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An aromatase polymorphism modulates the relationship between weight and estradiol levels in obese men

Fertility and sterility, 2010-10, Vol.94 (5), p.1734-1738

2010

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A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity

Journal of Obesity, 2015-01, Vol.2015, p.623431-7

2015

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Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides

Human genetics, 2005-09, Vol.117 (5), p.444-451

2005

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Sodium Bicarbonate Cotransporter Polymorphisms Are Associated With Baseline and 10-Year Follow-Up Blood Pressures

Hypertension (Dallas, Tex. 1979), 2006-03, Vol.47 (3, Part 2 Suppl), p.532-536

2006

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Two-dimensional, sex-specific autosomal linkage scan of the number of sodium pump sites

Journal of hypertension, 2010-04, Vol.28 (4), p.740-747

2010

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Evaluation of coronary risk factors in patients with heterozygous familial hypercholesterolemia

The American journal of cardiology, 2001-03, Vol.87 (5), p.547-553

2001

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Association of the FTO Gene With BMI

Obesity (Silver Spring, Md.), 2008-04, Vol.16 (4), p.902-904

2008

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APOH interacts with FTO to predispose to healthy thinness

Human genetics, 2016-02, Vol.135 (2), p.201-207

2016

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Apolipoprotein H Variant Modifies Plasma Triglyceride Phenotype in Familial Hypercholesterolemia: A Molecular Study in an Eight-generation Hyperlipidemic Family

Journal of Atherosclerosis and Thrombosis, 2003, Vol.10(2), pp.79-84

2003

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Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred

Journal of human genetics, 2002-12, Vol.47 (12), p.656-664

2002

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Polymorphisms in the NPY2R Gene Show Significant Associations With BMI That Are Additive to FTO, MC4R, and NPFFR2 Gene Effects

Obesity (Silver Spring, Md.), 2011-11, Vol.19 (11), p.2241-2247

2011

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Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: Intra-familial association study in an eight-generation hyperlipidemic kindred

American journal of medical genetics, 2003-08, Vol.121A (2), p.136-140

2003

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Restricted localization of L1 and N-CAM at sites of contact between Schwann cells and neurites in culture

Glia, 1994-01, Vol.10 (1), p.70-74

1994

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Neuronal pathways mediating head turning behavior in Aplysia

Neuroscience letters, 1995-02, Vol.186 (2), p.197-199

1995

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Lack of Association of Glutamate Decarboxylase 2 Gene Polymorphisms with Severe Obesity in Utah

Obesity (Silver Spring, Md.), 2006-04, Vol.14 (4), p.650-655

2006

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C-PR Neuron of Aplysia Has Differential Effects on "Feeding" Cerebral Interneurons, Including Myomodulin-Positive CBI-12

Journal of neurophysiology, 1999-02, Vol.81 (2), p.521-534

1999

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Cerebral-Abdominal Interganglionic Coordinating Neurons in Aplysia

Journal of neurophysiology, 2001-01, Vol.85 (1), p.174-186

2001

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Actions of a Pair of Identified Cerebral-Buccal Interneurons (CBI-8/9) in Aplysia That Contain the Peptide Myomodulin

Journal of neurophysiology, 1999-02, Vol.81 (2), p.507-520

1999

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An Identified Interneuron Contributes to Aspects of Six Different Behaviors in Aplysia

The Journal of neuroscience, 1996-08, Vol.16 (16), p.5266-5279

1996

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Multifunctional Neuron CC6 in Aplysia Exerts Actions Opposite to Those of Multifunctional Neuron CC5

Journal of neurophysiology, 2000-05, Vol.83 (5), p.2473-2481

2000

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Distribution in the central nervous system of Aplysia of afferent fibers arising from cell bodies located in the periphery

Journal of comparative neurology (1911), 1995-09, Vol.359 (4), p.627-643

1995

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A Pair of Identified Interneurons in Aplysia that Are Involved in Multiple Behaviors Are Necessary and Sufficient for the Arterial-Shortening Component of a Local Withdrawal Reflex

The Journal of neuroscience, 1996-07, Vol.16 (14), p.4518-4528

1996

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Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities

Journal of human genetics, 2000-01, Vol.45 (3), p.154-158

2000

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A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia

Journal of human genetics, 1999-01, Vol.44 (6), p.364-367

1999

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Ganglionic distribution of inputs and outputs of C-PR, a neuron involved in the generation of a food-induced arousal state in Aplysia

Invertebrate neuroscience, 1997-03, Vol.2 (4), p.235-244

1997

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An aromatase polymorphism modulates the relationship between weight and estradiol levels in obese men

A Copy Number Variant on Chromosome 20q13.3 Implicated in Thinness and Severe Obesity

Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides

Sodium Bicarbonate Cotransporter Polymorphisms Are Associated With Baseline and 10-Year Follow-Up Blood Pressures

Two-dimensional, sex-specific autosomal linkage scan of the number of sodium pump sites

Evaluation of coronary risk factors in patients with heterozygous familial hypercholesterolemia

Association of the FTO Gene With BMI

APOH interacts with FTO to predispose to healthy thinness

Apolipoprotein H Variant Modifies Plasma Triglyceride Phenotype in Familial Hypercholesterolemia: A Molecular Study in an Eight-generation Hyperlipidemic Family

Interaction between the LDL-receptor gene bearing a novel mutation and a variant in the apolipoprotein A-II promoter: molecular study in a 1135-member familial hypercholesterolemia kindred

Polymorphisms in the NPY2R Gene Show Significant Associations With BMI That Are Additive to FTO, MC4R, and NPFFR2 Gene Effects

Growth hormone receptor variant (L526I) modifies plasma HDL cholesterol phenotype in familial hypercholesterolemia: Intra-familial association study in an eight-generation hyperlipidemic kindred

Restricted localization of L1 and N-CAM at sites of contact between Schwann cells and neurites in culture

Neuronal pathways mediating head turning behavior in Aplysia

Lack of Association of Glutamate Decarboxylase 2 Gene Polymorphisms with Severe Obesity in Utah

C-PR Neuron of Aplysia Has Differential Effects on "Feeding" Cerebral Interneurons, Including Myomodulin-Positive CBI-12

Cerebral-Abdominal Interganglionic Coordinating Neurons in Aplysia

Actions of a Pair of Identified Cerebral-Buccal Interneurons (CBI-8/9) in Aplysia That Contain the Peptide Myomodulin

An Identified Interneuron Contributes to Aspects of Six Different Behaviors in Aplysia

Multifunctional Neuron CC6 in Aplysia Exerts Actions Opposite to Those of Multifunctional Neuron CC5

Distribution in the central nervous system of Aplysia of afferent fibers arising from cell bodies located in the periphery

A Pair of Identified Interneurons in Aplysia that Are Involved in Multiple Behaviors Are Necessary and Sufficient for the Arterial-Shortening Component of a Local Withdrawal Reflex

Co-segregation of elevated LDL with a novel mutation (D92K) of the LDL receptor in a kindred with multiple lipoprotein abnormalities

A novel LDLR mutation, H190Y, in a Utah kindred with familial hypercholesterolemia

Ganglionic distribution of inputs and outputs of C-PR, a neuron involved in the generation of a food-induced arousal state in Aplysia

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