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425 PR articles • 43,575 PR citations • Sorted by year • Download PDF (PDF by citations)
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1Translocations can drive expression changes of multiple genes in regulons covering entire chromosome arms15.50Citations (PDF)
2Assessing the impact of interregional mobility on COVID19 spread in Spain using transfer entropy
Scientific Reports, 2025, 15,
3.40Citations (PDF)
3Patient stratification reveals the molecular basis of disease co-occurrences7.54Citations (PDF)
4UNCAN.eu: Toward a European Federated Cancer Research Data Hub
Cancer Discovery, 2024, 14, 30-35
25.14Citations (PDF)
5DIRECTEUR: transcriptome-based prediction of small molecules that replace transcription factors for direct cell conversion
Bioinformatics, 2024, 40,
4.70Citations (PDF)
6Drug-target identification in COVID-19 disease mechanisms using computational systems biology approaches4.914Citations (PDF)
7Rare disease research workflow using multilayer networks elucidates the molecular determinants of severity in Congenital Myasthenic Syndromes13.714Citations (PDF)
8Immunization with V987H-stabilized Spike glycoprotein protects K18-hACE2 mice and golden Syrian hamsters upon SARS-CoV-2 infection13.71Citations (PDF)
9Frustraevo: a web server to localize and quantify the conservation of local energetic frustration in protein families
Nucleic Acids Research, 2024, 52, W233-W237
15.56Citations (PDF)
10p53 rapidly restructures 3D chromatin organization to trigger a transcriptional response13.725Citations (PDF)
113Dmapper: a command line tool for BioBank-scale mapping of variants to protein structures
Bioinformatics, 2024, 40,
4.70Citations (PDF)
12Lung Tissue Multilayer Network Analysis Uncovers the Molecular Heterogeneity of Chronic Obstructive Pulmonary Disease8.914Citations (PDF)
13Prevalence and differences in the co-administration of drugs known to interact: an analysis of three distinct and large populations
BMC Medicine, 2024, 22,
7.113Citations (PDF)
14Gene set proximity analysis: expanding gene set enrichment analysis through learned geometric embeddings, with drug-repurposing applications in COVID-19
Bioinformatics, 2023, 39,
4.710Citations (PDF)
15CanMethdb: a database for genome-wide DNA methylation annotation in cancers
Bioinformatics, 2023, 39,
4.75Citations (PDF)
16Efficient querying of genomic reference databases with gget
Bioinformatics, 2023, 39,
4.731Citations (PDF)
17CATHe: detection of remote homologues for CATH superfamilies using embeddings from protein language models
Bioinformatics, 2023, 39,
4.736Citations (PDF)
18Low input capture Hi-C (liCHi-C) identifies promoter-enhancer interactions at high-resolution13.717Citations (PDF)
19PANACEA: network-based methods for pharmacotherapy prioritization in personalized oncology
Bioinformatics, 2023, 39,
4.73Citations (PDF)
20Predicting protein stability changes upon mutation using a simple orientational potential
Bioinformatics, 2023, 39,
4.724Citations (PDF)
21LEGO-CSM: a tool for functional characterization of proteins
Bioinformatics, 2023, 39,
4.72Citations (PDF)
22Molecular bases of comorbidities: present and future perspectives
Trends in Genetics, 2023, 39, 773-786
9.815Citations (PDF)
23PC_ali: a tool for improved multiple alignments and evolutionary inference based on a hybrid protein sequence and structure similarity score
Bioinformatics, 2023, 39,
4.75Citations (PDF)
24PhysiBoSS 2.0: a sustainable integration of stochastic Boolean and agent-based modelling frameworks2.933Citations (PDF)
25Overview of DrugProt task at BioCreative VII: data and methods for large-scale text mining and knowledge graph generation of heterogenous chemical–protein relations2.722Citations (PDF)
26The PENGUIN approach to reconstruct protein interactions at enhancer-promoter regions and its application to prostate cancer13.71Citations (PDF)
27Local energetic frustration conservation in protein families and superfamilies13.739Citations (PDF)
28Limits and potential of combined folding and docking
Bioinformatics, 2022, 38, 954-961
4.720Citations (PDF)
29The structural coverage of the human proteome before and after AlphaFold
PLoS Computational Biology, 2022, 18, e1009818
3.1121Citations (PDF)
30Plotgardener: cultivating precise multi-panel figures in R
Bioinformatics, 2022, 38, 2042-2045
4.7116Citations (PDF)
31ExTRI: Extraction of transcription regulation interactions from literature2.414Citations (PDF)
32Parallel model exploration for tumor treatment simulations
Computational Intelligence, 2022, 38, 1379-1401
1.912Citations (PDF)
33Optimizing Dosage-Specific Treatments in a Multi-Scale Model of a Tumor Growth3.510Citations (PDF)
34Mortality in Persons With Autism Spectrum Disorder or Attention-Deficit/Hyperactivity Disorder
JAMA Pediatrics, 2022, 176, e216401
8.6114Citations (PDF)
35Detection of oncogenic and clinically actionable mutations in cancer genomes critically depends on variant calling tools
Bioinformatics, 2022, 38, 3181-3191
4.722Citations (PDF)
36Design and methodological characteristics of studies using observational routinely collected health data for investigating the link between cancer and neurodegenerative diseases: protocol for a meta-research study
BMJ Open, 2022, 12, e058738
1.91Citations (PDF)
37Evaluating the policy of closing bars and restaurants in Cataluña and its effects on mobility and COVID19 incidence
Scientific Reports, 2022, 12,
3.410Citations (PDF)
38TVAR: assessing tissue-specific functional effects of non-coding variants with deep learning
Bioinformatics, 2022, 38, 4697-4704
4.75Citations (PDF)
39A structural biology community assessment of AlphaFold2 applications8.8562Citations (PDF)
403D chromatin connectivity underlies replication origin efficiency in mouse embryonic stem cells
Nucleic Acids Research, 2022, 50, 12149-12165
15.515Citations (PDF)
41IntAPT: integrated assembly of phenotype-specific transcripts from multiple RNA-seq profiles
Bioinformatics, 2021, 37, 650-658
4.71Citations (PDF)
42Classification in biological networks with hypergraphlet kernels
Bioinformatics, 2021, 37, 1000-1007
4.724Citations (PDF)
43STAG2 loss-of-function affects short-range genomic contacts and modulates the basal-luminal transcriptional program of bladder cancer cells
Nucleic Acids Research, 2021, 49, 11005-11021
15.529Citations (PDF)
44Simulating SARS-CoV-2 epidemics by region-specific variables and modeling contact tracing app containment10.431Citations (PDF)
45Unraveling the molecular basis of host cell receptor usage in SARS-CoV-2 and other human pathogenic β-CoVs3.95Citations (PDF)
46Artificial intelligence in cancer research: learning at different levels of data granularity
Molecular Oncology, 2021, 15, 817-829
4.132Citations (PDF)
47The eTRANSAFE Project on Translational Safety Assessment through Integrative Knowledge Management: Achievements and Perspectives
Pharmaceuticals, 2021, 14, 237
4.229Citations (PDF)
48Protein contact map refinement for improving structure prediction using generative adversarial networks
Bioinformatics, 2021, 37, 3168-3174
4.712Citations (PDF)
49The multilayer community structure of medulloblastoma
IScience, 2021, 24, 102365
3.69Citations (PDF)
50Visual exploration of large metabolic models
Bioinformatics, 2021, 37, 4460-4468
4.79Citations (PDF)
51Mutational mechanisms shaping the coding and noncoding genome of germinal center derived B-cell lymphomas
Leukemia, 2021, 35, 2002-2016
7.752Citations (PDF)
