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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: Chromosomal contacts connect loci associated with autism, BMI and head circumference phenotypes
Author(s): Loviglio, M. N.; Leleu, M.; Männik, K.; et al.
Source: Mol Psychiatry Published: 2016
DOI: 10.1038/mp.2016.84 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/27240531
added
02-Jun-16
2. Title: CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
Author(s): Mercati, O.; Huguet, G.; Danckaert, A.; et al.
Source: Mol Psychiatry Published: 2016
DOI: 10.1038/mp.2016.61 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/27166760
added
12-May-16
3. Title: Complex Copy Number Variation of AMY1 does not Associate with Obesity in two East Asian Cohorts
Author(s): Yong, Rita Y. Y.; Mustaffa, Su'Aidah B.; Wasan, Pavandip S.; et al.
Source: Human Mutation Volume: 37 Issue: 7 Pages: 669-678 Published: JUL 2016
Times Cited: 0
DOI: 10.1002/humu.22996
added
07-Sep-16
4. Title: Copy-number variations are enriched for neurodevelopmental genes in children with developmental coordination disorder
Author(s): Mosca, S. J.; Langevin, L. M.; Dewey, D.; et al.
Source: J Med Genet Published: 2016
DOI: 10.1136/jmedgenet-2016-103818 / Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/27489308
added
09-Aug-16
5. Title: De novo large rare copy-number variations contribute to conotruncal heart disease in Chinese patients
Author(s): Mak, Christopher C. Y.; Chow, Pak Cheong; Liu, Anthony P. Y.; et al.
added
20-Sep-16
6. Title: Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index
Author(s): Hinney, A.; Kesselmeier, M.; Jall, S.; et al.
Source: Mol Psychiatry Published: 2016
DOI: 10.1038/mp.2016.71 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/27184124
added
30-May-16
7. Title: Genome-wide characteristics of de novo mutations in autism
Author(s): Yuen, Ryan K. C.; Merico, Daniele; Cao, Hongzhi; et al.
Source: Npj Genomic Medicine Volume: 1 Pages: 16027 Published: 2016
added
09-Aug-16
8. 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: 1
DOI: 10.1016/j.ijcard.2015.11.127
added
14-Jan-16
9. Title: Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell-Silver syndrome
Author(s): Cytrynbaum, C.; Chong, K.; Hannig, V.; et al.
Source: Am J Med Genet A Published: 2016
DOI: 10.1002/ajmg.a.37819 / Author-provided URL : https://www.ncbi.nlm.nih.gov/pubmed/27374371
added
12-Jul-16
10. Title: Genomic medicine goes mainstream
Author(s): Scherer, Stephen W.
Source: Npj Genomic Medicine Volume: 1 Pages: 150001 Published: 2016
added
15-Jan-16
publication(s)  
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