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BMC Medical Genomics|October 25, 2008
A global transcriptional view of apoptosis in human T-cell activationMin Wang, Dirk Windgassen, Eleftherios T Papoutsakis
BMC Medical Genomics|August 27, 2020
Genome-wide association meta-analysis for early age-related macular degeneration highlights novel loci and insights for advanced diseaseThomas W Winkler, Felix Grassmann, Caroline Brandl, et al.
BMC Medical Genomics|March 27, 2021
Novel biallelic variant in BBS9 causative of Bardet-Biedl syndrome: expanding the spectrum of disease-causing genetic alterationsJulia Suárez-González, Verónica Seidel, Cristina Andrés-Zayas, et al.
BMC Medical Genomics|April 20, 2023
Genetic disorders and pregnancy outcomes of non-immune hydrops fetalis in a tertiary referral centerDanhua Guo, Shuqiong He, Na Lin, et al.
BMC Medical Genomics|April 24, 2023
Clinical and genetic characteristics of children with COX20-associated mitochondrial disorder: case report and literature reviewLiqing Chen, Yan Liu
BMC Medical Genomics|April 5, 2023
Implementation and evaluation of personal genetic testing as part of genomics analysis courses in German universitiesTamara Slosarek, Susanne Ibing, Barbara Schormair, et al.
BMC Medical Genomics|April 6, 2023
Genetic liability to age at first sex and birth in relation to cardiovascular diseases: a Mendelian randomization studyMiao Chen, Zhen Wang, Hongfei Xu, et al.
BMC Medical Genomics|August 19, 2020
Clinical, genomics and networking analyses of a high-altitude native American Ecuadorian patient with congenital insensitivity to pain with anhidrosis: a case reportAndrés López-Cortés, Ana Karina Zambrano, Patricia Guevara-Ramírez, et al.
BMC Medical Genomics|August 22, 2020
Breast and prostate cancers harbor common somatic copy number alterations that consistently differ by race and are associated with survivalYalei Chen, Sudha M Sadasivan, Ruicong She, et al.
BMC Medical Genomics|May 1, 2023
The genetic landscape of inherited retinal dystrophies in ArabsLama Jaffal, Hawraa Joumaa, Jinane Noureldine, et al.
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