Anke Hinney

Q: What Schools Are Affiliated With Anke Hinney

Anke Hinney is affiliated with the following schools: Boston University, University of Marburg, Technical University of Munich, Massachusetts General Hospital, University of Vienna, University of Duisburg-Essen

Anke Hinney's AcademicInfluence.com Rankings

Anke Hinney

Psychology

#3458

World Rank

#3902

Historical Rank

Neuropsychology

#106

World Rank

#109

Historical Rank

Cognitive Science

#191

World Rank

#192

Historical Rank

Cognitive Psychology

#428

World Rank

#442

Historical Rank

psychology Degrees

Download Badge

Psychology

Anke Hinney's Degrees

Masters Cognitive Science University of Vienna
Bachelors Psychology University of Vienna

Similar Degrees You Can Earn

Best Online Bachelor's in Psychology 2025

Why Is Anke Hinney Influential?

(Suggest an Edit or Addition)

(See a Problem?)

Anke Hinney's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

[Obesity and overweight]. (2009) (3013)
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index (2010) (2011)
Common variants near MC4R are associated with fat mass, weight and risk of obesity (2008) (1307)
Association analyses of 249,796 individuals reveal eighteen new loci associated with body mass index (2010) (1179)
A Common Genetic Variant Is Associated with Adult and Childhood Obesity (2006) (739)
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders (2019) (724)
Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human (2012) (573)
Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture (2013) (568)
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolution (2007) (515)
Genome Wide Association (GWA) Study for Early Onset Extreme Obesity Supports the Role of Fat Mass and Obesity Associated Gene (FTO) Variants (2007) (510)
Mapping the human genetic architecture of COVID-19 (2021) (455)
Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans. (1999) (453)
A genome-wide association meta-analysis identifies new childhood obesity loci (2012) (375)
Significant Locus and Metabolic Genetic Correlations Revealed in Genome-Wide Association Study of Anorexia Nervosa. (2017) (357)
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 (2010) (337)
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (314)
A genome-wide association study of anorexia nervosa (2014) (284)
The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: Alternative biallelic variation in rhesus monkeys (2005) (242)
Association of BDNF with anorexia, bulimia and age of onset of weight loss in six European populations. (2004) (236)
From monogenic to polygenic obesity: recent advances (2010) (232)
Melanocortin-4 receptor gene variant I103 is negatively associated with obesity. (2004) (218)
Melanocortin-4 receptor gene: case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesity. (2003) (210)
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany. (2006) (202)
Genetic evidence of assortative mating in humans (2017) (199)
Meta‐analysis of genome‐wide linkage scans of attention deficit hyperactivity disorder (2008) (185)
Association between an agouti-related protein gene polymorphism and anorexia nervosa (2001) (175)
A role for β-melanocyte-stimulating hormone in human body-weight regulation (2006) (168)
Mutation screen of the brain derived neurotrophic factor gene (BDNF): Identification of several genetic variants and association studies in patients with obesity, eating disorders, and attention‐deficit/hyperactivity disorder (2005) (164)
The Association of a SNP Upstream of INSIG2 with Body Mass Index is Reproduced in Several but Not All Cohorts (2007) (163)
Systematic mutation screening of the estrogen receptor beta gene in probands of different weight extremes: identification of several genetic variants. (1998) (162)
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs (2006) (157)
Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. (2010) (155)
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 (2008) (154)
Interrogating the Genetic Determinants of Tourette's Syndrome and Other Tic Disorders Through Genome-Wide Association Studies. (2019) (153)
Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor gene. (1999) (148)
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. (2004) (147)
Association of BDNF with restricting anorexia nervosa and minimum body mass index: a family-based association study of eight European populations (2005) (147)
The V103I polymorphism of the MC4R gene and obesity: population based studies and meta-analysis of 29 563 individuals (2007) (145)
Environmental and genetic risk factors in obesity. (2009) (145)
Lifestyle Intervention in Obese Children With Variations in the Melanocortin 4 Receptor Gene (2009) (144)
Ghrelin gene: identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students. (2002) (141)
A Genetic Investigation of Sex Bias in the Prevalence of Attention-Deficit/Hyperactivity Disorder (2017) (136)
Melanocortin-4 receptor in energy homeostasis and obesity pathogenesis. (2013) (131)
Large quantitative effect of melanocortin-4 receptor gene mutations on body mass index (2004) (128)
Novel common copy number variation for early onset extreme obesity on chromosome 11q11 identified by a genome-wide analysis (2010) (125)
Transmission disequilibrium of polymorphic variants in the tryptophan hydroxylase-2 gene in children and adolescents with obsessive-compulsive disorder. (2006) (123)
Epidemic obesity: are genetic factors involved via increased rates of assortative mating? (2000) (121)
Serotonin transporter gene-linked polymorphic region: allele distributions in relationship to body weight and in anorexia nervosa. (1997) (121)
Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys (2005) (112)
