ResearcherID.com
ResearcherID Thomson Reuters  

Scherer, Stephen W
Create a ResearcherID badge for this researcher View publications analytics for this researcher
Close
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)  
First Page Previous Page Page   of  45  Go Next Page Last Page
  Sort by:    Results per page: 
1. Title: 15q11.2 Duplication Encompassing only the UBE3A Gene is Associated with Developmental Delay and Neuropsychiatric Phenotypes
Author(s): Noor, A.; Dupuis, L.; Mittal, K.; et al.
Source: Hum Mutat Published: 2015
DOI: 10.1002/humu.22800 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25884337
added
20-Apr-15
2. Title: A copy number variation map of the human genome
Author(s): Zarrei, Mehdi; MacDonald, Jeffrey R.; Merico, Daniele; et al.
Source: Nature Reviews Genetics Volume: 16 Issue: 3 Pages: 172-183 Published: MAR 2015
Times Cited: 1
DOI: 10.1038/nrg3871
added
26-Mar-15
3. Title: Ankrd11 Is a Chromatin Regulator Involved in Autism that Is Essential for Neural Development
Author(s): Gallagher, Denis; Voronova, Anastassia; Zander, Mark A.; et al.
Source: Developmental Cell Volume: 32 Issue: 1 Pages: 31-42 Published: JAN 12 2015
Times Cited: 0
DOI: 10.1016/j.devcel.2014.11.031
added
26-Mar-15
4. Title: Biallelic Mutations in BRCA1 Cause a New Fanconi Anemia Subtype
Author(s): Sawyer, Sarah L.; Tian, Lei; Kaehkoenen, Marketta; et al.
Source: Cancer Discovery Volume: 5 Issue: 2 Pages: 135-142 Published: FEB 2015
Times Cited: 0
DOI: 10.1158/2159-8290.CD-14-1156
added
01-May-15
5. Title: CAOS-Episodic Cerebellar Ataxia, Areflexia, Optic Atrophy, and Sensorineural Hearing Loss: A Third Allelic Disorder of the ATP1A3 Gene
Author(s): Heimer, G.; Sadaka, Y.; Israelian, L.; et al.
Source: J Child Neurol Published: 2015
DOI: 10.1177/0883073815579708 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25895915
added
04-May-15
6. Title: Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers
Author(s): Shlien, Adam; Campbell, Brittany B.; de Borja, Richard; et al.
Source: Nature Genetics Volume: 47 Issue: 3 Pages: 257-+ Published: MAR 2015
Times Cited: 2
DOI: 10.1038/ng.3202
added
02-Apr-15
7. 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: 3
DOI: 10.1016/j.biopsych.2014.05.011
added
28-Jan-15
8. Title: De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: A case report and a brief literature review
Author(s): Liu, Y.; Zhao, D.; Dong, R.; et al.
Source: Am J Med Genet A Published: 2015
DOI: 10.1002/ajmg.a.37050 / Author-provided URL : http://www.ncbi.nlm.nih.gov/pubmed/25851617
added
20-Apr-15
9. Title: Delineating the 15q13.3 microdeletion phenotype: a case series and comprehensive review of the literature
Author(s): Lowther, Chelsea; Costain, Gregory; Stavropoulos, Dimitri J.; et al.
Source: Genetics in Medicine Volume: 17 Issue: 2 Pages: 149-157 Published: FEB 2015
Times Cited: 0
DOI: 10.1038/gim.2014.83
added
26-Mar-15
10. Title: Individualized medicine enabled by genomics in Saudi Arabia.
Author(s): Abu-Elmagd, Muhammad; Assidi, Mourad; Schulten, Hans-Juergen; et al.
Source: BMC medical genomics Volume: 8 Pages: 531 Published: 2015
DOI: 10.1186/1755-8794-8-S1-S3
added
23-Apr-15
publication(s)  
First Page Previous Page Page   of  45  Go Next Page Last Page
  Sort by:    Results per page: