Alicia López‐Nevot

Author

Alicia López‐Nevot

Hospital Universitario Virgen de las Nieves

Also Known As

A López-Nevot, Alicia Lopez-Nevot, Alicia Lopez‐Nevot, Alicia López-Nevot, Alicia López‐Nevot, Haruhiko Sizuku

Publications

376

Citations

H-Index

Concepts

All Affiliations

Hospital Universitario Virgen de las Nieves Hospital de Poniente Complejo Hospitalario de Pontevedra Complejo Hospitalario Universitario de Santiago Pfizer-University of Granada-Junta de Andalucía Centre for Genomics and Oncological Research

About

Alicia López‐Nevot is an author at Hospital Universitario Virgen de las Nieves specializing in medicine, hearing loss, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	108
2	Pathology	2	2	38
3	Arts	1	1	20
4	Allergy	1	1	18
5	Immunology	1	1	70

Alicia López‐Nevot

Publications

367

Citations

H-Index

Page 1

	Year	Citations
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, American Journal of Medical Genetics Part A	2005	80
Allelic variants in TLR10 gene may influence bilateral affectation and clinical course of Meniere’s disease Teresa Requena, Irene Gázquez, Antonia Moreno, Immunogenetics Allelic VariantBilateral AffectationAutoimmune DiseaseGeneticsImmunology	2013	70
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, The Laryngoscope	2009	46
Absence of COCH mutations in patients with Meniere disease Elena Sánchez, José A. López‐Escámez, Miguel Ángel López‐Nevot, European Journal of Human Genetics Coch MutationsMendelian DisorderOphthalmologyGenetic DisorderNeurotology	2004	40
MICA-STR A.4 Is Associated With Slower Hearing Loss Progression in Patients With Ménière’s Disease Irene Gázquez, Antonia Moreno, Ismael Arán, Otology & Neurotology	2012	38
[Diagnosis of common causes of vertigo using a structured clinical history]. José A. López‐Escámez, Alicia López‐Nevot, Maria J. Gámiz, PubMed	2000	29
Functional variants of MIF, INFG and TFNA genes are not associated with disease susceptibility or hearing loss progression in patients with Ménière’s disease Irene Gázquez, Antonia Moreno, Teresa Requena, European Archives of Oto-Rhino-Laryngology Hearing Loss ProgressionGenetic DisorderGeneticsGenetic EpidemiologyAudiology	2012	20
Expression of A, B, C and DR antigens in definite Meniere's disease in a Spanish population José A. López‐Escámez, Alicia López‐Nevot, Rosario Mendoza Cortes, European Archives of Oto-Rhino-Laryngology Dr AntigensAllergySpanish PopulationPathologyDefinite Meniere	2002	18
Functional Variants in <i>NOS1</i> and <i>NOS2A</i> Are Not Associated with Progressive Hearing Loss in Ménière's Disease in a European Caucasian Population Irene Gázquez, José A. López‐Escámez, Antonia Ruíz Moreno, DNA and Cell Biology	2011	13
Poly(ADP-ribose) polymerase-1 (PARP-1) longer alleles spanning the promoter region may confer protection to bilateral Meniere's disease José A. López‐Escámez, Antonia Moreno, Mónica Bernal, Acta Oto-Laryngologica	2009	13

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