Citation Impact
Citing Papers
IgG marker of optic-spinal multiple sclerosis binds to the aquaporin-4 water channel
2005 Standout
The MR-Base platform supports systematic causal inference across the human phenome
2018 Standout
Hypoxia-Inducible Factors and the Response to Hypoxic Stress
2010 Standout
Does peroxisome proliferator-activated receptor γ genotype (Pro12ala) modify the association of physical activity and dietary fat with fasting insulin level?
2003
Pro12Ala Substitution in the Peroxisome Proliferator-Activated Receptor-Gamma Is Associated with Increased Leptin Levels in Women with Type-2 Diabetes mellitus
2002
Thiazolidinediones
2004 Standout
Genetic analysis of β-thalassemia intermedia in Israel: Diversity of mechanisms and unpredictability of phenotype
1997
Biochemistry and pathophysiology of intravascular and intracellular lipolysis
2013
Haplotype Structure and Population Genetic Inferences from Nucleotide-Sequence Variation in Human Lipoprotein Lipase
1998
The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
2000
Review article: the role of butyrate on colonic function
2007 Standout
Ulcerative Colitis
2011 Standout
Score Tests for Association between Traits and Haplotypes when Linkage Phase Is Ambiguous
2002 Standout
Studies of the Pro12Ala polymorphism of the peroxisome proliferator-activated receptor-γ2 (PPAR-γ2) gene in relation to insulin sensitivity among glucose tolerant Caucasians
2001
Overcoming the Winner’s Curse: Estimating Penetrance Parameters from Case-Control Data
2007
The β-Thalassemias
1999 Standout
The Human Obesity Gene Map: The 2005 Update
2006
Childhood obesity: public-health crisis, common sense cure
2002 Standout
Impact of the Pro12Ala polymorphism of the PPAR-γ2 gene on serum triacylglycerol response to n−3 fatty acid supplementation
2003
Natural product agonists of peroxisome proliferator-activated receptor gamma (PPARγ): a review
2014 Standout
6 β-Thalassaemia
1993
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
2008 Standout
Lipoprotein lipase: from gene to obesity
2009
Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene
1991 StandoutNature
Breastfeeding in the 21st century: epidemiology, mechanisms, and lifelong effect
2016 Standout
Inflammation, stress, and diabetes
2005 Standout
PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses
2007 Standout
Host Remodeling of the Gut Microbiome and Metabolic Changes during Pregnancy
2012 Standout
Role of Oxidative Modifications in Atherosclerosis
2004 Standout
Impaired expression of peroxisome proliferator-activated receptor γ in ulcerative colitis
2003
Candidate Genes for Type 2 Diabetes
2004
8 The population genetics of the haemoglobinopathies
1993
The Androgen Excess and PCOS Society criteria for the polycystic ovary syndrome: the complete task force report
2008 Standout
A comprehensive review of genetic association studies
2002
Initial sequence of the chimpanzee genome and comparison with the human genome
2005 StandoutNature
Power failure: why small sample size undermines the reliability of neuroscience
2013 Standout
Diagnosis of Sickle Cell Anemia and β-Thalassemia with Enzymatically Amplified DNA and Nonradioactive Allele-Specific Oligonucleotide Probes
1988
Mechanisms linking obesity to insulin resistance and type 2 diabetes
2006 StandoutNature
Sickle-cell disease
2010 Standout
Polycystic Ovary Syndrome
2005 Standout
Ulcerative colitis
2016 Standout
The genetical history of humans and the great apes
2002 StandoutNobel
The Human Obesity Gene Map: The 2001 Update
2002
Mechanisms of fatty acid-induced inhibition of glucose uptake.
1994 Standout
What We Talk About When We Talk About Fat
2014 Standout
Haplotype analysis of the PPARγ Pro12Ala and C1431T variants reveals opposing associations with body weight
2002
The Human Obesity Gene Map: The 2003 Update
2004
The Human Copper-Zinc Superoxide Dismutase Gene (SOD1) Proximal Promoter Is Regulated by Sp1, Egr-1, and WT1 via Non-canonical Binding Sites
1999
World distribution of factor V Leiden
1995 Standout
Superoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression
2002 Standout
Impact of Informing Overweight Individuals about the Role of Genetics in Obesity: An Online Experimental Study
2013 Standout
Genome-wide association studies for common diseases and complex traits
2005 Standout
Effects of the Type 2 Diabetes-AssociatedPPARGP12A Polymorphism on Progression to Diabetes and Response to Troglitazone
2007
Why are some genetic diseases common?