Common variants at 6q22 and 17q21 are associated with intracranial volume (2012) (110)
'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 (2008) (108)
Binge-eating episodes are not characteristic of carriers of melanocortin-4 receptor gene mutations (2004) (108)
An instance of clinical radiation morbidity and cellular radiosensitivity, not associated with ataxia-telangiectasia. (1990) (107)
Systematic mutation screening of the pro-opiomelanocortin gene: identification of several genetic variants including three different insertions, one nonsense and two missense point mutations in probands of different weight extremes. (1998) (107)
Chipping Away the ‘Missing Heritability’: GIANT Steps Forward in the Molecular Elucidation of Obesity – but Still Lots to Go (2010) (106)
Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects? (2009) (105)
The 5-HT2A −1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres (2001) (98)
Definable somatic disorders in overweight children and adolescents. (2007) (95)
5-HT2A promoter polymorphism −1438G/A in children and adolescents with obsessive-compulsive disorders (2002) (94)
5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity (1997) (93)
Interindividual Variation in DNA Methylation at a Putative POMC Metastable Epiallele Is Associated with Obesity. (2016) (93)
Lack of association between the –759C/T polymorphism of the 5-HT2C receptor gene and clozapine-induced weight gain among German schizophrenic individuals (2004) (89)
Perspectives: molecular genetic research in human obesity (2003) (89)
Genome‐wide association study in German patients with attention deficit/hyperactivity disorder (2011) (87)
Eating disorders: the current status of molecular genetic research (2009) (87)
Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals: Does Heterogeneity of Estimates Relate to Study Design? (2009) (85)
Impact of FTO genotypes on BMI and weight in polycystic ovary syndrome: a systematic review and meta-analysis (2012) (85)
Genome scan for childhood and adolescent obesity in German families. (2003) (84)
Molecular genetic aspects of weight regulation. (2013) (83)
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) (2010) (83)
Association and linkage of allelic variants of the dopamine transporter gene in ADHD (2007) (82)
β3-adrenergic-receptor allele distributions in children, adolescents and young adults with obesity, underweight or anorexia nervosa (1997) (81)
Sympathetic function in human carriers of melanocortin-4 receptor gene mutations. (2010) (80)
Association of the MC4R V103I Polymorphism With Obesity: A Chinese Case–control Study and Meta‐analysis in 55,195 Individuals (2010) (79)
Further lack of association between the 5-HT2A gene promoter polymorphism and susceptibility to eating disorders and a meta-analysis pertaining to anorexia nervosa (1999) (79)
Common obesity risk alleles in childhood attention‐deficit/hyperactivity disorder (2013) (77)
Association Studies on Ghrelin and Ghrelin Receptor Gene Polymorphisms With Obesity (2009) (77)
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder (2012) (76)
Hyperphagia, not hypometabolism, causes early onset obesity in melanocortin-4 receptor knockout mice. (2003) (74)
Candidate gene polymorphisms in eating disorders. (2000) (73)
Genetic aspects in attention-deficit/hyperactivity disorder (2008) (72)
Polygenic Obesity in Humans (2008) (72)
No evidence for involvement of polymorphisms of the dopamine D4 receptor gene in anorexia nervosa, underweight, and obesity. (1999) (70)
No evidence for involvement of the leptin gene in anorexia nervosa, bulimia nervosa, underweight or early onset extreme obesity: identification of two novel mutations in the coding sequence and a novel polymorphism in the leptin gene linked upstream region (1998) (68)
Independent confirmation of a major locus for obesity on chromosome 10. (2000) (66)
The genetics of obesity: practical implications (2001) (66)
Missense variants in the human peroxisome proliferator-activated receptor-gamma2 gene in lean and obese subjects. (1999) (64)
Association of the MC4R V103I Polymorphism With the Metabolic Syndrome: The KORA Study (2008) (64)
A novel nonsense mutation in the melanocortin-4 receptor associated with obesity in a Spanish population (2003) (62)
Genes and lifestyle factors in obesity: results from 12 462 subjects from MONICA/KORA (2010) (62)
Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder (2015) (61)
Lack of Support for the Association between GAD2 Polymorphisms and Severe Human Obesity (2005) (60)
Screening for mutations in the neuropeptide Y Y5 receptor gene in cohorts belonging to different weight extremes (1998) (60)
Combined family trio and case‐control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa (2004) (56)
Serotonin transporter gene polymorphism (5-HTTLPR), environmental conditions, and developing negative emotionality and fear in early childhood (2009) (56)
Evidence of an Influence of a Polymorphism Near the INSIG2 on Weight Loss During a Lifestyle Intervention in Obese Children and Adolescents (2008) (55)
Genetic Risk Factors in Eating Disorders (2004) (55)
Genetic variation of the ghrelin activator gene ghrelin O-acyltransferase (GOAT) is associated with anorexia nervosa. (2011) (51)
A Trans-ancestral Meta-Analysis of Genome-Wide Association Studies Reveals Loci Associated with Childhood Obesity. (2019) (51)
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample (2006) (51)
Lack of association of genetic variants in genes of the endocannabinoid system with anorexia nervosa (2008) (51)
Aggravating effect of INSIG2 and FTO on overweight reduction in a one-year lifestyle intervention (2009) (51)
