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Author Details
Full Name
Laurent Briollais
Affiliation
Institute of Health Policy, Dalla Lana School of Public Health, University of Toronto
ORCID
Career Start Year
1996
Papers
92
H Index
24
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36875483
Cord blood myostatin concentrations by gestational diabetes mellitus and fetal sex.
Front Endocrinol (Lausanne)
2023
37632107
Characterizing Risk Factors for Hospitalization and Clinical Characteristics in a Cohort of COVID-19 Patients Enrolled in the GENCOV Study.
Viruses
2023
37406717
Public knowledge of SARS-CoV-2 serological and viral lineage laboratory testing and result interpretation: A GENCOV study cross-sectional survey.
Clin Biochem
2023
36964717
Evaluating colonoscopy screening intervals in patients with Lynch syndrome from a large Canadian registry.
J Natl Cancer Inst
2023
36846925
Bayesian estimation of two-part joint models for a longitudinal semicontinuous biomarker and a terminal event with INLA: Interests for cancer clinical trial evaluation.
Biom J
2023
32282877
Two-part joint model for a longitudinal semicontinuous marker and a terminal event with application to metastatic colorectal cancer data.
Biostatistics
2022
35500004
DNA methylation profiles in the blood of newborn term infants born to mothers with obesity.
PLoS One
2022
35721735
Genome-Wide Placental Gene Methylations in Gestational Diabetes Mellitus, Fetal Growth and Metabolic Health Biomarkers in Cord Blood.
Front Endocrinol (Lausanne)
2022
35450913
Building knowledge, optimising physical and mental health and setting up healthier life trajectories in South African women (<i>Bukhali</i>): a preconception randomised control trial part of the Healthy Life Trajectories Initiative (HeLTI).
BMJ Open
2022
36585686
Genome-wide placental DNA methylations in fetal overgrowth and associations with leptin, adiponectin and fetal growth factors.
Clin Epigenetics
2022
36454756
Highly efficient reprogrammable mouse lines with integrated reporters to track the route to pluripotency.
Proc Natl Acad Sci U S A
2022
34986920
Maternal BMI, breastfeeding and perinatal factors that influence early childhood growth trajectories: a scoping review.
J Dev Orig Health Dis
2022
32277476
A Bayes factor approach with informative prior for rare genetic variant analysis from next generation sequencing data.
Biometrics
2021
33630024
Association of Risk-Reducing Salpingo-Oophorectomy With Breast Cancer Risk in Women With BRCA1 and BRCA2 Pathogenic Variants.
JAMA Oncol
2021
34937578
DNA methylation mediates the association between breastfeeding and early-life growth trajectories.
Clin Epigenetics
2021
34512212
FamEvent: An R Package for Generating and Modeling Time-to-Event Data in Family Designs.
J Stat Softw
2021
34232831
A competing risks model with binary time varying covariates for estimation of breast cancer risks in <i>BRCA1</i> families.
Stat Methods Med Res
2021
34196652
Bilateral Salpingo-Oophorectomy to Reduce Breast Cancer Risk in Women With Germline BRCA1 or BRCA2 Pathogenic Variants-Caution Needed-Reply.
JAMA Oncol
2021
32746960
Early life risk and resiliency factors and their influences on developmental outcomes and disease pathways: a rapid evidence review of systematic reviews and meta-analyses.
J Dev Orig Health Dis
2021
31347460
Joint nested frailty models for clustered recurrent and terminal events: An application to colonoscopy screening visits and colorectal cancer risks in Lynch Syndrome families.
Stat Methods Med Res
2020
32525877
Exclusive breastfeeding can attenuate body-mass-index increase among genetically susceptible children: A longitudinal study from the ALSPAC cohort.
PLoS Genet
2020
30380125
Risks of Colorectal Cancer and Cancer-Related Mortality in Familial Colorectal Cancer Type X and Lynch Syndrome Families.
