An estimation of global genetic prevalence of PLA2G6-associated neurodegeneration

Our estimates highlight the significant underdiagnosis of PLA2G6-associated neurodegeneration and underscores the need for increased awareness and diagnostic efforts. Furthermore, our study revealed a higher carrier frequency of PLA2G6 variants in African and Asian populations, stressing the importance of expanded genetic sequencing in non-European populations to ensure accurate and comprehensive diagnosis. Future research should focus on confirming our findings and implementing expanded sequencing strategies to facilitate maximal and accurate diagnosis, particularly in non-European populations.

Authors

Institutions

Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2024-10-18
DOI
https://doi.org/10.1186/s13023-024-03275-x
Citations
8
Primary Topic
Neurological diseases and metabolism
Type
article
Field-Weighted Citation Impact
1.98
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

An estimation of global genetic prevalence of PLA2G6-associated neurodegeneration

Amina Kurtović-Kozarić, Jordan C. Wood, Samantha Baxter, Moriel Singer‐Berk et al.
8 citations
Orphanet Journal of Rare Diseases
Neurological diseases and metabolism
1.98
article

An estimation of global genetic prevalence of PLA2G6-associated neurodegeneration

Amina Kurtović-Kozarić, Jordan C. Wood, Samantha Baxter, Moriel Singer‐Berk, Amanda Hope, Emily Evangelista, Leena Panwala, Mark J. Kiel, Stefanie M. Heinrich
article en
8 citations

Abstract

Our estimates highlight the significant underdiagnosis of PLA2G6-associated neurodegeneration and underscores the need for increased awareness and diagnostic efforts. Furthermore, our study revealed a higher carrier frequency of PLA2G6 variants in African and Asian populations, stressing the importance of expanded genetic sequencing in non-European populations to ensure accurate and comprehensive diagnosis. Future research should focus on confirming our findings and implementing expanded sequencing strategies to facilitate maximal and accurate diagnosis, particularly in non-European populations.

Orphanet Journal of Rare DiseasesVol. 19(1)
Broad Institute (US), Center for Genomic Science (IT)
Openalex Percentile: Top 13%
Neurological diseases and metabolism
1.98
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.