Michael P. Snyder

Michael P. Snyder's AcademicInfluence.com Rankings

Michael P. Snyder

Biology

#2303

World Rank

#3674

Historical Rank

#1033

USA Rank

Genetics

#206

World Rank

#250

Historical Rank

#107

USA Rank

biology Degrees

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Biology

Why Is Michael P. Snyder Influential?

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According to Wikipedia, Michael P. Snyder is an American genomicist and the Stanford B. Ascherman Professor, and since 2009, chair of genetics and director of genomics and personalized medicine at Stanford University. He is the former director of the Yale Center for Genomics and Proteomics. He was elected to the American Academy of Arts and Sciences in 2015. During his tenure as chair of the department at Stanford, U.S. News & World Report has ranked Stanford University first or tied for first in genetics, genomics and bioinformatics under his leadership.

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Michael P. Snyder'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

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) (5196)
Functional characterization of the S. cerevisiae genome by gene deletion and parallel analysis. (1999) (4002)
Genetic effects on gene expression across human tissues (2017) (2841)
The Transcriptional Landscape of the Yeast Genome Defined by RNA Sequencing (2008) (2513)
The ENCODE (ENCyclopedia Of DNA Elements) Project (2004) (2194)
An integrated encyclopedia of DNA elements in the human genome (2012) (2080)
ChIP-seq guidelines and practices of the ENCODE and modENCODE consortia (2012) (1701)
A User's Guide to the Encyclopedia of DNA Elements (ENCODE) (2011) (1467)
Single-cell chromatin accessibility reveals principles of regulatory variation (2015) (1435)
Genome-wide profiles of STAT1 DNA association using chromatin immunoprecipitation and massively parallel sequencing (2007) (1432)
High-Quality Binary Protein Interaction Map of the Yeast Interactome Network (2008) (1419)
Architecture of the human regulatory network derived from ENCODE data (2012) (1393)
A Bayesian Networks Approach for Predicting Protein-Protein Interactions from Genomic Data (2003) (1355)
A comparative encyclopedia of DNA elements in the mouse genome (2014) (1337)
CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing. (2011) (1294)
Paired-End Mapping Reveals Extensive Structural Variation in the Human Genome (2007) (1204)
Genomic binding sites of the yeast cell-cycle transcription factors SBF and MBF (2001) (1191)
Global Analysis of Protein Activities Using Proteome Chips (2001) (1185)
Extensive Promoter-Centered Chromatin Interactions Provide a Topological Basis for Transcription Regulation (2012) (1142)
Personal Omics Profiling Reveals Dynamic Molecular and Medical Phenotypes (2012) (1128)
Global Identification of Human Transcribed Sequences with Genome Tiling Arrays (2004) (1102)
Mapping copy number variation by population scale genome sequencing (2010) (1057)
Integrative Analysis of the Caenorhabditis elegans Genome by the modENCODE Project (2010) (931)
High-throughput sequencing technologies. (2015) (887)
Sequence features and chromatin structure around the genomic regions bound by 119 human transcription factors (2012) (817)
Lineage-specific and single cell chromatin accessibility charts human hematopoiesis and leukemia evolution (2016) (797)
Expanded encyclopaedias of DNA elements in the human and mouse genomes (2020) (765)
What is a gene, post-ENCODE? History and updated definition. (2007) (699)
Integrated Proteogenomic Characterization of Human High-Grade Serous Ovarian Cancer (2016) (672)
Predicting non-small cell lung cancer prognosis by fully automated microscopic pathology image features (2016) (653)
Defining functional DNA elements in the human genome (2014) (647)
Linking disease associations with regulatory information in the human genome (2012) (645)
Patient-Specific Induced Pluripotent Stem Cells as a Model for Familial Dilated Cardiomyopathy (2012) (612)
PeakSeq enables systematic scoring of ChIP-seq experiments relative to controls (2009) (611)
Variation in Transcription Factor Binding Among Humans (2010) (595)
Getting connected: analysis and principles of biological networks. (2007) (560)
HTRA1 promoter polymorphism in wet age-related macular degeneration. (2007) (539)
Large-scale analysis of gene expression, protein localization, and gene disruption in Saccharomyces cerevisiae. (1994) (518)
A single-molecule long-read survey of the human transcriptome (2013) (516)
Performance comparison of exome DNA sequencing technologies (2011) (503)
Biochemical and genetic analysis of the yeast proteome with a movable ORF collection. (2005) (491)
The NASA Twins Study: A multidimensional analysis of a year-long human spaceflight (2019) (491)
New insights into Acinetobacter baumannii pathogenesis revealed by high-density pyrosequencing and transposon mutagenesis. (2007) (484)
Landscape and variation of RNA secondary structure across the human transcriptome (2014) (476)
Molecular basis of cell integrity and morphogenesis in Saccharomyces cerevisiae. (1995) (463)
MAPK target networks in Arabidopsis thaliana revealed using functional protein microarrays. (2009) (461)
How many human proteoforms are there? (2018) (440)
An encyclopedia of mouse DNA elements (Mouse ENCODE) (2012) (438)
Deep sequencing of subcellular RNA fractions shows splicing to be predominantly co-transcriptional in the human genome but inefficient for lncRNAs (2012) (428)
The Integrative Human Microbiome Project (2019) (426)
A proposal for validation of antibodies (2016) (403)
Rapid analysis of the DNA-binding specificities of transcription factors with DNA microarrays (2004) (398)
C. elegans ORFeome version 1.1: experimental verification of the genome annotation and resource for proteome-scale protein expression (2003) (392)
Intrinsic histone-DNA interactions are not the major determinant of nucleosome positions in vivo (2009) (385)
Divergence of Transcription Factor Binding Sites Across Related Yeast Species (2007) (382)
HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration (2006) (377)
Deciphering Protein Kinase Specificity Through Large-Scale Analysis of Yeast Phosphorylation Site Motifs (2010) (368)
Proteogenomic Analysis of Human Colon Cancer Reveals New Therapeutic Opportunities (2019) (366)
Clinical interpretation and implications of whole-genome sequencing. (2014) (365)
Differential binding of calmodulin-related proteins to their targets revealed through high-density Arabidopsis protein microarrays (2007) (358)
The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies (2009) (355)
Extensive Variation in Chromatin States Across Humans (2013) (346)
Nim1-related kinases coordinate cell cycle progression with the organization of the peripheral cytoskeleton in yeast. (1999) (337)
The Human Proteome Project: Current State and Future Direction (2011) (328)
Compartmentalization of the cell cortex by septins is required for maintenance of cell polarity in yeast. (2000) (326)
A myelopoiesis-associated regulatory intergenic noncoding RNA transcript within the human HOXA cluster. (2009) (326)
Protein arrays and microarrays. (2001) (324)
Landscape of next-generation sequencing technologies. (2011) (319)
Variation and Genetic Control of Protein Abundance in Humans (2013) (317)
AlleleSeq: analysis of allele-specific expression and binding in a network framework (2011) (311)
RNA‐Seq: A Method for Comprehensive Transcriptome Analysis (2010) (311)
Performance comparison of whole-genome sequencing platforms (2011) (310)
The transcriptional activity of human Chromosome 22. (2003) (309)
Distribution of NF-κB-binding sites across human chromosome 22 (2003) (307)
Digital Health: Tracking Physiomes and Activity Using Wearable Biosensors Reveals Useful Health-Related Information (2017) (303)
Comparison of the transcriptional landscapes between human and mouse tissues (2014) (299)
Complex transcriptional circuitry at the G1/S transition in Saccharomyces cerevisiae. (2002) (295)
Non-equivalence of Wnt and R-spondin ligands during Lgr5+ intestinal stem cell self-renewal (2017) (294)
A Comprehensive Map of Mobile Element Insertion Polymorphisms in Humans (2011) (293)
A genomic study of the bipolar bud site selection pattern in Saccharomyces cerevisiae. (2001) (288)
PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data (2009) (286)
Longitudinal multi-omics of host–microbe dynamics in prediabetes (2019) (284)
Cell polarity and morphogenesis in budding yeast. (1998) (283)
Genetic Control of Chromatin States in Humans Involves Local and Distal Chromosomal Interactions (2015) (282)
The Chromosome-Centric Human Proteome Project for cataloging proteins encoded in the genome (2012) (281)
An Integrated Understanding of the Rapid Metabolic Benefits of a Carbohydrate-Restricted Diet on Hepatic Steatosis in Humans. (2018) (276)
Wearables and the medical revolution. (2018) (273)
H3K4me3 Breadth Is Linked to Cell Identity and Transcriptional Consistency (2015) (273)
High-throughput sequencing for biology and medicine (2013) (268)
The human body at cellular resolution: the NIH Human Biomolecular Atlas Program (2019) (265)
Identification of differentially expressed proteins in ovarian cancer using high-density protein microarrays (2007) (258)
A synthetic lethal screen identifies SLK1, a novel protein kinase homolog implicated in yeast cell morphogenesis and cell growth (1992) (258)
mTOR-mediated dedifferentiation of the retinal pigment epithelium initiates photoreceptor degeneration in mice. (2011) (254)
A Genome-Scale Resource for In Vivo Tag-Based Protein Function Exploration in C. elegans (2012) (253)
Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors (2012) (249)
DNA gyrase and topoisomerase IV on the bacterial chromosome: quinolone-induced DNA cleavage. (1996) (249)
Promise of personalized omics to precision medicine (2013) (244)
Genome-wide map of regulatory interactions in the human genome (2014) (242)
NuMA: an unusually long coiled-coil related protein in the mammalian nucleus (1992) (238)
Finding new components of the target of rapamycin (TOR) signaling network through chemical genetics and proteome chips. (2004) (237)
Diverse transcription factor binding features revealed by genome-wide ChIP-seq in C. elegans. (2011) (236)
The Human Tumor Atlas Network: Charting Tumor Transitions across Space and Time at Single-Cell Resolution (2020) (234)
Recurrent Somatic Mutations in Regulatory Regions of Human Cancer Genomes (2015) (234)
A major epigenetic programming mechanism guided by piRNAs. (2013) (233)
Macrophage de novo NAD+ synthesis specifies immune function in aging and inflammation (2018) (229)
Genomic analysis of mycosis fungoides and Sézary syndrome identifies recurrent alterations in TNFR2 (2015) (229)
A Longitudinal Big Data Approach for Precision Health (2019) (228)
Genome-scale measurement of off-target activity using Cas9 toxicity in high-throughput screens (2017) (226)
Pseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolution. (2007) (225)
Lineage-specific dynamic and pre-established enhancer–promoter contacts cooperate in terminal differentiation (2017) (225)
Rnnotator: an automated de novo transcriptome assembly pipeline from stranded RNA-Seq reads (2010) (224)
Targeting of Chitin Synthase 3 to Polarized Growth Sites in Yeast Requires Chs5p and Myo2p (1997) (222)
Sequencing Y Chromosomes Resolves Discrepancy in Time to Common Ancestor of Males Versus Females (2013) (221)
Pre-symptomatic detection of COVID-19 from smartwatch data (2020) (218)
Diverse Roles and Interactions of the SWI/SNF Chromatin Remodeling Complex Revealed Using Global Approaches (2011) (217)
Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis (2015) (216)
A question of size: the eukaryotic proteome and the problems in defining it. (2002) (215)
Mapping accessible chromatin regions using Sono-Seq (2009) (211)
The SPA2 protein of yeast localizes to sites of cell growth (1989) (211)
Defining a personal, allele-specific, and single-molecule long-read transcriptome (2014) (211)
Comprehensive annotation of the transcriptome of the human fungal pathogen Candida albicans using RNA-seq. (2010) (210)
TOS9 Regulates White-Opaque Switching in Candidaalbicans (2006) (208)