1993
Genetics of Food Intake Self-Regulation in Childhood: Literature Review and Research Opportunities
2013 Standout
The Pro12Ala polymorphism of PPARγ2 gene and susceptibility to type 2 diabetes mellitus in a Polish population
2003
Study of a new PPARγ2 promoter polymorphism and haplotype analysis in a French population
2005
The Human Obesity Gene Map: The 2004 Update
2005
The relative contributions of insulin resistance and beta-cell dysfunction to the pathophysiology of Type 2 diabetes
2003 Standout
Chronic Intermittent Hypoxia Induces Atherosclerosis via Activation of Adipose Angiopoietin-like 4
2013 StandoutNobel
Peroxisome Proliferator–Activated Receptor γ and Metabolic Disease
2001
Pathophysiology of Human Visceral Obesity: An Update
2013 Standout
Criteria for Defining Polycystic Ovary Syndrome as a Predominantly Hyperandrogenic Syndrome: An Androgen Excess Society Guideline
2006 Standout
A Mitochondrial Paradigm of Metabolic and Degenerative Diseases, Aging, and Cancer: A Dawn for Evolutionary Medicine
2005 Standout
The Inherited Basis of Diabetes Mellitus: Implications for the Genetic Analysis of Complex Traits
2003
Excess of Rare Amino Acid Polymorphisms in the Toll-like Receptor 4 in Humans
2001 StandoutNobel
Human evolution
1999 StandoutNobel
Obesity and Cardiovascular Disease: Pathophysiology, Evaluation, and Effect of Weight Loss
2005 Standout
Type 2 diabetes: principles of pathogenesis and therapy
2005 Standout
The Genetics of Type 2 Diabetes
2001
The Mechanisms of Action of PPARs
2002 Standout
Breast-Feeding Modulates the Influence of the Peroxisome Proliferator–Activated Receptor-γ (PPARG2) Pro12Ala Polymorphism on Adiposity in Adolescents
2009
Sex and Gender Differences in Risk, Pathophysiology and Complications of Type 2 Diabetes Mellitus
2016 Standout
Fat and Beyond: The Diverse Biology of PPARγ
2008 Standout
Genetics of obesity
2006
PPARγAND GLUCOSE HOMEOSTASIS
2002
Functional mapping of disease susceptibility loci using cell biology
2006 StandoutNobel
Beta‐thalassaemia intermedia: is it possible consistently to predict phenotype from genotype?
1998
Common polymorphisms of the PPAR-?2 (Pro12Ala) and PGC-1? (Gly482Ser) genes are associated with the conversion from impaired glucose tolerance to type 2 diabetes in the STOP-NIDDM trial
2004
Impact of Two Common Polymorphisms in the PPARγ Gene on Glucose Tolerance and Plasma Insulin Profiles in Monozygotic and Dizygotic Twins
2003
Inflammatory Bowel Disease
2010 Standout
Oxidative Stress: An Essential Factor in the Pathogenesis of Gastrointestinal Mucosal Diseases
2014 Standout
A Common Human β Globin Splicing Mutation Modeled in Mice
1998 StandoutNobel
Exon 6 and 2 Peroxisome Proliferator-Activated Receptor-γ Polymorphisms in Polycystic Ovary Syndrome
2003
Effects of oxidative stress on expression of extracellular superoxide dismutase, CuZn-superoxide dismutase and Mn-superoxide dismutase in human dermal fibroblasts
1994
Cellular Mechanisms for Insulin Resistance in Normal Pregnancy and Gestational Diabetes
2007
Molecular basis and prenatal diagnosis of beta-thalassemia
1988
Association Between Peroxisome Proliferator–Activated Receptor γ Haplotypes and the Metabolic Syndrome in French Men and Women
2005
Human evolution
1999 StandoutNobel
The gut flora as a forgotten organ
2006 Standout
Epigenetic Effects of Human Breast Milk
2014
Works of SS Deeb being referenced
Impact of the Peroxisome Proliferator Activated Receptor γ2 Pro12Ala polymorphism on adiposity, lipids and non-insulin-dependent diabetes mellitus
2000
Molecular basis of familial chylomicronemia: mutations in the lipoprotein lipase and apolipoprotein C-II genes.
1992
Loss of copper-zinc superoxide dismutase gene expression in differentiated cells of myelo-monocytic origin
1989
The molecular basis of beta-thalassemia in Lebanon: application to prenatal diagnosis
1987