Citation Impact
Citing Papers
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
2009 Standout
Evaluating plague and smallpox as historical selective pressures for the CCR5-Δ32 HIV-resistance allele
2003
The UK Biobank resource with deep phenotyping and genomic data
2018 StandoutNature
The promise and challenge of therapeutic genome editing
2020 StandoutNatureNobel
Long-Term Engraftment and Fetal Globin Induction upon BCL11A Gene Editing in Bone-Marrow-Derived CD34 + Hematopoietic Stem and Progenitor Cells
2017
Investigation of associations between Piezo1 mechanoreceptor gain-of-function variants and glaucoma-related phenotypes in humans and mice
2020 StandoutNobel
Programmable editing of a target base in genomic DNA without double-stranded DNA cleavage
2016 StandoutNature
Atopic Dermatitis
2008 Standout
A HapMap harvest of insights into the genetics of common disease
2008
Leptin stimulates fatty-acid oxidation by activating AMP-activated protein kinase
2002 StandoutNature
Asthma Genetics
2002
The Effect of Infections on Susceptibility to Autoimmune and Allergic Diseases
2002 Standout
Increased oxidative stress in obesity and its impact on metabolic syndrome
2004 Standout
Congenital leptin deficiency is associated with severe early-onset obesity in humans
1997 StandoutNature
Genetic loci controlling body fat, lipoprotein metabolism, and insulin levels in a multifactorial mouse model.
1998
Advances in autism genetics: on the threshold of a new neurobiology
2008
Foxp2 controls synaptic wiring of corticostriatal circuits and vocal communication by opposing Mef2c
2016 StandoutNobel
The genetics of psoriasis, psoriatic arthritis and atopic dermatitis
2004
Relatively low plasma leptin concentrations precede weight gain in Pima Indians
1997
Childhood obesity: public-health crisis, common sense cure
2002 Standout
Advances in the molecular genetics of obesity
1999
How reliable are empirical genomic scans for selective sweeps?
2006
The Leptin Receptor
1997
Natural regulatory mutations elevate the fetal globin gene via disruption of BCL11A or ZBTB7A binding
2018
Regulation of skeletal muscle mass in mice by a new TGF-p superfamily member
1997 StandoutNature
Modifier genes and sickle cell anemia
2006
Genetic modifiers of sickle cell disease
2012
Targeted Disruption of the Melanocortin-4 Receptor Results in Obesity in Mice
1997 Standout
Mapping and analysis of chromatin state dynamics in nine human cell types
2011 StandoutNature
Osf2/Cbfa1: A Transcriptional Activator of Osteoblast Differentiation
1997 Standout
A Cold-Inducible Coactivator of Nuclear Receptors Linked to Adaptive Thermogenesis
1998 Standout
Therapeutic genome editing: prospects and challenges
2015
The Rise and Fall of the Chemoattractant Receptor GPR33
2005 StandoutNobel
Association of All-Cause Mortality With Overweight and Obesity Using Standard Body Mass Index Categories
2013 Standout
The Human Obesity Gene Map: The 1996 Update
1997
Central nervous system control of food intake
2000 StandoutNature
Genome-wide association studies: potential next steps on a genetic journey
2008
Genome-wide RNAi analysis of Caenorhabditis elegans fat regulatory genes
2003 StandoutNatureNobel
The Molecular Genetics of Rodent Single Gene Obesities
1997
Search-and-replace genome editing without double-strand breaks or donor DNA
2019 StandoutNature
Endocrine Regulation of Energy Metabolism by the Skeleton
2007 Standout
Leptin modulates the T-cell immune response and reverses starvation-induced immunosuppression
1998 StandoutNature
Sickle-cell disease
2010 Standout
A major quantitative trait locus determining serum leptin levels and fat mass is located on human chromosome 2
1997
Rapid and Pervasive Changes in Genome-wide Enhancer Usage during Mammalian Development
2013
Adipogenesis and Obesity: Rounding Out the Big Picture
1996
Predicting Obesity in Young Adulthood from Childhood and Parental Obesity
1997 Standout
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
2018 Standout
A framework for variation discovery and genotyping using next-generation DNA sequencing data
2011 Standout
The Emerging Hallmarks of Cancer Metabolism
2016 Standout
Simultaneous Genotype Calling and Haplotype Phasing Improves Genotype Accuracy and Reduces False-Positive Associations for Genome-wide Association Studies
2009
Genome-wide association study of hematological and biochemical traits in a Japanese population
2010
