Associated Papers
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors.
Pankratz N et al.
Human Molecular Genetics, 2022
Somatic signature of brain-specific single nucleotide variations in sporadic Alzheimer's disease.
Parcerisas A et al.
Journal of Alzheimer's Disease : Jad, 2014
25024348 (PubMed )
Supplement: sj-xls-6-alz-10.3233_jad-140891.xls › P3H
Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels.
Antoni G et al.
Bmc Medical Genetics, 2011
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