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Alexander Hoischen

2006–2026 年に発表

158
論文数
22,827
被引用数
85
h 指数
149
i10 指数

被引用数

Alexander Hoischen の年別被引用数1986 年: 被引用 1 件1993 年: 被引用 1 件2002 年: 被引用 1 件2006 年: 被引用 1 件2007 年: 被引用 7 件2008 年: 被引用 17 件2009 年: 被引用 14 件2010 年: 被引用 60 件2011 年: 被引用 175 件2012 年: 被引用 249 件2013 年: 被引用 282 件2014 年: 被引用 316 件2015 年: 被引用 349 件2016 年: 被引用 349 件2017 年: 被引用 346 件2018 年: 被引用 291 件2019 年: 被引用 807 件2020 年: 被引用 905 件2021 年: 被引用 1,036 件2022 年: 被引用 773 件2023 年: 被引用 576 件2024 年: 被引用 823 件2025 年: 被引用 445 件2026 年: 被引用 14 件1987〜1992 年は被引用が無いため表示していません1994〜2001 年は被引用が無いため表示していません2003〜2005 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 3,086 件、この内訳の 21.7%イギリス: 引用元論文 1,162 件、この内訳の 8.2%オランダ: 引用元論文 991 件、この内訳の 7%ドイツ: 引用元論文 978 件、この内訳の 6.9%フランス: 引用元論文 708 件、この内訳の 5%中国: 引用元論文 691 件、この内訳の 4.8%イタリア: 引用元論文 623 件、この内訳の 4.4%カナダ: 引用元論文 595 件、この内訳の 4.2%オーストラリア: 引用元論文 492 件、この内訳の 3.4%スペイン: 引用元論文 417 件、この内訳の 2.9%ベルギー: 引用元論文 342 件、この内訳の 2.4%日本: 引用元論文 306 件、この内訳の 2.1%
0%21.7%その他 27%

機関

分野

  • Biochemistry, Genetics and Molecular Biology53.6%
  • Medicine31.4%
  • Immunology and Microbiology7.7%
  • Neuroscience5%
  • Agricultural and Biological Sciences0.7%
  • Psychology0.4%
  • その他1.2%

トピック

  • Genomics and Rare Diseases6.6%
  • Genomic variations and chromosomal abnormalities4.4%
  • Genetics and Neurodevelopmental Disorders4.2%
  • Cancer Genomics and Diagnostics2.3%
  • RNA modifications and cancer1.8%
  • Epigenetics and DNA Methylation1.5%
  • その他79.2%

共著者

全論文

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  1. Aberrant phase separation and nucleolar dysfunction in rare genetic diseases

    著者: Martin A. Mensah, Henri Niskanen, Alexandre P. Magalhães, Shaon Basu, Martin Kircher, Henrike L. Sczakiel, Alisa Maria Vittoria Reiter, Jonas Elsner, Peter Meinecke, Saskia Biskup, Brian Hon‐Yin Chung, Gregor Dombrowsky, Christel Eckmann-Scholz, Marc‐Phillip Hitz, Alexander Hoischen, Paul‐Martin Holterhus, Wiebke Hülsemann, Kimia Kahrizi, Vera M. Kalscheuer, Anita Sik Yau Kan, Mandy Krumbiegel, Ingo Kurth, Jonas Leubner, Ann Carolin Longardt, Jörg Detlev Moritz, Hossein Najmabadi, Karolina Skipalova, Lot Snijders Blok, Andreas Tzschach, Eberhard Wiedersberg, Martin Zenker, Carla Garcia‐Cabau, René Buschow, Xavier Salvatella, Matthew L. Kraushar, Stefan Mundlos, Almuth Caliebe, Malte Spielmann, Denise Horn, Denes Hnisz - Nature 2023 被引用: 152

