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List of works by Stacey S. Cherny

A Mendelian randomization study of testosterone and cognition in men

scientific article published on 11 February 2016

A first stage genome-wide screen for regions shared identical-by-descent in hutterite families with multiple sclerosis

scientific article published on 01 June 2008

A genetic variant in the gene encoding adrenomedullin predicts the development of dysglycemia over 6.4 years in Chinese

scientific article

A genetic variant in the gene encoding fibrinogen beta chain predicted development of hypertension in Chinese men.

scientific article published on 2 February 2010

A genome-wide linkage and association scan reveals novel loci for hypertension and blood pressure traits.

scientific article

A genome-wide scan for loci influencing adolescent cannabis dependence symptoms: evidence for linkage on chromosomes 3 and 9.

scientific article published on 13 December 2006

A genome-wide scan in forty large pedigrees with multiple sclerosis

scientific article published on 15 November 2007

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

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

scientific article

A maximum-likelihood model-fitting approach to conducting a Hayman analysis of diallel tables with complete or missing data

scientific article published on January 1993

A powerful and rapid approach to human genome scanning using small quantities of genomic DNA

scientific article published on 01 April 2001

Actionable secondary findings from whole-genome sequencing of 954 East Asians

scientific article published on 11 November 2017

Advances in Twin and Sib-Pair Analysis

scientific article published in September 2001

An Exome-Chip Association Analysis in Chinese Subjects Reveals a Functional Missense Variant of GCKR That Regulates FGF21 Levels.

scientific article published on 6 April 2017

An improved multipoint sib-pair analysis of quantitative traits

scientific article published on September 1996

Application of genome-wide SNP data for uncovering pairwise relationships and quantitative trait loci

scientific article

Association of BDNF Polymorphisms with the Risk of Epilepsy: a Multicenter Study

scientific article published on 16 April 2015

Association of CD247 with systemic lupus erythematosus in Asian populations

article

Association of F11 receptor gene polymorphisms with central obesity and blood pressure

article

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

scientific article

Association of a polymorphism in the lipin 1 gene with systolic blood pressure in men.

scientific article published on 13 March 2008

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

article

C-reactive protein as a predictor of hypertension in the Hong Kong Cardiovascular Risk Factor Prevalence Study (CRISPS) cohort

scientific article published on 27 January 2011

Chinese family with diffuse oesophageal leiomyomatosis: a new COL4A5/COL4A6 deletion and a case of gonosomal mosaicism

scientific article published on 16 July 2015

Combined linkage and association sib-pair analysis for quantitative traits

scientific article

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

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

scientific article (publication date: 7 October 2011)

Continuity and change in infant shyness from 14 to 20 months

scientific article published on July 1994

Contribution of GABRG2 Polymorphisms to Risk of Epilepsy and Febrile Seizure: a Multicenter Cohort Study and Meta-analysis.

scientific article

Cost effective assay choice for rare disease study designs

scientific article published on 4 February 2015

De novo mutations in Caudal Type Homeo Box transcription Factor 2 (CDX2) in patients with persistent cloaca

scientific article published on 21 November 2017

Deciphering the Causal Relationships Between Low Back Pain Complications, Metabolic Factors, and Comorbidities

scientific article published in 2022

Development genetic analysis of general cognitive ability from 1 to 12 years in a sample of adoptees, biological siblings, and twins

article

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

scientific article published in May 2009

Differential heritability across levels of cognitive ability

scientific article published on March 1992

ELF1 is associated with systemic lupus erythematosus in Asian populations

scientific article

Elevated plasma level of soluble F11 receptor/junctional adhesion molecule-A (F11R/JAM-A) in hypertension

scientific article published on 12 February 2009

Errata

scholarly article published in Behavior Genetics

Erratum: Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort

scientific article published on 18 August 2015

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

scientific article (publication date: 7 October 2010)

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

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

scientific article published on 03 March 2011

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

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

scientific article

Exome-chip association analysis reveals an Asian-specific missense variant in PAX4 associated with type 2 diabetes in Chinese individuals.

scientific article published on 15 October 2016

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

scientific article

Fine mapping of the 9q31 Hirschsprung's disease locus.

scientific article

Fine mapping of the NRG1 Hirschsprung's disease locus

scientific article

GENESiS: creating a composite index of the vulnerability to anxiety and depression in a community-based sample of siblings

scientific article published in December 2000

Gamma-glutamyl transferase level predicts the development of hypertension in Hong Kong Chinese

article

Gender-controlled measures of socially desirable responding

scientific article published on 01 September 1994

Gene network analysis of candidate loci for human anorectal malformations

scientific article

Gene-based meta-analysis of genome-wide association study data identifies independent single-nucleotide polymorphisms in ANXA6 as being associated with systemic lupus erythematosus in Asian populations.

scientific article

Genetic Analyses of a Three Generation Family Segregating Hirschsprung Disease and Iris Heterochromia.

scientific article

Genetic Architecture of Complex Diseases

scholarly article published 2011

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

scientific article

Genetic and environmental influences on cognition during childhood

Genetic and environmental influences on early childhood behavior

scientific article published on 01 January 1994

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

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

Genetic overlap between epilepsy and schizophrenia: Evidence from cross phenotype analysis in Hong Kong Chinese population

scientific article

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

scientific article

Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients

scientific article

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

scientific journal article

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

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

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

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

scientific article

Genome-wide copy number variation study in anorectal malformations.

