Carmen Martı́nez

Universidad Complutense de Madrid — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

21h-index3.0kcitations41works0.02yr avg
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Research Topics

Genomics, phytochemicals, and oxidative stress(8), Glutathione Transferases and Polymorphisms(7), Neuropeptides and Animal Physiology(6), Epigenetics and DNA Methylation(5), Heme Oxygenase-1 and Carbon Monoxide(4)

Publications41 total

Vasoactive Intestinal Peptide advances chondrogenesis and modulates pathogenic mediators in human osteoarthritis.
2025Open Access
Supplementary Table 1 from <i>TP53</i> and <i>KRAS2</i> Mutations in Plasma DNA of Healthy Subjects and Subsequent Cancer Occurrence: A Prospective Study
2023Open Access
Data from <i>TP53</i> and <i>KRAS2</i> Mutations in Plasma DNA of Healthy Subjects and Subsequent Cancer Occurrence: A Prospective Study
2023Open Access
Data from <i>TP53</i> and <i>KRAS2</i> Mutations in Plasma DNA of Healthy Subjects and Subsequent Cancer Occurrence: A Prospective Study
2023Open Access
Targeting Hedgehog Signaling with Glasdegib in Patients with Refractory Sclerotic Chronic Graft vs. Host Disease: A Report of Two Phase I/II Trials
Blood·2022
Anaesthesia management for emergency cesarean section in a patient with Aarskog-Scott syndrome.
2019
Data Quality in Rare Cancers Registration: The Report of the RARECARE Data Quality Study
Tumori Journal·2016· 30 citedOpen Access
Heme Oxygenase-1 and 2 Common Genetic Variants and Risk for Multiple Sclerosis
Scientific Reports·2016· 36 citedOpen Access
Heme Oxygenase 1 and 2 Common Genetic Variants and Risk for Essential Tremor
Medicine·2015· 23 citedOpen Access
The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis
Cellular and Molecular Immunology·2014· 7 citedOpen Access
NQO1gene rs1800566 variant is not associated with risk for multiple sclerosis
BMC Neurology·2014· 13 citedOpen Access
Hereditary Coproporphyria Associated with the Q306X Mutation in the Coproporphyrin Oxidase Gene Presenting with Acute Ataxia
Tremor and Other Hyperkinetic Movements·2013· 4 citedOpen Access
LINGO1 rs9652490 and rs11856808 polymorphisms are not associated with risk for multiple sclerosis
BMC Neurology·2013· 11 citedOpen Access
Hereditary Coproporphyria Associated with the Q306X Mutation in theCoproporphyrin Oxidase Gene Presenting with Acute Ataxia
PubMed·2012· 3 citedOpen Access
The Differential Effect of NAT2 Variant Alleles Permits Refinement in Phenotype Inference and Identifies a Very Slow Acetylation Genotype
PLoS ONE·2012· 53 citedOpen Access
Tears at the rotator cuff footprints: imaging characteristic on MRI and ultrasound, evolutions and clinical significance
2012
A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease
Pharmacogenetics and Genomics·2011· 26 cited
A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium
PLoS Genetics·2011· 318 citedOpen Access
Paraoxonase 1 (PON1) polymorphisms and risk for migraine
Journal of Neurology·2010· 21 cited
Paraoxonase 1 Polymorphisms Are Not Related with the Risk for Multiple Sclerosis
NeuroMolecular Medicine·2009· 20 cited
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Frequent Co-authors

Elena Garcı́a-Martı́n(22), José A. G. Agúndez(22), Hortensia Alonso‐Navarro(11), Félix Javier Jiménez‐Jiménez(11), José M. Ladero(6), Julián Benito‐León(6), José Francisco Plaza‐Nieto(6), Paolo Vineis(5), Mario Delgado(5), Rosa P. Gomariz(5), Manuel Díaz‐Rubio(5), María Elena Díaz Sánchez(5), Patricia Calleja(5), Diana Pisa(5), Lucía Ayuso‐Peralta(5), Eiliv Lund(4), Pierre Hainaut(4), Elio Ríboli(4), Javier Leceta(4), Domenico Palli(4)