List of works - Richard M. Myers

A genome-wide SNP genotyping array reveals patterns of global and repeated species-pair divergence in sticklebacks

scientific article

A physical map of the human genome

scientific article

A reference panel of 64,976 haplotypes for genotype imputation

scientific article

A role for a neo-sex chromosome in stickleback speciation

scientific article published on 27 September 2009

Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy

scientific article published on 07 January 2021

Adaptive evolution of pelvic reduction in sticklebacks by recurrent deletion of a Pitx1 enhancer

scientific article

Assembly of DNA sequencing data

scientific article

Assembly of the threespine stickleback Y chromosome reveals convergent signatures of sex chromosome evolution

scientific article published on 19 July 2020

Cathepsin B but not cathepsins L or S contributes to the pathogenesis of Unverricht-Lundborg progressive myoclonus epilepsy (EPM1)

scientific article (publication date: 15 September 2003)

ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia

scientific article

Characterizing the admixed African ancestry of African Americans

scientific article published in 2009

Coding potential of laboratory and clinical strains of human cytomegalovirus

scientific article

Coelacanth genome sequence reveals the evolutionary history of vertebrate genes

scientific article (publication date: December 2004)

Complete HOX cluster characterization of the coelacanth provides further evidence for slow evolution of its genome

scientific article (publication date: 23 February 2010)

Defining functional DNA elements in the human genome

scientific article

Dynamics of microRNA expression during mouse prenatal development

scientific article published on 23 October 2019

Education and personalized genomics: deciphering the public’s genetic health report

scientific article

Evolving New Skeletal Traits by cis-Regulatory Changes in Bone Morphogenetic Proteins

scientific journal article

Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data

scientific article

Expanded encyclopaedias of DNA elements in the human and mouse genomes

scientific article published on 29 July 2020

Extensive linkage disequilibrium, a common 16.7-kilobase deletion, and evidence of balancing selection in the human protocadherin alpha cluster

scientific article

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

Gene conversion and the evolution of protocadherin gene cluster diversity

scientific article published on March 2004

Generation and annotation of the DNA sequences of human chromosomes 2 and 4

scientific article

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

scientific article

Genetic architecture of variation in the lateral line sensory system of threespine sticklebacks.

scientific article

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

scientific article

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

scientific article published on 13 December 2019

Genome-wide analysis of transcription factor binding sites based on ChIP-Seq data

scientific article

Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations

scientific article

Genome-wide association study identifies 30 loci associated with bipolar disorder.

scientific article

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

scientific article published in June 2021

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

scientific article published in June 2007

Identification of promoter regions in the human genome by using a retroviral plasmid library-based functional reporter gene assay

scientific article

Initial sequencing and analysis of the human genome

scientific article published on 15 February 2001

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families

scientific article (publication date: 8 January 2002)

Model-based analysis of ChIP-Seq (MACS)

scientific article

PEA15 loss of function and defective cerebral development in the domestic cat

scientific article published on 08 December 2020

Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions

scientific article

Quality assessment of finished BAC sequences

scientific article published in January 2004

Quality assessment of the human genome sequence

scientific article

Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease

scientific article published on August 2014

STAT3 and GR cooperate to drive gene expression and growth of basal-like triple-negative breast cancer

scientific article published on 19 August 2020

Sequence finishing

scientific article published on 01 January 2004

Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling

scientific article published on 3 May 2006

Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging

scientific article published in October 2009

Serum response factor binding sites differ in three human cell types

scientific article

Signals of recent positive selection in a worldwide sample of human populations

scientific article

Systematic reanalysis of genomic data improves quality of variant interpretation.

scientific article published on 13 April 2018

The DNA sequence and biology of human chromosome 19

scientific article

The DNA sequence and comparative analysis of human chromosome 5

scientific article

The completion of the Mammalian Gene Collection (MGC).

scientific article published on 18 September 2009

The genomic basis of adaptive evolution in threespine sticklebacks

scientific article

The master sex-determination locus in threespine sticklebacks is on a nascent Y chromosome

scientific article

The role of geography in human adaptation

scientific article

The sequence and analysis of duplication-rich human chromosome 16

scientific article

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)

scientific article

Theria-specific homeodomain and cis-regulatory element evolution of the Dlx3-4 bigene cluster in 12 different mammalian species

scientific article published on 5 September 2012

List of works by Richard M. Myers

A genome-wide SNP genotyping array reveals patterns of global and repeated species-pair divergence in sticklebacks

A physical map of the human genome

A reference panel of 64,976 haplotypes for genotype imputation

A role for a neo-sex chromosome in stickleback speciation

Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy

Adaptive evolution of pelvic reduction in sticklebacks by recurrent deletion of a Pitx1 enhancer

Assembly of DNA sequencing data

Assembly of the threespine stickleback Y chromosome reveals convergent signatures of sex chromosome evolution

Cathepsin B but not cathepsins L or S contributes to the pathogenesis of Unverricht-Lundborg progressive myoclonus epilepsy (EPM1)

ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia

Characterizing the admixed African ancestry of African Americans

Coding potential of laboratory and clinical strains of human cytomegalovirus

Coelacanth genome sequence reveals the evolutionary history of vertebrate genes

Complete HOX cluster characterization of the coelacanth provides further evidence for slow evolution of its genome

Defining functional DNA elements in the human genome

Dynamics of microRNA expression during mouse prenatal development

Education and personalized genomics: deciphering the public’s genetic health report

Evolving New Skeletal Traits by cis-Regulatory Changes in Bone Morphogenetic Proteins

Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data

Expanded encyclopaedias of DNA elements in the human and mouse genomes

Extensive linkage disequilibrium, a common 16.7-kilobase deletion, and evidence of balancing selection in the human protocadherin alpha cluster

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

Gene conversion and the evolution of protocadherin gene cluster diversity

Generation and annotation of the DNA sequences of human chromosomes 2 and 4

Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences

Genetic architecture of variation in the lateral line sensory system of threespine sticklebacks.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles

Genome-wide analysis of transcription factor binding sites based on ChIP-Seq data

Genome-wide association studies of quantitatively measured skin, hair, and eye pigmentation in four European populations

Genome-wide association study identifies 30 loci associated with bipolar disorder.

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Identification of promoter regions in the human genome by using a retroviral plasmid library-based functional reporter gene assay

Initial sequencing and analysis of the human genome

Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families

Model-based analysis of ChIP-Seq (MACS)

PEA15 loss of function and defective cerebral development in the domestic cat

Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions

Quality assessment of finished BAC sequences

Quality assessment of the human genome sequence

Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease

STAT3 and GR cooperate to drive gene expression and growth of basal-like triple-negative breast cancer

Sequence finishing

Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling

Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney aging

Serum response factor binding sites differ in three human cell types

Signals of recent positive selection in a worldwide sample of human populations

Systematic reanalysis of genomic data improves quality of variant interpretation.

The DNA sequence and biology of human chromosome 19

The DNA sequence and comparative analysis of human chromosome 5

The completion of the Mammalian Gene Collection (MGC).

The genomic basis of adaptive evolution in threespine sticklebacks

The master sex-determination locus in threespine sticklebacks is on a nascent Y chromosome

The role of geography in human adaptation

The sequence and analysis of duplication-rich human chromosome 16

The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)

Theria-specific homeodomain and cis-regulatory element evolution of the Dlx3-4 bigene cluster in 12 different mammalian species