52Transcriptomic and Genetic Associations between Alzheimer’s Disease, Parkinson’s Disease, and Cancer
Cancers, 2021, 13, 2990
3.834Citations (PDF)
53Computational analysis of sense-antisense chimeric transcripts reveals their potential regulatory features and the landscape of expression in human cells2.219Citations (PDF)
54Co-evolutionary distance predictions contain flexibility information
Bioinformatics, 2021, 38, 65-72
4.718Citations (PDF)
55Systems biology at the giga-scale: Large multiscale models of complex, heterogeneous multicellular systems1.440Citations (PDF)
56MAX mutant small-cell lung cancers exhibit impaired activities of MGA-dependent noncanonical polycomb repressive complex7.512Citations (PDF)
57Assessing the accuracy of contact and distance predictions in CASP142.620Citations (PDF)
58A catalogue of 863 Rett-syndrome-causing MECP2 mutations and lessons learned from data integration
Scientific Data, 2021, 8,
5.729Citations (PDF)
59COVID19 Disease Map, a computational knowledge repository of virus–host interaction mechanisms6.777Citations (PDF)
60VINYL: Variant prIoritizatioN bY survivaL analysis
Bioinformatics, 2021, 36, 5590-5599
4.75Citations (PDF)
61COVID-19 Flow-Maps an open geographic information system on COVID-19 and human mobility for Spain
Scientific Data, 2021, 8,
5.725Citations (PDF)
62iScore: a novel graph kernel-based function for scoring protein–protein docking models
Bioinformatics, 2020, 36, 112-121
4.775Citations (PDF)
63PDBe-KB: a community-driven resource for structural and functional annotations
Nucleic Acids Research, 2020, 48, D344-D353
15.5127Citations (PDF)
64On the inconsistent treatment of gene-protein-reaction rules in context-specific metabolic models
Bioinformatics, 2020, 36, 1986-1988
4.77Citations (PDF)
65cd2sbgnml: bidirectional conversion between CellDesigner and SBGN formats
Bioinformatics, 2020, 36, 2620-2622
4.710Citations (PDF)
66Towards FAIR principles for research software
Data Science, 2020, 3, 37-59
1.2233Citations (PDF)
67Expanded encyclopaedias of DNA elements in the human and mouse genomes
Nature, 2020, 583, 699-710
37.92,189Citations (PDF)
68Formal axioms in biomedical ontologies improve analysis and interpretation of associated data
Bioinformatics, 2020, 36, 2229-2236
4.716Citations (PDF)
69Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples13.744Citations (PDF)
70Sex differences in oncogenic mutational processes13.786Citations (PDF)
71Interpreting molecular similarity between patients as a determinant of disease comorbidity relationships13.731Citations (PDF)
72Sex and gender differences and biases in artificial intelligence for biomedicine and healthcare10.4420Citations (PDF)
73A user guide for the online exploration and visualization of PCAWG data13.733Citations (PDF)
74The ELIXIR Core Data Resources: fundamental infrastructure for the life sciences
Bioinformatics, 2020, 36, 2636-2642
4.766Citations (PDF)
75Reconstructing evolutionary trajectories of mutation signature activities in cancer using TrackSig13.745Citations (PDF)
76iPAC: a genome-guided assembler of isoforms via phasing and combing paths
Bioinformatics, 2020, 36, 2712-2717
4.75Citations (PDF)
77Heterogeneous networks integration for disease–gene prioritization with node kernels
Bioinformatics, 2020, 36, 2649-2656
4.723Citations (PDF)
78Genomic footprints of activated telomere maintenance mechanisms in cancer13.7118Citations (PDF)
79A deep learning system accurately classifies primary and metastatic cancers using passenger mutation patterns13.7195Citations (PDF)
80High-coverage whole-genome analysis of 1220 cancers reveals hundreds of genes deregulated by rearrangement-mediated cis-regulatory alterations13.768Citations (PDF)
81Combined burden and functional impact tests for cancer driver discovery using DriverPower13.755Citations (PDF)
82Integrative pathway enrichment analysis of multivariate omics data13.7209Citations (PDF)
83Divergent mutational processes distinguish hypoxic and normoxic tumours13.7129Citations (PDF)
84Inferring structural variant cancer cell fraction13.745Citations (PDF)
85Pathway and network analysis of more than 2500 whole cancer genomes13.799Citations (PDF)
86The evolutionary history of 2,658 cancers
Nature, 2020, 578, 122-128
37.9978Citations (PDF)
87Patterns of somatic structural variation in human cancer genomes
Nature, 2020, 578, 112-121
37.9797Citations (PDF)
88The repertoire of mutational signatures in human cancer
Nature, 2020, 578, 94-101
37.93,137Citations (PDF)
89Analyses of non-coding somatic drivers in 2,658 cancer whole genomes
Nature, 2020, 578, 102-111
37.9570Citations (PDF)
90Pan-cancer analysis of whole genomes
Nature, 2020, 578, 82-93
37.92,826Citations (PDF)
91Genomic basis for RNA alterations in cancer
Nature, 2020, 578, 129-136
37.9385Citations (PDF)
92The landscape of viral associations in human cancers
Nature Genetics, 2020, 52, 320-330
25.2349Citations (PDF)
93Pan-cancer analysis of whole genomes identifies driver rearrangements promoted by LINE-1 retrotransposition
Nature Genetics, 2020, 52, 306-319
25.2422Citations (PDF)
94Disruption of chromatin folding domains by somatic genomic rearrangements in human cancer
Nature Genetics, 2020, 52, 294-305
25.2262Citations (PDF)
95Comprehensive analysis of chromothripsis in 2,658 human cancers using whole-genome sequencing
Nature Genetics, 2020, 52, 331-341
25.2640Citations (PDF)
96Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis4.4172Citations (PDF)
97Understanding oncogenicity of cancer driver genes and mutations in the cancer genomics era
FEBS Letters, 2020, 594, 4233-4246
2.746Citations (PDF)
98Unveiling new disease, pathway, and gene associations via multi-scale neural network
PLoS ONE, 2020, 15, e0231059
2.321Citations (PDF)
99PathExt: a general framework for path-based mining of omics-integrated biological networks
Bioinformatics, 2020, 37, 1254-1262
4.718Citations (PDF)
100Butler enables rapid cloud-based analysis of thousands of human genomes
Nature Biotechnology, 2020, 38, 288-292
29.813Citations (PDF)
101Comprehensive molecular characterization of mitochondrial genomes in human cancers
Nature Genetics, 2020, 52, 342-352
25.2398Citations (PDF)
102CoMeBack: DNA methylation array data analysis for co-methylated regions
Bioinformatics, 2020, 36, 2675-2683
4.760Citations (PDF)
103The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research
F1000Research, 2020, 9, 1229
0.56Citations (PDF)
104COVID-19 and beyond: a call for action and audacious solidarity to all the citizens and nations, it is humanity’s fight
F1000Research, 2020, 9, 1130
0.53Citations (PDF)
105ECCB2020: the 19th European Conference on Computational Biology
Bioinformatics, 2020, 36, i569-i572
4.71Citations (PDF)
106BIPSPI: a method for the prediction of partner-specific protein–protein interfaces
Bioinformatics, 2019, 35, 470-477
4.794Citations (PDF)
107Random walk with restart on multiplex and heterogeneous biological networks
Bioinformatics, 2019, 35, 497-505
4.7287Citations (PDF)
108The bio.tools registry of software tools and data resources for the life sciences
Genome Biology, 2019, 20,
8.162Citations (PDF)
109Next generation community assessment of biomedical entity recognition web servers: metrics, performance, interoperability aspects of BeCalm5.44Citations (PDF)
110Leveraging European infrastructures to access 1 million human genomes by 2022
Nature Reviews Genetics, 2019, 20, 693-701
47.083Citations (PDF)
111Intronic CNVs and gene expression variation in human populations
PLoS Genetics, 2019, 15, e1007902
3.285Citations (PDF)