Distance from sub-Saharan Africa predicts mutational load in diverse human genomes (2015) (208)
H3K4me3 Breadth Is Linked to Cell Identity and Transcriptional Consistency (2014) (204)
Mapping of transcription factor binding regions in mammalian cells by ChIP: comparison of array- and sequencing-based technologies. (2007) (204)
DNA gyrase on the bacterial chromosome: DNA cleavage induced by oxolinic acid. (1979) (202)
Genome-Wide Occupancy of SREBP1 and Its Partners NFY and SP1 Reveals Novel Functional Roles and Combinatorial Regulation of Distinct Classes of Genes (2008) (201)
Structured RNAs in the ENCODE selected regions of the human genome. (2007) (201)
Extensive In Vivo Metabolite-Protein Interactions Revealed by Large-Scale Systematic Analyses (2010) (199)
Genomic Binding Profiles of Functionally Distinct RNA Polymerase III Transcription Complexes in Human Cells (2010) (198)
The impact of rare variation on gene expression across tissues (2016) (197)
Genome-wide relationship between histone H3 lysine 4 mono- and tri-methylation and transcription factor binding. (2008) (196)
Dynamic transcriptomes during neural differentiation of human embryonic stem cells revealed by short, long, and paired-end sequencing (2010) (196)
Static and dynamic DNA loops form AP-1 bound activation hubs during macrophage development (2017) (195)
ChIP-chip: a genomic approach for identifying transcription factor binding sites. (2002) (193)
Quantitative analysis of RNA-protein interactions on a massively parallel array for mapping biophysical and evolutionary landscapes (2014) (193)
Cuticle protein genes of Drosophila: Structure, organization and evolution of four clustered genes (1982) (192)
Close association of RNA polymerase II and many transcription factors with Pol III genes (2010) (191)
Quantifying environmental adaptation of metabolic pathways in metagenomics (2009) (191)
Age-Dependent Pancreatic Gene Regulation Reveals Mechanisms Governing Human β Cell Function. (2016) (187)
Mass spectrometry-based metabolomics: a guide for annotation, quantification and best reporting practices (2021) (186)
The Cbk1p Pathway Is Important for Polarized Cell Growth and Cell Separation in Saccharomyces cerevisiae (2001) (185)
Ubiquitous heterogeneity and asymmetry of the chromatin environment at regulatory elements (2012) (184)
Index switching causes “spreading-of-signal” among multiplexed samples in Illumina HiSeq 4000 DNA sequencing (2017) (182)
CREB Binds to Multiple Loci on Human Chromosome 22 (2004) (181)
Target hub proteins serve as master regulators of development in yeast. (2006) (177)
Comparative analysis of regulatory information and circuits across distant species (2014) (177)
Whole-genome haplotyping using long reads and statistical methods (2014) (177)
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations. (2013) (176)
Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library (2010) (176)
Distribution of NF-kappaB-binding sites across human chromosome 22. (2003) (176)
Superhelical Escherichia coli DNA: relaxation by coumermycin. (1978) (176)
Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway (2014) (175)
Gaining comprehensive biological insight into the transcriptome by performing a broad-spectrum RNA-seq analysis (2017) (175)
A multipurpose transposon system for analyzing protein production, localization, and function in Saccharomyces cerevisiae. (1997) (173)
Physiological blood–brain transport is impaired with age by a shift in transcytosis (2020) (172)
Understanding transcriptional regulation by integrative analysis of transcription factor binding data (2012) (170)
Comprehensive transcriptome analysis using synthetic long-read sequencing reveals molecular co-association of distant splicing events (2015) (170)
Components required for cytokinesis are important for bud site selection in yeast (1993) (169)
GATA-1 binding sites mapped in the β-globin locus by using mammalian chIp-chip analysis (2002) (169)
Advances in functional protein microarray technology (2005) (169)
Molecular Transducers of Physical Activity Consortium (MoTrPAC): Mapping the Dynamic Responses to Exercise (2020) (169)
Microtubule capture by the cleavage apparatus is required for proper spindle positioning in yeast. (2002) (169)
Genome-Wide Identification of Binding Sites Defines Distinct Functions for Caenorhabditis elegans PHA-4/FOXA in Development and Environmental Response (2010) (168)
Efficient yeast ChIP-Seq using multiplex short-read DNA sequencing (2009) (167)
A highly divergent gamma-tubulin gene is essential for cell growth and proper microtubule organization in Saccharomyces cerevisiae (1995) (165)
Circular DNA elements of chromosomal origin are common in healthy human somatic tissue (2018) (162)
Molecular Mechanisms of Ethanol-Induced Pathogenesis Revealed by RNA-Sequencing (2010) (159)
Optimized Analytical Procedures for the Untargeted Metabolomic Profiling of Human Urine and Plasma by Combining Hydrophilic Interaction (HILIC) and Reverse-Phase Liquid Chromatography (RPLC)–Mass Spectrometry* (2015) (158)
Molecular Choreography of Acute Exercise (2020) (158)
Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease (2017) (158)
SWI/SNF Chromatin-remodeling Factors: Multiscale Analyses and Diverse Functions* (2012) (157)
Proteogenomic Landscape of Breast Cancer Tumorigenesis and Targeted Therapy (2020) (156)
High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays. (2006) (155)
Concerted genomic targeting of H3K27 demethylase REF6 and chromatin-remodeling ATPase BRM in Arabidopsis (2016) (153)
Major molecular differences between mammalian sexes are involved in drug metabolism and renal function. (2004) (152)
The SPA2 gene of Saccharomyces cerevisiae is important for pheromone- induced morphogenesis and efficient mating (1990) (150)
Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci. (2014) (150)
Analysis of copy number variants and segmental duplications in the human genome: Evidence for a change in the process of formation in recent evolutionary history. (2008) (150)
Integrative analysis of RNA, translation, and protein levels reveals distinct regulatory variation across humans (2015) (149)
Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence (2011) (149)
Systematic evaluation of variability in ChIP-chip experiments using predefined DNA targets. (2008) (147)
Patient-Specific iPSC-Derived Endothelial Cells Uncover Pathways that Protect against Pulmonary Hypertension in BMPR2 Mutation Carriers. (2017) (146)
Integrative Personal Omics Profiles during Periods of Weight Gain and Loss. (2018) (145)
Extensive genetic variation in somatic human tissues (2012) (145)
Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias. (2013) (144)
Selection of axial growth sites in yeast requires Axl2p, a novel plasma membrane glycoprotein. (1996) (143)
Studies concerning the temporal and genetic control of cell polarity in Saccharomyces cerevisiae (1991) (143)
Transcription interferes with elements important for chromosome maintenance in Saccharomyces cerevisiae (1988) (143)
A Quantitative Proteome Map of the Human Body (2019) (143)
Defective sphingosine-1-phosphate receptor 1 (S1P1) phosphorylation exacerbates TH17-mediated autoimmune neuroinflammation (2013) (142)
Personal aging markers and ageotypes revealed by deep longitudinal profiling (2020) (140)
Nuclear pore complex clustering and nuclear accumulation of poly(A)+ RNA associated with mutation of the Saccharomyces cerevisiae RAT2/NUP120 gene (1995) (139)
Defined culture conditions of human embryonic stem cells. (2006) (139)
Heterogeneity in old fibroblasts is linked to variability in reprogramming and wound healing (2019) (138)
DNA replication-timing analysis of human chromosome 22 at high resolution and different developmental states. (2004) (138)
Personal genome sequencing: current approaches and challenges. (2010) (136)
Dynamic trans-Acting Factor Colocalization in Human Cells (2013) (133)
The Rex system of bacteriophage lambda: tolerance and altruistic cell death. (1992) (130)
Microbial Synergy via an Ethanol-Triggered Pathway (2004) (129)
Localization of the Kar3 kinesin heavy chain-related protein requires the Cik1 interacting protein (1994) (127)
iPSC-derived cardiomyocytes reveal abnormal TGFβ signaling in left ventricular non-compaction cardiomyopathy (2016) (126)
Glucotypes reveal new patterns of glucose dysregulation (2018) (125)
Defining Genes in the Genomics Era (2003) (125)
Transcriptome Profiling of Patient-Specific Human iPSC-Cardiomyocytes Predicts Individual Drug Safety and Efficacy Responses In Vitro. (2016) (124)
p53 protects against genome instability following centriole duplication failure (2015) (124)
NHP6A and NHP6B, which encode HMG1-like proteins, are candidates for downstream components of the yeast SLT2 mitogen-activated protein kinase pathway (1994) (122)
A Nonerythroid Isoform of Protein 4.1R Interacts with the Nuclear Mitotic Apparatus (NuMA) Protein (1999) (121)
Integrated Network Analysis Reveals an Association between Plasma Mannose Levels and Insulin Resistance. (2016) (121)
Detecting and annotating genetic variations using the HugeSeq pipeline (2012) (120)
Polarized Growth Controls Cell Shape and Bipolar Bud Site Selection in Saccharomyces cerevisiae (2000) (120)
H 3 K 4 me 3 breadth is linked to cell identity and transcriptional consistency (2014) (119)
Predicting essential genes in fungal genomes. (2006) (119)
Global changes in STAT target selection and transcription regulation upon interferon treatments. (2005) (118)
RNA sequencing. (2011) (117)
Regulation of cytokinesis by the Elm1 protein kinase in Saccharomyces cerevisiae. (2000) (116)
The nuclear-mitotic apparatus protein is important in the establishment and maintenance of the bipolar mitotic spindle apparatus. (1992) (115)
Issues in the analysis of oligonucleotide tiling microarrays for transcript mapping. (2005) (115)
The current excitement about copy-number variation: how it relates to gene duplications and protein families. (2008) (115)
A small reservoir of disabled ORFs in the yeast genome and its implications for the dynamics of proteome evolution. (2002) (113)
Integrated systems analysis reveals a molecular network underlying autism spectrum disorders (2014) (109)
Histone variant H2A.J accumulates in senescent cells and promotes inflammatory gene expression (2017) (108)
Substrate specificity analysis of protein kinase complex Dbf2-Mob1 by peptide library and proteome array screening (2005) (108)
Exerkines in health, resilience and disease (2022) (108)
Two methods for full-length RNA sequencing for low quantities of cells and single cells (2012) (107)
SeqFold: Genome-scale reconstruction of RNA secondary structure integrating high-throughput sequencing data (2013) (107)
The Rho-GEF Rom2p localizes to sites of polarized cell growth and participates in cytoskeletal functions in Saccharomyces cerevisiae. (1997) (107)
RSEQtools: a modular framework to analyze RNA-Seq data using compact, anonymized data summaries (2010) (107)
Dynamic Human Environmental Exposome Revealed by Longitudinal Personal Monitoring (2018) (106)
Dynamic and complex transcription factor binding during an inducible response in yeast. (2009) (106)
Multiomics modeling of the immunome, transcriptome, microbiome, proteome and metabolome adaptations during human pregnancy (2018) (106)
High-Resolution Copy-Number Variation Map Reflects Human Olfactory Receptor Diversity and Evolution (2008) (106)
Mutation or deletion of the Saccharomyces cerevisiae RAT3/NUP133 gene causes temperature-dependent nuclear accumulation of poly(A)+ RNA and constitutive clustering of nuclear pore complexes. (1995) (106)
Measuring the Evolutionary Rewiring of Biological Networks (2011) (105)
CIK1: a developmentally regulated spindle pole body-associated protein important for microtubule functions in Saccharomyces cerevisiae. (1992) (104)
Regulatory analysis of the C. elegans genome with spatiotemporal resolution (2014) (103)
A global transcriptional network connecting noncoding mutations to changes in tumor gene expression (2018) (101)
Identification of phagocytosis regulators using magnetic genome-wide CRISPR screens (2018) (100)
A procedure for highly specific, sensitive, and unbiased whole-genome amplification (2008) (100)
The cuticle genes of Drosophila: A developmentally regulated gene cluster (1981) (99)