scientific article published on 29 October 2012

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

Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations

scientific article published on 10 April 2015

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

Haplotype analysis reveals a possible founder effect of RET mutation R114H for Hirschsprung's disease in the Chinese population.

scientific article

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

scientific article

Heritability of hallucinations in adolescent twins

scientific article published on 10 May 2012

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

scientific article published on October 2007

High-resolution mapping of quantitative trait loci in outbred mice

scientific article published on 01 March 1999

Homozygosity mapping on a single patient: identification of homozygous regions of recent common ancestry by using population data

scientific article

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

Identification of neuroglycan C and interacting partners as potential susceptibility genes for schizophrenia in a Southern Chinese population.

scientific article

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

scientific article

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

scientific article published on September 2010

Increase in power through multivariate analyses

scientific article published on 01 September 1998

Influence of Alzheimer's disease genes on cognitive decline: the Guangzhou Biobank Cohort Study

scientific article

Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot Study.

scientific article

Introduction to the Special Issue on Variance Components Methods for Mapping Quantitative Trait Loci

Introduction to the special issue: human linkage studies for behavioral traits

scientific article

Linkage analysis of a common oligogenic disease using selected sib pairs

scientific article published in January 1995

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

scientific article published on November 1, 1995

Longitudinal heritability of childhood aggression

scientific article published on 19 January 2016

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

scientific article

Mapping of a Hirschsprung's disease locus in 3p21

scientific article published on 20 February 2008

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

scientific article (publication date: 2002)

Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus.

scientific article published on 22 August 2014

Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus

scientific article

Multiple regression analysis of twin data: a model-fitting approach

scientific article published in July 1992

Mutational analysis ofSHHandGLI3in anorectal malformations

article

Mutations in the NRG1 gene are associated with Hirschsprung disease

article

No NRG1 V266L in Chinese patients with schizophrenia

article

Novel pre-mRNA splicing of intronically integrated HBV generates oncogenic chimera in hepatocellular carcinoma.

scientific article

Novel sib pair selection strategy increases power in quantitative association analysis

scientific article published in July 2009

Optimal selection strategies for QTL mapping using pooled DNA samples

Optimal sibship selection for genotyping in quantitative trait locus linkage analysis

scientific article published in January 2001

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

scientific article published in December 2000

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

article

Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis.

scientific article

Plasma adrenomedullin level is related to a single nucleotide polymorphism in the adrenomedullin gene

scientific article published on 28 July 2011

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

scientific article

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

scientific article published on 05 July 2002

QTL Methodology in Behavior Genetics

article

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

scientific article

RET and NRG1 interplay in Hirschsprung disease.

scientific article published on 12 February 2013

RET mutational spectrum in Hirschsprung disease: evaluation of 601 Chinese patients.

scientific article

Rare variants and de novo variants in mesial temporal lobe epilepsy with hippocampal sclerosis.

scientific article published on 11 June 2018

Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort

scientific article published on 2 December 2014

Relationship of plasma interleukin-6 and its genetic variants with hypertension in Hong Kong Chinese

scientific article

Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications.

scientific article

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

scientific article published on 03 October 2006

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

scientific article

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

scientific article

Role of Genetic Variants in the Gene Encoding Lipocalin-2 in the Development of Elevated Blood Pressure

article

SNP-based HLA allele tagging, imputation and association with antiepileptic drug-induced cutaneous reactions in Hong Kong Han Chinese.

scientific article published on 11 April 2017

Sacral agenesis: A pilot whole exome sequencing and copy number study

Sacral agenesis: a pilot whole exome sequencing and copy number study

scientific article

Screening of the RET gene of Vietnamese Hirschsprung patients identifies 2 novel missense mutations.

scientific article

Sharing of Genes and Pathways Across Complex Phenotypes: A Multilevel Genome-Wide Analysis.

scientific article

Significant linkage to migraine with aura on chromosome 11q24.

scientific article published on 29 July 2003

Sleep duration and memory in the elderly Chinese: longitudinal analysis of the Guangzhou Biobank Cohort Study

scientific article

Statistical Power and the Classical Twin Design

scientific article published on 01 April 2020

Targeted Next-Generation Sequencing on Hirschsprung Disease: A Pilot Study Exploits DNA Pooling

scientific article published on 20 June 2014

The analysis of causal relationships between blood lipid levels and BMD

The familial aggregation of depressive symptoms, antisocial behavior, and alcohol abuse

scientific article published on 01 April 1997

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

article

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

scientific article

Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians.

scientific article published on 2 September 2013

Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.

scientific article published on 3 October 2016

Two missense variants in UHRF1BP1 are independently associated with systemic lupus erythematosus in Hong Kong Chinese

article

Two subtypes of intervertebral disc degeneration distinguished by large-scale population-based study.

scientific article published on 5 May 2016

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

article

Uncovering the genetic lesions underlying the most severe form of Hirschsprung disease by whole-genome sequencing

scientific article published on 26 February 2018

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

scientific article

Using glycosylated hemoglobin to define the metabolic syndrome in United States adults

scientific article

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

scientific article

Variance Components and Related Methods for Mapping Quantitative Trait Loci

Variance-Components QTL linkage analysis of selected and non-normal samples: conditioning on trait values

scientific article published in January 2000

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

scholarly article

Whole exome sequencing coupled with unbiased functional analysis reveals new Hirschsprung disease genes

scientific article

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