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Kristien Verhoeven

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Kristl G Claeys; Stephan Zuchner; Marina Kennerson; José Berciano; Antonio Garcia; Kristien Verhoeven; Elsdon Storey; John R Merory; Henriette M E Bienfait; Martin Lammens; Eva Nelis; Jonathan Baets; Els De Vriendt; Zwi N Berneman; Ilse De Veuster; Jeffery Vance; Garth Nicholson; Vincent Timmerman; Peter De Jonghe
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.
Philip Van Damme; Elke Bogaert; Maarten Dewil; Nicole Hersmus; Dora Kiraly; Wendy Scheveneels; Ilse Bockx; Dries Braeken; Nathalie Verpoorten; Kristien Verhoeven; Vincent Timmerman; Paul Herijgers; Geert Callewaert; Peter Carmeliet; Ludo Van Den Bosch; Wim Robberecht
Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity.
Kristien Verhoeven; Vincent Timmerman; Barbara Mauko; Thomas R Pieber; Peter De Jonghe; Michaela Auer-Grumbach
Recent advances in hereditary sensory and autonomic neuropathies.

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All Publications

2009: Kristl G Claeys; Stephan Zuchner; Marina Kennerson; José Berciano; Antonio Garcia; Kristien Verhoeven; Elsdon Storey; John R Merory; Henriette M E Bienfait; Martin Lammens; Eva Nelis; Jonathan Baets; Els De Vriendt; Zwi N Berneman; Ilse De Veuster; Jeffery Vance; Garth Nicholson; Vincent Timmerman; Peter De Jonghe
Phenotypic spectrum of dynamin 2 mutations in Charcot-Marie-Tooth neuropathy.
Brain : a journal of neurology 2009;132(Pt 7):1741-52.
2007: Philip Van Damme; Elke Bogaert; Maarten Dewil; Nicole Hersmus; Dora Kiraly; Wendy Scheveneels; Ilse Bockx; Dries Braeken; Nathalie Verpoorten; Kristien Verhoeven; Vincent Timmerman; Paul Herijgers; Geert Callewaert; Peter Carmeliet; Ludo Van Den Bosch; Wim Robberecht
Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(37):14825-30.
2006: Kristien Verhoeven; Vincent Timmerman; Barbara Mauko; Thomas R Pieber; Peter De Jonghe; Michaela Auer-Grumbach
Recent advances in hereditary sensory and autonomic neuropathies.
Current opinion in neurology 2006;19(5):474-80.
2006: Stephan Zuchner; Peter De Jonghe; Albena Jordanova; Kristl G Claeys; Velina Guergueltcheva; Sylvia Cherninkova; Steven R Hamilton; Gregory P Van Stavern; Karen M Krajewski; Jason E Stajich; Ivailo Tournev; Kristien Verhoeven; Christine T Langerhorst; Marianne De Visser; Frank Baas; Thomas D Bird; Vincent Timmerman; chris hall; Jeffery Vance
Axonal neuropathy with optic atrophy is caused by mutations in mitofusin 2.
Annals of neurology 2006;59(2):276-81.
2005: Nathalie Verpoorten; Kristien Verhoeven; Stefan Weckx; An Jacobs; Sally Serneels; Jurgen Del-Favero; Chantal Ceuterick; Dirk R Van Bockstaele; Zwi N Berneman; Ludo Van Den Bosch; Wim Robberecht; Lucilla Nobbio; Angelo Schenone; Eric Dessaud; Odile deLapeyrière; Danny Huylebroeck; An Zwijsen; Peter De Jonghe; Vincent Timmerman
Synaptopodin and 4 novel genes identified in primary sensory neurons.
Molecular and cellular neurosciences 2005;30(3):316-25.
2005: P Kevin Legan; Victoria A Lukashkina; Richard J Goodyear; Andrei N Lukashkin; Kristien Verhoeven; Guy Van Camp; Ian J Russell; Guy P Richardson
A deafness mutation isolates a second role for the tectorial membrane in hearing.
Nature neuroscience 2005;8(8):1035-42.
2005: Tiziana Vigo; Lucilla Nobbio; Paul Van Hummelen; Michele Abbruzzese; Gianluigi Mancardi; Nathalie Verpoorten; Kristien Verhoeven; Michael W Sereda; Klaus-Armin Nave; Vincent Timmerman; Angelo Schenone
Experimental Charcot-Marie-Tooth type 1A: a cDNA microarrays analysis.
Molecular and cellular neurosciences 2005;28(4):703-14.
