Steven E. Brenner | Academic Influence

Steven E. Brenner's AcademicInfluence.com Rankings

Steven E. Brenner

Biology

#1043

World Rank

#1800

Historical Rank

Computational Biology

#47

World Rank

#47

Historical Rank

biology Degrees

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Biology

Steven E. Brenner's Degrees

PhD Biophysics Stanford University

Why Is Steven E. Brenner Influential?

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According to Wikipedia, Steven Elliot Brenner is a professor at the Department of Plant and Microbial Biology at the University of California Berkeley, adjunct professor at the Department of Bioengineering and Therapeutic Sciences at the University of California, and San Francisco Faculty scientist, Physical Biosciences at the Lawrence Berkeley National Laboratory.

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Steven E. Brenner'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

WebLogo: a sequence logo generator. (2004) (10269)
SCOP: a structural classification of proteins database for the investigation of sequences and structures. (1995) (6550)
The Transcriptional Landscape of the Mammalian Genome (2005) (3394)
The Bioperl toolkit: Perl modules for the life sciences. (2002) (1700)
Identification of Functional Elements and Regulatory Circuits by Drosophila modENCODE (2010) (1211)
Evidence for the widespread coupling of alternative splicing and nonsense-mediated mRNA decay in humans (2002) (1015)
Data growth and its impact on the SCOP database: new developments (2007) (985)
SCOP database in 2004: refinements integrate structure and sequence family data (2004) (970)
SCOP: a structural classification of proteins database (1998) (859)
The Sorcerer II Global Ocean Sampling Expedition: Expanding the Universe of Protein Families (2007) (855)
A large-scale evaluation of computational protein function prediction (2013) (784)
The Developmental Transcriptome of Drosophila melanogaster (2010) (766)
Biases in Illumina transcriptome sequencing caused by random hexamer priming (2010) (695)
KBase: The United States Department of Energy Systems Biology Knowledgebase (2018) (659)
SCOPe: Structural Classification of Proteins—extended, integrating SCOP and ASTRAL data and classification of new structures (2013) (617)
Unproductive splicing of SR genes associated with highly conserved and ultraconserved DNA elements (2007) (605)
The ASTRAL Compendium in 2004 (2003) (581)
Assessing sequence comparison methods with reliable structurally identified distant evolutionary relationships. (1998) (534)
The ASTRAL compendium for protein structure and sequence analysis (2000) (514)
SCOP database in 2002: refinements accommodate structural genomics (2002) (509)
The Impact of Structural Genomics: Expectations and Outcomes (2005) (388)
Errors in genome annotation. (1999) (367)
The evolving roles of alternative splicing. (2004) (324)
An expanded evaluation of protein function prediction methods shows an improvement in accuracy (2016) (316)
Selection of primers for optimal taxonomic classification of environmental 16S rRNA gene sequences (2012) (311)
Comparative Analysis of the Transcriptome across Distant Species (2014) (268)
SCOP: a Structural Classification of Proteins database (1999) (254)
Conservation of an RNA regulatory map between Drosophila and mammals. (2011) (246)
WebLogo: A sequence logo generator, Genome Research, (2004) (237)
The coupling of alternative splicing and nonsense-mediated mRNA decay. (2007) (236)
The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens (2019) (219)
Protein Molecular Function Prediction by Bayesian Phylogenomics (2005) (205)
Recommendations for application of the functional evidence PS3/BS3 criterion using the ACMG/AMP sequence variant interpretation framework (2019) (202)
RNA structural motifs: building blocks of a modular biomolecule (2005) (199)
An unappreciated role for RNA surveillance (2004) (194)
