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Expertise in Hearing Disorders: HELP
Amara Fatima
Based on 6 articles published since 2009
(Why 6 articles?)
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Expertise Level
The expertise of Amara Fatima ranks in the
  • Top 8.8%
  • ... of 62,471 published authors worldwide on Hearing Disorders
  • ... from 2009 through 2019
  • ... based on contributions to 6 articles on the topic.
Graphical view (beta)
Aliases Fatima, A   ·   Fatima, Amara
Work Locations
Details
Most likely:    University of the Punjab      
2017
  • School of Biological Sciences, University of the Punjab, Lahore, Pakistan. · Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, USA 20892. · Audiology Unit, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, USA 20892. · Genomics and Computational Biology Core, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, USA 20892. · Pubmed 27573290
2013
  • School of Biological Sciences, University of the Punjab, Quaid-i-Azam Campus, Lahore 54590, Pakistan. · Pubmed 23340767
2012
  • School of Biological Sciences, University of the Punjab, Lahore, Pakistan. · Pubmed 22617256
  • School of Biological Sciences, University of the Punjab, Quaid-i-Azam Campus, Lahore 54590, Pakistan. · Pubmed 22245518
2010
  • School of Biological Sciences, University of the Punjab, Lahore, Pakistan. · Pubmed 20811388
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 Amara Fatima in 2009-2019 about Hearing Disorders:

  • Genetic causes of moderate to severe hearing loss point to modifiers. 2017
  • The c.42_52del11 mutation in TPRN and progressive hearing loss in a family from Pakistan. 2013
  • A p.C343S missense mutation in PJVK causes progressive hearing loss. 2012
  • Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss. 2012
  • Mutations in CLDN14 are associated with different hearing thresholds. 2010
  • A frameshift mutation in SANS results in atypical Usher syndrome. 2010
Show List of Full Article Records
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University of the Punjab
Affiliation Timeline
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University of the Punjab
2017
  • School of Biological Sciences, University of the Punjab, Lahore, Pakistan. · Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, USA 20892. · Audiology Unit, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, USA 20892. · Genomics and Computational Biology Core, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, USA 20892. · Pubmed 27573290
2013
  • School of Biological Sciences, University of the Punjab, Quaid-i-Azam Campus, Lahore 54590, Pakistan. · Pubmed 23340767
2012
  • School of Biological Sciences, University of the Punjab, Lahore, Pakistan. · Pubmed 22617256
  • School of Biological Sciences, University of the Punjab, Quaid-i-Azam Campus, Lahore 54590, Pakistan. · Pubmed 22245518
2010
  • School of Biological Sciences, University of the Punjab, Lahore, Pakistan. · Pubmed 20811388
Yearly article counts 00100012020
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