Richard M. Myers | Academic Influence

Richard M. Myers's AcademicInfluence.com Rankings

Richard M. Myers

Biology

#3310

World Rank

#5078

Historical Rank

#1354

USA Rank

Genetics

#398

World Rank

#462

Historical Rank

#169

USA Rank

biology Degrees

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Biology

Richard M. Myers's Degrees

PhD Genetics Stanford University
Bachelors Biochemistry University of California, Berkeley

Why Is Richard M. Myers Influential?

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According to Wikipedia, Richard M. Myers is an American geneticist and biochemist known for his work on the Human Genome Project . The National Human Genome Research Institute says the HGP “[gave] the world a resource of detailed information about the structure, organization and function of the complete set of human genes.” Myers' genome center, in collaboration with the Joint Genome Institute, contributed more than 10 percent of the data in the project.

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Richard M. Myers's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Model-based Analysis of ChIP-Seq (MACS) (2008) (11787)
Integrated Genomic Analyses of Ovarian Carcinoma (2011) (6411)
Comprehensive genomic characterization defines human glioblastoma genes and core pathways (2008) (5775)
Genome-Wide Mapping of in Vivo Protein-DNA Interactions (2007) (2675)
The ENCODE (ENCyclopedia Of DNA Elements) Project (2004) (2194)
An integrated encyclopedia of DNA elements in the human genome (2012) (2080)
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs (2013) (2011)
Human Homolog of patched, a Candidate Gene for the Basal Cell Nevus Syndrome (1996) (1916)
Worldwide Human Relationships Inferred from Genome-Wide Patterns of Variation (2008) (1910)
Evolving gene/transcript definitions significantly alter the interpretation of GeneChip data (2005) (1891)
Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences (2002) (1846)
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia (2012) (1701)
The genomic basis of adaptive evolution in threespine sticklebacks (2012) (1560)
A User's Guide to the Encyclopedia of DNA Elements (ENCODE) (2011) (1467)
Architecture of the human regulatory network derived from ENCODE data (2012) (1393)
Widespread Parallel Evolution in Sticklebacks by Repeated Fixation of Ectodysplasin Alleles (2005) (1374)
Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes. (1989) (1346)
Candidate-gene approaches for studying complex genetic traits: practical considerations (2002) (1117)
A Gene Map of the Human Genome (1996) (1080)
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder (2017) (998)
A Validated Regulatory Network for Th17 Cell Specification (2012) (991)
Detection and localization of single base changes by denaturing gradient gel electrophoresis. (1987) (957)
Primary structure and functional expression of the 5HT3 receptor, a serotonin-gated ion channel. (1991) (948)
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 (2011) (929)
Adaptive Evolution of Pelvic Reduction in Sticklebacks by Recurrent Deletion of a Pitx1 Enhancer (2010) (927)
Structure and variability of human chromosome ends (1990) (864)
Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors (2012) (817)
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways (2015) (816)
Expanded encyclopaedias of DNA elements in the human and mouse genomes (2020) (765)
Genome-Wide Analysis of Transcription Factor Binding Sites Based on ChIP-Seq Data (2008) (760)
Signals of recent positive selection in a worldwide sample of human populations. (2009) (730)
A genomic screen of autism: evidence for a multilocus etiology. (1999) (693)
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways (2015) (676)
A physical map of 30,000 human genes. (1998) (670)
Defining functional DNA elements in the human genome (2014) (647)
Nearly all single base substitutions in DNA fragments joined to a GC-clamp can be detected by denaturing gradient gel electrophoresis. (1985) (633)
Radiation hybrid mapping: a somatic cell genetic method for constructing high-resolution maps of mammalian chromosomes. (1990) (629)
Dynamic DNA methylation across diverse human cell lines and tissues (2013) (627)
An abundance of bidirectional promoters in the human genome. (2003) (594)
Population analysis of large copy number variants and hotspots of human genetic disease. (2009) (589)
Altered cortical glutamatergic and GABAergic signal transmission with glial involvement in depression (2005) (571)
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (2004) (565)
A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation (1995) (526)
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes (2017) (517)
Widespread plasticity in CTCF occupancy linked to DNA methylation (2012) (515)
A neurodegeneration-specific gene-expression signature of acutely isolated microglia from an amyotrophic lateral sclerosis mouse model. (2013) (510)
Coding potential of laboratory and clinical strains of human cytomegalovirus (2003) (508)
Detection of single base substitutions by ribonuclease cleavage at mismatches in RNA:DNA duplexes. (1985) (501)
Genomic determination of the glucocorticoid response reveals unexpected mechanisms of gene regulation. (2009) (490)
Circadian patterns of gene expression in the human brain and disruption in major depressive disorder (2013) (464)
Selective Disruption of Lysosomes in HeLa Cells Triggers Apoptosis Mediated by Cleavage of Bid by Multiple Papain-like Lysosomal Cathepsins* (2004) (462)
From single-cell to cell-pool transcriptomes: Stochasticity in gene expression and RNA splicing (2014) (451)
Advancements in Next-Generation Sequencing. (2016) (422)
Genome-wide Analyses Identify KIF5A as a Novel ALS Gene (2018) (414)
The Role of Geography in Human Adaptation (2009) (406)
The Master Sex-Determination Locus in Threespine Sticklebacks Is on a Nascent Y Chromosome (2004) (394)
Genomic patterns of homozygosity in worldwide human populations. (2012) (373)
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects (2008) (372)
Dysregulation of the fibroblast growth factor system in major depression. (2004) (367)