Widespread predicted nonsense-mediated mRNA decay of alternatively-spliced transcripts of human normal and disease genes (2003) (191)
Distribution of protein folds in the three superkingdoms of life. (1999) (183)
A tour of structural genomics (2001) (179)
Comparative analysis of regulatory information and circuits across distant species (2014) (177)
Population statistics of protein structures: lessons from structural classifications. (1997) (171)
Newborn Sequencing in Genomic Medicine and Public Health (2017) (163)
ASTRAL compendium enhancements (2002) (150)
SCOP: a Structural Classification of Proteins database (2000) (140)
The COMBREX Project: Design, Methodology, and Initial Results (2013) (137)
Global analysis of positive and negative pre-mRNA splicing regulators in Drosophila. (2005) (136)
Outcome of a workshop on applications of protein models in biomedical research. (2009) (129)
Regulation of Splicing Factors by Alternative Splicing and NMD Is Conserved between Kingdoms Yet Evolutionarily Flexible (2015) (125)
Target selection for structural genomics (2000) (123)
SCOR: a Structural Classification of RNA database (2002) (122)
Hypothesis: decreased use of pediatric aspirin has contributed to the increasing prevalence of childhood asthma. (1998) (118)
SCOR: Structural Classification of RNA, version 2.0 (2004) (111)
Understanding protein structure: using scop for fold interpretation. (1996) (110)
Expectations from structural genomics (2008) (108)
Sulfotransferases and sulfatases in mycobacteria. (2002) (99)
SCOPe: classification of large macromolecular structures in the structural classification of proteins—extended database (2018) (98)
Protein folds in the all-beta and all-alpha classes. (1997) (97)
DNA recognition code of transcription factors. (1995) (95)
Association of gut microbiota with post-operative clinical course in Crohn’s disease (2013) (93)
WebLogo: A sequence logo generator - eScholarship (2004) (92)
Comparison of D. melanogaster and C. elegans developmental stages, tissues, and cells by modENCODE RNA-seq data (2014) (91)
Genome-Wide Identification of Alternative Splice Forms Down-Regulated by Nonsense-Mediated mRNA Decay in Drosophila (2009) (91)
The role of exome sequencing in newborn screening for inborn errors of metabolism (2020) (89)
Genome-wide analysis of alternative pre-mRNA splicing and RNA-binding specificities of the Drosophila hnRNP A/B family members. (2009) (89)
Gene duplications in H. influenzae (1995) (86)
Protein secondary structure: entropy, correlations and prediction. (2003) (85)
SCOPe: Manual Curation and Artifact Removal in the Structural Classification of Proteins - extended Database. (2017) (84)
Combined Immunodeficiency Due to MALT1 Mutations, Treated by Hematopoietic Cell Transplantation (2015) (81)
Newborn Screening for SCID Identifies Patients with Ataxia Telangiectasia (2012) (79)
Multisystem Anomalies in Severe Combined Immunodeficiency with Mutant BCL11B. (2016) (79)
The RNA Ontology Consortium: an open invitation to the RNA community. (2006) (78)
Regulation of alternative splicing in Drosophila by 56 RNA binding proteins (2015) (76)
Implications of structural genomics target selection strategies: Pfam5000, whole genome, and random approaches (2004) (70)
Three-dimensional motifs from the SCOR, structural classification of RNA database: extruded strands, base triples, tetraloops and U-turns. (2004) (67)
A novel human autoimmune syndrome caused by combined hypomorphic and activating mutations in ZAP-70 (2016) (65)
MeRNA: a database of metal ion binding sites in RNA structures (2005) (64)
The DOE Systems Biology Knowledgebase (KBase) (2016) (63)
Genome-wide analysis reveals an unexpected function for the Drosophila splicing factor U2AF50 in the nuclear export of intronless mRNAs. (2004) (63)
Genome-scale phylogenetic function annotation of large and diverse protein families. (2011) (59)
