Lista de obras - Josep Maria Mercader - Dominio Público Uruguay

A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians

artículo científico publicado en 2017

A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes

artículo científico publicado en 2017

A functional IFN-λ4-generating DNA polymorphism could protect older asthmatic women from aeroallergen sensitization and associate with clinical features of asthma

artículo científico publicado en 2017

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

artículo científico publicado en 2014

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

scientific article published on 13 April 2020

Aberrant brain microRNA target and miRISC gene expression in the anx/anx anorexia mouse model

artículo científico publicado en 2012

Altered Circulating miRNA Expression Profile in Pregestational and Gestational Obesity.

artículo científico publicado en 2015

Altered brain-derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia.

artículo científico publicado en 2007

Analysis of Glucocorticoid-Related Genes Reveal CCHCR1 as a New Candidate Gene for Type 2 Diabetes

scientific article published on 24 August 2020

Analysis of the multi-copy gene family FAM90A as a copy number variant in different ethnic backgrounds

article

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders

artículo científico publicado en 2008

Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population

artículo científico publicado en 2014

Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

artículo científico publicado en 2018

Blood levels of brain-derived neurotrophic factor correlate with several psychopathological symptoms in anorexia nervosa patients.

artículo científico publicado en 2007

Brain-derived neurotrophic factor Val66Met and psychiatric disorders: meta-analysis of case-control studies confirm association to substance-related disorders, eating disorders, and schizophrenia.

artículo científico publicado en 2007

Changes in circulating microRNAs are associated with childhood obesity.

artículo científico publicado en 2013

Circulating profiling reveals the effect of a polyunsaturated fatty acid-enriched diet on common microRNAs.

artículo científico publicado en 2015

Common genetic variants of surfactant protein-D (SP-D) are associated with type 2 diabetes

artículo científico publicado en 2013

Contribution of the serotoninergic system to anxious and depressive traits that may be partially responsible for the phenotypical variability of bulimia nervosa.

artículo científico publicado en 2006

Correction: Nucleotide, Cytogenetic and Expression Impact of the Human Chromosome 8p23.1 Inversion Polymorphism.

artículo científico publicado en 2010

Correlation of BDNF blood levels with interoceptive awareness and maturity fears in anorexia and bulimia nervosa patients.

artículo científico publicado en 2010

Decreased lipid metabolism but increased FA biosynthesis are coupled with changes in liver microRNAs in obese subjects with NAFLD.

artículo científico publicado en 2017

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Dysregulation of Placental miRNA in Maternal Obesity Is Associated With Pre- and Postnatal Growth

artículo científico publicado en 2017

Erratum to: Targeting the association of calgranulin B (S100A9) with insulin resistance and type 2 diabetes

scholarly article by Francisco J. Ortega et al published 8 March 2013 in Journal of Molecular Medicine

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

article by Jason Flannick et al published 22 May 2019 in Nature

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

artículo científico publicado en 2016

Genome-wide associations for birth weight and correlations with adult disease

artículo científico publicado en 2016

Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes

scientific article published on 28 June 2019

Hypothalamus transcriptome profile suggests an anorexia-cachexia syndrome in the anx/anx mouse model

artículo científico publicado en 2008

Identification of novel type 2 diabetes candidate genes involved in the crosstalk between the mitochondrial and the insulin signaling systems

artículo científico publicado en 2012

Inflammation triggers specific microRNA profiles in human adipocytes and macrophages and in their supernatants

artículo científico publicado en 2015

MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene

artículo científico publicado en 2007

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

artículo científico publicado en 2019

Mendelian Randomization Shows a Causal Effect of Low Vitamin D on Non-infectious Uveitis and Scleritis Risk

artículo científico publicado en 2022

Metformin alters the gut microbiome of individuals with treatment-naive type 2 diabetes, contributing to the therapeutic effects of the drug

artículo científico publicado en 2017

New insights into the expression profile and function of micro-ribonucleic acid in human spermatozoa

artículo científico

Nucleotide, cytogenetic and expression impact of the human chromosome 8p23.1 inversion polymorphism

artículo científico publicado en 2009

PAIRUP-MS: Pathway analysis and imputation to relate unknowns in profiles from mass spectrometry-based metabolite data

artículo científico publicado en 2019

Profiling of circulating microRNAs reveals common microRNAs linked to type 2 diabetes that change with insulin sensitization

artículo científico publicado en 2014

Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.

artículo científico publicado en 2018

Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes

artículo científico publicado en 2018

Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes

artículo científico publicado en 2022

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease

artículo científico publicado en 2010

SNPassoc: an R package to perform whole genome association studies

artículo científico publicado en 2007

Suicide attempts in bulimia nervosa: personality and psychopathological correlates

artículo científico publicado en 2008

Surgery-Induced Weight Loss Is Associated With the Downregulation of Genes Targeted by MicroRNAs in Adipose Tissue.

artículo científico publicado en 2015

Targeting the association of calgranulin B (S100A9) with insulin resistance and type 2 diabetes

artículo científico publicado en 2012

Targeting the circulating microRNA signature of obesity.

