Timothy D. O’Brien

Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels

Zhongming Zhao, P. Jia, M. Landi, 2018, Genome Medicine.

Characterization of genome-wide association study data reveals spatiotemporal heterogeneity of mental disorders

Zhongming Zhao, P. Jia, Guangsheng Pei, 2020, BMC Medical Genomics.

Inconsistency and features of single nucleotide variants detected in whole exome sequencing versus transcriptome sequencing: A case study in lung cancer.

Junfeng Xia, Peilin Jia, William Pao, 2015, Methods.

Lung Cancer: One Disease or Many

Zhongming Zhao, P. Jia, M. Aldrich, 2018, Human Heredity.

Weak sharing of genetic association signals in three lung cancer subtypes: evidence at the SNP, gene, regulation, and pathway levels

Zhongming Zhao, P. Jia, M. Landi, 2018, Genome Medicine.

Artificial intelligence (AI)-assisted exome reanalysis greatly aids in the identification of new positive cases and reduces analysis time in a clinical diagnostic laboratory.

C. Richards, Amiee B. Potter, A. Kulkarni, 2021, Genetics in medicine : official journal of the American College of Medical Genetics.

Population screening shows risk of inherited cancer and familial hypercholesterolemia in Oregon.

Andrew C. Adey, Asia D. Mitchell, B. O’Roak, 2023, American journal of human genetics.

Missense variant in RBM10 associated with mild and non‐lethal form of TARP syndrome

C. Richards, Amiee B. Potter, A. Kulkarni, 2023, Clinical genetics.