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BMC Medical Genomics|August 15, 2015
Design of a randomized controlled trial of disclosing genomic risk of coronary heart disease: the Myocardial Infarction Genes (MI-GENES) studyIftikhar J Kullo, Hayan Jouni, Janet E Olson, et al.
BMC Medical Genomics|August 17, 2015
Integrating microbial and host transcriptomics to characterize asthma-associated microbial communitiesEduardo Castro-Nallar, Ying Shen, Robert J Freishtat, et al.
BMC Medical Genomics|August 23, 2015
Development and verification of the PAM50-based Prosigna breast cancer gene signature assayBrett Wallden, James Storhoff, Torsten Nielsen, et al.
BMC Medical Genomics|May 1, 2019
LncRNA-miRNA-mRNA expression variation profile in the urine of calcium oxalate stone patientsXiongfa Liang, Yongchang Lai, Weizhou Wu, et al.
BMC Medical Genomics|September 27, 2018
Frequency and phenotype consequence of APOC3 rare variants in patients with very low triglyceride levelsDana C Crawford, Nicole A Restrepo, Kirsten E Diggins, et al.
BMC Medical Genomics|September 27, 2018
Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer's diseaseJason E Miller, Manu K Shivakumar, Younghee Lee, et al.
BMC Medical Genomics|May 11, 2019
Alternative cleavage and polyadenylation of genes associated with protein turnover and mitochondrial function are deregulated in Parkinson's, Alzheimer's and ALS diseaseRadhika Patel, Cillian Brophy, Mark Hickling, et al.
BMC Medical Genomics|May 18, 2019
NeoMutate: an ensemble machine learning framework for the prediction of somatic mutations in cancerIrantzu Anzar, Angelina Sverchkova, Richard Stratford, et al.
BMC Medical Genomics|October 18, 2018
Mitochondrial DNA 7908-8816 region mutations in maternally inherited essential hypertensive subjects in ChinaYe Zhu, Xiang Gu, Chao Xu
BMC Medical Genomics|April 27, 2018
WISARD: workbench for integrated superfast association studies for related datasetsSungyoung Lee, Sungkyoung Choi, Dandi Qiao, et al.
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