Fine structure genetic analysis of a beta-globin promoter. (1986) (360)
Detection of single base substitutions in total genomic DNA (1985) (359)
Polymorphisms within the C-reactive protein (CRP) promoter region are associated with plasma CRP levels. (2005) (339)
An STS-based radiation hybrid map of the human genome. (1997) (334)
A role for a neo-sex chromosome in stickleback speciation (2009) (327)
Progressive ataxia, myoclonic epilepsy and cerebellar apoptosis in cystatin B-deficient mice (1998) (325)
The role of heat shock transcription factor 1 in the genome-wide regulation of the mammalian heat shock response. (2003) (318)
Effect of agonal and postmortem factors on gene expression profile: quality control in microarray analyses of postmortem human brain (2004) (312)
Altered expression of glutamate signaling, growth factor and glia genes in the locus coeruleus of patients with major depression (2010) (311)
An integrated system CisGenome for analyzing ChIP-chip and ChIP-seq data (2008) (308)
Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry (2009) (304)
Diverse and specific gene expression responses to stresses in cultured human cells. (2004) (300)
Distinct DNA methylation patterns characterize differentiated human embryonic stem cells and developing human fetal liver. (2009) (299)
Comprehensive analysis of transcriptional promoter structure and function in 1% of the human genome. (2005) (298)
Analysis of DNA Methylation in a Three-Generation Family Reveals Widespread Genetic Influence on Epigenetic Regulation (2011) (297)
The DNA sequence and biology of human chromosome 19 (2004) (295)
Sequence census methods for functional genomics (2008) (281)
Mitochondrial involvement in psychiatric disorders (2008) (278)
Differential DNA methylation with age displays both common and dynamic features across human tissues that are influenced by CpG landscape (2013) (278)
Distinct properties of cell-type-specific and shared transcription factor binding sites. (2013) (260)
Modification of the melting properties of duplex DNA by attachment of a GC-rich DNA sequence as determined by denaturing gradient gel electrophoresis. (1985) (260)
High throughput sequencing reveals a complex pattern of dynamic interrelationships among human T cell subsets (2010) (259)
A general method for saturation mutagenesis of cloned DNA fragments. (1985) (243)
Systematic changes in gene expression in postmortem human brains associated with tissue pH and terminal medical conditions. (2004) (240)
Genome-wide association study of over 40,000 bipolar disorder cases provides new insights into the underlying biology (2021) (240)
A Genome-wide SNP Genotyping Array Reveals Patterns of Global and Repeated Species-Pair Divergence in Sticklebacks (2012) (230)
Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1 (1997) (227)
SV40 gene expression is modulated by the cooperative binding of T antigen to DNA (1981) (220)
DNA methylation profiling reveals novel biomarkers and important roles for DNA methyltransferases in prostate cancer. (2011) (218)
Gender-Specific Gene Expression in Post-Mortem Human Brain: Localization to Sex Chromosomes (2004) (217)
CTCF/cohesin-mediated DNA looping is required for protocadherin α promoter choice (2012) (212)
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2015) (206)
Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions. (2007) (206)
Mitochondrial Variants in Schizophrenia, Bipolar Disorder, and Major Depressive Disorder (2009) (201)
Susceptibility locus for clinical and subclinical coronary artery disease at chromosome 9p21 in the multi-ethnic ADVANCE study. (2008) (201)
Behavioral phenotypic variation in autism multiplex families: evidence for a continuous severity gradient. (2002) (200)
Regulation of simian virus 40 early transcription in vitro by a purified tumor antigen. (1980) (186)
Identification and functional analysis of human transcriptional promoters. (2003) (184)
Mitochondrial-related gene expression changes are sensitive to agonal-pH state: implications for brain disorders (2006) (174)
Genomic diagnosis for children with intellectual disability and/or developmental delay (2016) (165)
Comparative genomics modeling of the NRSF/REST repressor network: from single conserved sites to genome-wide repertoire. (2006) (163)
Functional analysis of transcription factor binding sites in human promoters (2012) (163)
The sequence and analysis of duplication-rich human chromosome 16 (2004) (160)
Exon trapping: a genetic screen to identify candidate transcribed sequences in cloned mammalian genomic DNA. (1990) (158)
Systematic evaluation of factors influencing ChIP-seq fidelity (2012) (153)
Construction and analysis of simian virus 40 origins defective in tumor antigen binding and DNA replication. (1980) (151)
A High-Resolution Radiation Hybrid Map of the Human Genome Draft Sequence (2001) (149)
Effects of sequence variation on differential allelic transcription factor occupancy and gene expression (2012) (148)
DDX5 and its associated lncRNA Rmrp modulate Th17 cell effector functions (2015) (147)
Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets. (2008) (147)
Microarray technology: a review of new strategies to discover candidate vulnerability genes in psychiatric disorders. (2003) (145)
Characterizing the admixed African ancestry of African Americans (2009) (143)
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. (2016) (143)
Role of CCCTC binding factor (CTCF) and cohesin in the generation of single-cell diversity of Protocadherin-α gene expression (2012) (140)
Circadian dysregulation of clock genes: clues to rapid treatments in major depressive disorder (2014) (140)
Transcription factor binding and modified histones in human bidirectional promoters. (2007) (139)
Recurrent read-through fusion transcripts in breast cancer (2014) (137)
Rapid mapping of zebrafish mutations with SNPs and oligonucleotide microarrays. (2002) (133)
The completion of the Mammalian Gene Collection (MGC). (2009) (132)
Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia (2017) (129)
Transcriptional regulation and binding of heat shock factor 1 and heat shock factor 2 to 32 human heat shock genes during thermal stress and differentiation (2004) (128)
