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Lisenka Vissers

Research Profile

Disorders

Physiology

Genes & Molecular Sequences

Procedures

Chemicals & Drugs

Anatomy

Chromosomes, Human, Pair 17

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Oligonucleotide Array Sequence Analysis

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Publications

TOP 3
Zafar Iqbal; Jamie M Kramer; Bonnie Nijhof; Hilde Peeters; Sheikh Riazuddin; Laura Tomas Roca; Muhammad Ansar; Judith A Besseling; Arjan P M de Brouwer; R Frank Kooy; Christian Gilissen; Céline Helsmoortel; Annette Schenck; Hans van Bokhoven; Nathalie Van der Aa; Monique van der Voet; Geert Vandeweyer; Joris A Veltman; Lisenka E L M Vissers; Anneke T Vulto-van Silfhout; Ali Muhammad Waryah; Muhammad Yasir Zahoor; Liesbeth Rooms
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
Janneke H M Schuurs-Hoeijmakers; Marloes Steehouwer; Mariëlle E M Swinkels; Hans van Bokhoven; Joris Veltman; Lisenka E L M Vissers; Michèl A Willemsen; Arjan P M de Brouwer; Bert B A de Vries; koenraad devriendt; Christian Gilissen; Maureen Holvoet; Nicholas Katsanis; Edwin C Oh; Han G Brunner
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.
Joep de Ligt; Bert B A de Vries; Petra de Vries; Marisol del Rosario; Christian Gilissen; Alexander Hoischen; Tjitske Kleefstra; David A Koolen; Thessa Kroes; Hans Scheffer; Bregje W M van Bon; Joris Veltman; Anneke T Vulto-van Silfhout; Marjolein H Willemsen; Helger G Yntema; Han G Brunner; Lisenka E L M Vissers
Diagnostic exome sequencing in persons with severe intellectual disability.

