Lisenka E L M Vissers (Lisenka Vissers, L E L M Vissers)

ResearcherID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 29

Top Topics

Intellectual Disability

Dna Methylation

Autism Spectrum Disorder

Top Venues

European journal of human genetics : EJHG

medRxiv : the preprint server for health sciences

Nature genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Sissy Bassani, Jacqueline Chrast, Giovanna Ambrosini, Norine Voisin, Frédéric Schütz, Alfredo Brusco, Fabio Sirchia, Lydia Turban, Susanna Schubert, Rami Abou Jamra, Jan-Ulrich Schlump, Desiree DeMille, Pinar Bayrak-Toydemir, Gary Rex Nelson, Kristen Nicole Wong, Laura Duncan, Mackenzie Mosera, Christian Gilissen, Lisenka E L M Vissers, Rolph Pfundt, Rogier Kersseboom, Hilde Yttervik, Geir Åsmund Myge Hansen, Marie Falkenberg Smeland, Kameryn M Butler, Michael J Lyons, Claudia M B Carvalho, Chaofan Zhang, James R. Lupski, Lorraine Potocki, Leticia Flores-Gallegos, Rodrigo Morales-Toquero, Florence Petit, Binnaz Yalcin, Annabelle Tuttle, Houda Zghal Elloumi, Lane Mccormick, Mary K Kukolich, Oliver Klaas, Judit Horvath, Marcello Scala, Michele Iacomino, Francesca Felicia Operto, Federico Zara, Karin Writzl, Ales Maver, Maria K Haanpää, Pia Pohjola, Harri Arikka, Christian Iseli, Nicolas Guex, Alexandre Reymond
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles. medRxiv : the preprint server for health sciences (2024)
Wouter Steyaert, Lydia Sagath, German Demidov, Vicente A Yépez, Anna Esteve-Codina, Julien Gagneur, Kornelia Ellwanger, Ronny Derks, Janneke M Weiss, Amber den Ouden, Simone van den Heuvel, Hilde Swinkels, Nick Zomer, Marloes Steehouwer, Luke O'Gorman, Galuh Astuti, Kornelia Neveling, Rebecca Schüle, Jishu Xu, Matthis Synofzik, Danique Beijer, Holger Hengel, Ludger Schöls, Kristl G Claeys, Jonathan Baets, Liedewei Van de Vondel, Alessandra Ferlini, Rita Selvatici, Heba Morsy, Marwa Saeed Abd Elmaksoud, Volker Straub, Juliane Müller, Veronica Pini, Luke Perry, Anna Sarkozy, Irina T Zaharieva, Francesco Muntoni, Enrico Bugiardini, Kiran Polavarapu, Rita Horvath, Evan Reid, Hanns Lochmüller, Marco Spinazzi, Marco Savarese, null null, null null, null null, null null, Leslie Matalonga, Steven Laurie, Han G Brunner, Holm Graessner, Sergi Beltran, Stephan Ossowski, Lisenka E L M Vissers, Christian Gilissen, Alexander Hoischen
Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing. medRxiv : the preprint server for health sciences (2024)
Sissy Bassani, Jacqueline Chrast, Giovanna Ambrosini, Norine Voisin, Frédéric Schütz, Alfredo Brusco, Fabio Sirchia, Lydia Turban, Susanna Schubert, Rami Abou Jamra, Jan-Ulrich Schlump, Desiree DeMille, Pinar Bayrak-Toydemir, Gary Rex Nelson, Kristen Nicole Wong, Laura Duncan, Mackenzie Mosera, Christian Gilissen, Lisenka E L M Vissers, Rolph Pfundt, Rogier Kersseboom, Hilde Yttervik, Geir Åsmund Myge Hansen, Marie Falkenberg Smeland, Kameryn M Butler, Michael J Lyons, Claudia M B Carvalho, Chaofan Zhang, James R. Lupski, Lorraine Potocki, Leticia Flores-Gallegos, Rodrigo Morales-Toquero, Florence Petit, Binnaz Yalcin, Annabelle Tuttle, Houda Zghal Elloumi, Lane Mccormick, Mary K Kukolich, Oliver Klaas, Judit Horvath, Marcello Scala, Michele Iacomino, Francesca Felicia Operto, Federico Zara, Karin Writzl, Ales Maver, Maria K Haanpää, Pia Pohjola, Harri Arikka, Christian Iseli, Nicolas Guex, Alexandre Reymond
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles. medRxiv : the preprint server for health sciences (2024)