Analysis of the site in CD4 that binds to the HIV envelope glycoprotein. (1990) (128)
Cancer cell proliferation is inhibited by specific modulation frequencies (2011) (125)
The Hypersensitive Glucocorticoid Response Specifically Regulates Period 1 and Expression of Circadian Genes (2012) (124)
Post-mortem molecular profiling of three psychiatric disorders (2016) (122)
Evolving New Skeletal Traits by cis-Regulatory Changes in Bone Morphogenetic Proteins (2016) (121)
NALP3 inflammasome up-regulation and CASP1 cleavage of the glucocorticoid receptor causes glucocorticoid resistance in leukemia cells (2015) (116)
The DNA sequence and comparative analysis of human chromosome 5 (2004) (116)
Identification and molecular cloning of a neuropeptide y homolog that produces prolonged inhibition in aplysia neurons (1992) (116)
Intricate interplay between astrocytes and motor neurons in ALS (2013) (115)
A map of the distal region of the long arm of human chromosome 21 constructed by radiation hybrid mapping and pulsed-field gel electrophoresis. (1991) (114)
Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans (2017) (112)
Gene conversion and the evolution of protocadherin gene cluster diversity. (2004) (110)
Genistein and bisphenol A exposure cause estrogen receptor 1 to bind thousands of sites in a cell type-specific manner (2012) (109)
Cathepsin B but not cathepsins L or S contributes to the pathogenesis of Unverricht-Lundborg progressive myoclonus epilepsy (EPM1). (2003) (108)
IκB kinase ε (IKKε) regulates the balance between type I and type II interferon responses (2011) (107)
Analysis of miR-137 expression and rs1625579 in dorsolateral prefrontal cortex. (2013) (107)
Glucocorticoid and mineralocorticoid receptor expression in the human hippocampus in major depressive disorder. (2013) (107)
Erratum: Initial sequencing and analysis of the human genome: International Human Genome Sequencing Consortium (Nature (2001) 409 (860-921)) (2001) (106)
CETCh-seq: CRISPR epitope tagging ChIP-seq of DNA-binding proteins (2015) (104)
Cystatin B-deficient mice have increased expression of apoptosis and glial activation genes. (2001) (103)
Genome-Wide Association Studies of Quantitatively Measured Skin, Hair, and Eye Pigmentation in Four European Populations (2012) (102)
Wild-type huntingtin participates in protein trafficking between the Golgi and the extracellular space. (2007) (102)
Sequence features that drive human promoter function and tissue specificity. (2010) (100)
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls (2018) (99)
Generation and annotation of the DNA sequences of human chromosomes 2 and 4 (2005) (98)
Segregation of the Huntington disease region of human chromosome 4 in a somatic cell hybrid. (1989) (97)
Lack of replication of thirteen single-nucleotide polymorphisms implicated in Parkinson's disease: a large-scale international study (2006) (96)
Expression of the MHC Class II Pathway in Triple-Negative Breast Cancer Tumor Cells Is Associated with a Good Prognosis and Infiltrating Lymphocytes (2016) (94)
Direct isolation and identification of promoters in the human genome. (2005) (92)
Absence of linkage and linkage disequilibrium to chromosome 15q11-q13 markers in 139 multiplex families with autism. (1999) (91)
Mutation Detection by PCR, GC-Clamps, and Denaturing Gradient Gel Electrophoresis (1989) (91)
Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary disease. (2007) (89)
Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. (2010) (89)
Detection of single base changes in DNA: ribonuclease cleavage and denaturing gradient gel electrophoresis. (1988) (86)
Transposase mediated construction of RNA-seq libraries. (2012) (86)
Early de novo DNA methylation and prolonged demethylation in the muscle lineage (2013) (84)
Serum response factor binding sites differ in three human cell types. (2007) (83)
Dynamic MicroRNA Gene Transcription and Processing during T Cell Development (2012) (82)
Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling. (2006) (82)
Evolutionary constraint facilitates interpretation of genetic variation in resequenced human genomes. (2010) (80)
Stress-induced changes in primate prefrontal profiles of gene expression (2007) (80)
Perspectives on ENCODE (2020) (79)
Variable telomere length across post-mortem human brain regions and specific reduction in the hippocampus of major depressive disorder (2015) (79)
Discrimination among potential activators of the beta-globin CACCC element by correlation of binding and transcriptional properties (1993) (79)
Neuropathological Changes in a Mouse Model of Progressive Myoclonus Epilepsy: Cystatin B Deficiency and Unverricht‐Lundborg Disease (2002) (78)
Gene Expression Changes in the Prefrontal Cortex, Anterior Cingulate Cortex and Nucleus Accumbens of Mood Disorders Subjects That Committed Suicide (2012) (77)
New genomic tools for molecular studies of evolutionary change in threespine sticklebacks (2004) (77)
Coelacanth genome sequence reveals the evolutionary history of vertebrate genes. (2004) (74)
Evidence for alterations of the glial syncytial function in major depressive disorder. (2016) (73)
Complete HOX cluster characterization of the coelacanth provides further evidence for slow evolution of its genome (2010) (71)
The genetic basis of divergent pigment patterns in juvenile threespine sticklebacks (2011) (70)
De Novo Mutations in SON Disrupt RNA Splicing of Genes Essential for Brain Development and Metabolism, Causing an Intellectual-Disability Syndrome. (2016) (68)
The complete sequence of human chromosome 5 (2004) (68)
Evidence from antibody studies that the CAG repeat in the Huntington disease gene is expressed in the protein. (1995) (66)
CCCTC‐Binding Factor Translates Interleukin 2‐ and &agr;‐Ketoglutarate‐Sensitive Metabolic Changes in T Cells into Context‐Dependent Gene Programs (2017) (65)
A radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci. (1991) (65)
Apoptosis caused by cathepsins does not require Bid signaling in an in vivo model of progressive myoclonus epilepsy (EPM1) (2003) (64)
DNA sequences involved in transcriptional regulation of the mouse beta-globin promoter in murine erythroleukemia cells (1988) (63)
