Published in Nucleic Acids Res on November 27, 2012
ClinVar: public archive of relationships among sequence variation and human phenotype. Nucleic Acids Res (2013) 9.31
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2012) 8.41
RefSeq: an update on mammalian reference sequences. Nucleic Acids Res (2013) 7.29
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2014) 3.55
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2015) 2.44
Gene: a gene-centered information resource at NCBI. Nucleic Acids Res (2014) 2.00
Prioritizing genomic applications for action by level of evidence: a horizon-scanning method. Clin Pharmacol Ther (2014) 1.93
The 2013 Nucleic Acids Research Database Issue and the online molecular biology database collection. Nucleic Acids Res (2012) 1.66
Preemptive clinical pharmacogenetics implementation: current programs in five US medical centers. Annu Rev Pharmacol Toxicol (2014) 1.58
Horizon scanning for translational genomic research beyond bench to bedside. Genet Med (2014) 1.54
The Human Phenotype Ontology in 2017. Nucleic Acids Res (2016) 1.01
Pharmacogenetic allele nomenclature: International workgroup recommendations for test result reporting. Clin Pharmacol Ther (2015) 0.95
Achieving high-sensitivity for clinical applications using augmented exome sequencing. Genome Med (2015) 0.94
Genetic epidemiology and nonsyndromic structural birth defects: from candidate genes to epigenetics. JAMA Pediatr (2014) 0.88
Minimum information for reporting next generation sequence genotyping (MIRING): Guidelines for reporting HLA and KIR genotyping via next generation sequencing. Hum Immunol (2015) 0.87
The pharmacogenetic control of antiplatelet response: candidate genes and CYP2C19. Expert Opin Drug Metab Toxicol (2015) 0.79
Histoimmunogenetics Markup Language 1.0: Reporting next generation sequencing-based HLA and KIR genotyping. Hum Immunol (2015) 0.78
MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search. Nucleic Acids Res (2016) 0.77
GeneSense: a new approach for human gene annotation integrated with protein-protein interaction networks. Sci Rep (2014) 0.77
Regulating whole exome sequencing as a diagnostic test. Hum Genet (2016) 0.76
GT2RDF: Semantic Representation of Genetic Testing Data. AMIA Annu Symp Proc (2017) 0.75
Annotating Mutational Effects on Proteins and Protein Interactions: Designing Novel and Revisiting Existing Protocols. Methods Mol Biol (2017) 0.75
Incidence of Exposure of Patients in the United States to Multiple Drugs for Which Pharmacogenomic Guidelines Are Available. PLoS One (2016) 0.75
FDA's Proposed Guidance for Laboratory Developed Tests: How Should Regulators Balance the Risks and Promise of Innovation in Clinical Genetics? FDLIs Food Drug Policy Forum (2015) 0.75
EHR based Genetic Testing Knowledge Base (iGTKB) Development. BMC Med Inform Decis Mak (2015) 0.75
Cost-effectiveness of pharmacogenetic-guided treatment: are we there yet? Pharmacogenomics J (2017) 0.75
Variant Interpretation: Functional Assays to the Rescue. Am J Hum Genet (2017) 0.75
The Universal Protein Resource (UniProt) in 2010. Nucleic Acids Res (2009) 19.70
NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy. Nucleic Acids Res (2011) 14.04
McKusick's Online Mendelian Inheritance in Man (OMIM). Nucleic Acids Res (2008) 12.83
CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network. Clin Pharmacol Ther (2011) 10.95
Entrez Gene: gene-centered information at NCBI. Nucleic Acids Res (2010) 9.09
The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. Am J Hum Genet (2008) 8.78
Pharmacogenomics knowledge for personalized medicine. Clin Pharmacol Ther (2012) 6.92
genenames.org: the HGNC resources in 2011. Nucleic Acids Res (2010) 5.77
GeneTests-GeneClinics: genetic testing information for a growing audience. Hum Mutat (2002) 2.97
Evaluation of the UMLS as a terminology and knowledge resource for biomedical informatics. Proc AMIA Symp (2002) 2.20
Describing structural changes by extending HGVS sequence variation nomenclature. Hum Mutat (2011) 1.62
Developing the blueprint for a genetic testing registry. Public Health Genomics (2009) 1.29
Registry of genetic tests: a critical stepping stone to improving the genetic testing system. Genet Test Mol Biomarkers (2009) 0.99
Initial sequencing and comparative analysis of the mouse genome. Nature (2002) 96.15
NCBI reference sequences (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins. Nucleic Acids Res (2006) 48.10
NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins. Nucleic Acids Res (2005) 37.39
NCBI Reference Sequences: current status, policy and new initiatives. Nucleic Acids Res (2008) 26.04
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2005) 22.98
