Article detail · 2019
The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance
Journal
Elsevier BVISSN 0002-9297
The ISSN points to another catalog journal; the name is from the YÖKSİS record.
YÖKSİS
OpenAlex
Open access · bronze
SJR Q1
JCR Q1
Citations 123
Top 10%
Percentile 98.4%
FWCI 8.41
- Year
- 2019
- Type
- article
Data source split
- YÖKSİS YÖKSİS article record
- YÖKSİS venue Elsevier BV
- Catalog match (ISSN) American Journal of Human Genetics
- 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.
123 citations
OpenAlex cited_by_count (cache / database)
43 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
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- High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population 2021
- Bi-allelic Pathogenic Variants in TUBGCP2 Cause Microcephaly and Lissencephaly Spectrum Disorders 2019
- Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability 2022
- Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability 2022
- The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders 2023
- Biallelic Novel USP53 Splicing Variant Disrupting the Gene Function that Causes Cholestasis Phenotype and Review of the Literature 2023
- Biallelic Novel USP53 Splicing Variant Disrupting the Gene Function that Causes Cholestasis Phenotype and Review of the Literature 2022