artículo científico publicado en 2013

The Genetic Basis of Type 2 Diabetes in Hispanics and Latin Americans: Challenges and Opportunities

artículo científico publicado en 2017

The power of genetic diversity in genome-wide association studies of lipids

Thyroid hormone receptor alpha gene variants increase the risk of developing obesity and show gene-diet interactions

artículo científico publicado en 2013

Transferrin receptor-1 gene polymorphisms are associated with type 2 diabetes

artículo científico publicado en 2010

Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

artículo científico publicado en 2017

Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: A soft clustering analysis

artículo científico publicado en 2018

Unravelling the hidden DNA structural/physical code provides novel insights on promoter location

artículo científico publicado en 2013

ZNRD1 (zinc ribbon domain-containing 1) is a host cellular factor that influences HIV-1 replication and disease progression

artículo científico publicado en 2010

miRNAs in cerebrospinal fluid identify patients with MS and specifically those with lipid-specific oligoclonal IgM bands

artículo científico publicado en 2017

Lista de obras de Josep Maria Mercader

A Genome-Wide Association Study Using a Custom Genotyping Array Identifies Variants in GPR158 Associated With Reduced Energy Expenditure in American Indians

A Loss-Of-Function Splice Acceptor Variant in IGF2 is Protective for Type 2 Diabetes

A functional IFN-λ4-generating DNA polymorphism could protect older asthmatic women from aeroallergen sensitization and associate with clinical features of asthma

A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

Aberrant brain microRNA target and miRISC gene expression in the anx/anx anorexia mouse model

Altered Circulating miRNA Expression Profile in Pregestational and Gestational Obesity.

Altered brain-derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia.

Analysis of Glucocorticoid-Related Genes Reveal CCHCR1 as a New Candidate Gene for Type 2 Diabetes

Analysis of the multi-copy gene family FAM90A as a copy number variant in different ethnic backgrounds

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders

Association of a low-frequency variant in HNF1A with type 2 diabetes in a Latino population

Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

Blood levels of brain-derived neurotrophic factor correlate with several psychopathological symptoms in anorexia nervosa patients.

Brain-derived neurotrophic factor Val66Met and psychiatric disorders: meta-analysis of case-control studies confirm association to substance-related disorders, eating disorders, and schizophrenia.

Changes in circulating microRNAs are associated with childhood obesity.

Circulating profiling reveals the effect of a polyunsaturated fatty acid-enriched diet on common microRNAs.

Common genetic variants of surfactant protein-D (SP-D) are associated with type 2 diabetes

Contribution of the serotoninergic system to anxious and depressive traits that may be partially responsible for the phenotypical variability of bulimia nervosa.

Correction: Nucleotide, Cytogenetic and Expression Impact of the Human Chromosome 8p23.1 Inversion Polymorphism.

Correlation of BDNF blood levels with interoceptive awareness and maturity fears in anorexia and bulimia nervosa patients.

Decreased lipid metabolism but increased FA biosynthesis are coupled with changes in liver microRNAs in obese subjects with NAFLD.

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Dysregulation of Placental miRNA in Maternal Obesity Is Associated With Pre- and Postnatal Growth

Erratum to: Targeting the association of calgranulin B (S100A9) with insulin resistance and type 2 diabetes

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

Genome-wide associations for birth weight and correlations with adult disease

Human pancreatic islet three-dimensional chromatin architecture provides insights into the genetics of type 2 diabetes

Hypothalamus transcriptome profile suggests an anorexia-cachexia syndrome in the anx/anx mouse model

Identification of novel type 2 diabetes candidate genes involved in the crosstalk between the mitochondrial and the insulin signaling systems

Inflammation triggers specific microRNA profiles in human adipocytes and macrophages and in their supernatants

MRPS18CP2 alleles and DEFA3 absence as putative chromosome 8p23.1 modifiers of hearing loss due to mtDNA mutation A1555G in the 12S rRNA gene

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors

Mendelian Randomization Shows a Causal Effect of Low Vitamin D on Non-infectious Uveitis and Scleritis Risk

Metformin alters the gut microbiome of individuals with treatment-naive type 2 diabetes, contributing to the therapeutic effects of the drug

New insights into the expression profile and function of micro-ribonucleic acid in human spermatozoa

Nucleotide, cytogenetic and expression impact of the human chromosome 8p23.1 inversion polymorphism

PAIRUP-MS: Pathway analysis and imputation to relate unknowns in profiles from mass spectrometry-based metabolite data

Profiling of circulating microRNAs reveals common microRNAs linked to type 2 diabetes that change with insulin sensitization

Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.

Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes

Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease

SNPassoc: an R package to perform whole genome association studies

Suicide attempts in bulimia nervosa: personality and psychopathological correlates

Surgery-Induced Weight Loss Is Associated With the Downregulation of Genes Targeted by MicroRNAs in Adipose Tissue.

Targeting the association of calgranulin B (S100A9) with insulin resistance and type 2 diabetes

Targeting the circulating microRNA signature of obesity.

The Genetic Basis of Type 2 Diabetes in Hispanics and Latin Americans: Challenges and Opportunities

The power of genetic diversity in genome-wide association studies of lipids

Thyroid hormone receptor alpha gene variants increase the risk of developing obesity and show gene-diet interactions

Transferrin receptor-1 gene polymorphisms are associated with type 2 diabetes

Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms

Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: A soft clustering analysis

Unravelling the hidden DNA structural/physical code provides novel insights on promoter location

ZNRD1 (zinc ribbon domain-containing 1) is a host cellular factor that influences HIV-1 replication and disease progression

miRNAs in cerebrospinal fluid identify patients with MS and specifically those with lipid-specific oligoclonal IgM bands