PuSH - Publication Server of Helmholtz Zentrum München

11 Records found.
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1.
Kesselmeier, M.* et al.: High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation. World J. Biol. Psychiatry 19, 187-199 (2018)
2.
Volckmar, A.L.* et al.: Analysis of genes involved in body weight regulation by targeted re-sequencing. PLoS ONE 11:e0147904 (2016)
3.
Volckmar, A.L.* et al.: Fine mapping of a GWAS-derived obesity candidate region on chromosome 16p11.2. PLoS ONE 10:e0125660 (2015)
4.
Jarick, I.* et al.: Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Mol. Psychiatry 19, 115–121 (2014)
5.
Albayrak, Ö.* et al.: Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder. Am. J. Med. Genet. B 162, 295-305 (2013)
6.
Berndt, S.I.* et al.: Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat. Genet. 45, 501-512 (2013)
7.
Hinney, A.* et al.: No impact of obesity susceptibility loci on weight regain after a lifestyle intervention in overweight children. J. Pediatr. Endocrinol. Metab. 26, 1209-1213 (2013)
8.
Schimmelmann, B.G.* et al.: Bipolar disorder risk alleles in children with ADHD. J. Neural Transm. 120, 1611-1617 (2013)
9.
Mühlhaus, J.* et al.: Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatedness. Horm. Res. Paediatr. 77, 358-368 (2012)
10.
Hinney, A.* et al.: Genome-wide association study in German patients with attention deficit/hyperactivity disorder. Am. J. Med. Genet. B 156B, 888-897 (2011)
11.
Pütter, C.* et al.: Missing heritability in the tails of quantitative traits? A simulation study on the impact of slightly altered true genetic models. Hum. Hered. 72, 173-181 (2011)