Lista de obras -

A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases

artículo científico publicado en 2014

APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathy ⬇️

artículo científico publicado el 13 de octubre de 2011

Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch-Schönlein purpura nephritis

artículo científico publicado en 2011

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

artículo científico publicado en 2021

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

artículo científico publicado en 2019

COL4A3 mutations cause focal segmental glomerulosclerosis

artículo científico publicado en 2014

Challenges in Rare Variant Association Studies for Complex Kidney Traits: CFHR5 and IgA Nephropathy

artículo científico publicado en 2016

Coiled Versus Straight Peritoneal Dialysis Catheters: A Randomized Controlled Trial and Meta-analysis ⬇️

artículo científico publicado el 27 de agosto de 2011

Copy-number disorders are a common cause of congenital kidney malformations

artículo científico publicado en 2012

Current Understanding of the Role of Complement in IgA Nephropathy

artículo científico publicado en 2015

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

artículo científico publicado en 2014

Donor APOL1 high-risk genotypes are associated with increased risk and inferior prognosis of de novo collapsing glomerulopathy in renal allografts

artículo científico publicado en 2018

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

artículo científico publicado en 2017

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

artículo científico publicado en 2017

Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

artículo científico publicado en 2020

Fine Mapping Implicates a Deletion of CFHR1 and CFHR3 in Protection from IgA Nephropathy in Han Chinese.

artículo científico publicado en 2016

GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway

artículo científico publicado en 2017

Genetic Complexities of the HLA Region and Idiopathic Membranous Nephropathy.

artículo científico publicado en 2017

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

artículo científico publicado en 2017

Genetic studies of IgA nephropathy: past, present, and future.

artículo científico publicado en 2010

Genetic studies of body mass index yield new insights for obesity biology

artículo científico publicado en 2015

Genetic susceptibility, HIV infection, and the kidney

artículo científico publicado en 2007

Genome-wide association study identifies susceptibility loci for IgA nephropathy

artículo científico publicado en 2011

Genome-wide association study in mice identifies loci affecting liver-related phenotypes including Sel1l influencing serum bile acids

artículo científico publicado en 2016

Genome-wide polygenic risk predictors for kidney disease

article

Genomic imbalances in pediatric patients with chronic kidney disease

artículo científico publicado en 2015

Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis

artículo científico publicado en 2012

Glomerular diseases: emerging tests and therapies for IgA nephropathy

artículo científico publicado en 2013

Identification of a Potential Susceptibility Locus for Macular Telangiectasia Type 2 ⬇️

artículo científico publicado el 31 de agosto de 2012

Inhibition of STAT3 Signaling Reduces IgA1 Autoantigen Production in IgA Nephropathy.

artículo científico publicado en 2017

Kidney Failure Risk Prediction Equations in IgA Nephropathy: A Multicenter Risk Assessment Study in Chinese Patients

artículo científico publicado en 2018

Lack of serologic evidence to link IgA nephropathy with celiac disease or immune reactivity to gluten

artículo científico publicado en 2014

New developments in the genetics, pathogenesis, and therapy of IgA nephropathy

artículo científico publicado en 2015

New genetic insights into kidney physiology and disease

artículo científico publicado en 2020

New genetic loci link adipose and insulin biology to body fat distribution

artículo científico publicado en 2015

Novel biomarkers in glomerular disease

artículo científico publicado en 2014

Novel mutations in the inverted formin 2 gene of Chinese families contribute to focal segmental glomerulosclerosis

artículo científico publicado en 2015

Pathogenesis of immunoglobulin A nephropathy: recent insight from genetic studies

artículo científico publicado en 2012

Precision Medicine for Acute Kidney Injury (AKI): Redefining AKI by Agnostic Kidney Tissue Interrogation and Genetics

artículo científico publicado en 2018

Predicting Progression of IgA Nephropathy: New Clinical Progression Risk Score ⬇️

artículo científico publicado el 14 de junio de 2012

Quantitative genetics of renal function: tackling complexities of the eGFR phenotype in gene mapping studies

artículo científico publicado en 2008

Renal function and genetic variation in dopamine D(1) receptor: is the case strong enough?

artículo científico publicado en 2009

Susceptibility loci for murine HIV-associated nephropathy encode trans-regulators of podocyte gene expression

scientific article published on 20 April 2009

The association between kidney disease and cardiovascular risk in a multiethnic cohort: findings from the Northern Manhattan Study (NOMAS).

artículo científico publicado en 2008

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

artículo científico publicado en 2018

The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1.

