Genome Medicine
ISSN: 1756-994X
Publisher: BMC
Publications (12)
Glioblastoma-instructed microglia transition to heterogeneous phenotypic states with phagocytic and dendritic cell-like features in patient tumors and patient-derived orthotopic xenografts (2024)
Yabo YA, Moreno-Sanchez PM, Pires-Afonso Y, Kaoma T, Nosirov B, Scafidi A, Ermini L, et al.
Journal article
Spatially resolved transcriptomic profiles reveal unique defining molecular features of infiltrative 5ALA-metabolizing cells associated with glioblastoma recurrence (2023)
Andrieux G, Das T, Griffin M, Straehle J, Paine SM, Beck J, Boerries M, et al.
Journal article
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry (2023)
Mueller SH, Lai AG, Valkovskaya M, Michailidou K, Bolla MK, Wang Q, Dennis J, et al.
Journal article
Network reconstruction for trans acting genetic loci using multi-omics data and prior information (2022)
Hawe JS, Saha A, Waldenberger M, Kunze S, Wahl S, Mueller-Nurasyid M, Prokisch H, et al.
Journal article
Clinical implementation of RNA sequencing for Mendelian disease diagnostics (2022)
Yépez VA, Gusic M, Kopajtich R, Mertes C, Smith NH, Alston CL, Ban R, et al.
Journal article
A novel molecular signature identifies mixed subtypes in renal cell carcinoma with poor prognosis and independent response to immunotherapy (2022)
Buettner FA, Winter S, Stuehler V, Rausch S, Hennenlotter J, Füssel S, Zastrow S, et al.
Journal article
Breast cancer risks associated with missense variants in breast cancer susceptibility genes (2022)
Dorling L, Carvalho S, Allen J, Parsons MT, Fortuno C, Gonzalez-Neira A, Heijl SM, et al.
Journal article
Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders (2021)
Mannucci I, Dang NDP, Huber H, Murry JB, Abramson J, Althoff T, Banka S, et al.
Journal article
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders (2021)
Gillentine MA, Wang T, Hoekzema K, Rosenfeld J, Liu P, Guo H, Kim CN, et al.
Journal article
Investigation of a nonsense mutation located in the complex KIV-2 copy number variation region of apolipoprotein(a) in 10,910 individuals (2020)
Di Maio S, Grüneis R, Streiter G, Lamina C, Maglione M, Schoenherr S, Öfner D, et al.
Journal article