Recent advances in the development of methods for detecting single-base substitutions associated with human genetic diseases. (1986) (63)
Whole-Exome Sequencing in Familial Parkinson Disease. (2016) (62)
Alterations in DNA helix stability due to base modifications can be evaluated using denaturing gradient gel electrophoresis. (1987) (62)
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease (2008) (60)
A directly repeated sequence in the beta-globin promoter regulates transcription in murine erythroleukemia cells (1990) (59)
Matrix metalloproteinase circulating levels, genetic polymorphisms, and susceptibility to acute myocardial infarction among patients with coronary artery disease. (2007) (58)
Genetic Architecture of Variation in the Lateral Line Sensory System of Threespine Sticklebacks (2012) (58)
Occupancy maps of 208 chromatin-associated proteins in one human cell type (2020) (56)
Construction of a 750-kb bacterial clone contig and restriction map in the region of human chromosome 21 containing the progressive myoclonus epilepsy gene. (1996) (56)
Extensive linkage disequilibrium, a common 16.7-kilobase deletion, and evidence of balancing selection in the human protocadherin alpha cluster. (2003) (56)
Assembly of the threespine stickleback Y chromosome reveals convergent signatures of sex chromosome evolution (2020) (56)
Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies. (2018) (56)
Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families. (2002) (55)
G protein-linked signaling pathways in bipolar and major depressive disorders (2013) (55)
Genomic regulation of invasion by STAT3 in triple negative breast cancer (2016) (54)
The ets-Related Transcription Factor GABP Directs Bidirectional Transcription (2007) (54)
Sequential Use of Transcriptional Profiling, Expression Quantitative Trait Mapping, and Gene Association Implicates MMP20 in Human Kidney Aging (2009) (53)
The molecular genetic bases of the progressive myoclonus epilepsies. (1999) (53)
Mutations in EBF3 Disturb Transcriptional Profiles and Cause Intellectual Disability, Ataxia, and Facial Dysmorphism. (2017) (52)
Inference of cell type content from human brain transcriptomic datasets illuminates the effects of age, manner of death, dissection, and psychiatric diagnosis (2018) (52)
DNA microarray analysis of functionally discrete human brain regions reveals divergent transcriptional profiles (2003) (51)
The microRNA network is altered in anterior cingulate cortex of patients with unipolar and bipolar depression. (2016) (50)
Glutamate transporters: a key piece in the glutamate puzzle of major depressive disorder. (2013) (50)
Integrating and mining the chromatin landscape of cell-type specificity using self-organizing maps (2013) (49)
A toolbox of immunoprecipitation-grade monoclonal antibodies to human transcription factors (2018) (49)
DNA methylation profiling reveals novel diagnostic biomarkers in renal cell carcinoma (2014) (49)
Longitudinal Analysis of T and B Cell Receptor Repertoire Transcripts Reveal Dynamic Immune Response in COVID-19 Patients (2020) (49)
A genome-wide association study identifies a novel locus at 6q22.1 associated with ulcerative colitis. (2014) (48)
A transcript map of the Down syndrome critical region on chromosome 21. (1994) (48)
Identification and characterization of the human homologue of SH3BP2, an SH3 binding domain protein within a common region of deletion at 4p16.3 involved in bladder cancer. (1997) (48)
TBCRC 019: A Phase II Trial of Nanoparticle Albumin-Bound Paclitaxel with or without the Anti-Death Receptor 5 Monoclonal Antibody Tigatuzumab in Patients with Triple-Negative Breast Cancer (2015) (48)
Identification of risk loci for Crohn's disease phenotypes using a genome-wide association study. (2015) (48)
Association of polymorphisms in platelet and hemostasis system genes with acute myocardial infarction. (2007) (47)
Batf Pioneers the Reorganization of Chromatin in Developing Effector T Cells via Ets1-Dependent Recruitment of Ctcf (2019) (47)
Predicting future from past: The genomic basis of recurrent and rapid stickleback evolution (2020) (45)
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease. (2008) (44)
Progressive myoclonus epilepsy EPM1 locus maps to a 175-kb interval in distal 21q. (1996) (44)
Isolation and characterization of the mouse cystatin B gene. (1996) (43)
Mitochondrial related gene expression changes are sensitive to agonal-pH state (2006) (42)
Fibroblast growth factor 9 is a novel modulator of negative affect (2015) (42)
Genome-wide DNA methylation measurements in prostate tissues uncovers novel prostate cancer diagnostic biomarkers and transcription factor binding patterns (2017) (42)
Isolation and field-inversion gel electrophoresis analysis of DNA markers located close to the Huntington disease gene. (1989) (41)
Integrated analysis of experimental data sets reveals many novel promoters in 1% of the human genome. (2007) (41)
Non-Coding and Loss-of-Function Coding Variants in TET2 are Associated with Multiple Neurodegenerative Diseases (2019) (40)
Mitochondrial Mutations in Subjects with Psychiatric Disorders (2015) (39)
Failure to replicate an association of SNPs in the oxidized LDL receptor gene (OLR1) with CAD (2008) (38)
Eliciting Preferences on Secondary Findings: The Preferences Instrument for Genomic Secondary Results (PIGSR) (2016) (38)
Genetic Variation in the Proximal Promoter of ABC and SLC Superfamilies: Liver and Kidney Specific Expression and Promoter Activity Predict Variation (2009) (37)
Genetic variation at the glycosaminoglycan metabolism pathway contributes to the risk of psoriatic arthritis but not psoriasis (2018) (37)
Altered choroid plexus gene expression in major depressive disorder (2014) (37)
Gastrogenomic delights: A movable feast (1997) (36)
Allele-specific distribution of RNA polymerase II on female X chromosomes. (2011) (36)
SON and Its Alternatively Spliced Isoforms Control MLL Complex-Mediated H3K4me3 and Transcription of Leukemia-Associated Genes. (2016) (35)
Oligomeric structure of a simian virus 40 T antigen in free form and bound to DNA. (1981) (35)