  2. Adult-onset autoinflammation caused by somatic mutations in UBA1: A Dutch case series of patients with VEXAS

    著者: Caspar I. van der Made, Judith Potjewijd, Annemiek Hoogstins, Huub P J Willems, Arjan J. Kwakernaak, Ruud G.L. de Sévaux, Paul Van Daele, Annet Simons, Marloes W Heijstek, David B. Beck, Mihai G. Netea, Pieter van Paassen, A. Elizabeth Hak, Lars T. van der Veken, Mariëlle van Gijn, Alexander Hoischen, Frank L. van de Veerdonk, Helen L. Leavis, Abraham Rutgers - Journal of Allergy and Clinical Immunology 2021 被引用: 211

  3. Presence of Genetic Variants Among Young Men With Severe COVID-19

    著者: Caspar I. van der Made, Annet Simons, Janneke Schuurs-Hoeijmakers, Guus van den Heuvel, Tuomo Mantere, Simone Kersten, Rosanne C. van Deuren, Marloes Steehouwer, Simon V. van Reijmersdal, Martin Jaeger, Tom Hofste, Galuh Astuti, Jordi Corominas Galbany, Vyne van der Schoot, Hans van der Hoeven, Wanda Hagmolen of ten Have, Eva Klijn, Catrien van den Meer, Jeroen Fiddelaers, Quirijn de Mast, Chantal P. Bleeker‐Rovers, Leo A. B. Joosten, Helger G. Yntema, Christian Gilissen, Marcel Nelen, J.W.M. van der Meer, Han G. Brunner, Mihai G. Netea, Frank L. van de Veerdonk, Alexander Hoischen - JAMA 2020 被引用: 832

  4. Long-Read Sequencing Emerging in Medical Genetics

    著者: Tuomo Mantere, Simone Kersten, Alexander Hoischen - Frontiers in Genetics 2019 被引用: 462

  5. Diagnostic Exome Sequencing in Persons With Severe Intellectual Disability

    著者: Joep de Ligt, Marjolein H. Willemsen, Bregje W.M. van Bon, Tjitske Kleefstra, Helger G. Yntema, Thessa Kroes, Anneke T. Vulto-van Silfhout, David A. Koolen, Petra de Vries, Christian Gilissen, Marisol del Rosario, Alexander Hoischen, Hans Scheffer, Bert B.A. de Vries, Han G. Brunner, Joris A. Veltman, Lisenka E.L.M. Vissers - New England Journal of Medicine 2012 被引用: 1,578

  6. Optical genome mapping enables constitutional chromosomal aberration detection

    著者: Tuomo Mantere, Kornelia Neveling, Céline Pebrel‐Richard, Marion Benoist, Guillaume van de Zande, Ellen Kater‐Baats, Imane Baatout, Ronald van Beek, Tony Yammine, Michiel Oorsprong, Faten Hsoumi, Daniel Olde-Weghuis, Wed Majdali, Susan Vermeulen, Marc Pauper, Aziza Lebbar, Marian Stevens‐Kroef, Damien Sanlaville, Jean‐Michel Dupont, Dominique Smeets, Alexander Hoischen, Caroline Schluth‐Bolard, Laïla El Khattabi - The American Journal of Human Genetics 2021 被引用: 253

  7. Refining analyses of copy number variation identifies specific genes associated with developmental delay

    著者: Bradley P. Coe, Kali Witherspoon, Jill A. Rosenfeld, Bregje W.M. van Bon, Anneke T. Vulto‐van Silfhout, Paolo Bosco, Kathryn Friend, Carl Baker, Serafino Buono, Lisenka E.L.M. Vissers, Janneke Schuurs-Hoeijmakers, Alexander Hoischen, Rolph Pfundt, Nik Krumm, Gemma L. Carvill, Deana Li, David G. Amaral, Natasha J. Brown, Paul J. Lockhart, Ingrid E. Scheffer, A Alberti, Marie Shaw, Rosa Pettinato, Raymond C. Tervo, Nicole de Leeuw, Margot R.F. Reijnders, Beth S. Torchia, Hilde Peeters, Elizabeth Thompson, Brian J. O’Roak, Marco Fichera, Jayne Y. Hehir‐Kwa, Jay Shendure, Heather C. Mefford, Eric Haan, Jozef Gécz, Bert B A de Vries, Corrado Romano, Evan E Eichler - Nature Genetics 2014 被引用: 758

