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Genetic Variants of the NF-κB Pathway: Unraveling the Genetic Architecture of Psoriatic Disease

International journal of molecular sciences, 2021-11, Vol.22 (23), p.13004

2021

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The IFIH1/MDA5 rs1990760 Gene Variant (946Thr) Differentiates Early- vs. Late-Onset Skin Disease and Increases the Risk of Arthritis in a Spanish Cohort of Psoriasis

International journal of molecular sciences, 2023-10, Vol.24 (19), p.14803

2023

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Unified Criteria for Ultrasonographic Diagnosis of ADPKD

Journal of the American Society of Nephrology, 2009, Vol.20 (1), p.205-212

2009

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Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

Nature communications, 2014-10, Vol.5 (1), p.5326-5326, Article 5326

2014

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Genetic variation at IL12B , IL23R and IL23A is associated with psoriasis severity, psoriatic arthritis and type 2 diabetes mellitus

Journal of dermatological science, 2014-09, Vol.75 (3), p.167-172

2014

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Transcriptomic clustering of critically ill COVID-19 patients

The European respiratory journal, 2023-01, Vol.61 (1), p.2200592

2023

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Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients

Circulation. Cardiovascular genetics, 2017-04, Vol.10 (2)

2017

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Pharmacogenetics of tacrolimus after renal transplantation: analysis of polymorphisms in genes encoding 16 drug metabolizing enzymes

Clinical chemistry and laboratory medicine, 2011-05, Vol.49 (5), p.825-833

2011

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Mutation Analysis of the Main Hypertrophic Cardiomyopathy Genes Using Multiplex Amplification and Semiconductor Next-Generation Sequencing

Circulation Journal, 2014/11/25, Vol.78(12), pp.2963-2971

2014

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MiRNA Profile in the Substantia Nigra of Parkinson’s Disease and Healthy Subjects

Journal of molecular neuroscience, 2014-12, Vol.54 (4), p.830-836

2014

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Pharmacogenetics of calcineurin inhibitors in renal transplantation

Transplantation, 2009-08, Vol.88 (3 Suppl), p.S62-S67

2009

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Association between single nucleotide polymorphisms IL17RA rs4819554 and IL17E rs79877597 and Psoriasis in a Spanish cohort

Journal of dermatological science, 2015-11, Vol.80 (2), p.111-115

2015

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Association study of serotonin 2A receptor (5-HT2A) and serotonin transporter (5-HTT) gene polymorphisms with schizophrenia

Progress in neuro-psychopharmacology & biological psychiatry, 2007-04, Vol.31 (3), p.741-745

2007

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Familial hypercholesterolaemia in twin brothers born using in-vitro fertilisation with donor semen and ovules

Anales de Pediatría, 2021-03, Vol.94 (3), p.179-180

2021

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Identification of host endotypes using peripheral blood transcriptomics in a prospective cohort of patients with endocarditis

International journal of infectious diseases, 2024-11, Vol.148, p.107235, Article 107235

2024

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A Single Nucleotide Polymorphism in the Il17ra Promoter Is Associated with Functional Severity of Ankylosing Spondylitis

PloS one, 2016-07, Vol.11 (7), p.e0158905-e0158905

2016

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A search for new CYP3A4 variants as determinants of tacrolimus dose requirements in renal-transplanted patients

Pharmacogenetics and genomics, 2013-08, Vol.23 (8), p.445-448

2013

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A labor- and cost-effective non-optical semiconductor (Ion Torrent) next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman's syndrome patients

Journal of human genetics, 2014-07, Vol.59 (7), p.376-380

2014

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Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease

Translational psychiatry, 2019-01, Vol.9 (1), p.55-55, Article 55

2019

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Genetic Variation in the H19 - IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function

DNA and cell biology, 2018-07, Vol.37 (7), p.617-625

2018

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RICORS2040: the need for collaborative research in chronic kidney disease

Clinical kidney journal, 2022-03, Vol.15 (3), p.372-387

Ortiz, Alberto

2022

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Mitochondrial DNA haplogroups and risk of new-onset diabetes among tacrolimus-treated renal transplanted patients

Gene, 2014-03, Vol.538 (1), p.195-198

2014

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Defining a Methylation Signature Associated With Operational Tolerance in Kidney Transplant Recipients

Frontiers in immunology, 2021-08, Vol.12, p.709164-709164

2021

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Cardiovascular risk factors influence response to biological therapies in psoriasis

Journal of the American Academy of Dermatology, 2015-08, Vol.73 (2), p.327-329

2015

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Genetic Variants of the NF-κB Pathway: Unraveling the Genetic Architecture of Psoriatic Disease

The IFIH1/MDA5 rs1990760 Gene Variant (946Thr) Differentiates Early- vs. Late-Onset Skin Disease and Increases the Risk of Arthritis in a Spanish Cohort of Psoriasis

Unified Criteria for Ultrasonographic Diagnosis of ADPKD

Mutations in filamin C cause a new form of familial hypertrophic cardiomyopathy

Genetic variation at IL12B , IL23R and IL23A is associated with psoriasis severity, psoriatic arthritis and type 2 diabetes mellitus

Effects of IFIH1 rs1990760 variants on systemic inflammation and outcome in critically ill COVID-19 patients in an observational translational study

Transcriptomic clustering of critically ill COVID-19 patients

Screening of the Filamin C Gene in a Large Cohort of Hypertrophic Cardiomyopathy Patients

Pharmacogenetics of tacrolimus after renal transplantation: analysis of polymorphisms in genes encoding 16 drug metabolizing enzymes

Mutation Analysis of the Main Hypertrophic Cardiomyopathy Genes Using Multiplex Amplification and Semiconductor Next-Generation Sequencing

MiRNA Profile in the Substantia Nigra of Parkinson’s Disease and Healthy Subjects

Pharmacogenetics of calcineurin inhibitors in renal transplantation

Association between single nucleotide polymorphisms IL17RA rs4819554 and IL17E rs79877597 and Psoriasis in a Spanish cohort

Association study of serotonin 2A receptor (5-HT2A) and serotonin transporter (5-HTT) gene polymorphisms with schizophrenia

Familial hypercholesterolaemia in twin brothers born using in-vitro fertilisation with donor semen and ovules

Identification of host endotypes using peripheral blood transcriptomics in a prospective cohort of patients with endocarditis

A Single Nucleotide Polymorphism in the Il17ra Promoter Is Associated with Functional Severity of Ankylosing Spondylitis

A search for new CYP3A4 variants as determinants of tacrolimus dose requirements in renal-transplanted patients

A labor- and cost-effective non-optical semiconductor (Ion Torrent) next-generation sequencing of the SLC12A3 and CLCNKA/B genes in Gitelman's syndrome patients

Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer’s disease

Genetic Variation in the H19 - IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function

RICORS2040: the need for collaborative research in chronic kidney disease

Mitochondrial DNA haplogroups and risk of new-onset diabetes among tacrolimus-treated renal transplanted patients

Defining a Methylation Signature Associated With Operational Tolerance in Kidney Transplant Recipients

Cardiovascular risk factors influence response to biological therapies in psoriasis

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