Associated Papers
Whole exome sequencing of 28 families of Danish descent reveals novel candidate genes and pathways in developmental dysplasia of the hip.
Dembic M et al.
Molecular Genetics and Genomics : Mgg, 2023
36454308 (PubMed )
Supplement: 438_2022_1980_MOESM4_ESM.xlsx › List_of_genes
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementia.
Wightman DP et al.
Scientific Reports, 2023
36750708 (PubMed )
Supplement: 41598_2023_29108_MOESM1_ESM.xlsx › Supp_T11
Evidence against a role for rare ADAM10 mutations in sporadic Alzheimer disease.
Cai G et al.
Neurobiology of Aging, 2012
Computational analysis and molecular dynamics simulation of high-risk single nucleotide polymorphisms of the ADAM10 gene.
Namme JN et al.
Journal of Biomolecular Structure & Dynamics, 0
36995110 (PubMed )
Supplement: supplement_1.zip › suppl_data › Supplementary_file_1_423_nsSNPs_10_tools.xlsx › Sheet1
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