Identifying digenic disease genes via machine learning in the Undiagnosed Diseases Network.
PMID:34529933
Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia.
PMID:32942984
Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.
PMID:27058588
Archaeal Clusters of Orthologous Genes (arCOGs): An Update and Application for Analysis of Shared Features between Thermococcales, Methanococcales, and Methanobacteriales.
PMID:25764277
The Hsp90-dependent proteome is conserved and enriched for hub proteins with high levels of protein-protein connectivity.
PMID:25316598
H-InvDB in 2013: an omics study platform for human functional gene and transcript discovery.
PMID:23197657
Revealing mammalian evolutionary relationships by comparative analysis of gene clusters.
PMID:22454131
Developing a community-based genetic nomenclature for anole lizards.
PMID:22077994
Distinct evolutionary patterns of Oryza glaberrima deciphered by genome sequencing and comparative analysis.
PMID:21323774
genenames.org: the HGNC resources in 2011.
PMID:20929869
Massive gene losses in Asian cultivated rice unveiled by comparative genome analysis.
PMID:20167122
H-InvDB in 2009: extended database and data mining resources for human genes and transcripts.
PMID:19933760
ProPhylER: a curated online resource for protein function and structure based on evolutionary constraint analyses.
PMID:19846609
G-compass: a web-based comparative genome browser between human and other vertebrate genomes.
PMID:19846439
Synorth: exploring the evolution of synteny and long-range regulatory interactions in vertebrate genomes.
PMID:19698106
The Chicken Gene Nomenclature Committee report.
PMID:19607656
Sexy gene conversions: locating gene conversions on the X-chromosome.
PMID:19487239
Low conservation and species-specific evolution of alternative splicing in humans and mice: comparative genomics analysis using well-annotated full-length cDNAs.
PMID:18838389
The H-Invitational Database (H-InvDB), a comprehensive annotation resource for human genes and transcripts.
PMID:18089548