112Large-scale analysis of human gene expression variability associates highly variable drug targets with lower drug effectiveness and safety
Bioinformatics, 2019, 35, 3028-3037
4.732Citations (PDF)
113Molecular Inverse Comorbidity between Alzheimer’s Disease and Lung Cancer: New Insights from Matrix Factorization4.415Citations (PDF)
114Association of Anorexia Nervosa With Risk of Cancer
JAMA Network Open, 2019, 2, e195313
6.619Citations (PDF)
115vulcanSpot: a tool to prioritize therapeutic vulnerabilities in cancer
Bioinformatics, 2019, 35, 4846-4848
4.710Citations (PDF)
116Interactive Extreme-Scale Analytics: Towards Battling Cancer0.35Citations (PDF)
117AlphaFold at CASP13
Bioinformatics, 2019, 35, 4862-4865
4.7300Citations (PDF)
118ResPRE: high-accuracy protein contact prediction by coupling precision matrix with deep residual neural networks
Bioinformatics, 2019, 35, 4647-4655
4.7164Citations (PDF)
119Transcriptomic metaanalyses of autistic brains reveals shared gene expression and biological pathway abnormalities with cancer
Molecular Autism, 2019, 10,
4.443Citations (PDF)
120Big data analytics for personalized medicine6.8226Citations (PDF)
121Protein multiple alignments: sequence-based versus structure-based programs
Bioinformatics, 2019, 35, 3970-3980
4.741Citations (PDF)
122PhenoPro: a novel toolkit for assisting in the diagnosis of Mendelian disease
Bioinformatics, 2019, 35, 3559-3566
4.731Citations (PDF)
123Gene expression models based on transcription factor binding events confer insight into functional <i>cis</i>-regulatory variants
Bioinformatics, 2019, 35, 2610-2617
4.719Citations (PDF)
124Protein–protein interaction sites prediction by ensemble random forests with synthetic minority oversampling technique
Bioinformatics, 2019, 35, 2395-2402
4.7157Citations (PDF)
125Characterization and identification of long non-coding RNAs based on feature relationship
Bioinformatics, 2019, 35, 2949-2956
4.7114Citations (PDF)
126The EVcouplings Python framework for coevolutionary sequence analysis
Bioinformatics, 2019, 35, 1582-1584
4.7286Citations (PDF)
127A natural upper bound to the accuracy of predicting protein stability changes upon mutations
Bioinformatics, 2019, 35, 1513-1517
4.741Citations (PDF)
128ConDo: protein domain boundary prediction using coevolutionary information
Bioinformatics, 2019, 35, 2411-2417
4.722Citations (PDF)
129<i>De novo</i>pattern discovery enables robust assessment of functional consequences of non-coding variants
Bioinformatics, 2019, 35, 1453-1460
4.721Citations (PDF)
130Precision medicine needs pioneering clinical bioinformaticians
Briefings in Bioinformatics, 2019, 20, 752-766
6.651Citations (PDF)
131Enhancing protein fold determination by exploring the complementary information of chemical cross-linking and coevolutionary signals
Bioinformatics, 2018, 34, 2201-2208
4.718Citations (PDF)
132Co-complex protein membership evaluation using Maximum Entropy on GO ontology and InterPro annotation
Bioinformatics, 2018, 34, 1884-1892
4.721Citations (PDF)
133DeepSF: deep convolutional neural network for mapping protein sequences to folds
Bioinformatics, 2018, 34, 1295-1303
4.7167Citations (PDF)
134Epigenetic and Transcriptional Variability Shape Phenotypic Plasticity
BioEssays, 2018, 40,
2.193Citations (PDF)
135Phenotypic stability and plasticity in GMP-derived cells as determined by their underlying regulatory network
Bioinformatics, 2018, 34, 1174-1182
4.714Citations (PDF)
136MemBrain-contact 2.0: a new two-stage machine learning model for the prediction enhancement of transmembrane protein residue contacts in the full chain
Bioinformatics, 2018, 34, 230-238
4.717Citations (PDF)
137DNCON2: improved protein contact prediction using two-level deep convolutional neural networks
Bioinformatics, 2018, 34, 1466-1472
4.7160Citations (PDF)
138High precision in protein contact prediction using fully convolutional neural networks and minimal sequence features
Bioinformatics, 2018, 34, 3308-3315
4.7179Citations (PDF)
139On the mechanisms of protein interactions: predicting their affinity from unbound tertiary structures
Bioinformatics, 2018, 34, 592-598
4.712Citations (PDF)
140Protein–protein interaction specificity is captured by contact preferences and interface composition
Bioinformatics, 2018, 34, 459-468
4.735Citations (PDF)
141APPRIS 2017: principal isoforms for multiple gene sets
Nucleic Acids Research, 2018, 46, D213-D217
15.5155Citations (PDF)
142Association Between Germline Mutations in BRF1, a Subunit of the RNA Polymerase III Transcription Complex, and Hereditary Colorectal Cancer
Gastroenterology, 2018, 154, 181-194.e20
0.933Citations (PDF)
143Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils
Cell Reports, 2018, 24, 2784-2794
6.3134Citations (PDF)
144Bio-knowledge-based filters improve residue–residue contact prediction accuracy
Bioinformatics, 2018, 34, 3675-3683
4.71Citations (PDF)
145LncRNAnet: long non-coding RNA identification using deep learning
Bioinformatics, 2018, 34, 3889-3897
4.798Citations (PDF)
146Sequential search leads to faster, more efficient fragment-basedde novoprotein structure prediction
Bioinformatics, 2018, 34, 1132-1140
4.712Citations (PDF)
147ProteomeVis: a web app for exploration of protein properties from structure to sequence evolution across organisms’ proteomes
Bioinformatics, 2018, 34, 3557-3565
4.77Citations (PDF)
148CommWalker: correctly evaluating modules in molecular networks in light of annotation bias
Bioinformatics, 2018, 34, 994-1000
4.710Citations (PDF)
149Germline variation in the oxidative DNA repair genesNUDT1andOGG1is not associated with hereditary colorectal cancer or polyposis
Human Mutation, 2018, 39, 1214-1225
4.512Citations (PDF)
150Prioritizing predictive biomarkers for gene essentiality in cancer cells with mRNA expression data and DNA copy number profile
Bioinformatics, 2018, 34, 3975-3982
4.74Citations (PDF)
151Deep convolutional networks for quality assessment of protein folds
Bioinformatics, 2018, 34, 4046-4053
4.796Citations (PDF)
152Increasing the accuracy of protein loop structure prediction with evolutionary constraints
Bioinformatics, 2018, 35, 2585-2592
4.79Citations (PDF)
153A pipeline for local assembly of minisatellite alleles from single-molecule sequencing data
Bioinformatics, 2017, 33, 650-653
4.72Citations (PDF)
154ISCB’s initial reaction to <i>New England Journal of Medicine</i> editorial on data sharing
Bioinformatics, 2017, 33, 2968-2968
4.71Citations (PDF)
155Genome-wide analysis of differential transcriptional and epigenetic variability across human immune cell types
Genome Biology, 2017, 18,
8.1113Citations (PDF)
156EigenTHREADER: analogous protein fold recognition by efficient contact map threading
Bioinformatics, 2017, 33, 2684-2690
4.765Citations (PDF)
157Capturing non-local interactions by long short-term memory bidirectional recurrent neural networks for improving prediction of protein secondary structure, backbone angles, contact numbers and solvent accessibility
Bioinformatics, 2017, 33, 2842-2849
4.7349Citations (PDF)
158Reliability of algorithmic somatic copy number alteration detection from targeted capture data
Bioinformatics, 2017, 33, 2791-2798
4.715Citations (PDF)
159Most Alternative Isoforms Are Not Functionally Important6.785Citations (PDF)
160A deep learning framework for improving long-range residue–residue contact prediction using a hierarchical strategy
Bioinformatics, 2017, 33, 2675-2683
4.741Citations (PDF)
161Annotating function to differentially expressed LincRNAs in myelodysplastic syndrome using a network-based method
