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A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism

The journal of clinical endocrinology and metabolism, 2016-03, Vol.101 (3), p.847-851

2016

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Two Novel Missense Mutations in G Protein-Coupled Receptor 54 in a Patient with Hypogonadotropic Hypogonadism

The journal of clinical endocrinology and metabolism, 2005-03, Vol.90 (3), p.1849-1855

2005

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Prolonged successful therapy for hyperinsulinaemic hypoglycaemia after gastric bypass: the pathophysiological role of GLP1 and its response to a somatostatin analogue

European journal of endocrinology, 2012-05, Vol.166 (5), p.951

2012

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Early childhood infection and atopic disorder

Thorax, 1998-11, Vol.53 (11), p.927-932

1998

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Functional characterization of human NTRK2 mutations identified in patients with severe early-onset obesity

International Journal of Obesity, 2007-02, Vol.31 (2), p.359-364

2007

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Effects of Recombinant Leptin Therapy in a Child with Congenital Leptin Deficiency

The New England journal of medicine, 1999-09, Vol.341 (12), p.879-884

1999

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Food images engage subliminal motivation to seek food

International Journal of Obesity, 2012-09, Vol.36 (9), p.1245-1247

2012

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New advances in the genetics of early onset obesity

International Journal of Obesity, 2005-10, Vol.29 (10), p.1149-1152

2005

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A frameshift mutation in MC4R associated with dominantly inherited human obesity

Nature genetics, 1998-10, Vol.20 (2), p.111-112

1998

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Increased body mass index is associated with specific regional alterations in brain structure

International Journal of Obesity, 2016-07, Vol.40 (7), p.1177-1182

2016

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Congenital leptin deficiency is associated with severe early-onset obesity in humans

Nature (London), 1997-06, Vol.387 (6636), p.903-908

1997

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Human obesity as a heritable disorder of the central control of energy balance

International Journal of Obesity, 2008-12, Vol.32 (7S), p.S55-S61

2008

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Genetic factors in human obesity

Obesity reviews, 2007-03, Vol.8 (s1), p.37-40

2007

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Studies of the SIM1 gene in relation to human obesity and obesity-related traits

International Journal of Obesity, 2007-03, Vol.31 (3), p.429-434

2007

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Monogenic human obesity syndromes

Recent progress in hormone research, 2004, Vol.59, p.409

2004

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TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency

European journal of endocrinology, 2004-10, Vol.151 (4), p.463

2004

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Uncoupling protein 3 genetic variants in human obesity : the c-55t promoter polymorphism is negatively correlated with body mass index in a UK Caucasian population

International Journal of Obesity, 2001-04, Vol.25 (4), p.472-477

2001

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Sequential alterations in haemorheology, endothelial dysfunction, platelet activation and thrombogenesis in relation to prognosis following acute stroke: The West Birmingham Stroke Project

Blood coagulation & fibrinolysis, 2002-06, Vol.13 (4), p.339-347

2002

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Genetic variation in the corticotrophin-releasing factor receptors: identification of single-nucleotide polymorphisms and association studies with obesity in UK Caucasians

International Journal of Obesity, 2004-03, Vol.28 (3), p.442-446

2004

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Homozygosity for a novel missense mutation in the leptin receptor gene (P316T) in two Egyptian cousins with severe early onset obesity

Molecular genetics and metabolism, 2011-04, Vol.102 (4), p.461-464

2011

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Genetics of body-weight regulation

Nature (London), 2000-04, Vol.404 (6778), p.644-651

2000

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Leptin Substitution Results in the Induction of Menstrual Cycles in an Adolescent with Leptin Deficiency and Hypogonadotropic Hypogonadism

Hormone research in paediatrics, 2012-01, Vol.77 (2), p.127-133

2012

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Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency

The Journal of clinical investigation, 2000-07, Vol.106 (2), p.271-279

2000

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The role of melanocortin signalling in the control of body weight: evidence from human and murine genetic models

QJM : An International Journal of Medicine, 2000-01, Vol.93 (1), p.7-14

2000

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A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

Human molecular genetics, 2002-08, Vol.11 (17), p.1997-2004

2002

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A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism

Two Novel Missense Mutations in G Protein-Coupled Receptor 54 in a Patient with Hypogonadotropic Hypogonadism

Prolonged successful therapy for hyperinsulinaemic hypoglycaemia after gastric bypass: the pathophysiological role of GLP1 and its response to a somatostatin analogue

Early childhood infection and atopic disorder

Functional characterization of human NTRK2 mutations identified in patients with severe early-onset obesity

Effects of Recombinant Leptin Therapy in a Child with Congenital Leptin Deficiency

Food images engage subliminal motivation to seek food

New advances in the genetics of early onset obesity

A frameshift mutation in MC4R associated with dominantly inherited human obesity

Increased body mass index is associated with specific regional alterations in brain structure

Congenital leptin deficiency is associated with severe early-onset obesity in humans

Human obesity as a heritable disorder of the central control of energy balance

Genetic factors in human obesity

Studies of the SIM1 gene in relation to human obesity and obesity-related traits

Monogenic human obesity syndromes

TPIT mutations are associated with early-onset, but not late-onset isolated ACTH deficiency

Uncoupling protein 3 genetic variants in human obesity : the c-55t promoter polymorphism is negatively correlated with body mass index in a UK Caucasian population

Sequential alterations in haemorheology, endothelial dysfunction, platelet activation and thrombogenesis in relation to prognosis following acute stroke: The West Birmingham Stroke Project

Genetic variation in the corticotrophin-releasing factor receptors: identification of single-nucleotide polymorphisms and association studies with obesity in UK Caucasians

Homozygosity for a novel missense mutation in the leptin receptor gene (P316T) in two Egyptian cousins with severe early onset obesity

Genetics of body-weight regulation

Leptin Substitution Results in the Induction of Menstrual Cycles in an Adolescent with Leptin Deficiency and Hypogonadotropic Hypogonadism

Dominant and recessive inheritance of morbid obesity associated with melanocortin 4 receptor deficiency

The role of melanocortin signalling in the control of body weight: evidence from human and murine genetic models

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism

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