Wolfgang Hofmeister
TitleCited byYear
Different mutations in PDE4D associated with developmental disorders with mirror phenotypes
A Lindstrand, G Grigelioniene, D Nilsson, M Pettersson, W Hofmeister, ...
Journal of medical genetics 51 (1), 45-54, 2014
CTNND2—a candidate gene for reading problems and mild intellectual disability
W Hofmeister, D Nilsson, A Topa, BM Anderlid, F Darki, H Matsson, ...
Journal of medical genetics 52 (2), 111-122, 2015
Whole‐genome sequencing of cytogenetically balanced chromosome translocations identifies potentially pathological gene disruptions and highlights the importance of …
D Nilsson, M Pettersson, P Gustavsson, A Förster, W Hofmeister, ...
Human mutation 38 (2), 180-192, 2017
WNT3 involvement in human bladder exstrophy and cloaca development in zebrafish
I Baranowska Körberg, W Hofmeister, E Markljung, J Cao, D Nilsson, ...
Human molecular genetics 24 (18), 5069-5078, 2015
Frizzled-3a and slit2 genetically interact to modulate midline axon crossing in the telencephalon
W Hofmeister, CA Devine, JA Rothnagel, B Key
Mechanisms of development 129 (5-8), 109-124, 2012
Identification of three novel FGF16 mutations in X‐linked recessive fusion of the fourth and fifth metacarpals and possible correlation with heart disease
T Laurell, D Nilsson, W Hofmeister, A Lindstrand, N Ahituv, J Vandermeer, ...
Molecular genetics & genomic medicine 2 (5), 402-411, 2014
Frizzled-3a and Wnt-8b genetically interact during forebrain commissural formation in embryonic zebrafish
W Hofmeister, B Key
Brain research 1506, 25-34, 2013
Distinct expression patterns of syndecans in the embryonic zebrafish brain
W Hofmeister, CA Devine, B Key
Gene Expression Patterns 13 (3-4), 126-132, 2013
Novel KIAA0753 mutations extend the phenotype of skeletal ciliopathies
A Hammarsjö, Z Wang, R Vaz, F Taylan, M Sedghi, KM Girisha, ...
Scientific reports 7 (1), 15585, 2017
Chemoattractant axon guidance cues regulate de novo axon trajectories in the embryonic forebrain of zebrafish
A Gaudin, W Hofmeister, B Key
Developmental biology 367 (2), 126-139, 2012
Targeted copy number screening highlights an intragenic deletion of WDR63 as the likely cause of human occipital encephalocele and abnormal CNS …
W Hofmeister, M Pettersson, D Kurtoglu, M Armenio, J Eisfeldt, ...
Human mutation 39 (4), 495-505, 2018
Further support linking the 22q11.2 microduplication to an increased risk of bladder exstrophy and highlighting LZTR1 as a candidate gene
J Lundin, E Markljung, I Baranowska Körberg, W Hofmeister, J Cao, ...
Molecular genetics & genomic medicine, e666, 2019
Zebrafish Models of Neurodevelopmental Disorders: Limitations and Benefits of Current Tools and Techniques
R Vaz, W Hofmeister, A Lindstrand
International journal of molecular sciences 20 (6), 1296, 2019
Alu‐Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasias
M Pettersson, R Vaz, A Hammarsjö, J Eisfeldt, CMB Carvalho, ...
Human mutation 39 (10), 1456-1467, 2018
Loss of zebrafish ctnnd2b results in disorganised forebrain neuron clusters
W Hofmeister, R Vaz, S Edwards, AD Rey, A Lindstrand
bioRxiv, 420828, 2018
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