Bioinformatics, 2017, 33, 2622-2630
4.714Citations (PDF)
162Information Retrieval and Text Mining Technologies for Chemistry
Chemical Reviews, 2017, 117, 7673-7761
52.6258Citations (PDF)
163HIPred: an integrative approach to predicting haploinsufficient genes
Bioinformatics, 2017, 33, 1751-1757
4.742Citations (PDF)
164Predicting accurate contacts in thousands of Pfam domain families using PconsC3
Bioinformatics, 2017, 33, 2859-2866
4.742Citations (PDF)
165LimTox: a web tool for applied text mining of adverse event and toxicity associations of compounds, drugs and genes
Nucleic Acids Research, 2017, 45, W484-W489
15.549Citations (PDF)
166ChiPPI: a novel method for mapping chimeric protein–protein interactions uncovers selection principles of protein fusion events in cancer
Nucleic Acids Research, 2017, 45, 7094-7105
15.535Citations (PDF)
167Elucidating the molecular basis of MSH2‐deficient tumors by combined germline and somatic analysis
International Journal of Cancer, 2017, 141, 1365-1380
4.328Citations (PDF)
168Comparison of algorithms for the detection of cancer drivers at subgene resolution
Nature Methods, 2017, 14, 782-788
24.677Citations (PDF)
169Correlated mutations select misfolded from properly folded proteins
Bioinformatics, 2017, 33, 1497-1504
4.73Citations (PDF)
170Epigenomic annotation-based interpretation of genomic data: from enrichment analysis to machine learning
Bioinformatics, 2017, 33, 3323-3330
4.736Citations (PDF)
171A molecular hypothesis to explain direct and inverse co-morbidities between Alzheimer’s Disease, Glioblastoma and Lung cancer3.4101Citations (PDF)
172Forecasting residue–residue contact prediction accuracy
Bioinformatics, 2017, 33, 3405-3414
4.74Citations (PDF)
173Automatic identification of informative regions with epigenomic changes associated to hematopoiesis
Nucleic Acids Research, 2017, 45, 9244-9259
15.522Citations (PDF)
174Extreme genomic erosion after recurrent demographic bottlenecks in the highly endangered Iberian lynx
Genome Biology, 2016, 17,
8.1173Citations (PDF)
175Conservation of coevolving protein interfaces bridges prokaryote–eukaryote homologies in the twilight zone7.540Citations (PDF)
176An expanded evaluation of protein function prediction methods shows an improvement in accuracy
Genome Biology, 2016, 17,
8.1367Citations (PDF)
177Integrating epigenomic data and 3D genomic structure with a new measure of chromatin assortativity
Genome Biology, 2016, 17,
8.159Citations (PDF)
178The BLUEPRINT Data Analysis Portal
Cell Systems, 2016, 3, 491-495.e5
5.8150Citations (PDF)
179The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease
Cell, 2016, 167, 1415-1429.e19
33.71,260Citations (PDF)
180CD8+ T Cells from Human Neonates Are Biased toward an Innate Immune Response
Cell Reports, 2016, 17, 2151-2160
6.377Citations (PDF)
181Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells
Cell, 2016, 167, 1398-1414.e24
33.7693Citations (PDF)
182KinMutRF: a random forest classifier of sequence variants in the human protein kinase superfamily
BMC Genomics, 2016, 17,
3.311Citations (PDF)
183The Markyt visualisation, prediction and benchmark platform for chemical and gene entity recognition at BioCreative/CHEMDNER challenge2.711Citations (PDF)
184Chromatin Regulators as a Guide for Cancer Treatment Choice
Molecular Cancer Therapeutics, 2016, 15, 1768-1777
1.919Citations (PDF)
185wKinMut-2: Identification and Interpretation of Pathogenic Variants in Human Protein Kinases
Human Mutation, 2016, 37, 36-42
4.510Citations (PDF)
186Epigenomic Co-localization and Co-evolution Reveal a Key Role for 5hmC as a Communication Hub in the Chromatin Network of ESCs
Cell Reports, 2016, 14, 1246-1257
6.343Citations (PDF)
187POLE and POLD1 mutations in 529 kindred with familial colorectal cancer and/or polyposis: review of reported cases and recommendations for genetic testing and surveillance
Genetics in Medicine, 2016, 18, 325-332
4.2234Citations (PDF)
188ISCB’s initial reaction to New England Journal of Medicine editorial on data sharing
F1000Research, 2016, 5, 157
0.51Citations (PDF)
189Identifying ELIXIR Core Data Resources
F1000Research, 2016, 5, 2422
0.555Citations (PDF)
190ISCB’s Initial Reaction to The New England Journal of Medicine Editorial on Data Sharing
PLoS Computational Biology, 2016, 12, e1004816
3.112Citations (PDF)
191CHEMDNER: The drugs and chemical names extraction challenge5.4213Citations (PDF)
192The CHEMDNER corpus of chemicals and drugs and its annotation principles5.4213Citations (PDF)
193Alternatively Spliced Homologous Exons Have Ancient Origins and Are Highly Expressed at the Protein Level
PLoS Computational Biology, 2015, 11, e1004325
3.186Citations (PDF)
194NOTCH pathway inactivation promotes bladder cancer progression10.6106Citations (PDF)
195Whole-genome fingerprint of the DNA methylome during human B cell differentiation
Nature Genetics, 2015, 47, 746-756
25.2321Citations (PDF)
196ChiTaRS 2.1—an improved database of the chimeric transcripts and RNA-seq data with novel sense–antisense chimeric RNA transcripts
Nucleic Acids Research, 2015, 43, D68-D75
15.529Citations (PDF)
197Alternative splicing and co-option of transposable elements: the case of TMPO/LAP2α and ZNF451 in mammals
Bioinformatics, 2015, 31, 2257-2261
4.738Citations (PDF)
198Structure-PPi: a module for the annotation of cancer-related single-nucleotide variants at protein–protein interfaces
Bioinformatics, 2015, 31, 2397-2399
4.740Citations (PDF)
199APPRIS WebServer and WebServices
Nucleic Acids Research, 2015, 43, W455-W459
15.520Citations (PDF)
200FUN-L: gene prioritization for RNAi screens
Bioinformatics, 2015, 31, 2052-2053
4.710Citations (PDF)
201Summary of the BioLINK SIG 2013 meeting at ISMB/ECCB 2013
Bioinformatics, 2015, 31, 297-298
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202Non-coding recurrent mutations in chronic lymphocytic leukaemia
Nature, 2015, 526, 519-524
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203Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair
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204Detection of significant protein coevolution
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205Higher gene expression variability in the more aggressive subtype of chronic lymphocytic leukemia
Genome Medicine, 2015, 7,
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206Most Highly Expressed Protein-Coding Genes Have a Single Dominant Isoform
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207From residue coevolution to protein conformational ensembles and functional dynamics7.5133Citations (PDF)
208The Evolutionary Fate of Alternatively Spliced Homologous Exons after Gene Duplication
Genome Biology and Evolution, 2015, 7, 1392-1403
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209The UBC-40 Urothelial Bladder Cancer cell line index: a genomic resource for functional studies
BMC Genomics, 2015, 16,
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210A computational approach inspired by simulated annealing to study the stability of protein interaction networks in cancer and neurological disorders2.77Citations (PDF)
211Conserved Clusters of Functionally Related Genes in Two Bacterial Genomes1.755Citations (PDF)
212Integration of biological data by kernels on graph nodes allows prediction of new genes involved in mitotic chromosome condensation
Molecular Biology of the Cell, 2014, 25, 2522-2536
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213CheNER: chemical named entity recognizer
