Nermin Başerer

Frequencies of gap‐ and tight‐junction mutations in Turkish families with autosomal‐recessive non‐syndromic hearing loss

M Emiroglu, Asadollah Ghanbari, Nermin Başerer et al. · Clinical Genetics · 2003 · 94 citations

Life Sciences, Genetics, Molecular Genetics +17

The novel R75Q mutation in the <i>GJB2</i> gene causes autosomal dominant hearing loss and palmoplantar keratoderma in a Turkish family

Turgut Tükel, Can Baykal, Hacer Eris et al. · Clinical Genetics · 2002 · 75 citations

Life Sciences, Genetics, Molecular Genetics +17

Mutations in the<i>lipoma HMGIC fusion partner-like 5 (LHFPL5)</i>gene cause autosomal recessive nonsyndromic hearing loss

Ersan Kalay, Yun Li, Abdullah Üzümcü et al. · Human Mutation · 2006 · 71 citations

Life Sciences, Genetics, Molecular Genetics +16

Does the Addition of Hyperbaric Oxygen Therapy to the Conventional Treatment Modalities Influence the Outcome of Sudden Deafness?

İsmet Aslan, Çağatay Oysu, Bayram Veyseller et al. · Otolaryngology · 2002 · 66 citations

Health Professions, Audiology, Otolaryngology +12

<i>MYO15A</i> (<i>DFNB3</i>) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation

Ersan Kalay, Abdullah Üzümcü, Elmar Krieger et al. · American Journal of Medical Genetics Part A · 2007 · 52 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17