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All Publications

2013: Zafar Iqbal; Jamie M Kramer; Bonnie Nijhof; Hilde Peeters; Sheikh Riazuddin; Laura Tomas Roca; Muhammad Ansar; Judith A Besseling; Arjan P M de Brouwer; R Frank Kooy; Christian Gilissen; Céline Helsmoortel; Annette Schenck; Hans van Bokhoven; Nathalie Van der Aa; Monique van der Voet; Geert Vandeweyer; Joris A Veltman; Lisenka E L M Vissers; Anneke T Vulto-van Silfhout; Ali Muhammad Waryah; Muhammad Yasir Zahoor; Liesbeth Rooms
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
Human molecular genetics 2013;22(10):1960-70.
2012: Janneke H M Schuurs-Hoeijmakers; Marloes Steehouwer; Mariëlle E M Swinkels; Hans van Bokhoven; Joris Veltman; Lisenka E L M Vissers; Michèl A Willemsen; Arjan P M de Brouwer; Bert B A de Vries; koenraad devriendt; Christian Gilissen; Maureen Holvoet; Nicholas Katsanis; Edwin C Oh; Han G Brunner
Recurrent de novo mutations in PACS1 cause defective cranial-neural-crest migration and define a recognizable intellectual-disability syndrome.
American journal of human genetics 2012;91(6):1122-7.
2012: Joep de Ligt; Bert B A de Vries; Petra de Vries; Marisol del Rosario; Christian Gilissen; Alexander Hoischen; Tjitske Kleefstra; David A Koolen; Thessa Kroes; Hans Scheffer; Bregje W M van Bon; Joris Veltman; Anneke T Vulto-van Silfhout; Marjolein H Willemsen; Helger G Yntema; Han G Brunner; Lisenka E L M Vissers
Diagnostic exome sequencing in persons with severe intellectual disability.
The New England journal of medicine 2012;367(20):1921-9.
2012: Tjitske Kleefstra; Tom S Koemans; Jamie M Kramer; Kornelia Neveling; Willy M Nillesen; Trine Prescott; Annette Schenck; Han G Brunner; Robin D Clark; Arjan P M de Brouwer; koenraad devriendt; Michaela Fenckova; Christian Gilissen; Nael Nadif Kasri; Willem M R van den Akker; Jeroen van Reeuwijk; Joris Veltman; Lisenka E L M Vissers; Marjolein H Willemsen; Willemijn Wissink-Lindhout; Huiqing Zhou; Hans van Bokhoven
Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability.
American journal of human genetics 2012;91(1):73-82.
2012: David A Koolen; Willy M Nillesen; Alyson Bradbury; Arjan P M de Brouwer; Nicole de Leeuw; Bert B A de Vries; Juliette Dupont; James Steer; Leo P Ten Kate; Simone P A van den Heuvel; Lisenka E L M Vissers; Michael J Parker
Two families with sibling recurrence of the 17q21.31 microdeletion syndrome due to low-grade mosaicism.
European journal of human genetics : EJHG 2012;20(7):729-33.
2012: David A Koolen; Jamie M Kramer; Valérie Malan; Sarah Martens; Heather L Moore-Barton; Kornelia Neveling; Willy M Nillesen; Hans Scheffer; Annette Schenck; Annick Toutain; Anne Chun-Hui Tsai; Joris Veltman; Eugene T P Verwiel; Lisenka E L M Vissers; Helger G Yntema; Jeanne Amiel; Ernie M H F Bongers; Han G Brunner; Sau Wai Cheung; Arjan P M de Brouwer; Petra de Vries; Frances V Elmslie; Ton Feuth; Christian Gilissen; Bert B A de Vries
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.
Nature genetics 2012;44(6):639-41.
2012: Andy Itsara; Robert B Jenkins; David A Koolen; Choli Lee; Kevin J Meyer; Karyn Meltz Steinberg; Joris Veltman; Lisenka E L M Vissers; Richard K Wilson; Michael C Zody; Carl Baker; Edwin Cuppen; Joep de Ligt; Tina A Graves; Evan E Eichler
Resolving the breakpoints of the 17q21.31 microdeletion syndrome with next-generation sequencing.
American journal of human genetics 2012;90(4):599-613.
2012: Marjolein H Willemsen; Han G Brunner; Joep de Ligt; Bert B A de Vries; Ben C J Hamel; Thessa Kroes; Dorien Lugtenberg; Jeroen Schoots; Hans van Bokhoven; Bregje W M van Bon; Joris Veltman; Lisenka E L M Vissers; Michèl A A P Willemsen; Tjitske Kleefstra
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects.
Journal of medical genetics 2012;49(3):179-83.
2012: Michael A Simpson; Lisenka E L M Vissers; Susan M White; Wesley J Woollard; Ernie M H F Bongers; Han G Brunner; Ruthy Cohen-Snuijf; Dimitra Dafou; Ronny Derks; Charu Deshpande; Gabriele Gillessen-Kaesbach; Lies Hoefsloot; Susan E Holder; Sarina G Kant; Willie Reardon; Richard C Trembath
De novo mutations of the gene encoding the histone acetyltransferase KAT6B cause Genitopatellar syndrome.
American journal of human genetics 2012;90(2):290-4.