Bioinformatics, 2014, 30, 1039-1040
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214Molecular Evidence for the Inverse Comorbidity between Central Nervous System Disorders and Cancers Detected by Transcriptomic Meta-analyses
PLoS Genetics, 2014, 10, e1004173
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215Predicting Protein Relationships to Human Pathways through a Relational Learning Approach Based on Simple Sequence Features2.93Citations (PDF)
216FireDB: a compendium of biological and pharmacologically relevant ligands
Nucleic Acids Research, 2014, 42, D267-D272
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217A common structural scaffold in CTD phosphatases that supports distinct catalytic mechanisms2.64Citations (PDF)
218Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia
Genome Research, 2014, 24, 212-226
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219Colorectal cancer classification based on gene expression is not associated with FOLFIRI response
Nature Medicine, 2014, 20, 1230-1231
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220Analyzing the First Drafts of the Human Proteome
Journal of Proteome Research, 2014, 13, 3854-3855
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221Transcriptional dissection of pancreatic tumors engrafted in mice
Genome Medicine, 2014, 6,
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222Integrated Next-Generation Sequencing and Avatar Mouse Models for Personalized Cancer Treatment
Clinical Cancer Research, 2014, 20, 2476-2484
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223Multiple evidence strands suggest that there may be as few as 19 000 human protein-coding genes
Human Molecular Genetics, 2014, 23, 5866-5878
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224BioCreative-IV virtual issue2.746Citations (PDF)
225Characterization of the DNA Methylome during Human B-Cell Differentiation
Blood, 2014, 124, 4346-4346
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226Subfunctionalization via Adaptive Evolution Influenced by Genomic Context: The Case of Histone Chaperones ASF1a and ASF1b
Molecular Biology and Evolution, 2013, 30, 1853-1866
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227Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy
Nature Genetics, 2013, 45, 1464-1469
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228Towards a detailed atlas of protein–protein interactions6.493Citations (PDF)
229The Functional Genomics Network in the evolution of biological text mining over the past decade
New Biotechnology, 2013, 30, 278-285
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230Emerging methods in protein co-evolution
Nature Reviews Genetics, 2013, 14, 249-261
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231Incorporating information on predicted solvent accessibility to the co-evolution-based study of protein interactions
Molecular BioSystems, 2013, 9, 70-76
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232Late-replicating CNVs as a source of new genes
Biology Open, 2013, 2, 1402-1411
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233APPRIS: annotation of principal and alternative splice isoforms
Nucleic Acids Research, 2013, 41, D110-D117
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234RUbioSeq: a suite of parallelized pipelines to automate exome variation and bisulfite-seq analyses
Bioinformatics, 2013, 29, 1687-1689
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235BioC: a minimalist approach to interoperability for biomedical text processing2.7143Citations (PDF)
236An Epistatic Interaction between the PAX8 and STK17B Genes in Papillary Thyroid Cancer Susceptibility
PLoS ONE, 2013, 8, e74765
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237Interpretation of the Consequences of Mutations in Protein Kinases: Combined Use of Bioinformatics and Text Mining2.89Citations (PDF)
238How to link ontologies and protein-protein interactions to literature: text-mining approaches and the BioCreative experience2.728Citations (PDF)
239JDet: interactive calculation and visualization of function-related conservation patterns in multiple sequence alignments and structures
Bioinformatics, 2012, 28, 584-586
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240Comparative Proteomics Reveals a Significant Bias Toward Alternative Protein Isoforms with Conserved Structure and Function
Molecular Biology and Evolution, 2012, 29, 2265-2283
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241ChiTaRS: a database of human, mouse and fruit fly chimeric transcripts and RNA-sequencing data
Nucleic Acids Research, 2012, 41, D142-D151
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242Text mining for the biocuration workflow2.7140Citations (PDF)
243Mirroring co-evolving trees in the light of their topologies
Bioinformatics, 2012, 28, 1202-1208
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244Novel domain combinations in proteins encoded by chimeric transcripts
Bioinformatics, 2012, 28, i67-i74
4.739Citations (PDF)
245BioCreative-2012 Virtual Issue2.719Citations (PDF)
246Getting personalized cancer genome analysis into the clinic: the challenges in bioinformatics
Genome Medicine, 2012, 13, 61
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247EnrichNet: network-based gene set enrichment analysis
Bioinformatics, 2012, 28, i451-i457
4.7289Citations (PDF)
248The Ras protein superfamily: Evolutionary tree and role of conserved amino acids
Journal of Cell Biology, 2012, 196, 189-201
5.4353Citations (PDF)
249GENCODE: The reference human genome annotation for The ENCODE Project
Genome Research, 2012, 22, 1760-1774
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250Chimeras taking shape: Potential functions of proteins encoded by chimeric RNA transcripts
Genome Research, 2012, 22, 1231-1242
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251MyMiner: a web application for computer-assisted biocuration and text annotation
Bioinformatics, 2012, 28, 2285-2287
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252Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia
Nature Genetics, 2012, 44, 1236-1242
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253Genome-wide analysis of Pax8 binding provides new insights into thyroid functions
BMC Genomics, 2012, 13,
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254Uncovering the Molecular Machinery of the Human Spindle—An Integration of Wet and Dry Systems Biology
PLoS ONE, 2012, 7, e31813
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255Evidence for Transcript Networks Composed of Chimeric RNAs in Human Cells
PLoS ONE, 2012, 7, e28213
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256Distinct DNA methylomes of newborns and centenarians7.5763Citations (PDF)
257BLUEPRINT to decode the epigenetic signature written in blood
Nature Biotechnology, 2012, 30, 224-226
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258Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
Nature, 2011, 475, 101-105
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259Towards the prediction of protein interaction partners using physical docking6.7105Citations (PDF)
260Selection of organisms for the co-evolution-based study of protein interactions
BMC Bioinformatics, 2011, 12,
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261No paradox, no progress: inverse cancer comorbidity in people with other complex diseases
Lancet Oncology, The, 2011, 12, 604-608
