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BMC Medical Genomics|September 4, 2021
RNA sequencing of blood in coronary artery disease: involvement of regulatory T cell imbalanceTimothy A McCaffrey, Ian Toma, Zhaoquing Yang, et al.
BMC Medical Genomics|May 9, 2015
Molecular genetics of human primary microcephaly: an overviewMuhammad Faheem, Muhammad Imran Naseer, Mahmood Rasool, et al.
BMC Medical Genomics|May 11, 2015
The cis and trans effects of the risk variants of coronary artery disease in the Chr9p21 regionWei Zhao, Jennifer A Smith, Guangmei Mao, et al.
BMC Medical Genomics|April 11, 2020
Prevalence of clinically actionable disease variants in exceptionally long-lived familiesPaige Carlson, Mary K Wojczynski, Todd Druley, et al.
BMC Medical Genomics|October 26, 2019
Gene-based analysis of ADHD using PASCAL: a biological insight into the novel associated genesAitana Alonso-Gonzalez, Manuel Calaza, Cristina Rodriguez-Fontenla, et al.
BMC Medical Genomics|October 25, 2019
A novel genomic panel as an adjunctive diagnostic tool for the characterization and profiling of breast Fibroepithelial lesionsYirong Sim, Gwendolene Xin Pei Ng, Cedric Chuan Young Ng, et al.
BMC Medical Genomics|August 13, 2021
Genetic basis of cannabis use: a systematic reviewAlannah Hillmer, Caroul Chawar, Stephanie Sanger, et al.
BMC Medical Genomics|August 28, 2021
Exome sequencing identifies novel and known mutations in families with intellectual disabilityMemoona Rasheed, Valeed Khan, Ricardo Harripaul, et al.
BMC Medical Genomics|November 18, 2021
Development and validation of an expanded targeted sequencing panel for non-invasive prenatal diagnosis of sporadic skeletal dysplasiaChing-Yuan Wang, Yen-An Tang, I-Wen Lee, et al.
BMC Medical Genomics|November 22, 2021
Noninvasive prenatal diagnosis of duchenne muscular dystrophy in five Chinese families based on relative mutation dosage approachGanye Zhao, Xiaofeng Wang, Lina Liu, et al.
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