2005: Stephan Zuchner; Maher A Noureddine; Marina L Kennerson; Kristien Verhoeven; Kristl G Claeys; Peter De Jonghe; John Merory; Sofia A Oliveira; Marcy C Speer; Judith E Stenger; Gina Walizada; Danqing Zhu; Margaret Pericak-Vance; Garth Nicholson; Vincent Timmerman; Jeffery Vance
Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease.
Nature genetics 2005;37(3):289-94.
2004: Kristien Verhoeven; Katrien Coen; Els De Vriendt; An Jacobs; Veerle Van Gerwen; Iris Smouts; A Pou-Serradell; Jean-Jacques Martin; Vincent Timmerman; Peter De Jonghe
SPTLC1 mutation in twin sisters with hereditary sensory neuropathy type I.
Neurology 2004;62(6):1001-2.
2003: Kristien Verhoeven; Peter De Jonghe; Tom Van de Putte; Eva Nelis; An Zwijsen; Nathalie Verpoorten; Els De Vriendt; An Jacobs; Veerle Van Gerwen; Annick Francis; Chantal Ceuterick; Danny Huylebroeck; Vincent Timmerman
Slowed conduction and thin myelination of peripheral nerves associated with mutant rho Guanine-nucleotide exchange factor 10.
American journal of human genetics 2003;73(4):926-32.
2003: Michaela Auer-Grumbach; Peter De Jonghe; Kristien Verhoeven; Vincent Timmerman; Klaus Wagner; Hans-Peter Hartung; Garth A Nicholson
Autosomal dominant inherited neuropathies with prominent sensory loss and mutilations: a review.
Archives of neurology 2003;60(3):329-34.
2003: Kristien Verhoeven; Peter De Jonghe; Katrien Coen; Nathalie Verpoorten; Michaela Auer-Grumbach; Jennifer M Kwon; David FitzPatrick; Eric Schmedding; Els De Vriendt; An Jacobs; Veerle Van Gerwen; Klaus Wagner; Hans-Peter Hartung; Vincent Timmerman
Mutations in the small GTP-ase late endosomal protein RAB7 cause Charcot-Marie-Tooth type 2B neuropathy.
American journal of human genetics 2003;72(3):722-7.
2002: Jennifer L Dawkins; Sonal Brahmbhatt; Michaela Auer-Grumbach; Klaus Wagner; Hans-Peter Hartung; Kristien Verhoeven; Vincent Timmerman; Peter De Jonghe; Marina L Kennerson; Eric LeGuern; Garth A Nicholson
Exclusion of serine palmitoyltransferase long chain base subunit 2 (SPTLC2) as a common cause for hereditary sensory neuropathy.
Neuromuscular disorders : NMD 2002;12(7-8):656-8.
2002: Joy Irobi; Eva Nelis; Kristien Verhoeven; Els De Vriendt; Ines Dierick; Peter De Jonghe; Christine Van Broeckhoven; Vincent Timmerman
Mutation analysis of 12 candidate genes for distal hereditary motor neuropathy type II (distal HMN II) linked to 12q24.3.
Journal of the peripheral nervous system : JPNS 2002;7(2):87-95.
2002: Paul J Govaerts; Geert De Ceulaer; Kristin Daemers; Kristien Verhoeven; Guy Van Camp; Isabelle Schatteman; Margriet Verstreken; Patrick J Willems; Thomas Somers; F Erwin Offeciers
Clinical presentation of DFNA8-DFNA12.
Advances in oto-rhino-laryngology 2002;61():60-5.
2001: Kristien Verhoeven; M Villanova; A Rossi; A Malandrini; Peter De Jonghe; Vincent Timmerman
Localization of the gene for the intermediate form of Charcot-Marie-Tooth to chromosome 10q24.1-q25.1.
American journal of human genetics 2001;69(4):889-94.
2001: Sigrid Wayne; Nahid G Robertson; Frank Declau; N Chen; Kristien Verhoeven; Sai Prasad; L Tranebjärg; Cynthia C Morton; A F Ryan; Guy Van Camp; Richard J H Smith
Mutations in the transcriptional activator EYA4 cause late-onset deafness at the DFNA10 locus.
Human molecular genetics 2001;10(3):195-200.
2000: Michaela Auer-Grumbach; Peter De Jonghe; Klaus Wagner; Kristien Verhoeven; Hans-Peter Hartung; Vincent Timmerman
Phenotype-genotype correlations in a CMT2B family with refined 3q13-q22 locus.
Neurology 2000;55(10):1552-7.