  8. Catecholamines Induce Trained Immunity in Monocytes In Vitro and In Vivo

    著者: Charlotte D.C.C. van der Heijden, Laszlo Groh, Samuel T. Keating, Charlotte Kaffa, Marlies P. Noz, Simone Kersten, Antonius E. van Herwaarden, Alexander Hoischen, Leo A. B. Joosten, Henri Timmers, Mihai G. Netea, Niels P. Riksen - Circulation Research 2020 被引用: 156

  9. Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

    著者: Mehul Sharma, Daniel Leung, Mana Momenilandi, Lauren C.W. Jones, Lucia Pacillo, Alyssa James, Jill R. Murrell, Selket Delafontaine, Jesmeen Maimaris, Maryam Vaseghi‐Shanjani, Kate L. Del Bel, Henry Y. Lu, Gilbert T. Chua, Silvia Di Cesare, Oriol Fornés, Zhongyi Liu, Gigliola Di Matteo, Maggie P. Fu, Donato Amodio, Issan Yee San Tam, Gavin S.W. Chan, Ashish Sharma, Joshua Dalmann, Robin van der Lee, Géraldine Blanchard‐Rohner, Susan Lin, Quentin Philippot, Phillip A. Richmond, Jessica J. Lee, Allison Matthews, Michael Seear, Alexandra K. Turvey, Rachael L. Philips, Terri F. Brown‐Whitehorn, Christopher Gray, Kosuke Izumi, James R. Treat, Kathleen H. Wood, Justin Lack, Asya Khleborodova, Julie E. Niemela, Xingtian Yang, Rui Liang, Lin Kui, Christina Sze Man Wong, Grace Wing-kit Poon, Alexander Hoischen, Caspar I. van der Made, Jing Yang, Koon Wing Chan, Jaime S. Rosa Duque, Pamela Lee, M. Ho, Brian Hon‐Yin Chung, Huong Thi Minh Le, Wanling Yang, Pejman Rohani, Ali Fouladvand, Hassan Rokni‐Zadeh, Majid Changi‐Ashtiani, Mohammad Miryounesi, Anne Puel, Mohammad Shahrooei, Andrea Finocchi, Paolo Rossi, Beatrice Rivalta, Cristina Cifaldi, Antonio Novelli, Chiara Passarelli, Stefania Arasi, Dominique Bullens, Kate Sauer, Tania Claeys, Catherine M. Biggs, Emma Morris, Sergio D. Rosenzweig, John J. O’Shea, Wyeth W. Wasserman, H. Melanie Bedford, Clara D.M. van Karnebeek, Paolo Palma, Siobhan O. Burns, Isabelle Meyts, Jean‐Laurent Casanova, Jonathan J. Lyons, Nima Parvaneh, Anh Thi Van Nguyen, Caterina Cancrini, Jennifer Heimall, Hanan Ahmed, Margaret L. McKinnon, YL Lau, Vivien Béziat, Stuart E. Turvey - The Journal of Experimental Medicine 2023 被引用: 112

  10. Next-generation cytogenetics: Comprehensive assessment of 52 hematological malignancy genomes by optical genome mapping

    著者: Kornelia Neveling, Tuomo Mantere, Susan Vermeulen, Michiel Oorsprong, Ronald van Beek, Ellen Kater‐Baats, Marc Pauper, Guillaume van de Zande, Dominique Smeets, Daniël Olde Weghuis, Marian Stevens‐Kroef, Alexander Hoischen - The American Journal of Human Genetics 2021 被引用: 200

