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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 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
2. 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: 0
DOI: 10.1038/mp.2013.187
added
09-Dec-14
3. 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
4. Title: Absent CNKSR2 causes seizures and intellectual, attention and language deficits
Author(s): Vaags, A. K.; Bowdin, S.; Smith, M. L.; et al.
Source: Ann Neurol Published: 2014
DOI: 10.1002/ana.24274 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25223753
added
17-Sep-14
5. 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
6. 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: 1
DOI: 10.1002/ajmg.b.32236
added
18-Jul-14
7. Title: Autism spectrum disorder: advances in evidence-based practice
Author(s): Anagnostou, Evdokia; Zwaigenbaum, Lonnie; Szatmari, Peter; et al.
Source: Canadian Medical Association Journal Volume: 186 Issue: 7 Pages: 509-519 Published: APR 15 2014
Times Cited: 0
DOI: 10.1503/cmaj.121756
added
30-May-14
8. Title: Biological Overlap of Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder: Evidence From Copy Number Variants
Author(s): Martin, Joanna; Cooper, Miriam; Hamshere, Marian L.; et al.
Source: Journal of the American Academy of Child and Adolescent Psychiatry Volume: 53 Issue: 7 Pages: 761-770 Published: JUL 2014
Times Cited: 0
DOI: 10.1016/j.jaac.2014.03.004
added
05-Aug-14
9. Title: Brain-expressed exons under purifying selection are enriched for de novo mutations in autism spectrum disorder
Author(s): Uddin, Mohammed; Tammimies, Kristiina; Pellecchia, Giovanna; et al.
Source: Nature Genetics Volume: 46 Issue: 7 Pages: 742-747 Published: JUL 2014
Times Cited: 2
DOI: 10.1038/ng.2980
added
05-Aug-14
10. Title: CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems
Author(s): Chenier, Sebastien; Yoon, Grace; Argiropoulos, Bob; et al.
Source: Journal of Neurodevelopmental Disorders Volume: 6 Published: APR 22 2014
Times Cited: 0
DOI: 10.1186/1866-1955-6-9
added
30-May-14
publication(s)  
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