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BMC Medical Genomics|May 16, 2020
ERα-related chromothripsis enhances concordant gene transcription on chromosome 17q11.1-q24.1 in luminal breast cancerChun-Lin Lin, Xi Tan, Meizhen Chen, et al.
BMC Medical Genomics|August 2, 2022
Candidate genes for infertility: an in-silico study based on cytogenetic analysisJatinder Singh Sahota, Bhavna Sharma, Kamlesh Guleria, et al.
BMC Medical Genomics|September 19, 2021
Ethnicity-stratified analysis of the association between XRCC3 Thr241Met polymorphism and leukemia: an updated meta-analysisZhengjun Xie, Wei Peng, Qiuhua Li, et al.
BMC Medical Genomics|August 5, 2022
Distinct non-clock-like signatures of the basal cell carcinomas from three sisters with a lethal Gorlin-Goltz syndromeLihua Ye, Li Wang, Kexin Peng, et al.
BMC Medical Genomics|August 5, 2022
Association of IKZF1 and CDKN2A gene polymorphisms with childhood acute lymphoblastic leukemia: a high-resolution melting analysisMahla Sattarzadeh Bardsiri, Shahrzad Zehtab, Najibe Karami, et al.
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.
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