Publications:

Integrating de novo and inherited variants in 42,607 autism cases identifies mutations in new moderate-risk genes.

Nature Genetics

Zhou, Xueya X; Feliciano, Pamela P; Shu, Chang C; Wang, Tianyun T; Astrovskaya, Irina I; Hall, Jacob B JB; Obiajulu, Joseph U JU; Wright, Jessica R JR; Murali, Shwetha C SC; Xu, Simon Xuming SX; Brueggeman, Leo L; Thomas, Taylor R TR; Marchenko, Olena O; Fleisch, Christopher C; Barns, Sarah D SD; Snyder, LeeAnne Green LG; Han, Bing B; Chang, Timothy S TS; Turner, Tychele N TN; Harvey, William T WT; Nishida, Andrew A; O'Roak, Brian J BJ; Geschwind, Daniel H DH; , ; Michaelson, Jacob J JJ; Volfovsky, Natalia N; Eichler, Evan E EE; Shen, Yufeng Y; Chung, Wendy K WK

Publication Date: 2022-09

Variant appearance in text: LRP1: 77C>A; T26N

PubMed Link: 35982159

Variant Present in the following documents:

• 41588_2022_1148_MOESM5_ESM.xlsx, sheet 1

View BVdb publication page

Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome.

Bmc Medical Genetics

Morgan, Thomas M TM; Xiao, Lan L; Lyons, Patrick P; Kassebaum, Bethany B; Krumholz, Harlan M HM; Spertus, John A JA

Publication Date: 2008-07-12

Variant appearance in text: LRP1: Thr26Asn

PubMed Link: 18620593

Variant Present in the following documents:

• Main text
• 1471-2350-9-66.pdf

View BVdb publication page