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Article detail · 2007 · article

Hearing Loss in Biotinidase Deficiency: Genotype-Phenotype Correlation

Journal The Journal of Pediatrics The ISSN points to another catalog journal; the name is from the YÖKSİS record.
ISSN0022-3476
YÖKSİS OpenAlex
Year2007
Citations49OpenAlex
Citations53Semantic Scholar · 1 influential
Percentile%60.8
FWCI0.491.00 = world average
Scopus (SJR)Q1
WoS (JCR)Q1
DOI10.1016/j.jpeds.2007.01.036 OpenAlexOpenAlex record

Data source split

  • YÖKSİSYÖKSİS article record
  • YÖKSİS venueThe Journal of Pediatrics
  • Catalog match (ISSN)Journal of Pediatrics
  • OpenAlexOpenAlex enrichment (abstract, citations, topics)
  • Semantic Scholarcitation count (not merged with OpenAlex)

Abstract

Abstract not compiled yet; it will appear after the DergiPark / OpenAlex queue runs.

Topics

Citations

OpenAlex cited_by_count. Not a WoS or Scopus citation count; those sources have no separate column here.

49citationsOpenAlex · cited_by_count (cache / database)

29 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).

  1. 2020 Biotinidase Deficiency: Prevalence, Impact And Management StrategiesCitations 90 · OpenAlex
  2. 2015 Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screeningCitations 40 · OpenAlex
  3. 2015 Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screeningCitations 40 · OpenAlex
  4. 2015 Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screeningCitations 40 · OpenAlex
  5. 2015 Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screeningCitations 40 · OpenAlex
  6. 2015 Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screeningCitations 40 · OpenAlex
  7. 2015 Detection of biotinidase gene mutations in Turkish patients ascertained by newborn and family screeningCitations 39 · OpenAlex
  8. 2018 Single center experience of biotinidase deficiency: 259 patients and six novel mutationsCitations 37 · OpenAlex
  9. 2018 Single center experience of biotinidase deficiency: 259 patients and six novel mutationsCitations 37 · OpenAlex
  10. 2018 Single center experience of biotinidase deficiency: 259 patients and six novel mutationsCitations 37 · OpenAlex

Authors

10
  1. SERAP SİVRİ HACETTEPE ÜNİVERSİTESİ 1
  2. genc aydan 2
  3. AYŞEGÜL TOKATLI 3
  4. ALİ DURSUN 4
  5. TURGAY COŞKUN 5
  6. HALİL İBRAHİM AYDIN 6
  7. sennaroglu levent 7
  8. EROL BELGİN ANKARA MEDİPOL ÜNİVERSİTESİ 8
  9. jensen karin 9
  10. wolf barry 10