Institute of Human Genetics


close-button

Types of publications

Journal article
Book chapter / Article in edited volumes
Authored book
Translation
Thesis
Edited Volume
Conference contribution
Other publication type
Unpublished / Preprint

Publication year

From
To

Abstract

Journal

PAX5 biallelic genomic alterations define a novel subgroup of B-cell precursor acute lymphoblastic leukemia (2019) Bastian L, Schroeder MP, Eckert C, Schlee C, Tanchez JO, Kämpf S, Wagner DL, et al. Journal article Transcription factor Fra-1 targets arginase-1 to enhance macrophage-mediated inflammation in arthritis (2019) Hannemann N, Cao S, Eriksson D, Schnelzer A, Jordan J, Eberhardt M, Schleicher U, et al. Journal article Habituation Learning Is a Widely Affected Mechanism in Drosophila Models of Intellectual Disability and Autism Spectrum Disorders (2019) Fenckova M, Blok LE, Asztalos L, Goodman DP, Cizek P, Singgih EL, Glennon JC, et al. Journal article Loss of function of SVBP leads to autosomal recessive intellectual disability, microcephaly, ataxia, and hypotonia (2019) Iqbal Z, Tawamie H, Ba W, Reis A, Halak BA, Sticht H, Uebe S, et al. Journal article Mitochondrial DNA copy number is associated with mortality and infections in a large cohort of patients with chronic kidney disease (2019) Fazzini F, Lamina C, Fendt L, Schultheiss UT, Kotsis F, Hicks AA, Meiselbach H, et al. Journal article Delineation of MidXq28-duplication syndrome distal to MECP2 and proximal to RAB39B genes (2019) Sinibaldi L, Parisi V, Lanciotti S, Fontana P, Kuechler A, Baujat G, Torres B, et al. Journal article PEDIA: prioritization of exome data by image analysis (2019) Hsieh TC, Mensah MA, Pantel JT, Aguilar D, Bar O, Bayat A, Becerra-Solano L, et al. Journal article Evolutionary conserved networks of human height identify multiple Mendelian causes of short stature (2019) Hauer N, Popp B, Taher L, Vogl C, Dhandapany PS, Büttner C, Uebe S, et al. Journal article Macrophage phosphoproteome analysis reveals MINCLE-dependent and-independent mycobacterial cord factor signaling (2019) Hansen M, Peltier J, Killy B, Amin B, Bodendorfer B, HäRtlova A, Uebel S, et al. Journal article TRIM28 haploinsufficiency predisposes to Wilms tumor (2019) Diets IJ, Hoyer J, Ekici AB, Popp B, Hoogerbrugge N, van Reijmersdal SV, Bhaskaran R, et al. Journal article