Miguel A. Moreno‐Pelayo

Author

Hospital Universitario Ramón y Cajal ORCID

Also Known As

M A Moreno-Pelayo, M Moreno-Pelayo, M. A. Moreno Pelayo, M. A. Moreno-Pelayo, M. A. Moreno‐Pelayo, M. Á Moreno-Pelayo, M.-A. Moreno-Pelayo, M.A. Moreno-Pelayo, M.A. Moreno‐Pelayo, M.Á. Moreno Pelayo

Publications

4.5K

Citations

H-Index

109

Concepts

All Affiliations

Hospital Universitario Ramón y Cajal Centre for Biomedical Network Research on Rare Diseases Instituto Ramón y Cajal de Investigación Sanitaria Centro de Investigación Biomédica en Red Instituto de Salud Carlos III

About

Miguel A. Moreno‐Pelayo is an author at Hospital Universitario Ramón y Cajal specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	26	1.8K
2	Arts	9	9	1.5K
3	Engineering	2	2	54
4	Health Sciences	2	2	129
5	Natural Sciences	1	1	28

Miguel A. Moreno‐Pelayo

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
A Deletion Involving the Connexin 30 Gene in Nonsyndromic Hearing Impairment Ignacio del Castillo, Manuela Villamar, Miguel A. Moreno‐Pelayo, New England Journal of Medicine	2002	582
Mutations in the seed region of human miR-96 are responsible for nonsyndromic progressive hearing loss Ángeles Mencía, Silvia Modamio‐Høybjør, Nick Redshaw, Nature Genetics Developmental BiologyGeneticsAudiologySeed RegionArts	2009	548
An ENU-induced mutation of miR-96 associated with progressive hearing loss in mice Morag A. Lewis, Elizabeth Quint, Anne M. Glazier, Nature Genetics Developmental BiologyGeneticsArtsAuditory PhysiologyMicrorna Detection	2009	301
Prevalence and Evolutionary Origins of the del(GJB6-D13S1830) Mutation in the DFNB1 Locus in Hearing-Impaired Subjects: a Multicenter Study Ignacio del Castillo, Miguel A. Moreno‐Pelayo, Francisco Castillo, The American Journal of Human Genetics Genetic DisorderGeneticsGenetic EpidemiologyAudiologyEvolutionary Origins	2003	289
Auditory neuropathy in patients carrying mutations in the otoferlin gene (<i>OTOF</i>) Montserrat Rodríguez-Ballesteros, Francisco Castillo, Yolanda Martín, Human Mutation	2003	196
A multicenter study on the prevalence and spectrum of mutations in the otoferlin gene (<i>OTOF</i>) in subjects with nonsyndromic hearing impairment and auditory neuropathy Montserrat Rodríguez-Ballesteros, Raúl Reynoso, M. A. Gil Olarte, Human Mutation	2008	178
KCNQ4 K+ channels tune mechanoreceptors for normal touch sensation in mouse and man Matthias Heidenreich, Stefan G. Lechner, Vitya Vardanyan, Nature Neuroscience Haptic FeedbackKcnq4 K+ ChannelsNeurophysiologyPhysiologyHaptic Technology	2011	111
Consensus interpretation of the p.Met34Thr and p.Val37Ile variants in GJB2 by the ClinGen Hearing Loss Expert Panel Jun Shen, Andrea M. Oza, Ignacio del Castillo, Genetics in Medicine GeneticsP.val37ile VariantsGenetic EpidemiologyPathologyCochlear Development	2019	98
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss Michael S. Hildebrand, Matías Morin, Nicole C. Meyer, Human Mutation GeneticsGenetic EpidemiologyPathologyNeurotologyMolecular Genetics	2011	92
ClinGen expert clinical validity curation of 164 hearing loss gene–disease pairs Marina T. DiStefano, Sarah E. Hemphill, Andrea M. Oza, Genetics in Medicine Genetic EpidemiologyAudiologyPathologyHearing DisordersNeurotology	2019	91

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