Fine-scale recombination patterns differ between chimpanzees and humans
2005 StandoutNobel
The causes of obesity: advances in molecular biology but stagnation on the genetic front
1996
The Human Obesity Gene Map: The 2001 Update
2002
The hormone resistin links obesity to diabetes
2001 StandoutNature
Impact of Valve Prosthesis-Patient Mismatch on Left Ventricular Mass Regression Following Aortic Valve Replacement
2005
Obesity and the Regulation of Energy Balance
2001 Standout
Reactivating Fetal Hemoglobin Expression in Human Adult Erythroblasts Through BCL11A Knockdown Using Targeted Endonucleases
2016
The Drosophila takeout Gene Is a Novel Molecular Link between Circadian Rhythms and Feeding Behavior
2000 StandoutNobel
Atherosclerosis
2000 StandoutNature
Leptin and the regulation of body weight in mammals
1998 StandoutNature
Leptin and OB-R: Body weight regulation by a cytokine receptor
1996
Obesity is associated with macrophage accumulation in adipose tissue
2003 Standout
Estimating recombination rates from population-genetic data
2003
A Neuroligin-4 Missense Mutation Associated with Autism Impairs Neuroligin-4 Folding and Endoplasmic Reticulum Export
2009 StandoutNobel
Tissue-Resident Macrophage Enhancer Landscapes Are Shaped by the Local Microenvironment
2014 Standout
Leptin, Leptin Receptors, and the Control of Body Weight
2009
Validating therapeutic targets through human genetics
2013
The Human Condition—A Molecular Approach
2014 StandoutNobel
Direct Promoter Repression by BCL11A Controls the Fetal to Adult Hemoglobin Switch
2018
Why Most Discovered True Associations Are Inflated
2008
Leptin Inhibits Bone Formation through a Hypothalamic Relay
2000 Standout
Genome-wide detection and characterization of positive selection in human populations
2007 StandoutNature
The Amyloid Hypothesis of Alzheimer's Disease: Progress and Problems on the Road to Therapeutics
2002 StandoutScience
Linkage of Plasma Aβ42 to a Quantitative Locus on Chromosome 10 in Late-Onset Alzheimer's Disease Pedigrees
2000 Science
DNA polymorphisms at the BCL11A , HBS1L-MYB , and β- globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease
2008
Biological Action of Leptin as an Angiogenic Factor
1998 StandoutScience
ACC/AHA 2006 Guidelines for the Management of Patients With Valvular Heart Disease
2006 Standout
Sickle cell disease and stroke
2009
Transcriptional regulation of fetal to adult hemoglobin switching: new therapeutic opportunities
2011
Metabolic reprogramming and cancer progression
2020 StandoutScience
Customizing the genome as therapy for the β-hemoglobinopathies
2016
Iron-Deficiency Anemia
2015 Standout
Obesity is associated with macrophage accumulation in adipose tissue
2003 Standout
Genetic treatment of a molecular disorder: gene therapy approaches to sickle cell disease
2016
Evaluating replicability of laboratory experiments in economics
2016 StandoutScience
A natural regulatory mutation in the proximal promoter elevates fetal globin expression by creating a de novo GATA1 site
2019
Targeted Therapeutic Strategies for Fetal Hemoglobin Induction
2011
Works of Chad Garner being referenced
Deep sequencing of 10,000 human genomes
2016
Wnt signaling directs a metabolic program of glycolysis and angiogenesis in colon cancer
2014 Nobel
Association Between Celiac Disease and Iron Deficiency in Caucasians, but Not Non-Caucasians
2013
Genotype determination for polymorphisms in linkage disequilibrium
2009
Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin
2005
On selecting markers for association studies: Patterns of linkage disequilibrium between two and three diallelic loci
2002
Upward bias in odds ratio estimates from genome‐wide association studies
2007
Natural selection and resistance to HIV
2001 Nature
Evidence of Genetic Interaction between the β-Globin Complex and Chromosome 8q in the Expression of Fetal Hemoglobin
2002
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15
2007
Localization of the Netherton Syndrome Gene to Chromosome 5q32, by Linkage Analysis and Homozygosity Mapping
2000
Genetic and Environmental Influences on Left Ventricular Mass
2000
Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults
2007
The Extent of Linkage Disequilibrium Caused by Selection on G6PD in Humans
2005
Quantitative trait locus on chromosome 8q influences the switch from fetal to adult hemoglobin
2004
Indication for Linkage of the Human OB Gene Region With Extreme Obesity
1996