Distinct gene regulatory programs define the inhibitory effects of liver X receptors and PPARG on cancer cell proliferation (2016) (35)
Mutational analysis of simian virus 40 large T antigen DNA binding sites. (1984) (35)
Mitochondrial Complex I Deficiency in Schizophrenia and Bipolar Disorder and Medication Influence (2017) (35)
Physical mapping of yeast artificial chromosomes containing sequences from the human beta-globin gene region. (1991) (34)
A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci. (1993) (34)
Fully automated high-throughput chromatin immunoprecipitation for ChIP-seq: Identifying ChIP-quality p300 monoclonal antibodies (2014) (34)
Evidence for Transcriptional Factor Dysregulation in the Dorsal Raphe Nucleus of Patients with Major Depressive Disorder (2012) (33)
Evidence of allelic imbalance in the schizophrenia susceptibility gene ZNF804A in human dorsolateral prefrontal cortex (2014) (33)
A simple and efficient method for attachment of a 40-base pair, GC-rich sequence to PCR-amplified DNA. (1992) (32)
Characterization of X-Linked SNP genotypic variation in globally distributed human populations (2010) (32)
Assessing mapping progress in the Human Genome Project. (1994) (32)
The end in sight for Huntington disease? (1991) (32)
The Multi-Partner Consortium to Expand Dementia Research in Latin America (ReDLat): Driving Multicentric Research and Implementation Science (2021) (32)
Systems Genomics Identifies a Key Role for Hypocretin/Orexin Receptor-2 in Human Heart Failure. (2015) (31)
Sensitization of stefin B‐deficient thymocytes towards staurosporin‐induced apoptosis is independent of cysteine cathepsins (2005) (31)
Neonatal Maternal Deprivation Response and Developmental Changes in Gene Expression Revealed by Hypothalamic Gene Expression Profiling in Mice (2010) (30)
REPLICATION IN MONKEY CELLS OF PLASMID DNA CONTAINING THE MINIMAL SV40 ORIGIN (1981) (30)
Promoter-distal RNA polymerase II binding discriminates active from inactive CCAAT/ enhancer-binding protein beta binding sites (2015) (30)
Identification of promoter regions in the human genome by using a retroviral plasmid library-based functional reporter gene assay. (2003) (29)
Pituitary cell line GH3 expresses two somatostatin receptor subtypes that inhibit adenylyl cyclase: functional expression of rat somatostatin receptor subtypes 1 and 2 in human embryonic kidney 293 cells. (1994) (29)
Genome-Wide Pathway Analysis Identifies Genetic Pathways Associated with Psoriasis. (2016) (28)
Mapping genome-wide transcription factor binding sites in frozen tissues (2013) (28)
In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes. (2014) (27)
Lack of association to a NRG1 missense polymorphism in schizophrenia or bipolar disorder in a Costa Rican population (2011) (25)
Tumour-specific amplitude-modulated radiofrequency electromagnetic fields induce differentiation of hepatocellular carcinoma via targeting Cav3.2 T-type voltage-gated calcium channels and Ca2+ influx (2019) (25)
Systematic reanalysis of genomic data improves quality of variant interpretation (2018) (25)
Multiple transcription start sites for FOXP2 with varying cellular specificities. (2008) (24)
Sample matching by inferred agonal stress in gene expression analyses of the brain (2007) (24)
Stage-specific epigenetic regulation of CD4 expression by coordinated enhancer elements during T cell development (2018) (24)
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes". (1995) (24)
A high resolution physical map of 2.5 Mbp of the Down syndrome region on chromosome 21. (1994) (24)
Genome sequencing for early-onset or atypical dementia: high diagnostic yield and frequent observation of multiple contributory alleles (2019) (23)
A radiation hybrid map of the region on human chromosome 22 containing the neurofibromatosis type 2 locus. (1992) (23)
Rare variants in the neuronal ceroid lipofuscinosis gene MFSD8 are candidate risk factors for frontotemporal dementia (2018) (23)
Exon expression in lymphoblastoid cell lines from subjects with schizophrenia before and after glucose deprivation (2009) (23)
aRNApipe: a balanced, efficient and distributed pipeline for processing RNA-seq data in high-performance computing environments (2017) (22)
Statistical refinement of primer design parameters (1999) (22)
A deletion at ADAMTS9-MAGI1 locus is associated with psoriatic arthritis risk (2015) (22)
Fluorescence in situ hybridization deletion mapping at 4p16.3 in bladder cancer cell lines refines the localisation of the critical interval to 30 kb (1996) (22)
Genetic origin of a large family with a novel PSEN1 mutation (Ile416Thr) (2019) (21)
Discovery and Validation of Circulating Biomarkers of Colorectal Adenoma by High-Depth Small RNA Sequencing (2018) (21)
RNA sequencing-based cell proliferation analysis across 19 cancers identifies a subset of proliferation-informative cancers with a common survival signature (2016) (21)
A cloned DNA segment from the telomeric region of human chromosome 4p is not detectably rearranged in Huntington disease patients. (1990) (20)
Construction of cosmid contigs and high-resolution restriction mapping of the Huntington disease region of human chromosome 4. (1993) (20)
Research resource: enhanced genome-wide occupancy of estrogen receptor α by the cochaperone p23 in breast cancer cells. (2012) (20)
The fibroblast growth factor family and mood disorders. (2008) (19)
Genomic sequencing identifies secondary findings in a cohort of parent study participants (2017) (19)
Kinase Gene Expression Profiling of Metastatic Clear Cell Renal Cell Carcinoma Tissue Identifies Potential New Therapeutic Targets (2016) (19)
Dynamics of microRNA expression during mouse prenatal development (2018) (19)
Blocking of targeted microRNAs from next-generation sequencing libraries (2015) (19)
powerTCR: A model-based approach to comparative analysis of the clone size distribution of the T cell receptor repertoire (2018) (19)
De novo mutations in the GTP/GDP-binding region of RALA, a RAS-like small GTPase, cause intellectual disability and developmental delay (2018) (18)
Application of microarray technology in primate behavioral neuroscience research. (2006) (18)