Glucose induces cAMP-independent growth-related changes in stationary-phase cells of Saccharomyces cerevisiae. (1991) (98)
A high-stringency blueprint of the human proteome (2020) (98)
Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome (2007) (98)
Matrix stiffness induces a tumorigenic phenotype in mammary epithelium through changes in chromatin accessibility (2019) (98)
The NUF1 gene encodes an essential coiled-coil related protein that is a potential component of the yeast nucleoskeleton (1992) (96)
Specification of sites for polarized growth in Saccharomyces cerevisiae and the influence of external factors on site selection. (1992) (96)
Construction and Analysis of an Integrated Regulatory Network Derived from High-Throughput Sequencing Data (2011) (95)
EBNA1 regulates cellular gene expression by binding cellular promoters (2009) (94)
Distinct genomic aberrations associated with ERG rearranged prostate cancer (2009) (93)
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole genome sequencing studies at scale (2020) (93)
The development of protein microarrays and their applications in DNA-protein and protein-protein interaction analyses of Arabidopsis transcription factors. (2008) (92)
Systematic functional regulatory assessment of disease-associated variants (2013) (89)
Modeling ChIP Sequencing In Silico with Applications (2008) (89)
Global analysis of gene expression in yeast (2002) (89)
Genome-Wide Temporal Profiling of Transcriptome and Open Chromatin of Early Cardiomyocyte Differentiation Derived From hiPSCs and hESCs (2017) (88)
Cell polarity and morphogenesis in Saccharomyces cerevisiae. (1992) (88)
Lambda gt 11: gene isolation with antibody probes and other applications. (1987) (86)
A filamentous growth response mediated by the yeast mating pathway. (2001) (86)
Global analysis of the glycoproteome in Saccharomyces cerevisiae reveals new roles for protein glycosylation in eukaryotes (2009) (85)
Systematic identification of silencers in human cells (2020) (84)
Landscape of cohesin-mediated chromatin loops in the human genome (2020) (84)
Association of Omics Features with Histopathology Patterns in Lung Adenocarcinoma. (2017) (82)
Windows Into Human Health Through Wearables Data Analytics. (2019) (81)
Omics Profiling in Precision Oncology* (2016) (81)
Network analyses identify liver‐specific targets for treating liver diseases (2017) (81)
Carbon source induces growth of stationary phase yeast cells, independent of carbon source metabolism (1993) (81)
ChIA-PET2: a versatile and flexible pipeline for ChIA-PET data analysis (2016) (80)
Perspectives on ENCODE (2020) (79)
Perspectives on ENCODE (2020) (79)
Spatial mapping of protein composition and tissue organization: a primer for multiplexed antibody-based imaging (2021) (78)
Identification of significantly mutated regions across cancer types highlights a rich landscape of functional molecular alterations (2015) (78)
A highly integrated and complex PPARGC1A transcription factor binding network in HepG2 cells (2012) (77)
Identification of genomic indels and structural variations using split reads (2011) (77)
Global Analysis of Cdc14 Phosphatase Reveals Diverse Roles in Mitotic Processes* (2010) (76)
Incorporating Motif Analysis into Gene Co-expression Networks Reveals Novel Modular Expression Pattern and New Signaling Pathways (2013) (75)
Mapping the chromosomal targets of STAT1 by Sequence Tag Analysis of Genomic Enrichment (STAGE). (2007) (75)
A core erythroid transcriptional network is repressed by a master regulator of myelo-lymphoid differentiation (2012) (75)
Prediction and characterization of noncoding RNAs in C. elegans by integrating conservation, secondary structure, and high-throughput sequencing and array data. (2011) (74)
Recommendations from the 2008 International Summit on Proteomics Data Release and Sharing Policy: the Amsterdam principles. (2009) (73)
RNA Sequencing Analysis Detection of a Novel Pathway of Endothelial Dysfunction in Pulmonary Arterial Hypertension. (2015) (73)
Full-Length Isoform Sequencing Reveals Novel Transcripts and Substantial Transcriptional Overlaps in a Herpesvirus (2016) (72)
An integrative ENCODE resource for cancer genomics (2019) (72)
Statistical analysis of the genomic distribution and correlation of regulatory elements in the ENCODE regions. (2007) (71)
VAT: a computational framework to functionally annotate variants in personal genomes within a cloud-computing environment (2012) (70)
Pharmacological rescue of diabetic skeletal stem cell niches (2017) (69)
A genome-wide atlas of co-essential modules assigns function to uncharacterized genes (2019) (69)
Genomic analysis of fibrolamellar hepatocellular carcinoma. (2015) (69)
ChIP‐Seq: A Method for Global Identification of Regulatory Elements in the Genome (2010) (68)
Segregation of the nucleolus during mitosis in budding and fission yeast. (1991) (68)
EPHB4 kinase–inactivating mutations cause autosomal dominant lymphatic-related hydrops fetalis (2016) (68)
Arabidopsis RTNLB1 and RTNLB2 Reticulon-Like Proteins Regulate Intracellular Trafficking and Activity of the FLS2 Immune Receptor[C][W] (2011) (68)
Identification of STAT5A and STAT5B Target Genes in Human T Cells (2014) (68)
Mitigation of off-target toxicity in CRISPR-Cas9 screens for essential non-coding elements (2019) (67)
Diverse protein kinase interactions identified by protein microarrays reveal novel connections between cellular processes. (2011) (67)
Linking DNA-binding proteins to their recognition sequences by using protein microarrays. (2006) (67)
Wearable sensors enable personalized predictions of clinical laboratory measurements (2021) (67)
Genome-Wide Mapping of Copy Number Variation in Humans: Comparative Analysis of High Resolution Array Platforms (2011) (67)
High-throughput methods of regulatory element discovery. (2006) (65)
Exome Sequencing of Neonatal Blood Spots and the Identification of Genes Implicated in Bronchopulmonary Dysplasia. (2015) (65)
Induced Pluripotent Stem Cell Model of Pulmonary Arterial Hypertension Reveals Novel Gene Expression and Patient Specificity (2017) (63)
Molecular and functional resemblance of differentiated cells derived from isogenic human iPSCs and SCNT-derived ESCs (2017) (63)
Synthetic long read sequencing reveals the composition and intraspecies diversity of the human microbiome (2015) (63)
A high throughput embryonic stem cell screen identifies Oct-2 as a bifunctional regulator of neuronal differentiation. (2009) (63)
Accurate Identification and Analysis of Human mRNA Isoforms Using Deep Long Read Sequencing (2013) (62)
Effects of cellular origin on differentiation of human induced pluripotent stem cell-derived endothelial cells. (2016) (62)
The Kar3p kinesin-related protein forms a novel heterodimeric structure with its associated protein Cik1p. (2000) (62)
Large-scale mutagenesis of the yeast genome using a Tn7-derived multipurpose transposon. (2004) (62)
Systematic analysis of transcribed loci in ENCODE regions using RACE sequencing reveals extensive transcription in the human genome (2008) (61)
Design optimization methods for genomic DNA tiling arrays. (2005) (61)
Progress on Identifying and Characterizing the Human Proteome: 2018 Metrics from the HUPO Human Proteome Project. (2018) (61)
Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data (2022) (60)
Cross-Platform Comparison of Untargeted and Targeted Lipidomics Approaches on Aging Mouse Plasma (2018) (59)
Succinate and its G-protein-coupled receptor stimulates osteoclastogenesis (2017) (59)
Extensive Transcript Diversity and Novel Upstream Open Reading Frame Regulation in Yeast (2013) (59)
Yeast as a Model for Human Disease (2006) (59)
Transglutaminase 4 as a prostate autoantigen in male subfertility (2015) (59)
A High-Resolution Whole-Genome Map of Key Chromatin Modifications in the Adult Drosophila melanogaster (2011) (59)
Integrated Proteomic and Glycoproteomic Characterization of Human High-Grade Serous Ovarian Carcinoma. (2020) (58)
Shared functions of plant and mammalian StAR-related lipid transfer (START) domains in modulating transcription factor activity (2014) (58)
modENCODE Project Genome by the Caenorhabditis elegans Integrative Analysis of the (2011) (57)
Long-Read Isoform Sequencing Reveals a Hidden Complexity of the Transcriptional Landscape of Herpes Simplex Virus Type 1 (2017) (57)
Design and Implementation of the International Genetics and Translational Research in Transplantation Network (2015) (56)
The Spa2-related protein, Sph1p, is important for polarized growth in yeast. (1998) (56)
Decoding the Genomics of Abdominal Aortic Aneurysm (2018) (56)
Integrative Analysis of Longitudinal Metabolomics Data from a Personal Multi-Omics Profile (2013) (55)
Population-scale tissue transcriptomics maps long non-coding RNAs to complex disease (2021) (54)
Long-Read Sequencing - A Powerful Tool in Viral Transcriptome Research. (2019) (54)
Personalized sequencing and the future of medicine: discovery, diagnosis and defeat of disease. (2014) (54)
Novel nonsense gain-of-function NFKB2 mutations associated with a combined immunodeficiency phenotype. (2017) (54)
Selection of polarized growth sites in yeast. (1996) (54)
Gene-Environment Interaction in the Era of Precision Medicine (2019) (54)
Long-Read Sequencing of Human Cytomegalovirus Transcriptome Reveals RNA Isoforms Carrying Distinct Coding Potentials (2017) (54)
A transposable element that splits the promoter region inactivates a Drosophila cuticle protein gene. (1982) (54)
A genomic analysis of RNA polymerase II modification and chromatin architecture related to 3' end RNA polyadenylation. (2008) (54)
Classifying non-small cell lung cancer types and transcriptomic subtypes using convolutional neural networks (2020) (53)
Microfluidic isoform sequencing shows widespread splicing coordination in the human transcriptome (2018) (53)
Global identification of protein kinase substrates by protein microarray analysis (2009) (53)
Tilescope: online analysis pipeline for high-density tiling microarray data (2007) (53)
ProCAT: a data analysis approach for protein microarrays (2006) (52)
High-Coverage Whole-Exome Sequencing Identifies Candidate Genes for Suicide in Victims with Major Depressive Disorder (2017) (52)
Extended lifespan and reduced adiposity in mice lacking the FAT10 gene (2014) (52)
Achieving high-sensitivity for clinical applications using augmented exome sequencing (2015) (52)
Personal phenotypes to go with personal genomes (2009) (52)
Smooth Muscle Contact Drives Endothelial Regeneration by BMPR2-Notch1–Mediated Metabolic and Epigenetic Changes (2019) (52)
Proteome-wide survey of the autoimmune target repertoire in autoimmune polyendocrine syndrome type 1 (2016) (51)
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder (2018) (51)
Systems biology from a yeast omics perspective (2009) (50)
Comparative annotation of functional regions in the human genome using epigenomic data (2013) (50)
Structured elements drive extensive circular RNA translation. (2021) (50)
Minimum information about a protein affinity reagent (MIAPAR) (2010) (50)
Tissue-specific direct targets of Caenorhabditis elegans Rb/E2F dictate distinct somatic and germline programs (2013) (50)
Evidence against a genomic code for nucleosome positioning Reply to “Nucleosome sequence preferences influence in vivo nucleosome organization” (2010) (49)
Drivers and passengers wanted! the role of kinesin-associated proteins. (2000) (49)
Multi-Platform Sequencing Approach Reveals a Novel Transcriptome Profile in Pseudorabies Virus (2018) (49)
A Large Gene Network in Immature Erythroid Cells Is Controlled by the Myeloid and B Cell Transcriptional Regulator PU.1 (2011) (49)
Lifelong physical activity is associated with promoter hypomethylation of genes involved in metabolism, myogenesis, contractile properties and oxidative stress resistance in aged human skeletal muscle (2019) (49)
Integrated trajectories of the maternal metabolome, proteome, and immunome predict labor onset (2021) (49)
Transcriptome variation in human tissues revealed by long-read sequencing (2021) (48)
Chromosome segregation in yeast. (1993) (47)
Genome-wide chromatin occupancy analysis reveals a role for ASH2 in transcriptional pausing (2011) (47)
Engineering Genetic Predisposition in Human Neuroepithelial Stem Cells Recapitulates Medulloblastoma Tumorigenesis (2019) (46)
