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Scherer, Stephen W
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ResearcherID: B-3785-2013
Other Names: Scherer, S.; Scherer, S.W.
URL: http://www.researcherid.com/rid/B-3785-2013
Subject: Behavioral Sciences; Biochemistry & Molecular Biology; Genetics & Heredity; Science & Technology - Other
Keywords: genome sciences
ORCID: http://orcid.org/0000-0002-8326-1999
My Institutions (more details)
Primary Institution:
Sub-org/Dept: Genetics and Genome Biology
Role:
Joint Affiliation:
Sub-org/Dept:
Role:
My URLs: http://www.tcag.ca/scherer/
 
 

This list contains papers that I have authored.

publication(s)  
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1. Title: Complex Copy Number Variation Of Amy1 Does not Associate With Obesity in Two East Asian Cohorts
Author(s): Yong, R. Y.; Mustaffa, S. B.; Wasan, P. S.; et al.
Source: Hum Mutat Published: 2016
DOI: 10.1002/humu.22996 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/27068483
added
21-Apr-16
2. Title: Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries
Author(s): Costain, Gregory; Lionel, Anath C.; Ogura, Lucas; et al.
Source: International Journal of Cardiology Volume: 204 Pages: 115-121 Published: FEB 1 2016
Times Cited: 0
DOI: 10.1016/j.ijcard.2015.11.127
added
14-Jan-16
3. Title: Genomic medicine goes mainstream
Author(s): Scherer, Stephen W.
Source: Npj Genomic Medicine Volume: 1 Pages: 150001 Published: 2016
added
15-Jan-16
4. Title: Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L
Author(s): Yoon, G.; Malam, Z.; Paton, T.; et al.
Source: J Pediatr Published: 2016
DOI: 10.1016/j.jpeds.2015.12.060 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/26825290
added
03-Feb-16
5. Title: Microduplications at the pseudoautosomal SHOX locus in autism spectrum disorders and related neurodevelopmental conditions
Author(s): Tropeano, M.; Howley, D.; Gazzellone, M. J.; et al.
Source: J Med Genet Published: 2016
DOI: 10.1136/jmedgenet-2015-103621 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/27073233
added
21-Apr-16
6. Title: Phenotypic Association Analyses With Copy Number Variation in Recurrent Depressive Disorder
Author(s): Rucker, James J. H.; Tansey, Katherine E.; Rivera, Margarita; et al.
Source: Biological Psychiatry Volume: 79 Issue: 4 Pages: 329-336 Published: FEB 15 2016
Times Cited: 0
DOI: 10.1016/j.biopsych.2015.02.025
added
09-Mar-16
7. Title: Prevalence of Creatine Deficiency Syndromes in Children With Nonsyndromic Autism
Author(s): Schulze, Andreas; Bauman, Margaret; Tsai, Anne Chun-Hui; et al.
Source: Pediatrics Volume: 137 Issue: 1 Published: JAN 2016
Times Cited: 0
DOI: 10.1542/peds.2015-2672
added
21-Apr-16
8. Title: Rare Copy Number Variants Identified Suggest the Regulating Pathways in Hypertension-Related Left Ventricular Hypertrophy
Author(s): Boon-Peng, Hoh; Jusoh, Julia Ashazila Mat; Marshall, Christian R.; et al.
Source: Plos One Volume: 11 Issue: 3 Published: MAR 1 2016
Times Cited: 0
DOI: 10.1371/journal.pone.0148755
added
21-Apr-16
9. Title: Rare copy number variations in an adult with transposition of the great arteries emphasize the importance of updated genetic assessments in syndromic congenital cardiac disease
Author(s): Costain, Gregory; Roche, S. Lucy; Scherer, Stephen W.; et al.
Source: International Journal of Cardiology Volume: 203 Pages: 516-518 Published: JAN 15 2016
Times Cited: 0
DOI: 10.1016/j.ijcard.2015.10.216
added
14-Jan-16
10. Title: The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD
Author(s): Richard, A. C.; Rovelet-Lecrux, A.; Delaby, E.; et al.
Source: Am J Med Genet B Neuropsychiatr Genet Published: 2016
DOI: 10.1002/ajmg.b.32416 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/26978485
added
21-Mar-16
publication(s)  
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