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BMC Medical Genomics|July 30, 2022
PO2RDF: representation of real-world data for precision oncology using resource description frameworkYiqing Zhao, Anastasios Dimou, Feichen Shen, et al.
BMC Medical Genomics|April 16, 2022
Comment on Balsamo et al.: Birt-Hogg-Dubé syndrome with simultaneous hyperplastic polyposis of the gastrointestinal tract: case report and review of the literatureIrma van de Beek, Maurice A M van Steensel, Arjan C Houweling
BMC Medical Genomics|April 5, 2022
Expression profile of circRNA in peripheral blood mononuclear cells of patients with rheumatoid arthritisHuangxin Lu, Yifan Yang, Dong Kuang, et al.
BMC Medical Genomics|November 2, 2021
A KRT6A mutation p.Ile462Asn in a Chinese family with pachyonychia congenita, and identification of maternal mosaicism: a case reportYue Li, Yumeng Wang, Yan Ming, et al.
BMC Medical Genomics|January 25, 2022
Case-control study on TP73 rs1801173 C > T gene polymorphism and susceptibility to gastric cancer in a Chinese Han populationHuiwen Pan, Xuyu Gu, Xiaoyan Wang, et al.
BMC Medical Genomics|December 19, 2009
A taxonomy of epithelial human cancer and their metastasesOlivier Gevaert, Anneleen Daemen, Bart De Moor, et al.
BMC Medical Genomics|June 12, 2019
Comprehensive genomic characterization of breast tumors with BRCA1 and BRCA2 mutationsAvantika Lal, Daniele Ramazzotti, Ziming Weng, et al.
BMC Medical Genomics|June 13, 2014
On the identification of potential regulatory variants within genome wide association candidate SNP setsChih-Yu Chen, I-Shou Chang, Chao A Hsiung, et al.
BMC Medical Genomics|October 13, 2012
Defining the genomic signature of the parous breastSuraj Peri, Ricardo López de Cicco, Julia Santucci-Pereira, et al.
BMC Medical Genomics|September 1, 2021
Multiple malignant tumors in a patient with familial chordoma, a case reportNuttavut Sumransub, Paari Murugan, Shelly Marette, et al.
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