  11. Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

    著者: Birte Zurek, Kornelia Ellwanger, Lisenka E.L.M. Vissers, Rebecca Schüle, Matthis Synofzik, Ana Töpf, Richarda M. de Voer, Steven Laurie, Leslie Matalonga, Christian Gilissen, Stephan Ossowski, Peter A.C. ’t Hoen, Antonio Vitobello, Julia M. Schulze‐Hentrich, Olaf Rieß, Han G. Brunner, Anthony J. Brookes, Ana Rath, Gisèle Bonne, Gulcin Gumus, Alain Verloès, Nicoline Hoogerbrugge, Teresinha Evangelista, Tina Harmuth, Morris A. Swertz, Dylan Spalding, Alexander Hoischen, Sergi Beltrán, Holm Graeßner, T. Haack, Birte Zurek, Kornelia Ellwanger, German Demidov, Marc Sturm, Christoph Keßler, Melanie Wayand, Carlo Wilke, Andreas Traschütz, Lüdger Schöls, Holger Hengel, Peter Heutink, Han G. Brunner, Hans Scheffer, Wouter Steyaert, Karolis Sablauskas, Richarda M. de Voer, Erik-Jan Kamsteeg, Bart van de Warrenburg, Nienke van Os, Iris te Paske, Erik Janssen, Elke de Boer, Marloes Steehouwer, Burcu Yaldız, Tjitske Kleefstra, Colin Veal, Spencer Gibson, Marc Wadsley, Mehdi Mehtarizadeh, Umar Riaz, Greg Warren, Farid Yavari Dizjikan, Thomas Shorter, Volker Straub, C. Marini Bettolo, Sabine Specht, Jill Clayton‐Smith, Siddharth Banka, Elizabeth Alexander, Adam Jackson, Laurence Faivre, Christel Thauvin, Antonio Vitobello, Anne‐Sophie Denommé‐Pichon, Yannis Duffourd, Émilie Tisserant, Ange‐Line Bruel, Christine Peyron, Aurore Pélissier, Sergi Beltrán, Marta Gut, Steven Laurie, Davide Piscia, Leslie Matalonga, Anastasios Papakonstantinou, Gemma Bullich, Alberto Corvò, Carles García, Marcos Fernandez-Callejo, Carles Hernandéz-Ferrer, Daniel Picó, Ida Paramonov, Hanns Lochmüller, Gulcin Gumus, Virginie Bros‐Facer, Marc Hanauer, Annie Olry, David Lagorce, Svitlana Havrylenko, Katia Izem ほか 123 名 - European Journal of Human Genetics 2021 被引用: 103

  12. Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling

    著者: Lot Snijders Blok, Erik Madsen, Jane Juusola, Christian Gilissen, Diana Baralle, Margot R.F. Reijnders, Hanka Venselaar, Céline Helsmoortel, Megan T. Cho, Alexander Hoischen, Lisenka E.L.M. Vissers, Tom S. Koemans, W.M. Wissink-Lindhout, Evan E. Eichler, Corrado Romano, Hilde Van Esch, Connie T. R. M. Stumpel, Maaike Vreeburg, Eric Smeets, Karin Oberndorff, Bregje W.M. van Bon, Marie Shaw, Jozef Gécz, Eric Haan, Melanie Bienek, Corinna Jensen, Bart Loeys, Anke Van Dijck, A. Micheil Innes, Hilary Racher, Sascha Vermeer, Nataliya Di Donato, Andreas Rump, Katrina Tatton‐Brown, Michael Parker, Alex Henderson, Sally Ann Lynch, Alan Fryer, Alison Ross, Pradeep Vasudevan, Usha Kini, Ruth Newbury‐Ecob, Kate Chandler, Alison Male, Sybe Dijkstra, Jolanda Schieving, Jacques C. Giltay, Koen L.I. van Gassen, Janneke Schuurs-Hoeijmakers, Perciliz L. Tan, Igor Pediaditakis, Stefan A. Haas, Kyle Retterer, Patrick Reed, Kristin G. Monaghan, Eden Haverfield, Marvin R. Natowicz, Angela Myers, Michael C. Kruer, Quinn Stein, Kevin A. Strauss, Karlla W. Brigatti, Katherine E. Keating, Barbara K. Burton, Katherine H. Kim, Joel Charrow, Jennifer Norman, Audrey Foster‐Barber, Antonie D. Kline, Amy Kimball, Elaine H. Zackai, Margaret Harr, Joyce E. Fox, Julie McLaughlin, Kristin Lindstrom, Katrina Haude, Kees van Roozendaal, Han G. Brunner, Wendy K. Chung, R. Frank Kooy, Rolph Pfundt, Vera M. Kalscheuer, Sarju Mehta, Nicholas Katsanis, Tjitske Kleefstra - The American Journal of Human Genetics 2015 被引用: 339

