Article detail · 2014
MCM9 Mutations Are Associated with Ovarian Failure, Short Stature, and Chromosomal Instability
Journal
The American Journal of Human GeneticsISSN 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 237
Top 10%
Percentile 97.5%
FWCI 6.3
- Year
- 2014
- Type
- article
Data source split
- YÖKSİS YÖKSİS article record
- YÖKSİS venue The American Journal of Human Genetics
- 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.
237 citations
OpenAlex cited_by_count (cache / database)
11 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
- Mutations in the mitochondrial ribosomal protein MRPS22 lead to primary ovarian insufficiency 2018
- Oocyte maturation abnormalities - A systematic review of the evidence and mechanisms in a rare but difficult to manage fertility pheneomina 2022
- Oocyte maturation abnormalities - A systematic review of the evidence and mechanisms in a rare but difficult to manage fertility pheneomina 2022
- Pathogenic Variants in ZSWIM7 Cause Primary Ovarian Insufficiency 2022
- Oocyte maturation abnormalities - A systematic review of the evidence and mechanisms in a rare but difficult to manage fertility pheneomina 2022
- Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency 2022
- Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency 2022
- Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency 2021
- Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadism 2021
- Clinical characteristics and molecular genetic analysis of a cohort with idiopathic congenital hypogonadism 2021