Heritability and Genomics of Gene Expression in Peripheral Blood
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P. Sullivan | F. Wright | A. Shabalin | J. Tzeng | B. Penninx | G. Willemsen | P. Gallins | D. Boomsma | E. D. de Geus | Yi‐Hui Zhou | J. Hottenga | J. Smit | Wei Sun | F. Zou | A. Abdellaoui | M. Kattenberg | K. Xia | Wei Wang | Weibo Wang | Ting-Huei Chen | Shunping Huang | J. Vink | A. Brooks | V. Madar | R. Jansen | Wonil Chung | Sandra Batista | Casey Butler | Guanhua Chen | David D’Ambrosio | M. Ha | J. Kochar | C. Middeldorp | Ani Qu | J. Tischfield | Laura Todd | G. van Grootheest | Qi Wang | Zhaoyu Yin | Wen Wang | Jung‐Ying Tzeng | D. Boomsma | Andy Brooks | Jung-Ying Tzeng | Gerard van Grootheest | Yi-Hui Zhou
[1] H. Grüneberg,et al. Introduction to quantitative genetics , 1960 .
[2] L. Buchanan. Mental retardation. , 1972, The Medical journal of Australia.
[3] Nature Genetics , 1991, Nature.
[4] Robin Thompson,et al. Average information REML: An efficient algorithm for variance parameter estimation in linear mixed models , 1995 .
[5] J. Rashbass. Online Mendelian Inheritance in Man. , 1995, Trends in genetics : TIG.
[6] The phenotypic difference discards sib-pair QTL linkage information. , 1997 .
[7] F. Wright. The phenotypic difference discards sib-pair QTL linkage information. , 1997, American journal of human genetics.
[8] David J. Groggel,et al. Practical Nonparametric Statistics , 2000, Technometrics.
[9] G. Abecasis,et al. Merlin—rapid analysis of dense genetic maps using sparse gene flow trees , 2002, Nature Genetics.
[10] M. Daly,et al. PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes , 2003, Nature Genetics.
[11] C. Pál,et al. The evolutionary dynamics of eukaryotic gene order , 2004, Nature Reviews Genetics.
[12] Cameron S. Osborne,et al. Active genes dynamically colocalize to shared sites of ongoing transcription , 2004, Nature Genetics.
[13] Jennifer K Inlow,et al. Molecular and comparative genetics of mental retardation. , 2004, Genetics.
[14] Timothy B Sackton,et al. A Scan for Positively Selected Genes in the Genomes of Humans and Chimpanzees , 2005, PLoS biology.
[15] Andrew B. Nobel,et al. Significance analysis of functional categories in gene expression studies: a structured permutation approach , 2005, Bioinform..
[16] Nick Gilbert,et al. The role of chromatin structure in regulating the expression of clustered genes , 2005, Nature Reviews Genetics.
[17] Manuel A. R. Ferreira,et al. Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings , 2006, PLoS genetics.
[18] Danielle Posthuma,et al. Netherlands Twin Register: From Twins to Twin Families , 2006, Twin Research and Human Genetics.
[19] D. Reich,et al. Principal components analysis corrects for stratification in genome-wide association studies , 2006, Nature Genetics.
[20] J. Pritchard,et al. A Map of Recent Positive Selection in the Human Genome , 2006, PLoS biology.
[21] David Bryant,et al. DAVID Bioinformatics Resources: expanded annotation database and novel algorithms to better extract biology from large gene lists , 2007, Nucleic Acids Res..
[22] Kathryn E. Hentges,et al. Regional Variation in the Density of Essential Genes in Mice , 2007, PLoS genetics.
[23] V. McKusick. Mendelian Inheritance in Man and Its Online Version, OMIM , 2007, The American Journal of Human Genetics.
[24] R. Redon,et al. Relative Impact of Nucleotide and Copy Number Variation on Gene Expression Phenotypes , 2007, Science.
[25] P. Donnelly,et al. New models of collaboration in genome-wide association studies: the Genetic Association Information Network , 2007, Nature Genetics.
[26] Joshua T. Burdick,et al. Common genetic variants account for differences in gene expression among ethnic groups , 2007, Nature Genetics.
[27] Jeffrey T Leek,et al. On the design and analysis of gene expression studies in human populations , 2007, Nature Genetics.
[28] John D. Storey,et al. Capturing Heterogeneity in Gene Expression Studies by Surrogate Variable Analysis , 2007, PLoS genetics.
[29] P. Sullivan,et al. Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projects , 2008, European Journal of Human Genetics.
[30] P. Cuijpers,et al. The Netherlands Study of Depression and Anxiety (NESDA): rationale, objectives and methods , 2008, International journal of methods in psychiatric research.