Longitudinal personal DNA methylome dynamics in a human with a chronic condition (2018) (46)
The genetic predisposition to bronchopulmonary dysplasia (2016) (46)
Genomics. Defining genes in the genomics era. (2003) (44)
ExpressYourself: a modular platform for processing and visualizing microarray data (2003) (44)
RNA polymerase II stalling: loading at the start prepares genes for a sprint (2008) (44)
Phosphorylation of gamma-tubulin regulates microtubule organization in budding yeast. (2001) (44)
Sbe2p and sbe22p, two homologous Golgi proteins involved in yeast cell wall formation. (2000) (43)
MSB: a mean-shift-based approach for the analysis of structural variation in the genome. (2008) (43)
Whole-Exome Enrichment with the Agilent SureSelect Human All Exon Platform. (2015) (43)
MISTERMINATE Mechanistically Links Mitochondrial Dysfunction with Proteostasis Failure (2019) (42)
Mutagenesis of murine cytomegalovirus using a Tn3-based transposon. (2000) (42)
Identification of Human Neuronal Protein Complexes Reveals Biochemical Activities and Convergent Mechanisms of Action in Autism Spectrum Disorders. (2015) (42)
Disease Variant Landscape of a Large Multiethnic Population of Moyamoya Patients by Exome Sequencing (2015) (42)
Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension (2020) (42)
Physical exercise is a risk factor for amyotrophic lateral sclerosis: Convergent evidence from Mendelian randomisation, transcriptomics and risk genotypes (2020) (41)
Systematic Identification of Host Cell Regulators of Legionella pneumophila Pathogenesis Using a Genome-wide CRISPR Screen. (2019) (41)
Progress on Identifying and Characterizing the Human Proteome: 2018-2019 Metrics from the HUPO Human Proteome Project. (2019) (41)
Integrated analysis of experimental data sets reveals many novel promoters in 1% of the human genome. (2007) (41)
A supervised hidden markov model framework for efficiently segmenting tiling array data in transcriptional and chIP-chip experiments: systematically incorporating validated biological knowledge (2006) (41)
Single cell transcriptomics reveals unanticipated features of early hematopoietic precursors (2016) (41)
Genetic Characterization and Role in Virulence of the Ribonucleotide Reductases of Streptococcus sanguinis * ♦ (2013) (40)
Characterization of the Dynamic Transcriptome of a Herpesvirus with Long-read Single Molecule Real-Time Sequencing (2017) (40)
Two gene families clustered in a small region of the Drosophila genome. (1983) (40)
Proteomic approaches for the global analysis of proteins. (2002) (40)
Specific Protein Targeting during Cell Differentiation: Polarized Localization of Fus1p during Mating Depends on Chs5p in Saccharomyces cerevisiae (2003) (40)
An exercise-inducible metabolite that suppresses feeding and obesity (2022) (40)
Investigating metabolite-protein interactions: an overview of available techniques. (2012) (40)
Centromere-Like Regions in the Budding Yeast Genome (2013) (40)
Personal Omics for Precision Health (2018) (39)
A chromosome-centric human proteome project (C-HPP) to characterize the sets of proteins encoded in chromosome 17. (2013) (38)
Multiomic immune clockworks of pregnancy (2020) (37)
Systematic Identification of Regulators of Oxidative Stress Reveals Non-canonical Roles for Peroxisomal Import and the Pentose Phosphate Pathway. (2020) (37)
Distinct splice variants and pathway enrichment in the cell-line models of aggressive human breast cancer subtypes. (2014) (36)
Real-time alerting system for COVID-19 and other stress events using wearable data (2021) (36)
Cumulative Lifetime Burden of Cardiovascular Disease From Early Exposure to Air Pollution (2020) (36)
HAT1 Coordinates Histone Production and Acetylation via H4 Promoter Binding. (2019) (36)
Nat1 Deficiency Is Associated with Mitochondrial Dysfunction and Exercise Intolerance in Mice. (2016) (36)
Altered Cardiac Energetics and Mitochondrial Dysfunction in Hypertrophic Cardiomyopathy. (2021) (35)
Large-scale mutagenesis: yeast genetics in the genome era. (2001) (35)
Simul-seq: combined DNA and RNA sequencing for whole-genome and transcriptome profiling (2016) (35)
High-throughput methods for the large-scale analysis of gene function by transposon tagging. (2000) (35)
Early Detection Of COVID-19 Using A Smartwatch (2020) (35)
Assessing the performance of different high-density tiling microarray strategies for mapping transcribed regions of the human genome. (2007) (35)
Sequencing The Transcriptional Landscape of the Yeast Genome Defined by RNA (2013) (34)
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss (2014) (34)
Bisulfite-independent analysis of CpG island methylation enables genome-scale stratification of single cells (2017) (34)
Multiple Long-Read Sequencing Survey of Herpes Simplex Virus Dynamic Transcriptome (2019) (33)
Multi-platform analysis reveals a complex transcriptome architecture of a circovirus. (2017) (33)
MOTIPS: Automated Motif Analysis for Predicting Targets of Modular Protein Domains (2010) (33)
X chromosome-wide analyses of genomic DNA methylation states and gene expression in male and female neutrophils (2010) (33)
Characterization of Novel Transcripts in Pseudorabies Virus (2015) (33)
Genome-wide mutant collections: toolboxes for functional genomics. (2000) (33)
Multiomics Characterization of Preterm Birth in Low- and Middle-Income Countries (2020) (33)
The MEK5-ERK5 kinase axis controls lipid metabolism in small cell lung cancer. (2020) (33)
The carboxy terminus of Tub4p is required for gamma-tubulin function in budding yeast. (2000) (33)
COVID-19–Induced New-Onset Diabetes: Trends and Technologies (2021) (32)
Transcriptomic and epigenomic differences in human induced pluripotent stem cells generated from six reprogramming methods (2017) (32)
Single-cell analyses define a continuum of cell state and composition changes in the malignant transformation of polyps to colorectal cancer (2021) (32)
Spindle Checkpoint Maintenance Requires Ame1 and Okp1 (2005) (31)
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis (2020) (31)
Longitudinal linked-read sequencing reveals ecological and evolutionary responses of a human gut microbiome during antibiotic treatment (2019) (31)
Proteomics and genomics (2004) (31)
Research on The Human Proteome Reaches a Major Milestone: >90% of Predicted Human Proteins Now Credibly Detected, according to the HUPO Human Proteome Project. (2020) (30)
Transcription factor binding site identification in yeast: a comparison of high-density oligonucleotide and PCR-based microarray platforms (2007) (30)
The dynamic, combinatorial cis-regulatory lexicon of epidermal differentiation (2020) (30)
The gut microbiome: a key player in the complexity of amyotrophic lateral sclerosis (ALS) (2021) (30)
Transposon mutagenesis for the analysis of protein production, function, and localization. (1999) (30)
A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth (2018) (29)
Dynamic transcriptome profiling dataset of vaccinia virus obtained from long-read sequencing techniques (2018) (29)
The DART classification of unannotated transcription within the ENCODE regions: associating transcription with known and novel loci. (2007) (29)
CTLA-4 expression by B-1a B cells is essential for immune tolerance (2021) (29)
Strain Kaplan of Pseudorabies Virus Genome Sequenced by PacBio Single-Molecule Real-Time Sequencing Technology (2014) (28)
De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease (2017) (28)
Systematic investigation of protein–small molecule interactions (2013) (27)
Phenotypically-Silent Bone Morphogenetic Protein Receptor 2 (Bmpr2) Mutations Predispose Rats to Inflammation-Induced Pulmonary Arterial Hypertension by Enhancing The Risk for Neointimal Transformation. (2019) (27)
Prospects and Challenges in Proteomics (2005) (27)
A Case Report of Hypoglycemia and Hypogammaglobulinemia: DAVID Syndrome in a Patient With a Novel NFKB2 Mutation (2017) (27)
PPARγ-p53-Mediated Vasculoregenerative Program to Reverse Pulmonary Hypertension. (2020) (27)
Value of Circulating Cytokine Profiling During Submaximal Exercise Testing in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (2018) (27)
SETD7 Drives Cardiac Lineage Commitment through Stage-Specific Transcriptional Activation. (2018) (27)
Mutations in PRG1, a yeast proteasome-related gene, cause defects in nuclear division and are suppressed by deletion of a mitotic cyclin gene. (1994) (27)
Nuclear pore complex antigens delineate nuclear envelope dynamics in vegetative and conjugating Saccharomyces cerevisiae (1993) (27)
Introduction and Historical Overview of DNA Sequencing (2011) (26)
Template-switching artifacts resemble alternative polyadenylation (2019) (25)
Long-read sequencing of the human cytomegalovirus transcriptome with the Pacific Biosciences RSII platform (2017) (25)
Genomic analysis of insertion behavior and target specificity of mini-Tn7 and Tn3 transposons in Saccharomyces cerevisiae (2006) (25)
Identification of Genes Critical for Resistance to Infection by West Nile Virus Using RNA-Seq Analysis (2013) (25)
Fetal de novo mutations and preterm birth (2017) (25)
Deep learning-based detection of COVID-19 using wearables data (2021) (25)
The conserved histone deacetylase Rpd3 and its DNA binding subunit Ume6 control dynamic transcript architecture during mitotic growth and meiotic development (2014) (25)
Deep longitudinal multiomics profiling reveals two biological seasonal patterns in California (2020) (24)
iPSC Modeling of RBM20-Deficient DCM Identifies Upregulation of RBM20 as a Therapeutic Strategy (2020) (24)
Genome-Wide Profiling of Cap-Independent Translation Enhancing Elements in the Human Genome (2013) (24)
Sequence to Medical Phenotypes: A Framework for Interpretation of Human Whole Genome DNA Sequence Data (2015) (24)
Recent developments in analytical and functional protein microarrays. (2003) (24)
Global metabolic profiling to model biological processes of aging in twins (2019) (24)
A machine-compiled database of genome-wide association studies (2019) (24)
Tandem duplications of the rII region of bacteriophage T4D. (1972) (23)
Haplotype structure and positive selection at TLR1 (2013) (23)
Discovery of Stress Responsive DNA Regulatory Motifs in Arabidopsis (2012) (23)
Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation (2017) (23)
Natural Selection Has Differentiated the Progesterone Receptor among Human Populations. (2018) (22)
Precision Medicine: Role of Proteomics in Changing Clinical Management and Care. (2018) (22)
Quality-control mechanisms targeting translationally stalled and C-terminally extended poly(GR) associated with ALS/FTD (2020) (22)
MITI minimum information guidelines for highly multiplexed tissue images (2021) (22)
Global, distinctive, and personal changes in molecular and microbial profiles by specific fibers in humans. (2022) (22)
Rare Variant Burden Analysis within Enhancers Identifies CAV1 as an ALS Risk Gene (2020) (22)
Metabolome progression during early gut microbial colonization of gnotobiotic mice (2015) (22)
Transcriptome Signature and Regulation in Human Somatic Cell Reprogramming (2015) (22)
NF90/ILF3 is a transcription factor that promotes proliferation over differentiation by hierarchical regulation in K562 erythroleukemia cells (2017) (22)
Fast Optimal Genome Tiling with Applications to Microarray Design and Homology Search (2002) (21)
A limited set of transcriptional programs define major cell types (2019) (21)
Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration (2013) (21)
Cross-Laboratory Standardization of Preclinical Lipidomics Using Differential Mobility Spectrometry and Multiple Reaction Monitoring (2021) (21)
Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2020) (21)
Exploring the phenotypic consequences of tissue specific gene expression variation inferred from GWAS summary statistics (2018) (21)
Disruption of mesoderm formation during cardiac differentiation due to developmental exposure to 13-cis-retinoic acid (2018) (20)
Precision Neoantigen Discovery Using Large-scale Immunopeptidomes and Composite Modeling of MHC Peptide Presentation (2021) (20)
Classifying Non-Small Cell Lung Cancer Histopathology Types and Transcriptomic Subtypes using Convolutional Neural Networks (2019) (20)
Dissecting phosphorylation networks: lessons learned from yeast (2011) (20)
