Search research articles
Contact Us
Filters
Showing results (61-70 of 144) with videos related to
Page
of 15
Sort By:
Translational Psychiatry
|
February 2, 2021
Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia
Bahareh A Mojarad, Yue Yin, Roozbeh Manshaei, et al.
Journal of Psychiatric Research
|
July 21, 2010
Clinically detectable copy number variations in a Canadian catchment population of schizophrenia
Anne S Bassett, Gregory Costain, Wai Lun Alan Fung, et al.
Seizure
|
March 17, 2023
Epilepsy surgery outcomes in patients with GATOR1 gene complex variants: Report of new cases and review of literature
Ahmed N Sahly, Robyn Whitney, Gregory Costain, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2020
A novel intronic variant in UBE3A identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome
Meredith Curtis, Danielle Baribeau, Susan Walker, et al.
Plos Genetics
|
August 23, 2012
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways
Candice K Silversides, Anath C Lionel, Gregory Costain, et al.
Genome Medicine
|
December 1, 2017
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia
Chelsea Lowther, Daniele Merico, Gregory Costain, et al.
NPJ Genomic Medicine
|
February 26, 2024
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders
Kristen M Wigby, Deanna Brockman, Gregory Costain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 1, 2014
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature
Chelsea Lowther, Gregory Costain, Dimitri J Stavropoulos, et al.
Epilepsia
|
April 18, 2026
An n-of-1 gene-directed drug repurposing trial for an ultrarare genetic condition
Vedika Jha, Christina Tsetsos, Mark Bedford, et al.
The British Journal of Dermatology
|
November 23, 2024
Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmenti
Neta Pipko, Rachel Youjin Oh, Aiyana Kaplan, et al.
Page
of 15
Search research articles
Search
Showing results (61-70 of 144) with videos related to
Sort By:
Page
of 15
Translational Psychiatry
|
February 2, 2021
Genome sequencing broadens the range of contributing variants with clinical implications in schizophrenia
Bahareh A Mojarad, Yue Yin, Roozbeh Manshaei, et al.
Journal of Psychiatric Research
|
July 21, 2010
Clinically detectable copy number variations in a Canadian catchment population of schizophrenia
Anne S Bassett, Gregory Costain, Wai Lun Alan Fung, et al.
Seizure
|
March 17, 2023
Epilepsy surgery outcomes in patients with GATOR1 gene complex variants: Report of new cases and review of literature
Ahmed N Sahly, Robyn Whitney, Gregory Costain, et al.
American Journal of Medical Genetics. Part A
|
July 12, 2020
A novel intronic variant in UBE3A identified by genome sequencing in a patient with an atypical presentation of Angelman syndrome
Meredith Curtis, Danielle Baribeau, Susan Walker, et al.
Plos Genetics
|
August 23, 2012
Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways
Candice K Silversides, Anath C Lionel, Gregory Costain, et al.
Genome Medicine
|
December 1, 2017
Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia
Chelsea Lowther, Daniele Merico, Gregory Costain, et al.
NPJ Genomic Medicine
|
February 26, 2024
Evidence review and considerations for use of first line genome sequencing to diagnose rare genetic disorders
Kristen M Wigby, Deanna Brockman, Gregory Costain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 1, 2014
Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature
Chelsea Lowther, Gregory Costain, Dimitri J Stavropoulos, et al.
Epilepsia
|
April 18, 2026
An n-of-1 gene-directed drug repurposing trial for an ultrarare genetic condition
Vedika Jha, Christina Tsetsos, Mark Bedford, et al.
The British Journal of Dermatology
|
November 23, 2024
Genome sequencing reveals novel IKBKG structural variants associated with incontinentia pigmenti
Neta Pipko, Rachel Youjin Oh, Aiyana Kaplan, et al.
Page
of 15