Ohcanbohtosat - Hoischen, Alexander

Long-Read Sequencing Emerging in Medical Genetics Dahkki Mantere, Tuomo, Kersten, Simone, Hoischen, Alexander

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Prioritization of neurodevelopmental disease genes by discovery of new mutations Dahkki Hoischen, Alexander, Krumm, Niklas, Eichler, Evan E.

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New insights into the generation and role of de novo mutations in health and disease Dahkki Acuna-Hidalgo, Rocio, Veltman, Joris A., Hoischen, Alexander

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Postzygotic mosaicism in cerebral cavernous malformation Dahkki Rath, Matthias, Pagenstecher, Axel, Hoischen, Alexander, Felbor, Ute

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Solving the unsolved rare diseases in Europe Dahkki Graessner, Holm, Zurek, Birte, Hoischen, Alexander, Beltran, Sergi

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Unlocking Mendelian disease using exome sequencing Dahkki Gilissen, Christian, Hoischen, Alexander, Brunner, Han G, Veltman, Joris A

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Disease gene identification strategies for exome sequencing Dahkki Gilissen, Christian, Hoischen, Alexander, Brunner, Han G, Veltman, Joris A

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Next-Generation Sequencing in the Field of Primary Immunodeficiencies: Current Yield, Challenges, and Future Perspectives Dahkki Vorsteveld, Emil E., Hoischen, Alexander, van der Made, Caspar I.

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Shotgun metagenomic data reveals significant abundance but low diversity of “Candidatus Scalindua” marine anammox bacteria in the Arabian Sea oxygen minimum zone Dahkki Villanueva, Laura, Speth, Daan R., van Alen, Theo, Hoischen, Alexander, Jetten, Mike S. M.

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Quantification of differential gene expression by multiplexed targeted resequencing of cDNA Dahkki Arts, Peer, van der Raadt, Jori, van Gestel, Sebastianus H.C., Steehouwer, Marloes, Shendure, Jay, Hoischen, Alexander, Albers, Cornelis A.

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Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment Dahkki Chen, Xiaowei Sylvia, Reader, Rose H., Hoischen, Alexander, Veltman, Joris A., Simpson, Nuala H., Francks, Clyde, Newbury, Dianne F., Fisher, Simon E.

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Circulating interleukin-37 declines with aging in healthy humans: relations to healthspan indicators and IL37 gene SNPs Dahkki Brunt, Vienna E., Ikoba, Akpevweoghene P., Ziemba, Brian P., Ballak, Dov B., Hoischen, Alexander, Dinarello, Charles A., Ehringer, Marissa A., Seals, Douglas R.

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Cantú Syndrome Resulting from Activating Mutation in the KCNJ8 Gene Dahkki Cooper, Paige E., Reutter, Heiko, Woelfle, Joachim, Engels, Hartmut, Grange, Dorothy K., van Haaften, Gijs, van Bon, Bregje W., Hoischen, Alexander, Nichols, Colin G.

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Comprehensive Characterization of Genomic Aberrations in Gangliogliomas by CGH, Array‐based CGH and Interphase FISH Dahkki Hoischen, Alexander, Ehrler, Marion, Fassunke, Jana, Simon, Matthias, Baudis, Michael, Landwehr, Christina, Radlwimmer, Bernhard, Lichter, Peter, Schramm, Johannes, Becker, Albert J., Weber, Ruthild G.

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A novel marine nitrite-oxidizing Nitrospira species from Dutch coastal North Sea water Dahkki Haaijer, Suzanne C. M., Ji, Ke, van Niftrik, Laura, Hoischen, Alexander, Speth, Daan, Jetten, Mike S. M., Damsté, Jaap S. Sinninghe, Op den Camp, Huub J. M.

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Syndromic X-linked intellectual disability segregating with a missense variant in RLIM Dahkki Tønne, Elin, Holdhus, Rita, Stansberg, Christine, Stray-Pedersen, Asbjørg, Petersen, Kjell, Brunner, Han G, Gilissen, Christian, Hoischen, Alexander, Prescott, Trine, Steen, Vidar M, Fiskerstrand, Torunn

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Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation Dahkki Acuna-Hidalgo, Rocio, Bo, Tan, Kwint, Michael P., van de Vorst, Maartje, Pinelli, Michele, Veltman, Joris A., Hoischen, Alexander, Vissers, Lisenka E.L.M., Gilissen, Christian

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Progressive multifocal leukoencephalopathy in an immunocompetent patient Dahkki van der Kolk, Nicolien M., Arts, Peer, van Uden, Ingeborg W. M., Hoischen, Alexander, van de Veerdonk, Frank L., Netea, Mihai G., de Jong, Brigit A.

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Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life Dahkki Acuna-Hidalgo, Rocio, Sengul, Hilal, Steehouwer, Marloes, van de Vorst, Maartje, Vermeulen, Sita H., Kiemeney, Lambertus A.L.M., Veltman, Joris A., Gilissen, Christian, Hoischen, Alexander

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Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis Dahkki Cnossen, Wybrich R., te Morsche, René H. M., Hoischen, Alexander, Gilissen, Christian, Chrispijn, Melissa, Venselaar, Hanka, Mehdi, Soufi, Bergmann, Carsten, Veltman, Joris A., Drenth, Joost P. H.

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