Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders

Mendelian Inheritance in Man: A Catalog of Human Genes and Genetic Disorders

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Human Gene Mutation Database (HGMD®): 2003 update

Stenson, P., Ball, E. V., Mort, M., Phillips, A. D., Shiel, J. A., Thomas, N., Abeysinghe, S. S., Krawczak, M., & Cooper, D. (2003) · Human Mutation · doi:10.1002/humu.10212 · Cited by 1,887

The harmonizome: a collection of processed datasets gathered to serve and mine knowledge about genes and proteins

Rouillard, A. D., Gundersen, G. W., Fernandez, N. F., Wang, Z., Monteiro, C. D., McDermott, M. G., & Ma’ayan, A. (2016) · Database · doi:10.1093/database/baw100 · Cited by 1,515

Rare and common variants: twenty arguments

Gibson, G. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3118 · Cited by 1,278

Walking the Interactome for Prioritization of Candidate Disease Genes

Köhler, S., Bauer, S., Horn, D., & Robinson, P. N. (2008) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2008.02.013 · Cited by 1,268

Network Pharmacology Databases for Traditional Chinese Medicine: Review and Assessment

Zhang, R., Zhu, X. H., Bai, H., & Ning, K. (2019) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.00123 · Cited by 1,293

Development of Human Protein Reference Database as an Initial Platform for Approaching Systems Biology in HumansPreprint

Peri, S., Navarro, J. D., Amanchy, R., Kristiansen, T. Z., Jonnalagadda, C. K., Surendranath, V., Niranjan, V., Muthusamy, B., Gandhi, T. K. B., Grønborg, M., et al. (2003) · Genome Research · doi:10.1101/gr.1680803 · Cited by 1,086

Network pharmacology, a promising approach to reveal the pharmacology mechanism of Chinese medicine formula

Zhao, L., Zhang, H., Li, N., Chen, J., Xu, H. N., Wang, Y., & Liang, Q. (2023) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2023.116306 · Cited by 1,041

The Genetic Association Database

Becker, K. G., Barnes, K. C., Bright, T. J., & Wang, S. A. (2004) · Nature Genetics · doi:10.1038/ng0504-431 · Cited by 971

The Catalogue of Somatic Mutations in Cancer (COSMIC)

Forbes, S. A., Bhamra, G., Bamford, S., Dawson, E., Kok, C. Y., Clements, J., Menzies, A. H., Teague, J. W., Futreal, P. A., & Stratton, M. R. (2008) · Current Protocols in Human Genetics · doi:10.1002/0471142905.hg1011s57 · Cited by 899

PREDICT: a method for inferring novel drug indications with application to personalized medicine

Gottlieb, A., Stein, G. Y., Ruppin, E., & Sharan, R. (2011) · Molecular Systems Biology · doi:10.1038/msb.2011.26 · Cited by 900

Associating Genes and Protein Complexes with Disease via Network Propagation

Vanunu, O., Magger, O., Ruppin, E., Shlomi, T., & Sharan, R. (2010) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1000641 · Cited by 864

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy

Towbin, J. A., McKenna, W. J., Abrams, D. J., Ackerman, M. J., Calkins, H. G., Darrieux, F., Daubert, J. P., de Chillou, C., DePasquale, E. C., Desai, M. Y., et al. (2019) · Heart Rhythm · doi:10.1016/j.hrthm.2019.05.007 · Cited by 878

Database resources of the National Center for Biotechnology Information

Wheeler, D. L., Barrett, T., Benson, D. A., Bryant, S. H., Canese, K., Chetvernin, V., Church, D. M., DiCuccio, M., Edgar, R., Federhen, S., et al. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkl1031 · Cited by 734

A text-mining analysis of the human phenome

van Driel, M. A., Bruggeman, J., Vriend, G., Brunner, H. G., & Leunissen, J. A. M. (2006) · European Journal of Human Genetics · doi:10.1038/sj.ejhg.5201585 · Cited by 664

Characterising and Predicting Haploinsufficiency in the Human Genome

Huang, N., Lee, I., Marcotte, E. M., & Hurles, M. E. (2010) · PLoS Genetics · doi:10.1371/journal.pgen.1001154 · Cited by 659

Review of Drug Repositioning Approaches and Resources

Xue, H., Li, J., Xie, H., & Wang, Y. (2018) · International Journal of Biological Sciences · doi:10.7150/ijbs.24612 · Cited by 613

