Article detail · 2009 · article
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations
ISSN0165-5876
YÖKSİS
OpenAlex
Year2009
Citations62OpenAlex
Percentile%72.2
FWCI1.11.00 = world average
Scopus (SJR)Q1
WoS (JCR)Q3
Data source split
- YÖKSİSYÖKSİS article record
- YÖKSİS venueInternational Journal of Pediatric Otorhinolaryngology
- Catalog match (ISSN)International Journal of Pediatric Otorhinolaryngology
- OpenAlexOpenAlex enrichment (abstract, citations, topics)
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Topics
Citations
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62citationsOpenAlex · cited_by_count (cache / database)
8 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
- 2012 Autosomal recessive nonsyndromic deafness genes a reviewCitations 151 · OpenAlex
- 2012 Autosomal recessive nonsyndromic deafness genes: a reviewCitations 151 · OpenAlex
- 2011 Screening of 38 Genes Identifies Mutations in 62 of Families with Nonsyndromic Deafness in TurkeyCitations 91 · OpenAlex
- 2011 Screening of 38 Genes Identifies Mutations in 62 of Families with Nonsyndromic Deafness in TurkeyCitations 91 · OpenAlex
- 2011 Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in TurkeyCitations 91 · OpenAlex
- 2011 Screening of 38 Genes Identifies Mutations in 62 of Families with Nonsyndromic Deafness in TurkeyCitations 90 · OpenAlex
- 2015 Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing LossCitations 68 · OpenAlex
- 2015 Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing LossCitations 68 · OpenAlex