26 – IDENTIFYING DNA POLYMORPHISMS BY DENATURING GRADIENT GEL ELECTROPHORESIS (1990) (18)
Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011)) (2016) (17)
Identification of polymorphisms by genomic denaturing gradient gel electrophoresis: application to the proximal region of human chromosome 21. (1991) (17)
Cloning of the Huntington disease region in yeast artificial chromosomes. (1992) (17)
Genome-wide pathway analysis identifies VEGF pathway association with oral ulceration in systemic lupus erythematosus (2017) (16)
Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (16)
Identification and characterization of a beta-globin promoter-binding factor from murine erythroleukemia cells (1993) (15)
Does simian virus 40 T antigen unwind DNA? (1981) (15)
Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease (2014) (15)
Splice-Break: exploiting an RNA-seq splice junction algorithm to discover mitochondrial DNA deletion breakpoints and analyses of psychiatric disorders (2019) (15)
Quantitative Trait Locus and Brain Expression of HLA-DPA1 Offers Evidence of Shared Immune Alterations in Psychiatric Disorders (2016) (15)
Identification of a Functional In Vivo p53 Response Element in the Coding Sequence of the Xeroderma Pigmentosum Group C Gene. (2012) (15)
- 1-Sequential Use of Transcriptional Profiling , Expression Quantitative Trait Mapping and Gene Association Implicates MMP 20 in Human Kidney Aging Running Head : eQTLs and Kidney Aging (2009) (14)
A new approach for rare variation collapsing on functional protein domains implicates specific genic regions in ALS (2019) (14)
CRISPR/Cas9-targeted removal of unwanted sequences from small-RNA sequencing libraries (2018) (13)
A genome-wide association study identifies SLC8A3 as a susceptibility locus for ACPA-positive rheumatoid arthritis. (2016) (13)
Decoding transcriptional enhancers: Evolving from annotation to functional interpretation. (2016) (13)
Connective Tissue Growth Factor Is a Novel Prodepressant (2018) (12)
Transmembrane Protein Aptamer Induces Cooperative Signaling by the EPO Receptor and the Cytokine Receptor β-Common Subunit (2019) (12)
HDAC2 Regulates Site-Specific Acetylation of MDM2 and Its Ubiquitination Signaling in Tumor Suppression (2019) (12)
Quantitative validation of immunofluorescence and lectin staining using reduced CLARITY acrylamide formulations (2018) (11)
Aberrant regulation of a poison exon caused by a non-coding variant in a mouse model of Scn1a-associated epileptic encephalopathy (2021) (11)
Retraction Note: DDX5 and its associated lncRNA Rmrp modulate TH17 cell effector functions (2018) (11)
Three dimensional modeling of biologically relevant fluid shear stress in human renal tubule cells mimics in vivo transcriptional profiles (2021) (11)
A map to the future (1996) (10)
Dissecting the regulatory activity and sequence content of loci with exceptional numbers of transcription factor associations (2019) (9)
Methylation at the Huntington disease-linked D4S95 locus. (1989) (9)
Coding SNPs included in exon arrays for the study of psychiatric disorders (2008) (9)
S14-03 From trait to base pairs: Parallel evolution of pelvic reduction in three-spined sticklebacks occurs by repeated deletion of a tissue-specific pelvic enhancer at Pitx1 (2009) (9)
Identification of IRX1 as a Risk Locus for Rheumatoid Factor Positivity in Rheumatoid Arthritis in a Genome‐Wide Association Study (2016) (8)
Localization of the alpha 2-macroglobulin receptor-associated protein 1 gene (LRPAP1) and other gene fragments to human chromosome 4p16.3 by direct cDNA selection. (1994) (8)
STAT3 and GR Cooperate to Drive Gene Expression and Growth of Basal-Like Triple-Negative Breast Cancer (2020) (8)
A genome-wide interactome of DNA-associated proteins in the human liver (2017) (8)
Assembly of a young vertebrate Y chromosome reveals convergent signatures of sex chromosome evolution (2019) (8)
Education and personalized genomics: deciphering the public's genetic health report. (2009) (7)
Pooled CRISPR screening in pancreatic cancer cells implicates co-repressor complexes as a cause of multiple drug resistance via regulation of epithelial-to-mesenchymal transition (2019) (7)
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. (2016) (7)
Targeting of the CD80/86 proinflammatory axis as a therapeutic strategy to prevent severe COVID-19 (2021) (7)
P Lack of Association Between the Trp 719 Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies (2010) (7)
Electrophysiological evaluation of extracellular spermine and alkaline pH on synaptic human GABAA receptors (2019) (6)
Genetic linkage analysis of bipolar affective disorder in an Old Order Amish pedigree (1992) (6)
Stress amplifies sex differences in primate prefrontal profiles of gene expression (2017) (6)
Inference of Cell Type Composition from Human Brain Transcriptomic Datasets Illuminates the Effects of Age, Manner of Death, Dissection, and Psychiatric Diagnosis (2016) (6)
Multi-tissue integrative analysis of personal epigenomes (2021) (6)
Genetic and biochemical analysis of the mouse beta-major globin promoter. (1989) (6)
Quality assessment of the human genome sequence Schmutz, Jeremy Wheeler, Jane Grimwood, Mark Dickson, Joan Yang, Chenier Caoile, Eva Bajorek, Stacey Black, Yee Man Chan, (2004) (5)
TBCRC 002: a phase II, randomized, open-label trial of preoperative letrozole with or without bevacizumab in postmenopausal women with newly diagnosed stage 2/3 hormone receptor-positive and HER2-negative breast cancer (2020) (5)
A study of elective genome sequencing and pharmacogenetic testing in an unselected population (2021) (5)
Exome sequencing identifies rare damaging variants in the ATP8B4 and ABCA1 genes as novel risk factors for Alzheimer’s Disease (2020) (5)
The Therapeutic Odyssey: Positioning Genomic Sequencing in the Search for a Child’s Best Possible Life (2021) (5)
Theria-specific homeodomain and cis-regulatory element evolution of the Dlx3-4 bigene cluster in 12 different mammalian species. (2012) (5)
Quantitative Trait Locus and Brain Expression of HLA-DPA1 Offers Evidence of Shared Immune Alterations in Psychiatric Disorders. (2016) (4)
Corrigendum: DDX5 and its associated lncRNA Rmrp modulate TH17 cell effector functions (2016) (4)
