Showing 1 - 20 results of 23 for search 'T. Haer', query time: 0.06s
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Law, Story and Boundaries of Difference in Bringing Them Home by Steven de Haer
Published 2013-06-01
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A spatially-dependent synthetic global dataset of extreme sea level events by Huazhi Li, Toon Haer, Anaïs Couasnon, Alejandra R. Enríquez, Sanne Muis, Philip J. Ward
Published 2023-09-01
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Solenoidal Micromagnetic Stimulation Enables Activation of Axons With Specific Orientation by Laleh Golestanirad, Laleh Golestanirad, John T. Gale, Nauman F. Manzoor, Nauman F. Manzoor, Hyun-Joo Park, Lyall Glait, Lyall Glait, Frederick Haer, James A. Kaltenbach, Giorgio Bonmassar, Giorgio Bonmassar
Published 2018-07-01
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Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation by Wouter Steyaert, Lonneke Haer-Wigman, Rolph Pfundt, Debby Hellebrekers, Marloes Steehouwer, Juliet Hampstead, Elke de Boer, Alexander Stegmann, Helger Yntema, Erik-Jan Kamsteeg, Han Brunner, Alexander Hoischen, Christian Gilissen
Published 2023-10-01
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Genotype and Phenotype Analyses of a Novel <i>WFS1</i> Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38 by Hedwig M. Velde, Xanne J. J. Huizenga, Helger G. Yntema, Lonneke Haer-Wigman, Andy J. Beynon, Jaap Oostrik, Sjoert A. H. Pegge, Hannie Kremer, Cris P. Lanting, Ronald J. E. Pennings
Published 2023-02-01
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A coupled agent-based model to analyse human-drought feedbacks for agropastoralists in dryland regions by Ileen N. Streefkerk, Jens de Bruijn, Jens de Bruijn, Toon Haer, Anne F. Van Loon, Edisson A. Quichimbo, Marthe Wens, Khalid Hassaballah, Jeroen C. J. H. Aerts, Jeroen C. J. H. Aerts
Published 2023-01-01
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The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement by Graeme C. Black, Panagiotis Sergouniotis, Andrea Sodi, Bart P. Leroy, Caroline Van Cauwenbergh, Petra Liskova, Karen Grønskov, Artur Klett, Susanne Kohl, Gita Taurina, Marius Sukys, Lonneke Haer-Wigman, Katarzyna Nowomiejska, João Pedro Marques, Dorothée Leroux, Frans P. M. Cremers, Elfride De Baere, Hélène Dollfus, ERN-EYE study group
Published 2021-03-01
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Whole genome sequencing and in vitro splice assays reveal genetic causes for inherited retinal diseases by Zeinab Fadaie, Laura Whelan, Tamar Ben-Yosef, Adrian Dockery, Zelia Corradi, Christian Gilissen, Lonneke Haer-Wigman, Jordi Corominas, Galuh D. N. Astuti, Laura de Rooij, L. Ingeborgh van den Born, Caroline C. W. Klaver, Carel B. Hoyng, Niamh Wynne, Emma S. Duignan, Paul F. Kenna, Frans P. M. Cremers, G. Jane Farrar, Susanne Roosing
Published 2021-11-01
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