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Author Details

Ondrej Libiger
The Qualcomm Institute, University of California
2005
45
24
PMIDPaper TitleJournal TitlePublished Year
35436670Design, synthesis and preclinical evaluation of bio-conjugated amylinomimetic peptides as long-acting amylin receptor agonists.Eur J Med Chem2022
32789669Impacts of personal DNA ancestry testing.J Community Genet2021
33984181Longitudinal CSF proteomics identifies NPTX2 as a prognostic biomarker of Alzheimer's disease.Alzheimers Dement2021
31871053Comprehensive engineering of the tarantula venom peptide huwentoxin-IV to inhibit the human voltage-gated sodium channel hNa<sub>v</sub>1.7.J Biol Chem2020
27846195Genome-wide association study of paliperidone efficacy.Pharmacogenet Genomics2017
25953057Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing children.Brain Imaging Behav2016
27578802A statistical method for the detection of variants from next-generation resequencing of DNA pools.Bioinformatics2016
26810587Toward clinical genomics in everyday medicine: perspectives and recommendations.Expert Rev Mol Diagn2016
26183468Anxiety is related to indices of cortical maturation in typically developing children and adolescents.Brain Struct Funct2016
25937488The Pediatric Imaging, Neurocognition, and Genetics (PING) Data Repository.Neuroimage2016
25592880Fast individual ancestry inference from DNA sequence data leveraging allele frequencies for multiple populations.BMC Bioinformatics2015
26734061Partial Least Squares Regression Can Aid in Detecting Differential Abundance of Multiple Features in Sets of Metagenomic Samples.Front Genet2015
25821911Family income, parental education and brain structure in children and adolescents.Nat Neurosci2015
23999524Evidence for the role of EPHX2 gene variants in anorexia nervosa.Mol Psychiatry2014
25270064Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol-related phenotypes in a Native American community sample.Am J Med Genet B Neuropsychiatr Genet2014
25060271Admixture and clinical phenotypic variation.Hum Hered2014
24757035Correlation analysis of genetic admixture and social identification with body mass index in a Native American community.Am J Hum Biol2014
24521671Chip-based direct genotyping of coding variants in genome wide association studies: utility, issues and prospects.Gene2014
24219608The NIH Toolbox Cognition Battery: results from a large normative developmental sample (PING).Neuropsychology2014
23335941A Method for Inferring an Individual's Genetic Ancestry and Degree of Admixture Associated with Six Major Continental Populations.Front Genet2013
23815888Inference of human continental origin and admixture proportions using a highly discriminative ancestry informative 41-SNP panel.Investig Genet2013
24024963Genome-wide association study of shared components of reading disability and language impairment.Genes Brain Behav2013
23734161Genomic risk models improve prediction of longitudinal lipid levels in children and young adults.Front Genet2013
23467092Patterns of population epigenomic diversity.Nature2013
23516368Complex patterns of genomic admixture within southern Africa.PLoS Genet2013
22363593Nonparametric evaluation of quantitative traits in population-based association studies when the genetic model is unknown.PLoS One2012
23169628Long-term influence of normal variation in neonatal characteristics on human brain development.Proc Natl Acad Sci U S A2012
23125845Clinical implications of human population differences in genome-wide rates of functional genotypes.Front Genet2012
23150548Multimodal imaging of the self-regulating developing brain.Proc Natl Acad Sci U S A2012
22808950Model-specific tests on variance heterogeneity for detection of potentially interacting genetic loci.BMC Genet2012
22440735Characterization of circulating endothelial cells in acute myocardial infarction.Sci Transl Med2012
21121035An application and empirical comparison of statistical analysis methods for associating rare variants to a complex phenotype.Pac Symp Biocomput2011
21921155Transgenerational epigenetic instability is a source of novel methylation variants.Science2011
21653520A probabilistic method for the detection and genotyping of small indels from population-scale sequence data.Bioinformatics2011
21423666Global developmental gene expression and pathway analysis of normal brain development and mouse models of human neuronal migration defects.PLoS Genet2011
20940738Statistical analysis strategies for association studies involving rare variants.Nat Rev Genet2010
20067366Comparison of genetic distance measures using human SNP genotype data.Hum Biol2009
18252218Accommodating linkage disequilibrium in genetic-association analyses via ridge regression.Am J Hum Genet2008
18572020Identification of EpCAM as the gene for congenital tufting enteropathy.Gastroenterology2008
17411342Generalized analysis of molecular variance.PLoS Genet2007
17609390Detecting genetic variation in microarray expression data.Genome Res2007
17700628A simulation-based analysis of chromosome segment sharing among a group of arbitrarily related individuals.Eur J Hum Genet2007
17266112Comprehensive linkage and linkage heterogeneity analysis of 4344 sibling pairs affected with hypertension from the Family Blood Pressure Program.Genet Epidemiol2007
17324278DNA variation and brain region-specific expression profiles exhibit different relationships between inbred mouse strains: implications for eQTL mapping studies.Genome Biol2007
16451645Simulation-based homozygosity mapping with the GAW14 COGA dataset on alcoholism.BMC Genet2005
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Collaborators

Nicholas J Schork
University of California San Diego
Co-authored papers 35
Cinnamon Bloss
University of California
Co-authored papers 11
Bj Casey
Barnard College of Columbia University
Co-authored papers 8
Natacha Akshoomoff
University of California San Diego
Co-authored papers 8
Linda Chang
University of Maryland School of Medicine
Co-authored papers 8
Walter E Kaufmann
Emory University School of Medicine
Co-authored papers 8
Anders M Dale
University of California San Diego
Co-authored papers 8
Sarah S Murray
University of California San Diego Health System
Co-authored papers 8
Jeffrey R Gruen
Yale Medical School
Co-authored papers 8
Thomas Ernst
University of Maryland School of Medicine
Co-authored papers 8
David G Amaral
University of California
Co-authored papers 8
Stewart H Mostofsky
Johns Hopkins University School of Medicine
Co-authored papers 8
Jean A Frazier
university of massachusetts amherst Chan Medical School
Co-authored papers 8
Tal Kenet
Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital
Co-authored papers 7
Terry L Jernigan
Center for Human Development, University of California
Co-authored papers 7
Elizabeth R Sowell
Children's Hospital Los Angeles
Co-authored papers 7
Vikas Bansal
University of California San Diego
Co-authored papers 7
Joshua M Kuperman
University of California
Co-authored papers 7
Timothy T Brown
University of California San Diego
Co-authored papers 6
Donald J Hagler
Center for Multimodal Imaging and Genetics, University of California San Diego
Co-authored papers 6
Burcu F Darst
Fred Hutchinson Cancer Center
Co-authored papers 5
Hauke Bartsch
Haukeland University Hospital
Co-authored papers 5
Connor J McCabe
University of Washington.
Co-authored papers 5
David N Kennedy
University of Massachusetts Chan Medical School
Co-authored papers 4
Jae Yoon Chung
Boston University School of Medicine
Co-authored papers 4
Ali Torkamani
Scripps Science Institute
Co-authored papers 4
Caroline M Nievergelt
VA San Diego Healthcare System (VASDHS)
Co-authored papers 4
Nathan E Wineinger
Scripps Research Translational Institute, The Scripps Research Institute
Co-authored papers 4
Phillip Pham
Duke University
Co-authored papers 3
Guangfa Zhang
Sichuan Agricultural University
Co-authored papers 3
Release 1.2