Article detail · 2010
Disruption of ALX1 Causes Extreme Microphthalmia and Severe Facial Clefting Expanding the Spectrum of Autosomal Recessive ALX Related Frontonasal Dysplasia
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 157
Top 10%
Percentile 96.4%
FWCI 5.59
- Year
- 2010
- 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.
157 citations
OpenAlex cited_by_count (cache / database)
34 publications in the local catalog that cite this work (OpenAlex reference match; not the full global list).
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- Disruption of PTPRO Causes Childhood Onset Nephrotic Syndrome 2011
- Disruption of PTPRO Causes Childhood Onset Nephrotic Syndrome 2011
- Disruption of PTPRO Causes Childhood Onset Nephrotic Syndrome 2011
- Disruption of PTPRO Causes Childhood Onset Nephrotic Syndrome 2011
- STK4 MST1 deficiency in two siblings with autoimmune cytopenias A novel mutation 2015