Gustavo Pérez de Nanclares

Author

Also Known As

A. Vela, Alejandro García Castaño, Ana Belén de la Hoz, G Perez-Nanclares, G Pérez-Nanclares, G. Perez Nanclares, G. Perez-Nanclares, G. Perez‐Nanclares, G. Pérez de Nanclares Leal, G. Pérez-Nanclares

Publications

1.1K

Citations

H-Index

Concepts

All Affiliations

Hospital de Cruces BioCruces Health research Institute Centre for Biomedical Network Research on Rare Diseases University of the Basque Country Centro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas

About

Gustavo Pérez de Nanclares is an author at Hospital de Cruces specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	207
2	Cell Biology	2	2	28
3	Health Sciences	1	1	18
4	Public Health	1	1	18
5	Blood Transplantation	1	1	15

Gustavo Pérez de Nanclares

Publications

Citations

H-Index

Page 1

	Year	Citations
Immunogenicity and reactogenicity of BNT162b2 booster in ChAdOx1-S-primed participants (CombiVacS): a multicentre, open-label, randomised, controlled, phase 2 trial Alberto M. Borobia, Antonio J. Carcas, Mayte Pérez‐Olmeda, The Lancet	2021	384
Novel mutations in <i>MEN1</i> , <i>CDKN1B</i> and <i>AIP</i> genes in patients with multiple endocrine neoplasia type 1 syndrome in Spain Oihana Belar, Carmen de la Hoz, Gustavo Pérez de Nanclares, Clinical Endocrinology	2011	69
MICA response to gliadin in intestinal mucosa from celiac patients Ainhoa Martín‐Pagola, Gustavo Pérez de Nanclares, Lourdes Ortíz, Immunogenetics Mica ResponseAutoimmune DiseaseMucosal ImmunologyImmunologyGastroenterology	2004	50
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
Poor phenotype-genotype association in a large series of patients with Type III Bartter syndrome Alejandro García‐Castaño, Gustavo Pérez de Nanclares, Leire Madariaga, PLoS ONE	2017	43
Molecular diagnosis of distal renal tubular acidosis in Tunisian patients: proposed algorithm for Northern Africa populations for the ATP6V1B1, ATP6V0A4 and SCL4A1genes Donia Elhayek, Gustavo Pérez de Nanclares, Slaheddine Chouchane, BMC Medical Genetics	2013	41
Exclusion of the <i>GNAS</i> locus in PHP-Ib patients with broad <i>GNAS</i> methylation changes: Evidence for an autosomal recessive form of PHP-Ib? Eduardo Fernández‐Rebollo, Guiomar Pérez de Nanclares, Beatriz Lecumberri, Journal of Bone and Mineral Research	2011	38
A founder mutation in the CLCNKB gene causes Bartter syndrome type III in Spain Juan Rodríguez‐Soriano, Alfredo Vallo, Gustavo Pérez de Nanclares, Pediatric Nephrology Founder MutationMendelian DisorderGenetic DisorderGeneticsPathogenesis	2005	38
FGFs-1 and -2, and TGFβ 1 as Inductive Signals Modulating in vitro Odontoblast Differentiation Fernando Unda, Amaya Martín, Carlos Ernesto Hernández Hernández, Advances in Dental Research	2001	36
Analysis of the Expression of MICA in Small Intestinal Mucosa of Patients with Celiac Disease Ainhoa Martín‐Pagola, Lourdes Ortíz, Gustavo Pérez de Nanclares, Journal of Clinical Immunology Autoimmune DiseasePathogenesisImmunologyGastroenterologyPathology	2003	29

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