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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: A copy number variation map of the human genome
Author(s): Zarrei, M.; MacDonald, J. R.; Merico, D.; et al.
Source: Nat Rev Genet Published: 2015
DOI: 10.1038/nrg3871 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25645873
added
04-Feb-15
2. Title: Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers
Author(s): Shlien, A.; Campbell, B. B.; de Borja, R.; et al.
Source: Nat Genet Published: 2015
DOI: 10.1038/ng.3202 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25642631
added
03-Feb-15
3. Title: Copy Number Variable MicroRNAs in Schizophrenia and Their Neurodevelopmental Gene Targets
Author(s): Warnica, William; Merico, Daniele; Costain, Gregory; et al.
Source: Biological Psychiatry Volume: 77 Issue: 2 Pages: 158-166 Published: JAN 15 2015
Times Cited: 2
DOI: 10.1016/j.biopsych.2014.05.011
added
28-Jan-15
4. Title: Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
Author(s): Maier, R.; Moser, G.; Chen, G. B.; et al.
Source: Am J Hum Genet Published: 2015
DOI: 10.1016/j.ajhg.2014.12.006 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25640677
added
03-Feb-15
5. Title: Performance of case-control rare copy number variation annotation in classification of autism.
Author(s): Engchuan W.; Dhindsa K.; Lionel AC.; et al.
Source: BMC Genomics Volume: 8 Pages: S7 Published: 2015
added
03-Feb-15
6. Title: Single cell-derived clonal analysis of human glioblastoma links functional and genomic heterogeneity
Author(s): Meyer, M.; Reimand, J.; Lan, X.; et al.
Source: Proc Natl Acad Sci U S A Published: 2015
DOI: 10.1073/pnas.1320611111 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25561528
added
12-Jan-15
7. Title: Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome.
Author(s): Marshall CR.; Farrell SA.; Cushing D.; et al.
Source: BMC Genomics Volume: 16 Pages: S1 Published: 2015
added
03-Feb-15
8. Title: Whole-genome sequencing of quartet families with autism spectrum disorder
Author(s): Yuen, R. K.; Thiruvahindrapuram, B.; Merico, D.; et al.
Source: Nat Med Published: 2015
DOI: 10.1038/nm.3792 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25621899
added
28-Jan-15
9. Title: A CGG-Repeat Expansion Mutation in ZNF713 Causes FRA7A: Association with Autistic Spectrum Disorder in Two Families
Author(s): Metsu, Sofie; Rainger, Jacqueline K.; Debacker, Kim; et al.
Source: Human Mutation Volume: 35 Issue: 11 Pages: 1295-1300 Published: NOV 2014
Times Cited: 0
DOI: 10.1002/humu.22683
added
09-Dec-14
10. Title: A genome-wide association study of anorexia nervosa
Author(s): Boraska, V.; Franklin, C. S.; Floyd, J. A. B.; et al.
Source: Molecular Psychiatry Volume: 19 Issue: 10 Pages: 1085-1094 Published: OCT 2014
Times Cited: 4
DOI: 10.1038/mp.2013.187
added
09-Dec-14
publication(s)  
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