Lista de obras - Anke Hinney - Dominio Público Uruguay

'Fat mass and obesity associated' gene (FTO): no significant association of variant rs9939609 with weight loss in a lifestyle intervention and lipid metabolism markers in German obese children and adolescents

artículo científico publicado en 2008

A consultation with genetic information about obesity decreases self-blame about eating and leads to realistic weight loss goals in obese individuals

artículo científico publicado en 2008

A genome-wide association meta-analysis identifies new childhood obesity loci

artículo científico publicado en 2012

A novel SP1/SP3 dependent intronic enhancer governing transcription of the UCP3 gene in brown adipocytes

artículo científico publicado en 2013

Absence of leptin deficiency mutation in extremely obese German children and adolescents ⬇️

artículo científico publicado el 1 de diciembre de 1997

Analysis of Genes Involved in Body Weight Regulation by Targeted Re-Sequencing

artículo científico publicado en 2016

Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents

artículo científico publicado en 2007

Association analyses for dopamine receptor gene polymorphisms and weight status in a longitudinal analysis in obese children before and after lifestyle intervention

artículo científico publicado en 2013

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations

artículo científico publicado en 2004

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders

artículo científico publicado en 2008

Association of common variants identified by recent genome-wide association studies with obesity in Chinese children: a case-control study

artículo científico publicado en 2016

Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin

artículo científico publicado en 2010

Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder

artículo científico publicado en 2014

Catechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responses

artículo científico publicado en 2014

Changes of peripheral alpha-melanocyte-stimulating hormone in childhood obesity

artículo científico publicado en 2009

Child and adolescent psychiatric genetics

scientific article published on 06 February 2010

Common variants near MC4R are associated with fat mass, weight and risk of obesity

artículo científico publicado en 2008

DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder

artículo científico publicado en 2012

Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human

scientific journal article

Eating disorders: the current status of molecular genetic research

artículo científico publicado en 2009

Environmental and genetic risk factors in obesity

artículo científico publicado en 2009

Estrogen receptor 1 gene (ESR1) is associated with restrictive anorexia nervosa

artículo científico publicado en 2010

Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa

artículo científico publicado en 2017

Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2.

artículo científico publicado en 2015

Food Addiction in Gambling Disorder: Frequency and Clinical Outcomes

artículo científico publicado en 2017

From monogenic to polygenic obesity: recent advances

artículo científico publicado en 2010

Further support for linkage of extreme obesity to the obese gene in a study group of obese children and adolescents ⬇️

artículo científico publicado el 1 de enero de 1997

Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity

artículo científico publicado en 2013

Genes and the hypothalamic control of metabolism in humans

artículo científico

Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesity

scientific journal article

Genetic factors for overweight and CAD.

artículo científico publicado en 2006

Genetic findings in anorexia and bulimia nervosa

artículo científico publicado en 2010

Genetic risk factors in eating disorders

artículo científico publicado en 2004

Genetic variation of the ghrelin activator gene ghrelin O-acyltransferase (GOAT) is associated with anorexia nervosa

artículo científico publicado en 2010

Genetics of eating disorders

artículo científico

Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants

artículo científico publicado en 2007

Genome-wide association study in German patients with attention deficit/hyperactivity disorder

artículo científico publicado en 2011

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

scientific journal article

Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature

artículo científico publicado en 2004

Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity

artículo científico publicado en 2005

Increased constraints on MC4R during primate and human evolution

artículo científico publicado en 2008

Indications for potential parent-of-origin effects within the FTO gene

artículo científico publicado en 2015

Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with Obesity

artículo científico publicado en 2016

Investigation of a genome wide association signal for obesity: synthetic association and haplotype analyses at the melanocortin 4 receptor gene locus

artículo científico publicado en 2010

Is information on genetic determinants of obesity helpful or harmful for obese people?--A randomized clinical trial

artículo científico publicado en 2007

Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa

artículo científico publicado en 2008

Lack of support for the association between GAD2 polymorphisms and severe human obesity

artículo científico publicado en 2005

Large effects on body mass index and insulin resistance of fat mass and obesity associated gene (FTO) variants in patients with polycystic ovary syndrome (PCOS).

artículo científico publicado en 2010

Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study

artículo científico publicado en 2008

Melanocortin-4 receptor gene variant I103 is negatively associated with obesity

artículo científico publicado en 2004

Melanocortin-4 receptor in energy homeostasis and obesity pathogenesis

artículo científico

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

artículo científico publicado en 2008

Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design?

artículo científico publicado en 2009

Meta-analysis on the effect of the N363S polymorphism of the glucocorticoid receptor gene (GRL) on human obesity

artículo científico publicado en 2006

Mitochondrial DNA variants in obesity

artículo científico publicado en 2014

Molecular genetic aspects of weight regulation

artículo científico publicado en 2013

Mutation analysis of the MCHR1 gene in human obesity

artículo científico publicado en 2005

Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity

artículo científico publicado en 2010

Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.

