Lista de obras - Peter I - Dominio Público Uruguay

A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.

artículo científico publicado en 2016

A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci

scientific journal article

Age-Related Changes in Echocardiographic Measurements

An increase in LRRK2 suppresses autophagy and enhances Dectin-1-induced immunity in a mouse model of colitis

artículo científico publicado en 2018

Association of Infection with Chronic Hepatitis C Virus and Myocardial Infarction in People Living with HIV in the United States

scientific article published on 12 November 2019

Can genetic pleiotropy replicate common clinical constellations of cardiovascular disease and risk?

artículo científico publicado en 2012

Candidate gene polymorphisms in patients with acetaminophen-induced acute liver failure

artículo científico publicado en 2013

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

correction of a scientific article; published on 30 May 2019

Defects in NADPH Oxidase Genes NOX1 and DUOX2 in Very Early Onset Inflammatory Bowel Disease

artículo científico publicado en 2015

Effect of Genetic African Ancestry on eGFR and Kidney Disease

artículo científico publicado en 2014

Expanded genetic screening panel for the Ashkenazi Jewish population.

artículo científico publicado en 2015

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease

artículo científico publicado en 2018

Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

artículo científico publicado en 2013

Genetic architecture of cardiometabolic risks in people living with HIV

artículo científico publicado en 2020

Genome-wide data from medieval German Jews show that the Ashkenazi founder event pre-dated the 14 century

artículo científico publicado en 2022

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

artículo científico publicado en 2014

High-depth whole genome sequencing of a large population-specific reference panel: Enhancing sensitivity, accuracy, and imputation

High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation.

artículo científico publicado en 2018

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

preprint published 25 September 2016

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

artículo científico publicado en 2018

Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.

artículo científico publicado en 2012

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

artículo científico publicado en 2012

Mortality following myocardial infarction among HIV-infected persons: the Center for AIDS Research Network Of Integrated Clinical Systems (CNICS)

artículo científico publicado en 2019

Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophrenia

artículo científico publicado en 2021

Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins

artículo científico publicado en 2014

The KCNMB1 E65K variant is associated with reduced central pulse pressure in the community-based Framingham Offspring Cohort

artículo científico publicado en 2009

The UDP-glucuronosyltransferase (UGT) 1A polymorphism c.2042C>G (rs8330) is associated with increased human liver acetaminophen glucuronidation, increased UGT1A exon 5a/5b splice variant mRNA ratio, and decreased risk of unintentional acetaminophen-

artículo científico publicado en 2013

Types of Myocardial Infarction Among Human Immunodeficiency Virus-Infected Individuals in the United States

artículo científico publicado en 2017

Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.

artículo científico publicado en 2015

Lista de obras de Peter I

A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSF.

A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility loci

Age-Related Changes in Echocardiographic Measurements

An increase in LRRK2 suppresses autophagy and enhances Dectin-1-induced immunity in a mouse model of colitis

Association of Infection with Chronic Hepatitis C Virus and Myocardial Infarction in People Living with HIV in the United States

Can genetic pleiotropy replicate common clinical constellations of cardiovascular disease and risk?

Candidate gene polymorphisms in patients with acetaminophen-induced acute liver failure

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Defects in NADPH Oxidase Genes NOX1 and DUOX2 in Very Early Onset Inflammatory Bowel Disease

Effect of Genetic African Ancestry on eGFR and Kidney Disease

Expanded genetic screening panel for the Ashkenazi Jewish population.

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease

Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations

Genetic architecture of cardiometabolic risks in people living with HIV

Genome-wide data from medieval German Jews show that the Ashkenazi founder event pre-dated the 14 century

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes

High-depth whole genome sequencing of a large population-specific reference panel: Enhancing sensitivity, accuracy, and imputation

High-depth whole genome sequencing of an Ashkenazi Jewish reference panel: enhancing sensitivity, accuracy, and imputation.

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci.

Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci

Mortality following myocardial infarction among HIV-infected persons: the Center for AIDS Research Network Of Integrated Clinical Systems (CNICS)

Novel ultra-rare exonic variants identified in a founder population implicate cadherins in schizophrenia

Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins

The KCNMB1 E65K variant is associated with reduced central pulse pressure in the community-based Framingham Offspring Cohort

The UDP-glucuronosyltransferase (UGT) 1A polymorphism c.2042C>G (rs8330) is associated with increased human liver acetaminophen glucuronidation, increased UGT1A exon 5a/5b splice variant mRNA ratio, and decreased risk of unintentional acetaminophen-

Types of Myocardial Infarction Among Human Immunodeficiency Virus-Infected Individuals in the United States

Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.