A high-resolution wind damage model for Europe

por Koks, E. E., Haer., T.
Publicado 2020

Analyzing the microfoundations of human violence in the DRC - intrinsic and extrinsic rewards and the prediction of appetitive aggression

por Haer, Roos, Banholzer, Lilli, Elbert, Thomas, Weierstall, Roland
Publicado 2013

Transcriptome-wide analysis of alternative mRNA splicing signature in the diagnosis and prognosis of stomach adenocarcinoma

por Shi, Yu, Chen, Zuhua, Gao, Juanjuan, Wu, Si, Gao, Haer, Feng, Guoshuang
Publicado 2018

Structure and compositional analysis of aluminum oxyhydroxide adsorbed pertussis vaccine

por Duprez, Jessica, Kalbfleisch, Kristen, Deshmukh, Sasmit, Payne, Jessie, Haer, Manjit, Williams, Wayne, Durowoju, Ibrahim, Kirkitadze, Marina
Publicado 2020

Solenoidal Micromagnetic Stimulation Enables Activation of Axons With Specific Orientation

por Golestanirad, Laleh, Gale, John T., Manzoor, Nauman F., Park, Hyun-Joo, Glait, Lyall, Haer, Frederick, Kaltenbach, James A., Bonmassar, Giorgio
Publicado 2018

The network structure of posttraumatic stress symptoms in war‐affected children and adolescents

por Scharpf, Florian, Saupe, Laura, Crombach, Anselm, Haer, Roos, Ibrahim, Hawkar, Neuner, Frank, Peltonen, Kirsi, Qouta, Samir, Saile, Regina, Hecker, Tobias
Publicado 2022

Percutaneous versus open pedicle screw instrumentation in treatment of thoracic and lumbar spine fractures: A systematic review and meta-analysis

por Tian, Feng, Tu, Lai-Yong, Gu, Wen-Fei, Zhang, En-Feng, Wang, Zhen-Bin, Chu, Ge, Ka, Haer, Zhao, Jiang
Publicado 2018

In-line monitoring of surfactant clearance in viral vaccine downstream processing

por Payne, Jessie, Cronin, James, Haer, Manjit, Krouse, Jason, Prosperi, William, Drolet-Vives, Katherine, Lieve, Matthew, Soika, Michael, Balmer, Matthew, Kirkitadze, Marina
Publicado 2021

A coupled agent-based model for France for simulating adaptation and migration decisions under future coastal flood risk

por Tierolf, Lars, Haer, Toon, Botzen, W. J. Wouter, de Bruijn, Jens A., Ton, Marijn J., Reimann, Lena, Aerts, Jeroen C. J. H.
Publicado 2023

Identification of a Complex Allele in IMPG2 as a Cause of Adult-Onset Vitelliform Macular Dystrophy

por Vázquez-Domínguez, Irene, Li, Catherina H. Z., Fadaie, Zeinab, Haer-Wigman, Lonneke, Cremers, Frans P. M., Garanto, Alejandro, Hoyng, Carel B., Roosing, Susanne
Publicado 2022

Robust and accurate detection and sizing of repeats within the DMPK gene using a novel TP-PCR test

por Leferink, Maike, Wong, Daphne P. W., Cai, Shiwei, Yeo, Minli, Ho, Jocelin, Lian, Mulias, Kamsteeg, Erik-Jan, Chong, Samuel S., Haer-Wigman, Lonneke, Guan, Ming
Publicado 2019

Hypoxia potentiates monocyte-derived dendritic cells for release of tumor necrosis factor α via MAP3K8

por Paardekooper, Laurent M., Bendix, Maura B., Ottria, Andrea, de Haer, Lieke W., ter Beest, Martin, Radstake, Timothy R.D.J., Marut, Wioleta, van den Bogaart, Geert
Publicado 2018

