Citation Impact
Citing Papers
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
2009 Standout
Identifying Allelic Loss and Homozygous Deletions in Pancreatic Cancer without Matched Normals Using High-Density Single-Nucleotide Polymorphism Arrays
2006
ZBTB1 is a determinant of lymphoid development
2011 StandoutNobel
Diagnosis and management of acute myeloid leukemia in adults: recommendations from an international expert panel, on behalf of the European LeukemiaNet
2009 Standout
A Robust Algorithm for Copy Number Detection Using High-Density Oligonucleotide Single Nucleotide Polymorphism Genotyping Arrays
2005
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
FoxOs Enforce a Progression Checkpoint to Constrain mTORC1-Activated Renal Tumorigenesis
2010 StandoutNobel
In silico method for inferring genotypes in pedigrees
2006
[9] TM4 Microarray Software Suite
2006 Standout
Single Nucleotide Polymorphism in the Aetiology of Caries: Systematic Literature Review
2017 Standout
Quantitative trait locus association scan of early reading disability and ability using pooled DNA and 100K SNP microarrays in a sample of 5760 children
2007
Increasing power in association studies by using linkage disequilibrium structure and molecular function as prior information
2008
Genome-wide analysis of genetic alterations in acute lymphoblastic leukaemia
2007 Nature
Mechanisms of Thrombus Formation
2008 Standout
Genome-wide screen for asthma in Puerto Ricans: evidence for association with 5q23 region
2008
Integrated analysis of somatic mutations and focal copy-number changes identifies key genes and pathways in hepatocellular carcinoma
2012 Standout
Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients
2009
PIWI Associated siRNAs and piRNAs Specifically Require the Caenorhabditis elegans HEN1 Ortholog henn-1
2012 StandoutNobel
Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays
2006
A HapMap harvest of insights into the genetics of common disease
2008
Leveraging Polygenic Functional Enrichment to Improve GWAS Power
2018 Standout
Recent Developments in Genomewide Association Scans: A Workshop Summary and Review
2005
The Fontan procedure: analysis of cohorts and late complications
2000
HLA Has Strongest Association with IgA Nephropathy in Genome-Wide Analysis
2010 StandoutNobel
Relative Contribution of Genetic and Nongenetic Modifiers to Intestinal Obstruction in Cystic Fibrosis
2006
Cancer drug resistance: an evolving paradigm
2013 Standout
GMAP: a genomic mapping and alignment program for mRNA and EST sequences
2005 Standout
Malignant astrocytic glioma: genetics, biology, and paths to treatment
2007 Standout
Hematopoiesis: An Evolving Paradigm for Stem Cell Biology
2008 Standout
Whole-genome genotyping with the single-base extension assay
2005
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
2008 Standout
Efficient target-selected mutagenesis in Caenorhabditis elegans: Toward a knockout for every gene
2007
22q11.21 Deletion Syndromes: A Review of Proximal, Central, and Distal Deletions and Their Associated Features
2015 Standout
MARA: a novel approach for highly multiplexed locus-specific SNP genotyping using high-density DNA oligonucleotide arrays
2004
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
2007 Standout
Highly parallel genomic assays
2006
Oncogenic mutations of ALK kinase in neuroblastoma
2008 Nature
Principal components analysis corrects for stratification in genome-wide association studies
2006 Standout
The Mammalian Epigenome
2007 Standout
A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
2009 Standout
DNA methylation landscapes: provocative insights from epigenomics
2008 Standout
Rapid and Accurate Haplotype Phasing and Missing-Data Inference for Whole-Genome Association Studies By Use of Localized Haplotype Clustering
2007 Standout
Rapid and cost-effective polymorphism identification and genotyping using restriction site associated DNA (RAD) markers
2006
A missense mutation in the Kv1.1 voltage-gated potassium channel–encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia
2009
Evaluating and improving power in whole-genome association studies using fixed marker sets
2006
Cystic fibrosis genetics: from molecular understanding to clinical application
2014 Standout
FOXO1 and TCF7L2 genes involved in metastasis and poor prognosis in clear cell renal cell carcinoma
2010
Macrolides and airway inflammation in children
2005
Sequencing by Cyclic Ligation and Cleavage (CycLiC) directly on a microarray captured template
2008
Transactivation of miR-34a by p53 Broadly Influences Gene Expression and Promotes Apoptosis
2007 Standout
Multi-ethnic reference values for spirometry for the 3–95-yr age range: the global lung function 2012 equations
2012 Standout
Prescribing Personalized Nutrition for Cardiovascular Health: Are We Ready?
