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B. Alonso · SciRah

Researcher profile · Semantic Scholar

B. Alonso

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B. Alonso — researcher profile on SciRah

h-index: 19
Works: 42
Citations: 936

Most-cited papers

Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients
Juan Gómez, Rebeca Lorca, J. Reguero, C. Morís +8 more
2017Circulation: Cardiovascular Genetics83 citations Open access
Semantic Scholar
Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor next-generation sequencing.
Juan Gómez, J. Reguero, C. Morís, María Martín +4 more
2014Circulation Journal71 citations Open access
Semantic Scholar
[Mutations in sarcomeric genes MYH7, MYBPC3, TNNT2, TNNI3, and TPM1 in patients with hypertrophic cardiomyopathy].
M. García-Castro, E. Coto, J. Reguero, J. Berrazueta +5 more
2009Revista Española de Cardiología63 citations
Semantic Scholar
Mutational spectrum of the SPG4 (SPAST) and SPG3A (ATL1) genes in Spanish patients with hereditary spastic paraplegia
V. Álvarez, Elena Sánchez-Ferrero, C. Beetz, M. Díaz +16 more
2010BMC Neurology58 citations Open access
Semantic Scholar
FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients.
L. de Mena, L. Cardo, E. Coto, A. Miar +8 more
2010Neuroscience Letters52 citations Open access
Semantic Scholar
Espectro mutacional de los genes sarcoméricos MYH7, MYBPC3, TNNT2, TNNI3 y TPM1 en pacientes con miocardiopatía hipertrófica
Mónica García-Castro, E. Coto, J. Reguero, J. Berrazueta +5 more
200947 citations
Semantic Scholar
Late-onset Alzheimer's disease is associated with mitochondrial DNA 7028C/haplogroup H and D310 poly-C tract heteroplasmy
E. Coto, Juan Gómez, B. Alonso, A. Corao +6 more
2011Neurogenetics43 citations Open access
Semantic Scholar
IL17RA gene variants and anti-TNF response among psoriasis patients
A. Batalla, E. Coto, J. Gómez, N. Eirís +13 more
2016The Pharmacogenomics Journal41 citations
Semantic Scholar
Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function.
E. Coto, C. Díaz‐Corte, S. Tranche, Juan Gómez +5 more
2018Human Immunology40 citations Open access
Semantic Scholar
Mitochondrial DNA and TFAM gene variation in early-onset myocardial infarction: evidence for an association to haplogroup H.
M. Palacín, V. Álvarez, María Martín, M. Díaz +14 more
2011Mitochondrion (Amsterdam. Print)40 citations Open access
Semantic Scholar
Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease.
E. Coto, J. Reguero, P. Avanzas, I. Pascual +9 more
2019Immunology Letters33 citations Open access
Semantic Scholar
Common and rare CARD14 gene variants affect the antitumour necrosis factor response among patients with psoriasis
P. Coto-Segura, D. González-Fernández, A. Batalla, Juan Gómez +5 more
2016British Journal of Dermatology31 citations Open access
Semantic Scholar
KCNQ1 gene variants in the risk for type 2 diabetes and impaired renal function in the Spanish Renastur cohort.
C. Riobello, Juan Gómez, H. Gil-Peña, S. Tranche +11 more
2016Molecular and Cellular Endocrinology26 citations Open access
Semantic Scholar
Resequencing the whole MYH7 gene (including the intronic, promoter, and 3' UTR sequences) in hypertrophic cardiomyopathy.
E. Coto, J. Reguero, M. Palacín, Juan Gómez +11 more
2012Journal of Molecular Diagnostics25 citations Open access
Semantic Scholar
Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy.
Juan Gómez, Rebeca Lorca, J. Reguero, María Martín +6 more
2018Epigenomics24 citations Open access
Semantic Scholar
CDKAL1 gene variants affect the anti-TNF response among Psoriasis patients.
P. Coto-Segura, A. Batalla, D. González-Fernández, Juan Gómez +5 more
2015International Immunopharmacology22 citations Open access
Semantic Scholar
Functional polymorphisms in the CYP3A4, CYP3A5, and CYP21A2 genes in the risk for hypertension in pregnancy.
E. Coto, B. Tavira, R. Marín, F. Ortega +7 more
2010Biochemical and Biophysical Research Communications - BBRC21 citations Open access
Semantic Scholar
Lack of association between protocadherin 11-X/Y (PCDH11X and PCDH11Y) polymorphisms and late onset Alzheimer's disease.
A. Miar, V. Álvarez, A. Corao, B. Alonso +6 more
2011Brain Research20 citations Open access
Semantic Scholar
Influence of endothelial nitric oxide synthase polymorphisms in psoriasis risk
P. Coto-Segura, E. Coto, A. Mas‐Vidal, B. Morales +4 more
2011Archives of Dermatological Research20 citations Open access
Semantic Scholar
FURIN gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID‐19
E. Coto, G. Albaiceta, L. Amado-Rodríguez, M. García-Clemente +11 more
2022Journal of Medical Virology16 citations Open access
Semantic Scholar
The CCR5-delta32 variant might explain part of the association between COVID-19 and the chemokine-receptor gene cluster
Juan Gómez, Elías Cuesta-Llavona, G. Albaiceta, M. García-Clemente +11 more
2020medRxiv15 citations Open access