Human protein reference database as a discovery resource for proteomics

Peri, S. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh070 · Cited by 611

Human protein reference database--2006 update

Mishra, G. (2005) · Nucleic Acids Research · doi:10.1093/nar/gkj141 · Cited by 601

GeneCodis3: a non-redundant and modular enrichment analysis tool for functional genomics

Tabas‐Madrid, D., Nogales‐Cadenas, R., & Pascual-Montano, A. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks402 · Cited by 537

TreeFam: a curated database of phylogenetic trees of animal gene families

Li, H. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkj118 · Cited by 523

Drug repositioning based on comprehensive similarity measures and Bi-Random walk algorithm

Luo, H., Wang, J., Li, M., Luo, J., Peng, X., Wu, F., & Pan, Y. F. (2016) · Bioinformatics · doi:10.1093/bioinformatics/btw228 · Cited by 479

SOURCE: a unified genomic resource of functional annotations, ontologies, and gene expression data

Diehn, M. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg014 · Cited by 428

PANTHER version 6: protein sequence and function evolution data with expanded representation of biological pathways

Mi, H., Guo, N., Kejariwal, A., & Thomas, P. D. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl869 · Cited by 372

Pan-genomics in the human genome era

Sherman, R. M., & Salzberg, S. L. (2020) · Nature Reviews Genetics · doi:10.1038/s41576-020-0210-7 · Cited by 375

Applications of Network Pharmacology in Traditional Chinese Medicine Research

Zhou, Z., Chen, B., Chen, S., Lin, M., Chen, Y., Jin, S., Chen, W., & Zhang, Y. (2020) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2020/1646905 · Cited by 358

Integrative Annotation of 21,037 Human Genes Validated by Full-Length cDNA Clones

Imanishi, T., Itoh, T., Suzuki, Y., O’Donovan, C., Fukuchi, S., Koyanagi, K. O., Barrero, R. A., Tamura, T., Yamaguchi‐Kabata, Y., Tanino, M., et al. (2004) · PLoS Biology · doi:10.1371/journal.pbio.0020162 · Cited by 331

The UCSC genome browser database: update 2007

Kuhn, R. M., Karolchik, D., Zweig, A. S., Trumbower, H., Thomas, D. J., Thakkapallayil, A., Sugnet, C. W., Stanke, M., Smith, K. E., Siepel, A. C., et al. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl928 · Cited by 279

Computational drug repositioning using low-rank matrix approximation and randomized algorithms

Luo, H., Li, M., Wang, S., Liu, Q., Li, Y., & Wang, J. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty013 · Cited by 266

Molecular and Comparative Genetics of Mental Retardation

Inlow, J. K., & Restifo, L. L. (2004) · Genetics · doi:10.1534/genetics.166.2.835 · Cited by 264

A critical assessment of Mus musculusgene function prediction using integrated genomic evidence

Peña-Castillo, L., Tasan, M., Myers, C. L., Lee, H., Joshi, T., Zhang, C., Guan, Y., Leone, M., Pagnani, A., Kim, W. K., et al. (2008) · Genome Biology · doi:10.1186/gb-2008-9-s1-s2 · Cited by 248

PolySearch: a web-based text mining system for extracting relationships between human diseases, genes, mutations, drugs and metabolites

Cheng, D., Knox, C., Young, N., Stothard, P., Damaraju, S., & Wishart, D. S. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn296 · Cited by 254

Modeling 3D Facial Shape from DNA

Claes, P., Liberton, D. K., Daniels, K., Rosana, K. M., Quillen, E. E., Pearson, L. N., McEvoy, B., Bauchet, M., Zaidi, A. A., Yao, W., et al. (2014) · PLoS Genetics · doi:10.1371/journal.pgen.1004224 · Cited by 202

Speeding disease gene discovery by sequence based candidate prioritization

Adie, E. A., Adams, R. R., Evans, K. L., Porteous, D. J., & Pickard, B. S. (2005) · BMC Bioinformatics · doi:10.1186/1471-2105-6-55 · Cited by 249

TCM-Mesh: The database and analytical system for network pharmacology analysis for TCM preparations

Zhang, R., Yu, S., Bai, H., & Ning, K. (2017) · Scientific Reports · doi:10.1038/s41598-017-03039-7 · Cited by 234

Genome-wide prioritization of disease genes and identification of disease-disease associations from an integrated human functional linkage network