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262Characterization of pathogenic germline mutations in human Protein Kinases
BMC Bioinformatics, 2011, 12,
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263Overview of the BioCreative III Workshop
BMC Bioinformatics, 2011, 12,
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264The Protein-Protein Interaction tasks of BioCreative III: classification/ranking of articles and linking bio-ontology concepts to full text
BMC Bioinformatics, 2011, 12,
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265Text Mining for Drugs and Chemical Compounds: Methods, Tools and Applications
Molecular Informatics, 2011, 30, 506-519
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266Assessment of copy number variation using the Illumina Infinium 1M SNP-array: a comparison of methodological approaches in the Spanish Bladder Cancer/EPICURO study
Human Mutation, 2011, 32, 240-248
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267Long-Range Epigenetic Silencing Associates with Deregulation of Ikaros Targets in Colorectal Cancer Cells
Molecular Cancer Research, 2011, 9, 1139-1151
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268firestar —advances in the prediction of functionally important residues
Nucleic Acids Research, 2011, 39, W235-W241
15.559Citations (PDF)
269Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
Nature Genetics, 2011, 44, 47-52
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270Extending pathways and processes using molecular interaction networks to analyse cancer genome data
BMC Bioinformatics, 2010, 11,
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271Predicted residue–residue contacts can help the scoring of 3D models2.631Citations (PDF)
272Mutated genes, pathways and processes in tumours
EMBO Reports, 2010, 11, 805-810
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273The FEBS Letters/BioCreative II.5 experiment: making biological information accessible
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274FragKB: Structural and Literature Annotation Resource of Conserved Peptide Fragments and Residues
PLoS ONE, 2010, 5, e9679
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275Inference of Functional Relations in Predicted Protein Networks with a Machine Learning Approach
PLoS ONE, 2010, 5, e9969
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276MidA is a putative methyltransferase that is required for mitochondrial complex I function
Journal of Cell Science, 2010, 123, 1674-1683
2.454Citations (PDF)
277Protein interactions and ligand binding: From protein subfamilies to functional specificity7.5142Citations (PDF)
278An Overview of BioCreative II.52.988Citations (PDF)
279TopoGSA: network topological gene set analysis
Bioinformatics, 2010, 26, 1271-1272
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280The dynamic DNA methylomes of double-stranded DNA viruses associated with human cancer
Genome Research, 2009, 19, 438-451
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281Bionemo: molecular information on biodegradation metabolism
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282PLAN2L: a web tool for integrated text mining and literature-based bioentity relation extraction
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283EcID. A database for the inference of functional interactions in E. coli
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284Automated Alphabet Reduction for Protein Datasets
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285Extraction of human kinase mutations from literature, databases and genotyping studies
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286An integrated approach to the interpretation of Single Amino Acid Polymorphisms within the framework of CATH and Gene3D
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287Cancer‐associated mutations are preferentially distributed in protein kinase functional sites2.626Citations (PDF)
288From cancer genomes to cancer models: bridging the gaps
EMBO Reports, 2009, 10, 359-366
5.234Citations (PDF)
289Systemic approaches to biodegradation
FEMS Microbiology Reviews, 2009, 33, 98-108
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290Creating Reference Datasets for Systems Biology Applications Using Text Mining4.013Citations (PDF)
291Structure-Based Prediction of the Saccharomyces cerevisiae SH3–Ligand Interactions
Journal of Molecular Biology, 2009, 388, 902-916
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292Translational disease interpretation with molecular networks
Genome Biology, 2009, 10, 221
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293Sequence-based feature prediction and annotation of proteins
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294Bioinformatics and cancer research: building bridges for translational research2.116Citations (PDF)
295À la carte transcriptional regulators: unlocking responses of the prokaryotic enhancer-binding protein XylR to non-natural effectors
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2.561Citations (PDF)
296Predicting functional residues in Plasmodium falciparum plasmepsins by combining sequence and structural analysis with molecular dynamics simulations2.620Citations (PDF)
297Protein co-evolution, co-adaptation and interactions
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298Enhancing the prediction of protein pairings between interacting families using orthology information3.024Citations (PDF)
299Defining functional distances over Gene Ontology3.057Citations (PDF)
300Co‐evolution and co‐adaptation in protein networks
FEBS Letters, 2008, 582, 1225-1230
2.742Citations (PDF)
301A text‐mining perspective on the requirements for electronically annotated abstracts
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302Linking genes to literature: text mining, information extraction, and retrieval applications for biology
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303Evaluation of text-mining systems for biology: overview of the Second BioCreative community challenge
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304Proteomics studies confirm the presence of alternative protein isoforms on a large scale
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305Text mining for biology - the way forward: opinions from leading scientists
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306Overview of the protein-protein interaction annotation extraction task of BioCreative II
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307High-confidence prediction of global interactomes based on genome-wide coevolutionary networks7.5179Citations (PDF)
308Determination and validation of principal gene products
Bioinformatics, 2008, 24, 11-17
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309Progress and challenges in predicting protein-protein interaction sites
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310Interoperability with Moby 1.0--It's better than sharing your toothbrush!
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311iHOP web services
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312The implications of alternative splicing in the ENCODE protein complement7.5209Citations (PDF)
313firestar--prediction of functionally important residues using structural templates and alignment reliability
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314CARGO: a web portal to integrate customized biological information
