Wolfgang Hofmeister

Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation

Daniel Nilsson, Maria Pettersson, Peter Gustavsson et al. · Human Mutation · 2016 · 78 citations · Full text

Cytogenetics, Genetics, Genomic Mechanism +16

Different mutations in <i>PDE4D</i> associated with developmental disorders with mirror phenotypes

Anna Lindstrand, Giedré Grigelioniené, Daniel Nilsson et al. · Journal of Medical Genetics · 2013 · 64 citations

<i>CTNND2</i>—a candidate gene for reading problems and mild intellectual disability

Wolfgang Hofmeister, Daniel Nilsson, Alexandra Topa et al. · Journal of Medical Genetics · 2014 · 42 citations

Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies

Anna Hammarsjö, Z. Wang, Raquel Vaz et al. · Scientific Reports · 2017 · 35 citations · Full text

WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish

Izabella Baranowska Körberg, Wolfgang Hofmeister, Ellen Markljung et al. · Human Molecular Genetics · 2015 · 30 citations · Full text

Cloaca Development, Genetics, Genetic Epidemiology +21