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: MLH1: 1358A>C

PubMed Link: 35982159

Variant Present in the following documents:

• 41588_2022_1148_MOESM5_ESM.xlsx, sheet 1

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Candidate SNP Markers of Atherogenesis Significantly Shifting the Affinity of TATA-Binding Protein for Human Gene Promoters show stabilizing Natural Selection as a Sum of Neutral Drift Accelerating Atherogenesis and Directional Natural Selection Slowing It.

International Journal Of Molecular Sciences

Ponomarenko, Mikhail M; Rasskazov, Dmitry D; Chadaeva, Irina I; Sharypova, Ekaterina E; Drachkova, Irina I; Oshchepkov, Dmitry D; Ponomarenko, Petr P; Savinkova, Ludmila L; Oshchepkova, Evgeniya E; Nazarenko, Maria M; Kolchanov, Nikolay N

Publication Date: 2020-02-05

Variant appearance in text: rs1424963586

PubMed Link: 32033288

Variant Present in the following documents:

• Main text
• ijms-21-01045.pdf

View BVdb publication page