Sissy Bassani, Jacqueline Chrast, Giovanna Ambrosini, Norine Voisin, Frédéric Schütz, Alfredo Brusco, Fabio Sirchia, Lydia Turban, Susanna Schubert, Rami Abou Jamra, Jan-Ulrich Schlump, Desiree DeMille, Pinar Bayrak-Toydemir, Gary Rex Nelson, Kristen Nicole Wong, Laura Duncan, Mackenzie Mosera, Christian Gilissen, Lisenka E L M Vissers, Rolph Pfundt, Rogier Kersseboom, Hilde Yttervik, Geir Åsmund Myge Hansen, Marie Falkenberg Smeland, Kameryn M Butler, Michael J Lyons, Claudia M B Carvalho, Chaofan Zhang, James R. Lupski, Lorraine Potocki, Leticia Flores-Gallegos, Rodrigo Morales-Toquero, Florence Petit, Binnaz Yalcin, Annabelle Tuttle, Houda Zghal Elloumi, Lane Mccormick, Mary K Kukolich, Oliver Klaas, Judit Horvath, Marcello Scala, Michele Iacomino, Francesca Felicia Operto, Federico Zara, Karin Writzl, Ales Maver, Maria K Haanpää, Pia Pohjola, Harri Arikka, Christian Iseli, Nicolas Guex, Alexandre Reymond
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles. medRxiv : the preprint server for health sciences (2024)
Anouk E J Janssen, Rebekka M Koeck, Rick Essers, Ping Cao, Wanwisa van Dijk, Marion Drüsedau, Jeroen Meekels, Burcu Yaldiz, Maartje van de Vorst, Bart de Koning, Debby M E I Hellebrekers, Servi J C Stevens, Su Ming Sun, Malou Heijligers, Sonja A de Munnik, Chris M J van Uum, Jelle Achten, Lars Hamers, Marjan Naghdi, Lisenka E L M Vissers, Ron J T van Golde, Guido M W R De Wert, Jos C F M Dreesen, Christine de Die-Smulders, Edith Coonen, Han G Brunner, Arthur van den Wijngaard, Aimée D C Paulussen, Masoud Zamani Esteki
Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing. Nature communications 15 (1) (2024)
Sissy Bassani, Jacqueline Chrast, Giovanna Ambrosini, Norine Voisin, Frédéric Schütz, Alfredo Brusco, Fabio Sirchia, Lydia Turban, Susanna Schubert, Rami Abou Jamra, Jan-Ulrich Schlump, Desiree DeMille, Pinar Bayrak-Toydemir, Gary Rex Nelson, Kristen Nicole Wong, Laura Duncan, Mackenzie Mosera, Christian Gilissen, Lisenka E L M Vissers, Rolph Pfundt, Rogier Kersseboom, Hilde Yttervik, Geir Åsmund Myge Hansen, Marie Falkenberg Smeland, Kameryn M Butler, Michael J Lyons, Claudia M B Carvalho, Chaofan Zhang, James R. Lupski, Lorraine Potocki, Leticia Flores-Gallegos, Rodrigo Morales-Toquero, Florence Petit, Binnaz Yalcin, Annabelle Tuttle, Houda Zghal Elloumi, Lane Mccormick, Mary K Kukolich, Oliver Klaas, Judit Horvath, Marcello Scala, Michele Iacomino, Francesca Felicia Operto, Federico Zara, Karin Writzl, Ales Maver, Maria K Haanpää, Pia Pohjola, Harri Arikka, Christian Iseli, Nicolas Guex, Alexandre Reymond
Variant-specific pathophysiological mechanisms of AFF3 differently influence transcriptome profiles. medRxiv : the preprint server for health sciences (2024)
Robin Wijngaard, German Demidov, Luke O'Gorman, Jordi Corominas-Galbany, Burcu Yaldiz, Wouter Steyaert, Elke de Boer, Lisenka E L M Vissers, Erik-Jan Kamsteeg, Rolph Pfundt, Hilde Swinkels, Amber den Ouden, Iris B A W Te Paske, Richarda M de Voer, Laurence Faivre, Anne Sophie Denommé-Pichon, Yannis Duffourd, Antonio Vitobello, Martin Chevarin, Volker Straub, Ana Topf, Anneke J van der Kooi, Francesca Magrinelli, Clarissa Rocca, Michael G Hanna, Jana Vandrovcova, null null, Stephan Ossowski, Steven Laurie, Christian Gilissen
Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples. European journal of human genetics : EJHG (2023)
Sandra Jansen, Lisenka E L M Vissers, Bert B A de Vries
The Genetics of Intellectual Disability. Brain sciences 13 (2) (2023)
