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BMC Medical Genomics|June 28, 2021
Association between STAT4 gene polymorphism and type 2 diabetes risk in Chinese Han populationJiaqi Cui, Rui Tong, Jing Xu, et al.
BMC Medical Genomics|July 11, 2021
Genetic susceptibility to multiple sclerosis: interactions between conserved extended haplotypes of the MHC and other susceptibility regionsD S Goodin, P Khankhanian, P A Gourraud, et al.
BMC Medical Genomics|July 12, 2021
Diagnostic challenges in a CMMRD patient with a novel mutation in the PMS2 gene: a case reportShiqing Tan, Xiaoting Wu, Aoxue Wang, et al.
BMC Medical Genomics|June 14, 2021
Novel combined variants of WT1 and TET2 in a refractory and recurrent AML patientQiang Ma, Yixian Guo, Xiaoxi Lan, et al.
BMC Medical Genomics|June 13, 2021
Bi-allelic variants in MTMR5/SBF1 cause Charcot-Marie-Tooth type 4B3 featuring mitochondrial dysfunctionBeatrice Berti, Giovanna Longo, Francesco Mari, et al.
BMC Medical Genomics|June 15, 2021
New familial cases of karyomegalic interstitial nephritis with mutations in the FAN1 geneImen Rejeb, Mouna Jerbi, Houweyda Jilani, et al.
BMC Medical Genomics|May 21, 2022
Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK BiobankKatherine A Fawcett, German Demidov, Nick Shrine, et al.
BMC Medical Genomics|May 13, 2022
The correlation between promoter hypermethylation of VDR, CLDN, and CasR genes and recurrent stone formationFatemeh Khatami, Alireza Gorji, Mahdi Khoshchehreh, et al.
BMC Medical Genomics|May 13, 2022
Identifying key genes and functionally enriched pathways in Th2-high asthma by weighted gene co-expression network analysisYao Cao, Yi Wu, Li Lin, et al.
BMC Medical Genomics|May 16, 2022
Identification of a novel CNV at the EYA4 gene in a Chinese family with autosomal dominant nonsyndromic hearing lossWeixun Zhang, Jing Song, Busheng Tong, et al.
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