User profiles for "author:Iván Galván-Femenía"
Iván Galván-FemeníaInstitute for Research in Biomedicine (IRB Barcelona) Verified email at irbbarcelona.org Cited by 3416 |
[HTML][HTML] The chromatin network helps prevent cancer-associated mutagenesis at transcription-replication conflicts
A Bayona-Feliu, E Herrera-Moyano… - Nature …, 2023 - nature.com
Genome instability is a feature of cancer cells, transcription being an important source of
DNA damage. This is in large part associated with R-loops, which hamper replication …
DNA damage. This is in large part associated with R-loops, which hamper replication …
ADAR1 affects HCV infection by modulating innate immune response
The hepatitis C virus (HCV) is a globally prevalent infectious pathogen. As many as 80% of
people infected with HCV do not control the virus and develop a chronic infection. Response …
people infected with HCV do not control the virus and develop a chronic infection. Response …
GCAT| Genomes for life: a prospective cohort study of the genomes of Catalonia
M Obón-Santacana, M Vilardell, A Carreras, X Duran… - BMJ open, 2018 - bmjopen.bmj.com
Purpose The prevalence of chronic non-communicable diseases (NCDs) is increasing
worldwide. NCDs are the leading cause of both morbidity and mortality, and it is estimated …
worldwide. NCDs are the leading cause of both morbidity and mortality, and it is estimated …
Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort
I Galván-Femenía, M Obón-Santacana… - Journal of Medical …, 2018 - jmg.bmj.com
Background Heritability estimates have revealed an important contribution of SNP variants
for most common traits; however, SNP analysis by single-trait genome-wide association …
for most common traits; however, SNP analysis by single-trait genome-wide association …
[HTML][HTML] Disease networks identify specific conditions and pleiotropy influencing multimorbidity in the general population
Multimorbidity is an emerging topic in public health policy because of its increasing
prevalence and socio-economic impact. However, the age-and gender-dependent trends of …
prevalence and socio-economic impact. However, the age-and gender-dependent trends of …
[HTML][HTML] Identification of intergenerational epigenetic inheritance by whole genome DNA methylation analysis in trios
A Díez-Villanueva, B Martín, F Moratalla-Navarro… - Scientific Reports, 2023 - nature.com
Genome-wide association studies have identified thousands of loci associated with common
diseases and traits. However, a large fraction of heritability remains unexplained. Epigenetic …
diseases and traits. However, a large fraction of heritability remains unexplained. Epigenetic …
Revisiting the UK Genetic Severity Score for NF2: a proposal for the addition of a functional genetic component
N Catasús, B Garcia, I Galván-Femenía… - Journal of Medical …, 2022 - jmg.bmj.com
Background Neurofibromatosis type 2 (NF2) is an autosomal dominant disorder
characterised by the development of multiple schwannomas, especially on vestibular …
characterised by the development of multiple schwannomas, especially on vestibular …
Single nucleotide polymorphisms in PNPLA3, ADAR-1 and IFIH1 are associated with advanced liver fibrosis in patients co-infected with HIV-1//hepatitis C virus
Objective: Nonalcoholic fatty liver disease (NAFLD), insulin resistance and liver fibrosis are
prevalent in individuals co-infected with HIV type 1 (HIV-1)/hepatitis C virus (HCV), even …
prevalent in individuals co-infected with HIV type 1 (HIV-1)/hepatitis C virus (HCV), even …
[HTML][HTML] A likelihood ratio approach for identifying three-quarter siblings in genetic databases
I Galván-Femenía, C Barceló-Vidal, L Sumoy… - Heredity, 2021 - nature.com
The detection of family relationships in genetic databases is of interest in various scientific
disciplines such as genetic epidemiology, population and conservation genetics, forensic …
disciplines such as genetic epidemiology, population and conservation genetics, forensic …
Assessment of kinship detection using RNA-seq data
Abstract Analysis of RNA sequencing (RNA-seq) data from related individuals is widely used
in clinical and molecular genetics studies. Prediction of kinship from RNA-seq data would be …
in clinical and molecular genetics studies. Prediction of kinship from RNA-seq data would be …