Back
Top 0.7%
16.5%
Top 1%
11.0%
#1
8.4%
Top 3%
6.0%
Top 21%
5.5%
Top 59%
4.7%
Top 0.4%
4.7%
Top 3%
4.7%
Top 0.5%
3.9%
Top 0.7%
3.6%
Top 0.3%
3.6%
Top 0.2%
2.8%
Top 4%
1.8%
Top 0.8%
1.8%
Top 2%
1.8%
Top 94%
1.8%
Top 7%
1.2%
Top 10%
0.9%
Top 48%
0.9%
Top 8%
0.7%
Top 11%
0.7%
Top 5%
0.7%
Top 8%
0.7%
Top 12%
0.7%
Rare genetic variants in SEC24D modify orofacial cleft phenotypes
2023-03-27
genetic and genomic medicine
Title + abstract only
View on medRxiv
Show abstract
As one of the most common structural birth defects, orofacial clefts (OFCs) have been studied for decades, and recent studies have demonstrated that there are genetic differences between the different phenotypic presentations of OFCs. However, the contribution of rare genetic variation genome-wide to different subtypes of OFCs has been understudied, with most studies focusing on common genetic variation or rare variation within targeted regions of the genome. Therefore, we used whole-genome sequ...
Predicted journal destinations
1
Genetics in Medicine
57 training papers
2
The American Journal of Human Genetics
77 training papers
3
Human Genetics and Genomics Advances
39 training papers
4
Nature Genetics
72 training papers
5
Nature Communications
483 training papers
6
Scientific Reports
701 training papers
7
PLOS Genetics
39 training papers
8
Genome Medicine
56 training papers
9
European Journal of Human Genetics
25 training papers
10
Human Molecular Genetics
28 training papers
11
Journal of Medical Genetics
22 training papers
12
npj Genomic Medicine
18 training papers
13
Cell Genomics
34 training papers
14
Genes
21 training papers
15
Frontiers in Genetics
32 training papers
16
PLOS ONE
1737 training papers
17
iScience
74 training papers
18
Translational Psychiatry
94 training papers
19
eLife
262 training papers
20
Cell Reports Medicine
49 training papers
21
Brain
69 training papers
22
Bioinformatics
24 training papers
23
International Journal of Molecular Sciences
39 training papers
24
Nature
58 training papers