Author Search Results

1

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

Published 2019

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

Published 2014

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

Published 2016

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4

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

Published 2020

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

Published 2021

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

Published 2011

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7

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

Published 2012

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8

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

Published 2021

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9

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

Published 2014

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10

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

Published 2017

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11

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

Published 2017

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12

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

Published 2022

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13

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

Published 2014

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14

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

Published 2008

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15

A novel marine nitrite-oxidizing Nitrospira species from Dutch coastal North Sea water by 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.

Published 2013

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16

Syndromic X-linked intellectual disability segregating with a missense variant in RLIM by 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

Published 2015

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17

Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation by 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

Published 2015

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18

Progressive multifocal leukoencephalopathy in an immunocompetent patient by 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.

Published 2016

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19

Ultra-sensitive Sequencing Identifies High Prevalence of Clonal Hematopoiesis-Associated Mutations throughout Adult Life by 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

Published 2017

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20

Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis by 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.

Published 2014

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Search Results - Hoischen, Alexander

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

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

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

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

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

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

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

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

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

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

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

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

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

A novel marine nitrite-oxidizing Nitrospira species from Dutch coastal North Sea water by 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.

Syndromic X-linked intellectual disability segregating with a missense variant in RLIM by 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

Post-zygotic Point Mutations Are an Underrecognized Source of De Novo Genomic Variation by 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

Progressive multifocal leukoencephalopathy in an immunocompetent patient by 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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