Transcriptome-wide survey of pseudorabies virus using next- and third-generation sequencing platforms (2018) (19)
A DMS Shotgun Lipidomics Workflow Application to Facilitate High-Throughput, Comprehensive Lipidomics. (2021) (19)
Identification of Potential Glycan Cancer Markers with Sialic Acid Attached to Sialic Acid and Up-regulated Fucosylated Galactose Structures in Epidermal Growth Factor Receptor Secreted from A431 Cell Line* (2013) (19)
Statins Are Associated With Increased Insulin Resistance and Secretion (2021) (19)
iNetModels 2.0: an interactive visualization and database of multi-omics data (2019) (18)
High-frequency actionable pathogenic exome variants in an average-risk cohort (2018) (18)
Secure cloud computing for genomic data (2016) (18)
SLK1, a yeast homolog of MAP kinase activators, has a RAS/cAMP-independent role in nutrient sensing (1994) (18)
Long-Read Sequencing Revealed an Extensive Transcript Complexity in Herpesviruses (2018) (18)
Integrating Sequencing Technologies in Personal Genomics: Optimal Low Cost Reconstruction of Structural Variants (2009) (18)
Genome sequencing unveils a regulatory landscape of platelet reactivity (2019) (18)
Rapid mapping of antigenic coding regions and constructing insertion mutations in yeast genes by mini-Tn10 "transplason" mutagenesis. (1986) (17)
Arabidopsis RTNLB 1 and RTNLB 2 Reticulon-Like Proteins Regulate Intracellular Trafficking and Activity of the FLS 2 Immune Receptor (2011) (17)
Understanding health disparities (2018) (17)
Can Metabolic Profiles Be Used as a Phenotypic Readout of the Genome to Enhance Precision Medicine? (2016) (17)
High Throughput Sequencing and Assessing Disease Risk. (2018) (17)
Metadata Checklist for the Integrated Personal Omics Study: Proteomics and Metabolomics Experiments (2013) (17)
Challenges and recommendations for epigenomics in precision health (2017) (17)
Prediction of Immunotherapy Response in Melanoma through Combined Modeling of Neoantigen Burden and Immune-Related Resistance Mechanisms (2021) (16)
Human‐engineered Treg‐like cells suppress FOXP3‐deficient T cells but preserve adaptive immune responses in vivo (2020) (16)
Cell Type-Specific Chromatin Signatures Underline Regulatory DNA Elements in Human Induced Pluripotent Stem Cells and Somatic Cells (2017) (16)
Correction: AGAPE (Automated Genome Analysis PipelinE) for Pan-Genome Analysis of Saccharomyces cerevisiae (2015) (16)
Genomic era diagnosis and management of hereditary and sporadic colon cancer. (2014) (16)
A scalable, secure, and interoperable platform for deep data-driven health management (2021) (16)
Distinct transcriptomic and exomic abnormalities within myelodysplastic syndrome marrow cells (2018) (15)
Whole-Exome Enrichment with the Illumina TruSeq Exome Enrichment Platform. (2015) (15)
Reply to Brunet and Doolittle: Both selected effect and causal role elements can influence human biology and disease (2014) (15)
Transcriptomic study of Herpes simplex virus type-1 using full-length sequencing techniques (2018) (15)
Systematic Protein Prioritization for Targeted Proteomics Studies through Literature Mining. (2018) (15)
A common class of transcripts with 5′-intron depletion, distinct early coding sequence features, and N1-methyladenosine modification (2016) (14)
Supporting Online Material for HTRA 1 Promoter Polymorphism in Wet Age-Related Macular Degeneration (2006) (14)
Isolated Congenital Anosmia and CNGA2 Mutation (2017) (14)
Extrapolating traditional DNA microarray statistics to tiling and protein microarray technologies. (2006) (14)
Annotation of Spatially Resolved Single-cell Data with STELLAR (2021) (14)
WISP3 mutation associated with pseudorheumatoid dysplasia (2018) (14)
Integrative analysis of RNA, translation and protein levels reveals distinct regulatory variation across humans (2015) (14)
Omics AnalySIs System for PRecision Oncology (OASISPRO): a web-based omics analysis tool for clinical phenotype prediction (2018) (14)
Genome-wide transposon mutagenesis in yeast. (2001) (13)
Metformin Improves Diabetic Bone Health by Re-Balancing Catabolism and Nitrogen Disposal (2015) (13)
Positional artifacts in microarrays: experimental verification and construction of COP, an automated detection tool (2006) (13)
Full Genome Sequence of the Western Reserve Strain of Vaccinia Virus Determined by Third-Generation Sequencing (2018) (13)
Dual Platform Long-Read RNA-Sequencing Dataset of the Human Cytomegalovirus Lytic Transcriptome (2018) (13)
A homolog of the proteasome-related RING10 gene is essential for yeast cell growth. (1992) (13)
Comprehensive whole-genome sequencing of an early-stage primary myelofibrosis patient defines low mutational burden and non-recurrent candidate genes (2013) (13)
ALDH1A3 Coordinates Metabolism With Gene Regulation in Pulmonary Arterial Hypertension (2021) (13)
Genetic definition of two functional elements in a bacteriophage T4 host-range "cassette". (1989) (13)
The carboxy terminus of Tub 4 p is required for γ-tubulin function in budding yeast (12)
The genetic constitution of tandem duplications on the rII of bacteriophage T4D. (1973) (12)
Molecular basis of cell integrity and morphogenesis in Saccharomyces cerevisiae (1995) (12)
Association of AHSG with alopecia and mental retardation (APMR) syndrome (2017) (12)
Long-read assays shed new light on the transcriptome complexity of a viral pathogen (2020) (12)
SHC1, a high pH inducible gene required for growth at alkaline pH in Saccharomyces cerevisiae. (1999) (12)
Multiplatform next-generation sequencing identifies novel RNA molecules and transcript isoforms of the endogenous retrovirus isolated from cultured cells (2018) (12)
Personalized Metabolomics. (2019) (12)
Whole-Exome Enrichment with the Roche NimbleGen SeqCap EZ Exome Library SR Platform. (2015) (12)
KLF4 recruits SWI/SNF to increase chromatin accessibility and reprogram the endothelial enhancer landscape under laminar shear stress (2020) (12)
Precision environmental health monitoring by longitudinal exposome and multi-omics profiling (2021) (12)
Mismatch oligonucleotides in human and yeast: guidelines for probe design on tiling microarrays (2008) (12)
Discovery of Novel Human Gene Regulatory Modules from Gene Co-expression and Promoter Motif Analysis (2017) (11)
Plasma sterols and depressive symptom severity in a population-based cohort (2017) (11)
Much ado about nothing: A qualitative study of the experiences of an average‐risk population receiving results of exome sequencing (2019) (11)
Cloud-based interactive analytics for terabytes of genomic variants data (2017) (11)
Mutations in NGLY 1 Cause an Inherited Disorder of the Endoplasmic Reticulum-Associated Degradation ( ERAD ) Pathway (2014) (11)
Decoding personal biotic and abiotic airborne exposome (2021) (10)
Towards personalized medicine in maternal and child health: integrating biologic and social determinants (2020) (10)
Atlas of transcriptionally active transposable elements in human adult tissues (2019) (10)
Reassessment of Piwi binding to the genome and Piwi impact on RNA polymerase II distribution. (2015) (10)
Serine biosynthesis as a novel therapeutic target for dilated cardiomyopathy. (2022) (10)
Novel transcribed regions in the human genome. (2006) (10)
Chromatin accessibility associates with protein-RNA correlation in human cancer (2021) (10)
A Customizable Analysis Flow in Integrative Multi-Omics (2020) (9)
Corrigendum: Performance comparison of whole-genome sequencing platforms (2012) (9)
Applying genomics in heart transplantation (2018) (9)
The human proteome project: Current state and future direction. (2011) (9)
Metformin Affects Heme Function as a Possible Mechanism of Action (2018) (9)
Immunologic effects of forest fire exposure show increases in IL‐1β and CRP (2020) (9)
Improvement in Glucose Regulation Using a Digital Tracker and Continuous Glucose Monitoring in Healthy Adults and Those with Type 2 Diabetes (2021) (8)
Evaluating Common Humoral Responses against Fungal Infections with Yeast Protein Microarrays. (2015) (8)
A Droplet Microfluidics Based Platform for Mining Metagenomic Libraries for Natural Compounds (2017) (8)
Temporal changes in soluble angiotensin-converting enzyme 2 associated with metabolic health, body composition, and proteome dynamics during a weight loss diet intervention: a randomized trial with implications for the COVID-19 pandemic (2021) (8)
Network biology bridges the gaps between quantitative genetics and multi-omics to map complex diseases. (2021) (8)
Chromatin immunoprecipitation and multiplex sequencing (ChIP-Seq) to identify global transcription factor binding sites in the nematode Caenorhabditis elegans. (2014) (8)
Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays (2019) (8)
High-Resolution Bisulfite-Sequencing of Peripheral Blood DNA Methylation in Early-Onset and Familial Risk Breast Cancer Patients (2019) (8)
Specific Plasma Autoantibody Reactivity in Myelodysplastic Syndromes (2013) (8)
A Cloud-Based Metabolite and Chemical Prioritization System for the Biology/Disease-Driven Human Proteome Project. (2018) (8)
Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis (2018) (8)
The metabolomics of human aging: Advances, challenges, and opportunities (2022) (7)
Target gene identification: target specific transcriptional activation by three murine homeodomain/VP16 hybrid proteins in Saccharomyces cerevisiae. (1996) (7)
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Simultaneous RNA purification and size selection using on-chip isotachophoresis with an ionic spacer. (2019) (7)
Deep Characterization of the Human Antibody Response to Natural Infection Using Longitudinal Immune Repertoire Sequencing* (2019) (7)
Precision medicine in women with epilepsy: The challenge, systematic review, and future direction (2021) (7)
Multimodal Dynamic Profiling of Healthy and Diseased States for Future Personalized Health Care (2013) (7)
iPOP and its role in participatory medicine (2014) (7)
metID: A R package for automatable compound annotation for LC−MS-based data (2021) (7)
Integrated Proteomic and Genomic Analysis of Gastric Cancer Patient Tissues. (2015) (7)
metID: an R package for automatable compound annotation for LC−MS-based data (2021) (7)
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The Exposome in the Era of the Quantified Self. (2021) (7)
A Method for Intelligent Allocation of Diagnostic Testing by Leveraging Data from Commercial Wearable Devices: A Case Study on COVID-19 (2022) (7)
A cancer-associated RNA polymerase III identity drives robust transcription and expression of snaR-A noncoding RNA (2021) (7)
Real-time Alerting System for COVID-19 Using Wearable Data (2021) (7)
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Probing High-density Functional Protein Microarrays to Detect Protein-protein Interactions. (2015) (7)
Metadata checklist for the integrated personal OMICS study: proteomics and metabolomics experiments. (2014) (7)
Humans Are Selectively Exposed to Pneumocystis jirovecii (2020) (6)
High Resolution Single Cell Maps Reveals Distinct Cell Organization and Function Across Different Regions of the Human Intestine (2021) (6)
Protein substrates of the arginine methyltransferase Hmt1 identified by proteome arrays (2016) (6)
Wireless, closed-loop, smart bandage with integrated sensors and stimulators for advanced wound care and accelerated healing. (2022) (6)
10 Transposon Tagging I: A Novel System for Monitoring Protein Production, Function and Localization (1998) (6)
Multi-tissue integrative analysis of personal epigenomes (2021) (6)
Early detection of SARS‐CoV‐2 and other infections in solid organ transplant recipients and household members using wearable devices (2021) (6)
The variable somatic genome (2013) (6)
Meta-analytic approach for transcriptome profiling of herpes simplex virus type 1 (2020) (6)
Combined nanopore and single-molecule real-time sequencing survey of human betaherpesvirus 5 transcriptome (2021) (6)
Unbiased metabolome screen leads to personalized medicine strategy for amyotrophic lateral sclerosis (2022) (5)
TidyMass an object-oriented reproducible analysis framework for LC–MS data (2022) (5)
High Frequency Actionable Pathogenic Exome Mutations in an Average-Risk Cohort (2017) (5)
Cross-species blastocyst chimerism between nonhuman primates using iPSCs (2019) (5)
Q & A: the Snyderome (2012) (5)