Michelle van Slobbe, Arie van Haeringen, Lisenka E L M Vissers, Emilia K Bijlsma, Julie W Rutten, Manon Suerink, Esther A R Nibbeling, Claudia A L Ruivenkamp, Saskia Koene
Reanalysis of whole-exome sequencing (WES) data of children with neurodevelopmental disorders in a standard patient care context. European journal of pediatrics (2023)
Alan P Tenney, Silvio Alessandro Di Gioia, Bryn D Webb, Wai-Man Chan, Elke de Boer, Sarah J Garnai, Brenda J Barry, Tammy Ray, Michael Kosicki, Caroline D Robson, Zhongyang Zhang, Thomas E Collins, Alon Gelber, Brandon M Pratt, Yuko Fujiwara, Arushi Varshney, Monkol Lek, Peter E Warburton, Carol Van Ryzin, Tanya J Lehky, Christopher Zalewski, Kelly A King, Carmen C Brewer, Audrey Thurm, Joseph Snow, Flavia M Facio, Narisu Narisu, Lori L Bonnycastle, Amy Swift, Peter S Chines, Jessica L Bell, Suresh Mohan, Mary C Whitman, Sandra E Staffieri, James E Elder, Joseph L Demer, Alcy Torres, Elza Rachid, Christiane Al-Haddad, Rose-Mary N Boustany, David A Mackey, Angela F Brady, María Fenollar-Cortés, Melanie Fradin, Tjitske Kleefstra, George W Padberg, Salmo Raskin, Mario Teruo Sato, Stuart H Orkin, Stephen C J Parker, Tessa A Hadlock, Lisenka E L M Vissers, Hans van Bokhoven, Ethylin Wang Jabs, Francis S Collins, Len A Pennacchio, Irini Manoli, Elizabeth C Engle
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis. Nature genetics (2023)
Sandra Jansen, Lisenka E L M Vissers, Bert B A de Vries
The Genetics of Intellectual Disability. Brain sciences 13 (2) (2023)
Richelle A C M Olde Keizer, Abderrahim Marouane, Wilhelmina S Kerstjens-Frederikse, A Chantal Deden, Klaske D Lichtenbelt, Tinneke Jonckers, Marieke Vervoorn, Maaike Vreeburg, Lidewij Henneman, Linda S de Vries, Richard J Sinke, Rolph Pfundt, Servi J C Stevens, Peter Andriessen, Richard A van Lingen, Marcel Nelen, Hans Scheffer, Daphne Stemkens, Cor Oosterwijk, Hans Kristian Ploos van Amstel, Willem P de Boode, Wendy A G van Zelst-Stams, Gerardus W J Frederix, Lisenka E L M Vissers, null null
Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder: results of a prospective multicenter clinical utility study in the Netherlands. European journal of pediatrics (2023)
Alexander J M Dingemans, Max Hinne, Kim M G Truijen, Lia C M J Goltstein, Jeroen van Reeuwijk, Nicole de Leeuw, Janneke Schuurs-Hoeijmakers, Rolph Pfundt, Illja J Diets, Joery den Hoed, Elke de Boer, Jet Coenen-van der Spek, Sandra Jansen, Bregje W van Bon, Noraly Jonis, Charlotte W Ockeloen, Anneke T Vulto-van Silfhout, Tjitske Kleefstra, David A Koolen, Philippe M Campeau, Emma Elizabeth Palmer, Hilde Van Esch, Gholson J Lyon, Fowzan Sami Alkuraya, Anita Rauch, Ronit Marom, Diana Baralle, Pleuntje J van der Sluijs, Gijs W E Santen, R Frank Kooy, Marcel A J van Gerven, Lisenka E L M Vissers, Bert B A de Vries
PhenoScore quantifies phenotypic variation for rare genetic diseases by combining facial analysis with other clinical features using a machine-learning framework. Nature genetics (2023)
Linda Zhang, Joanne I Hsu, Etienne D Braekeleer, Chun-Wei Chen, Tajhal D Patel, Hidetaka Urya, Anna G Guzman, Alejandra G Martell, Sarah M Waldvogel, Ayala Tovy, Elsa Callen, Rebecca Murdaugh, Rosemary Richard, Sandra Jansen, Lisenka E L M Vissers, Bert B A de Vries, Andre Nussenzweig, Shixia Huang, Cristian Coarfa, Jamie N Anastas, Koichi Takahashi, George S Vassiliou, Margaret A Goodell
SOD1 is a synthetic lethal target in PPM1D -mutant leukemia cells. bioRxiv : the preprint server for biology (2023)