J Natl Cancer Inst
2019
30646839
sim1000G: a user-friendly genetic variant simulator in R for unrelated individuals and family-based designs.
BMC Bioinformatics
2019
27378229
Modeling of successive cancer risks in Lynch syndrome families in the presence of competing risks using copulas.
Biometrics
2017
30053077
Response.
J Natl Cancer Inst
2017
28429508
Immunophenotyping and activation status of maternal peripheral blood leukocytes during pregnancy and labour, both term and preterm.
J Cell Mol Med
2017
28376164
Germline Mutations in the Kallikrein 6 Region and Predisposition for Aggressive Prostate Cancer.
J Natl Cancer Inst
2017
29040503
The role of early life growth development, the FTO gene and exclusive breastfeeding on child BMI trajectories.
Int J Epidemiol
2017
26169714
Improving customized fetal biometry by longitudinal modelling.
J Matern Fetal Neonatal Med
2016
33907591
A BAYESIAN GRAPHICAL MODEL FOR GENOME-WIDE ASSOCIATION STUDIES (GWAS).
Ann Appl Stat
2016
27333071
Maternal Whole Blood Gene Expression at 18 and 28 Weeks of Gestation Associated with Spontaneous Preterm Birth in Asymptomatic Women.
PLoS One
2016
26969751
International Genome-Wide Association Study Consortium Identifies Novel Loci Associated With Blood Pressure in Children and Adolescents.
Circ Cardiovasc Genet
2016
25479140
Prevalence of germline mutations in cancer predisposition genes in patients with pancreatic cancer.
Gastroenterology
2015
25953783
A genome-wide association study of body mass index across early life and childhood.
Int J Epidemiol
2015
23946183
Estimating successive cancer risks in Lynch Syndrome families using a progressive three-state model.
Stat Med
2014
25519347
Mixed-effects models for joint modeling of sequence data in longitudinal studies.
BMC Proc
2014
25342289
Inferring gene network from candidate SNP association studies using a Bayesian graphical model: application to a breast cancer case-control study from ontario.
Hum Hered
2014
25153607
Robustness of the linear mixed effects model to error distribution assumptions and the consequences for genome-wide association studies.
Stat Appl Genet Mol Biol
2014
24770874
Application of quantile regression to recent genetic and -omic studies.
Hum Genet
2014
24691024
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
23349760
Modelling BMI trajectories in children for genetic association studies.
PLoS One
2013
25054682
Polymorphisms in genes within the IGF-axis influence antenatal and postnatal growth.
J Dev Orig Health Dis
2013
24244521
Association of a body mass index genetic risk score with growth throughout childhood and adolescence.
PLoS One
2013
24200906
Genetic influences on trajectories of systolic blood pressure across childhood and adolescence.
Circ Cardiovasc Genet
2013
23549870
Altered DNA methylation landscapes of polycomb-repressed loci are associated with prostate cancer progression and ERG oncogene expression in prostate cancer.
Clin Cancer Res
2013
23301017
Discovery, validation and characterization of Erbb4 and Nrg1 haplotypes using data from three genome-wide association studies of schizophrenia.
PLoS One
2013
22363742
Comparison of pathway analysis approaches using lung cancer GWAS data sets.
PLoS One
2012
25101807
Fat mass and obesity-associated obesity-risk genotype is associated with lower foetal growth: an effect that is reversed in the offspring of smoking mothers.
J Dev Orig Health Dis
2012
23154192
The impact of breastfeeding on FTO-related BMI growth trajectories: an application to the Raine pregnancy cohort study.
Int J Epidemiol
2012
22874102
Quantitative DNA methylation analysis of genes coding for kallikrein-related peptidases 6 and 10 as biomarkers for prostate cancer.
Epigenetics
2012
1 - 50 of 92
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Bristol Medical School, University of Bristol
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George Davey Smith
University of Bristol
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John Trachtenberg
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John R McLaughlin
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Alexandre R Zlotta
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3
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Steven Gallinger
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Albert Hofman
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