Sonia Mayo - Concepedia

Author

Sonia Mayo

Hospital Universitari i Politècnic La Fe ORCID

Also Known As

Mayo, S., S. Mayo, Sonia Mayo, Sonia Mayo de Andrés

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Hospital Universitari i Politècnic La Fe Universitat de València Instituto de Investigación de Enfermedades Raras University of York Hospital Universitario Doctor Peset

About

Sonia Mayo is an author at Hospital Universitari i Politècnic La Fe specializing in medicine, genetics, and gene expression.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	414
2	Natural Sciences	2	2	126
3	Biology	2	2	74
4	Engineering	1	1	35
5	Biostatistics	1	1	24

Sonia Mayo

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
The Arabidopsis heavy metal P‐type ATPase HMA5 interacts with metallochaperones and functions in copper detoxification of roots Nuria Andrés‐Colás, Vicente Sancenón, Susana Rodríguez‐Navarro, The Plant Journal	2005	335
High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing Francisco Martı́nez, Alfonso Caro‐Llopis, Mónica Rosello, Journal of Medical Genetics	2016	128
Identification of Intellectual Disability Genes in Female Patients with a Skewed X-Inactivation Pattern Nathalie Fieremans, Hilde Van Esch, Maureen Holvoet, Human Mutation X-inactivation PatternsGeneticsGenetic EpidemiologyDisease Gene IdentificationEpigenetics	2016	125
Copy-Number Gains of HUWE1 Due to Replication- and Recombination-Based Rearrangements Guy Froyen, Stefanie Belet, Francisco Martı́nez, The American Journal of Human Genetics Genome InstabilityCell DivisionNatural SciencesGeneticsDna Replication	2012	87
Clinical laboratory automated urinalysis: comparison among automated microscopy, flow cytometry, two test strips analyzers, and manual microscopic examination of the urine sediments Sonia Mayo, Delia Acevedo, Carmen Quiñones‐Torrelo, Journal of Clinical Laboratory Analysis	2008	68
Novel mutations of NFIX gene causing Marshall-Smith syndrome or Sotos-like syndrome: one gene, two phenotypes Francisco Martı́nez, Purificación Marín Reina, A. Sanchís Calvo, Pediatric Research Mendelian DisorderDisease MechanismMarshall-smith SyndromeMedicineGenetics	2015	48
Detection of Hypomethylation Syndrome among Patients with Epigenetic Alterations at the<i>GNAS</i>Locus Gustavo Pérez de Nanclares, Valeria Romanelli, Sonia Mayo, The Journal of Clinical Endocrinology & Metabolism	2012	45
De novo mutations in genes of mediator complex causing syndromic intellectual disability: mediatorpathy or transcriptomopathy? Alfonso Caro‐Llopis, Mónica Rosello, Carmen Orellana, Pediatric Research Mendelian DisorderGenetic DisorderGeneticsFragile X SpectrumDegenerative Disease	2016	43
Prenatal Diagnosis of a Female Fetus with Ring Chromosome 9, 46,XX,r(9)(p24q34), and a de novo Interstitial 9p Deletion Vanessa Penacho, Francisco Galán, Tina-A. Martín-Bayón, Cytogenetic and Genome Research	2014	41
Modulation of copper deficiency responses by diurnal and circadian rhythms in<i>Arabidopsis thaliana</i> Ana Perea‐García, Amparo Andrés-Bordería, Sonia Mayo, Journal of Experimental Botany BotanyMolecular RegulationGeneticsCryptochromeEpigenetics	2015	39

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