Robin Wijngaard, German Demidov, Luke O'Gorman, Jordi Corominas-Galbany, Burcu Yaldiz, Wouter Steyaert, Elke de Boer, Lisenka E L M Vissers, Erik-Jan Kamsteeg, Rolph Pfundt, Hilde Swinkels, Amber den Ouden, Iris B A W Te Paske, Richarda M de Voer, Laurence Faivre, Anne Sophie Denommé-Pichon, Yannis Duffourd, Antonio Vitobello, Martin Chevarin, Volker Straub, Ana Topf, Anneke J van der Kooi, Francesca Magrinelli, Clarissa Rocca, Michael G Hanna, Jana Vandrovcova, null null, Stephan Ossowski, Steven Laurie, Christian Gilissen
Correction: Mobile element insertions in rare diseases: a comparative benchmark and reanalysis of 60,000 exome samples. European journal of human genetics : EJHG (2023)
Sandra Jansen, Lisenka E L M Vissers, Bert B A de Vries
The Genetics of Intellectual Disability. Brain sciences 13 (2) (2023)
Manon S Oud, R M Smits, H E Smith, F Kumara Mastrorosa, G S Holt, B J Houston, P F de Vries, B K S Alobaidi, L E Batty, H Ismail, J Greenwood, Harsh J Sheth, A Mikulasova, G D N Astuti, Christian Gilissen, K McEleny, H Turner, Jonathan M Coxhead, S Cockell, Didi D M Braat, K Fleischer, K W M D'Hauwers, E Schaafsma, null null, Liina Nagirnaja, Donald F Conrad, C Friedrich, Sabine Kliesch, K I Aston, A Riera-Escamilla, C Krausz, C Gonzaga-Jauregui, M Santibanez-Koref, D J Elliott, Lisenka E L M Vissers, Frank Tüttelmann, Brendan J Houston, Liliana Ramos, Miguel J Xavier, Godfried W van der Heijden, Joris A Veltman
A de novo paradigm for male infertility. Nature communications 13 (1) (2022)
Bart P G H van der Sanden, Gaby Schobers, Jordi Corominas Galbany, David A Koolen, Margje Sinnema, Jeroen van Reeuwijk, Connie T R M Stumpel, Tjitske Kleefstra, Bert B A de Vries, Martina Ruiterkamp-Versteeg, Nico Leijsten, Michael Kwint, Ronny Derks, Hilde Swinkels, Amber den Ouden, Rolph Pfundt, Tuula Rinne, Nicole de Leeuw, Alexander P A Stegmann, Servi J C Stevens, Arthur van den Wijngaard, Han G Brunner, Helger G Yntema, Christian Gilissen, Marcel R Nelen, Lisenka E L M Vissers
The performance of genome sequencing as a first-tier test for neurodevelopmental disorders. European journal of human genetics : EJHG (2022)
Liselot van der Laan, Kathleen Rooney, Mariëlle Alders, Raissa Relator, Haley McConkey, Jennifer Kerkhof, Michael A Levy, Peter Lauffer, Mio Aerden, Miel Theunis, Eric Legius, Matthew L Tedder, Lisenka E L M Vissers, Saskia Koene, Claudia Ruivenkamp, Mariette J V Hoffer, Dagmar Wieczorek, Nuria C Bramswig, Theresia Herget, Vanesa López González, Fernando Santos-Simarro, Pernille Mathiesen Torring, Anne Sophie Denommé-Pichon, Bertrand Isidor, Boris Keren, Sophie Julia, Elise Schaefer, Christine Francannet, Pierre-Yves Maillard, Mala Misra-Isrie, Hilde Van Esch, Marcel M A M Mannens, Bekim Sadikovic, Mieke M van Haelst, Peter Henneman
Episignature Mapping of TRIP12 Provides Functional Insight into Clark-Baraitser Syndrome. International journal of molecular sciences 23 (22) (2022)
Richelle A C M Olde Keizer, Lidewij Henneman, Hans Kristian Ploos van Amstel, Lisenka E L M Vissers, Gerardus W J Frederix
Economic evaluations of exome and genome sequencing in pediatric genetics: considerations towards a consensus strategy. Journal of medical economics 24 (sup1) (2021)
Cenna Doornbos, Ronald van Beek, Ernie M H F Bongers, Dorien Lugtenberg, Peter H M Klaren, Lisenka E L M Vissers, Ronald Roepman, Machteld M Oud
Cell-based assay for ciliopathy patients to improve accurate diagnosis using ALPACA. European journal of human genetics : EJHG 29 (11) (2021)
