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  • Showing results for zollner s. Search instead for Zllner S (1 item)
1.

Inhibition of the oncogenic fusion protein EWS-FLI1 causes G2-M cell cycle arrest and enhanced vincristine sensitivity in Ewing's sarcoma.

Zöllner SK, Selvanathan SP, Graham GT, Commins RMT, Hong SH, Moseley E, Parks S, Haladyna JN, Erkizan HV, Dirksen U, Hogarty MD, Üren A, Toretsky JA.

Sci Signal. 2017 Oct 3;10(499). pii: eaam8429. doi: 10.1126/scisignal.aam8429.

PMID:
28974650
2.

An efficient algorithm for generating the internal branches of a Kingman coalescent.

Reppell M, Zöllner S.

Theor Popul Biol. 2017 Jul 11. pii: S0040-5809(16)30120-4. doi: 10.1016/j.tpb.2017.05.002. [Epub ahead of print]

PMID:
28709926
3.

Observation of Phase-Filling Singularities in the Optical Dielectric Function of Highly Doped n-Type Ge.

Xu C, Fernando NS, Zollner S, Kouvetakis J, Menéndez J.

Phys Rev Lett. 2017 Jun 30;118(26):267402. doi: 10.1103/PhysRevLett.118.267402. Epub 2017 Jun 27.

PMID:
28707902
4.

Genome-wide significance testing of variation from single case exomes.

Wilfert AB, Chao KR, Kaushal M, Jain S, Zöllner S, Adams DR, Conrad DF.

Nat Genet. 2016 Dec;48(12):1455-1461. doi: 10.1038/ng.3697. Epub 2016 Oct 24.

5.

[Atypical wet AMD].

Zollner S, Ulbig MW.

Ophthalmologe. 2017 Mar;114(3):266-268. doi: 10.1007/s00347-016-0339-0. German. No abstract available.

PMID:
27514521
6.

Social work after stroke: identifying demand for support by recording stroke patients' and carers' needs in different phases after stroke.

Padberg I, Knispel P, Zöllner S, Sieveking M, Schneider A, Steinbrink J, Heuschmann PU, Wellwood I, Meisel A.

BMC Neurol. 2016 Jul 20;16:111. doi: 10.1186/s12883-016-0626-z.

7.

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.

Hou L, Bergen SE, Akula N, Song J, Hultman CM, Landén M, Adli M, Alda M, Ardau R, Arias B, Aubry JM, Backlund L, Badner JA, Barrett TB, Bauer M, Baune BT, Bellivier F, Benabarre A, Bengesser S, Berrettini WH, Bhattacharjee AK, Biernacka JM, Birner A, Bloss CS, Brichant-Petitjean C, Bui ET, Byerley W, Cervantes P, Chillotti C, Cichon S, Colom F, Coryell W, Craig DW, Cruceanu C, Czerski PM, Davis T, Dayer A, Degenhardt F, Del Zompo M, DePaulo JR, Edenberg HJ, Étain B, Falkai P, Foroud T, Forstner AJ, Frisén L, Frye MA, Fullerton JM, Gard S, Garnham JS, Gershon ES, Goes FS, Greenwood TA, Grigoroiu-Serbanescu M, Hauser J, Heilbronner U, Heilmann-Heimbach S, Herms S, Hipolito M, Hitturlingappa S, Hoffmann P, Hofmann A, Jamain S, Jiménez E, Kahn JP, Kassem L, Kelsoe JR, Kittel-Schneider S, Kliwicki S, Koller DL, König B, Lackner N, Laje G, Lang M, Lavebratt C, Lawson WB, Leboyer M, Leckband SG, Liu C, Maaser A, Mahon PB, Maier W, Maj M, Manchia M, Martinsson L, McCarthy MJ, McElroy SL, McInnis MG, McKinney R, Mitchell PB, Mitjans M, Mondimore FM, Monteleone P, Mühleisen TW, Nievergelt CM, Nöthen MM, Novák T, Nurnberger JI Jr, Nwulia EA, Ösby U, Pfennig A, Potash JB, Propping P, Reif A, Reininghaus E, Rice J, Rietschel M, Rouleau GA, Rybakowski JK, Schalling M, Scheftner WA, Schofield PR, Schork NJ, Schulze TG, Schumacher J, Schweizer BW, Severino G, Shekhtman T, Shilling PD, Simhandl C, Slaney CM, Smith EN, Squassina A, Stamm T, Stopkova P, Streit F, Strohmaier J, Szelinger S, Tighe SK, Tortorella A, Turecki G, Vieta E, Volkert J, Witt SH, Wright A, Zandi PP, Zhang P, Zollner S, McMahon FJ.

Hum Mol Genet. 2016 Aug 1;25(15):3383-3394. doi: 10.1093/hmg/ddw181. Epub 2016 Jun 21.

8.

Transmission of human mtDNA heteroplasmy in the Genome of the Netherlands families: support for a variable-size bottleneck.