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315Modular organization in the reductive evolution of protein-protein interaction networks
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316Assessment of intramolecular contact predictions for CASP72.672Citations (PDF)
317Assessment of predictions submitted for the CASP7 function prediction category2.655Citations (PDF)
318Filamin-A regulates actin-dependent clustering of HIV receptors
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319Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
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320Title is missing!
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321The three-dimensional structure of an eukaryotic glutamine synthetase: Functional implications of its oligomeric structure
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322Title is missing!
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323Phylogeny-independent detection of functional residues
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324Bioinformatics in the human interactome project
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325TSEMA: interactive prediction of protein pairings between interacting families
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326TreeDet: a web server to explore sequence space
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327Semantic Mining in Biomedicine (Introduction to the papers selected from the SMBM 2005 Symposium, Hinxton, U.K., April 2005)
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328Death inducer obliterator protein 1 in the context of DNA regulation. Sequence analyses of distant homologues point to a novel functional role
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329Text-mining approaches in molecular biology and biomedicine
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330Automatic annotation of protein function6.4112Citations (PDF)
331Scoring docking models with evolutionary information2.641Citations (PDF)
332Domain definition and target classification for CASP62.626Citations (PDF)
333Assessment of predictions submitted for the CASP6 comparative modeling category2.6103Citations (PDF)
334CASP6 assessment of contact prediction2.687Citations (PDF)
335Implementing the iHOP concept for navigation of biomedical literature
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336A framework for computational and experimental methods: Identifying dimerization residues in CCR chemokine receptors
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337Do you do text?
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338EVAcon: a protein contact prediction evaluation service
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339Title is missing!
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340SQUARE--determining reliable regions in sequence alignments
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341MetaRouter: bioinformatics for bioremediation
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342YAdumper: extracting and translating large information volumes from relational databases to structured flat files
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343HCAD, closing the gap between breakpoints and genes
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344IntAct: an open source molecular interaction database
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345A gene network for navigating the literature
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346Identification of amino acid residues crucial for chemokine receptor dimerization
Nature Immunology, 2004, 5, 216-223
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347The small GTP-binding protein, Rhes, regulates signal transduction from G protein-coupled receptors
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348Title is missing!
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349Solution structure of the hypothetical protein Mth677 fromMethanobacterium thermoautotrophicum: A novel α+β fold
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350Structural model of carnitine palmitoyltransferase I based on the carnitine acetyltransferase crystal
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351Phage-display and correlated mutations identify an essential region of subdomain 1C involved in homodimerization of Escherichia coli FtsA2.636Citations (PDF)
352Protein interaction: same network, different hubs
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353Life cycles of successful genes
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354The single tryptophan of the PsbQ protein of photosystem II is at the end of a 4-α-helical bundle domain
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355Automatic annotation of protein function based on family identification2.653Citations (PDF)
356CAFASP3 in the spotlight of EVA2.632Citations (PDF)
357The organization of the microbial biodegradation network from a systems‐biology perspective
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358Early bioinformatics: the birth of a discipline--a personal view
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359Automatic Methods for Predicting Functionally Important Residues
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360Predicting Reliable Regions in Protein Alignments from Sequence Profiles
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361META, METAN AND CYBER SERVERS
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362Structural (βα)8 TIM Barrel Model of 3-Hydroxy-3-methylglutaryl-Coenzyme A Lyase
Journal of Biological Chemistry, 2003, 278, 29016-29023
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363EVA: evaluation of protein structure prediction servers
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364Identification of Conserved Amino Acid Residues in Rat Liver Carnitine Palmitoyltransferase I Critical for Malonyl-CoA Inhibition
Journal of Biological Chemistry, 2003, 278, 9058-9063
2.266Citations (PDF)
365Reductive genome evolution in Buchnera aphidicola7.5488Citations (PDF)
366Involvement of Intramolecular Interactions in the Regulation of G Protein-Coupled Receptor Kinase 2
Molecular Pharmacology, 2003, 64, 629-639
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367Evaluation of annotation strategies using an entire genome sequence
Bioinformatics, 2003, 19, 717-726
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368Structural Model of a Malonyl-CoA-binding Site of Carnitine Octanoyltransferase and Carnitine Palmitoyltransferase I
Journal of Biological Chemistry, 2002, 277, 11473-11480
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369Bioinformatics in structural genomics
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370BIOINFORMATICS: BIOLOGY BY OTHER MEANS
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371Information extraction in molecular biology
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372Clustering of proximal sequence space for the identification of protein families
Bioinformatics, 2002, 18, 908-921
4.758Citations (PDF)
373Bioinformatics methods for the analysis of expression arrays: data clustering and information extraction
Journal of Biotechnology, 2002, 98, 269-283
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374MARVEL: a conserved domain involved in membrane apposition events6.7222Citations (PDF)
375Computational methods for the prediction of protein interactions6.4331Citations (PDF)