2014 Standout
10 Years of GWAS Discovery: Biology, Function, and Translation
2017 Standout
Identification of a candidate genetic variant for the high prevalence of type II diabetes in Polynesians
2007
Normalization of Illumina Infinium whole-genome SNP data improves copy number estimates and allelic intensity ratios
2008
How culture shaped the human genome: bringing genetics and the human sciences together
2010 Standout
High-resolution Global Genomic Survey of 178 Gliomas Reveals Novel Regions of Copy Number Alteration and Allelic Imbalances
2006
[1] The Affymetrix GeneChip® Platform: An Overview
2006
Genome-wide genetic marker discovery and genotyping using next-generation sequencing
2011 Standout
High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays
2009
The prognostic landscape of genes and infiltrating immune cells across human cancers
2015 Standout
Genome-wide efficient mixed-model analysis for association studies
2012 Standout
Genetics of Food Intake Self-Regulation in Childhood: Literature Review and Research Opportunities
2013 Standout
AID-induced T-lymphoma or B-leukemia/lymphoma in a mouse BMT model
2010 StandoutNobel
Genome Wide Sampling Sequencing for SNP Genotyping: Methods, Challenges and Future Development
2015
Sequencing technologies — the next generation
2009 Standout
Mixed linear model approach adapted for genome-wide association studies
2010 Standout
Rapid SNP Discovery and Genetic Mapping Using Sequenced RAD Markers
2008 Standout
Common Variation in NLRP3 Is Associated With Early Death and Elevated Inflammasome Biomarkers Among Advanced HIV/TB Co-infected Patients in Botswana
2018 StandoutNobel
A comprehensive assay for targeted multiplex amplification of human DNA sequences
2008
Stacks: Building and Genotyping Loci De Novo From Short-Read Sequences
2011 Standout
Treatment of Plastic Bronchitis in a Fontan Patient With Tissue Plasminogen Activator: A Case Report and Review of the Literature
2002
Magnesium in Man: Implications for Health and Disease
2014 Standout
Incorporating prior information into association studies
2012
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease
2008 Standout
GEL: a novel genotype calling algorithm using empirical likelihood
2006
A Common NLRC4 Gene Variant Associates With Inflammation and Pulmonary Function in Human Immunodeficiency Virus and Tuberculosis
2019 StandoutNobel
Excavating Neandertal and Denisovan DNA from the genomes of Melanesian individuals
2016 StandoutScienceNobel
ACC/AHA 2008 Guidelines for the Management of Adults With Congenital Heart Disease: Executive Summary
2008 Standout
Genomewide Rapid Association Using Mixed Model and Regression: A Fast and Simple Method For Genomewide Pedigree-Based Quantitative Trait Loci Association Analysis
2007
Testing Untyped Alleles (TUNA)—applications to genome‐wide association studies
2006
The International Workshop on Meibomian Gland Dysfunction: Report of the Subcommittee on Management and Treatment of Meibomian Gland Dysfunction
2011 Standout
Drug Resistance in Cancer: An Overview
2014 Standout
Macrophages, Inflammation, and Insulin Resistance
2010 Standout
Works of Henry Hui being referenced
Genotyping over 100,000 SNPs on a pair of oligonucleotide arrays
2004
Bronchial casts in children: a proposed classification based on nine cases and a review of the literature.
1997