A method for the alignment of heterogeneous macromolecules from electron microscopy. (2009) (53)
Bootstrapping and normalization for enhanced evaluations of pairwise sequence comparison (2002) (48)
Planning the Human Variome Project: The Spain report (2009) (48)
Reports from CAGI: The Critical Assessment of Genome Interpretation (2017) (47)
The PRESAGE database for structural genomics (1999) (47)
The evolution of function within the Nudix homology clan (2017) (45)
Measurements of protein sequence–structure correlations (2004) (44)
The increase in allergic respiratory diseases: survival of the fittest? (2002) (43)
SIFTER search: a web server for accurate phylogeny-based protein function prediction (2015) (42)
SCOP, Structural Classification of Proteins database: applications to evaluation of the effectiveness of sequence alignment methods and statistics of protein structural data. (1998) (41)
PLoS Computational Biology: A New Community Journal (2005) (41)
Survey of large protein complexes in D. vulgaris reveals great structural diversity (2009) (38)
Automated multi-model reconstruction from single-particle electron microscopy data. (2010) (37)
A generalized affine gap model significantly improves protein sequence alignment accuracy (2004) (37)
Working toward precision medicine: Predicting phenotypes from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges (2017) (36)
Reports from the fifth edition of CAGI: The Critical Assessment of Genome Interpretation (2019) (35)
Statistical evaluation of pairwise protein sequence comparison with the Bayesian bootstrap (2005) (34)
Classification of multi‐helical DNA‐binding domains and application to predict the DBD structures of σ factor, LysR, OmpR/PhoB, CENP‐B, Rap1, and XylS/Ada/AraC (1995) (33)
Computational prediction of membrane-tethered transcription factors (2001) (32)
Transcriptomic variation of pharmacogenes in multiple human tissues and lymphoblastoid cell lines (2016) (31)
Common sense for our genomes (2007) (29)
Target selection and deselection at the Berkeley Structural Genomics Center (2005) (29)
An immunologic mechanism for the association between obesity and asthma. (2000) (28)
Structural Genomics of Minimal Organisms and Protein Fold Space (2005) (26)
A novel plant enzyme with dual activity: an atypical Nudix hydrolase and a dipeptidyl peptidase III (2017) (26)
Be prepared for the big genome leak (2013) (26)
A graphical model for predicting protein molecular function (2006) (25)
Registered access: authorizing data access (2018) (25)
SCOPe: improvements to the structural classification of proteins – extended database to facilitate variant interpretation and machine learning (2021) (25)
Personalized medicine: from genotypes, molecular phenotypes and the quantified self, towards improved medicine. (2014) (25)
Structural studies of the Nudix hydrolase DR1025 from Deinococcus radiodurans and its ligand complexes. (2004) (25)
High-throughput Isolation and Characterization of Untagged Membrane Protein Complexes: Outer Membrane Complexes of Desulfovibrio vulgaris (2012) (25)
Opportunities and challenges for the computational interpretation of rare variation in clinically important genes (2021) (24)
Nijmegen Breakage Syndrome Detected by Newborn Screening for T Cell Receptor Excision Circles (TRECs) (2015) (24)
An alternative model of amino acid replacement (2004) (23)
StrVCTVRE: A supervised learning method to predict the pathogenicity of human genome structural variants (2020) (22)
Regulation of Gene Expression by Coupling of Alternative Splicing and NMD (2013) (21)
Using metabolic pathway databases for functional annotation. (1998) (20)
VIPdb, a genetic Variant Impact Predictor Database (2019) (20)
Putting benchmarks in their rightful place: The heart of computational biology (2018) (20)
The value of protein structure classification information—Surveying the scientific literature (2015) (19)