Linghu, B., Snitkin, E. S., Hu, Z., Xia, Y., & DeLisi, C. (2009) · Genome biology · doi:10.1186/gb-2009-10-9-r91 · Cited by 236

SUSPECTS: enabling fast and effective prioritization of positional candidates

Adie, E. A., Adams, R. R., Evans, K. L., Porteous, D. J., & Pickard, B. S. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btk031 · Cited by 232

POCUS: mining genomic sequence annotation to predict disease genes

Turner, F. S., Clutterbuck, D. R., & Semple, C. A. M. (2003) · Genome biology · doi:10.1186/gb-2003-4-11-r75 · Cited by 227

ENDEAVOUR update: a web resource for gene prioritization in multiple species

Tranchevent, L.-C., Barriot, R., Yu, S., Vooren, S. V., Loo, P. V., Coessens, B., Moor, B. D., Aerts, S., & Moreau, Y. (2008) · Nucleic Acids Research · doi:10.1093/nar/gkn325 · Cited by 216

Prediction and Validation of Disease Genes Using HeteSim Scores

Zeng, X., Liao, Y., Liu, Y., & Zou, Q. (2017) · IEEE/ACM Transactions on Computational Biology and Bioinformatics · doi:10.1109/tcbb.2016.2520947 · Cited by 208

TFCat: the curated catalog of mouse and human transcription factors

Fulton, D. L., Sundararajan, S., Badis, G., Hughes, T. R., Wasserman, W. W., Roach, J. C., & SLADEK, R. M. (2009) · Genome biology · doi:10.1186/gb-2009-10-3-r29 · Cited by 205

A new grammar for drug discovery

Fishman, M. C., & Porter, J. A. (2005) · Nature · doi:10.1038/437491a · Cited by 193

Network Medicine in the Age of Biomedical Big Data

Sonawane, A. R., Weiss, S. T., Glass, K., & Sharma, A. (2019) · Frontiers in Genetics · doi:10.3389/fgene.2019.00294 · Cited by 197

Drug repositioning based on bounded nuclear norm regularization

Yang, M., Luo, H., Li, Y., & Wang, J. (2019) · Bioinformatics · doi:10.1093/bioinformatics/btz331 · Cited by 185

Drug repositioning based on the heterogeneous information fusion graph convolutional network

Cai, L., Lu, C., Xu, J., Meng, Y., Wang, P., Fu, X., Zeng, X., & Su, Y. (2021) · Briefings in Bioinformatics · doi:10.1093/bib/bbab319 · Cited by 180

Rediscovering the sweet spot in drug discovery

Brown, D., & Superti‐Furga, G. (2003) · Drug Discovery Today · doi:10.1016/s1359-6446(03)02902-7 · Cited by 180

Bioinformatics for Clinical Next Generation Sequencing

Oliver, G. R., Hart, S. N., & Klee, E. W. (2014) · Clinical Chemistry · doi:10.1373/clinchem.2014.224360 · Cited by 188

From syndrome families to functional genomics

Brunner, H. G., & van Driel, M. A. (2004) · Nature Reviews Genetics · doi:10.1038/nrg1383 · Cited by 175

MitoProteome: mitochondrial protein sequence database and annotation system

Cotter, D. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh048 · Cited by 175

Enzymes and auxiliary factors for GPI lipid anchor biosynthesis and post‐translational transfer to proteins

Eisenhaber, B., Maurer‐Stroh, S., Novatchkova, M., Schneider, G., & Eisenhaber, F. (2003) · BioEssays · doi:10.1002/bies.10254 · Cited by 168

Analyzing Effects of Naturally Occurring Missense Mutations

Zhang, Z., Miteva, M. A., Wang, L., & Alexov, E. (2012) · Computational and Mathematical Methods in Medicine · doi:10.1155/2012/805827 · Cited by 173

Drug Repositioning by Kernel-Based Integration of Molecular Structure, Molecular Activity, and Phenotype Data

Wang, Y., Chen, S., Deng, N.-Y., & Wang, Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0078518 · Cited by 165

ESTHER, the database of the / -hydrolase fold superfamily of proteins

Hôtelier, T. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkh141 · Cited by 165

An update on Drug Repurposing: Re-written saga of the drug’s fate

S, H. S. G. N., Saraswathy, G. R., Murahari, M., & Krishnamurthy, M. (2018) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2018.11.127 · Cited by 164

UTRdb and UTRsite: a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs

Mignone, F. (2004) · Nucleic Acids Research · doi:10.1093/nar/gki021 · Cited by 161

