>is required for cochlear development in humans and mice

Güney Bademci, Clemer Abad, Armağan İncesulu et al. · Human Molecular Genetics · 2018 · 41 citations

Genetics, Genomic Mechanism, Human Cochlea +19

Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability

Megan McSherry, Katherine E. Masih, Nursel Elçioğlu et al. · PLoS ONE · 2018 · 25 citations · Full text

Genetics, Genetic Epidemiology, Whole Exome +17

A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss

Claire J. Sineni, Muzeyyen Yildirim‐Baylan, Shengru Guo et al. · Human Genetics · 2019 · 23 citations · Full text

Genetic Disorder, Genetics, Audiology +6

Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development

Güney Bademci, Clemer Abad, Filiz Başak Cengiz et al. · Journal of Clinical Investigation · 2020 · 18 citations · Full text

Long-range Cis-regulatory Elements, Ear Development, Genetics +19

Novel variant p.E269K confirms causative role of <i>PLS1</i> mutations in autosomal dominant hearing loss

Oscar Diaz‐Horta, Güney Bademci, Suna Tokgöz-Yılmaz et al. · Clinical Genetics · 2019 · 16 citations