List of works - Adam P. Levine

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

scientific article published on July 2016

A New Look at Familial Risk of Inflammatory Bowel Disease in the Ashkenazi Jewish Population

scientific article published on 03 September 2018

Alkalinity of neutrophil phagocytic vacuoles is modulated by HVCN1 and has consequences for myeloperoxidase activity

scientific article (publication date: 2015)

An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils

scientific article published on 28 February 2017

Characterization of expression quantitative trait loci in the human colon

scientific article published on February 2015

Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.

scientific article published on 10 March 2015

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

Corrigendum: An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils.

scientific article published on 11 October 2017

Defective tumor necrosis factor release from Crohn's disease macrophages in response to Toll-like receptor activation: relationship to phenotype and genome-wide association susceptibility loci

scientific article

Disruption of macrophage pro-inflammatory cytokine release in Crohn's disease is associated with reduced optineurin expression in a subset of patients

scientific article

Elevation in Cell Cycle and Protein Metabolism Gene Transcription in Inactive Colonic Tissue From Icelandic Patients With Ulcerative Colitis

article

Endoscopy, but not as we know it

scientific article published on 01 March 2011

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

scientific article published in January 2018

Galactosylation of IgA1 Is Associated with Common Variation in C1GALT1.

scientific article published on 16 February 2017

Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families

scientific article

Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome

scientific article published on 01 July 2019

Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients

scientific article published on 20 April 2023

Imaging the Neutrophil Phagosome and Cytoplasm Using a Ratiometric pH Indicator.

scientific article published on 5 April 2017

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.

scientific article

Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy

scientific article published on 09 January 2020

Mucosal transcriptomics implicates under expression of BRINP3 in the pathogenesis of ulcerative colitis

scientific article

Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease

scientific article published on 22 August 2018

Seqfam: A python package for analysis of Next Generation Sequencing DNA data in families

The Human Salivary Microbiome Is Shaped by Shared Environment Rather than Genetics: Evidence from a Large Family of Closely Related Individuals.

scientific article published on 12 September 2017

The LRRC8A Mediated "Swell Activated" Chloride Conductance Is Dispensable for Vacuolar Homeostasis in Neutrophils

scientific article published on 12 May 2017

The NADPH Oxidase and Microbial Killing by Neutrophils, With a Particular Emphasis on the Proposed Antimicrobial Role of Myeloperoxidase within the Phagocytic Vacuole

scientific article

The human oral microbiome is shaped by shared environment rather than genetics: evidence from a large family of closely-related individuals

article

Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments

scientific article

What is wrong with granulocytes in inflammatory bowel diseases?

scientific article

Whole-genome sequencing of patients with rare diseases in a national health system

scientific article published on 24 June 2020

ZODET: software for the identification, analysis and visualisation of outlier genes in microarray expression data

scientific article

List of works by Adam P. Levine

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

A New Look at Familial Risk of Inflammatory Bowel Disease in the Ashkenazi Jewish Population

Alkalinity of neutrophil phagocytic vacuoles is modulated by HVCN1 and has consequences for myeloperoxidase activity

An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils

Characterization of expression quantitative trait loci in the human colon

Combinatorial Conflicting Homozygosity (CCH) analysis enables the rapid identification of shared genomic regions in the presence of multiple phenocopies.

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

Corrigendum: An Exploration of Charge Compensating Ion Channels across the Phagocytic Vacuole of Neutrophils.

Defective tumor necrosis factor release from Crohn's disease macrophages in response to Toll-like receptor activation: relationship to phenotype and genome-wide association susceptibility loci

Disruption of macrophage pro-inflammatory cytokine release in Crohn's disease is associated with reduced optineurin expression in a subset of patients

Elevation in Cell Cycle and Protein Metabolism Gene Transcription in Inactive Colonic Tissue From Icelandic Patients With Ulcerative Colitis

Endoscopy, but not as we know it

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

Galactosylation of IgA1 Is Associated with Common Variation in C1GALT1.

Genetic Complexity of Crohn's Disease in Two Large Ashkenazi Jewish Families

Genetic Identification of Two Novel Loci Associated with Steroid-Sensitive Nephrotic Syndrome

Identifying high-impact variants and genes in exomes of Ashkenazi Jewish inflammatory bowel disease patients

Imaging the Neutrophil Phagosome and Cytoplasm Using a Ratiometric pH Indicator.

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 Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy

Mucosal transcriptomics implicates under expression of BRINP3 in the pathogenesis of ulcerative colitis

Rare coding variant analysis in a large cohort of Ashkenazi Jewish families with inflammatory bowel disease

Seqfam: A python package for analysis of Next Generation Sequencing DNA data in families

The Human Salivary Microbiome Is Shaped by Shared Environment Rather than Genetics: Evidence from a Large Family of Closely Related Individuals.

The LRRC8A Mediated "Swell Activated" Chloride Conductance Is Dispensable for Vacuolar Homeostasis in Neutrophils

The NADPH Oxidase and Microbial Killing by Neutrophils, With a Particular Emphasis on the Proposed Antimicrobial Role of Myeloperoxidase within the Phagocytic Vacuole

The human oral microbiome is shaped by shared environment rather than genetics: evidence from a large family of closely-related individuals

Using genetic prediction from known complex disease Loci to guide the design of next-generation sequencing experiments

What is wrong with granulocytes in inflammatory bowel diseases?

Whole-genome sequencing of patients with rare diseases in a national health system

ZODET: software for the identification, analysis and visualisation of outlier genes in microarray expression data