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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: 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: 0
DOI: 10.1016/j.biopsych.2014.05.011
added
28-Jan-15
2. 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
3. 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
4. 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
5. 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: 1
DOI: 10.1038/mp.2013.187
added
09-Dec-14
6. Title: A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locus
Author(s): Oei, Ling; Hsu, Yi-Hsiang; Styrkarsdottir, Unnur; et al.
Source: Journal of Medical Genetics Volume: 51 Issue: 2 Pages: 122-131 Published: FEB 2014
Times Cited: 2
DOI: 10.1136/jmedgenet-2013-102064
added
02-May-14
7. Title: A high-resolution copy-number variation resource for clinical and population genetics
Author(s): Uddin, M.; Thiruvahindrapuram, B.; Walker, S.; et al.
Source: Genet Med Published: 2014
DOI: 10.1038/gim.2014.178 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25503493
added
23-Dec-14
8. Title: Absent CNKSR2 Causes Seizures and Intellectual, Attention, and Language Deficits
Author(s): Vaags, Andrea K.; Bowdin, Sarah; Smith, Mary-Lou; et al.
Source: Annals of Neurology Volume: 76 Issue: 5 Pages: 758-764 Published: NOV 2014
Times Cited: 0
DOI: 10.1002/ana.24274
added
23-Dec-14
9. Title: Adult expression of a 3q13.31 microdeletion
Author(s): Lowther, Chelsea; Costain, Gregory; Melvin, Rebecca; et al.
Source: Molecular Cytogenetics Volume: 7 Published: MAR 20 2014
Times Cited: 1
DOI: 10.1186/1755-8166-7-23
added
30-May-14
10. Title: Adult Neuropsychiatric Expression and Familial Segregation of 2q13 Duplications
Author(s): Costain, Gregory; Lionel, Anath C.; Fu, Fiona; et al.
Source: American Journal of Medical Genetics Part B-Neuropsychiatric Genetics Volume: 165 Issue: 4 Pages: 337-344 Published: JUN 2014
Times Cited: 2
DOI: 10.1002/ajmg.b.32236
added
18-Jul-14
publication(s)  
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