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sim1000G: a user-friendly genetic variant simulator in R for unrelated individuals and family-based designs

BMC bioinformatics, 2019-01, Vol.20 (1), p.26-26, Article 26

2019

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Application of quantile regression to recent genetic and -omic studies

Human genetics, 2014-08, Vol.133 (8), p.951-966

2014

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DNA methylation profiles in the blood of newborn term infants born to mothers with obesity

PloS one, 2022-05, Vol.17 (5), p.e0267946-e0267946

2022

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Exclusive breastfeeding can attenuate body-mass-index increase among genetically susceptible children: A longitudinal study from the ALSPAC cohort

PLoS genetics, 2020-06, Vol.16 (6), p.e1008790-e1008790

2020

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FamEvent: An R Package for Generating and Modeling Time-to-Event Data in Family Designs

Journal of statistical software, 2021-03, Vol.97 (7)

2021

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Large-scale whole exome sequencing studies identify two genes,CTSL and APOE, associated with lung cancer

PLoS genetics, 2023-09, Vol.19 (9), p.e1010902-e1010902

2023

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A competing risks model with binary time varying covariates for estimation of breast cancer risks in BRCA1 families

Statistical methods in medical research, 2021-10, Vol.30 (9), p.2165-2183

2021

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Cord blood myostatin concentrations by gestational diabetes mellitus and fetal sex

Frontiers in endocrinology (Lausanne), 2023-02, Vol.14, p.1018779-1018779

2023

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Maternal Whole Blood Gene Expression at 18 and 28 Weeks of Gestation Associated with Spontaneous Preterm Birth in Asymptomatic Women

PloS one, 2016-06, Vol.11 (6), p.e0155191-e0155191

2016

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Joint nested frailty models for clustered recurrent and terminal events: An application to colonoscopy screening visits and colorectal cancer risks in Lynch Syndrome families

Statistical methods in medical research, 2020-05, Vol.29 (5), p.1466-1479

2020

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Building knowledge, optimising physical and mental health and setting up healthier life trajectories in South African women (Bukhali): a preconception randomised control trial part of the Healthy Life Trajectories Initiative (HeLTI)

BMJ open, 2022-04, Vol.12 (4), p.e059914-e059914

2022

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Genome-Wide Placental Gene Methylations in Gestational Diabetes Mellitus, Fetal Growth and Metabolic Health Biomarkers in Cord Blood

Frontiers in endocrinology (Lausanne), 2022-05, Vol.13, p.875180-875180

2022

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SNP-SNP interactions in breast cancer susceptibility

BMC cancer, 2006-05, Vol.6 (1), p.114-114, Article 114

2006

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Alternative Splicing Variant of Kallikrein-Related Peptidase 8 as an Independent Predictor of Unfavorable Prognosis in Lung Cancer

Clinical chemistry (Baltimore, Md.), 2010-06, Vol.56 (6), p.987-997

2010

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Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia

PloS one, 2013-01, Vol.8 (1), p.e53042-e53042

2013

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Association of a body mass index genetic risk score with growth throughout childhood and adolescence

PloS one, 2013-11, Vol.8 (11), p.e79547-e79547

2013

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Discovery of novel hypermethylated genes in prostate cancer using genomic CpG island microarrays

PloS one, 2009-03, Vol.4 (3), p.e4830

2009

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Comparison of pathway analysis approaches using lung cancer GWAS data sets

PloS one, 2012-02, Vol.7 (2), p.e31816-e31816

2012

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Modelling BMI trajectories in children for genetic association studies

PloS one, 2013-01, Vol.8 (1), p.e53897-e53897

2013

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Investigation of genetic variants, birthweight and hypothalamic-pituitary-adrenal axis function suggests a genetic variant in the SERPINA6 gene is associated with corticosteroid binding globulin in the western Australia pregnancy cohort (Raine) study

PloS one, 2014-04, Vol.9 (4), p.e92957-e92957

2014

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Quantitative DNA methylation analysis of genes coding for kallikrein-related peptidases 6 and 10 as biomarkers for prostate cancer

Epigenetics, 2012-09, Vol.7 (9), p.1037-1045

2012

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Polymorphisms XRCC1-R399Q and XRCC3-T241M and the Risk of Breast Cancer at the Ontario Site of the Breast Cancer Family Registry

Cancer epidemiology, biomarkers & prevention, 2004-04, Vol.13 (4), p.583-591

2004

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Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario

BMC medicine, 2007-08, Vol.5 (1), p.22-22, Article 22

2007

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A marginalized two‐part joint model for a longitudinal biomarker and a terminal event with application to advanced head and neck cancers

Pharmaceutical statistics : the journal of the pharmaceutical industry, 2024-01, Vol.23 (1), p.60-80

2024

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sim1000G: a user-friendly genetic variant simulator in R for unrelated individuals and family-based designs

Application of quantile regression to recent genetic and -omic studies

DNA methylation profiles in the blood of newborn term infants born to mothers with obesity

Exclusive breastfeeding can attenuate body-mass-index increase among genetically susceptible children: A longitudinal study from the ALSPAC cohort

FamEvent: An R Package for Generating and Modeling Time-to-Event Data in Family Designs

Large-scale whole exome sequencing studies identify two genes,CTSL and APOE, associated with lung cancer

A competing risks model with binary time varying covariates for estimation of breast cancer risks in BRCA1 families

Cord blood myostatin concentrations by gestational diabetes mellitus and fetal sex

Maternal Whole Blood Gene Expression at 18 and 28 Weeks of Gestation Associated with Spontaneous Preterm Birth in Asymptomatic Women

Joint nested frailty models for clustered recurrent and terminal events: An application to colonoscopy screening visits and colorectal cancer risks in Lynch Syndrome families

Building knowledge, optimising physical and mental health and setting up healthier life trajectories in South African women (Bukhali): a preconception randomised control trial part of the Healthy Life Trajectories Initiative (HeLTI)

Genome-Wide Placental Gene Methylations in Gestational Diabetes Mellitus, Fetal Growth and Metabolic Health Biomarkers in Cord Blood

SNP-SNP interactions in breast cancer susceptibility

Alternative Splicing Variant of Kallikrein-Related Peptidase 8 as an Independent Predictor of Unfavorable Prognosis in Lung Cancer

Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia

Association of a body mass index genetic risk score with growth throughout childhood and adolescence

Characterizing Risk Factors for Hospitalization and Clinical Characteristics in a Cohort of COVID-19 Patients Enrolled in the GENCOV Study

Discovery of novel hypermethylated genes in prostate cancer using genomic CpG island microarrays

Comparison of pathway analysis approaches using lung cancer GWAS data sets

Modelling BMI trajectories in children for genetic association studies

Investigation of genetic variants, birthweight and hypothalamic-pituitary-adrenal axis function suggests a genetic variant in the SERPINA6 gene is associated with corticosteroid binding globulin in the western Australia pregnancy cohort (Raine) study

Quantitative DNA methylation analysis of genes coding for kallikrein-related peptidases 6 and 10 as biomarkers for prostate cancer

Polymorphisms XRCC1-R399Q and XRCC3-T241M and the Risk of Breast Cancer at the Ontario Site of the Breast Cancer Family Registry

Methodological issues in detecting gene-gene interactions in breast cancer susceptibility: a population-based study in Ontario

A marginalized two‐part joint model for a longitudinal biomarker and a terminal event with application to advanced head and neck cancers

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