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Alexander Hoischen

Active 2006–2026

158
Papers
22,827
Citations
85
h-index
149
i10-index

Citations

Citations per year for Alexander Hoischen1986: 1 citations1993: 1 citations2002: 1 citations2006: 1 citations2007: 7 citations2008: 17 citations2009: 14 citations2010: 60 citations2011: 175 citations2012: 249 citations2013: 282 citations2014: 316 citations2015: 349 citations2016: 349 citations2017: 346 citations2018: 291 citations2019: 807 citations2020: 905 citations2021: 1,036 citations2022: 773 citations2023: 576 citations2024: 823 citations2025: 445 citations2026: 14 citations1987–1992: no citations, so these years are not shown1994–2001: no citations, so these years are not shown2003–2005: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,086 citing papers, 21.7% of this breakdownUnited Kingdom: 1,162 citing papers, 8.2% of this breakdownNetherlands: 991 citing papers, 7% of this breakdownGermany: 978 citing papers, 6.9% of this breakdownFrance: 708 citing papers, 5% of this breakdownChina: 691 citing papers, 4.8% of this breakdownItaly: 623 citing papers, 4.4% of this breakdownCanada: 595 citing papers, 4.2% of this breakdownAustralia: 492 citing papers, 3.4% of this breakdownSpain: 417 citing papers, 2.9% of this breakdownBelgium: 342 citing papers, 2.4% of this breakdownJapan: 306 citing papers, 2.1% of this breakdown
0%21.7%Other 27%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology53.6%
  • Medicine31.4%
  • Immunology and Microbiology7.7%
  • Neuroscience5%
  • Agricultural and Biological Sciences0.7%
  • Psychology0.4%
  • Other1.2%

Topics

  • 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%
  • Other79.2%

Coauthors

All papers

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

    Authors: 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 cited by 152

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

    Authors: 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 cited by 211

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

    Authors: 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 cited by 832

  4. Long-Read Sequencing Emerging in Medical Genetics

    Authors: Tuomo Mantere, Simone Kersten, Alexander Hoischen - Frontiers in Genetics 2019 cited by 462

  5. Diagnostic Exome Sequencing in Persons With Severe Intellectual Disability

    Authors: 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 cited by 1,578

  6. Optical genome mapping enables constitutional chromosomal aberration detection

    Authors: 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 cited by 253

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

    Authors: 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 cited by 758

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

    Authors: 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 cited by 156

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

    Authors: 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 cited by 112

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

    Authors: 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 cited by 200

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

    Authors: 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 and 123 more - European Journal of Human Genetics 2021 cited by 103

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

    Authors: 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 cited by 339

  13. Genome sequencing identifies major causes of severe intellectual disability

    Authors: 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 cited by 1,159

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

    Authors: 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 cited by 373

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

    Authors: 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 cited by 86

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

    Authors: 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 cited by 65

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

    Authors: Rocío Acuña‐Hidalgo, Joris A. Veltman, Alexander Hoischen - Genome biology 2016 cited by 491

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

    Authors: 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 cited by 83

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

    Authors: 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 cited by 270

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

    Authors: 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 cited by 139

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

    Authors: 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 cited by 142

  22. A de novo paradigm for mental retardation

    Authors: 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 cited by 854

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

    Authors: 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 cited by 58

  24. STAT1 Mutations in Autosomal Dominant Chronic Mucocutaneous Candidiasis

    Authors: 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 cited by 656