Enhancing the Prioritization of Disease-Causing Genes through Tissue Specific Protein Interaction Networks

Magger, O., Waldman, Y. Y., Ruppin, E., & Sharan, R. (2012) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1002690 · Cited by 158

Computational approaches to disease‐gene prediction: rationale, classification and successes

Piro, R. M., & Cunto, F. D. (2012) · FEBS Journal · doi:10.1111/j.1742-4658.2012.08471.x · Cited by 156

SNPeffect: a database mapping molecular phenotypic effects of human non-synonymous coding SNPs

Reumers, J. (2004) · Nucleic Acids Research · doi:10.1093/nar/gki086 · Cited by 156

Analysis of protein sequence and interaction data for candidate disease gene prediction

George, R. A., Liu, J. Y., Feng, L. L., Bryson‐Richardson, R. J., Fatkin, D., & Wouters, M. A. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl707 · Cited by 155

Computationally Driven, Quantitative Experiments Discover Genes Required for Mitochondrial Biogenesis

Hess, D. C., Myers, C. L., Huttenhower, C., Hibbs, M., Hayes, A. P., Paw, J., Clore, J. J., Mendoza, R. M., Luis, B.-J. S., Nislow, C., et al. (2009) · PLoS Genetics · doi:10.1371/journal.pgen.1000407 · Cited by 152

Prediction of CircRNA-Disease Associations Using KATZ Model Based on Heterogeneous Networks

Fan, C., Lei, X., & Wu, F. (2018) · International Journal of Biological Sciences · doi:10.7150/ijbs.28260 · Cited by 155

Evolutionary conservation and selection of human disease gene orthologs in the rat and mouse genomes

Huang, H., Winter, E. E., Wang, H., Weinstock, K. G., Xing, H., Goodstadt, L., Stenson, P. D., Cooper, D. N., Smith, D., Albà, M. M., et al. (2004) · Genome biology · doi:10.1186/gb-2004-5-7-r47 · Cited by 153

ASAP: the Alternative Splicing Annotation Project

Lee, C. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg029 · Cited by 154

DRUG TARGET PREDICTIONS BASED ON HETEROGENEOUS GRAPH INFERENCE

Wang, W., Yang, S., & Li, J. (2012) · Pacific Symposium on Biocomputing (PSB) · doi:10.1142/9789814447973_0006 · Cited by 141

Germ-line DNA copy number variation frequencies in a large North American population

Zogopoulos, G., Ha, K., Naqib, F., Moore, S., Kim, H., Montpetit, A., Robidoux, F., Laflamme, P., Cotterchio, M., Greenwood, C. M. T., et al. (2007) · Human Genetics · doi:10.1007/s00439-007-0404-5 · Cited by 131

Genetic Models of Mechanotransduction: The NematodeCaenorhabditis elegans

Syntichaki, P., & Tavernarakis, N. (2004) · Physiological Reviews · doi:10.1152/physrev.00043.2003 · Cited by 130

IndiGenomes: a comprehensive resource of genetic variants from over 1000 Indian genomes

Jain, A. K., Bhoyar, R. C., Pandhare, K., Mishra, A., Sharma, D., Imran, M., Senthivel, V., Divakar, M. K., Rophina, M., Jolly, B., et al. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa923 · Cited by 127

Modeling Effects of Human Single Nucleotide Polymorphisms on Protein-Protein Interactions

Teng, S., Madej, T., Panchenko, A. R., & Alexov, E. G. (2009) · Biophysical Journal · doi:10.1016/j.bpj.2008.12.3904 · Cited by 125

Gene function analysis in complex data sets using ErmineJ

Gillis, J. A., Mistry, M., & Pavlidis, P. (2010) · Nature Protocols · doi:10.1038/nprot.2010.78 · Cited by 122

Network pharmacology-based strategy to investigate pharmacological mechanisms of Zuojinwan for treatment of gastritis

Yu, G.-H., Wang, W., Wang, X., Xu, M., Zhang, L.-L., Ding, L., Guo, R., & Shi, Y. (2018) · BMC Complementary and Alternative Medicine · doi:10.1186/s12906-018-2356-9 · Cited by 108

A genome-wide map of human genetic interactions inferred from radiation hybrid genotypesPreprint

Lin, A., Wang, R. T., Ahn, S., Park, C. C., & Smith, D. (2010) · Genome Research · doi:10.1101/gr.104216.109 · Cited by 112