Li M, Rothwell R, Vermaat M, Wachsmuth M, Schröder R, Laros JF, van Oven M, de Bakker PI, Bovenberg JA, van Duijn CM, van Ommen GJ, Slagboom PE, Swertz MA, Wijmenga C; Genome of Netherlands Consortium, Kayser M, Boomsma DI, Zöllner S, de Knijff P, Stoneking M.

Genome Res. 2016 Apr;26(4):417-26. doi: 10.1101/gr.203216.115. Epub 2016 Feb 25.

9.

Safety, pharmacokinetics and pharmacodynamics of the anti-hepcidin Spiegelmer lexaptepid pegol in healthy subjects.

Boyce M, Warrington S, Cortezi B, Zöllner S, Vauléon S, Swinkels DW, Summo L, Schwoebel F, Riecke K.

Br J Pharmacol. 2016 May;173(10):1580-8. doi: 10.1111/bph.13433. Epub 2016 Apr 8.

10.

A new strategy for enhancing imputation quality of rare variants from next-generation sequencing data via combining SNP and exome chip data.

Kim YJ, Lee J, Kim BJ; T2D-Genes Consortium, Park T.

BMC Genomics. 2015 Dec 29;16:1109. doi: 10.1186/s12864-015-2192-y.

11.

Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese.

Tang CS, Zhang H, Cheung CY, Xu M, Ho JC, Zhou W, Cherny SS, Zhang Y, Holmen O, Au KW, Yu H, Xu L, Jia J, Porsch RM, Sun L, Xu W, Zheng H, Wong LY, Mu Y, Dou J, Fong CH, Wang S, Hong X, Dong L, Liao Y, Wang J, Lam LS, Su X, Yan H, Yang ML, Chen J, Siu CW, Xie G, Woo YC, Wu Y, Tan KC, Hveem K, Cheung BM, Zöllner S, Xu A, Eugene Chen Y, Jiang CQ, Zhang Y, Lam TH, Ganesh SK, Huo Y, Sham PC, Lam KS, Willer CJ, Tse HF, Gao W.

Nat Commun. 2015 Dec 22;6:10206. doi: 10.1038/ncomms10206.

12.

Choosing Subsamples for Sequencing Studies by Minimizing the Average Distance to the Closest Leaf.

Kang JT, Zhang P, Zöllner S, Rosenberg NA.

Genetics. 2015 Oct;201(2):499-511. doi: 10.1534/genetics.115.176909. Epub 2015 Aug 24.

13.

Synovial sarcoma is a gateway to the role of chromatin remodeling in cancer.

Zöllner SK, Rössig C, Toretsky JA.

Cancer Metastasis Rev. 2015 Sep;34(3):417-28. doi: 10.1007/s10555-015-9575-z. Review.

PMID:
26277104
14.

Whole-genome sequencing of uropathogenic Escherichia coli reveals long evolutionary history of diversity and virulence.

Lo Y, Zhang L, Foxman B, Zöllner S.

Infect Genet Evol. 2015 Aug;34:244-50. doi: 10.1016/j.meegid.2015.06.023. Epub 2015 Jun 23.

15.

Beyond two-stage models for lung carcinogenesis in the Mayak workers: implications for plutonium risk.

Zöllner S, Sokolnikov ME, Eidemüller M.

PLoS One. 2015 May 22;10(5):e0126238. doi: 10.1371/journal.pone.0126238. eCollection 2015.

16.

Robust and Powerful Affected Sibpair Test for Rare Variant Association.

Lin KH, Zöllner S.

Genet Epidemiol. 2015 Jul;39(5):325-33. doi: 10.1002/gepi.21903. Epub 2015 May 13.

17.

Comparing variant calling algorithms for target-exon sequencing in a large sample.

Lo Y, Kang HM, Nelson MR, Othman MI, Chissoe SL, Ehm MG, Abecasis GR, Zöllner S.

BMC Bioinformatics. 2015 Mar 7;16:75. doi: 10.1186/s12859-015-0489-0.

18.

Genetic and childhood trauma interaction effect on age of onset in bipolar disorder: An exploratory analysis.

Anand A, Koller DL, Lawson WB, Gershon ES, Nurnberger JI; BiGS Collaborative.

J Affect Disord. 2015 Jul 1;179:1-5. doi: 10.1016/j.jad.2015.02.029. Epub 2015 Mar 10.

PMID:
25837715
19.

Characteristics of Bipolar I patients grouped by externalizing disorders.

Swaminathan S, Koller DL, Foroud T, Edenberg HJ, Xuei X, Niculescu AB 3rd; Bipolar Genome Study (BiGS) Consortium,, Nurnberger JI Jr.

J Affect Disord. 2015 Jun 1;178:206-14. doi: 10.1016/j.jad.2015.03.011. Epub 2015 Mar 14.

20.

Utility of a high VWF: FVIII ratio in preventing FVIII accumulation: a study in VWF-deficient mice.

Raquet E, Stockschlaeder M, Mueller-Cohrs J, Zollner S, Pragst I, Dickneite G.

Blood Coagul Fibrinolysis. 2015 Jul;26(5):515-21. doi: 10.1097/MBC.0000000000000269.

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