Multiple breast cancer risk variants are associated with differential transcript isoform expression in tumors (2015) (18)
Identification and experimental validation of splicing regulatory elements in Drosophila melanogaster reveals functionally conserved splicing enhancers in metazoans. (2011) (18)
Post-Transcriptional Gene Regulation: RNA-Protein Interactions, RNA Processing, mRNA Stability and Localization (2008) (18)
Pairwise alignment incorporating dipeptide covariation (2005) (17)
Application of full-genome analysis to diagnose rare monogenic disorders (2020) (17)
Serial segmental bronchoalveolar lavage in individual rats. (1999) (16)
Bacterial Interactomes: Interacting Protein Partners Share Similar Function and Are Validated in Independent Assays More Frequently Than Previously Reported* (2016) (15)
BLAST, Blitz, BLOCKS and BEAUTY: sequence comparison on the net. (1995) (15)
Evaluating the predictions of the protein stability change upon single amino acid substitutions for the FXN CAGI5 challenge (2019) (15)
Evidence-based calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for clinical use of PP3/BP4 criteria (2022) (15)
Practical database searching (1998) (14)
An SF1 affinity model to identify branch point sequences in human introns (2010) (14)
A quantitative methodology for the de novo design of proteins (1994) (13)
Phylogenetic molecular function annotation. (2009) (12)
The Early and Late Asthmatic Response to Allergen (2008) (11)
Predicting venous thromboembolism risk from exomes in the Critical Assessment of Genome Interpretation (CAGI) challenges (2019) (11)
Matching phenotypes to whole genomes: Lessons learned from four iterations of the personal genome project community challenges (2017) (11)
SCOP database in 2002 (2002) (10)
CAGI SickKids challenges: Assessment of phenotype and variant predictions derived from clinical and genomic data of children with undiagnosed diseases (2019) (10)
The Cyclooxygenase-2 Theory of Atopy and Asthma (1999) (10)
Quantitative Tagless Copurification: A Method to Validate and Identify Protein-Protein Interactions* (2016) (10)
Performance of in silico tools for the evaluation of p16INK4a (CDKN2A) variants in CAGI (2017) (10)
Population statistics of protein structures (1997) (10)
Substrate specificity characterization for eight putative nudix hydrolases. Evaluation of criteria for substrate identification within the Nudix family (2016) (9)
PRECISION MEDICINE: DATA AND DISCOVERY FOR IMPROVED HEALTH AND THERAPY. (2016) (8)
Assessing the performance of in silico methods for predicting the pathogenicity of variants in the gene CHEK2, among Hispanic females with breast cancer (2019) (8)
Performance of computational methods for the evaluation of pericentriolar material 1 missense variants in CAGI‐5 (2019) (8)
Alignment-free local structural search by writhe decomposition (2007) (8)
Introduction to Cgi/Perl: Getting Started With Web Scripts (1995) (7)
Genomic Analysis of Historical Cases with Positive Newborn Screens for Short-Chain Acyl-CoA Dehydrogenase Deficiency Shows That a Validated Second-Tier Biochemical Test Can Replace Future Sequencing (2020) (7)
Structural genomics and structural biology: compare and contrast (2004) (7)
The modENCODE Consortium modENCODE Drosophila Identification of Functional Elements and Regulatory Circuits (2011) (7)
Assessment of patient clinical descriptions and pathogenic variants from gene panel sequences in the CAGI‐5 intellectual disability challenge (2019) (7)
Molecular function prediction for a family exhibiting evolutionary tendencies toward substrate specificity swapping: Recurrence of tyrosine aminotransferase activity in the Iα subfamily (2013) (7)
Pathogenicity Interpretation in the Age of Precision Medicine: The 2015 Annual Scientific Meeting of the Human Genome Variation Society (2016) (6)
Assessing computational predictions of the phenotypic effect of cystathionine‐beta‐synthase variants (2019) (6)
