Back
Top 0.4%
21.7%
Top 13%
11.6%
Top 2%
7.6%
Top 19%
5.8%
Top 3%
5.8%
Top 0.3%
4.9%
Top 0.4%
4.1%
Top 0.2%
3.8%
Top 89%
3.1%
Top 4%
3.0%
Top 2%
2.7%
Top 7%
1.5%
Top 3%
1.5%
Top 0.9%
1.5%
Top 7%
1.5%
Top 5%
1.5%
Top 5%
1.3%
Top 4%
0.9%
Top 9%
0.9%
Top 21%
0.7%
Top 4%
0.7%
Top 11%
0.7%
Top 8%
0.7%
A Phenotypic Paradigm for Cerebral Palsy Genetics
2026-01-18
genetic and genomic medicine
Title + abstract only
View on medRxiv
Show abstract
Disease-causing genetic variants can be found in a subset of individuals with cerebral palsy (CP), with variants deemed causal of CP having been published for at least 515 genes. We develop a statistical approach that treats CP as a phenotypic feature for which some genetic disorders confer an increased risk. Based on comprehensive literature curation we show that the null hypothesis of no CP association can be rejected for only 89 of the 515 genes. We applied these findings to the analysis of a...
Predicted journal destinations
1
Genetics in Medicine
57 training papers
2
Scientific Reports
701 training papers
3
The American Journal of Human Genetics
77 training papers
4
Nature Communications
483 training papers
5
Nature Genetics
72 training papers
6
Human Genetics and Genomics Advances
39 training papers
7
European Journal of Human Genetics
25 training papers
8
Journal of Medical Genetics
22 training papers
9
PLOS ONE
1737 training papers
10
Genome Medicine
56 training papers
11
PLOS Genetics
39 training papers
12
Translational Psychiatry
94 training papers
13
Human Molecular Genetics
28 training papers
14
npj Genomic Medicine
18 training papers
15
Brain
69 training papers
16
Cell Genomics
34 training papers
17
Frontiers in Genetics
32 training papers
18
Genes
21 training papers
19
Molecular Psychiatry
84 training papers
20
Proceedings of the National Academy of Sciences
100 training papers
21
Bioinformatics
24 training papers
22
Nature
58 training papers
23
Movement Disorders
49 training papers