  13. Genome sequencing identifies major causes of severe intellectual disability

    著者: Christian Gilissen, Jayne Y. Hehir‐Kwa, Djie Tjwan Thung, Maartje van de Vorst, Bregje W.M. van Bon, Marjolein H. Willemsen, Michael Kwint, Irene M. Janssen, Alexander Hoischen, Annette Schenck, Richard A. Leach, Robert J. Klein, Rick Tearle, Tan Bo, Rolph Pfundt, Helger G. Yntema, Bert B.A. de Vries, Tjitske Kleefstra, Han G. Brunner, Lisenka E.L.M. Vissers, Joris A. Veltman - Nature 2014 被引用: 1,159

  14. Parent-of-origin-specific signatures of de novo mutations

    著者: Jakob M. Goldmann, Wendy S.W. Wong, Michele Pinelli, Terry Farrah, Dale L. Bodian, Anna Stittrich, Gustavo Glusman, Lisenka E.L.M. Vissers, Alexander Hoischen, Jared C. Roach, Joseph G. Vockley, Joris A. Veltman, Benjamin D. Solomon, Christian Gilissen, John E. Niederhuber - Nature Genetics 2016 被引用: 373

  15. Comprehensive SMN1 and SMN2 profiling for spinal muscular atrophy analysis using long-read PacBio HiFi sequencing

    著者: Xiao Chen, John Harting, Emily Farrow, Isabelle Thiffault, Dalia Kasperavičiūtė, Alexander Hoischen, Christian Gilissen, Tomi Pastinen, Michael A. Eberle - The American Journal of Human Genetics 2023 被引用: 86

  16. oxLDL-Induced Trained Immunity Is Dependent on Mitochondrial Metabolic Reprogramming

    著者: Laszlo Groh, Anaísa V. Ferreira, Leonie Helder, Charlotte D.C.C. van der Heijden, Boris Novakovic, Els van de Westerlo, Vasiliki Matzaraki, Simone J.C.F.M. Moorlag, L. Charlotte de Bree, Valerie A. C. M. Koeken, Vera P. Mourits, Samuel T. Keating, Jelmer H. van Puffelen, Alexander Hoischen, Leo A. B. Joosten, Mihai G. Netea, Werner J.H. Koopman, Niels P. Riksen - Immunometabolism 2021 被引用: 65

  17. New insights into the generation and role of de novo mutations in health and disease

    著者: Rocío Acuña‐Hidalgo, Joris A. Veltman, Alexander Hoischen - Genome biology 2016 被引用: 491

  18. Familial long-read sequencing increases yield of de novo mutations

    著者: Michelle D. Noyes, William T. Harvey, David Porubskỳ, Arvis Sulovari, Ruiyang Li, Nicholas R. Rose, Peter A. Audano, Katherine M. Munson, Alexandra P. Lewis, Kendra Hoekzema, Tuomo Mantere, Tina A. Graves-Lindsay, Ashley D. Sanders, Sara Goodwin, Melissa Kramer, Younes Mokrab, Michael C. Zody, Alexander Hoischen, Jan O. Korbel, W. Richard McCombie, Evan E. Eichler - The American Journal of Human Genetics 2022 被引用: 83

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

    著者: Rocío Acuña‐Hidalgo, Hilal Sengül, Marloes Steehouwer, Maartje van de Vorst, Sita H. Vermeulen, Lambertus A. Kiemeney, Joris A. Veltman, Christian Gilissen, Alexander Hoischen - The American Journal of Human Genetics 2017 被引用: 270

  20. Transcriptional and functional insights into the host immune response against the emerging fungal pathogen Candida auris

