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Alexandre Bureau

Showing results (61-70 of 69) with videos related to

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Plos One|May 27, 2015
A genome-wide copy number variant study of suicidal behaviorJeffrey A Gross, Alexandre Bureau, Jordie Croteau, et al.
American Journal of Human Genetics|August 5, 2005
Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplificationKym M Boycott, Shauna Flavelle, Alexandre Bureau, et al.
Patient Education and Counseling|March 4, 2026
Assessment of pregnant women's intention to use a mobile application-based decision aid for prenatal screening for trisomies 21, 18 and 13: A mixed-methods cross-sectional studySehouenou Albéric Candide Ahouehome, Alexandre Bureau, Samira Abbasgholizadeh Rahimi, et al.
Genetic Epidemiology|September 25, 2018
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variantsAlexandre Bureau, Ferdouse Begum, Margaret A Taub, et al.
BMC Medical Informatics and Decision Making|July 21, 2021
Exploring polypharmacy with artificial intelligence: data analysis protocolCaroline Sirois, Richard Khoury, Audrey Durand, et al.
BMC Public Health|May 23, 2022
Time trends in social contacts before and during the COVID-19 pandemic: the CONNECT studyMélanie Drolet, Aurélie Godbout, Myrto Mondor, et al.
Genetic Epidemiology|December 3, 2016
Whole exome association of rare deletions in multiplex oral cleft familiesJack Fu, Terri H Beaty, Alan F Scott, et al.
International Journal of Molecular Sciences|October 16, 2025
CTCF Mediates the Cis-Regulatory Hubs in Mouse HeartsMick Lee, Loïc Mangnier, Cory C Padilla, et al.
Genetics|May 6, 2014
Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral cleftsAlexandre Bureau, Margaret M Parker, Ingo Ruczinski, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
Plos One|May 27, 2015
A genome-wide copy number variant study of suicidal behaviorJeffrey A Gross, Alexandre Bureau, Jordie Croteau, et al.
American Journal of Human Genetics|August 5, 2005
Homozygous deletion of the very low density lipoprotein receptor gene causes autosomal recessive cerebellar hypoplasia with cerebral gyral simplificationKym M Boycott, Shauna Flavelle, Alexandre Bureau, et al.
Patient Education and Counseling|March 4, 2026
Assessment of pregnant women's intention to use a mobile application-based decision aid for prenatal screening for trisomies 21, 18 and 13: A mixed-methods cross-sectional studySehouenou Albéric Candide Ahouehome, Alexandre Bureau, Samira Abbasgholizadeh Rahimi, et al.
Genetic Epidemiology|September 25, 2018
Inferring disease risk genes from sequencing data in multiplex pedigrees through sharing of rare variantsAlexandre Bureau, Ferdouse Begum, Margaret A Taub, et al.
BMC Medical Informatics and Decision Making|July 21, 2021
Exploring polypharmacy with artificial intelligence: data analysis protocolCaroline Sirois, Richard Khoury, Audrey Durand, et al.
BMC Public Health|May 23, 2022
Time trends in social contacts before and during the COVID-19 pandemic: the CONNECT studyMélanie Drolet, Aurélie Godbout, Myrto Mondor, et al.
Genetic Epidemiology|December 3, 2016
Whole exome association of rare deletions in multiplex oral cleft familiesJack Fu, Terri H Beaty, Alan F Scott, et al.
International Journal of Molecular Sciences|October 16, 2025
CTCF Mediates the Cis-Regulatory Hubs in Mouse HeartsMick Lee, Loïc Mangnier, Cory C Padilla, et al.
Genetics|May 6, 2014
Whole exome sequencing of distant relatives in multiplex families implicates rare variants in candidate genes for oral cleftsAlexandre Bureau, Margaret M Parker, Ingo Ruczinski, et al.
Pageof 7