<style face="normal" font="default" size="100%">Association of a single nucleotide polymorphism in the ubxn6 gene with long-term non-progression phenotype in HIV-positive individuals.</style>

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<style face="normal" font="default" size="100%">Association of a single nucleotide polymorphism in the ubxn6 gene with long-term non-progression phenotype in HIV-positive individuals.</style>

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<style face="normal" font="default" size="100%">Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies.</style>

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<style face="normal" font="default" size="100%">Identification of the Photoreceptor Transcriptional Co-Repressor SAMD11 as Novel Cause of Autosomal Recessive Retinitis Pigmentosa.</style>

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<style face="normal" font="default" size="100%">The Mutational Landscape of Acute Promyelocytic Leukemia Reveals an Interacting Network of Co-Occurrences and Recurrent Mutations.</style>

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<style face="normal" font="default" size="100%">Progress in pharmacogenetics: consortiums and new strategies.</style>

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<style face="normal" font="default" size="100%">A Pan-Cancer Catalogue of Cancer Driver Protein Interaction Interfaces.</style>

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<style face="normal" font="default" size="100%">Pathways systematically associated to Hirschsprung's disease.</style>

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<style face="normal" font="default" size="100%">SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants.</style>

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<style face="normal" font="default" size="100%">VARIANT: Command Line, Web service and Web interface for fast and accurate functional characterization of variants found by Next-Generation Sequencing.</style>

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<style face="normal" font="default" size="100%">Exploring the link between germline and somatic genetic alterations in breast carcinogenesis.</style>

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<style face="normal" font="default" size="100%">Mutation spectrum of EYS in Spanish patients with autosomal recessive retinitis pigmentosa.</style>

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<style face="normal" font="default" size="100%">Gene set-based analysis of polymorphisms: finding pathways or biological processes associated to traits in genome-wide association studies.</style>

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<style face="normal" font="default" size="100%">Joint annotation of coding and non-coding single nucleotide polymorphisms and mutations in the SNPeffect and PupaSuite databases.</style>

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<style face="normal" font="default" size="100%">SNP and haplotype mapping for genetic analysis in the rat.</style>

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<style face="normal" font="default" size="100%">Use of estimated evolutionary strength at the codon level improves the prediction of disease-related protein mutations in humans.</style>