Published in Int J Obes Relat Metab Disord on May 01, 2001
PPARalpha L162V underlies variation in serum triglycerides and subcutaneous fat volume in young males. BMC Med Genet (2007) 0.99
Next-generation sequence analysis of genes associated with obesity and nonalcoholic fatty liver disease-related cirrhosis in extreme obesity. Hum Hered (2013) 0.82
Effect of GAS6 and AXL Gene Polymorphisms on Adiposity, Systemic Inflammation, and Insulin Resistance in Adolescents. Int J Endocrinol (2014) 0.78
The paradoxes of body weight. Dtsch Arztebl Int (2008) 0.75
The V103I polymorphism of the MC4R gene and obesity: population based studies and meta-analysis of 29 563 individuals. Int J Obes (Lond) (2007) 2.37
Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology. Mol Psychiatry (2013) 2.25
Genome-wide association scan for childhood caries implicates novel genes. J Dent Res (2011) 2.05
Increased body-mass index in patients with narcolepsy. Lancet (2000) 1.78
Several mutations in the melanocortin-4 receptor gene including a nonsense and a frameshift mutation associated with dominantly inherited obesity in humans. J Clin Endocrinol Metab (1999) 1.67
The 5-HT transporter gene-linked polymorphic region (5-HTTLPR) in evolutionary perspective: alternative biallelic variation in rhesus monkeys. Rapid communication. J Neural Transm (Vienna) (1997) 1.65
Arterial blood gas tensions and acid-base balance in the management of the respiratory distress syndrome. J Pediatr (1966) 1.61
Exploring the genetic link between RLS and ADHD. J Psychiatr Res (2009) 1.55
Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys. J Med Genet (2005) 1.29
A genome-wide scan for attention-deficit/hyperactivity disorder in 155 German sib-pairs. Mol Psychiatry (2006) 1.29
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. Am J Med Genet B Neuropsychiatr Genet (2005) 1.22
Systematic mutation screening of the estrogen receptor beta gene in probands of different weight extremes: identification of several genetic variants. J Clin Endocrinol Metab (1998) 1.09
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? Mol Psychiatry (2008) 1.07
Genes and lifestyle factors in obesity: results from 12,462 subjects from MONICA/KORA. Int J Obes (Lond) (2010) 1.04
Epidemic obesity: are genetic factors involved via increased rates of assortative mating? Int J Obes Relat Metab Disord (2000) 1.02
Independent confirmation of a major locus for obesity on chromosome 10. J Clin Endocrinol Metab (2000) 1.01
Large quantitative effect of melanocortin-4 receptor gene mutations on body mass index. J Med Genet (2004) 1.01
Association between an agouti-related protein gene polymorphism and anorexia nervosa. Mol Psychiatry (2001) 0.98
Biological studies on Brazilian plants used in wound healing. J Ethnopharmacol (2009) 0.97
Association and linkage of allelic variants of the dopamine transporter gene in ADHD. Mol Psychiatry (2007) 0.96
Aggravating effect of INSIG2 and FTO on overweight reduction in a one-year lifestyle intervention. Arch Dis Child (2009) 0.95
Binge-eating episodes are not characteristic of carriers of melanocortin-4 receptor gene mutations. Mol Psychiatry (2004) 0.93
An instance of clinical radiation morbidity and cellular radiosensitivity, not associated with ataxia-telangiectasia. Br J Radiol (1990) 0.93
Phenotypes in three pedigrees with autosomal dominant obesity caused by haploinsufficiency mutations in the melanocortin-4 receptor gene. Am J Hum Genet (1999) 0.92
Perspectives: molecular genetic research in human obesity. Obes Rev (2003) 0.90
A novel nonsense mutation in the melanocortin-4 receptor associated with obesity in a Spanish population. Int J Obes Relat Metab Disord (2003) 0.90
Genetic aspects in attention-deficit/hyperactivity disorder. J Neural Transm (Vienna) (2008) 0.90