[31] P. Chiurazzi,et al. XLMR genes: update 2007 , 2008, European Journal of Human Genetics.
[32] Mark D. Adams,et al. Human PAML browser: a database of positive selection on human genes using phylogenetic methods , 2007, Nucleic Acids Res..
[33] Manuel A. R. Ferreira,et al. Practical aspects of imputation-driven meta-analysis of genome-wide association studies. , 2008, Human molecular genetics.
[34] Elliott Kieff,et al. Genetic Analysis of Human Traits In Vitro: Drug Response and Gene Expression in Lymphoblastoid Cell Lines , 2008, PLoS genetics.
[35] W. G. Hill,et al. Heritability in the genomics era — concepts and misconceptions , 2008, Nature Reviews Genetics.
[36] John D. Rioux,et al. Genome-wide association studies: a new window into immune-mediated diseases , 2008, Nature Reviews Immunology.
[37] D. Reich,et al. Effects of cis and trans Genetic Ancestry on Gene Expression in African Americans , 2008, PLoS genetics.
[38] Benjamin M Neale,et al. The Positives , Protocols , and Perils of Genome-Wide Association , 2008 .
[39] Andrew B. Nobel,et al. A statistical framework for testing functional categories in microarray data , 2008, 0803.3881.
[40] H. Stefánsson,et al. Genetics of gene expression and its effect on disease , 2008, Nature.
[41] Cole Trapnell,et al. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome , 2009, Genome Biology.
[42] Daniel Sinnett,et al. Population genomics in a disease targeted primary cell model. , 2009, Genome research.
[43] L. Liang,et al. Mapping complex disease traits with global gene expression , 2009, Nature Reviews Genetics.
[44] Steven J. M. Jones,et al. Circos: an information aesthetic for comparative genomics. , 2009, Genome research.
[45] Guy Sella,et al. Pervasive Hitchhiking at Coding and Regulatory Sites in Humans , 2009, PLoS genetics.
[46] Jeremiah D. Degenhardt,et al. Targets of balancing selection in the human genome. , 2009, Molecular biology and evolution.
[47] F. Real,et al. Interaction between Hhex and SOX13 Modulates Wnt/TCF Activity , 2009, The Journal of Biological Chemistry.
[48] F. Collins,et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits , 2009, Proceedings of the National Academy of Sciences.
[49] Andrew Starkey,et al. Evidence of uneven selective pressure on different subsets of the conserved human genome; implications for the significance of intronic and intergenic DNA , 2009, BMC Genomics.
[50] N. Wray,et al. Genomewide Association for Major Depressive Disorder: A possible role for the presynaptic protein Piccolo , 2008, Molecular Psychiatry.
[51] Silke Szymczak,et al. Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility , 2010, PloS one.
[52] R. Guigó,et al. Transcriptome genetics using second generation sequencing in a Caucasian population , 2010, Nature.
[53] M. Eileen Dolan,et al. Chemotherapeutic drug susceptibility associated SNPs are enriched in expression quantitative trait loci , 2010, Proceedings of the National Academy of Sciences.
[54] David M. Simcha,et al. Tackling the widespread and critical impact of batch effects in high-throughput data , 2010, Nature Reviews Genetics.
[55] Ayellet V. Segrè,et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height , 2010, Nature.
[56] A. Nobel,et al. Heading Down the Wrong Pathway: on the Influence of Correlation within Gene Sets , 2010, BMC Genomics.
[57] Or Zuk,et al. A Composite of Multiple Signals Distinguishes Causal Variants in Regions of Positive Selection , 2010, Science.
[58] N. Cox,et al. Trait-Associated SNPs Are More Likely to Be eQTLs: Annotation to Enhance Discovery from GWAS , 2010, PLoS genetics.
[59] Joseph K. Pickrell,et al. Understanding mechanisms underlying human gene expression variation with RNA sequencing , 2010, Nature.
[60] Tanya M. Teslovich,et al. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index , 2010 .
[61] D. Altshuler,et al. A map of human genome variation from population-scale sequencing , 2010, Nature.
[62] T. Lehner,et al. The Netherlands Twin Register Biobank: A Resource for Genetic Epidemiological Studies , 2010, Twin Research and Human Genetics.
[63] Sharon R Grossman,et al. Integrating common and rare genetic variation in diverse human populations , 2010, Nature.
[64] Daniel Rios,et al. Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor , 2022 .
[65] Cisca Wijmenga,et al. Analysis of SNPs with an effect on gene expression identifies UBE2L3 and BCL3 as potential new risk genes for Crohn's disease. , 2010, Human molecular genetics.
[66] J. Ibrahim,et al. Genomewide Multiple-Loci Mapping in Experimental Crosses by Iterative Adaptive Penalized Regression , 2010, Genetics.
