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Mapping genes through the use of Linkage Disequilibrium generated by genetic drift:
’Drift Mapping’ in small populations with no demographic expansion.
J. Terwilliger, S. Zöllner, M. Laan, and S. Pääbo, Hum Hered 1998; 48:138-154
Coalescent approach to study Linkage Disequilibrium between Single Nucleotide Polymorphisms.
S. Zöllner and A. von Haeseler, Am. J. Hum. Genet. 66:615-628, 2000
Coalescent approach to study Linkage Disequilibrium between Single Nucleotide Polymorphisms.
S. Zöllner and A. von Haeseler, Am. J. Hum. Genet. 66:615-628, 2000
Extensive Linkage Disequilibrium in Small Human Populations in Eurasia.
H. Kaessmann*, S. Zöllner*,
A. C. Gustafsson, V. Wiebe, M. Laan et al., Am. J. Hum. Genet. 70:673-685, 2002
* denotes equal contribution
Signatures of domain shuffling in the human genome.
H. Kaessmann, S. Zöllner, A. Nekrutenku, W.-H. Li, Genome Res. 12: 1642-1650, 2002
Selection on Human Genes as revealed by comparison to Chimpanzee DNA.
I. Hellmann, S. Zöllner, W.Enard, I. Ebersberger, B. Nickel and S.Pääbo,
Genome Res. 13: 831-837, 2003
Evidence for extensive transmission distortion in the human genome.
S. Zöllner, X. Wen, N. Hanchard, M. Herbert, C. Ober and J. K. Pritchard,
Am. J. Hum. Genet. 70:673-685, 2004
A coalescent based approach for disease mapping.
S. Zöllner and J. K. Pritchard, Lecture Notes in Computer Science, Springer-Verlag, Heidelberg, Germany
(ISBN: 3-540-21249-3),2004
Coalescent-based association mapping and fine mapping of complex trait loci.
S. Zöllner and J. K. Pritchard, Genetics,169: 1071-1092, 2005
TREEMAP, a program for association mapping and fine mapping of complex trait loci.
S. Zöllner, X. Wen and J. K. Pritchard, Bioinformatics 21: 3168-3170, 2005
Overcoming the winner's curse: Estimating penetrance parameters from case-control data.
S. Zöllner and J. K. Pritchard, Am J Hum Genet 80: 605-615, 2007
GENOME: a rapid coalescent-based whole genome simulator.
L. Liang, S. Zöllner, G. R. Abecasis, Bioinformatics 23:1565-1567, 2007.
Family - based SNP Association Study on 8q24 in Bipolar Disorder.
P.P. Zandi, S. Zöllner, D. Avramopoulos, V. L. Willour, Z. S. Qin, M. Burmeister, K. Miao,
S. Gopalakrishnan, J. B. Potash, J. R. DePaulo, M. G. McInnis, Am J Med Genet B Neuropsychatr Genet. 147B(5): 612-618, 2008
Extensive Copy Number Variation of Mouse Segmental Duplications.
X. She, Z. Cheng, S. Zöllner, D. Church, E. E. Eichler, Nat Genet 40: 909-914, 2008
Psychiatric Genetics: Progress among Controversies.
M. Burmeister, M.G. McInnis, S. Zöllner, Nat Rev Genet 9: 527-540, 2008
EM Algorithm for scoring polymorphic deletions from SNP data and application to a common CNV on 8q24.
S. Zöllner, G. Su, Y. Chen, M. G. McInnis, M. Burmeister, In revision
Catalog of mouse Copy Number Variations and gene expression reveals long distance effects of CNVs on expression levels.
C. N. Henrichsen*, N. Vinckenbosch *, S. Zöllner *, E. Chaignat, S. Pradervand, M. Ruedi, H. Kaessmann, A. Reymond, Submitted
* denotes equal contribution
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