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Author Details
Full Name
Vladimir Vacic
Affiliation
Stanley Institute for Cognitive Genomics
ORCID
Career Start Year
2005
Papers
41
H Index
29
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36732511
Author Correction: Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.
Nat Commun
2023
33748968
Advancing drug discovery using the power of the human genome.
J Pathol
2021
33888516
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease.
Gut
2021
31023376
Sequencing and curation strategies for identifying candidate glioblastoma treatments.
BMC Med Genomics
2019
31375115
Correction to: Sequencing and curation strategies for identifying candidate glioblastoma treatments.
BMC Med Genomics
2019
30804565
Genome-wide analysis of insomnia in 1,331,010 individuals identifies new risk loci and functional pathways.
Nat Genet
2019
29563502
Placenta and appetite genes GDF15 and IGFBP7 are associated with hyperemesis gravidarum.
Nat Commun
2018
30271907
Genome-wide somatic variant calling using localized colored de Bruijn graphs.
Commun Biol
2018
28740869
Comparing sequencing assays and human-machine analyses in actionable genomics for glioblastoma.
Neurol Genet
2017
27260402
Differential burden of rare protein truncating variants in Alzheimer's disease patients compared to centenarians.
Hum Mol Genet
2016
26666262
Integrative genetic analysis of mouse and human AML identifies cooperating disease alleles.
J Exp Med
2016
27854363
Indel variant analysis of short-read sequencing data with Scalpel.
Nat Protoc
2016
27646943
Genetic Determinants of Cisplatin Resistance in Patients With Advanced Germ Cell Tumors.
J Clin Oncol
2016
27354699
Conpair: concordance and contamination estimator for matched tumor-normal pairs.
Bioinformatics
2016
26198764
Genome-wide association study of schizophrenia in Ashkenazi Jews.
Am J Med Genet B Neuropsychiatr Genet
2015
26391891
The Influence of Microdeletions and Microduplications of 16p11.2 on Global Transcription Profiles.
J Child Neurol
2015
26181256
Whole-Exome Sequencing of Metastatic Cancer and Biomarkers of Treatment Response.
JAMA Oncol
2015
24722188
Protein interaction network of alternatively spliced isoforms from brain links genetic risk factors for autism.
Nat Commun
2014
25333069
Disease variants in genomes of 44 centenarians.
Mol Genet Genomic Med
2014
25164765
Comparative sequencing analysis reveals high genomic concordance between matched primary and metastatic colorectal cancer lesions.
Genome Biol
2014
24842889
Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.
Hum Mol Genet
2014
24578576
Detection of a recurrent DNAJB1-PRKACA chimeric transcript in fibrolamellar hepatocellular carcinoma.
Science
2014
23267057
The variance of identity-by-descent sharing in the Wright-Fisher model.
Genetics
2013
22080206
Disease mutations in disordered regions--exception to the rule?
Mol Biosyst
2012
23055912
Disease-associated mutations disrupt functionally important regions of intrinsic protein disorder.
PLoS Comput Biol
2012
21346763
Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia.
Nature
2011
22196331
High frequencies of de novo CNVs in bipolar disorder and schizophrenia.
Neuron
2011
19722269
Identification, analysis, and prediction of protein ubiquitination sites.
Proteins
2010
20078397
Graphlet kernels for prediction of functional residues in protein structures.
J Comput Biol
2010
19915147
Immune profile and mitotic index of metastatic melanoma lesions enhance clinical staging in predicting patient survival.
Proc Natl Acad Sci U S A
2009
19855392
Microduplications of 16p11.2 are associated with schizophrenia.
Nat Genet
2009
18194570
Small RNAs and the regulation of cis-natural antisense transcripts in Arabidopsis.
BMC Mol Biol
2008
18831774
The unfoldomics decade: an update on intrinsically disordered proteins.
BMC Genomics
2008
18229677
A probabilistic method for small RNA flowgram matching.
Pac Symp Biocomput
2008
17145717
DisProt: the Database of Disordered Proteins.
Nucleic Acids Res
2007
17990975
MSOAR: a high-throughput ortholog assignment system based on genome rearrangement.
J Comput Biol
2007
17578581
Composition Profiler: a tool for discovery and visualization of amino acid composition differences.
BMC Bioinformatics
2007
17488107
Characterization of molecular recognition features, MoRFs, and their binding partners.
J Proteome Res
2007
16632492
Two Sample Logo: a graphical representation of the differences between two sets of sequence alignments.
Bioinformatics
2006
16935303
Analysis of molecular recognition features (MoRFs).
J Mol Biol
2006
15310560
DisProt: a database of protein disorder.
Bioinformatics
2005
1 - 41 of 41
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