An Integrated Sequencing Approach for Updating the Pseudorabies Virus Transcriptome (2021) (5)
Multiomic analysis reveals cell-type-specific molecular determinants of COVID-19 severity (2022) (5)
Longitudinal Analysis of Serum Cytokine Levels and Gut Microbial Abundance Links IL-17/IL-22 With Clostridia and Insulin Sensitivity in Humans (2020) (5)
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis (2019) (5)
Whole-exome sequencing data of suicide victims who had suffered from major depressive disorder (2019) (5)
Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity (2021) (5)
Tet enzymes are essential for early embryogenesis and completion of embryonic genome activation (2021) (5)
Time-course transcriptome analysis of host cell response to poxvirus infection using a dual long-read sequencing approach (2021) (4)
Chromosome-level de novo assembly of the pig-tailed macaque genome using linked-read sequencing and HiC proximity scaffolding (2019) (4)
Evaluation of the impact of ul54 gene-deletion on the global transcription and DNA replication of pseudorabies virus (2017) (4)
Chromatin Remodeling in Response to BRCA2-Crisis. (2019) (4)
Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies (2022) (4)
Robust and generalizable segmentation of human functional tissue units (2021) (4)
Analysis of the Complete Genome Sequence of a Novel, Pseudorabies Virus Strain Isolated in Southeast Europe (2019) (4)
Non-invasive wearables for remote monitoring of HbA1c and glucose variability: proof of concept (2021) (4)
iPSC Model of Pulmonary Arterial Hypertension Reveals Novel Gene Expression and Patient Specificity. (2016) (4)
Exploring disease interrelationships in patients with lymphatic disorders: A single center retrospective experience (2022) (4)
PRC2 clock: a universal epigenetic biomarker of aging and rejuvenation (2022) (4)
NF 90 / ILF 3 is a transcription factor that promotes proliferation over differentiation by hierarchical regulation in K 562 erythroleukemia cells (2017) (4)
Endogenous Retroviral Elements Generate Pathologic Neutrophils in Pulmonary Arterial Hypertension (2022) (4)
RobNorm: model-based robust normalization method for labeled quantitative mass spectrometry proteomics data (2019) (4)
Cell Polarity in the Budding Yeast Saccharomyces Cerevisiae (1998) (4)
Resource Dynamic transActing Factor Colocalization in Human Cells (2013) (4)
gamma-Tubulin of budding yeast. (2000) (4)
Multiple Pairwise Analysis of Non-homologous Centromere Coupling Reveals Preferential Chromosome Size-Dependent Interactions and a Role for Bouquet Formation in Establishing the Interaction Pattern (2016) (4)
Long-Read Sequencing Reveals a GC Pressure during the Evolution of Porcine Endogenous Retrovirus (2017) (4)
Temporal dynamics of the multi-omic response to endurance exercise training across tissues (2022) (4)
Systematic identification of significantly mutated regions reveals a rich landscape of functional molecular alterations across cancer genomes (2015) (3)
A small reservoir of disabled ORFs in the Saccharomyces cerevisiae genome and its implications for the dynamics of proteome evolution (2001) (3)
AdaReg: data adaptive robust estimation in linear regression with application in GTEx gene expressions (2019) (3)
Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals (2022) (3)
Analysis of Genomic Tiling Microarrays for Transcript Mapping and the Identification of Transcription Factor Binding Sites (2005) (3)
Erratum: A single-molecule long-read survey of the human transcriptome (2014) (3)
Prevention of Severe Intestinal Barrier Dysfunction Through a Single-Species Probiotics Is Associated With the Activation of Microbiome-Mediated Glutamate-Glutamine Biosynthesis. (2020) (3)
Master lineage transcription factors anchor trans mega transcriptional complexes at highly accessible enhancer sites to promote long-range chromatin clustering and transcription of distal target genes (2021) (3)
Human exposome assessment platform (2021) (3)
Phenotypic characteristics of peripheral immune cells of Myalgic encephalomyelitis/chronic fatigue syndrome via transmission electron microscopy: A pilot study (2022) (3)
A limited set of transcriptional programs define major histological types and provide the molecular basis for a cellular taxonomy of the human body (2019) (3)
Obesity Drives Delayed Infarct Expansion, Inflammation, and Distinct Gene Networks in a Mouse Stroke Model (2020) (3)
Patient-derived gene and protein expression signatures of NGLY1 deficiency. (2021) (3)
Evolution of diapause in the African turquoise killifish by remodeling ancient gene regulatory landscape (2021) (3)
In-depth triacylglycerol profiling using MS3 Q-Trap mass spectrometry. (2021) (3)
Human genome meeting 2016 (2016) (3)
Old fibroblasts secrete inflammatory cytokines that drive variability in reprogramming efficiency and may affect wound healing between old individuals (2018) (3)
Identification of novel functional elements in the human genome. (2003) (3)
Longitudinal multi-omics of host–microbe dynamics in prediabetes (2019) (3)
Identification of non-coding silencer elements and their regulation of gene expression. (2022) (3)
Patient-derived gene and protein expression signatures of NGLY1 deficiency (2021) (2)
Identification and mitigation of pervasive off-target activity in CRISPR-Cas9 screens for essential non-coding elements (2019) (2)
An XML application for genomic data interoperation (2001) (2)
MOBN: an interactive database of multi-omics biological networks (2019) (2)
CORRIGENDUM: Mutations in NGLY1 cause an inherited disorder of the endoplasmic reticulum–associated degradation pathway (2014) (2)
Systematic evaluation of variability in ChIP-chip experiments using data (2008) (2)
Candidate variants in TUB are associated with familial tremor (2020) (2)
Long-read sequencing of SARS-CoV-2 reveals novel transcripts and a diverse complex transcriptome landscape (2021) (2)
Learning Personal Food Preferences via Food Logs Embedding (2021) (2)
A machine learning algorithm with subclonal sensitivity reveals widespread pan-cancer human leukocyte antigen loss of heterozygosity (2022) (2)
Gut microbiota analyses of Saudi populations for type 2 diabetes-related phenotypes reveals significant association (2021) (2)
Rare variant burden analysis within enhancers identifies CAV1 as an ALS risk gene. (2021) (2)
BoCaTFBS: a boosted cascade learner to refine the binding sites suggested by ChIP-chip experiments (2006) (2)
Chimpanzee and pig-tailed macaque iPSCs: Improved culture and generation of primate cross-species embryos. (2022) (2)
Protein-Protein Interactions from Genomic Data A Bayesian Networks Approach for Predicting (2006) (2)
Multiomics Longitudinal Modeling of Preeclamptic Pregnancies (2021) (2)
Precision Medicine Approaches to Mental Healthcare. (2022) (2)
The EN-TEx resource of multi-tissue personal epigenomes & variant-impact models (2022) (2)
Identification of a novel mutation in the APTX gene associated with ataxia-oculomotor apraxia (2017) (2)
Adverse childhood experiences, diabetes and associated conditions, preventive care practices and healthcare access: A population-based study. (2022) (2)
Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes (2022) (2)
Tissue-specific direct targets of Caenorhabditis elegans Rb/E2F dictate distinct somatic and germline programs (2013) (2)
Protein Microarrays (2009) (2)
HAT1 drives a gene-metabolite circuit that links nutrient metabolism to histone production (2019) (2)
Endogenous Retroviral Elements Generate Pathologic Neutrophils and Elastase Rich Exosomes in Pulmonary Arterial Hypertension (2021) (2)
An acetyl-click screening platform identifies a small molecule inhibitor of Histone Acetyltransferase 1 (HAT1) with anti-tumor activity (2021) (2)
Transcriptomic Evaluation of CD34+ Marrow Cells from Myelodysplastic Syndrome (MDS) Patients (2014) (2)
Design and Methods of the Validating Injury to the Renal Transplant Using Urinary Signatures (VIRTUUS) Study in Children (2021) (2)
Recurrent repeat expansions in human cancer genomes (2022) (2)
Ultra high-throughput whole-genome methylation sequencing reveals trajectories in precancerous polyps to early colorectal adenocarcinoma (2022) (2)
Exposome-wide Association Study for Metabolic Syndrome (2021) (2)
Dual isoform sequencing reveals complex transcriptomic and epitranscriptomic landscapes of a prototype baculovirus (2022) (2)
A lipid droplet-peroxisome network drives longevity by monounsaturated fatty acids via modulating ether lipid synthesis and ferroptosis (2021) (2)
Swarm: A federated cloud framework for large-scale variant analysis (2021) (2)
The CRIT framework for identifying cross patterns in systems biology and application to chemogenomics (2011) (2)
Whole transcriptome profiling of prospective endomyocardial biopsies reveals prognostic and diagnostic signatures of cardiac allograft rejection. (2022) (1)
DE NOVO NAD+ SYNTHESIS RESCUES NEUROINFLAMMATION AND ALZHEIMER’S DISEASE PHENOTYPES: MODULATING IMMUNE CELL RESPONSES AND MITOCHONDRIAL BIOENERGETICS (2018) (1)
The X chromosome from telomere to telomere: key achievements and future opportunities. (2021) (1)
Prediction of gestational age using urinary metabolites in term and preterm pregnancies (2022) (1)
KMT2D-NOTCH Mediates Coronary Abnormalities in Hypoplastic Left Heart Syndrome (2022) (1)
RobNorm: Model-Based Robust Normalization for High-Throughput Proteomics from Mass Spectrometry Platform (2019) (1)
Response to Hulman and colleagues regarding “Glucotypes reveal new patterns of glucose dysregulation” (2021) (1)
Tyrosine kinase inhibitors induce mitochondrial dysfunction during cardiomyocyte differentiation through alteration of GATA4-mediated networks (2020) (1)
Understanding how biologic and social determinants affect disparities in preterm birth and outcomes of preterm infants in the NICU. (2021) (1)
Deep Learning-based Pseudo-Mass Spectrometry Imaging Analysis for Precision Medicine (2022) (1)
Deep Characterization of the Human Antibody Response to Natural Infection Using Longitudinal Immune Repertoire Sequencing. (2020) (1)
A genome-wide atlas of recurrent repeat expansions in human cancer (2022) (1)
Divergent patterns of selection on metabolite levels and gene expression (2021) (1)
2017 NIH-wide workshop report on “The Human Microbiome: Emerging Themes at the Horizon of the 21st Century” (2019) (1)
massDatabase: utilities for the operation of the public compound and pathway database (2022) (1)
Convergent mutations in tissue-specific regulatory regions reveal novel cancer drivers (2020) (1)
AdaTiSS: A Novel Data-Adaptive Robust Method for Quantifying Tissue Specificity Scores (2019) (1)
Chromatin Structure and Transcription of the Human alpha Globin Locus in Erythroid and Non-Erythroid Environments. (2007) (1)
Time-Course Transcriptome Profiling of a Poxvirus Using Long-Read Full-Length Assay (2021) (1)
Lipid droplets and peroxisomes are co-regulated to drive lifespan extension in response to mono-unsaturated fatty acids. (2023) (1)
A CLUSTER OF DROSOPHILA CUTICLE GENES (1981) (1)
Workshop I – Global Analysis of Protein Activities Using Protein Chips (2003) (1)
Large-scale analysis of gene expression, protein localization, and gene dlsrupuon in Saccharomyces cerevisiae (2007) (1)
Kinase Substrate Identification Using Yeast Protein Microarrays (2007) (1)
Corrigendum: Long-read sequencing of the human cytomegalovirus transcriptome with the pacific biosciences RSII platform (2018) (1)
Abstract 3616: Fix the fixation: effect of formalin fixation on targeted sequencing, variant calling and gene expression (2016) (1)
Genetic Adaptation of Porcine Circovirus Type 1 to Cultured Porcine Kidney Cells Revealed by Single-Molecule Long-Read Sequencing Technology (2017) (1)
Saccharomyces cerevisiae Complex transcriptional circuitry at the G 1 / S transition in data (2006) (1)
Lawrence Berkeley National Laboratory Recent Work Title Identification of genes critical for resistance to infection by West Nile virus using RNA-Seq analysis Permalink (2013) (1)
Corrigendum: Regulatory analysis of the C. elegans genome with spatiotemporal resolution (2015) (1)
Identification of Transcription Factor LIN-15B::GFP Binding Regions in L3 (2011) (1)
Multi-omic Analysis of Familial Adenomatous Polyposis Reveals Molecular Pathways and Polyclonal Spreading Associated with Early Tumorigenesis (2021) (1)