2011: Lisenka E L M Vissers; Giuseppina Timpani; Sheila Unger; Joris Veltman; Domenico Barbuti; Luisa Bonafé; Han G Brunner; Belinda Campos-Xavier; Tae-Joon Cho; Carlo Dionisi Vici; Ahmet Dursun; Virginia Fano; Ok Hwa Kim; Sun Hee Lee; Diego Martinelli; Gen Nishimura; Jörn Oliver Sass; Andrea Superti-Furga
Whole-exome sequencing detects somatic mutations of IDH1 in metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria (MC-HGA).
American journal of medical genetics. Part A 2011;155A(11):2609-16.
2011: Jayne Hehir-Kwa; Luis A Pérez Jurado; Rolph Pfundt; Benjamín Rodríguez-Santiago; Jan K Buitelaar; Nicole de Leeuw; Lisenka E L M Vissers; Joris Veltman
De novo copy number variants associated with intellectual disability have a paternal origin and age bias.
Journal of medical genetics 2011;48(11):776-8.
2011: Lisenka E L M Vissers; Fenny Wiradjaja; Garima Yagnik; Kiyotoshi Sekiguchi; Kieran M Short; Ian Smyth; Hans van Bokhoven; Joris Veltman; Peter J Anderson; Debora Bertola; Simeon Boyd; Michael F Buckley; Timothy C Cox; Michael L Cunningham; Irene M Janssen; Fernanda Jehee; Daiji Kiyozumi; Jia Liu; A. Murat Maga; Carlo Marcelis; Maria Rita Passos-Bueno; Tony Roscioli
Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice.
PLoS genetics 2011;7(9):e1002278.
2011: Alexander Hoischen; Irene Janssen; Susanne Kjaergaard; Ruth McGowan; Ruth Newbury-Ecob; Maarit Peippo; Anita Rauch; Benjamín Rodríguez-Santiago; Sarah F Smithson; Bregje W M van Bon; Bart van Lier; Joris Veltman; Lisenka E L M Vissers; Dagmar Wieczorek; Deborah Bartholdi; Han G Brunner; Jan M Cobben; Petra de Vries; Christian Gilissen; Gabriele Gillessen-Kaesbach; Judith Goodship; Rob Hastings; Bert B A de Vries
De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome.
Nature genetics 2011;43(8):729-31.
2011: Lisenka E L M Vissers; Ekkehart Lausch; Sheila Unger; Ana Belinda Campos-Xavier; Christian Gilissen; Antonio Rossi; Marisol Del Rosario; Hanka Venselaar; Ute Knoll; Sheela Nampoothiri; Mohandas Nair; Jürgen Spranger; Han G Brunner; Luisa Bonafé; Joris Veltman; Bernhard Zabel; andrea superti-furga
Chondrodysplasia and abnormal joint development associated with mutations in IMPAD1, encoding the Golgi-resident nucleotide phosphatase, gPAPP.
American journal of human genetics 2011;88(5):608-15.
2010: Lisenka E L M Vissers; Joep de Ligt; Christian Gilissen; Irene 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 Veltman
A de novo paradigm for mental retardation.
Nature genetics 2010;42(12):1109-12.
2010: Lisenka E L M Vissers; Bert B A de Vries; Joris Veltman
Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis.
Journal of medical genetics 2010;47(5):289-97.
2009: Lisenka E L M Vissers; samarth Bhatt; Irene M Janssen; Zhilian Xia; Seema R Lalani; Rolph Pfundt; Katarzyna Derwinska; Bert B A de Vries; Christian Gilissen; Alexander Hoischen; Monika Nesteruk; Barbara Wisniowiecka-Kowalnik; Marta Smyk; Han G Brunner; Sau Wai Cheung; Ad Geurts van Kessel; Joris Veltman; Pawel Stankiewicz
Rare pathogenic microdeletions and tandem duplications are microhomology-mediated and stimulated by local genomic architecture.
Human molecular genetics 2009;18(19):3579-93.
2008: Mariëlle E M Swinkels; Annet Simons; Dominique Smeets; Lisenka E L M Vissers; Joris Veltman; Rolph Pfundt; Bert B A de Vries; B H W Faas; C T R M Schrander-Stumpel; Emma McCann; Elizabeth Sweeney; Paul May; Jos M Th Draaisma; Nine V A M Knoers; Ad Geurts van Kessel; Conny van Ravenswaaij-Arts
Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: Delineation of the critical region for a consensus phenotype.
American journal of medical genetics. Part A 2008;146A(11):1430-8.
2007: Ilse Feenstra; Lisenka E L M Vissers; Mirjam Orsel; Ad Geurts van Kessel; Han G Brunner; Joris Veltman; Conny van Ravenswaaij-Arts
Genotype-phenotype mapping of chromosome 18q deletions by high-resolution array CGH: an update of the phenotypic map.
American journal of medical genetics. Part A 2007;143A(16):1858-67.
2007: Lisenka E L M Vissers; Pawel Stankiewicz; Svetlana A Yatsenko; E Crawford; H Creswick; V K Proud; Bert B A de Vries; Rolph Pfundt; C L M Marcelis; J Zackowski; Weimin Bi; Ad Geurts van Kessel; James R Lupski; Joris Veltman
Complex chromosome 17p rearrangements associated with low-copy repeats in two patients with congenital anomalies.
