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Mapping of Mcs30, a new mammary carcinoma susceptibility quantitative trait locus (QTL30) on rat chromosome 12: identification of fry as a candidate Mcs genePositional cloning of "Lisch-Like", a candidate modifier of susceptibility to type 2 diabetes in miceBioinformatics for personal genome interpretationNew in protein structure and function annotation: hotspots, single nucleotide polymorphisms and the 'Deep Web'.Correlating protein function and stability through the analysis of single amino acid substitutions.MuD: an interactive web server for the prediction of non-neutral substitutions using protein structural dataEvolutionary history of redox metal-binding domains across the tree of life.Common sequence variants affect molecular function more than rare variants?Functional analyses of variants reveal a significant role for dominant negative and common alleles in oligogenic Bardet-Biedl syndromeSNPdbe: constructing an nsSNP functional impacts database.SNP-SIG Meeting 2011: identification and annotation of SNPs in the context of structure, function, and disease.Disease-related mutations predicted to impact protein function.Collective judgment predicts disease-associated single nucleotide variantsPredictProtein--an open resource for online prediction of protein structural and functional features.SNAP: predict effect of non-synonymous polymorphisms on function.Chapter 15: disease gene prioritization.Thoughts from SNP-SIG 2012: future challenges in the annotation of genetic variations.Comprehensive in silico mutagenesis highlights functionally important residues in proteins.SNAP predicts effect of mutations on protein function.In silico mutagenesis: a case study of the melanocortin 4 receptorBetter prediction of functional effects for sequence variants.Functional Basis of Microorganism Classification.COMPUTATIONAL APPROACHES TO STUDY MICROBES AND MICROBIOMES.VarI-SIG 2015: methods for personalized medicine - the role of variant interpretation in research and diagnostics.Predicted Molecular Effects of Sequence Variants Link to System Level of Diseaseclubber: removing the bioinformatics bottleneck in big data analyses.Whole exome sequencing identifies novel candidate genes that modify chronic obstructive pulmonary disease susceptibility.Association of functionally significant Melanocortin-4 but not Melanocortin-3 receptor mutations with severe adult obesity in a large North American case-control study.Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studiesNeutral and weakly nonneutral sequence variants may define individuality.Computational prediction shines light on type III secretion origins.News from the protein mutability landscape.Building a genome analysis pipeline to predict disease risk and prevent disease.Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI.Protein function in precision medicine: deep understanding with machine learning.Comparative genomic and physiological analysis provides insights into the role of Acidobacteria in organic carbon utilization in Arctic tundra soils.The young PI buzz: learning from the organizers of the Junior Principal Investigator Meeting at ISMB-ECCB 2013.VarI-SIG 2014--From SNPs to variants: interpreting different types of genetic variants.Conserved amino acids within the adenovirus 2 E3/19K protein differentially affect downregulation of MHC class I and MICA/B proteins.TrAnsFuSE refines the search for protein function: oxidoreductases.
P50
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P50
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научный исследователь
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հետազոտող
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Yana Bromberg
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Yana Bromberg
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Yana Bromberg
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Яна Бромберг
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Yana Bromberg
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Yana Bromberg
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Yana Bromberg
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Yana Bromberg
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Яна Бромберг
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Yana Bromberg
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Yana Bromberg
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Yana Bromberg
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Yana Bromberg
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Yana Bromberg
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Яна Бромберг
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P108
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P2456
P31
P496
0000-0002-8351-0844