Identification and analysis of functional elements in 1 % of the human genome by the ENCODE pilot project The ENCODE Project Consortium * (2007) (1)
Integration and comparison of multi-omics profiles of NGLY1 deficiency plasma and cellular models to identify clinically relevant molecular phenotypes (2021) (1)
Hummingbird: efficient performance prediction for executing genomic applications in the cloud (2021) (1)
Interactive Analytics for Very Large Scale Genomic Data (2015) (1)
Leveraging Mobile Technology for Public Health Promotion: A Multidisciplinary Perspective. (2022) (1)
modENCODE consortia ChIP-seq guidelines and practices of the ENCODE and Material Supplemental (2012) (1)
Identification of Transcription Factor GEI-1::GFP Binding Regions in L4 (2011) (1)
Identification of Transcription Factor EGL-27::GFP Binding Regions in L1 (2011) (1)
Five-year pediatric use of a digital wearable fitness device: lessons from a pilot case study (2020) (1)
Multi-omics microsampling for the profiling of lifestyle-associated changes in health. (2023) (1)
Real-time alerting system for COVID-19 and other stress events using wearable data (2021) (1)
Validated machine learning algorithm with sub-clonal sensitivity reveals widespread pan-cancer human leukocyte antigen loss of heterozygosity (2021) (1)
Association of HLA loss of heterozygosity with allele-specific neoantigen expansion in response to immunotherapy. (2021) (1)
Wireless closed-loop smart bandage for chronic wound management and accelerated tissue regeneration (2022) (1)
Predicting Non-Small Cell Lung Cancer Diagnosis and Prognosis by Fully Automated Microscopic Pathology Image Features (2017) (1)
Identification of phagocytosis regulators using magnetic genome-wide CRISPR screens (2018) (1)
Copy Number Variation detection from 1000 Genomes project exon capture sequencing data (2012) (1)
Shared functions of plant and mammalian StAR-related lipid transfer (START) domains in modulating transcription factor activity (2014) (1)
A global transcriptional network connecting noncoding mutations to changes in tumor gene expression (2018) (1)
Personal aging markers and ageotypes revealed by deep longitudinal profiling (2020) (1)
Value of Circulating Cytokine Profiling During Submaximal Exercise Testing in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (2018) (0)
Introduction (2007) (0)
07-Cell cycle and DNA replication (2007) (0)
Proteomic Assessment of Fluid Shifts and Association with Visual Impairment and Intracranial Pressure in Twin Astronauts (2016) (0)
Towards the full understanding of yeast transcription factor binding sites in genomic level (2011) (0)
Evaluation of the impact of ul54 gene-deletion on the global transcription and DNA replication of pseudorabies virus (2017) (0)
Adapting skills from genetic counseling to wearables technology research during the COVID‐19 pandemic: Poised for the pivot (2021) (0)
Multiomic immune clockworks of pregnancy (2020) (0)
C . elegans genome-wide ChIP-seq in Diverse transcription factor binding features revealed by Material Supplemental (2011) (0)
Metabolomics as a robust tool in systems biology and personalized medicine: an open letter to the metabolomics community (2013) (0)
Abnormal Differentiation and Proliferation of Coronary Arterial Endothelium in Hypoplastic Left Heart Syndrome (2021) (0)
Longitudinal interactions between levels of serum cytokine and the microbiome from four body sites (2022) (0)
Systems Analysis of de novo Mutations in Congenital Heart Diseases Identified a Molecular Network in Hypoplastic Left Heart Syndrome (2022) (0)
Probing Yeast Protein Microarrays for Protein-protein Interactions Using V5-epitope Tagged Fusion Protein Probes (2012) (0)
Abstract 15808: Whole Exome Sequencing and Hypertrophic Cardiomyopathy (2011) (0)
Exome Sequencing Unravels Novel Candidate Genes in Familial Multiple Sclerosis (P2.219) (2015) (0)
Staining with Calcofluor , Hoechst 3325 & and Anti-SPA 2 Antibodies (2002) (0)
Discovery of Cancer and Autoimmune Biomarkers Utilizing Serum Antibody Profiling on Protein Microarrays (2007) (0)
Longitudinal Urine Metabolic Profiling and Gestational Age Prediction in Pregnancy (2022) (0)
Identification of Transcription Factor MEP-1::GFP Binding Regions in Embryos (2011) (0)
analysis of transcription , and evolution Pseudogenes in the ENCODE regions : Consensus annotation , Material Supplemental (2007) (0)
Human Transcription Factors Running title : Analysis of Sites of 119 TFs in the Human Genome (2012) (0)
Techniques for the analysis of complex genomes: edited by Rakesh Anand Academic Press, 1992. £19.95 (xii + 239 pages) ISBN 0 12 057620 1 (1992) (0)
Discovering CNVs from read depth analysis of next generation sequencing data (2009) (0)
Vision Statement for Plant Physiology Prospects and Challenges in Proteomics (2005) (0)
Yeast Interactome Network High-Quality Binary Protein Interaction (2009) (0)
Global Analysis of Small Molecule Interactions with Proteins Online ESI-MS Analysis of Biomolecules Two-Dimensional Liquid Chromatography Coupled with ESI-MS for Protein Identification and Quantification (2009) (0)
inefficient for lncRNAs predominantly co-transcriptional in the human genome but Deep sequencing of subcellular RNA fractions shows splicing to be Material Supplemental (2012) (0)
Practical Guidelines for Secure Cloud Computing for Genomic Data (2015) (0)
Physiological blood–brain transport is impaired with age by a shift in transcytosis (2020) (0)
SEGIEGATION IN YEAST (1993) (0)
Meta-analytic approach for transcriptome profiling of herpes simplex virus type 1 (2020) (0)
Benchmarking workflows to assess performance and suitability of germline variant calling pipelines in clinical diagnostic assays (2021) (0)
Proteomics for Elucidating Protein Function, Regulatory Networks and Improving Human Health (2007) (0)
Low expression of EXOSC2 protects against clinical COVID-19 and impedes SARS-CoV-2 replication (2022) (0)
Systematic identification of silencers in human cells (2020) (0)
Discovery of Novel Human Gene Regulatory Modules from Gene Co-expression and Promoter Motif Analysis (2017) (0)
Deploying wearable sensors for pandemic mitigation (2022) (0)
Time-course transcriptome analysis of host cell response to poxvirus infection using a dual long-read sequencing approach (2021) (0)
Viewpoints Personal Omics for Precision Health (2018) (0)
Author Correction: Prediction of gestational age using urinary metabolites in term and preterm pregnancies (2022) (0)
using RNA-seq Candida albicans fungal pathogen Comprehensive annotation of the transcriptome of the human Material (2010) (0)
A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth (2018) (0)
Longitudinal personal DNA methylome dynamics in a human with a chronic condition (2018) (0)
Multi-tissue integrative analysis of personal epigenomes [preprint] Multi-tissue integrative analysis of personal epigenomes [preprint] you. (2021) (0)
Consumer Wearable Devices for Health Surveillance and Disease Monitoring (2017) (0)
Deploying wearable sensors for pandemic mitigation: A counterfactual modelling study of Canada’s second COVID-19 wave (2022) (0)
yeast Target hub proteins serve as master regulators of development in data (2006) (0)
Ecological and Genetic Variation Among Populations of Boechera caeruleamontana sp. nov. (Brassicaceae) from Blue Mountain and Dinosaur National Monumentin Eastern Utah and Western Colorado (2017) (0)
E-GEOD-25798.processed.2.zip (2011) (0)
A method for intelligent allocation of diagnostic testing by leveraging data from commercial wearable devices: a case study on COVID-19 (2022) (0)
Longitudinally tracking personal physiomes for precision management of childhood epilepsy (2022) (0)
Proteome Chips Global Analysis of Protein Activities Using (2009) (0)
by high-density pyrosequencing and transposon mutagenesis pathogenesis revealed Acinetobacter baumannii New insights into (2007) (0)
Organism-wide secretome mapping uncovers pathways of tissue crosstalk in exercise (2022) (0)
Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis (2019) (0)
The IgG Antibody Paradox in Insulin Resistance: Pathogenic and Therapeutic (2021) (0)
Long-Read Sequencing of Human Cytomegalovirus Transcriptome Reveals RNA Isoforms Carrying Distinct Coding Potentials (2017) (0)
Distinct factors associated with short-term and long-term weight loss induced by low-fat or low-carbohydrate diet intervention (2022) (0)
Effects of an immersive psychosocial training program on depression and well-being: A randomized clinical trial (2022) (0)
Simultaneous Profiling of Host Expression and Microbial Abundance by Spatial Meta-Transcriptome Sequencing (2022) (0)
variation in the genome MSB : A mean-shift-based approach for the analysis of structural (2008) (0)
Performance effectiveness of vital parameter combinations for early warning of sepsis—an exhaustive study using machine learning (2022) (0)
Abstract 10300: Crosstalk Between GATA4 and Mitochondria During Cardiomyocyte Differentiation Upon Exposure to Tyrosine Kinase Inhibitors (2018) (0)
Remodeling of active endothelial enhancers is associated with aberrant gene-regulatory networks in pulmonary arterial hypertension (2020) (0)
Adverse childhood experiences, diabetes and associated conditions, preventive care practices and health care access: A population-based study (0)
genome Structured RNAs in the ENCODE selected regions of the human Related Content (2007) (0)
Challenging obesity and sex based differences in resting energy expenditure using allometric modeling, a sub-study of the DIETFITS clinical trial. (2022) (0)
Leveraging Physiology and Artificial Intelligence to Deliver Advancements in Healthcare. (2023) (0)
SAT-LB25 A Multi-Omics Analysis of Advanced Papillary Thyroid Cancer (2020) (0)
The Roles and Mechanisms of Gut Microbiota in Food Allergy (2023) (0)
Transcriptomewidesurvey of pseudorabies virususing next- and third-generationsequencing platforms (2018) (0)
Abstract 5640: Mono-allelic immunopeptidomics data from 109 MHC-I alleles reveals variability in binding preferences and improves neoantigen prediction algorithm (2022) (0)
Achieving high-sensitivity for clinical applications using augmented exome sequencing (2015) (0)
Divergent patterns of selection on metabolite levels and gene expression (2021) (0)
Template-switching artifacts resemble alternative polyadenylation (2019) (0)
Robust prediction of response to immunotherapy in a mixed cohort of previously treated and immunotherapy-naive melanoma patients. (2021) (0)
EXTENSIVELY VALIDATED HLA LOH ALGORITHM DEMONSTRATES AN ASSOCIATION BETWEEN HLA LOH AND GENOMIC INSTABILITY (2021) (0)
Design Issues inImplementing aPortable SampleTracking andAnalysis Research Support (STARS) System forPCRBasedMicroarray Research (2006) (0)
Clustering reveals ubiquitous heterogeneity and asymmetry of genomic signals at functional elements (2013) (0)
Exome sequencing and genome-wide copy number variant mapping reveal novel associations with sensorineural hereditary hearing loss (2014) (0)
Quantifying and Improving Clinical-grade Coverage and Accuracy using Augmented Exome Sequencing (2015) (0)
79 Extensively validated HLA LOH algorithm demonstrates an association between HLA LOH and genomic instability (2021) (0)
A Machine-Curated Database of Genome-Wide 1 Association Studies 2 (2018) (0)
Precision neoantigen discovery using large-scale immunopeptidomes and composite modeling of MHC peptide presentation. (2023) (0)
Whole Genome Sequence Analysis of Primary Myelofibrosis. (2012) (0)
Is this really the end? Template-switching artifacts resemble alternative polyadenylation (2019) (0)
Demand for Multiplatform and Meta-analytic Approaches in Transcriptome Profiling (2019) (0)
Effects of Habitual Sleep on Glucose Regulation in Individuals at Risk for Type 2 Diabetes (2020) (0)
591-P: Glucose Dynamics during OGTT Identify Metabolic Subphenotypes in Individuals with Glucose Dysregulation (2021) (0)
Abstract 3899: Integrating RNA/DNA analysis with a comprehensive cancer panel to improve interpretations of stage four metastatic renal cell carcinoma (2015) (0)
transcript within the human HOXA cluster A myelopoiesis-associated regulatory intergenic non-coding RNA (2009) (0)
61-OR: Machine Learning Framework Predicts Metabolic Subphenotypes Using Glucose Dynamics during Oral Glucose Tolerance Test (2022) (0)