Investigation of a Genome Wide Association Signal for Obesity: Synthetic Association and Haplotype Analyses at the Melanocortin 4 Receptor Gene Locus (2010) (50)
Meta-analysis on the effect of the N363S polymorphism of the glucocorticoid receptor gene (GRL) on human obesity (2006) (50)
Transmission disequilibrium studies in children and adolescents with obsessive-compulsive disorders pertaining to polymorphisms of genes of the serotonergic pathway (2004) (49)
No evidence for an involvement of variants in the cannabinoid receptor gene (CNR1) in obesity in German children and adolescents. (2007) (47)
Association of the melanocortin 4 receptor with feed intake and daily gain in F2 Mangalitsa x Piétrain pigs. (2006) (47)
Evaluation of a Cys23Ser mutation within the human 5-HT2C receptor gene: no evidence for an association of the mutant allele with obesity or underweight in children, adolescents and young adults. (1997) (47)
Case-control and combined family trios analysis of three polymorphisms in the ghrelin gene in European patients with anorexia and bulimia nervosa. (2006) (47)
No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD (2007) (46)
Genetic predisposition to obesity in bulimia nervosa: a mutation screen of the melanocortin-4 receptor gene (2002) (46)
A role for beta-melanocyte-stimulating hormone in human body-weight regulation. (2006) (45)
Contribution of common non-synonymous variants in PCSK1 to body mass index variation and risk of obesity: a systematic review and meta-analysis with evidence from up to 331 175 individuals. (2015) (45)
Transmission disequilibrium studies in early onset of obsessive–compulsive disorder for polymorphisms in genes of the dopaminergic system (2008) (44)
Catechol-O-Methyltransferase Val158Met Polymorphism Is Associated with Somatosensory Amplification and Nocebo Responses (2014) (44)
Changes of peripheral alpha-melanocyte-stimulating hormone in childhood obesity. (2010) (44)
Several mutations in the melanocortin 4 receptor gene are associated with obesity in Chinese children and adolescents (2006) (44)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (43)
Evidence for involvement of the vitamin D receptor gene in idiopathic short stature via a genome-wide linkage study and subsequent association studies. (2006) (42)
Estrogen Receptor 1 Gene (ESR1) is Associated with Restrictive Anorexia Nervosa (2010) (42)
Mutation analysis of the MCHR1 gene in human obesity. (2005) (42)
Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders. (2008) (41)
Preferential reciprocal transfer of paternal/maternal DLK1 alleles to obese children: first evidence of polar overdominance in humans (2008) (41)
Fat Mass and Obesity-Associated Gene (FTO) in Eating Disorders: Evidence for Association of the rs9939609 Obesity Risk Allele with Bulimia nervosa and Anorexia nervosa (2012) (40)
Rescue of Melanocortin 4 Receptor (MC4R) Nonsense Mutations by Aminoglycoside‐Mediated Read‐Through (2012) (40)
Vitamin D and the Risk of Depression: A Causal Relationship? Findings from a Mendelian Randomization Study (2019) (39)
Decreased melanocortin‐4 receptor function conferred by an infrequent variant at the human melanocortin receptor accessory protein 2 gene (2016) (39)
No evidence for an involvement of alleles of polymorphisms in the serotonin1Dβ and 7 receptor genes in obesity, underweight or anorexia nervosa (1999) (39)
Association analyses for dopamine receptor gene polymorphisms and weight status in a longitudinal analysis in obese children before and after lifestyle intervention (2013) (39)
Genetics of Eating Disorders (2013) (39)
A consultation with genetic information about obesity decreases self-blame about eating and leads to realistic weight loss goals in obese individuals. (2009) (38)
Functional variants of the serotonin receptor type 3A and B gene are associated with eating disorders (2009) (38)
Short-term metreleptin treatment of patients with anorexia nervosa: rapid on-set of beneficial cognitive, emotional, and behavioral effects (2020) (38)
Is Information on Genetic Determinants of Obesity Helpful or Harmful for Obese People?—A Randomized Clinical Trial (2007) (38)
Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach (2016) (37)
Associations Between Attention-Deficit/Hyperactivity Disorder and Various Eating Disorders: A Swedish Nationwide Population Study Using Multiple Genetically Informative Approaches (2019) (37)
Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants (2012) (36)
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index (2017) (36)
Analysis of the uncoupling protein-1 (UCP1) gene in obese and lean subjects: Identification of four amino acid variants (1998) (36)
Genetic variation at the CELF1 (CUGBP, elav‐like family member 1 gene) locus is genome‐wide associated with Alzheimer's disease and obesity (2014) (36)
Brain-derived neurotrophic factor V66M polymorphism in childhood-onset obsessive-compulsive disorder. (2005) (34)
Using ancestry-informative markers to identify fine structure across 15 populations of European origin (2014) (34)
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index (2017) (34)
Food Addiction in Gambling Disorder: Frequency and Clinical Outcomes (2017) (34)
Evidence for an influence of TCF7L2 polymorphism rs7903146 on insulin resistance and sensitivity indices in overweight children and adolescents during a lifestyle intervention (2008) (34)
Further support for linkage of extreme obesity to the obese gene in a study group of obese children and adolescents. (2009) (33)
The 103I variant of the melanocortin 4 receptor is associated with low serum triglyceride levels. (2006) (33)
