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Methylation and Transcripts Expression at the Imprinted GNAS Locus in Human Embryonic and Induced Pluripotent Stem Cells and Their Derivatives

Stem cell reports, 2014-09, Vol.3 (3), p.432-443

2014

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Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature

Clinical epigenetics, 2022-05, Vol.14 (1), p.65-65, Article 65

2022

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Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3

Human molecular genetics, 2017-10, Vol.26 (20), p.3883-3894

2017

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Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney Complex

The Journal of biological chemistry, 2015-11, Vol.290 (46), p.27816-27828

2015

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Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children

Diabetes (New York, N.Y.), 2008-02, Vol.57 (2), p.494-502

2008

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Fetal growth is associated with CpG methylation in the P2 promoter of the IGF1 gene

Clinical epigenetics, 2018-04, Vol.10 (1), p.57-57, Article 57

2018

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The insulin gene VNTR is associated with fasting insulin levels and development of juvenile obesity

Nature genetics, 2000-12, Vol.26 (4), p.444-446

2000

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A common promoter variant of the leptin gene is associated with changes in the relationship between serum leptin and fat mass in obese girls

Diabetes (New York, N.Y.), 2000-12, Vol.49 (12), p.2196-2200

2000

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Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity

Nature genetics, 2001-09, Vol.29 (1), p.96-99

2001

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Correction to: Fetal growth is associated with CpG methylation in the P2 promoter of the IGF1 gene

Clinical epigenetics, 2018-06, Vol.10 (1), p.74-74, Article 74

2018

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The human MC4R promoter: Characterization and role in obesity

Diabetes (New York, N.Y.), 2003-12, Vol.52 (12), p.2996-3000

2003

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The Common −866 G/A Polymorphism in the Promoter of Uncoupling Protein 2 Is Associated With Increased Carbohydrate and Decreased Lipid Oxidation in Juvenile Obesity

Diabetes (New York, N.Y.), 2004-01, Vol.53 (1), p.235-239

2004

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Genetic Study of the Melanin-Concentrating Hormone Receptor 2 in Childhood and Adulthood Severe Obesity

The journal of clinical endocrinology and metabolism, 2007-11, Vol.92 (11), p.4403-4409

2007

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Increased Insulin Resistance in Obese Children Who Have Both 972 IRS-1 and 1057 IRS-2 Polymorphisms

Diabetes (New York, N.Y.), 2002-12, Vol.51 (suppl 3), p.S304-S307

2002

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Long-Term Disease Prevention with a Gene Therapy Targeting Oligodendrocytes in a Mouse Model of Adrenomyeloneuropathy

Human gene therapy, 2022-09, Vol.33 (17-18), p.936

2022

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Correction of a knock-in mouse model of acrodysostosis with gene therapy using a rAAV9-CAG-human PRKAR1A vector

Gene therapy, 2022-08, Vol.29 (7-8), p.441-448

2022

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Knock‐In of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP‐Dependent Protein Kinase A Activation: A Model of Type 1 Acrodysostosis

Journal of bone and mineral research, 2017-02, Vol.32 (2), p.333-346

2017

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Molecular Genetics of Human Obesity-Associated MC4R Mutations

Annals of the New York Academy of Sciences, 2003-06, Vol.994 (1), p.49-57

2003

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Endocrine Manifestations of the Rapid-Onset Obesity with Hypoventilation, Hypothalamic, Autonomic Dysregulation, and Neural Tumor Syndrome in Childhood

The journal of clinical endocrinology and metabolism, 2008-10, Vol.93 (10), p.3971-3980

2008

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SAT-039 GNAS-miRNAs Are Likely Involved in the Phenotype of Patients with Pseudohypoparathyroidism 1B/iPPSD3

Journal of the Endocrine Society, 2019-04, Vol.3 (Supplement_1)

2019

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The Human MC4R Promoter

Diabetes (New York, N.Y.), 2003-12, Vol.52 (12), p.2996-3000

2003

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A Homozygous Null Mutation Delineates the Role of the Melanocortin-4 Receptor in Humans

The journal of clinical endocrinology and metabolism, 2004-05, Vol.89 (5), p.2028-2032

2004

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A single-nucleotide polymorphism in the p110beta gene promoter is associated with partial protection from insulin resistance in severely obese adolescents

The journal of clinical endocrinology and metabolism, 2008-01, Vol.93 (1), p.212-215

2008

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Methylation and Transcripts Expression at the Imprinted GNAS Locus in Human Embryonic and Induced Pluripotent Stem Cells and Their Derivatives

Differentially methylated CpGs in response to growth hormone administration in children with idiopathic short stature

Mutations causing acrodysostosis-2 facilitate activation of phosphodiesterase 4D3

Functional Characterization of PRKAR1A Mutations Reveals a Unique Molecular Mechanism Causing Acrodysostosis but Multiple Mechanisms Causing Carney Complex

Association Analysis Indicates That a Variant GATA-Binding Site in the PIK3CB Promoter Is a Cis-Acting Expression Quantitative Trait Locus for This Gene and Attenuates Insulin Resistance in Obese Children

Fetal growth is associated with CpG methylation in the P2 promoter of the IGF1 gene

The insulin gene VNTR is associated with fasting insulin levels and development of juvenile obesity

A common promoter variant of the leptin gene is associated with changes in the relationship between serum leptin and fat mass in obese girls

Paternal transmission of the very common class I INS VNTR alleles predisposes to childhood obesity

Correction to: Fetal growth is associated with CpG methylation in the P2 promoter of the IGF1 gene

The human MC4R promoter: Characterization and role in obesity

The Common −866 G/A Polymorphism in the Promoter of Uncoupling Protein 2 Is Associated With Increased Carbohydrate and Decreased Lipid Oxidation in Juvenile Obesity

Genetic Study of the Melanin-Concentrating Hormone Receptor 2 in Childhood and Adulthood Severe Obesity

Increased Insulin Resistance in Obese Children Who Have Both 972 IRS-1 and 1057 IRS-2 Polymorphisms

Long-Term Disease Prevention with a Gene Therapy Targeting Oligodendrocytes in a Mouse Model of Adrenomyeloneuropathy

Variation in FTO contributes to childhood obesity and severe adult obesity

Correction of a knock-in mouse model of acrodysostosis with gene therapy using a rAAV9-CAG-human PRKAR1A vector

Knock‐In of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP‐Dependent Protein Kinase A Activation: A Model of Type 1 Acrodysostosis

Common nonsynonymous variants in PCSK1 confer risk of obesity

Molecular Genetics of Human Obesity-Associated MC4R Mutations

Endocrine Manifestations of the Rapid-Onset Obesity with Hypoventilation, Hypothalamic, Autonomic Dysregulation, and Neural Tumor Syndrome in Childhood

SAT-039 GNAS-miRNAs Are Likely Involved in the Phenotype of Patients with Pseudohypoparathyroidism 1B/iPPSD3

The Human MC4R Promoter

A Homozygous Null Mutation Delineates the Role of the Melanocortin-4 Receptor in Humans

A single-nucleotide polymorphism in the p110beta gene promoter is associated with partial protection from insulin resistance in severely obese adolescents

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