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BMC Medical Genomics|June 20, 2022
A Japanese case of castration-resistant prostate cancer with BRCA2 and RB1 co-loss and TP53 mutation: a case reportTomohiro Iwasawa, Takeo Kosaka, Shinya Morita, et al.
BMC Medical Genomics|June 10, 2021
Unraveling synonymous and deep intronic variants causing aberrant splicing in two genetically undiagnosed epilepsy familiesQiang Li, Yiting Wang, Yijun Pan, et al.
BMC Medical Genomics|December 14, 2020
Identification of KRAS mutation in a patient with linear nevus sebaceous syndrome: a case reportChun Pan, Xiaowei Zhou, Anlan Hong, et al.
BMC Medical Genomics|January 8, 2021
Genome-wide survey of tandem repeats by nanopore sequencing shows that disease-associated repeats are more polymorphic in the general populationSatomi Mitsuhashi, Martin C Frith, Naomichi Matsumoto
BMC Medical Genomics|May 28, 2017
Quantitative analysis of cryptic splicing associated with TDP-43 depletionJack Humphrey, Warren Emmett, Pietro Fratta, et al.
BMC Medical Genomics|June 8, 2017
Identifying subtype-specific associations between gene expression and DNA methylation profiles in breast cancerGaram Lee, Lisa Bang, So Yeon Kim, et al.
BMC Medical Genomics|June 8, 2017
Taking promoters out of enhancers in sequence based predictions of tissue-specific mammalian enhancersJulia Herman-Izycka, Michal Wlasnowolski, Bartek Wilczynski
BMC Medical Genomics|September 15, 2016
Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cellsAndréanne Morin, Tony Kwan, Bing Ge, et al.
BMC Medical Genomics|February 6, 2022
A case report of pediatric acute lymphoblastic leukemia with e8a2 BCR/ABL1 fusion transcriptAleksandra Mroczkowska, Bożena Jaźwiec, Justyna Urbańska-Rakus, et al.
BMC Medical Genomics|October 22, 2021
Association between genetic variants of the cholinergic system and postoperative delirium and cognitive dysfunction in elderly patientsMaria Heinrich, Miriam Sieg, Jochen Kruppa, et al.
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