Jesús Solera

Universidad Autónoma de Madrid — Spain

Biochemistry, Genetics and Molecular Biology · Life Sciences

14h-index727citations43works8.02yr avg
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Research Topics

BRCA gene mutations in cancer(6), Lysosomal Storage Disorders Research(6), Glycogen Storage Diseases and Myoclonus(6), Virus-based gene therapy research(5), Cancer Genomics and Diagnostics(5)

Publications43 total

Tetrahedral DNA nanostructures, graphene and carbon nanodots-based electrochemiluminescent biosensor for BRCA1 gene mutation detection
Talanta·2024· 8 citedOpen Access
Genetic analysis of 76 Spanish Pompe disease patients: Identification of 12 novel pathogenic GAA variants and functional characterization of splicing variants
Gene·2021· 4 cited
Expression and Characterization of the Naturally Occurring Mutation L394R in Human γ-Glutamyl Carboxylase
UNC Libraries·2021Open Access
Functionalization of a Few-Layer Antimonene with Oligonucleotides for DNA Sensing
ACS Applied Nano Materials·2020· 36 cited
Reevaluating the pathogenicity of the mutation c.1194 +5 G>A in GAA gene by functional analysis of RNA in a 61-year-old woman diagnosed with Pompe disease by muscle biopsy
Neuromuscular Disorders·2018· 2 cited
Evaluation of Breast Cancer Patients with Genetic Risk in a University Hospital: Before and After the Implementation of a Heredofamilial Cancer Unit
Journal of Genetic Counseling·2017· 8 cited
La ley del Corazón: Los lugares de la luz
Cameraman: Revista técnica cinematográfica·2017
Five Years of Multidisciplinary Care in Hereditary Cancer: Our Experience in a Spanish University Hospital
Oncology·2016· 3 cited
Compliance and impact of screening on individuals at high risk of breast and ovarian cancer syndrome (BOCS).
Journal of Clinical Oncology·2016
PanGen-Fam: Spanish registry of hereditary pancreatic cancer
European Journal of Cancer·2015· 44 cited
First one thousand families: Our multidisciplinary experience in the heredo-familial cancer unit from a Spanish University Hospital.
Journal of Clinical Oncology·2015· 1 cited
Targeted screening for the detection of Pompe disease in patients with unclassified limb-girdle muscular dystrophy or asymptomatic hyperCKemia using dried blood: A Spanish cohort
Neuromuscular Disorders·2015· 59 cited
Genetic and phenotypic characterization of families with familial pancreatic cancer and screening of high-risk individuals.
Journal of Clinical Oncology·2015
Dried Blood Spot for Screening for Late-Onset Pompe Disease: A Spanish Cohort
Journal of Neuromuscular Diseases·2015· 3 citedOpen Access
A Multidisciplinary Approach to Heredofamilial Cancer Syndromes: Evaluation of the First Four Years of Experience at a Spanish University Hospital
Annals of Oncology·2014
Novel mutation in the<i>PTCH1</i>gene in a patient with Gorlin syndrome with prominent clinical features
Clinical and Experimental Dermatology·2014· 2 cited
Goya y Velázquez la condición humana
Dialnet (Universidad de la Rioja)·2014
Primary Dermal Melanoma: A Case Report and a Review of the Literature
Actas Dermo-Sifiliográficas·2013· 6 citedOpen Access
Noninvasive Diagnosis of Hypolactasia With 4-Galactosylxylose (Gaxilose)
Journal of Clinical Gastroenterology·2013· 28 cited
Recurrence of Hirschsprung disease due to maternal mosaicism of a novel <i><scp>RET</scp></i> gene mutation
Clinical Genetics·2013· 3 cited
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Frequent Co-authors

Darrel W. Stafford(5), Cinthia Amiñoso(5), Sara López‐Tarruella(4), Santiago Lizarraga(4), Oscar Bueno(4), Iván Márquez‐Rodas(4), Benjamin Brenner(3), Beatriz Sánchez-Vega(3), Eduardo Gutiérrez‐Rivas(3), Isabel Illa(3), Adolfo López de Munaín(3), Luís Jiménez(3), Carmen Guillén‐Ponce(3), Julie Earl(3), Miguel Martín(3), J.A. Pajares(3), Andrés J. Muñoz Martín(3), Sheue-Mei Wu(2), Naomi Lanir(2), Juan J. Vílchez(2)