376Analysis of the Cellular Functions of Escherichia coli Operons and Their Conservation in Bacillus subtilis1.737Citations (PDF)
377Prediction of protein-protein interaction sites in heterocomplexes with neural networks
FEBS Journal, 2002, 269, 1356-1361
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378In silico two-hybrid system for the selection of physically interacting protein pairs2.6247Citations (PDF)
379Bioinformatics and Computational Biology at the crossroads of post-genomic technology
Phytochemistry Reviews, 2002, 1, 209-214
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380Search and retrieve
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381A hierarchical unsupervised growing neural network for clustering gene expression patterns
Bioinformatics, 2001, 17, 126-136
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382Mining functional information associated with expression arrays2.964Citations (PDF)
383Escherichia coli FtsZ polymers contain mostly GTP and have a high nucleotide turnover
Molecular Microbiology, 2001, 41, 83-91
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384Threading structural model of the manganese-stabilizing protein PsbO reveals presence of two possible ?-sandwich domains2.621Citations (PDF)
385CAFASP2: The second critical assessment of fully automated structure prediction methods2.6132Citations (PDF)
386Improvement in affinity and HIV-1 neutralization by somatic mutation in the heavy chain first complementarity-determining region of antibodies triggered by HIV-1 infection3.25Citations (PDF)
387Bringing gene order into bacterial shape
Trends in Genetics, 2001, 17, 124-126
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388Intrinsic errors in genome annotation
Trends in Genetics, 2001, 17, 429-431
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389Similarity of phylogenetic trees as indicator of protein–protein interaction2.6449Citations (PDF)
390Structural Model of the Catalytic Core of Carnitine Palmitoyltransferase I and Carnitine Octanoyltransferase (COT)
Journal of Biological Chemistry, 2001, 276, 45001-45008
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391Prediction of contact maps with neural networks and correlated mutations2.6176Citations (PDF)
392Practical limits of function prediction2.6317Citations (PDF)
393Three-dimensional view of the surface motif associated with the P-loop structure: cis and trans cases of convergent evolution 1 1Edited by J. Thornton
Journal of Molecular Biology, 2000, 303, 455-465
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394Title is missing!
Genome Biology, 2000, 2, interactions0001.1
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395A platform for integrating threading results with protein family analyses
Bioinformatics, 1999, 15, 1062-1063
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396Effector Recognition by the Small GTP-binding Proteins Ras and Ral
Journal of Biological Chemistry, 1999, 274, 17763-17770
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397Molecular analysis of HIV-1 gp120 antibody response using isotype IgM and IgG phage display libraries from a long-term non-progressor HIV-1-infected individual
European Journal of Immunology, 1999, 29, 2666-2675
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398Model of the Ran-RCC1 Interaction using Biochemical and Docking Experiments
Journal of Molecular Biology, 1999, 289, 1119-1130
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399Effective use of sequence correlation and conservation in fold recognition 1 1Edited by J. M. Thornton
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400Structural model of Dex protein fromPenicillium minioluteumand its implications in the mechanism of catalysis
1998, 31, 345-354
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401Structural model for family 32 of glycosyl-hydrolase enzymes
1998, 33, 383-395
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402Shaping of Drosophila Alcohol Dehydrogenase Through Evolution: Relationship with Enzyme Functionality1.724Citations (PDF)
403Distribution and functional diversification of the ras superfamily inSaccharomyces cerevisiae
FEBS Letters, 1998, 434, 219-225
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404Mutations in the DnaK chaperone affecting interaction with the DnaJ cochaperone7.5171Citations (PDF)
405Sequence analysis of the Methanococcus jannaschii genome and the prediction of protein function
Bioinformatics, 1997, 13, 481-483
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406Correlated mutations contain information about protein-protein interaction 1 1Edited by A. R. Fersht
Journal of Molecular Biology, 1997, 271, 511-523
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407Classification of protein families and detection of the determinant residues with an improved self-organizing map
Biological Cybernetics, 1997, 76, 441-450
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408Genomes with distinct function composition
FEBS Letters, 1996, 389, 96-101
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409Computational comparisons of model genomes
Trends in Biotechnology, 1996, 14, 280-285
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410Novelties from the complete genome of Mycoplasma genitalium
Molecular Microbiology, 1996, 20, 898-900
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411A method to predict functional residues in proteins8.8398Citations (PDF)
412Eukaryotic translation elongation factor 1γ contains a glutathione transferase domain—Study of a diverse, ancient protein super family using motif search and structural modeling
Protein Science, 1994, 3, 2045-2055
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413Correlated mutations and residue contacts in proteins2.6839Citations (PDF)
414A conserved loop in the ATPase domain of the DnaK chaperone is essential for stable binding of GrpE8.8125Citations (PDF)
415Convergent evolution of similar enzymatic function on different protein folds: The hexokinase, ribokinase, and galactokinase families of sugar kinases
Protein Science, 1993, 2, 31-40
5.9371Citations (PDF)
416A new ATP-binding fold in actin, hexokinase and Hsc70
Trends in Cell Biology, 1993, 3, 53-59
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417How does the switch II region of G-domains work?
FEBS Letters, 1993, 320, 1-6
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418The ras protein family: evolutionary tree and role of conserved amino acids
Biochemistry, 1991, 30, 4637-4648
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419<i>MIB2</i>variants altering NOTCH signalling result in left ventricle hypertrabeculation/non-compaction and are associated with Ménétrier-like gastropathy2.97Citations (PDF)
420The pseudo GTPase CENP-M drives human kinetochore assembly
ELife, 0, 3,
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421Patient-specific Boolean models of signalling networks guide personalised treatments
ELife, 0, 11,
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422myAURA : a personalized health library for epilepsy management via knowledge graph sparsification and visualization3.52Citations (PDF)
423Constraint based modeling of drug induced metabolic changes in a cancer cell line2.90Citations (PDF)
424Antidepressant and Antipsychotic Drug Use and Cancer Risk: Protocol for an Overview of Systematic Reviews and Meta-Analyses0.00Citations (PDF)
425Sex-specific transcriptome similarity networks elucidate comorbidity relationships4.50Citations (PDF)