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Your search keyword '"Scherag S"' showing total 49 results

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1. A genome-wide association study of anorexia nervosa

4. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

7. Association study in eating disorders: TPH2 associates with anorexia nervosa and self-induced vomiting

8. Using ancestry-informative markers to identify fine structure across 15 populations of European origin

9. A genome-wide association study of anorexia nervosa

10. 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

11. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

12. A genome-wide association study of anorexia nervosa

13. Using ancestry-informative markers to identify fine structure across 15 populations of European origin

14. Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes

15. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

16. Genomweite Assoziationsstudien für Anorexia nervosa - warum finden wir so wenig? Symposium: 'Neue Erkenntnisse zu Genetik, Epigenetik und Neurobiologie bei Anorexia nervosa'

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

18. Molecular genetics of attention-deficit/hyperactivity disorder: an overview.

19. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

20. Molecular genetics of attention-deficit/hyperactivity disorder: an overview

21. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

22. Addendum: Genome-wide association study in German patients with attention deficit/hyperactivity disorder

23. Association study in eating disorders: TPH2 associates with anorexia nervosa and self-induced vomiting

24. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

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

26. 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)

27. Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

28. Causal relationship between obesity and vitamin D status: bi-directional Mendelian randomization analysis of multiple cohorts

29. Genome-Wide Association Analysis Identifies Variants Associated with Nonalcoholic Fatty Liver Disease That Have Distinct Effects on Metabolic Traits

30. Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index

31. Effects of the DRD4 genotype on neural networks associated with executive functions in children and adolescents.

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

33. Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatedness.

34. 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.

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

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

37. Relationship between MTNR1B (melatonin receptor 1B gene) polymorphism rs10830963 and glucose levels in overweight children and adolescents.

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

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

40. 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.

41. Common variants near MC4R: exploring gender effects in overweight and obese children and adolescents participating in a lifestyle intervention.

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

43. The 5-HTTLPR polymorphism, platelet serotonin transporter activity and platelet serotonin content in underweight and weight-recovered females with anorexia nervosa.

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

45. 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.

46. Sympathetic function in human carriers of melanocortin-4 receptor gene mutations.

47. Molecular genetics of attention-deficit/hyperactivity disorder: an overview.

48. Eating disorders: the current status of molecular genetic research.

49. Genetic findings in anorexia and bulimia nervosa.

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