    著者: Mariolina Bruno, Simone Kersten, Judith M. Bain, Martin Jaeger, Diletta Rosati, Michael Kruppa, Douglas W. Lowman, Peter J. Rice, Bridget Graves, Zuchao Ma, Yue Ning Jiao, Anuradha Chowdhary, George Renieris, Frank L. van de Veerdonk, Bart Jan Kullberg, Evangelos J. Giamarellos‐Bourboulis, Alexander Hoischen, Neil A. R. Gow, Alistair J. P. Brown, Jacques F. Meis, David L. Williams, Mihai G. Netea - Nature Microbiology 2020 被引用: 139

  21. Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics

    著者: Mubeen Khan, Stéphanie S. Cornelis, Marta l De Pozo-Valero, Laura Whelan, Esmee H. Runhart, Ketan Mishra, Femke Bults, Yahya AlSwaiti, Alaa AlTalbishi, Elfride De Baere, Sandro Banfi, Eyal Banin, Miriam Bauwens, Tamar Ben‐Yosef, Camiel J. F. Boon, L. Ingeborgh van den Born, Sabine Defoort, Aurore Devos, Adrian Dockery, Ľubica Ďuďáková, Ana Fakin, G. Jane Farrar, Juliana Maria Ferraz Sallum, Kaoru Fujinami, Christian Gilissen, Damjan Glavač, Michael B. Gorin, Jacquie Greenberg, Takaaki Hayashi, Ymkje M. Hettinga, Alexander Hoischen, Carel B. Hoyng, Karsten Hufendiek, Herbert Jägle, Smaragda Kamakari, Marianthi Karali, Ulrich Kellner, Caroline C. W. Klaver, Bohdan Kousal, Tina M. Lamey, Ian M. MacDonald, Anna Matynia, Terri L. McLaren, Marcela Mena, Isabelle Meunier, Rianne Miller, Hadas Newman, Buhle Ntozini, Monika Ołdak, Marc Pieterse, Osvaldo L. Podhajcer, Bernard Puech, Raj Ramesar, Klaus Rüther, Manar Salameh, Mariana Vallim Salles, Dror Sharon, Francesca Simonelli, Georg Spital, Marloes Steehouwer, Jacek P. Szaflik, Jennifer A. Thompson, C. Thuillier, Anna M. Tracewska, Martine van Zweeden, Andrea L. Vincent, Xavier Zanlonghi, Petra Lišková, Heidi Stöhr, John N. De Roach, Carmen Ayuso, Lisa Roberts, Bernhard H. F. Weber, Claire‐Marie Dhaenens, Frans P.M. Cremers - Genetics in Medicine 2020 被引用: 142

  22. A de novo paradigm for mental retardation

    著者: Lisenka E.L.M. Vissers, Joep de Ligt, Christian Gilissen, Irene M. Janssen, Marloes Steehouwer, Petra de Vries, Bart van Lier, Peer Arts, Nienke Wieskamp, Marisol del Rosario, Bregje W.M. van Bon, Alexander Hoischen, Bert B.A. de Vries, Han G. Brunner, Joris A. Veltman - Nature Genetics 2010 被引用: 854

  23. Comprehensive de novo mutation discovery with HiFi long-read sequencing

    著者: Erdi Küçük, Bart van der Sanden, Luke O’Gorman, Michael Kwint, Ronny Derks, Aaron M. Wenger, Christine Lambert, Shreyasee Chakraborty, Primo Baybayan, William J. Rowell, Han G. Brunner, Lisenka E.L.M. Vissers, Alexander Hoischen, Christian Gilissen - Genome Medicine 2023 被引用: 58

  24. STAT1 Mutations in Autosomal Dominant Chronic Mucocutaneous Candidiasis

    著者: Frank L. van de Veerdonk, Theo S. Plantinga, Alexander Hoischen, Sanne P. Smeekens, Leo A. B. Joosten, Christian Gilissen, Peer Arts, Diana C. Rosentul, Andrew Carmichael, Chantal A.A. Smits-van der Graaf, Bart Jan Kullberg, J.W.M. van der Meer, Desa Lilić, Joris A. Veltman, Mihai G. Netea - New England Journal of Medicine 2011 被引用: 656