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2007) 22.53
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2008) 21.36
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2006) 18.85
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2006) 18.84
The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes. Genome Res (2009) 14.90
NCBI Reference Sequences (RefSeq): current status, new features and genome annotation policy. Nucleic Acids Res (2011) 14.04
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. Am J Hum Genet (2010) 13.70
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2009) 12.51
Prepublication data sharing. Nature (2009) 12.24
Managing incidental findings in human subjects research: analysis and recommendations. J Law Med Ethics (2008) 12.10
NCBI Reference Sequence project: update and current status. Nucleic Acids Res (2003) 11.30
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2010) 10.97
ClinVar: public archive of relationships among sequence variation and human phenotype. Nucleic Acids Res (2013) 9.31
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res (2004) 9.18
Database resources of the National Center for Biotechnology Information. Nucleic Acids Res (2011) 8.62
Public expectations for return of results from large-cohort genetic research. Am J Bioeth (2008) 7.63
RefSeq: an update on mammalian reference sequences. Nucleic Acids Res (2013) 7.29
Subjects matter: a survey of public opinions about a large genetic cohort study. Genet Med (2008) 4.52
ClinGen--the Clinical Genome Resource. N Engl J Med (2015) 4.45
p53 regulates hematopoietic stem cell quiescence. Cell Stem Cell (2009) 4.30
Locus Reference Genomic sequences: an improved basis for describing human DNA variants. Genome Med (2010) 4.19
New models for large prospective studies: is there a better way? Am J Epidemiol (2012) 3.85
Transcatheter valve-in-valve implantation for failed bioprosthetic heart valves. Circulation (2010) 3.65
Human immunodeficiency virus type 1, human protein interaction database at NCBI. Nucleic Acids Res (2008) 3.54
The Fanconi anaemia gene FANCC promotes homologous recombination and error-prone DNA repair. Mol Cell (2004) 3.44
IgBLAST: an immunoglobulin variable domain sequence analysis tool. Nucleic Acids Res (2013) 3.33
Predictive factors for glaucomatous visual field progression in the Advanced Glaucoma Intervention Study. Ophthalmology (2004) 3.14
Extreme diving of beaked whales. J Exp Biol (2006) 2.95
Public perspectives on informed consent for biobanking. Am J Public Health (2009) 2.93
Confidentiality, privacy, and security of genetic and genomic test information in electronic health records: points to consider. Genet Med (2008) 2.84
A prospective, randomized, multicenter trial of amnioreduction vs selective fetoscopic laser photocoagulation for the treatment of severe twin-twin transfusion syndrome. Am J Obstet Gynecol (2007) 2.73
The vertebrate Hef ortholog is a component of the Fanconi anemia tumor-suppressor pathway. Nat Struct Mol Biol (2005) 2.55
Lung cancer screening with sputum cytologic examination, chest radiography, and computed tomography: an update for the U.S. Preventive Services Task Force. Ann Intern Med (2004) 2.53
Deep-diving foraging behaviour of sperm whales (Physeter macrocephalus). J Anim Ecol (2006) 2.41
The completion of the Mammalian Gene Collection (MGC). Genome Res (2009) 2.21
Current status and new features of the Consensus Coding Sequence database. Nucleic Acids Res (2013) 2.19
A double-blind randomized controlled clinical trial to assess the effect of Doppler optimized intraoperative fluid management on outcome following radical cystectomy. J Urol (2011) 2.19
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants. Nucleic Acids Res (2013) 2.18
A QTL resource and comparison tool for pigs: PigQTLDB. Mamm Genome (2005) 2.11
A web server for performing electronic PCR. Nucleic Acids Res (2004) 2.02
Mapping infant brain myelination with magnetic resonance imaging. J Neurosci (2011) 1.97
What everybody should know about the rat genome and its online resources. Nat Genet (2008) 1.94
Established human papillomavirus type 16-expressing tumors are effectively eradicated following vaccination with long peptides. J Immunol (2002) 1.93
Control of spin precession in a spin-injected field effect transistor. Science (2009) 1.93
Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinion. Am J Med Genet C Semin Med Genet (2008) 1.92
Ocular biomechanics and biotransport. Annu Rev Biomed Eng (2004) 1.91
Reducing DUI among US college students: results of an environmental prevention trial. Addiction (2005) 1.87
Mechanisms and treatment of cardiovascular disease in Williams-Beuren syndrome. J Clin Invest (2008) 1.86
