Alzheimer's Disease
Genetics Consortium

ADGC Publications

Found 3 results

Filters: Author is Roeder, Kathryn [Clear All Filters]

2014

Samocha KE, Robinson EB, Sanders SJ, Stevens C, Sabo A, McGrath LM, Kosmicki JA, Rehnström K, Mallick S, Kirby A et al.. 2014. A framework for the interpretation of de novo mutation in human disease.. Nat Genet. 46(9):944-50.

2013

Schafer CM, Campbell NG, Cai G, Yu F, Makarov V, Yoon S, Daly MJ, Gibbs RA, Schellenberg GD, Devlin B et al.. 2013. Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.. Genomics. 102(4):270-7.

2012

Whitcomb DC, LaRusch J, Krasinskas AM, Klei L, Smith JP, Brand RE, Neoptolemos JP, Lerch MM, Tector M, Sandhu BS et al.. 2012. Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis.. Nat Genet. 44(12):1349-54.