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akaturk Academic measurement

Article detail · 2018

Genetics of intellectual disability in consanguineous families

Journal

Molecular Psychiatry

ISSN 1359-4184

YÖKSİS OpenAlex Open access · green SJR Q1 JCR Q1 Citations 226 Top 1% Percentile 99.5% FWCI 16.16
Year
2018
Type
article

Data source split

  • YÖKSİS YÖKSİS article record
  • YÖKSİS venue Molecular Psychiatry
  • Catalog match (ISSN) Molecular Psychiatry
  • OpenAlex OpenAlex enrichment (abstract, citations, topics)

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.

226 citations

OpenAlex cited_by_count (cache / database)

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

  1. High Prevalence of Multilocus Pathogenic Variation in Neurodevelopmental Disorders in the Turkish Population 2021 Citations 107 · OpenAlex
  2. High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population 2021 Citations 107 · OpenAlex
  3. High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population 2021 Citations 107 · OpenAlex
  4. Malonyl coenzyme A decarboxylase deficiency with a novel mutation 2021 Citations 107 · OpenAlex
  5. Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability. 2018 Citations 26 · OpenAlex
  6. Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability 2018 Citations 26 · OpenAlex
  7. Biallelic missense variants in ZBTB11 can cause intellectual disability in humans 2018 Citations 25 · OpenAlex
  8. Biallelic missense variants in ZBTB11 can cause intellectual disability in humans 2018 Citations 25 · OpenAlex
  9. Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases 2023 Citations 16 · OpenAlex
  10. Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly 2023 Citations 12 · OpenAlex

Authors

  1. FARZANEH LARTI KADİR HAS ÜNİVERSİTESİ