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Expertise in Autistic Disorder: HELP
Stanley F. Nelson
Based on 5 articles published since 2008
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Expertise Level
The expertise of Stanley F. Nelson ranks in the
  • Top 6.1%
  • ... of 26,233 published authors worldwide on Autistic Disorder
  • ... from 2008 through 2019
  • ... based on contributions to 5 articles on the topic.
Graphical view (beta)
Uncounted papers?
Aliases Nelson, S F   ·   Nelson, Stanley F
Work Locations
Details
Most likely:    UCLA   Contact    
2014
  • Department of Pathology and Laboratory Medicine. · Department of Physiology. · Department of Psychiatry, Department of Molecular and Medical Pharmacology, Department of Pediatrics. · Department of Pathology and Laboratory Medicine, Department of Human Genetics, University of California, Los Angeles, CA 90095, USA · Pubmed 24501278
2010
  • Department of Human Genetics, University of California-Los Angeles, 695 Charles E. Young Dr. South, Los Angeles, CA 90095, USA. · Pubmed 20552678
  • Department of Human Genetics, University of California, Los Angeles, CA 90095-7088, USA. · Pubmed 19455149
2008
  • UCLA Center for Autism Research and Treatment, Semel Institute of Neuroscience, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA. · Pubmed 18179893
Possible:    Trinity College Dublin      
2010
  • Department of Psychiatry, School of Medicine, Trinity College, Dublin 8, Ireland. · Pubmed 20663923
Specific Interests

In the titles of their published articles, experts often reveal their very specific interests.

Here are the titles of all articles written by Stanley F. Nelson in 2008-2019 about Autistic Disorder:

  • Exome sequencing identifies de novo gain of function missense mutation in KCND2 in identical twins with autism and seizures that slows potassium channel inactivation. 2014
  • A genome-wide scan for common alleles affecting risk for autism. 2010
  • Accuracy of phenotyping of autistic children based on Internet implemented parent report. 2010
  • High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene. 2010
  • Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene. 2008
Show List of Full Article Records
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UCLA
2014
  • Department of Pathology and Laboratory Medicine. · Department of Physiology. · Department of Psychiatry, Department of Molecular and Medical Pharmacology, Department of Pediatrics. · Department of Pathology and Laboratory Medicine, Department of Human Genetics, University of California, Los Angeles, CA 90095, USA · Pubmed 24501278
2010
  • Department of Human Genetics, University of California-Los Angeles, 695 Charles E. Young Dr. South, Los Angeles, CA 90095, USA. · Pubmed 20552678
  • Department of Human Genetics, University of California, Los Angeles, CA 90095-7088, USA. · Pubmed 19455149
2008
  • UCLA Center for Autism Research and Treatment, Semel Institute of Neuroscience, David Geffen School of Medicine at UCLA, Los Angeles, CA 90095, USA. · Pubmed 18179893
Trinity College Dublin
2010
  • Department of Psychiatry, School of Medicine, Trinity College, Dublin 8, Ireland. · Pubmed 20663923
Yearly article counts 000001000301
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