PRECISION MEDICINE: DATA AND DISCOVERY FOR IMPROVED HEALTH AND THERAPY. (2017) (6)
Update on the Pfam5000 Strategy for Selection of Structural Genomics Targets (2005) (6)
Revealing molecular pathways for cancer cell fitness through a genetic screen of the cancer translatome (2021) (6)
Understanding protein structure (1996) (5)
Networks of Splice Factor Regulation by Unproductive Splicing Coupled With Nonsense Mediated mRNA Decay (2020) (5)
Assessment of predicted enzymatic activity of α‐N‐acetylglucosaminidase variants of unknown significance for CAGI 2016 (2019) (5)
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulation (2019) (5)
A novel PRRT2 pathogenic variant in a family with paroxysmal kinesigenic dyskinesia and benign familial infantile seizures (2018) (5)
A continuous fluorescence assay for the characterization of Nudix hydrolases (2013) (5)
Antioxidants and risk of Alzheimer disease. (2002) (5)
Beneficial effect of nonsteroidal anti-inflammatory drugs and cyclooxygenase-2 inhibitors in patients with asthma during viral infection. (2002) (5)
Newborn screening for neurodevelopmental diseases: Are we there yet? (2022) (4)
Automated particle correspondence and accurate tilt-axis detection in tilted-image pairs. (2014) (4)
PRECISION MEDICINE: FROM DIPLOTYPES TO DISPARITIES TOWARDS IMPROVED HEALTH AND THERAPIES. (2018) (4)
INFLAMMATORY MEDIATORS IN EXERCISE-INDUCED ASTHMA (1999) (4)
Transcriptome analysis of alternative splicing-coupled nonsense-mediated mRNA decay in human cells reveals broad regulatory potential (2020) (4)
Calibration of computational tools for missense variant pathogenicity classification and ClinGen recommendations for PP3/BP4 criteria (2022) (4)
Performance of in silico tools for the evaluation of p 16 INK 4 a ( CDKN 2 A ) variants in CAGI (2017) (3)
DNA from dried blood spots yields high quality sequences for exome analysis (2020) (3)
Personalized medicine: from genotypes and molecular phenotypes towards therapy- session introduction. (2013) (3)
Automobile traffic, atmospheric pollution, and childhood asthma. (2001) (3)
Perturbation robustness analyses reveal important parameters in variant interpretation pipelines (2020) (3)
Computational Structural Genomics of a Complete Minimal Organism (2002) (3)
Unproductive splicing of SR genes associated with highly-and ultraconserved DNA elements (2007) (3)
ANDY: a general, fault-tolerant tool for database searching on computer clusters (2005) (2)
When Biology Gets Personal: Hidden Challenges of Privacy and Ethics in Biological Big Data (2018) (2)
Protein Molecular Function Prediction (2005) (2)
Software Discovery Index Workshop Report (2015) (2)
Polysome fractionation analysis reveals features important for human nonsense-mediated mRNA decay (2020) (2)
Network sequence retrieval (1995) (2)
Use of Genome Data in Newborns as a Starting Point for Life-Long Precision Medicine (2016) (2)
Methods and tools for assessing the impact of genetic variations: The 2017 Annual Scientific Meeting of the Human Genome Variation Society (2018) (2)
Ten Years of PLoS‡ Computational Biology: A Decade of Appreciation and Innovation (2015) (2)
Dysregulation of hippocampal adult-born immature neurons disrupts a brain-wide network for spatial memory (2020) (2)
A bifunctional plant enzyme: an isopentenyl diphosphate hydrolase fused to a dipeptidyl peptidase III (2017) (1)
PERSONALIZED MEDICINE: FROM GENOTYPES AND MOLECULAR PHENOTYPES TOWARDS COMPUTED THERAPY. (2013) (1)
Quantitative tagless co-purification : a method to validate and identify protein-protein interactions (2016) (1)
A prototype computer system for de novo protein design. (1994) (1)
Computational Challenges and Artificial Intelligence in Precision Medicine (2020) (1)
PERSONALIZED MEDICINE: FROM GENOTYPES AND MOLECULAR PHENOTYPES TOWARDS COMPUTED THERAPY. (2011) (1)
Optimal and fast rotational alignment of volumes with missing data in Fourier space. (2013) (1)
Precision Medicine: Improving health through high-resolution analysis of personal data. (2018) (1)
A rust-fungus Nudix hydrolase effector decaps mRNA in vitro and interferes with plant immune pathways. (2023) (1)
SCOR : Structural Classi ® cation of RNA , version 2 . 0 (1)
Identification and annotation of genetic variants in the context of structure , function , and disease (2014) (1)
Sequences and topology: a decade of genomes (2005) (1)
PLOS Computational Biology 2017 Reviewer and Editorial Board Thank You (2018) (1)
PLOS Computational Biology 2016 Reviewer and Editorial Board Thank You (2017) (1)
Non‐Coding Variation: The 2016 Annual Scientific Meeting of the Human Genome Variation Society (2017) (1)
Methods and algorithms for the design of proteins (1994) (1)
An unappreciated role for RNA surveillance - eScholarship (2004) (1)
Meta-Align: A Novel HMM-based Algorithm for Pairwise Alignment of Error-Prone Sequencing Reads (2020) (1)
Another Good Reason to Live in Cleveland, Ohio (2006) (1)
Protein Design by Optimization of a Sequence-Structure Quality Function (1994) (1)
CAGI: The critical assessment of genome interpretation, a community experiment to evaluate phenotype prediction (2020) (1)
Re: Locke et al.— risk factors for irritable bowel syndrome (2000) (1)
An alternative explanation for the inverse relationship between atopy and myocardial infarction. (2013) (1)
A Specification for Defining and Annotating Regions of Macromolecular Structures (1995) (1)
REGULATORY RNA. (2016) (0)
FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulation (2019) (0)
Registered access: authorizing data access (2018) (0)
Crystal Structure of NUDIX HYDROLASE DR1025 FROM DEINOCOCCUS RADIODURANS (2004) (0)
Newborn Screening for SCID Identifies Patients with Ataxia Telangiectasia (2012) (0)
New Tools for Understanding, Composition and Dynamics of Microbial Communities, Project (2014) (0)
Precision Medicine: Using Artificial Intelligence to Improve Diagnostics and Healthcare. (2021) (0)
The Evolution of Function within the Nudix Superfamily: 46-PDB sequence alignment in FASTA format (2015) (0)
Curation and Artifact Removal in the Structural Classification of Proteins – extended Database ndonia (2016) (0)
Lawrence Berkeley National Laboratory Title The Sorcerer II Global Ocean Sampling Expedition : Expanding the Universe of Protein Families Permalink (2007) (0)
Back Cover, Volume 40, Issue 9 (2019) (0)
mammals and Drosophila Conservation of an RNA regulatory map between Material (2010) (0)
Faculty Opinions recommendation of Secondary structure switching in Cro protein evolution. (2004) (0)
Developing Computational Biology (2007) (0)
Novel Presentation of Recurrent Infection in a Family with NOD2 Mutation (2015) (0)
Paracetamol and asthma. (2000) (0)
Huxley, Thomas Henry (2001) (0)
Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders (2021) (0)
Genome annotation and protein structure (2002) (0)
Abstract LB-250: The Critical Assessment of Genome Interpretation: A community experiment that informs use of methods for germline cancer variant impact prediction (2020) (0)
Navigating ethical quandaries with the privacy dilemma of biomedical datasets (2019) (0)
Transcriptome Analysis Reveals Extensive Alternative Splicing-Coupled Nonsense-Mediated mRNA Decay in a Human Cell Line (2015) (0)
CRYSTAL STRUCTURE OF NUDIX HYDROLASE DR1025 IN COMPLEX WITH SM+3 (2004) (0)
Crick, Francis Harry Compton (2001) (0)
Interpreting new born genomes (2018) (0)
Session Introduction (2003) (0)
Running head: ANDY: database searching on computer clusters (2006) (0)
ClinVar and HGMD genomic variant classification accuracy has improved over time, as measured by implied disease burden (2022) (0)
Abstract 3295: CAGI: The Critical Assessment of Genome Interpretation, a community experiment to evaluate phenotype prediction: implications for predicting impact of variants in cancer (2018) (0)
