نتائج البحث

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

• Authors : Jarick, I; Volckmar, A-L; Pütter, C

• Source: Jarick, I; Volckmar, A-L; Pütter, C; Pechlivanis, S; Nguyen, T T; Dauvermann, M R; Beck, S; Albayrak, O; Scherag, S; Gilsbach, S; Cichon,

تفاصيل العنوان

Analysis of genes involved in body weight regulation by targeted re-sequencing.

• Authors : Volckmar, A.L.; Han, C.T.; Pütter, C.

• Source: PLoS ONE 11:e0147904 (2016)

تفاصيل العنوان

Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index

• Authors : Hoggart, C; Venturini, G; Mangino, M

تفاصيل العنوان

Bipolar disorder risk alleles in children with ADHD

• Authors : Schimmelmann, B. G.; Hinney, A.; Scherag, A.

Subjects: 150 Psychology; 610 Medicine & health

• Source: Schimmelmann, B. G.; Hinney, A.; Scherag, A.; Pütter, C.; Pechlivanis, S.; Cichon, S.; Jöckel, K.-H.; Schreiber, S.; Wichmann, H. E.;

تفاصيل العنوان

Fine mapping of a GWAS-derived obesity candidate region on chromosome 16p11.2.

• Authors : Volckmar, A.L.; Song, J.Y.; Jarick, I.

• Source: PLoS ONE 10:e0125660 (2015)

تفاصيل العنوان

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

• Authors : Jarick, I.; Volckmar, A. L.; Pütter, C.

Subjects: ddc:610

تفاصيل العنوان

Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index

• Authors : Hoggart, CJ; Venturini, G; Ascari, G

• Source: PLoS Genetics , 10 (7) , Article e1004508. (2014)

تفاصيل العنوان

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

• Authors : Berndt, S.I.; Gustafsson, S.; Mägi, R.

Subjects: /dk/atira/pure/keywords/cohort_studies/netherlands_twin_register_ntr_; name=Netherlands Twin Register (NTR); /dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being

• Source: Berndt , S I , Gustafsson , S , Mägi , R , Ganna , A , Wheeler , E , Feitosa , M F , Justice , A E , Monda , K L , Croteau-Chonka , D C , Day , F R , Esko , T , Fall ,

تفاصيل العنوان

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

• Authors : Jarick, I; Volckmar, A-L; Pütter, C

Subjects: Cellular and Molecular Neuroscience; Psychiatry and Mental health; Molecular Biology

• Source: Molecular Psychiatry ; volume 19, issue 1, page 115-121 ; ISSN 1359-4184 1476-5578

تفاصيل العنوان

Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up study.

• Authors : Thomas, S¹; Pütter, C²; Weber, S¹

• Source: British Journal of Cancer. 3/13/2012, Vol. 106 Issue 6, p1171-1176. 6p. 3 Charts, 2 Graphs.

تفاصيل العنوان