Article detail · 2018
Genetics of intellectual disability in consanguineous families
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).
- High Prevalence of Multilocus Pathogenic Variation in Neurodevelopmental Disorders in the Turkish Population 2021
- High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population 2021
- High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population 2021
- Malonyl coenzyme A decarboxylase deficiency with a novel mutation 2021
- Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability. 2018
- Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability 2018
- Biallelic missense variants in ZBTB11 can cause intellectual disability in humans 2018
- Biallelic missense variants in ZBTB11 can cause intellectual disability in humans 2018
- Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases 2023
- Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly 2023