Summary: In analyses of exome data, candidate gene selection can be challenging in the absence of variants in known disease-causing genes. We calculated the putative biologically closest known disease-causing genes for 13,005 human genes not currently reported to be disease-causing. We used these data to construct the Closest Disease-Causing Genes (CDG) server, which can be used to infer the closest associated disease-causing genes and phenotypes for lists of candidate genes. This resource will be a considerable asset for ascertaining the poten-tial relevance of lists of genes to specific diseases of interest
The recent improvement in high throughput sequencing technologies has led to the sharp decrease in t...
Genome-wide association studies (GWASs) have identified hundreds of loci associated with Crohn’s dis...
Background: The observation that the genetic variants identified in genome-wide association studies ...
Summary: In analyses of exome data, candidate gene selection can be challenging in the absence of va...
High-throughput genomic technologies yield about 20,000 variants in the protein-coding exome of each...
<p>High-throughput genomic technologies yield about 20,000 variants in the protein-coding exome of e...
International audienceBACKGROUND: Identifying the genotypes underlying human disease phenotypes is a...
Background: Common variable immunodeficiency (CVID), the most prevalent form of primary immunodefici...
Common Variable Immunodeficiency Disorders (CVIDs) are the most prevalent cause of primary antibody ...
CITATION: Schlechter, N. et al. 2017. Exome sequencing identifies a novel MAP3K14 mutation in recess...
Background: Pinpointing genes involved in inherited human diseases remains a great challenge in the ...
Primary immunodeficiencies (PIDs) refer to a clinically, immunologically, and genetically heterogene...
Introduction: Next Generation Sequencing (NGS) has driven the rapid increase in the number of recogn...
Background Primary immunodeficiency diseases (PIDDs) are clinically and genetically heterogeneous di...
We are deeply grateful to the affected individuals who participated in this study and their families...
The recent improvement in high throughput sequencing technologies has led to the sharp decrease in t...
Genome-wide association studies (GWASs) have identified hundreds of loci associated with Crohn’s dis...
Background: The observation that the genetic variants identified in genome-wide association studies ...
Summary: In analyses of exome data, candidate gene selection can be challenging in the absence of va...
High-throughput genomic technologies yield about 20,000 variants in the protein-coding exome of each...
<p>High-throughput genomic technologies yield about 20,000 variants in the protein-coding exome of e...
International audienceBACKGROUND: Identifying the genotypes underlying human disease phenotypes is a...
Background: Common variable immunodeficiency (CVID), the most prevalent form of primary immunodefici...
Common Variable Immunodeficiency Disorders (CVIDs) are the most prevalent cause of primary antibody ...
CITATION: Schlechter, N. et al. 2017. Exome sequencing identifies a novel MAP3K14 mutation in recess...
Background: Pinpointing genes involved in inherited human diseases remains a great challenge in the ...
Primary immunodeficiencies (PIDs) refer to a clinically, immunologically, and genetically heterogene...
Introduction: Next Generation Sequencing (NGS) has driven the rapid increase in the number of recogn...
Background Primary immunodeficiency diseases (PIDDs) are clinically and genetically heterogeneous di...
We are deeply grateful to the affected individuals who participated in this study and their families...
The recent improvement in high throughput sequencing technologies has led to the sharp decrease in t...
Genome-wide association studies (GWASs) have identified hundreds of loci associated with Crohn’s dis...
Background: The observation that the genetic variants identified in genome-wide association studies ...