Association of common variants identified by recent genome-wide association studies with obesity in Chinese children: a case-control study (2016) (33)
Common Variants Near MC4R: Exploring Gender Effects in Overweight and Obese Children and Adolescents Participating in a Lifestyle Intervention (2011) (32)
Selection of unrelated bone marrow donors by PCR-SSP typing and subsequent nonradioactive sequence-based typing for HLA DRB1/3/4/5, DQB1, and DPB1 alleles. (1994) (32)
A Heterozygous Mutation in the Third Transmembrane Domain Causes a Dominant-Negative Effect on Signalling Capability of the MC4R (2008) (32)
No evidence for involvement of the promoter polymorphism -866 G/A of the UCP2 gene in childhood-onset obesity in humans. (2003) (30)
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 (2007) (30)
Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (30)
DCLK1 Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder (2012) (29)
Increased constraints on MC4R during primate and human evolution (2008) (29)
Mitochondrial DNA Variants in Obesity (2014) (29)
Exploring the genetic link between RLS and ADHD. (2009) (28)
Genetic association and gene expression analysis identify FGFR1 as a new susceptibility gene for human obesity. (2011) (28)
Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents (1998) (27)
Genetic findings in anorexia and bulimia nervosa. (2010) (26)
Synaptic processes and immune-related pathways implicated in Tourette syndrome (2020) (26)
Association study in eating disorders: TPH2 associates with anorexia nervosa and self‐induced vomiting (2011) (26)
A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesity. (2007) (26)
SDCCAG8 Obesity Alleles and Reduced Weight Loss After a Lifestyle Intervention in Overweight Children and Adolescents (2012) (25)
Successful methylphenidate treatment of early onset extreme obesity in a child with a melanocortin-4 receptor gene mutation and attention deficit/hyperactivity disorder. (2011) (25)
Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesity. (2005) (25)
Comparison of metabolic profiles of acutely ill and short-term weight recovered patients with anorexia nervosa reveals alterations of 33 out of 163 metabolites. (2012) (24)
Familiality and molecular genetics of attention networks in ADHD (2009) (24)
Causal attributions of obese men and women in genetic testing: Implications of genetic/biological attributions (2009) (24)
Effect of an vitamin D deficiency on depressive symptoms in child and adolescent psychiatric patients – a randomized controlled trial: study protocol (2018) (24)
Assessing causal links between metabolic traits, inflammation and schizophrenia: a univariable and multivariable, bidirectional Mendelian-randomization study (2019) (24)
Relationship between MTNR1B (melatonin receptor 1B gene) polymorphism rs10830963 and glucose levels in overweight children and adolescents † (2011) (24)
Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry (2009) (23)
Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin. (2010) (23)
High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation (2018) (23)
Lack of Association of CD36 SNPs With Early Onset Obesity: A Meta‐Analysis in 9,973 European Subjects (2011) (23)
The 5-HT transporter genel inked polymorphic region ( 5H T T L P R ) in evolut ionary perspective : alternative biallelic variation in rhesus m o n k e y s Rapid Communication (23)
Child and adolescent psychiatric genetics (2010) (23)
Variants in the human β1‐,β2‐ and β3‐adrenergic receptor genes are not associated with morbid obesity in children and adolescents (2004) (22)
Gastric inhibitory polypeptide receptor: association analyses for obesity of several polymorphisms in large study groups (2009) (22)
Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity (2010) (21)
Shared Genetic Risk between Eating Disorder- and Substance-Use-Related Phenotypes: Evidence from Genome-Wide Association Studies (2019) (20)
Association of the rs10830963 Polymorphism in MTNR1B with Fasting Glucose Levels in Chinese Children and Adolescents (2011) (20)
A novel mutation Thr162Arg of the melanocortin 4 receptor gene in a Spanish children and adolescent population (2007) (20)
Genetische Befunde bei der Aufmerksamkeitsdefizit- und Hyperaktivitätsstörung (ADHS) (2006) (20)
No evidence for involvement of alleles of the 825-C/T polymorphism of the G-protein subunit beta 3 in body weight regulation. (2001) (19)
Three at One Swoop! (2009) (19)
Effect of vitamin D deficiency on depressive symptoms in child and adolescent psychiatric patients: results of a randomized controlled trial (2020) (18)
Analysis of sequence variations in the suppressor of cytokine signaling (SOCS)-3 gene in extremely obese children and adolescents (2007) (18)
Successful Treatment with Atomoxetine of an Adolescent Boy with Attention Deficit/Hyperactivity Disorder, Extreme Obesity, and Reduced Melanocortin 4 Receptor Function (2013) (18)
Bipolar disorder risk alleles in children with ADHD (2013) (17)
Estimated prevalence of potentially damaging variants in the leptin gene (2017) (17)
Screening for variability in the ciliary neurotrophic factor (CNTF) gene: no evidence for association with human obesity. (2009) (17)
Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents (2000) (17)
Rapid amelioration of anorexia nervosa in a male adolescent during metreleptin treatment including recovery from hypogonadotropic hypogonadism (2021) (17)
Genes and the hypothalamic control of metabolism in humans. (2014) (16)
A Novel SP1/SP3 Dependent Intronic Enhancer Governing Transcription of the UCP3 Gene in Brown Adipocytes (2013) (16)
Absence of leptin deficiency mutation in extremely obese German children and adolescents (1997) (15)