Cystic adenomatoid malformation volume ratio predicts outcome in prenatally diagnosed cystic adenomatoid malformation of the lung. J Pediatr Surg (2002) 1.84
Identifying early glaucoma with optical coherence tomography. Am J Ophthalmol (2004) 1.84
Aging, age-related macular degeneration, and the response-to-retention of apolipoprotein B-containing lipoproteins. Prog Retin Eye Res (2009) 1.80
Tracking and coordinating an international curation effort for the CCDS Project. Database (Oxford) (2012) 1.78
The changing paradigm of outflow resistance generation: towards synergistic models of the JCT and inner wall endothelium. Exp Eye Res (2008) 1.77
Preparing for a consumer-driven genomic age. N Engl J Med (2010) 1.72
The oil spill in ageing Bruch membrane. Br J Ophthalmol (2011) 1.62
Cataloguing the HIV type 1 human protein interaction network. AIDS Res Hum Retroviruses (2008) 1.61
Geneticists' views on science policy formation and public outreach. Am J Med Genet A (2005) 1.53
Characterising the complexity of medication safety using a human factors approach: an observational study in two intensive care units. BMJ Qual Saf (2013) 1.52
Circadian regulation of cortisol release in behaviorally split golden hamsters. Endocrinology (2011) 1.50
Expression profiles of osteosarcoma that can predict response to chemotherapy. Cancer Res (2005) 1.49
Multidetector computed tomography in transcatheter aortic valve implantation. JACC Cardiovasc Imaging (2011) 1.47
FANCE: the link between Fanconi anaemia complex assembly and activity. EMBO J (2002) 1.47
The mechanism of increasing outflow facility during washout in the bovine eye. Invest Ophthalmol Vis Sci (2002) 1.44
Residency training in preventive medicine: challenges and opportunities. Am J Prev Med (2005) 1.44
Optic disk appearance in advanced age-related macular degeneration. Am J Ophthalmol (2004) 1.43
Apoptosis and autophagy: BIM as a mediator of tumour cell death in response to oncogene-targeted therapeutics. FEBS J (2009) 1.41
Apolipoprotein B-containing lipoproteins in retinal aging and age-related macular degeneration. J Lipid Res (2009) 1.41
On-film formation of bi nanowires with extraordinary electron mobility. Nano Lett (2009) 1.38
Can the Kattan nomogram still accurately predict prognosis in renal cell carcinoma using the revised 2010 tumor-nodes-metastasis reclassification? Int J Urol (2012) 1.38
Quick-freeze/deep-etch visualization of age-related lipid accumulation in Bruch's membrane. Invest Ophthalmol Vis Sci (2003) 1.36
Veterans' attitudes regarding a database for genomic research. Genet Med (2009) 1.36
Expression of Bcl-2 family proteins in advanced laryngeal squamous cell carcinoma: correlation with response to chemotherapy and organ preservation. Laryngoscope (2002) 1.35
The genes induced by signal transducer and activators of transcription (STAT)3 and STAT5 in mammary epithelial cells define the roles of these STATs in mammary development. Mol Endocrinol (2005) 1.33
Individual right whales call louder in increased environmental noise. Biol Lett (2010) 1.31
Sequencing and analysis of 10,967 full-length cDNA clones from Xenopus laevis and Xenopus tropicalis reveals post-tetraploidization transcriptome remodeling. Genome Res (2006) 1.31
Quality of interaction between at-risk infants and caregiver at 12-15 months is associated with 3-year autism outcome. J Child Psychol Psychiatry (2012) 1.27
Civilian and military genetics: nondiscrimination policy in a post-GINA world. Am J Hum Genet (2008) 1.24
Secreted proteins from Mycobacterium tuberculosis gain access to the cytosolic MHC class-I antigen-processing pathway. J Immunol (2006) 1.24
Physician competencies for prescribing lifestyle medicine. JAMA (2010) 1.23
Parent-infant interaction in infant siblings at risk of autism. Res Dev Disabil (2012) 1.22
Transcatheter closure of paravalvular defects using a purpose-specific occluder. JACC Cardiovasc Interv (2010) 1.20
Aortic annulus diameter determination by multidetector computed tomography: reproducibility, applicability, and implications for transcatheter aortic valve implantation. JACC Cardiovasc Interv (2011) 1.20
Direct-to-consumer genetic tests, government oversight, and the First Amendment: what the government can (and can't) do to protect the public's health. Oklahoma Law Rev (2004) 1.19
Conditional deletion of Pkd1 in osteocytes disrupts skeletal mechanosensing in mice. FASEB J (2011) 1.16
A cell number-counting factor regulates the cytoskeleton and cell motility in Dictyostelium. Proc Natl Acad Sci U S A (2002) 1.16
The effect of intrauterine myelomeningocele repair on the incidence of shunt-dependent hydrocephalus. Pediatr Neurosurg (2003) 1.15