One step forward toward identification of the genetic signature of glioblastomas. (2009) (4)
Blocking of the CD80/86 axis as a therapeutic approach to prevent progression to more severe forms of COVID-19. (2020) (3)
Variable telomere length across post-mortem human brain regions and specific reduction in the hippocampus of major depressive disorder. (2016) (3)
PEA15 loss of function and defective cerebral development in the domestic cat (2020) (3)
Regional Collapsing of Rare Variation Implicates Specific Genic Regions in ALS (2018) (3)
Assessing the quality of finished genomic sequence. (2003) (3)
MHC II antigen presentation pathway expression in triple-negative breast cancer. (2015) (3)
Identification of positive modulators of TRPM5 channel from a high-throughput screen using a fluorescent membrane potential assay. (2021) (3)
aRNApipe: A balanced, efficient and distributed pipeline for processing RNA-seq data in high performance computing environments (2016) (3)
A White Paper Advocating Complete Sequencing of the Genome of the Common Chimpanzee , Pan Troglodytes (2002) (2)
bind thousands of sites in a cell type-specific manner Genistein and bisphenol A exposure cause estrogen receptor 1 to Material Supplemental (2012) (2)
Sequence finishing. (2004) (2)
Corrigendum: Longitudinal Analysis of T and B Cell Receptor Repertoire Transcripts Reveal Dynamic Immune Response in COVID-19 Patients (2020) (2)
Epitope Tagging ChIP-Seq of DNA Binding Proteins Using CETCh-Seq. (2020) (2)
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype. (2022) (2)
Tumour-speci fi c amplitude-modulated radiofrequency electromagnetic fi elds induce differentiation of hepatocellular carcinoma via targeting Cav 3 . 2 T-type voltage-gated calcium channels and Ca 2 + in fl ux (2019) (2)
expression and RNA splicing From single-cell to cell-pool transcriptomes : Stochasticity in gene Material Supplemental (2014) (2)
specificity using self-organizing maps Integrating and mining the chromatin landscape of cell-type Material Supplemental (2013) (2)
Systematic evaluation of variability in ChIP-chip experiments using data (2008) (2)
Mapping genome-wide transcription factor binding sites in frozen tissues (2013) (2)
Report and abstracts of the Third International Workshop on Human Chromosome 4 Mapping. Palo Alto, California, July 10-11, 1993. (1994) (2)
Genome sequencing for early-onset dementia: high diagnostic yield and frequent observation of multiple contributory alleles (2019) (2)
Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes (2022) (2)
Mo-P6:419 A common novel SNP in the peroxisome proliferative activated receptor gamma gene is associated with early-onset coronary artery disease (2006) (1)
Taql RFLP at D21S137 (1991) (1)
Functional analysis of transcription factor binding sites in human promoters (2012) (1)
Supplementary material for : The role of geography in human adaptation (2009) (1)
modENCODE consortia ChIP-seq guidelines and practices of the ENCODE and Material Supplemental (2012) (1)
Overrepresentation of Neuronal Development Pathways in Heart Failure Patients Who Dramatically Responded to Pharmaceutical Therapy (2008) (1)
Differential DNA methylation with age displays both common and dynamic features across human tissues that are influenced by CpG landscape (2013) (1)
Genome-wide strand asymmetry in massively parallel reporter activity favors genic strands (2020) (1)
variation in globally distributed human populations (2010) (1)
Transposase mediated construction of RNA-seq libraries (Genome Research (2012) 22, (134-141)) (2012) (1)
MAPPING ENHANCER REGIONS FOR GENES ASSOCIATED WITH NEURODEGENERATIVE DISEASES (2018) (1)
Assembly of DNA sequencing data. (2004) (1)
Mutations in EBF3 disturb transcriptional profiles and underlie a novel syndrome of intellectual disability, ataxia and facial dysmorphism (2016) (1)
Identification and analysis of functional elements in 1 % of the human genome by the ENCODE pilot project The ENCODE Project Consortium * (2007) (1)
Methods for “ The effects of genome sequence on differential allelic transcription factor occupancy and gene expression ” (2012) (1)
Report ping Array Reveals Patterns of Global and Repeated Species-Pair Divergence in Sticklebacks (2012) (1)
HOX clusters of Latimeria : Complete characterization provides further evidence for slow evolution of the coelacanth genome (2009) (1)
human populations Signals of recent positive selection in a worldwide sample of Material Supplemental (2009) (1)
Mitochondria Genetics of Schizophrenia and Bipolar Disorder (2021) (1)
Aberrant regulation of a poison exon caused by a non-coding variant in Scn1a-associated epileptic encephalopathy (2020) (1)
REANALYSIS OF WHOLE EXOME AND GENOME DATA LEADS TO NEW DIAGNOSES IN CHILDREN WITH INTELLECTUAL DISABILITY AND DEVELOPMENTAL DELAY (2017) (0)
Abstract 5135: Genome-wide CRISPR-based screening reveals ABCG2 as a novel drug resistance gene in pancreatic cancer (2019) (0)
Dissecting the regulatory activity and key sequence elements of loci with exceptional numbers of transcription factor associations (2019) (0)
Human Genome Draft Sequence A High-Resolution Radiation Hybrid Map of the (2010) (0)
Comprehensive and semi-quantitative TCR repertoire analysis with a novel multiplex PCR method and 454 sequencing (85.3) (2010) (0)
Identification of cis‐regulatory elements associated with MAPT expression in human induced pluripotent stem cell derived neural cells. (2022) (0)
mtDNA copy number, mtDNA total somatic deletions, Complex I activity, synapse number and synaptic mitochondria number are altered in schizophrenia and bipolar disorder (2022) (0)
Erratum: Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling (Genome Research (2006) 16, (796-803)) (2006) (0)
Genome Improvement at JGI-HAGSC (2012) (0)
R10K update: NGS of immune repertoire for biomarker discoveries (P3241) (2013) (0)
Protein-6 and Coronary Artery Disease in 19 Case-Control Studies Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like (2012) (0)
Lack of Association Between the Trp 719 Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control (2017) (0)