artículo científico publicado en 2007

Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants

artículo científico publicado en 2012

Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry

artículo científico publicado en 2009

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis

artículo científico publicado en 2010

Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach

artículo científico publicado en 2016

Polygenic obesity in humans

artículo científico publicado en 2008

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

artículo científico publicado en 2017

Relevance of polymorphisms in MC4R and BDNF in short normal stature

scientific article published on 22 August 2018

Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-through

artículo científico publicado en 2011

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease

artículo científico publicado en 2010

Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa

artículo científico publicado en 2017

Successful methylphenidate treatment of early onset extreme obesity in a child with a melanocortin-4 receptor gene mutation and attention deficit/hyperactivity disorder ⬇️

artículo científico publicado el 3 de enero de 2011

The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts

artículo científico publicado en 2007

The association of serum leptin levels with food addiction is moderated by weight status in adolescent psychiatric inpatients

artículo científico publicado en 2018

The promise of new anti-obesity therapies arising from knowledge of genetic obesity traits

artículo científico publicado en 2022

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups

scientific journal article

Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cachexia

artículo científico publicado en 2008

Where in the genome are significant single nucleotide polymorphisms from genome-wide association studies located?

artículo científico

Lista de obras de Anke Hinney

'Fat mass and obesity associated' gene (FTO): no significant association of variant rs9939609 with weight loss in a lifestyle intervention and lipid metabolism markers in German obese children and adolescents

A consultation with genetic information about obesity decreases self-blame about eating and leads to realistic weight loss goals in obese individuals

A genome-wide association meta-analysis identifies new childhood obesity loci

A novel SP1/SP3 dependent intronic enhancer governing transcription of the UCP3 gene in brown adipocytes

Absence of leptin deficiency mutation in extremely obese German children and adolescents ⬇️

Analysis of Genes Involved in Body Weight Regulation by Targeted Re-Sequencing

Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents

Association analyses for dopamine receptor gene polymorphisms and weight status in a longitudinal analysis in obese children before and after lifestyle intervention

Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders

Association of common variants identified by recent genome-wide association studies with obesity in Chinese children: a case-control study

Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin

Case-control genome-wide association study of persistent attention-deficit hyperactivity disorder identifies FBXO33 as a novel susceptibility gene for the disorder

Catechol-O-methyltransferase Val158Met polymorphism is associated with somatosensory amplification and nocebo responses

Changes of peripheral alpha-melanocyte-stimulating hormone in childhood obesity

Child and adolescent psychiatric genetics

Common variants near MC4R are associated with fat mass, weight and risk of obesity

DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder

Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human

Eating disorders: the current status of molecular genetic research

Environmental and genetic risk factors in obesity

Estrogen receptor 1 gene (ESR1) is associated with restrictive anorexia nervosa

Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa

Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2.

Food Addiction in Gambling Disorder: Frequency and Clinical Outcomes

From monogenic to polygenic obesity: recent advances

Further support for linkage of extreme obesity to the obese gene in a study group of obese children and adolescents ⬇️

Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity

Genes and the hypothalamic control of metabolism in humans

Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesity

Genetic factors for overweight and CAD.

Genetic findings in anorexia and bulimia nervosa

Genetic risk factors in eating disorders

Genetic variation of the ghrelin activator gene ghrelin O-acyltransferase (GOAT) is associated with anorexia nervosa

Genetics of eating disorders

Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants

Genome-wide association study in German patients with attention deficit/hyperactivity disorder

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Ghrelin receptor gene: identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal stature

Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity

Increased constraints on MC4R during primate and human evolution

Indications for potential parent-of-origin effects within the FTO gene

Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with Obesity

Investigation of a genome wide association signal for obesity: synthetic association and haplotype analyses at the melanocortin 4 receptor gene locus

Is information on genetic determinants of obesity helpful or harmful for obese people?--A randomized clinical trial

Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa

Lack of support for the association between GAD2 polymorphisms and severe human obesity

Large effects on body mass index and insulin resistance of fat mass and obesity associated gene (FTO) variants in patients with polycystic ovary syndrome (PCOS).

Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study

Melanocortin-4 receptor gene variant I103 is negatively associated with obesity

Melanocortin-4 receptor in energy homeostasis and obesity pathogenesis

Meta-analysis of genome-wide linkage scans of attention deficit hyperactivity disorder

Meta-analysis of the INSIG2 association with obesity including 74,345 individuals: does heterogeneity of estimates relate to study design?

Meta-analysis on the effect of the N363S polymorphism of the glucocorticoid receptor gene (GRL) on human obesity

Mitochondrial DNA variants in obesity

Molecular genetic aspects of weight regulation

Mutation analysis of the MCHR1 gene in human obesity

Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity

Mutation screen and association studies in the diacylglycerol O-acyltransferase homolog 2 gene (DGAT2), a positional candidate gene for early onset obesity on chromosome 11q13.

Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants

Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry

Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis

Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach

Polygenic obesity in humans

Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity

Relevance of polymorphisms in MC4R and BDNF in short normal stature

Rescue of melanocortin 4 receptor (MC4R) nonsense mutations by aminoglycoside-mediated read-through

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease

Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa

Successful methylphenidate treatment of early onset extreme obesity in a child with a melanocortin-4 receptor gene mutation and attention deficit/hyperactivity disorder ⬇️

The association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohorts

The association of serum leptin levels with food addiction is moderated by weight status in adolescent psychiatric inpatients

The promise of new anti-obesity therapies arising from knowledge of genetic obesity traits

Two new Loci for body-weight regulation identified in a joint analysis of genome-wide association studies for early-onset extreme obesity in French and german study groups

Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cachexia

Where in the genome are significant single nucleotide polymorphisms from genome-wide association studies located?