Combined Immunodeficiency Due to MALT1 Mutations, Treated by Hematopoietic Cell Transplantation (2015) (0)
The role of exome sequencing in newborn screening for inborn errors of metabolism (2020) (0)
Characterization of Illumina Sequencing Errors: Implications for Investigations of the Gut Microbiota (2011) (0)
Regulatory RNA: Session Introduction (2016) (0)
Lawrence Berkeley National Laboratory Recent Work Title Quantitative tagless copurification : A method to validate and identify protein-protein interactions Permalink (2016) (0)
FISH (Fluorescent In Situ Hybridization) (2001) (0)
PERSONALIZED MEDICINE: FROM GENOTYPES AND MOLECULAR PHENOTYPES TOWARDS THERAPY. (2014) (0)
Revealing New Molecular Pathways for Cancer Cell Fitness Through a Genetic Screen of the Cancer Translatome (2020) (0)
Local Structural Comparison with Global Structural Descriptors (2006) (0)
CRYSTAL STRUCTURE OF THE NUDIX HYDROLASE DR1025 IN COMPLEX WITH ATP (2004) (0)
Precision Medicine: Addressing the Challenges of Sharing, Analysis, and Privacy at Scale. (2019) (0)
733 Angiodema—Unusual causes (1996) (0)
Biomedical research in the Cloud: considerations for researchers and organizations moving to (or adding) cloud computing resources. (2022) (0)
Hypothesis hygiene: Does atopy prevent infections? (2002) (0)
The Future of Genome-Based Medicine (2012) (0)
Session Introduction: Precision Medicine: Using Artificial Intelligence to Improve Diagnostics and Healthcare. (2023) (0)
splicing enhancers in metazoans reveals functionally conserved Drosophila melanogaster elements in Identification and experimental validation of splicing regulatory Material (2011) (0)
Title A continuous fluorescence assay for the characterization of Nudix hydrolases Permalink (2013) (0)
Figure 1, [Some alternatively spliced transcripts are...]. (2013) (0)
Opportunities and Challenges for Interpreting Rare Variation in Clinically Important Genes (2020) (0)
Sequences and topology: a decade of genomes Editorial overview (2005) (0)
Issue Information (2019) (0)
Pervasive unproductive splicing of SR proteins associated with ultraconserved elements (2004) (0)
ratssegmental bronchoalveolar lavage in individual (2015) (0)
Protein complex analysis project (PCAP): Project overview (2007) (0)
Title Regulation of alternative splicing in Drosophila by 56 RNA binding proteins (2015) (0)
Investigation of the causal etiology in a patient with T-B+NK+ immunodeficiency (2022) (0)
W1828 Studying the Intestinal Microbiome: Illumina Sequencing Technology Can Be Used to Accurately Classify Human Gut Samples With Moderate Taxonomic and Phylogenetic Resolution (2010) (0)
High Throughput Identification, Purification and Structural Characterization of Water Soluble Protein Complexes in Desulfovibrio vulgaris (2010) (0)
Publisher Correction: Application of full-genome analysis to diagnose rare monogenic disorders (2021) (0)
DBDS Workshop in Biostatistics and in pervasive population (2022) (0)
Social, Technical, and Ethical Challenges in Biomedical Data Privacy (2021) (0)
CRYSTAL STRUCTURE OF NUDIX HYDROLASE DR1025 IN COMPLEXED WITH GNP AND MG+2 (2004) (0)
Nijmegen Breakage Syndrome Detected by Newborn Screening for T Cell Receptor Excision Circles (TRECs) (2015) (0)
The CAFA challenge reports improved protein function prediction and new functional annotations for hundreds of genes through experimental screens (2019) (0)
The Evolution of Function within the Nudix Superfamily: Full Nudix clan alignment in FASTA format (2015) (0)
Crosstalk Sulfotransferases and Sulfatases in Mycobacteria (2002) (0)
Proposal SAMPLE 1 : Improved Scoring Schemes for Profile-HMMs applied to Protein Analysis (0)
Advair prevents alcohol-induced asthma (2003) (0)
Session Introduction: TOWARDS ETHICAL BIOMEDICAL INFORMATICS: LEARNING FROM OLELO NOEAU, HAWAIIAN PROVERBS. (2022) (0)

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