C. Greenwood

发表

A hierarchical clustering method for estimating copy number variation.

S. Bull, Baifang Xing, C. Greenwood, 2007, Biostatistics.

Two-step jackknife bias reduction for logistic regression mles

Walter W. Hauck, Shelley B. Bull, S. Bull, 1994 .

Design considerations for association studies of candidate genes in families

S. Bull, C. Greenwood, G. Darlington, 2001, Genetic epidemiology.

Imprinting and deviation from Mendelian transmission ratios.

C. Greenwood, A. Naumova, K. Morgan, 2001, Genome.

A rare variant association test in family‐based designs and non‐normal quantitative traits

C. Greenwood, L. Lakhal-Chaieb, K. Oualkacha, 2016, Statistics in medicine.

Inheritance patterns of maternal alleles in imprinted regions of the mouse genome at different stages of development

C. Greenwood, Fleur Huang, A. Naumova, 2001, Mammalian Genome.

HostSeq: a Canadian whole genome sequencing and clinical data resource

A. Paterson, J. Brooks, I. Birol, 2022, BMC Genomic Data.

More on Dietary Sodium and Blood Pressure-Reply

A. Logan, C. Greenwood, J. Midgley, 1997 .

Dietary Sodium and Blood Pressure-Reply

A. Logan, C. Greenwood, J. Midgley, 1996 .

Statistical Genetic Modeling and Analysis of Complex Traits

S. Bull, C. Greenwood, J. Graham, 2014 .

Efficiency of reduced logistic regression models

Allan Donner, Celia M. T. Greenwood, Shelley B. Bull, 1994 .

Salt, blood pressure, and cointervention.

A. Logan, C. Greenwood, 1997, Archives of internal medicine.

Identity-by-descent sharing using Markov chain Monte Carlo in subsets of the asthma Hutterite pedigree

D. Goldstein, A. Bureau, C. Greenwood, 2001 .

Effect of reduced dietary sodium on blood pressure: a meta-analysis of randomized controlled trials.

A. Logan, C. Greenwood, J. Midgley, 1996, JAMA.

Statistical power in COVID-19 case-control host genomic study design

Jennifer D. Brooks, A. Paterson, S. Bull, 2020, Genome medicine.

On Statistical Power for Case-Control Host Genomic Studies of COVID-19

Jennifer D. Brooks, A. Paterson, S. Bull, 2020, medRxiv.

Pedigree Selection and Tests of Linkage in a Hutterite Asthma Pedigree

Alexandre Bureau, D. Goldstein, A. Bureau, 2001, Genetic epidemiology.

Evaluation of genetic and environmental effects using GEE and APM methods

S. Bull, C. Greenwood, N. Chapman, 1995, Genetic epidemiology.

Epigenetics and Complex Traits

C. Greenwood, A. Naumova, 2013, Springer New York.

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells

C. Laprise, F. Martínez, C. Greenwood, 2018, Biology of Sex Differences.

Parental Effect of DNA (Cytosine-5) Methyltransferase 1 on Grandparental-Origin-Dependent Transmission Ratio Distortion in Mouse Crosses and Human Families

A. Bélisle, C. Greenwood, A. Naumova, 2008, Genetics.

Model-free linkage analysis of a binary trait.

Wei Xu, Lucia Mirea, Shelley B Bull, 2012, Methods in molecular biology.

Linkage of tuberculosis to chromosome 2q35 loci, including NRAMP1, in a large aboriginal Canadian family.

C. Greenwood, M. Miller, E. Schurr, 2000, American journal of human genetics.

A modified score function estimator for multinomial logistic regression in small samples

Celia M. T. Greenwood, Shelley B. Bull, Carment Mak, 2002 .

Analysis of affected sib pairs, with covariates--with and without constraints.

S. Bull, C. Greenwood, 1999, American journal of human genetics.

Down-weighting of multiple affected sib pairs leads to biased likelihood-ratio tests, under the assumption of no linkage.

S. Bull, C. Greenwood, 1999, American journal of human genetics.

Incorporation of covariates into genome scanning using sib‐pair analysis in bipolar affective disorder

S. Bull, C. Greenwood, 1997, Genetic epidemiology.

The impact of transmission-ratio distortion on allele sharing in affected sibling pairs.

C. Greenwood, K. Morgan, 2000, American journal of human genetics.

Statistical Issues in a Metaregression Analysis of Randomized Trials: Impact on the Dietary Sodium Intake and Blood Pressure Relationship

A. Logan, C. Greenwood, J. Midgley, 1999, Biometrics.

Regression models for allele sharing: analysis of accumulating data in affected sib pair studies

S. Bull, C. Greenwood, L. Mirea, 2002, Statistics in medicine.

Effect of genome-wide genotyping and reference panels on rare variants imputation.

Celia M T Greenwood, J Brent Richards, Hou-Feng Zheng, 2012, Journal of genetics and genomics = Yi chuan xue bao.

Genetic architecture: the shape of the genetic contribution to human traits and disease

C. Greenwood, N. Timpson, D. Lawson, 2017, Nature Reviews Genetics.

The genetic analysis of a founder Northern American population of European descent identifies FANCI as a candidate familial ovarian cancer risk gene

J. Ragoussis, C. Greenwood, A. Mes-Masson, 2020, medRxiv.

A tree‐based model for allele‐sharing‐based linkage analysis in human complex diseases

F. McMahon, T. Schulze, S. Bull, 2006, Genetic epidemiology.

X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells

C. Laprise, F. Martínez, C. Greenwood, 2018, Biology of Sex Differences.

Corrections to the parameterization of constraints on allele sharing in sibling pairs alter covariate-parameter estimates but not sharing-probability estimates or power of tests for linkage.

S. Bull, C. Greenwood, 2005, American Journal of Human Genetics.

Variants of the SFTPA1 and SFTPA2 genes and susceptibility to tuberculosis in Ethiopia

C. Greenwood, J. Beyene, T. Eguale, 2006, Human Genetics.