artículo científico publicado en 2013

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

artículo científico publicado en 2020

The genetics and immunobiology of IgA nephropathy

artículo científico publicado en 2014

The genetics of albuminuria: from haplotype association mapping in mice to genetic causation in humans

artículo científico publicado en 2010

The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression

artículo científico publicado en 2012

The molecular pathogenesis of HIV-1 associated nephropathy: recent advances

artículo científico publicado en 2011

Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study

artículo científico publicado en 2017

Lista de obras de

A panel of serum biomarkers differentiates IgA nephropathy from other renal diseases

APOL1 variants increase risk for FSGS and HIVAN but not IgA nephropathy ⬇️

Aberrant glycosylation of IgA1 is inherited in both pediatric IgA nephropathy and Henoch-Schönlein purpura nephritis

Age-dependent impact of the major common genetic risk factor for COVID-19 on severity and mortality

Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract

COL4A3 mutations cause focal segmental glomerulosclerosis

Challenges in Rare Variant Association Studies for Complex Kidney Traits: CFHR5 and IgA Nephropathy

Coiled Versus Straight Peritoneal Dialysis Catheters: A Randomized Controlled Trial and Meta-analysis ⬇️

Copy-number disorders are a common cause of congenital kidney malformations

Current Understanding of the Role of Complement in IgA Nephropathy

Discovery of new risk loci for IgA nephropathy implicates genes involved in immunity against intestinal pathogens

Donor APOL1 high-risk genotypes are associated with increased risk and inferior prognosis of de novo collapsing glomerulopathy in renal allografts

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations

Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19

Fine Mapping Implicates a Deletion of CFHR1 and CFHR3 in Protection from IgA Nephropathy in Han Chinese.

GWAS for serum galactose-deficient IgA1 implicates critical genes of the O-glycosylation pathway

Genetic Complexities of the HLA Region and Idiopathic Membranous Nephropathy.

Genetic Drivers of Kidney Defects in the DiGeorge Syndrome

Genetic studies of IgA nephropathy: past, present, and future.

Genetic studies of body mass index yield new insights for obesity biology

Genetic susceptibility, HIV infection, and the kidney

Genome-wide association study identifies susceptibility loci for IgA nephropathy

Genome-wide association study in mice identifies loci affecting liver-related phenotypes including Sel1l influencing serum bile acids

Genome-wide polygenic risk predictors for kidney disease

Genomic imbalances in pediatric patients with chronic kidney disease

Geographic differences in genetic susceptibility to IgA nephropathy: GWAS replication study and geospatial risk analysis

Glomerular diseases: emerging tests and therapies for IgA nephropathy

Identification of a Potential Susceptibility Locus for Macular Telangiectasia Type 2 ⬇️

Inhibition of STAT3 Signaling Reduces IgA1 Autoantigen Production in IgA Nephropathy.

Kidney Failure Risk Prediction Equations in IgA Nephropathy: A Multicenter Risk Assessment Study in Chinese Patients

Lack of serologic evidence to link IgA nephropathy with celiac disease or immune reactivity to gluten

New developments in the genetics, pathogenesis, and therapy of IgA nephropathy

New genetic insights into kidney physiology and disease

New genetic loci link adipose and insulin biology to body fat distribution

Novel biomarkers in glomerular disease

Novel mutations in the inverted formin 2 gene of Chinese families contribute to focal segmental glomerulosclerosis

Pathogenesis of immunoglobulin A nephropathy: recent insight from genetic studies

Precision Medicine for Acute Kidney Injury (AKI): Redefining AKI by Agnostic Kidney Tissue Interrogation and Genetics

Predicting Progression of IgA Nephropathy: New Clinical Progression Risk Score ⬇️

Quantitative genetics of renal function: tackling complexities of the eGFR phenotype in gene mapping studies

Renal function and genetic variation in dopamine D(1) receptor: is the case strong enough?

Susceptibility loci for murine HIV-associated nephropathy encode trans-regulators of podocyte gene expression

The association between kidney disease and cardiovascular risk in a multiethnic cohort: findings from the Northern Manhattan Study (NOMAS).

The copy number variation landscape of congenital anomalies of the kidney and urinary tract

The emerging role of genomics in the diagnosis and workup of congenital urinary tract defects: a novel deletion syndrome on chromosome 3q13.31-22.1.

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

The genetics and immunobiology of IgA nephropathy

The genetics of albuminuria: from haplotype association mapping in mice to genetic causation in humans

The level of galactose-deficient IgA1 in the sera of patients with IgA nephropathy is associated with disease progression

The molecular pathogenesis of HIV-1 associated nephropathy: recent advances

Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study