Systematic analysis of paralogous regions in 41,755 exomes uncovers clinically relevant variation

por Steyaert, Wouter, Haer-Wigman, Lonneke, Pfundt, Rolph, Hellebrekers, Debby, Steehouwer, Marloes, Hampstead, Juliet, de Boer, Elke, Stegmann, Alexander, Yntema, Helger, Kamsteeg, Erik-Jan, Brunner, Han, Hoischen, Alexander, Gilissen, Christian
Publicado 2023

Genotype and Phenotype Analyses of a Novel WFS1 Variant (c.2512C>T p.(Pro838Ser)) Associated with DFNA6/14/38

por Velde, Hedwig M., Huizenga, Xanne J. J., Yntema, Helger G., Haer-Wigman, Lonneke, Beynon, Andy J., Oostrik, Jaap, Pegge, Sjoert A. H., Kremer, Hannie, Lanting, Cris P., Pennings, Ronald J. E.
Publicado 2023

An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS

por Tracewska-Siemiątkowska, Anna, Haer-Wigman, Lonneke, Bosch, Danielle G. M., Nickerson, Deborah, Bamshad, Michael J., van de Vorst, Maartje, Rendtorff, Nanna Dahl, Möller, Claes, Kjellström, Ulrika, Andréasson, Sten, Cremers, Frans P. M., Tranebjærg, Lisbeth
Publicado 2017

Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals

por van der Schoot, Vyne, Haer-Wigman, Lonneke, Feenstra, Ilse, Tammer, Femke, Oerlemans, Anke J. M., van Koolwijk, Martine P. A., van Agt, Frans, Arens, Yvonne H. J. M., Brunner, Han G., Vissers, Lisenka E. L. M., Yntema, Helger G.
Publicado 2021

Long-read technologies identify a hidden inverted duplication in a family with choroideremia

por Fadaie, Zeinab, Neveling, Kornelia, Mantere, Tuomo, Derks, Ronny, Haer-Wigman, Lonneke, den Ouden, Amber, Kwint, Michael, O’Gorman, Luke, Valkenburg, Dyon, Hoyng, Carel B., Gilissen, Christian, Vissers, Lisenka E.L.M., Nelen, Marcel, Cremers, Frans P.M., Hoischen, Alexander, Roosing, Susanne
Publicado 2021

The need for widely available genomic testing in rare eye diseases: an ERN-EYE position statement

por Black, Graeme C., Sergouniotis, Panagiotis, Sodi, Andrea, Leroy, Bart P., Van Cauwenbergh, Caroline, Liskova, Petra, Grønskov, Karen, Klett, Artur, Kohl, Susanne, Taurina, Gita, Sukys, Marius, Haer-Wigman, Lonneke, Nowomiejska, Katarzyna, Marques, João Pedro, Leroux, Dorothée, Cremers, Frans P. M., De Baere, Elfride, Dollfus, Hélène
Publicado 2021

Diagnostic analysis of the highly complex OPN1LW/OPN1MW gene cluster using long-read sequencing and MLPA

por Haer-Wigman, Lonneke, den Ouden, Amber, van Genderen, Maria M., Kroes, Hester Y., Verheij, Joke, Smailhodzic, Dzenita, Hoekstra, Attje S., Vijzelaar, Raymon, Blom, Jan, Derks, Ronny, Tjon-Pon-Fong, Menno, Yntema, Helger G., Nelen, Marcel R., Vissers, Lisenka E.L.M., Lugtenberg, Dorien, Neveling, Kornelia
Publicado 2022

Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT)

por Haer-Wigman, Lonneke, Newman, Hadas, Leibu, Rina, Bax, Nathalie M., Baris, Hagit N, Rizel, Leah, Banin, Eyal, Massarweh, Amir, Roosing, Susanne, Lefeber, Dirk J., Zonneveld-Vrieling, Marijke N., Isakov, Ofer, Shomron, Noam, Sharon, Dror, Den Hollander, Anneke I., Hoyng, Carel B., Cremers, Frans P.M., Ben-Yosef, Tamar
Publicado 2015