Genome-Wide Association Study Reveals First Locus for Anorexia Nervosa and Metabolic Correlations (2016) (15)
Analyses of non-synonymous obesity risk alleles in SH2B1 (rs7498665) and APOB48R (rs180743) in obese children and adolescents undergoing a 1-year lifestyle intervention. (2013) (15)
FTO Gene: Association to Weight Regain after Lifestyle Intervention in Overweight Children (2014) (15)
Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease. (2010) (15)
The role of genetic variation of human metabolism for BMI, mental traits and mental disorders (2018) (14)
The Fatty Acid Amide Hydrolase (FAAH) Gene Variant rs324420 AA/AC is not Associated with Weight Loss in a 1-Year Lifestyle Intervention for Obese Children and Adolescents (2011) (14)
No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight children (2013) (14)
Detailed stratified GWAS analysis for severe COVID-19 in four European populations (2022) (13)
New susceptibility loci for severe COVID-19 by detailed GWAS analysis in European populations (2021) (13)
Analysis of the HLA‐DR gene locus by temperature gradient gel electrophoresis and its application for the rapid selection of unrelated bone marrow donors (1994) (13)
The promise of new anti-obesity therapies arising from knowledge of genetic obesity traits (2022) (13)
Identification of a deletion variant in the gene encoding the human alpha(2A)-adrenergic receptor. (2001) (13)
Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa (2017) (13)
Variants in the human beta 1-, beta 2-, and beta 3-adrenergic receptor genes are not associated with morbid obesity in children and adolescents. (2004) (12)
Confidence Intervals for Genotype Relative Risks and Allele Frequencies from the Case Parent Trio Design for Candidate-Gene Studies (2003) (12)
The Role of Genetic Variation of BMI, Body Composition, and Fat Distribution for Mental Traits and Disorders: A Look-Up and Mendelian Randomization Study (2020) (12)
Analysis of Genes Involved in Body Weight Regulation by Targeted Re-Sequencing (2016) (12)
The involvement of the canonical Wnt‐signaling receptor LRP5 and LRP6 gene variants with ADHD and sexual dimorphism: Association study and meta‐analysis (2018) (11)
Glucose Transporter 4 Gene (2002) (11)
No evidence for involvement of the calpain-10 gene 'high-risk' haplotype combination for non-insulin-dependent diabetes mellitus in early onset obesity. (2002) (11)
Evaluation of the Obesity Genes FTO and MC4R and the Type 2 Diabetes Mellitus Gene TCF7L2 for Contribution to Stroke Risk: The Mannheim-Heidelberg Stroke Study (2011) (11)
Gene Set of Nuclear-Encoded Mitochondrial Regulators Is Enriched for Common Inherited Variation in Obesity (2013) (11)
Indications for Potential Parent-of-Origin Effects within the FTO Gene (2015) (11)
The Effect of SH2B1 Variants on Expression of Leptin- and Insulin-Induced Pathways in Murine Hypothalamus (2018) (10)
Die Gewichtsregulation im Rahmen der Anorexia nervosa unter besonderer Berücksichtigung der Leptinsekretion (1999) (10)
No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in Germans. (2007) (10)
P0343 - Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders (2008) (10)
Genetische Ursachen der Adipositas (2010) (9)
Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation (2001) (9)
The association of serum leptin levels with food addiction is moderated by weight status in adolescent psychiatric inpatients (2018) (9)
Where in the genome are significant single nucleotide polymorphisms from genome-wide association studies located? (2011) (9)
Val103Ile polymorphism of the melanocortin-4 receptor gene (MC4R) in cancer cachexia (2008) (9)
TCF7L2 polymorphism rs7903146 and predisposition for type 2 diabetes mellitus in obese children. (2008) (9)
Gain‐of‐function variants in the melanocortin 4 receptor gene confer susceptibility to binge eating disorder in subjects with obesity: a systematic review and meta‐analysis (2018) (9)
Fine Mapping of a GWAS-Derived Obesity Candidate Region on Chromosome 16p11.2 (2015) (9)
Molekulare Grundlagen der Adipositas (2001) (8)
Prävalenz von Melanocortin-4-Rezeptor(MC4R)-Mutationen und Polymorphismen bei adipösen Kindern und Jugendlichen in einer konsekutiven pädiatrischen Inanspruchnahmepopulation (2005) (8)
Temperature gradient gel electrophoresis: Rapid detection of alpha‐1‐antitrypsin deficiency carriers (1992) (8)
[Prevalence of melanocortin 4 receptor (MC4R) mutations and polymorphismsin consecutively ascertained obese children and adolescents from a pediatric health care utilization population]. (2005) (8)
Genetische Aspekte der Adipositas (2008) (8)
Genetik und Epigenetik der Adipositas (2015) (8)
Glucose transporter 4 gene: association studies pertaining to alleles of two polymorphisms in extremely obese children and adolescents and in normal and underweight controls. (2002) (8)
[Genetic findings in Attention-Deficit and Hyperactivity Disorder (ADHD)]. (2006) (8)
Serotonin transporter gene polymorphism (5-HTTLPR), environmental conditions, and developing negative emotionality and fear in early childhood (2009) (7)
Missense variants in the human cholecystokinin type A receptor gene: no evidence for association with early-onset obesity. (1999) (7)
Correction: 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 (2008) (7)
Response to Comments on "A Common Genetic Variant Is Associated with Adult and Childhood Obesity" (2007) (7)
[Genetic and epigenetic mechanisms in obesity]. (2015) (7)
Elevated Common Variant Genetic Risk for Tourette Syndrome in a Densely Affected Pedigree (2021) (7)
Lack of Evidence for a Relationship Between the Hypothalamus-Pituitary-Adrenal and the Hypothalamus-Pituitary-Thyroid Axis in Adolescent Depression (2021) (6)