Evidence for an influence of TCF7L2 polymorphism rs7903146 on insulin resistance and sensitivity indices in overweight children and adolescents during a lifestyle intervention. Int J Obes (Lond) (2008) 0.87
FDG PET findings leading to diagnosis of neurosarcoidosis. Clin Neurol Neurosurg (2012) 0.87
The 5-HT(2A) -1438G/A polymorphism in anorexia nervosa: a combined analysis of 316 trios from six European centres. Mol Psychiatry (2002) 0.85
No evidence for preferential transmission of common valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor gene (BDNF) in ADHD. J Neural Transm (Vienna) (2007) 0.85
Genetic predisposition to obesity in bulimia nervosa: a mutation screen of the melanocortin-4 receptor gene. Mol Psychiatry (2002) 0.85
On the total expected study cost in two-stage genome-wide search designs for linkage analysis using the mean test for affected sib pairs. Genet Epidemiol (2001) 0.85
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample. J Neural Transm (Vienna) (2006) 0.85
Analysis of the uncoupling protein-1 (UCP1) gene in obese and lean subjects: identification of four amino acid variants. Int J Obes Relat Metab Disord (1998) 0.83
Objective measurement of hyperactivity, impulsivity, and inattention in children with hyperkinetic disorders before and after treatment with methylphenidate. Eur Child Adolesc Psychiatry (2004) 0.83
Missense variants in the human peroxisome proliferator-activated receptor-gamma2 gene in lean and obese subjects. Eur J Endocrinol (1999) 0.82
Several mutations in the melanocortin 4 receptor gene are associated with obesity in Chinese children and adolescents. J Endocrinol Invest (2006) 0.82
Comparison of metabolic profiles of acutely ill and short-term weight recovered patients with anorexia nervosa reveals alterations of 33 out of 163 metabolites. J Psychiatr Res (2012) 0.82
Variants in the human beta 1-, beta 2-, and beta 3-adrenergic receptor genes are not associated with morbid obesity in children and adolescents. Diabetes Obes Metab (2004) 0.82
Further support for linkage of extreme obesity to the obese gene in a study group of obese children and adolescents. Exp Clin Endocrinol Diabetes (1997) 0.82
A novel non-synonymous mutation in the melanocortin-4 receptor gene (MC4R) in a 2-year-old Austrian girl with extreme obesity. Exp Clin Endocrinol Diabetes (2007) 0.82
No evidence for involvement of the promoter polymorphism -866 G/A of the UCP2 gene in childhood-onset obesity in humans. Exp Clin Endocrinol Diabetes (2003) 0.81
Prevalence of obesity in adolescent and young adult patients with and without schizophrenia and in relationship to antipsychotic medication. J Psychiatr Res (2001) 0.81
Transmission disequilibrium studies in children and adolescents with obsessive-compulsive disorders pertaining to polymorphisms of genes of the serotonergic pathway. J Neural Transm (Vienna) (2004) 0.81
Further lack of association between the 5-HT2A gene promoter polymorphism and susceptibility to eating disorders and a meta-analysis pertaining to anorexia nervosa. Mol Psychiatry (1999) 0.81
Combined family trio and case-control analysis of the COMT Val158Met polymorphism in European patients with anorexia nervosa. Am J Med Genet B Neuropsychiatr Genet (2004) 0.81
5-HT2A promoter polymorphism -1438G/A in children and adolescents with obsessive-compulsive disorders. Mol Psychiatry (2002) 0.81
No evidence for involvement of alleles of the 825-C/T polymorphism of the G-protein subunit beta 3 in body weight regulation. Exp Clin Endocrinol Diabetes (2001) 0.81
Effects of unfractionated and fractionated heparin on platelet function. Haemostasis (1988) 0.80
TCF7L2 polymorphism rs7903146 and predisposition for type 2 diabetes mellitus in obese children. Horm Metab Res (2008) 0.80
Transmission disequilibrium and sequence variants at the leptin receptor gene in extremely obese German children and adolescents. Hum Genet (1998) 0.80
