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Authors whose works are in public domain in at least one jurisdiction

List of works by Stacey S. Cherny

1-50 of 148 results

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees

scientific article (publication date: 2002)

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

scholarly article

Combined linkage and association sib-pair analysis for quantitative traits

scientific article published on 01 January 1999

Evaluating the effective numbers of independent tests and significant p-value thresholds in commercial genotyping arrays and public imputation reference datasets

scientific article published on 6 December 2011

Diabetes prevalence and therapeutic target achievement in the United States, 1999 to 2006.

scientific article published in May 2009

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

scientific article published on 05 July 2002

Evaluating the heritability explained by known susceptibility variants: a survey of ten complex diseases

scientific article published on 03 March 2011

High-resolution mapping of quantitative trait loci in outbred mice

scientific article published on 01 March 1999

Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

scientific article

Association of JAG1 with bone mineral density and osteoporotic fractures: a genome-wide association study and follow-up replication studies.

scientific article

Quantitative-trait locus for specific language and reading deficits on chromosome 6p

scientific article published on 01 January 1999

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

scientific journal article

Genetic determinants of common epilepsies: a meta-analysis of genome-wide association studies

scientific article

Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations

scientific article

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

scientific article

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

article

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

scientific article published on September 2010

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.

scientific article

Linkage between sexual orientation and chromosome Xq28 in males but not in females

scientific article published on November 1, 1995

Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds.

scientific article published on 03 October 2006

European bone mineral density loci are also associated with BMD in East-Asian populations

scientific article (publication date: 7 October 2010)

Increase in power through multivariate analyses

scientific article published on 01 September 1998

Significant linkage to migraine with aura on chromosome 11q24.

scientific article published on 29 July 2003

An improved multipoint sib-pair analysis of quantitative traits

scientific article published on September 1996

The relationship between CAG repeat length and age of onset differs for Huntington's disease patients with juvenile onset or adult onset.

scientific article

Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4.

scientific article published on 27 March 2013

Genetic and environmental contributions to general cognitive ability through the first 16 years of life

scientific article

Genome-wide linkage analysis of a composite index of neuroticism and mood-related scales in extreme selected sibships

scientific article published on 6 September 2004

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

scientific article (publication date: 7 October 2011)

A germline mutation (A339V) in thyroid transcription factor-1 (TITF-1/NKX2.1) in patients with multinodular goiter and papillary thyroid carcinoma

scientific journal article

Utility of the trnH-psbA intergenic spacer region and its combinations as plant DNA barcodes: a meta-analysis

scientific article

Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant.

scientific article

Heritability of longitudinal measures of body mass index and lipid and lipoprotein levels in aging twins

scientific article published on October 2007

Association of genetic variants in the adiponectin gene with adiponectin level and hypertension in Hong Kong Chinese

article

Risk prediction of complex diseases from family history and known susceptibility loci, with applications for cancer screening

scientific article

Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds

scientific article published in July 2008

Replication study of SNP associations for colorectal cancer in Hong Kong Chinese

scientific article

Genetic influences on the difference in variability of height, weight and body mass index between Caucasian and East Asian adolescent twins

scientific article published on 09 September 2008

ELF1 is associated with systemic lupus erythematosus in Asian populations

scientific article

Hedgehog/Notch-induced premature gliogenesis represents a new disease mechanism for Hirschsprung disease in mice and humans

scientific article

A knowledge-based weighting framework to boost the power of genome-wide association studies

scientific article

Parent ratings of temperament in twins: explaining the 'too low' DZ correlations

scientific article published in December 2000

Identification of IGF1, SLC4A4, WWOX, and SFMBT1 as hypertension susceptibility genes in Han Chinese with a genome-wide gene-based association study

scientific article published in 2012

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

article

RET and NRG1 interplay in Hirschsprung disease.

scientific article published on 12 February 2013

Common genetic variants regulating ADD3 gene expression alter biliary atresia risk.

scientific article published on 19 July 2013

Common variants on Xq28 conferring risk of schizophrenia in Han Chinese

scientific article

Exome chip meta-analysis identifies novel loci and East Asian-specific coding variants that contribute to lipid levels and coronary artery disease

scientific article published on 30 October 2017

Genome-wide copy number analysis uncovers a new HSCR gene: NRG3

scientific article

Mutations in the NRG1 gene are associated with Hirschsprung disease

article