loci ENCODE regions : Associating transcription with known and novel The DART classification of unannotated transcription within the Material Supplemental (2007) (0)
161-OR: Cognitive Impairment in Individuals with Post-Bariatric Hypoglycemia (2022) (0)
Meal Timing-Based Dietary Patterns Are Associated With Glucose Regulation, Insulin Resistance, and Incretin Effect in Individuals at Risk for Type 2 Diabetes (2021) (0)
regulatory elements in the ENCODE regions Statistical analysis of the genomic distribution and correlation of Material Supplemental (2007) (0)
Whole-exome sequencing data of suicide victims who had suffered from major depressive disorder (2019) (0)
Functional characterization of GWAS loci associated with fracture risk (2013) (0)
Low expression of EXOSC2 protects against clinical COVID-19 and impedes SARS-CoV-2 replication (2022) (0)
University of Groningen Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci Tragante, (2014) (0)
High-Coverage Whole-Exome Sequencing Identifies Candidate Genes for Suicide in Victims with Major Depressive Disorder (2017) (0)
Korbel Human Genome Paired-End Mapping Reveals Extensive Structural Variation in the (2012) (0)
Systems analysis of de novo mutations in congenital heart diseases identified a protein network in the hypoplastic left heart syndrome. (2022) (0)
A machine-compiled database of genome-wide association studies (2019) (0)
Resource Large-Scale Analyses of HumanMicrobiomes Reveal Thousands of Small , Novel Genes Graphical (2019) (0)
De novo and rare mutations in the HSPA1L heat shock gene associated with inflammatory bowel disease (2017) (0)
A vast resource of allelic expression data spanning human tissues (2020) (0)
Identification of Transcription Factor CEH-30::GFP Binding Regions in Late Embyros (2011) (0)
Abstract 13600: RNAseq Analysis of Pulmonary Arterial Endothelial Cells from Patients with Idiopathic Pulmonary Arterial Hypertension Reveals Dysregulation of Angiogenic Factors (2012) (0)
Clonal haematopoiesis and risk of chronic liver disease (2023) (0)
Genetic and non-genetic factors affecting the expression of COVID-19-relevant genes in the large airway epithelium (2021) (0)
The genetic basis of cross-phenotype correlation with bone fracture risk: the GEFOS consortium (2013) (0)
Variant-specific inflation factors for assessing population stratification at the phenotypic variance level (2021) (0)
SA94MACHINE LEARNING ANALYSIS OF ULTRA-DEEP WHOLE-GENOME SEQUENCING IN HUMAN BRAIN REVEALS SOMATIC GENOMIC RETROTRANSPOSITION IN GLIA AS WELL AS IN NEURONS (2019) (0)
Systematic screening for environmental and behavioral determinants identifies factors detrimental to skeletal health (2017) (0)
Author Correction: Inherited causes of clonal haematopoiesis in 97,691 whole genomes (2021) (0)
Title: Multiomics Longitudinal Modeling of Preeclamptic Pregnancies (2021) (0)
Classification of human genomic regions based on experimentally determined binding sites of more than 100 transcription-related factors (2012) (0)
Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale (2020) (0)
Evaluation of whole exome sequencing as an alternative to BeadChip and whole genome sequencing in human population genetic analysis (2018) (0)
Abstract B2-42: Systematic dissection of multi-scale mutational hotspots across 21 cancer types reveals a rich landscape of functionally targeted oncogenic disruptions (2015) (0)
mTOR-Mediated Dedifferentiation of the RPE Initiates Photoreceptor Degeneration (2011) (0)
Heterochronic Parabiosis Rejuvenates Aged Bones (2014) (0)
Analysis of Health Using Advanced Technologies. (2019) (0)
Data Descriptor: Whole-exome sequencing data of suicide victims who had suffered from major depressive disorder (2019) (0)
Multiomic identification of key transcriptional regulatory programs during endurance exercise training (2023) (0)
Tomoichiro Miyoshi Length Fission Yeast Pot 1-Tpp 1 Protects Telomeres and Regulates Telomere (2014) (0)
Dual Isoform Sequencing Reveals a Multifaceted Transcriptional Architecture of a Prototype Baculovirus (2021) (0)
Abstract 97: Epigenetic Signatures Contribute to the Superior Endothelial Cell Identity in Human Induced Pluripotent Stem Cells Derived From Endothelial Cells (2015) (0)
Global Analysis of Gene Networks Involved in Hematopoiesis. (2004) (0)
Scientists find new, rare mutations linked to inflammatory bowel disease (2021) (0)
Pooled Short Hairpin (shRNA) Library Screen Coupled with Next-Generation Sequencing Efficiently Uncover Transcriptional Network in Neural Lineage Development of Human Embryonic Stem Cells (P02.016) (2012) (0)
human genome Linking disease associations with regulatory information in the Material Supplemental (2012) (0)
Embryonic Stem Cells: Discovery, Development, and Current Trends (2011) (0)
Topological organization and dynamic regulation of human tRNA genes during macrophage differentiation (2017) (0)
62 Proteomic screening for plasma autoantibody biomarkers in MDS using protein microarrays (2011) (0)
AdaTiSS: a novel data-Adaptive robust method for identifying Tissue Specificity Scores (2021) (0)
Wnt Signaling Interactor WTIP (Wilms Tumor Interacting Protein) Underlies Novel Mechanism for Cardiac Hypertrophy (2022) (0)
Lipidomic profiling reveals age-dependent changes in complex plasma membrane lipids that regulate neural stem cell aging (2022) (0)
Michael Snyder (2012) (0)
Disruption of mesoderm formation during cardiac differentiation due to developmental exposure to 13-cis-retinoic acid (2018) (0)
Abstract 19076: ATAC-seq Implicates Epigenome-wide CTCF Dissociation in the Progression of Cardiac Ischemia (2015) (0)
Genome interpretation and assembly-recent progress and next steps. (2012) (0)
Ning Sun Dilated Cardiomyopathy Patient-Specific Induced Pluripotent Stem Cells as a Model for Familial (2012) (0)
Abstract 248: Aberrant TGFβ Signaling as an Etiology of Left Ventricular Non-compaction Cardiomyopathy (2015) (0)
Author Correction: Perspectives on ENCODE (2022) (0)
Author Correction: Perspectives on ENCODE (2022) (0)
Unraveling the Molecular Basis of Lung Adenocarcinoma Dedifferentiation and Prognosis by Integrating Omics and Histopathology (2018) (0)
Abstract 235: Hypertrophic Cardiomyopathy, a Disease of Altered Cardiac Energetics (2020) (0)
Matrix stiffness induces a tumorigenic phenotype in mammary epithelium through changes in chromatin accessibility (2019) (0)
Supplemental Information SETD 7 Drives Cardiac Lineage Commitment through Stage-Speci fi c Transcriptional Activation (2018) (0)
Author Correction: Perspectives on ENCODE (2022) (0)
Transcriptomic and epigenomic differences in human induced pluripotent stem cells generated from six reprogramming methods (2017) (0)
Genome-wide effects of social status on DNA methylation in the brain of a cichlid fish, Astatotilapia burtoni (2019) (0)
Stem cell plasticity, acetylation of H3K14, and de novo gene activation rely on KAT7. (2023) (0)
Global loss of fine-scale chromatin architecture and rebalancing of gene expression during early colorectal cancer development (2022) (0)
An exercise-inducible metabolite that suppresses feeding and obesity (2022) (0)
THEME 1 EPIDEMIOLOGY AND INFORMATICS EPI-01 Unbiased metabolomics by Mendelian randomisation links serum isoleucine to risk of amyotrophic lateral sclerosis (0)
Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes (2022) (0)
Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes (2022) (0)
Identification of end‐stage renal disease metabolic signatures from human perspiration (2023) (0)
Extensive dynamic changes in omics profiles during normal and disease states (2012) (0)
Abstract 3497: The polyclonal path to malignant transformation in familial adenomatous polyposis (2023) (0)
Systematic evaluation of the impact of ChIP-seq read designs on genome coverage, peak identification, and allele-specific binding detection (2016) (0)
Proinflammatory polarization of monocytes by particulate air pollutants is mediated by induction of trained immunity in pediatric asthma. (2023) (0)
Correction (2013) (0)
Abstract 12501: Abnormal Activation of TGFβ Signaling as a Pathogenesis of Left Ventricular Non-compaction Cardiomyopathy (2015) (0)
Abstract 289: Transcriptomic Analysis of Inter- and Intra-patient Variation in Human iPSCs: Platform for Precision Medicine to Predict Drug Toxicity (2016) (0)
Gaining comprehensive biological insight into the transcriptome by performing a broad-spectrum RNA-seq analysis (2017) (0)
Design of a Lunar Rover Utilizing Hydrogen-Oxygen Fuel Cell Technologies (2011) (0)
Circular DNA elements of chromosomal origin are common in healthy human somatic tissue (2018) (0)
Decoding personal biotic and abiotic airborne exposome (2021) (0)
Organism-wide, cell-type-specific secretome mapping of exercise training in mice. (2023) (0)
Mitochondrial function determines severity but not risk of amyotrophic lateral sclerosis (2022) (0)
Integration of spatial and single-cell data across modalities with weak linkage (2023) (0)
DSIF modulates RNA polymerase II occupancy according to template G + C content (2022) (0)
Acetyl-Click Screening Platform Identifies Small-Molecule Inhibitors of Histone Acetyltransferase 1 (HAT1). (2023) (0)
Abstract 15020: Transcriptomic and Epigenomic Resemblance of Terminally Differentiated Cells Derived From Isogenic Human iPSCs and Nuclear Transfer Derived ESCs (2016) (0)
Gpr124 is essential for blood–brain barrier integrity in central nervous system disease (2017) (0)
Macrophage de novo NAD+ synthesis specifies immune function in aging and inflammation (2018) (0)
Reply to ‘Lactate as a major myokine and exerkine’ (2022) (0)
Association of AHSG with alopecia and mental retardation (APMR) syndrome (2017) (0)
Isolated Congenital Anosmia and CNGA2 Mutation (2017) (0)
E-GEOD-25800.processed.1.zip (2011) (0)
regulation upon interferon treatments Global changes in STAT target selection and transcription data (2005) (0)
Enhancing GTEx by bridging the gaps between genotype, gene expression, and disease (2017) (0)
E-GEOD-25798.additional.1.zip (2011) (0)
Transcription interference networks examined by single molecule long read sequencing technology (2015) (0)
Lifelong physical activity is associated with promoter hypomethylation of genes involved in metabolism, myogenesis, contractile properties and oxidative stress resistance in aged human skeletal muscle (2019) (0)
High-Resolution Whole-Genome Mapping of the Piwi/piRNA-Mediated Epigenetic Pathway in Drosophila (2009) (0)
Author response: Comment on 'AIRE-deficient patients harbor unique high-affinity disease-ameliorating autoantibodies' (2019) (0)
throughput sequencing and array data by integrating conservation , secondary structure and high Prediction and characterization of non-coding RNAs in C . elegans (2010) (0)
Cross-Platform Comparison of Untargeted and Targeted Lipidomics Approaches on Aging Mouse Plasma (2018) (0)
Erratum: Regulatory analysis of the C. elegans genome with spatiotemporal resolution (Nature (2014) 512 (400-405) DOI:10.1038/nature13497) (2015) (0)
Mining biological complexity: cross integration of large-scale metagenomics, environmental, and chemical datasets (2009) (0)
Scientists � nd new , rare mutations linked to in � ammatory bowel disease (2021) (0)
Genomics and Proteomics Issue: Introduction (2007) (0)
Analysis of Genomic Enrichment ( STAGE ) Mapping the chromosomal targets of STAT 1 by Sequence Tag data (2007) (0)
An Integrated Understand ing of the Rapid Metabolic Benefits of a Carbohydrate-Restricted Diet on Hepatic Steatosis in Humans Graphical (2018) (0)
The Out of Africa expansion affected accumulation of deleterious alleles in human genomes (2015) (0)
CL-01 Translation of Clinical Proteomics : Opportunities and Challenges (2013) (0)
Predicting essential genes in fungal genomes data (2006) (0)
Comprehensive Longitudinal Multi-omic Profiling in Weight Gain and Insulin Resistance (2016) (0)
RNA-Seq transcriptomics (2012) (0)
Robust identification of temporal biomarkers in longitudinal omics studies (2021) (0)
The International Genomics & Translational Research in Transplantation Network (iGeneTrain).: Abstract# A521 (2014) (0)
An Integrated Sequencing Approach for Updating of Pseudorabies Virus Transcriptome (2020) (0)

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