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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, 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
4. 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
5. 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
6. 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
7. Title: Genomic medicine goes mainstream
Author(s): Scherer, Stephen W.
Source: Npj Genomic Medicine Volume: 1 Pages: 150001 Published: 2016
added
15-Jan-16
8. Title: Indexing Effects of Copy Number Variation on Genes Involved in Developmental Delay.
Author(s): Uddin, Mohammed; Pellecchia, Giovanna; Thiruvahindrapuram, Bhooma; et al.
Source: Scientific reports Volume: 6 Pages: 28663 Published: 2016
DOI: 10.1038/srep28663
added
12-Jul-16
9. Title: Lethal Disorder of Mitochondrial Fission Caused by Mutations in DNM1L
Author(s): Yoon, Grace; Malam, Zeenat; Paton, Tara; et al.
Source: Journal of Pediatrics Volume: 171 Pages: 313-+ Published: APR 2016
Times Cited: 0
DOI: 10.1016/j.jpeds.2015.12.060
added
12-May-16
10. Title: MED23-associated refractory epilepsy successfully treated with the ketogenic diet
Author(s): Lionel, A. C.; Monfared, N.; Scherer, S. W.; et al.
Source: Am J Med Genet A Published: 2016
DOI: 10.1002/ajmg.a.37802 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/27311965
added
21-Jun-16
publication(s)  
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