Human genetics 2007;121(6):697-709.
2007: Silke Schlaubitz; Svetlana A Yatsenko; Laurie D Smith; Kory L Keller; Lisenka E L M Vissers; Daryl A Scott; Wei-Wen Cai; William Reardon; Omar A Abdul-Rahman; Edward J Lammer; Caroline A Lifchez; Ellen Magenis; Joris Veltman; Pawel Stankiewicz; Bernhard Zabel; Brendan Lee
Ovotestes and XY sex reversal in a female with an interstitial 9q33.3-q34.1 deletion encompassing NR5A1 and LMX1B causing features of Genitopatellar syndrome.
American journal of medical genetics. Part A 2007;143A(10):1071-81.
2007: Stefan J White; Lisenka E L M Vissers; Ad Geurts van Kessel; Renée X de Menezes; E Kalay; A E Lehesjoki; P C Giordano; Esther van de Vosse; M H Breuning; Han G Brunner; Johan T den Dunnen; Joris Veltman
Variation of CNV distribution in five different ethnic populations.
Cytogenetic and genome research 2007;118(1):19-30.
2006: David A Koolen; Lisenka E L M Vissers; Rolph Pfundt; Nicole de Leeuw; Samantha J L Knight; Regina Regan; R Frank Kooy; Edwin Reyniers; Corrado Romano; Marco Fichera; Albert Schinzel; Alessandra Baumer; Britt-Marie Anderlid; Jacqueline Schoumans; Nine V A M Knoers; Ad Geurts van Kessel; Erik A Sistermans; Joris Veltman; Han G Brunner; Bert B A de Vries
A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism.
Nature genetics 2006;38(9):999-1001.
2006: Marjolijn Jongmans; Ronald J C Admiraal; Kim P van der Donk; Lisenka E L M Vissers; A F Baas; Livia Kapusta; J M van Hagen; D Donnai; T J de Ravel; Joris Veltman; Ad Geurts van Kessel; Bert B A de Vries; Han G Brunner; Lies Hoefsloot; Conny van Ravenswaaij-Arts
CHARGE syndrome: the phenotypic spectrum of mutations in the CHD7 gene.
Journal of medical genetics 2006;43(4):306-14.
2005: Lisenka E L M Vissers; Joris Veltman; Ad Geurts van Kessel; Han G Brunner
Identification of disease genes by whole genome CGH arrays.
Human molecular genetics 2005;14 Spec No. 2():R215-23.
2005: Bert B A de Vries; Rolph Pfundt; Martijn A R Leisink; David A Koolen; Lisenka E L M Vissers; Irene M Janssen; Simon van Reijmersdal; Willy M Nillesen; Erik H L P G Huys; Nicole de Leeuw; Dominique Smeets; Erik A Sistermans; Ton Feuth; Conny van Ravenswaaij-Arts; Ad Geurts van Kessel; Eric F P M Schoenmakers; Han G Brunner; Joris Veltman
Diagnostic genome profiling in mental retardation.
American journal of human genetics 2005;77(4):606-16.
2004: Lisenka E L M Vissers; Conny van Ravenswaaij-Arts; Ronald J C Admiraal; Jane A Hurst; Bert B A de Vries; Irene M Janssen; Walter A Van Der Vliet; Erik H L P G Huys; Pieter J de Jong; Ben C J Hamel; Eric F P M Schoenmakers; Han G Brunner; Joris Veltman; Ad Geurts van Kessel
Mutations in a new member of the chromodomain gene family cause CHARGE syndrome.
Nature genetics 2004;36(9):955-7.
2004: David A Koolen; Lisenka E L M Vissers; Willy M Nillesen; Dominique Smeets; Conny van Ravenswaaij-Arts; Erik A Sistermans; Joris Veltman; Bert B A de Vries; B D A de Vries
A novel microdeletion, del(2)(q22.3q23.3) in a mentally retarded patient, detected by array-based comparative genomic hybridization.
Clinical genetics 2004;65(5):429-32.
2003: Lisenka E L M Vissers; Bert B A de Vries; Kazutoyo Osoegawa; Irene M Janssen; Ton Feuth; Chik On Choy; huub straatman; Walter A Van Der Vliet; Erik H L P G Huys; Anke van Rijk; Dominique Smeets; Conny van Ravenswaaij-Arts; Nine V A M Knoers; Ineke van der Burgt; Pieter J de Jong; Han G Brunner; Ad Geurts van Kessel; Eric F P M Schoenmakers; Joris Veltman
Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.
American journal of human genetics 2003;73(6):1261-70.
2003: Imke M Veltman; Joris Veltman; Ger Arkesteijn; Irene M Janssen; Lisenka E L M Vissers; Pieter J de Jong; Ad Geurts van Kessel; Eric F P M Schoenmakers
Chromosomal breakpoint mapping by arrayCGH using flow-sorted chromosomes.
BioTechniques 2003;35(5):1066-70.
2003: Gaetano Zafarana; Beata Grygalewicz; Ad J M Gillis; Lisenka E L M Vissers; Walter van de Vliet; Ruud van Gurp; hans stoop; Maria Debiec-Rychter; J Wolter Oosterhuis; Ad Geurts van Kessel; Eric F P M Schoenmakers; Leendert H J Looijenga; Joris Veltman
12p-amplicon structure analysis in testicular germ cell tumors of adolescents and adults by array CGH.
Oncogene 2003;22(48):7695-701.