A role for b-melanocyte-stimulating hormone in human bodyweight regulation (6)
Alterations in B cell subsets correlate with body composition parameters in female adolescents with anorexia nervosa (2021) (6)
[Genetic determinants of obesity. Current issues]. (2010) (6)
Genetische Faktoren bei Adipositas (2012) (5)
Waist-hip ratio related genetic loci are associated with risk of impaired fasting glucose in Chinese children: a case control study (2018) (5)
Genetic studies of antithrombin III with IEF and ASO hybridization (1992) (5)
Genetic Factors for Overweight and CAD (2006) (5)
A mendelian randomization study on causal effects of 25(OH)vitamin D levels on attention deficit/hyperactivity disorder (2020) (5)
Adipositas: Genetik und Gen-Umwelt-Interaktionen (2004) (5)
Zur Erblichkeit der Adipositas im Kindes- und Jugendalter (2000) (5)
Genetik und Gen-Umwelt-Interaktionen (2005) (5)
[Body weight regulation in anorexia nervosa with special attention to leptin secretion]. (1999) (5)
Genetic and epigenetic findings in anorexia nervosa (2020) (4)
Kurzzeitige Behandlung von Patient_innen mit Anorexia nervosa mit rekombinant hergestelltem Human-Leptin (Metreleptin): Rasch einsetzende positive Effekte auf Stimmung, Kognition und Verhalten (2021) (4)
Suggestive Evidence for Causal Effect of Leptin Levels on Risk for Anorexia Nervosa: Results of a Mendelian Randomization Study (2021) (4)
Evaluation of Metabolic Profiles of Patients with Anorexia Nervosa at Inpatient Admission, Short- and Long-Term Weight Regain—Descriptive and Pattern Analysis (2020) (4)
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p (2022) (4)
Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation (2018) (3)
Procolipase Gene: No Association with Early-Onset Obesity or Fat Intake (2009) (3)
Common Genetic Variation and Age of Onset of Anorexia Nervosa (2021) (3)
Do Common Variants Separate between Obese Melanocortin-4 Receptor Gene Mutation Carriers and Non-Carriers? The Impact of Cryptic Relatedness (2012) (3)
No Effect of Thyroid Dysfunction and Autoimmunity on Health-Related Quality of Life and Mental Health in Children and Adolescents: Results From a Nationwide Cross-Sectional Study (2020) (3)
[Relevance of the melanocortinergic system for body weight regulation]. (2003) (3)
Relevance of polymorphisms in MC4R and BDNF in short normal stature (2018) (3)
Das Körpergewicht im Rahmen der Schizophrenie unter besonderer Berücksichtigung der clozapin-induzierten Gewichtszunahme und dem damit einhergehenden Anstieg der Leptinsekretion (1999) (3)
Genetische Ursachen der Adipositas (2017) (2)
Klotho KL-VS haplotype does not improve cognition in a population-based sample of adults age 55–87 years (2021) (2)
Size Matters: The CAG Repeat Length of the Androgen Receptor Gene, Testosterone, and Male Adolescent Depression Severity (2021) (2)
PTBP2 – a gene with relevance for both Anorexia nervosa and body weight regulation (2022) (2)
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity (2017) (2)
Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa (2017) (2)
Gene Variants and Obesity (2006) (2)
Erratum: Common variants at 6q22 and 17q21 are associated with intracranial volume (2013) (2)
22nd European Congress on Obesity (ECO2015), Prague, Czech Republic, May 6-9, 2015: Abstracts (2015) (2)
Genetische Aspekte der Essstörungen (2015) (2)
Abstract 1879: Genetic Variation at Chromosome 1p13.3 Affects Sortilin mRNA Expression, Cellular LDL Uptake and Serum LDL Levels Which Translates to the Risk of Coronary Artery Disease (2009) (2)
Causal Effect of Age at Menarche on the Risk for Depression: Results From a Two-Sample Multivariable Mendelian Randomization Study (2022) (2)
[Nutrition and mental health - how findings from genetic studies can support the identification of dietary effects]. (2021) (1)
Mutational screening of the human type II deiodinase gene. (2001) (1)
Prevalence estimates of putatively pathogenic leptin variants in the gnomAD database (2022) (1)
Impact of Genetic Markers on Overweight Reduction in a Lifestyle Intervention (2008) (1)
Genetic aspects of obesity. (2003) (1)
Nonradioactive Approach to Type DNA by Minisatellite Variant Repeats (1994) (1)
[Perspectives of genetic research in eating disorders using the example of anorexia nervosa]. (2015) (1)
Evidence for correlations between BMI-associated SNPs and circRNAs (2022) (1)
A NOVEL MUTATION Thr 162 Arg OF THE MELANOCORTIN 4 RECEPTOR GENE IN A SPANISH CHILDREN AND ADOLESCENTS POPULATION (2010) (1)
Age at menarche relates to depression in adolescent girls: Comparing a clinical sample to the general pediatric population. (2022) (1)
The adrenal steroid profile in adolescent depression: a valuable bio-readout? (2022) (1)
Association and Linkage Studies in Caucasians (2007) (1)
Sex differences in anxiety and depression in children with attention deficit hyperactivity disorder: Investigating genetic liability and comorbidity (2021) (1)
Will leptin provide an insight into weight regulation of patients with anorexia nervosa (1997) (1)
Adiposity in the first half of life. Abstracts of the 27th Annual Meeting of the German Society for Obesity Research. October 6-8, 2011. Bochum, Germany. (2011) (1)
Nutrient-Gene Interactions Human Galanin ( GAL ) and Galanin 1 Receptor ( GALR 1 ) Variations Are Not Involved in Fat Intake and Early Onset Obesity 1 , 2 (2005) (1)
Evidenz für die Assoziation von Adipositas mit genetischen Varianten des FTO-Gens in familien- und populationsbasierten Studien (2007) (1)
Genetische Aspekte in der Adipositas-Beratung – Auswirkungen auf Körperakzeptanz und subjektives Wohlbefinden (2006) (1)
Einfluss genetischer Marker auf den Erfolg einer Lifestyle-Intervention (2008) (1)
Genetische Aspekte von Adipositas (2015) (1)