VisANT: an integrative framework for networks in systems biology

Hu, Z., Snitkin, E. S., & DeLisi, C. (2008) · Briefings in Bioinformatics · doi:10.1093/bib/bbn020 · Cited by 120

Comparative analysis of cancer genes in the human and chimpanzee genomes

Puente, X. S., Velasco, G., Gutiérrez‐Fernández, A., Bertranpetit, J., King, M., & López-Otı́n, C. (2006) · BMC Genomics · doi:10.1186/1471-2164-7-15 · Cited by 118

Extending the mutual information measure to rank inferred literature relationships

Wren, J. D. (2004) · BMC Bioinformatics · doi:10.1186/1471-2105-5-145 · Cited by 117

Polypharmacology modelling using proteochemometrics (PCM): recent methodological developments, applications to target families, and future prospects

Cortés‐Ciriano, I., Ain, Q. U., Subramanian, V., Lenselink, E. B., Méndez‐Lucio, O., IJzerman, A. P., Wohlfahrt, G., Prūsis, P., Malliavin, T. E., van Westen, G. J. P., et al. (2014) · MedChemComm · doi:10.1039/c4md00216d · Cited by 119

Searching NCBI's dbSNP Database

Bhagwat, M. (2010) · Current Protocols in Bioinformatics · doi:10.1002/0471250953.bi0119s32 · Cited by 116

Recent additions and improvements to the Onto-Tools

Khatri, P., Sellamuthu, S., Malhotra, P., Amin, K., Done, A., & Drăghici, S. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki472 · Cited by 114

Human genetic variation alters CRISPR-Cas9 on- and off-targeting specificity at therapeutically implicated loci

Lessard, S., Francioli, L. C., Alföldi, J., Tardif, J., Ellinor, P. T., MacArthur, D. G., Lettre, G., Orkin, S. H., & Canver, M. C. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1714640114 · Cited by 115

NOPdb: Nucleolar Proteome Database

Leung, A. K. L. (2005) · Nucleic Acids Research · doi:10.1093/nar/gkj004 · Cited by 111

Exploiting Protein-Protein Interaction Networks for Genome-Wide Disease-Gene Prioritization

Güney, E., & Oliva, B. (2012) · PLoS ONE · doi:10.1371/journal.pone.0043557 · Cited by 109

Dominating Biological Networks

Milenković, T., Memišević, V., Bonato, A., & Pržulj, N. (2011) · PLoS ONE · doi:10.1371/journal.pone.0023016 · Cited by 107

Computational drug repositioning based on multi-similarities bilinear matrix factorization

Yang, M., Wu, G., Zhao, Q., Li, Y., & Wang, J. (2020) · Briefings in Bioinformatics · doi:10.1093/bib/bbaa267 · Cited by 109

Mining FDA drug labels using an unsupervised learning technique - topic modeling

Bişğin, H., Liu, Z., Fang, H., Xu, X., & Tong, W. (2011) · BMC Bioinformatics · doi:10.1186/1471-2105-12-s10-s11 · Cited by 107

Characterization of protein-interaction networks in tumors

Platzer, A., Perco, P., Lukas, A., & Mayer, B. (2007) · BMC Bioinformatics · doi:10.1186/1471-2105-8-224 · Cited by 106

Metabolic dysregulation in monogenic disorders and cancer — finding method in madness

Erez, A., & DeBerardinis, R. J. (2015) · Nature Reviews Cancer · doi:10.1038/nrc3949 · Cited by 105

Differences in the evolutionary history of disease genes affected by dominant or recessive mutations

Furney, S. J., Albà, M. M., & López-Bigas, N. (2006) · BMC Genomics · doi:10.1186/1471-2164-7-165 · Cited by 105

The Nuclear Protein Database (NPD): sub-nuclear localisation and functional annotation of the nuclear proteome

Dellaire, G. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg018 · Cited by 102

PupaSNP Finder: a web tool for finding SNPs with putative effect at transcriptional level

Conde, L., Vaquerizas, J. M., Santoyo, J., Al‐Shahrour, F., Ruiz‐Llorente, S., Robledo, M., & Dopazo, J. (2004) · Nucleic Acids Research · doi:10.1093/nar/gkh438 · Cited by 100

Systems-level cancer gene identification from protein interaction network topology applied to melanogenesis-related functional genomics data

