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Lista de obras de Stacey S. Cherny

A Mendelian randomization study of testosterone and cognition in men

artículo científico publicado en 2016

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

artículo científico publicado en 2008

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

artículo científico publicado en 2010

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

artículo científico publicado en 2010

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

artículo científico publicado en 2012

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

artículo científico publicado en 2006

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

artículo científico publicado en 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

artículo científico publicado en 2010

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

artículo científico publicado en 1993

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

artículo científico publicado en 2001

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

artículo científico publicado en 2017

Advances in Twin and Sib-Pair Analysis

artículo científico publicado en 2001

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

artículo científico publicado en 2017

An improved multipoint sib-pair analysis of quantitative traits

artículo científico publicado en 1996

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

artículo científico publicado en 2009

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

artículo científico publicado en 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.

artículo científico publicado en 2010

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

artículo científico publicado en 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

artículo científico publicado en 2011

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

artículo científico publicado en 2015

Combined linkage and association sib-pair analysis for quantitative traits

artículo científico publicado en 1999

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

artículo científico publicado en 2013

Common variants on Xq28 conferring risk of schizophrenia in Han Chinese

artículo científico publicado en 2013

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

artículo científico publicado en 2011

Continuity and change in infant shyness from 14 to 20 months

artículo científico publicado en 1994

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

artículo científico publicado en 2015

Cost effective assay choice for rare disease study designs

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 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.

artículo científico publicado en 2009

Differential heritability across levels of cognitive ability

artículo científico publicado en 1992

ELF1 is associated with systemic lupus erythematosus in Asian populations

artículo científico publicado en 2010

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

artículo científico publicado en 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

artículo científico publicado en 2015

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

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

artículo científico publicado en 2011

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

artículo científico publicado en 2017

Exome sequencing reveals a high genetic heterogeneity on familial Hirschsprung disease

artículo científico publicado en 2015

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

artículo científico publicado en 2016

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

artículo científico publicado en 2015

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

artículo científico publicado en 2010

Fine mapping of the NRG1 Hirschsprung's disease locus

artículo científico publicado en 2011

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

artículo científico publicado en 2000

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

article

Gender-controlled measures of socially desirable responding

artículo científico publicado en 1994

Gene network analysis of candidate loci for human anorectal malformations

artículo científico publicado en 2013

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.

artículo científico publicado en 2015

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

artículo científico publicado en 2013

Genetic Architecture of Complex Diseases

scholarly article published 2011

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

artículo científico publicado en 2004

Genetic and environmental influences on cognition during childhood

Genetic and environmental influences on early childhood behavior

artículo científico publicado en 1994

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

artículo científico publicado en 2014

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

artículo científico publicado en 2008

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

artículo científico publicado en 2017

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

artículo científico publicado en 2016

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

artículo científico publicado en 2017

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.

artículo científico publicado en 2010

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

artículo científico publicado en 2013

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

artículo científico publicado en 2012

Genome-wide copy number variation study in anorectal malformations.

artículo científico publicado en 2012

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

artículo científico publicado en 2004

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

artículo científico publicado en 2015

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

artículo científico publicado en 2008

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

Heritability of hallucinations in adolescent twins

artículo científico publicado en 2012

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

artículo científico publicado en 2007

High-resolution mapping of quantitative trait loci in outbred mice

artículo científico publicado en 1999

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

artículo científico publicado en 2011

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

artículo científico publicado en 2012

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

artículo científico publicado en 2010

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

artículo científico publicado en 2014

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

artículo científico publicado en 2010

Increase in power through multivariate analyses

artículo científico publicado en 1998

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

artículo científico publicado en 2014

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

artículo científico publicado en 2016

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

artículo científico publicado en 2006

Linkage analysis of a common oligogenic disease using selected sib pairs

artículo científico publicado en 1995

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

artículo científico publicado el 1 de noviembre de 1995

Longitudinal heritability of childhood aggression

artículo científico publicado en 2016

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

artículo científico publicado en 2013

Mapping of a Hirschsprung's disease locus in 3p21

artículo científico publicado en 2008

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

artículo científico publicado en 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.

artículo científico publicado en 2014

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

artículo científico publicado en 2015

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

artículo científico publicado en 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.

artículo científico publicado en 2016

Novel sib pair selection strategy increases power in quantitative association analysis

artículo científico publicado en 2009

Optimal selection strategies for QTL mapping using pooled DNA samples

Optimal sibship selection for genotyping in quantitative trait locus linkage analysis

artículo científico publicado en 2001

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

artículo científico publicado en 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.

artículo científico publicado en 2017

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

artículo científico publicado en 2011

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

artículo científico publicado en 2000

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

artículo científico publicado en 1999

RET and NRG1 interplay in Hirschsprung disease.

artículo científico publicado en 2013

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

artículo científico publicado en 2011

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

artículo científico publicado en 2018

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

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

artículo científico publicado en 2009

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

artículo científico publicado en 2006

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

artículo científico publicado en 2010

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

artículo científico publicado en 2011

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.

artículo científico publicado en 2017

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

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

artículo científico publicado en 2016

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

artículo científico publicado en 2012

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

artículo científico publicado en 2017

Significant linkage to migraine with aura on chromosome 11q24.

artículo científico publicado en 2003

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

artículo científico publicado en 2014

Statistical Power and the Classical Twin Design

artículo científico publicado en 2020

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

artículo científico publicado en 2014

The analysis of causal relationships between blood lipid levels and BMD

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

artículo científico publicado en 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.

artículo científico publicado en 2006

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

artículo científico publicado en 2013

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

artículo científico publicado en 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.

artículo científico publicado en 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

artículo científico publicado en 2018

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

artículo científico publicado en 2003

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

artículo científico publicado en 2010

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

artículo científico publicado en 2012

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

artículo científico publicado en 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

artículo científico publicado en 2017

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