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Primate evolution of the recombination regulator PRDM9
Download from dx.doi.orgDisruptive CHD8 mutations define a subtype of autism early in development
Download from www.ncbi.nlm.nih.govDecoding long nanopore sequencing reads of natural DNA
Download from www.nature.comMIPgen: Optimized Modeling and Design of Molecular Inversion Probes for Targeted Resequencing
Download from academic.oup.comSpecies-Level Deconvolution of Metagenome Assemblies with Hi-C–Based Contact Probability Maps
Download from academic.oup.comMutations in PIEZO2 Cause Gordon Syndrome, Marden-Walker Syndrome, and Distal Arthrogryposis Type 5
Download from www.ncbi.nlm.nih.govGuidelines for investigating causality of sequence variants in human disease
Download from www.nature.comAdaptive Gene Amplification As an Intermediate Step in the Expansion of Virus Host Range
Download from dx.doi.orgGABRA1 and STXBP1: Novel genetic causes of Dravet syndrome
Download from www.ncbi.nlm.nih.govA general framework for estimating the relative pathogenicity of human genetic variants
Download from www.nature.comMutations in TBC1D24, a Gene Associated With Epilepsy, Also Cause Nonsyndromic Deafness DFNB86
Download from www.ncbi.nlm.nih.govA de novo convergence of autism genetics and molecular neuroscience
Download from www.ncbi.nlm.nih.govMissing publications? Search for publications with a matching author name.