5-HT2A receptor gene polymorphisms, anorexia nervosa, and obesity. Lancet (1997) 0.80
Association of the melanocortin 4 receptor with feed intake and daily gain in F2 Mangalitsa x Piétrain pigs. Anim Genet (2006) 0.80
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. Tissue Antigens (1994) 0.79
A bivariate Haseman-Elston method and application to the analysis of asthma-related phenotypes on chromosome 5q. Genet Epidemiol (2001) 0.79
[Occupational and non-occupational risk factors in bladder cancer patients in an industrialized area located in former East-Germany]. Aktuelle Urol (2005) 0.79
Screening for mutations in the neuropeptide Y Y5 receptor gene in cohorts belonging to different weight extremes. Int J Obes Relat Metab Disord (1998) 0.79
Missense variants in the human cholecystokinin type A receptor gene: no evidence for association with early-onset obesity. Horm Metab Res (1999) 0.78
Screening for variability in the ciliary neurotrophic factor (CNTF) gene: no evidence for association with human obesity. Exp Clin Endocrinol Diabetes (1998) 0.78
Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents. Acta Diabetol (2000) 0.78
Mutational screening of the human type II deiodinase gene. Horm Metab Res (2001) 0.78
[Prevalence of melanocortin 4 receptor (MC4R) mutations and polymorphismsin consecutively ascertained obese children and adolescents from a pediatric health care utilization population]. Klin Padiatr (2005) 0.78
Absence of leptin deficiency mutation in extremely obese German children and adolescents. Int J Obes Relat Metab Disord (1997) 0.77
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. Horm Metab Res (2011) 0.77
Analyses of non-synonymous obesity risk alleles in SH2B1 (rs7498665) and APOB48R (rs180743) in obese children and adolescents undergoing a 1-year lifestyle intervention. Exp Clin Endocrinol Diabetes (2013) 0.77
No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in Germans. Horm Metab Res (2007) 0.77
Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Mol Psychiatry (2016) 0.77
Association study in eating disorders: TPH2 associates with anorexia nervosa and self-induced vomiting. Genes Brain Behav (2010) 0.76
Bipolar disorder risk alleles in children with ADHD. J Neural Transm (Vienna) (2013) 0.76
Glutathione transferase activities in renal carcinomas and adjacent normal renal tissues: factors influencing renal carcinogenesis induced by xenobiotics. Arch Toxicol (2001) 0.76
5-HT2A gene promoter polymorphism and anorexia nervosa. Lancet (1999) 0.75
[Relevance of the melanocortinergic system for body weight regulation]. Dtsch Med Wochenschr (2003) 0.75
A novel mutation Thr162Arg of the melanocortin 4 receptor gene in a Spanish children and adolescent population. Clin Endocrinol (Oxf) (2007) 0.75
Systematic screening for mutations in the human necdin gene (NDN): identification of two naturally occurring polymorphisms and association analysis in body weight regulation. Int J Obes Relat Metab Disord (2001) 0.75
Liposomes as a tool in experimental pharmacology and toxicology. Pharmazie (1995) 0.75
Innovative application of skin staplers in operations for burns. Surg Gynecol Obstet (1982) 0.75
Genetic studies of antithrombin III with IEF and ASO hybridization. Hum Genet (1992) 0.75
[Genetic determinants of obesity. Current issues]. Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz (2010) 0.75
Analysis of the HLA-DR gene locus by temperature gradient gel electrophoresis and its application for the rapid selection of unrelated bone marrow donors. Electrophoresis (1995) 0.75
N-acetyltransferase 2 phenotype in painters with bladder cancer and controls. Ann Acad Med Singapore (2001) 0.75
Detection of two hypervariable (ATTTT)n loci in the human genome. Electrophoresis (1995) 0.75