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Congenital Hypopituitarism: Current Agnostic Genetics Faces Its Limits

The journal of clinical endocrinology and metabolism, 2024-06

Bougnères, Pierre

2024

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Genome-Wide Methylation Analysis Identifies Specific Epigenetic Marks In Severely Obese Children

Scientific reports, 2017-04, Vol.7 (1), p.46311-46311, Article 46311

2017

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Letter to the Editor from Bougnères: "Reproductive Hormone Concentrations and Associated Anatomical Responses: Does Soy Formula Affect Minipuberty in Boys?"

The journal of clinical endocrinology and metabolism, 2022-02, Vol.107 (2), p.e890-e891

Bougneres, Pierre

2022

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Letter to the Editor: “A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness”

The journal of clinical endocrinology and metabolism, 2021-01, Vol.106 (1), p.e397-e398

Bougneres, Pierre

2021

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The Half-Empty Glass of GH Treatment in Dyschondrosteosis

Hormone research in paediatrics, 2022-10, Vol.95 (4), p.402-403

Bougnères, Pierre

2022

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Correction: Increased CpG methylation at the CDH1 locus in inflamed ileal mucosa of patients with Crohn disease

Clinical epigenetics, 2024-03, Vol.16 (1), p.43-43, Article 43

2024

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A common polymorphism of the growth hormone receptor is associated with increased responsiveness to growth hormone

Nature genetics, 2004-07, Vol.36 (7), p.720-724

2004

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A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

Nature (London), 1998-03, Vol.392 (6674), p.398-401

1998

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Low-dose IL-2 in children with recently diagnosed type 1 diabetes: a Phase I/II randomised, double-blind, placebo-controlled, dose-finding study

Diabetologia, 2020-09, Vol.63 (9), p.1808-1821

2020

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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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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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Long-Term Follow-Up of Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy

Human gene therapy, 2021-10, Vol.32 (19-20), p.1260-1269

2021

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Global epidemiology of type 1 diabetes in young adults and adults: a systematic review

BMC public health, 2015-03, Vol.15 (1), p.255-255, Article 255

2015

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Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control study

BMC public health, 2016-09, Vol.16 (1), p.1021-1021, Article 1021

2016

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Editorial: Genotypic and Phenotypic Complexity at the Insulin Variable Number of Tandem Repeats Locus

The journal of clinical endocrinology and metabolism, 2006-11, Vol.91 (11), p.4246-4249

BOUGNERES, Pierre

2006

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XPG and XPF Endonucleases Trigger Chromatin Looping and DNA Demethylation for Accurate Expression of Activated Genes

Molecular cell, 2012-08, Vol.47 (4), p.622-632

2012

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Recurrent PRKAR1A Mutation in Acrodysostosis with Hormone Resistance

The New England journal of medicine, 2011-06, Vol.364 (23), p.2218-2226

2011

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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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Exploring the risk of hypospadias in children born from mothers living close to a vineyard

PloS one, 2021-04, Vol.16 (4), p.e0249800-e0249800

2021

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Towards a new developmental synthesis: adaptive developmental plasticity and human disease

The Lancet (British edition), 2009-05, Vol.373 (9675), p.1654-1657

2009

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Increased CpG methylation at the CDH1 locus in inflamed ileal mucosa of patients with Crohn disease

Clinical epigenetics, 2024-02, Vol.16 (1), p.28-28, Article 28

2024

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Early varicella infection is associated with a delayed onset of childhood type 1 diabetes

Diabetes & metabolism, 2022-11, Vol.48 (6), p.101394-101394, Article 101394

2022

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Prenatal loss of father during World War One is predictive of a reduced lifespan in adulthood

Proceedings of the National Academy of Sciences - PNAS, 2017-04, Vol.114 (16), p.4201-4206

2017

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Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes

PloS one, 2012-05, Vol.7 (5), p.e36278-e36278

2012

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Congenital Hypopituitarism: Current Agnostic Genetics Faces Its Limits

Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I

Genome-Wide Methylation Analysis Identifies Specific Epigenetic Marks In Severely Obese Children

Letter to the Editor from Bougnères: "Reproductive Hormone Concentrations and Associated Anatomical Responses: Does Soy Formula Affect Minipuberty in Boys?"

Letter to the Editor: “A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness”

The Half-Empty Glass of GH Treatment in Dyschondrosteosis

Correction: Increased CpG methylation at the CDH1 locus in inflamed ileal mucosa of patients with Crohn disease

A common polymorphism of the growth hormone receptor is associated with increased responsiveness to growth hormone

A mutation in the human leptin receptor gene causes obesity and pituitary dysfunction

Low-dose IL-2 in children with recently diagnosed type 1 diabetes: a Phase I/II randomised, double-blind, placebo-controlled, dose-finding study

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

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

Long-Term Follow-Up of Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy

Global epidemiology of type 1 diabetes in young adults and adults: a systematic review

Association of environmental markers with childhood type 1 diabetes mellitus revealed by a long questionnaire on early life exposures and lifestyle in a case-control study

Editorial: Genotypic and Phenotypic Complexity at the Insulin Variable Number of Tandem Repeats Locus

XPG and XPF Endonucleases Trigger Chromatin Looping and DNA Demethylation for Accurate Expression of Activated Genes

Recurrent PRKAR1A Mutation in Acrodysostosis with Hormone Resistance

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

Exploring the risk of hypospadias in children born from mothers living close to a vineyard

Towards a new developmental synthesis: adaptive developmental plasticity and human disease

Increased CpG methylation at the CDH1 locus in inflamed ileal mucosa of patients with Crohn disease

Early varicella infection is associated with a delayed onset of childhood type 1 diabetes

Prenatal loss of father during World War One is predictive of a reduced lifespan in adulthood

Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes

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