Milenković, T., Memišević, V., Ganesan, A. K., & Pržulj, N. (2009) · Journal of The Royal Society Interface · doi:10.1098/rsif.2009.0192 · Cited by 95

OMIA (Online Mendelian Inheritance in Animals): an enhanced platform and integration into the Entrez search interface at NCBI

Lenffer, J. (2005) · Nucleic Acids Research · doi:10.1093/nar/gkj152 · Cited by 98

Variant effect prediction tools assessed using independent, functional assay-based datasets: implications for discovery and diagnostics

Mahmood, K., Jung, C., Philip, G. K., Georgeson, P., Chung, J., Pope, B. J., & Park, D. J. (2017) · Human Genomics · doi:10.1186/s40246-017-0104-8 · Cited by 96

Domains, motifs and clusters in the protein universe

Liu, J., & Rost, B. (2003) · Current Opinion in Chemical Biology · doi:10.1016/s1367-5931(02)00003-0 · Cited by 97

MitoP2: the mitochondrial proteome database--now including mouse data

Prokisch, H. (2005) · Nucleic Acids Research · doi:10.1093/nar/gkj127 · Cited by 95

GeneSeeker: extraction and integration of human disease-related information from web-based genetic databases

van Driel, M. A., Cuelenaere, K., Kemmeren, P., Leunissen, J. A. M., Brunner, H. G., & Vriend, G. (2005) · Nucleic Acids Research · doi:10.1093/nar/gki435 · Cited by 94

Correction: Prediction of microRNAs Associated with Human Diseases Based on Weighted k Most Similar Neighbors

Xuan, P., Han, K., Guo, M., Guo, Y., Li, J., Ding, J., Liu, Y., Dai, Q., Li, J., Teng, Z., et al. (2013) · PLoS ONE · doi:10.1371/annotation/28592478-72f5-4937-919b-b2342d6ceda0 · Cited by 94

Inferring new indications for approved drugs via random walk on drug-disease heterogenous networks

Liu, H., Song, Y., Guan, J., Luo, L., & Zhuang, Z. (2016) · BMC Bioinformatics · doi:10.1186/s12859-016-1336-7 · Cited by 94

Defining the Role of Essential Genes in Human Disease

Dickerson, J. E., Zhu, A., Robertson, D. L., & Hentges, K. E. (2011) · PLoS ONE · doi:10.1371/journal.pone.0027368 · Cited by 91

The Human Gene Mutation Database (HGMD) and Its Exploitation in the Study of Mutational Mechanisms

Cooper, D. N., Stenson, P. D., & Chuzhanova, N. A. (2005) · Current Protocols in Bioinformatics · doi:10.1002/0471250953.bi0113s12 · Cited by 90

Predicting Potential Drugs for Breast Cancer based on miRNA and Tissue Specificity

Yu, L., Zhao, J. K., & Gao, L. (2018) · International Journal of Biological Sciences · doi:10.7150/ijbs.23350 · Cited by 87

Online Mendelian Inheritance in Animals (OMIA): a comparative knowledgebase of genetic disorders and other familial traits in non-laboratory animals

Nicholas, F. W. (2003) · Nucleic Acids Research · doi:10.1093/nar/gkg074 · Cited by 88

Network Pharmacology-Based Strategy to Investigate the Pharmacologic Mechanisms of Atractylodes macrocephala Koidz. for the Treatment of Chronic Gastritis

Yang, S., Zhang, J., Yan, Y., Yang, M., Li, C., Li, J., Zhong, L., Qian-feng, G., & Yu, H. (2020) · Frontiers in Pharmacology · doi:10.3389/fphar.2019.01629 · Cited by 87

Mutation nomenclature extensions and suggestions to describe complex mutations: A discussion

den Dunnen, J. T., & Antonarakis, S. E. (2000) · Human Mutation · doi:10.1002/(sici)1098-1004(200001)15:1 · Cited by 1,757

Online Mendelian Inheritance in Man

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Content and Access

Maglott, D. R., Amberger, J. S., & Hamosh, A. (2012)

McKusick's Online Mendelian Inheritance in Man (OMIM(R))

Amberger, J., Bocchini, C. A., Scott, A. F., & Hamosh, A. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkn665 · Cited by 717

Searching Online Mendelian Inheritance in Man ( OMIM ) for Information on Genetic Loci Involved in Human Disease

Baxevanis, A. D. (2012) · Current Protocols in Human Genetics · doi:10.1002/0471142905.hg0913s73 · Cited by 22