| Year |
Citation |
Score |
| 2022 |
Khrystoforova I, Shochat-Carvalho C, Harari R, Henke K, Woronowicz K, Harris MP, Karasik D. Zebrafish mutants reveal unexpected role of Lrp5 in osteoclast regulation. Frontiers in Endocrinology. 13: 985304. PMID 36120446 DOI: 10.3389/fendo.2022.985304 |
0.645 |
|
| 2022 |
Meyer-Miner A, Van Gennip JLM, Henke K, Harris MP, Ciruna B. Resolving primary pathomechanisms driving idiopathic-like spinal curvature using a new scoliosis model. Iscience. 25: 105028. PMID 36105588 DOI: 10.1016/j.isci.2022.105028 |
0.613 |
|
| 2021 |
Hawkins MB, Henke K, Harris MP. Latent developmental potential to form limb-like skeletal structures in zebrafish. Cell. PMID 33545089 DOI: 10.1016/j.cell.2021.01.003 |
0.673 |
|
| 2020 |
Peskin B, Henke K, Cumplido N, Treaster S, Harris MP, Bagnat M, Arratia G. Notochordal Signals Establish Phylogenetic Identity of the Teleost Spine. Current Biology : Cb. PMID 32559448 DOI: 10.1016/J.Cub.2020.05.037 |
0.722 |
|
| 2020 |
Caetano-Lopes J, Henke K, Urso K, Duryea J, Charles JF, Warman ML, Harris MP. Correction: Unique and non-redundant function of paralogues in regulation and evolution of post-embryonic development of the zebrafish. Development (Cambridge, England). 147. PMID 32423978 DOI: 10.1242/dev.192211 |
0.624 |
|
| 2020 |
Rose CD, Pompili D, Henke K, Van Gennip JLM, Meyer-Miner A, Rana R, Gobron S, Harris MP, Nitz M, Ciruna B. SCO-Spondin Defects and Neuroinflammation Are Conserved Mechanisms Driving Spinal Deformity across Genetic Models of Idiopathic Scoliosis. Current Biology : Cb. PMID 32386528 DOI: 10.1016/J.Cub.2020.04.020 |
0.656 |
|
| 2020 |
Coulter ME, Musaev D, DeGennaro EM, Zhang X, Henke K, James KN, Smith RS, Hill RS, Partlow JN, Muna Al-Saffar, Kamumbu AS, Hatem N, Barkovich AJ, Aziza J, Chassaing N, et al. Regulation of human cerebral cortical development by EXOC7 and EXOC8, components of the exocyst complex, and roles in neural progenitor cell proliferation and survival. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32103185 DOI: 10.1038/S41436-020-0758-9 |
0.593 |
|
| 2020 |
Li C, Barton C, Henke K, Daane J, Treaster S, Caetano-Lopez J, Tanguay RL, Harris M. Celsr1a is essential for tissue homeostasis and onset of aging phenotypes in the zebrafish. Elife. 9. PMID 31985398 DOI: 10.7554/Elife.50523 |
0.628 |
|
| 2020 |
Caetano-Lopes J, Henke K, Urso K, Duryea J, Charles JF, Warman ML, Harris MP. Unique and non-redundant function of paralogues in regulation and evolution of post-embryonic development of the zebrafish. Development (Cambridge, England). PMID 31932352 DOI: 10.1242/Dev.181834 |
0.658 |
|
| 2019 |
Webster KA, Henke K, Ingalls DM, Nahrin A, Harris MP, Siegfried KR. Cyclin-dependent kinase 21 is a novel regulator of proliferation and meiosis in the male germ line of zebrafish. Reproduction (Cambridge, England). PMID 30763280 DOI: 10.1530/Rep-18-0386 |
0.627 |
|
| 2018 |
Gistelinck C, Kwon RY, Malfait F, Symoens S, Harris MP, Henke K, Hawkins MB, Fisher S, Sips P, Guillemyn B, Bek JW, Vermassen P, De Saffel H, Witten PE, Weis M, et al. Zebrafish type I collagen mutants faithfully recapitulate human type I collagenopathies. Proceedings of the National Academy of Sciences of the United States of America. PMID 30082390 DOI: 10.1073/Pnas.1722200115 |
0.639 |
|
| 2017 |
Henke K, Daane JM, Hawkins MB, Dooley CM, Busch-Nentwich EM, Stemple DL, Harris MP. Genetic Screen for Post-embryonic Development in the Zebrafish (Danio rerio): Dominant Mutations Affecting Adult Form. Genetics. PMID 28835471 DOI: 10.1534/Genetics.117.300187 |
0.678 |
|
| 2017 |
Charles JF, Sury M, Tsang K, Urso K, Henke K, Huang Y, Russell R, Duryea J, Harris MP. Utility of quantitative micro-computed tomographic analysis in zebrafish to define gene function during skeletogenesis. Bone. PMID 28476577 DOI: 10.1016/J.Bone.2017.05.001 |
0.64 |
|
| 2014 |
Hu WF, Pomp O, Ben-Omran T, Kodani A, Henke K, Mochida GH, Yu TW, Woodworth MB, Bonnard C, Raj GS, Tan TT, Hamamy H, Masri A, Shboul M, Al Saffar M, et al. Katanin p80 regulates human cortical development by limiting centriole and cilia number. Neuron. 84: 1240-57. PMID 25521379 DOI: 10.1016/J.Neuron.2014.12.017 |
0.667 |
|
| 2013 |
Henke K, Bowen ME, Harris MP. Identification of mutations in zebrafish using next-generation sequencing. Current Protocols in Molecular Biology / Edited by Frederick M. Ausubel ... [Et Al.]. 104: Unit 7.13. PMID 24510885 DOI: 10.1002/0471142727.Mb0713S104 |
0.61 |
|
| 2013 |
Henke K, Bowen ME, Harris MP. Perspectives for identification of mutations in the zebrafish: making use of next-generation sequencing technologies for forward genetic approaches. Methods (San Diego, Calif.). 62: 185-96. PMID 23748111 DOI: 10.1016/J.Ymeth.2013.05.015 |
0.638 |
|
| 2012 |
Dauber A, Lafranchi SH, Maliga Z, Lui JC, Moon JE, McDeed C, Henke K, Zonana J, Kingman GA, Pers TH, Baron J, Rosenfeld RG, Hirschhorn JN, Harris MP, Hwa V. Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein ninein. The Journal of Clinical Endocrinology and Metabolism. 97: E2140-51. PMID 22933543 DOI: 10.1210/Jc.2012-2150 |
0.6 |
|
| 2012 |
Bowen ME, Henke K, Siegfried KR, Warman ML, Harris MP. Efficient mapping and cloning of mutations in zebrafish by low-coverage whole-genome sequencing. Genetics. 190: 1017-24. PMID 22174069 DOI: 10.1534/Genetics.111.136069 |
0.654 |
|
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