Stacey S Cherny

Statistical Power and the Classical Twin Design

Michael C Neale, Shaun M Purcell, Benjamin M Neale, 2020, Twin Research and Human Genetics.

Comparisons of seven algorithms for pathway analysis using the WTCCC Crohn's Disease dataset

Hongsheng Gui, Stacey S Cherny, Miaoxin Li, 2011, BMC Research Notes.

Use of multivariate linkage analysis for dissection of a complex cognitive trait.

Simon E Fisher, Stacey S Cherny, Lon R Cardon, 2003, American journal of human genetics.

Homozygosity Mapping on a Single Patient—Identification of Homozygous Regions of Recent Common Ancestry by Using Population Data

Pak Chung Sham, Lu Zhang, Wanling Yang, 2011, Human mutation.

The impact of genotyping error on family-based analysis of quantitative traits

Stacey S Cherny, Gonçalo R Abecasis, Lon R Cardon, 2001, European Journal of Human Genetics.

Fine Mapping of the NRG1 Hirschsprung's Disease Locus

Stacey S Cherny, Man-Ting So, Benjamin Hon-Kei Yip, 2011, PloS one.

Venezuelan kindreds reveal that genetic and environmental factors modulate Huntington's disease age of onset.

Karen Marder, Norman Arnheim, Ira Shoulson, 2004, Proceedings of the National Academy of Sciences of the United States of America.

Common variants on Xq28 conferring risk of schizophrenia in Han Chinese.

Eric Y H Chen, Hon-Cheong So, Shaun M Purcell, 2014, Schizophrenia bulletin.

Impaired intellect and memory: a missing link between genetic risk and schizophrenia?

Daniel R Weinberger, Timothea Toulopoulou, Daniel Stahl, 2010, Archives of general psychiatry.

Powerful regression-based quantitative-trait linkage analysis of general pedigrees.

Shaun Purcell, Pak C Sham, Stacey S Cherny, 2002, American journal of human genetics.

Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese.

Pak Chung Sham, Wanling Yang, Patrick Kwan, 2012, Human molecular genetics.