PuSH - Publication Server of Helmholtz Zentrum München

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1.
Giuranna, J.* et al.: The effect of SH2B1 variants on expression of leptin- and insulin-induced pathways in murine hypothalamus. Obes. Facts 11, 93-108 (2018)
2.
Huckins, L.M.* et al.: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa. Mol. Psychiatry 23, 1169-1180 (2018)
3.
Huckins, L.M.* et al.: Correction: Investigation of common, low-frequency and rare genome-wide variation in anorexia nervosa. Mol. Psychiatry 23:1 (2018)
4.
Kesselmeier, M.* et al.: High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation. World J. Biol. Psychiatry 19, 187-199 (2018)
5.
Duncan, L.* et al.: Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa. Am. J. Psychiatry 174, 850-858 (2017)
6.
Hinney, A.* et al.: Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Mol. Psychiatry 22, 192-201 (2017)
7.
Hinney, A.* et al.: Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index (vol 22, pg 192, 2017). Mol. Psychiatry 22, 321-322 (2017)
8.
Mooney, M.A.* et al.: Pathway analysis in attention deficit hyperactivity disorder: An ensemble approach. Am. J. Med. Genet. B 171, 815-826 (2016)
9.
Volckmar, A.L.* et al.: Analysis of genes involved in body weight regulation by targeted re-sequencing. PLoS ONE 11:e0147904 (2016)
10.
Wang, H.J.* et al.: Association of common variants identified by recent genome-wide association studies with obesity in Chinese children: A case-control study. BMC Med. Genet. 17:7 (2016)
11.
Nead, K.T.* et al.: 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. Hum. Mol. Genet. 24, 3582-3594 (2015)
12.
Volckmar, A.L.* et al.: Fine mapping of a GWAS-derived obesity candidate region on chromosome 16p11.2. PLoS ONE 10:e0125660 (2015)
13.
Boraska, V.* et al.: A genome-wide association study of anorexia nervosa. Mol. Psychiatry 19, 1085-1094 (2014)
14.
Hinney, A.* et al.: Genetic variation at the CELF1 (CUGBP, elav-like family member 1 gene) locus is genome-wide associated with Alzheimer's disease and obesity. Am. J. Med. Genet. B 165, 283-293 (2014)
15.
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)
16.
Knoll, N.* et al.: Mitochondrial DNA variants in obesity. PLoS ONE 9:e94882 (2014)
17.
Albayrak, Ö.* et al.: Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder. Am. J. Med. Genet. B 162, 295-305 (2013)
18.
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)
19.
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)
20.
Knoll, N.* et al.: Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity. PLoS ONE 8:e55884 (2013)