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Multilocus Genetic Profile for Dopamine Signaling Predicts Ventral Striatum Reactivity

Neuropsychopharmacology (New York, N.Y.), 2011-08, Vol.36 (9), p.1940-1947

2011

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Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers

PLoS genetics, 2009-02, Vol.5 (2), p.e1000337-e1000337

2009

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Deficiency of Subsarcolemmal Mitochondria in Obesity and Type 2 Diabetes

Diabetes (New York, N.Y.), 2005-01, Vol.54 (1), p.8-14

2005

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Genetic variation in human NPY expression affects stress response and emotion

Nature, 2008-04, Vol.452 (7190), p.997-1001

2008

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Insulin Resistance Is Associated With Higher Intramyocellular Triglycerides in Type I but Not Type II Myocytes Concomitant With Higher Ceramide Content

Diabetes (New York, N.Y.), 2010-01, Vol.59 (1), p.80-88

2010

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Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment

Clinical cancer research, 2012-04, Vol.18 (8), p.2382-2390

2012

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Polymorphic variation in the dopamine D4 receptor predicts delay discounting as a function of childhood socioeconomic status: evidence for differential susceptibility

Social cognitive and affective neuroscience, 2013-06, Vol.8 (5), p.499-508

2013

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Haptoglobin genotype and functional outcome after aneurysmal subarachnoid hemorrhage

Journal of neurosurgery, 2014-02, Vol.120 (2), p.386-390

2014

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DRD4 polymorphism moderates the effect of alcohol consumption on social bonding

PloS one, 2012-02, Vol.7 (2), p.e28914

2012

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PER2 rs2304672 Polymorphism Moderates Circadian-Relevant Reward Circuitry Activity in Adolescents

Biological psychiatry (1969), 2012-03, Vol.71 (5), p.451-457

2012

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Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk

BMC medical genetics, 2008-07, Vol.9 (1), p.59-59

2008

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Haptoglobin Genotype and Renal Function Decline in Type 1 Diabetes

Diabetes (New York, N.Y.), 2009-12, Vol.58 (12), p.2904-2909

2009

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C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes

PloS one, 2008-05, Vol.3 (5), p.e2199-e2199

2008

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Haptoglobin genotype and cerebrovascular disease incidence in type 1 diabetes

Diabetes & vascular disease research, 2014-09, Vol.11 (5), p.335-342

2014

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MIF (Macrophage Migration Inhibitory Factor) Promoter Polymorphisms and Susceptibility to Severe Malarial Anemia

The Journal of infectious diseases, 2009-08, Vol.200 (4), p.629-637

2009

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Characteristics of skeletal muscle mitochondrial biogenesis induced by moderate-intensity exercise and weight loss in obesity

Journal of applied physiology (1985), 2007-07, Vol.103 (1), p.21-27

2007

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Brain-Derived Neurotrophic Factor Serum Levels and Genotype: Association with Depression during Interferon-α Treatment

Neuropsychopharmacology (New York, N.Y.), 2013-05, Vol.38 (6), p.985-995

2013

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Multilocus genetic profile for dopamine signaling predicts ventral striatum reactivity

Neuropsychopharmacology (New York, N.Y.), 2011-08, Vol.36 (9), p.1940-1947

2011

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Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM)

PloS one, 2011-08, Vol.6 (8), p.e22297-e22297

2011

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Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men

Journal of bone and mineral research, 2010-02, Vol.25 (2), p.330-338

2010

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Decreased STAT1 Expression by Promoter Methylation in Squamous Cell Carcinogenesis

JNCI : Journal of the National Cancer Institute, 2006-02, Vol.98 (3), p.181-189

2006

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Genome-wide linkage scan to identify loci associated with type 2 diabetes and blood lipid phenotypes in the Sikh Diabetes Study

PloS one, 2011-06, Vol.6 (6), p.e21188

2011

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Racial Disparities and Sex-Based Outcomes Differences after Severe Injury

Journal of the American College of Surgeons, 2012-06, Vol.214 (6), p.973-980

2012

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Susceptibility Genes for Age-Related Maculopathy on Chromosome 10q26

American journal of human genetics, 2005-09, Vol.77 (3), p.389-407

2005

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HGF and MET mutations in primary and secondary lymphedema

Lymphatic research and biology, 2008-06, Vol.6 (2), p.65-68

2008

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Multilocus Genetic Profile for Dopamine Signaling Predicts Ventral Striatum Reactivity

Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiers

Deficiency of Subsarcolemmal Mitochondria in Obesity and Type 2 Diabetes

Genetic variation in human NPY expression affects stress response and emotion

Insulin Resistance Is Associated With Higher Intramyocellular Triglycerides in Type I but Not Type II Myocytes Concomitant With Higher Ceramide Content

Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment

Polymorphic variation in the dopamine D4 receptor predicts delay discounting as a function of childhood socioeconomic status: evidence for differential susceptibility

Haptoglobin genotype and functional outcome after aneurysmal subarachnoid hemorrhage

DRD4 polymorphism moderates the effect of alcohol consumption on social bonding

PER2 rs2304672 Polymorphism Moderates Circadian-Relevant Reward Circuitry Activity in Adolescents

Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk

Haptoglobin Genotype and Renal Function Decline in Type 1 Diabetes

C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genes

Haptoglobin genotype and cerebrovascular disease incidence in type 1 diabetes

MIF (Macrophage Migration Inhibitory Factor) Promoter Polymorphisms and Susceptibility to Severe Malarial Anemia

Characteristics of skeletal muscle mitochondrial biogenesis induced by moderate-intensity exercise and weight loss in obesity

Brain-Derived Neurotrophic Factor Serum Levels and Genotype: Association with Depression during Interferon-α Treatment

Multilocus genetic profile for dopamine signaling predicts ventral striatum reactivity

Evaluation of 15 functional candidate genes for association with chronic otitis media with effusion and/or recurrent otitis media (COME/ROM)

Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men

Decreased STAT1 Expression by Promoter Methylation in Squamous Cell Carcinogenesis

Genome-wide linkage scan to identify loci associated with type 2 diabetes and blood lipid phenotypes in the Sikh Diabetes Study

Racial Disparities and Sex-Based Outcomes Differences after Severe Injury

Susceptibility Genes for Age-Related Maculopathy on Chromosome 10q26

HGF and MET mutations in primary and secondary lymphedema

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