Applying Genomic and Genetic Tools to Understand and Mitigate Damage from Exposure to Toxins (2011) (0)
Protocadherin Gene Clusters Comparative DNA Sequence Analysis of Mouse and Human (2001) (0)
Sequencing and analysis of 10967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis (2005) (0)
High-throughput identification of genes involved in single and multi-drug resistance in pancreatic cancer with pooled CRISPR screening (2019) (0)
Pooled CRISPR screening in pancreatic cancer cells implicates co-repressor complexes as a cause of multiple drug resistance via regulation of epithelial-to-mesenchymal transition (2021) (0)
Linkage analysis for autism and chromosomal markers located in the PWS/Angelman syndrome region (1997) (0)
Processing during T Cell Development Dynamic MicroRNA Gene Transcription and (2012) (0)
CORRIGENDUM (2020) (0)
YAC STS-content maps of human chromosome 4 (1994) (0)
P665 A genome-wide association study identifies DSE-FAM26F as a risk locus for ulcerative colitis (2014) (0)
Global Genomic Analysis of Prostate, Breast and Pancreatic Cancer (2012) (0)
Diurnal Gene Expression in Retinal Pigment Epithelium (2005) (0)
Correction: Investigating rare pathogenic/likely pathogenic exonic variation in bipolar disorder (2021) (0)
A toolbox of immunoprecipitation-grade monoclonal antibodies against human transcription factors (2017) (0)
Bridging the gaps (1992) (0)
Abstract 16018: Genetic variation near HCRTR2 associates with dramatic improvement of heart function in patients with heart failure (2013) (0)
LOSS-OF-FUNCTION CODING AND NON-CODING VARIANTS IN TET2 ARE ASSOCIATED WITH NEURODEGENERATIVE DISEASES (2019) (0)
Interval in Distal 21q (1996) (0)
Quality assessment of finished BAC sequences. (2004) (0)
Erratum: Mitochondrial involvement in psychiatric disorders (Annals of Medicine (2008) 40 (281-295)) (2011) (0)
Dorsal lateral prefrontal cortex and mediodorsal thalamus in schizophrenic brains show concordant and discordant alterations in gene expression (2003) (0)
Human Transcription Factors Running title : Analysis of Sites of 119 TFs in the Human Genome (2012) (0)
Response to Holstege et al. (2020) (0)
UTILITY OF GENOMIC SEQUENCING IN CASES OF EARLY-ONSET AND FAMILIAL DEMENTIA (2019) (0)
Transposase mediated construction of RNA-seq libraries Material Supplemental (2011) (0)
R10K: an international collaborative project for biomarker discovery (58.7) (2012) (0)
David R. Cox 1946–2013 (2013) (0)
Abstract P1-15-02: Long term follow-up of the neo-adjuvant pilot trial evaluating activity of letrozole in combination with bevacizumab in post-menopausal women with newly diagnosed estrogen and/or progesterone receptor positive primary breast cancer (2013) (0)
Supplemental Information Distinct Properties of Cell-Type-Specific and Shared Transcription Factor Binding Sites (2013) (0)
MAPT expression is mediated by long-range interactions with cis-regulatory elements (2023) (0)
Evidence that a proposed repeated segment of glutamine residues is expressed in the Huntington disease protein (1994) (0)
STAT3 and GR cooperate to drive basal-like triple negative breast cancer gene expression and proliferation (2019) (0)
network: From single conserved sites to genome-wide repertoire Comparative genomics modeling of the NRSF/REST repressor (2007) (0)
Modification ofthemelting properties ofduplex DNAbyattachment ofaGC-rich DNA sequence asdetermined bydenaturing gradient gelelectrophoresis (1985) (0)
Genome-Wide Patterns of Variation Worldwide Human Relationships Inferred from (2008) (0)
FGF2 related methods to diagnose and treat depression (2006) (0)
Signature of Glioblastomas One Step Forward Toward Identification of the Genetic (2012) (0)
Genome-wide DNA methylation measurements in prostate tissues uncovers novel prostate cancer diagnostic biomarkers and transcription factor binding patterns (2017) (0)
Tu1943a A Genome-Wide Association Study Identifies DSE-FAM26F As a Risk Locus for Ulcerative Colitis (2014) (0)
Stage-specific epigenetic regulation of CD4 expression by coordinated enhancer elements during T cell development (2018) (0)
Next-generation sequencing technologies are beginning to facilitate genome sequencing. But in addition, new applications and new assay concepts have emerged that are vastly increasing our ability to understand genome function. (2008) (0)
Acknowledgments Constant Ratio Approximations of the Weighted Feedback Vertex Set Problem for Undirected Graphs, Proc. Sixth Annual Symposium on Algorithms and Computation (isaac 95) . 13 Data Set Old N New N Old Time New Time Speedup (1997) (0)
genome Direct isolation and identification of promoters in the human data (2005) (0)
Occupancy patterns of 208 DNA-associated proteins in a single human cell type (2018) (0)
FGF-2 related methods for the diagnosis and treatment of depression (2006) (0)
Clonal Integration of a Polyomavirus in Human Merkel Cell Carcinoma (2008) (0)
Abstract LB-412: TargetRich cancer gene panels: targeted next generation sequencing in cancer samples (2012) (0)
GENETIC DETERMINANTS OF DRAMATIC IMPROVEMENT IN LEFT VENTRICULAR FUNCTION IN PATIENTS WITH HEART FAILURE (2011) (0)
Abstracts of papers presented at the 1993 Meeting on Genome Mapping and Sequencing, May 12-May 16, 1993 (1990) (0)
Oligonucleotide Microarrays Rapid Mapping of Zebrafish Mutations With SNPs and Material (2002) (0)
Abstract 1319: Epigenome-wide association study reveals differential DNA methylation consistent with progression of multiple myeloma (2017) (0)
Post-mortem molecular profiling of three psychiatric disorders (2017) (0)
P3-142 STRATIFICATION OFALZHEIMER’S PATIENTS USING POSTMORTEM BRAIN CO-EXPRESSION DATA REVEALS NOVEL GENETIC MODIFIERS MEDIATING INFLAMMATORYAGING (2019) (0)
Amplitude-modulated radiofrequency electromagnetic fields target hepatocellular carcinoma stem cells through activation of Cav 3.2 T-type calcium channels. (2018) (0)
Abstract P1-05-25: Patterns of translational dysregulation in models of estrogen receptor(+) and (-) breast cancer (2017) (0)
Identification of cis‐regulatory elements associated with MAPT expression in human induced pluripotent stem cell derived neural cells (2021) (0)

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