Semantic Scholar
NFKBIZ in Psoriasis: Assessing the association with gene polymorphisms and report of a new transcript variant.
P. Coto-Segura, L. González-Lara, Juan Gómez, N. Eirís +7 more
2017Human Immunology15 citations Open access
Semantic Scholar
Spectrum of Mutations in Hypertrophic Cardiomyopathy Genes Among Tunisian Patients
Nawel Jaafar, Juan Gómez, I. Kammoun, I. Zairi +7 more
2016Genetic Testing and Molecular Biomarkers15 citations Open access
Semantic Scholar
Common European Mitochondrial Haplogroups in the Risk for Psoriasis and Psoriatic Arthritis
P. Coto-Segura, J. Santos-Juanes, Juan Gómez, V. Álvarez +4 more
2012Genetic Testing and Molecular Biomarkers12 citations
Semantic Scholar
Gene Variant in the NF-κB Pathway Inhibitor NFKBIA Distinguishes Patients with Psoriatic Arthritis within the Spectrum of Psoriatic Disease
P. Coto-Segura, E. Coto, L. González-Lara, B. Alonso +3 more
2019BioMed Research International11 citations Open access
Semantic Scholar
A new SLC12A3 founder mutation (p.Val647Met) in Gitelman's syndrome patients of Roma ancestry.
H. Gil-Peña, E. Coto, F. Santos, M. Espino +8 more
2017Nefrología11 citations Open access
Semantic Scholar
A Next-Generation Sequencing of the NOTCH3 and HTRA1 Genes in CADASIL Patients
Ángela Fernández, Juan Gómez, B. Alonso, S. Iglesias +1 more
2015Journal of Molecular Neuroscience10 citations Open access
Semantic Scholar
The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain).
J. Reguero, J. Gómez, María Martín, J. P. Flórez +5 more
2013International Journal of Cardiology10 citations Open access
Semantic Scholar
A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients.
B. Tavira, Juan Gómez, S. Málaga, F. Santos +8 more
2015Gene8 citations Open access
Semantic Scholar
Amyloid Precursor Protein Gene (APP) Variation in Late-Onset Alzheimer’s Disease
A. Miar, V. Álvarez, A. Corao, M. Díaz +6 more
2011Journal of Molecular Neuroscience8 citations Open access
Semantic Scholar
Association of the Genetic Variation in the Long Non-Coding RNA FENDRR with the Risk of Developing Hypertrophic Cardiomyopathy
E. Cuesta-Llavona, Rebeca Lorca, Valeria Rolle, B. Alonso +8 more
2022Life7 citations Open access
Semantic Scholar
Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function
E. Coto, Carmen Díaz Corte, S. Tranche, Juan Gómez +6 more
2018DNA and Cell Biology6 citations Open access
Semantic Scholar
An elderly Jervell and Lange‐Nielsen patient heterozygous compound for two new KCNQ1 mutations
E. Coto, F. García-Fernández, D. Calvo, R. Salgado-Aranda +4 more
2017American Journal of Medical Genetics. Part A6 citations Open access
Semantic Scholar
Next generation sequencing of the NOTCH3 gene in a cohort of pulmonary hypertension patients.
Juan Gómez, J. Reguero, M. Junquera, C. Alvarez +4 more
2016International Journal of Cardiology5 citations Open access
Semantic Scholar
ABCB1 (MDR-1) pharmacogenetics of tacrolimus in renal transplanted patients: a Next Generation Sequencing approach
B. Tavira, Juan Gómez, C. Díaz‐Corte, B. Suarez +7 more
2015Clinical Chemistry and Laboratory Medicine5 citations Open access
Semantic Scholar
Functional polymorphisms in the CYP 3 A 4 , CYP 3 A 5 , and CYP 21 A 2 genes in the risk for hypertension in pregnancy
E. Coto, B. Tavira, R. Marín, F. Ortega +7 more
20105 citations
Semantic Scholar
Genetic Screening of a Large Panel of Genes Associated with Cardiac Disease in a Spanish Heart Transplanted Cohort
E. Cuesta-Llavona, Rebeca Lorca, B. Díaz-Molina, J. Lambert-Rodríguez +7 more
2022Cardiogenetics4 citations Open access
Semantic Scholar
The APOB polymorphism rs1801701 A/G (p.R3638Q) is an independent risk factor for early-onset coronary artery disease: Data from a Spanish cohort.
E. Coto, Rebeca Lorca, J. Rodríguez-Reguero, María Martín +10 more
2021NMCD. Nutrition Metabolism and Cardiovascular Diseases4 citations
Semantic Scholar
DNA variation in myoMIRs of the 1, 133, and 208 families in hypertrophic cardiomyopathy
M. Palacín, E. Coto, J. Reguero, María Martín +5 more
20112 citations Open access
Semantic Scholar
FRI0461 GENETIC ANALYSIS OF THE NF-KB PATHWAY CAN BE USEFUL TO DISTINGUISH PATIENTS AT RISK OF PSORIATIC ARTHRITIS WITHIN THE SPECTRUM OF PSORIATIC DISEASE
Rubén Queiró Silva, P. Coto-Segura, L. González-Lara, B. Alonso +3 more
2019Psoriatic arthritis1 citations Open access
Semantic Scholar
Next generation sequencing search for uromodulin gene variants related with impaired renal function
Juan Gómez, C. Díaz‐Corte, S. Tranche, F. Álvarez +3 more
2015Molecular Biology Reports1 citations Open access
Semantic Scholar
Next generation sequencing search for uromodulin gene variants related with impaired renal function
Juan Gómez, C. Díaz‐Corte, S. Tranche, F. Álvarez +3 more
2015Molecular Biology Reports0 citations Open access
Semantic Scholar

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