Nowak-Göttl U - Search Results

1

Targeted resequencing of a locus for heparin-induced thrombocytopenia on chromosome 5 identified in a genome-wide association study.

Witten A, Bolbrinker J, Barysenka A, Huber M, Rühle F, Nowak-Göttl U, Garbe E, Kreutz R, Stoll M. Witten A, et al. J Mol Med (Berl). 2018 Aug;96(8):765-775. doi: 10.1007/s00109-018-1661-6. Epub 2018 Jun 22. J Mol Med (Berl). 2018. PMID: 29934777

2

ADAMTS12, a new candidate gene for pediatric stroke.

Witten A, Rühle F, de Witt M, Barysenka A, Stach M, Junker R, Nowak-Göttl U, Stoll M. Witten A, et al. PLoS One. 2020 Aug 20;15(8):e0237928. doi: 10.1371/journal.pone.0237928. eCollection 2020. PLoS One. 2020. PMID: 32817637 Free PMC article.

3

A genome-wide association study identifies a gene network of ADAMTS genes in the predisposition to pediatric stroke.

Arning A, Hiersche M, Witten A, Kurlemann G, Kurnik K, Manner D, Stoll M, Nowak-Göttl U. Arning A, et al. Blood. 2012 Dec 20;120(26):5231-6. doi: 10.1182/blood-2012-07-442038. Epub 2012 Sep 18. Blood. 2012. PMID: 22990015 Free article.

4

Advances in understanding stroke risk in children--a geneticist's view.

Stoll M, Rühle F, Nowak-Göttl U. Stoll M, et al. Br J Haematol. 2014 Mar;164(5):636-45. doi: 10.1111/bjh.12706. Epub 2013 Dec 19. Br J Haematol. 2014. PMID: 24354735 Free article. Review.

5

Rare Variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric Stroke.

Stoll M, Rühle F, Witten A, Barysenka A, Arning A, Strauss C, Nowak-Göttl U. Stoll M, et al. Circ Cardiovasc Genet. 2016 Aug;9(4):357-67. doi: 10.1161/CIRCGENETICS.115.001184. Epub 2016 Jul 13. Circ Cardiovasc Genet. 2016. PMID: 27412500

6

Rare genetic variants in SMAP1, B3GAT2, and RIMS1 contribute to pediatric venous thromboembolism.

Rühle F, Witten A, Barysenka A, Huge A, Arning A, Heller C, Krümpel A, Mesters R, Franke A, Lieb W, Riemenschneider M, Hiersche M, Limperger V, Nowak-Göttl U, Stoll M. Rühle F, et al. Blood. 2017 Feb 9;129(6):783-790. doi: 10.1182/blood-2016-07-728840. Epub 2016 Dec 23. Blood. 2017. PMID: 28011674 Free article.

7

Single- and Multimarker Genome-Wide Scans Evidence Novel Genetic Risk Modifiers for Venous Thromboembolism.

Herrera-Rivero M, Stoll M, Hegenbarth JC, Rühle F, Limperger V, Junker R, Franke A, Hoffmann P, Shneyder M, Stach M, Nowak-Göttl U. Herrera-Rivero M, et al. Thromb Haemost. 2021 Sep;121(9):1169-1180. doi: 10.1055/s-0041-1723988. Epub 2021 Feb 16. Thromb Haemost. 2021. PMID: 33592630

8

Role of prothrombin 19911 A>G polymorphism, blood group and male gender in patients with venous thromboembolism: Results of a German cohort study.

Limperger V, Kenet G, Kiesau B, Köther M, Schmeiser M, Langer F, Juhl D, Shneyder M, Franke A, Klostermeier UK, Mesters R, Rühle F, Stoll M, Steppat D, Kowalski D, Rocke A, Kuta P, Bajorat T, Torge A, Neuner B, Junker R, Nowak-Göttl U. Limperger V, et al. J Thromb Thrombolysis. 2021 Feb;51(2):494-501. doi: 10.1007/s11239-020-02169-6. J Thromb Thrombolysis. 2021. PMID: 32594420 Free PMC article.

9

Association of the protein Z ATG haplotype with symptomatic nonvascular stroke or thromboembolism in white children: a family-based cohort study.

Nowak-Göttl U, Fröhlich B, Thedieck S, Huge A, Stoll M. Nowak-Göttl U, et al. Blood. 2009 Mar 5;113(10):2336-41. doi: 10.1182/blood-2008-10-181461. Epub 2008 Dec 2. Blood. 2009. PMID: 19050305 Free article.

10

Plasma glutathione peroxidase in pediatric stroke families.

Nowak-Göttl U, Fiedler B, Huge A, Niederstadt T, Thedieck S, Seehafer T, Stoll M. Nowak-Göttl U, et al. J Thromb Haemost. 2011 Jan;9(1):33-8. doi: 10.1111/j.1538-7836.2010.04103.x. J Thromb Haemost. 2011. PMID: 20946167 Free article.

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