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 | 110 | 2019 |
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 | 65 | 2017 |
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 | 62 | 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 | 48 | 2015 |
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 | 32 | 2015 |
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 | 30 | 2017 |
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 | 19 | 2014 |
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 | 18 | 2018 |
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 | 16 | 2012 |
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 | 15 | 2018 |
Frizzled-3a and Wnt-8b genetically interact during forebrain commissural formation in embryonic zebrafish W Hofmeister, B Key Brain research 1506, 25-34, 2013 | 15 | 2013 |
A morphogenetic EphB/EphrinB code controls hepatopancreatic duct formation MI Thestrup, S Caviglia, J Cayuso, RLS Heyne, R Ahmad, W Hofmeister, ... Nature Communications 10 (1), 5220, 2019 | 14 | 2019 |
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 | 13 | 2013 |
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 7 (6), e666, 2019 | 10 | 2019 |
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 | 8 | 2012 |
A systematic exposition of methods used for quantification of heart regeneration after apex resection in zebrafish H Juul Belling, W Hofmeister, DC Andersen Cells 9 (3), 548, 2020 | 7 | 2020 |
Apex Resection in Zebrafish (Danio rerio) as a Model of Heart Regeneration: A Video-Assisted Guide DG Ellman, IM Slaiman, SB Mathiesen, KS Andersen, W Hofmeister, ... International Journal of Molecular Sciences 22 (11), 5865, 2021 | 6 | 2021 |
Loss of ctnnd2b affects neuronal differentiation and behavior in zebrafish R Vaz, S Edwards, A Dueñas-Rey, W Hofmeister, A Lindstrand Frontiers in Neuroscience 17, 1205653, 2023 | 2 | 2023 |
Loss of zebrafish ctnnd2b results in disorganised forebrain neuron clusters W Hofmeister, R Vaz, S Edwards, A Dueñas Rey, A Lindstrand bioRxiv, 420828, 2018 | 1 | 2018 |
Intragenic deletion of WDR63 results in a dominant negative ciliopathy disorder W Hofmeister, D Kurtoglo, M Pettersson, M Armenio, J Eisfeldt, ... EUROPEAN JOURNAL OF HUMAN GENETICS 26, 510-511, 2018 | | 2018 |