Genome-wide association study identifies eight risk loci and implicates metabo-psychiatric origins for anorexia nervosa (2019) (0)
Allele frequencies of three 5-HT2A receptor gene polymorphisms in patients with anorexia nervosa, and in healthy underweight and obese individuals (1997) (0)
Faculty Opinions recommendation of SH2B1 CpG-SNP is associated with body weight reduction in obese subjects following a dietary restriction program. (2015) (0)
The complexity of eating disorders: insight into recent research venues in molecular genetics, neuropsychology, neuroimaging, and social sciences (2015) (0)
Editorial Board (2011) (0)
Contents Vol. 77, 2012 (2012) (0)
expression in brown and white adipocytes in rat pups Mechanisms for LEPR-mediated regulation of leptin (2015) (0)
Melanocortin-4-receptor gene variants: hotspot or identical by descent? (2009) (0)
A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
Erratum (2018) (0)
Faculty Opinions recommendation of Genome-wide association study of problematic opioid prescription use in 132,113 23andMe research participants of European ancestry. (2022) (0)
Functional characterization of naturally occurring mutations in the melanocortin receptor accesory protein 2 (MRAP2) (2016) (0)
Herz Genetic Factors for Overweight and CAD (0)
Identifying Genes Underlying Child and Adolescent Psychiatric Disorders. (2006) (0)
Genetics of monogenic obesity: part 1 of 2 (2015) (0)
Faculty Opinions recommendation of The obesity-associated SNPs in intron 1 of the FTO gene affect primary transcript levels. (2010) (0)
Genetics of monogenic obesity 2 (2015) (0)
Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity (2021) (0)
' s report Title : Marginal Impact of Phenotypic Selection on Detecting MC 4 R Mutations in Italian Obese Children Version : 1 Date : 13 November 2008 (0)
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deﬁcit/hyperactivity disorder (2013) (0)
Expression of CXCR4 on CD4+ T cells predicts body composition parameters in female adolescents with anorexia nervosa (2022) (0)
A heterozygous MC4R mutation in the third transmembrane domain causes a dominant-negative effect (2006) (0)
Faculty Opinions recommendation of Common genetic variation near MC4R is associated with waist circumference and insulin resistance. (2008) (0)
Title : Association analyses for dopamine receptor gene polymorphisms and weight status : a cross-sectional case-control study and longitudinal analysis in obese children before and after lifestyle intervention Running title : Dopamine receptor polymorphisms and obesity (2013) (0)
Dysfunctionof lipid sensorGPR120 leads to obesity in both mouse and human (2020) (0)
Title Pages / Table of Contents (2011) (0)
Genetic Sum Score of Risk Alleles Associated with Body- Mass-Index Interacts with Socioeconomic Status in the Heinz Nixdorf Recall Study (2019) (0)
Genetische Faktoren der Adipositas und koronaren Herzerkrankung (KHK) (2006) (0)
S.01.03 Anorexia nervosa and body mass index: combined GWAS and functional ex-vivo studies (2017) (0)
Bestimmung von Gen x Gen Wechselwirkungen zwischen etablierten Adipositas assozierten Polymorphismen des Insulin Induced 2 (INSIG2) und des Melanocortin-4 Rezeptor (MC4R) Gens (2006) (0)
POMC DNA Hypermethylation Variant is Highly Associated with Obesity in Adults (2015) (0)
Association Sessions (2012) (0)
A combined population and family-based study of eight European populations demonstrates association between BDNF and eating disorders. (2003) (0)
Supplementary Material for: Common Variants Near MC4R: Exploring Gender Effects in Overweight and Obese Children and Adolescents Participating in a Lifestyle Intervention (2017) (0)
Sympathetic nervous activity in carriers of MC4R mutations (2006) (0)
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
Screening for mutations in the glucose-dependent insulinotrophic polypeptide receptor gene (GIPR) in obese patients with disturbed glucose tolerance (2008) (0)
Lipocalin 2 – mutation screen and serum levels in patients with anorexia nervosa or obesity and in lean individuals (2023) (0)
Faculty Opinions recommendation of Transcriptional requirements of the distal heavy-strand promoter of mtDNA. (2013) (0)
Association of obesity risk alleles with childhood Attention-Deficit/Hyperactivity Disorder: A cross-disorder analysis (2012) (0)
Mutationssuche im Brain Derived Neurotrophic Factor Gen (BDNF): Identifizierung verschiedener genetischer Varianten in Patienten mit Adipositas und Eßstörungen (2004) (0)
Acknowledgement to Reviewers (2016) (0)
Tribute to Lodewijk Sandkuijl (2003) (0)
Molecular insights in dysfunctions of the human melanocortin-4-receptor (MC4R) caused by mutations in the third transmembrane domain (TM3) and the second intracellular loop (2008) (0)
Isolation of a (ATTTT)n Positive Locus by Cloning, PCR Cycle Sequencing and Nonradioactive Direct Blotting Electrophoresis (1994) (0)
Polygenic risk score-based phenome-wide association study identifies novel associations for Tourette syndrome (2022) (0)
obesity in melanocortin-4 receptor knockout mice Hyperphagia, not hypometabolism, causes early onset (2015) (0)
List of Contributors (2019) (0)
M83 ASSESSING CAUSAL LINKS BETWEEN METABOLIC TRAITS, INFLAMMATION AND SCHIZOPHRENIA: A UNIVARIABLE AND MULTIVARIABLE BIDIRECTIONAL MENDELIAN RANDOMIZATION STUDY (2019) (0)
Title Page / Table of Contents (2010) (0)
Changes of peripheral [alpha]-melanocortin stimulating hormone ([alpha]-MSH) in childhood craniopharyngioma patients in comparison with other forms of childhood obesity (2012) (0)
Faculty Opinions recommendation of Adipose circular RNAs exhibit dynamic regulation in obesity and functional role in adipogenesis. (2021) (0)
