Zöllner S - Search Results

1

Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans.

Carlson J, Locke AE, Flickinger M, Zawistowski M, Levy S, Myers RM, Boehnke M, Kang HM, Scott LJ, Li JZ, Zöllner S; BRIDGES Consortium. Carlson J, et al. Among authors: zollner s. Nat Commun. 2018 Sep 14;9(1):3753. doi: 10.1038/s41467-018-05936-5. Nat Commun. 2018. PMID: 30218074 Free PMC article.

2

Family-based SNP association study on 8q24 in bipolar disorder.

Zandi PP, Zöllner S, Avramopoulos D, Willour VL, Chen Y, Qin ZS, Burmeister M, Miao K, Gopalakrishnan S, McEachin R, Potash JB, Depaulo JR Jr, McInnis MG. Zandi PP, et al. Among authors: zollner s. Am J Med Genet B Neuropsychiatr Genet. 2008 Jul 5;147B(5):612-8. doi: 10.1002/ajmg.b.30651. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18163389 Free PMC article.

3

Psychiatric genetics: progress amid controversy.

Burmeister M, McInnis MG, Zöllner S. Burmeister M, et al. Among authors: zollner s. Nat Rev Genet. 2008 Jul;9(7):527-40. doi: 10.1038/nrg2381. Nat Rev Genet. 2008. PMID: 18560438 Review.

4

Bayesian EM algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24.

Zöllner S, Su G, Stewart WC, Chen Y, McInnis MG, Burmeister M. Zöllner S, et al. Genet Epidemiol. 2009 May;33(4):357-68. doi: 10.1002/gepi.20391. Genet Epidemiol. 2009. PMID: 19085946 Free article.

5

A map of human genome variation from population-scale sequencing.

1000 Genomes Project Consortium; Abecasis GR, Altshuler D, Auton A, Brooks LD, Durbin RM, Gibbs RA, Hurles ME, McVean GA. 1000 Genomes Project Consortium, et al. Nature. 2010 Oct 28;467(7319):1061-73. doi: 10.1038/nature09534. Nature. 2010. PMID: 20981092 Free PMC article.

6

Extending rare-variant testing strategies: analysis of noncoding sequence and imputed genotypes.

Zawistowski M, Gopalakrishnan S, Ding J, Li Y, Grimm S, Zöllner S. Zawistowski M, et al. Among authors: zollner s. Am J Hum Genet. 2010 Nov 12;87(5):604-17. doi: 10.1016/j.ajhg.2010.10.012. Am J Hum Genet. 2010. PMID: 21070896 Free PMC article.

7

Family-based association analysis to finemap bipolar linkage peak on chromosome 8q24 using 2,500 genotyped SNPs and 15,000 imputed SNPs.

Zhang P, Xiang N, Chen Y, Sliwerska E, McInnis MG, Burmeister M, Zöllner S. Zhang P, et al. Among authors: zollner s. Bipolar Disord. 2010 Dec;12(8):786-92. doi: 10.1111/j.1399-5618.2010.00883.x. Bipolar Disord. 2010. PMID: 21176025 Free PMC article.

8

Variation in genome-wide mutation rates within and between human families.

Conrad DF, Keebler JE, DePristo MA, Lindsay SJ, Zhang Y, Casals F, Idaghdour Y, Hartl CL, Torroja C, Garimella KV, Zilversmit M, Cartwright R, Rouleau GA, Daly M, Stone EA, Hurles ME, Awadalla P; 1000 Genomes Project. Conrad DF, et al. Nat Genet. 2011 Jun 12;43(7):712-4. doi: 10.1038/ng.862. Nat Genet. 2011. PMID: 21666693 Free PMC article.

9

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4.

Psychiatric GWAS Consortium Bipolar Disorder Working Group. Psychiatric GWAS Consortium Bipolar Disorder Working Group. Nat Genet. 2011 Sep 18;43(10):977-83. doi: 10.1038/ng.943. Nat Genet. 2011. PMID: 21926972 Free PMC article.

10

FTEC: a coalescent simulator for modeling faster than exponential growth.

Reppell M, Boehnke M, Zöllner S. Reppell M, et al. Among authors: zollner s. Bioinformatics. 2012 May 1;28(9):1282-3. doi: 10.1093/bioinformatics/bts135. Epub 2012 Mar 21. Bioinformatics. 2012. PMID: 22441586 Free PMC article.

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