List of works - Dan Andrews

A high-resolution survey of deletion polymorphism in the human genome

2005 scientific article

An overview of Ensembl

scientific article (publication date: May 2004)

DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

scientific article

The DNA sequence and analysis of human chromosome 6

scientific article

The DNA sequence and biological annotation of human chromosome

scientific article

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

scientific article

Comparison of predicted and actual consequences of missense mutations

scientific article

Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.

scientific article

Genome-wide dFOXO targets and topology of the transcriptomic response to stress and insulin signalling

scientific article

DNA sequence and analysis of human chromosome 9

scientific article

Interplay of dFOXO and two ETS-family transcription factors determines lifespan in Drosophila melanogaster

scientific article

The RNA-binding protein hnRNPLL induces a T cell alternative splicing program delineated by differential intron retention in polyadenylated RNA.

scientific article

Rasgrp1 mutation increases naive T-cell CD44 expression and drives mTOR-dependent accumulation of Helios⁺ T cells and autoantibodies.

scientific article published on 12 December 2013

Zinc-finger protein ZFP318 is essential for expression of IgD, the alternatively spliced Igh product made by mature B lymphocytes.

scientific article

Brief Report: Identification of a Pathogenic Variant in TREX1 in Early-Onset Cerebral Systemic Lupus Erythematosus by Whole-Exome Sequencing

scientific article published on 01 December 2014

Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome

scientific article published on 2 June 2015

Understanding the immunological impact of the human mutation explosion

scientific article published on January 16, 2013

Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1

scientific article published on 01 July 2020

TLR7 gain-of-function genetic variation causes human lupus

scientific article published on 27 April 2022

Finding new immune regulatory genes by ENU mutagenesis

scientific article published on 28 November 2012

List of works by Dan Andrews

A high-resolution survey of deletion polymorphism in the human genome

An overview of Ensembl

DNA methylation profiling of the human major histocompatibility complex: a pilot study for the human epigenome project

The DNA sequence and analysis of human chromosome 6

The DNA sequence and biological annotation of human chromosome

Breaking the waves: improved detection of copy number variation from microarray-based comparative genomic hybridization.

Comparison of predicted and actual consequences of missense mutations

Massively parallel sequencing of the mouse exome to accurately identify rare, induced mutations: an immediate source for thousands of new mouse models.

Genome-wide dFOXO targets and topology of the transcriptomic response to stress and insulin signalling

DNA sequence and analysis of human chromosome 9

Interplay of dFOXO and two ETS-family transcription factors determines lifespan in Drosophila melanogaster

The RNA-binding protein hnRNPLL induces a T cell alternative splicing program delineated by differential intron retention in polyadenylated RNA.

Rasgrp1 mutation increases naive T-cell CD44 expression and drives mTOR-dependent accumulation of Helios⁺ T cells and autoantibodies.

Zinc-finger protein ZFP318 is essential for expression of IgD, the alternatively spliced Igh product made by mature B lymphocytes.

Brief Report: Identification of a Pathogenic Variant in TREX1 in Early-Onset Cerebral Systemic Lupus Erythematosus by Whole-Exome Sequencing

Novel and rare functional genomic variants in multiple autoimmune syndrome and Sjögren's syndrome

Understanding the immunological impact of the human mutation explosion

Absence of mucosal-associated invariant T cells in a person with a homozygous point mutation in MR1

TLR7 gain-of-function genetic variation causes human lupus

Finding new immune regulatory genes by ENU mutagenesis