2000: Margriet Verstreken; Frank Declau; Isabelle Schatteman; D Van Velzen; Kristien Verhoeven; Guy Van Camp; Patrick J Willems; E W Kuhweide; E Verhaert; P D'Haese; Floris L Wuyts; Paul H Van De Heyning
Audiometric analysis of a Belgian family linked to the DFNA10 locus.
The American journal of otology 2000;21(5):675-81.
2000: Kristien Verhoeven; T Fagerheim; Sai Prasad; Sigrid Wayne; F De Clau; Wendy Balemans; Margriet Verstreken; Isabelle Schatteman; B Solem; Paul Van de Heyning; L Tranebjärg; Richard J H Smith; Guy Van Camp
Refined localization and two additional linked families for the DFNA10 locus for nonsyndromic hearing impairment.
Human genetics 2000;107(1):7-11.
2000: Guy Van Camp; Paul J Coucke; Peter Van Hauwe; Lut Van Laer; Kristien Verhoeven; Floris L Wuyts; Richard J H Smith
DFNA 2, 5, 8, 12.
Advances in oto-rhino-laryngology 2000;56():68-77.
1999: Ludo Van Den Bosch; Kristien Verhoeven; Humbert De Smedt; Frank Wuytack; Ludwig Missiaen; Wim Robberecht
Calcium handling proteins in isolated spinal motoneurons.
Life sciences 1999;65(15):1597-606.
1999: Kristien Verhoeven; Robbert J H Ensink; V Tiranti; Patrick Huygen; DF Johnson; Isabelle Schatteman; Lut Van Laer; Margriet Verstreken; Paul Van de Heyning; Nathan Fischel-Ghodsian; M Zeviani; Cor W R J Cremers; Patrick J Willems; Guy Van Camp
Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
European journal of human genetics : EJHG 1999;7(1):45-51.
1998: Paul J Govaerts; Geert De Ceulaer; Kristin Daemers; Kristien Verhoeven; Guy Van Camp; Isabelle Schatteman; Margriet Verstreken; Patrick J Willems; Thomas Somers; F Erwin Offeciers
A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.
The American journal of otology 1998;19(6):718-23.
1998: Robbert J H Ensink; Kristien Verhoeven; Henri Marres; Patrick Huygen; G W Padberg; H ter Laak; Guy Van Camp; P J Willems; Cor W R J Cremers
Early-onset sensorineural hearing loss and late-onset neurologic complaints caused by a mitochondrial mutation at position 7472.
Archives of otolaryngology--head & neck surgery 1998;124(8):886-91.
1998: Daryl A Scott; John H Greinwald; JR Marietta; Stacy Drury; Ruth E Swiderski; A Viñas; Margaret DeAngelis; Rivka Carmi; Arabandi Ramesh; ML Kraft; Khalil Elbedour; A B Skworak; R A Friedman; Srikumari Srisailapathy; Kristien Verhoeven; G Van Gamp; Michael Lovett; Prescott L Deininger; Mark A Batzer; Cynthia C Morton; Bronya J B Keats; Richard J H Smith; Val C Sheffield
Identification and mutation analysis of a cochlear-expressed, zinc finger protein gene at the DFNB7/11 and dn hearing-loss loci on human chromosome 9q and mouse chromosome 19.
Gene 1998;215(2):461-9.
1998: Kristien Verhoeven; Lut Van Laer; Karin Kirschhofer; P Kevin Legan; David Hughes; Isabelle Schatteman; Margriet Verstreken; Peter Van Hauwe; P Coucke; A Chen; Richard J H Smith; Thomas Somers; F Erwin Offeciers; Paul Van de Heyning; Guy P Richardson; Franz J Wachtler; William J Kimberling; Patrick J Willems; Paul J Govaerts; Guy Van Camp
Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.
Nature genetics 1998;19(1):60-2.
1998: AH Chen; Robert F Mueller; Sai D Prasad; John H Greinwald; Jose M Manaligod; A C Muilenburg; Kristien Verhoeven; Guy Van Camp; Richard J H Smith
Presymptomatic diagnosis of nonsyndromic hearing loss by genotyping.
Archives of otolaryngology--head & neck surgery 1998;124(1):20-4.
1997: Kristien Verhoeven; Guy Van Camp; Paul J Govaerts; Wendy Balemans; Isabelle Schatteman; Margriet Verstreken; Lut Van Laer; Richard J H Smith; MR Brown; Paul H Van De Heyning; Thomas Somers; F Erwin Offeciers; Patrick J Willems
A gene for autosomal dominant nonsyndromic hearing loss (DFNA12) maps to chromosome 11q22-24.
American journal of human genetics 1997;60(5):1168-73.