Meta-analysis of genome-wide association studies on ADHD: A dimensional approach (2013) (0)
Erratum to: Impact of FTO genotypes on BMI and weight in polycystic ovary syndrome: a systematic review and meta-analysis (2012) (0)
Contents of Forthcoming Issues (2008) (0)
pathway in eating disorders (2008) (0)
Dickes Erbe – Genetische Faktoren der Adipositas im Kindes- und Jugendalter (2005) (0)
Genetic variation in the melanocortinergic system in relationship to body weight (2003) (0)
www.ssoar.info From monogenic to polygenic obesity: recent advances (2021) (0)
Contents Vol. 54, 2002 (2003) (0)
Faculty Opinions recommendation of Genome-wide association studies of obesity and metabolic syndrome. (2014) (0)
Detection of two hypervariable (ATTTT)n loci in the human genome (1995) (0)
Genetic variation at three genetic loci involved in anorexia nervosa are associated with body weight regulation (2015) (0)
F53GENETIC AND GENE EXPRESSION ANALYSIS IN CTBP2: A GENE DERIVED FROM GENOME-WIDE DATA IN ANOREXIA NERVOSA AND BODY WEIGHT REGULATION (2019) (0)
Erratum: A genome-wide association study of anorexia nervosa suggests a risk locus implicated in dysregulated leptin signaling (2017) (0)
Subjective reward processing and catechol-O- methyltransferase Val158Met polymorphism as potential research domain criteria in addiction: A pilot study (2022) (0)
Faculty Opinions recommendation of The genetic contribution to non-syndromic human obesity. (2009) (0)
Epigenetik – was man vom ‘schönen Schafhintern' (Callipyge) über Adipositas lernen kann (2006) (0)
Neue Junior-Herausgeber_innen (2023) (0)
Aktuelle genetische Befunde zu Adipositas: INSIG2 und UCP3 (2006) (0)
Genetic Markers, Weight Reduction, and Behavioral Changes in Lifestyle (2011) (0)
Contents Vol. 81, 2014 (2014) (0)
Meetings and Conferences · Tagungen und Kongresse (2009) (0)
Keine Assoziation von genetischen Varianten im Cannabinoidrezeptor 1 Gen (CNR1) mit frühmanifester Adipositas bei deutschen Kindern und Jugendlichen (2007) (0)
Perspektiven der genetischen Forschung bei Essstörungen am Beispiel der Anorexia nervosa (2015) (0)
Gene, die wahren Dickmacher? (2006) (0)
Title Pages / 28. Jahrestagung der Deutschen Adipositas-Gesellschaft / Table of Contents (2012) (0)
Subject Index Vol. 54, 2002 (2003) (0)
Restoration of signalling capabilities in total loss of function MC4R mutations (2007) (0)
Genetische Mechanismen bei der Gewichtsregulation (2018) (0)
Mutationsscreening des PTBP2-Gens – Ein Gen, das sowohl für AN als auch für die Gewichtsregulierung von Bedeutung ist (#20) (2022) (0)
Ebenen der genetischen Analyse komplexer Phänotypen am Beispiel der Anorexia nervosa und der Varianz des Körpergewichts (2021) (0)
Genetik in der Kinder- und Jugendpsychiatrie (2021) (0)
Addendum: Genome‐wide association study in German patients with attention deficit/hyperactivity disorder (2012) (0)
Korrelationen zwischen BMI-assoziierten genetischen Varianten und zirkulären RNAs (#19) (2022) (0)
Die genetischen Grundlagen der Aufmerksamkeitsdefizit‐Hyperaktivitätsstörung (ADHS) (2007) (0)
No evidence for intervention-associated DNA methylation changes in monocytes of patients with posttraumatic stress disorder (2020) (0)
Molekulargenetische Analysen zur Adipositas (2006) (0)
Alterations in B cell subsets correlate with body composition parameters in female adolescents with anorexia nervosa (2021) (0)
Genetic variants in genes involved in creatine biosynthesis in patients with severe obesity or anorexia nervosa (2023) (0)
Ernährungseffekten auf der Spur – Wie die Genetik helfen kann, Zusammenhänge zwischen Ernährung und seelischer Gesundheit aufzudecken (2021) (0)
Subject Index Vol. 77, 2012 (2012) (0)
Polygene Varianten und Epigenetik bei Adipositas (2017) (0)
Melanocortinerges System und Adipositas: Die bislang unterschätzte Rolle des beta-MSH (2006) (0)
Evolutionary Perspective of MC4R (2006) (0)
Polygene Formen der Adipositas und Störungs-übergreifende Analysen (2018) (0)
S.18.03 Genetics of obesity (2010) (0)
TGGE and HIEF: a comparison of two methods in the detection of carriers of the Z mutation of the alpha-1-antitrypsin gene (1994) (0)
TO JMG Large quantitative effect of melanocortin-4 receptor gene mutations on body mass index (2004) (0)
Genetics of Eating and Weight Disorders (2019) (0)
Faculty Opinions recommendation of Associations of the FTO rs9939609 variant with discrete body fat depots and dietary intake in a multi-ethnic cohort. (2012) (0)
University of Groningen Investigation of common , low-frequency and rare genome-wide variation in anorexia nervosa Kas (2017) (0)
DCLK1Variants Are Associated across Schizophrenia and Attention Deficit/Hyperactivity Disorder (0)
Mutation screen in the GWAS derived obesity gene SH2B1including functional analyses of detected variants (2012) (0)
Sympathetic function in carriers of MC4R mutations (2006) (0)
[Genetic Analyses of Complex Phenotypes Through the Example of Anorexia Nervosa and Bodyweight Regulation]. (2021) (0)
Lawrence Berkeley National Laboratory Lawrence Berkeley National Laboratory Title Lack of Support for the Association Between GAD 2 Polymorphisms and Severe Human Obesity Permalink (2005) (0)
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder (2018) (0)
3. Ursachen der Adipositas (2017) (0)

This paper list is powered by the following services:

What Schools Are Affiliated With Anke Hinney?

Anke Hinney is affiliated with the following schools:

Anke Hinney's Academic­Influence.com Rankings

Anke Hinney's Degrees

Similar Degrees You Can Earn

Why Is Anke Hinney Influential?

Anke Hinney's Published Works

Published Works

What Schools Are Affiliated With Anke Hinney?

Anke Hinney's AcademicInfluence.com Rankings