Alicia López‐Nevot

High prevalence of the <i>W24X</i> mutation in the gene encoding connexin‐26 (<i>GJB2</i>) in Spanish Romani (gypsies) with autosomal recessive non‐syndromic hearing loss

Araceli Álvarez, Ignacio del Castillo, Manuela Villamar et al. · American Journal of Medical Genetics Part A · 2005 · 81 citations

Life Sciences, Genetics, Molecular Genetics +17

Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere’s disease

Teresa Requena, Irene Gázquez, Antonia Moreno et al. · Immunogenetics · 2013 · 73 citations · Full text

Life Sciences, Genetics, Neurology +12

Association of a functional polymorphism of <i>PTPN22</i> encoding a lymphoid protein phosphatase in bilateral Meniere's disease

José A. López‐Escámez, Pablo Sáenz-López, Lourdes Acosta et al. · The Laryngoscope · 2009 · 48 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Absence of COCH mutations in patients with Meniere disease

Elena Sánchez, José A. López‐Escámez, Miguel Ángel López‐Nevot et al. · European Journal of Human Genetics · 2004 · 41 citations

Medicine, Genetics, Otolaryngology +14

MICA-STR A.4 Is Associated With Slower Hearing Loss Progression in Patients With Ménière’s Disease

Irene Gázquez, Antonia Moreno, Ismael Arán et al. · Otology & Neurotology · 2012 · 39 citations

Life Sciences, Genetics, Immunology +17