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Andrei L Turinsky

Showing results (31-40 of 44) with videos related to

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Nucleic Acids Research|September 30, 2010
DAnCER: disease-annotated chromatin epigenetics resourceAndrei L Turinsky, Brian Turner, Rosanne C Borja, et al.
Nature Communications|July 13, 2024
Early human fetal lung atlas reveals the temporal dynamics of epithelial cell plasticityHenry Quach, Spencer Farrell, Ming Jia Michael Wu, et al.
Journal of Neurodevelopmental Disorders|August 18, 2020
Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variationSarah J Goodman, Christie L Burton, Darci T Butcher, et al.
Clinical Epigenetics|August 15, 2019
DNA methylation signature is prognostic of choroid plexus tumor aggressivenessMalgorzata Pienkowska, Sanaa Choufani, Andrei L Turinsky, et al.
Clinical Epigenetics|October 23, 2019
Correction to: DNA methylation signature is prognostic of choroid plexus tumor aggressivenessMalgorzata Pienkowska, Sanaa Choufani, Andrei L Turinsky, et al.
Inflammatory Bowel Diseases|February 11, 2026
Primary infliximab failure in pediatric colonic inflammatory bowel disease: Development of a proteomics predictive model using a prospective Canadian cohortAmanda Ricciuto, Andrei L Turinsky, Anne M Griffiths, et al.
BMC Medical Genomics|January 30, 2013
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5CDaria Grafodatskaya, Barian H Y Chung, Darci T Butcher, et al.
American Journal of Human Genetics|May 6, 2017
CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping ConditionsDarci T Butcher, Cheryl Cytrynbaum, Andrei L Turinsky, et al.
Cell Reports|July 2, 2014
Human-chromatin-related protein interactions identify a demethylase complex required for chromosome segregationEdyta Marcon, Zuyao Ni, Shuye Pu, et al.
Human Mutation|February 19, 2022
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discoveryHannah G Driver, Taila Hartley, E Magda Price, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Nucleic Acids Research|September 30, 2010
DAnCER: disease-annotated chromatin epigenetics resourceAndrei L Turinsky, Brian Turner, Rosanne C Borja, et al.
Nature Communications|July 13, 2024
Early human fetal lung atlas reveals the temporal dynamics of epithelial cell plasticityHenry Quach, Spencer Farrell, Ming Jia Michael Wu, et al.
Journal of Neurodevelopmental Disorders|August 18, 2020
Obsessive-compulsive disorder and attention-deficit/hyperactivity disorder: distinct associations with DNA methylation and genetic variationSarah J Goodman, Christie L Burton, Darci T Butcher, et al.
Clinical Epigenetics|August 15, 2019
DNA methylation signature is prognostic of choroid plexus tumor aggressivenessMalgorzata Pienkowska, Sanaa Choufani, Andrei L Turinsky, et al.
Clinical Epigenetics|October 23, 2019
Correction to: DNA methylation signature is prognostic of choroid plexus tumor aggressivenessMalgorzata Pienkowska, Sanaa Choufani, Andrei L Turinsky, et al.
Inflammatory Bowel Diseases|February 11, 2026
Primary infliximab failure in pediatric colonic inflammatory bowel disease: Development of a proteomics predictive model using a prospective Canadian cohortAmanda Ricciuto, Andrei L Turinsky, Anne M Griffiths, et al.
BMC Medical Genomics|January 30, 2013
Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5CDaria Grafodatskaya, Barian H Y Chung, Darci T Butcher, et al.
American Journal of Human Genetics|May 6, 2017
CHARGE and Kabuki Syndromes: Gene-Specific DNA Methylation Signatures Identify Epigenetic Mechanisms Linking These Clinically Overlapping ConditionsDarci T Butcher, Cheryl Cytrynbaum, Andrei L Turinsky, et al.
Cell Reports|July 2, 2014
Human-chromatin-related protein interactions identify a demethylase complex required for chromosome segregationEdyta Marcon, Zuyao Ni, Shuye Pu, et al.
Human Mutation|February 19, 2022
Genomics4RD: An integrated platform to share Canadian deep-phenotype and multiomic data for international rare disease gene discoveryHannah G Driver, Taila Hartley, E Magda Price, et al.
Pageof 5