Alexander J M Dingemans, Kim M G Truijen, Jung-Hyun Kim, Zahide Alaçam, Laurence Faivre, Kathleen M Collins, Erica H Gerkes, Mieke van Haelst, Ingrid M B H van de Laar, Kristin Lindstrom, Mathilde Nizon, James Pauling, Edyta Heropolitańska-Pliszka, Astrid S Plomp, Caroline Racine, Rani Sachdev, Margje Sinnema, Jon Skranes, Hermine E Veenstra-Knol, Eline A Verberne, Anneke T Vulto-van Silfhout, Marlon E F Wilsterman, Eun-Young Erin Ahn, Bert B A de Vries, Lisenka E L M Vissers
Establishing the phenotypic spectrum of ZTTK syndrome by analysis of 52 individuals with variants in SON. European journal of human genetics : EJHG (2021)
Vyne van der Schoot, Lonneke Haer-Wigman, Ilse Feenstra, Femke Tammer, Anke J M Oerlemans, Martine P A van Koolwijk, Frans van Agt, Yvonne H J M Arens, Han G Brunner, Lisenka E L M Vissers, Helger G Yntema
Lessons learned from unsolicited findings in clinical exome sequencing of 16,482 individuals. European journal of human genetics : EJHG (2021)
Leslie Matalonga, Carles Hernandez-Ferrer, Davide Piscia, null null, Rebecca Schüle, Matthis Synofzik, Ana Töpf, Lisenka E L M Vissers, Richarda M de Voer, null null, null null, null null, null null, Raul Tonda, Steven Laurie, Marcos Fernandez-Callejo, Daniel Picó, Carles Garcia-Linares, Anastasios Papakonstantinou, Alberto Corvó, Ricky Joshi, Hector Diez, Ivo Glynne Gut, Alexander Hoischen, Holm Graessner, Sergi Beltran, null null
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data. European journal of human genetics : EJHG 29 (9) (2021)
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 Verloes, Nicoline Hoogerbrugge, Teresinha Evangelista, Tina Harmuth, Morris Swertz, J Dylan Spalding, Alexander Hoischen, Sergi Beltran, Holm Graessner, null null
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases. European journal of human genetics : EJHG 29 (9) (2021)
Alexander J M Dingemans, Diante E Stremmelaar, Roos van der Donk, Lisenka E L M Vissers, David A Koolen, Patrick Rump, Jayne Y Hehir-Kwa, Bert B A de Vries
Quantitative facial phenotyping for Koolen-de Vries and 22q11.2 deletion syndrome. European journal of human genetics : EJHG 29 (9) (2021)
Elke de Boer, Charlotte W Ockeloen, Leslie Matalonga, Rita Horvath, null null, Richard J T Rodenburg, Marieke J H Coenen, Mirian Janssen, Dylan Henssen, Christian Gilissen, Wouter Steyaert, Ida Paramonov, null null, Aurélien Trimouille, Tjitske Kleefstra, Alain Verloes, Lisenka E L M Vissers
A MT-TL1 variant identified by whole exome sequencing in an individual with intellectual disability, epilepsy, and spastic tetraparesis. European journal of human genetics : EJHG 29 (9) (2021)
Marc Pauper, Erdi Kucuk, Aaron M Wenger, Shreyasee Chakraborty, Primo Baybayan, Michael Kwint, Bart P G H van der Sanden, Marcel R Nelen, Ronny Derks, Han G Brunner, Alexander Hoischen, Lisenka E L M Vissers, Christian Gilissen
Long-read trio sequencing of individuals with unsolved intellectual disability. European journal of human genetics : EJHG 29 (4) (2020)
Lisenka E L M Vissers, Kirsten J M van Nimwegen, Jolanda H Schieving, Erik-Jan Kamsteeg, Tjitske Kleefstra, Helger G Yntema, Rolph Pfundt, Gert Jan van der Wilt, Gert Jan van der Wilt, Han G Brunner, Simone van der Burg, Janneke Grutters, Joris A Veltman, Michèl A A P Willemsen
A clinical utility study of exome sequencing versus conventional genetic testing in pediatric neurology. Genetics in medicine : official journal of the American College of Medical Genetics 19 (9) (2017)