[67] Luigi Ferrucci,et al. Abundant Quantitative Trait Loci Exist for DNA Methylation and Gene Expression in Human Brain , 2010, PLoS genetics.
[68] Jacek Majewski,et al. The study of eQTL variations by RNA-seq: from SNPs to phenotypes. , 2011, Trends in genetics : TIG.
[69] M. Daly,et al. Proteins Encoded in Genomic Regions Associated with Immune-Mediated Disease Physically Interact and Suggest Underlying Biology , 2011, PLoS genetics.
[70] Christian Gieger,et al. The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits , 2011, PloS one.
[71] Emmanouil Collab. A map of human genome variation from population-scale sequencing , 2011, Nature.
[72] P. Visscher,et al. GCTA: a tool for genome-wide complex trait analysis. , 2011, American journal of human genetics.
[73] Albert J. Vilella,et al. A high-resolution map of human evolutionary constraint using 29 mammals , 2011, Nature.
[74] C. Betancur,et al. Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting , 2011, Brain Research.
[75] F. Agakov,et al. Abundant pleiotropy in human complex diseases and traits. , 2011, American journal of human genetics.
[76] Christopher D. Brown,et al. Identification, Replication, and Functional Fine-Mapping of Expression Quantitative Trait Loci in Primary Human Liver Tissue , 2011, PLoS genetics.
[77] Gregory M. Cooper,et al. A Copy Number Variation Morbidity Map of Developmental Delay , 2011, Nature Genetics.
[78] Heping Zhang,et al. Statistical Inference in Mixed Models and Analysis of Twin and Family Data , 2011, Biometrics.
[79] Jingyuan Fu,et al. Trans-eQTLs Reveal That Independent Genetic Variants Associated with a Complex Phenotype Converge on Intermediate Genes, with a Major Role for the HLA , 2011, PLoS genetics.
[80] F. Vannberg,et al. GENETICS OF GENE EXPRESSION IN PRIMARY IMMUNE CELLS IDENTIFIES CELL-SPECIFIC MASTER REGULATORS AND ROLES OF HLA ALLELES , 2012, Nature Genetics.
[81] Patrick F. Sullivan,et al. Genetic architectures of psychiatric disorders: the emerging picture and its implications , 2012, Nature Reviews Genetics.
[82] Fred A. Wright,et al. seeQTL: a searchable database for human eQTLs , 2011, Bioinform..
[83] Joseph K. Pickrell,et al. DNaseI sensitivity QTLs are a major determinant of human expression variation , 2011, Nature.
[84] P. Deloukas,et al. Patterns of Cis Regulatory Variation in Diverse Human Populations , 2012, PLoS genetics.
[85] K. Hao,et al. Bayesian method to predict individual SNP genotypes from gene expression data , 2012, Nature Genetics.
[86] Simon C. Potter,et al. Mapping cis- and trans-regulatory effects across multiple tissues in twins , 2012, Nature Genetics.
[87] Yuan Tian,et al. Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders. , 2012, American journal of human genetics.
[88] Wiepke Cahn,et al. Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes , 2012, European Journal of Human Genetics.
[89] Nathan C. Sheffield,et al. The accessible chromatin landscape of the human genome , 2012, Nature.
[90] P. Visscher,et al. Genetic control of gene expression in whole blood and lymphoblastoid cell lines is largely independent. , 2012, Genome research.
[91] Shane J. Neph,et al. Systematic Localization of Common Disease-Associated Variation in Regulatory DNA , 2012, Science.
[92] Andrey A. Shabalin,et al. Matrix eQTL: ultra fast eQTL analysis via large matrix operations , 2011, Bioinform..
[93] Dorret I. Boomsma,et al. The continuing value of twin studies in the omics era , 2012, Nature Reviews Genetics.
[94] M. Peters,et al. Systematic identification of trans eQTLs as putative drivers of known disease associations , 2013, Nature Genetics.
[95] Psychiatric genetics: are we there yet? , 2013, JAMA psychiatry.
[96] M. Stephens,et al. A Statistical Framework for Joint eQTL Analysis in Multiple Tissues , 2012, PLoS genetics.
[97] Eric S. Lander,et al. Identifying Recent Adaptations in Large-Scale Genomic Data , 2013, Cell.
[98] Joseph E. Powell,et al. Congruence of Additive and Non-Additive Effects on Gene Expression Estimated from Pedigree and SNP Data , 2013, PLoS genetics.
[99] T. Manolio,et al. eXclusion: toward integrating the X chromosome in genome-wide association analyses. , 2013, American journal of human genetics.
[100] R Core Team,et al. R: A language and environment for statistical computing. , 2014 .
[101] G. Hong,et al. Nucleic Acids Research , 2015, Nucleic Acids Research.