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Researcher
Bart Dermaut
Profile
Projects
Publications
Activities
Awards & Distinctions
136
Results
2024
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability
Maria del Rocio Pérez Baca
Eva Jacobs
Lies Vantomme
Pontus LeBlanc
Elke Bogaert
Annelies Dheedene
Laurenz De Cock
Sadegheh Haghshenas
Aidin Foroutan
Michael A Levy
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2024
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder
Maria del Rocio Pérez Baca
Maria Palomares
Michiel Vanhooydonck
Eva D'haene
Eva Z. Jacobs
Lies Vantomme
Fernando Santos-Simarro
Roser Lleuger-Pujol
Sixto García-Miñaúr
Itsaso Losantos-García
et al.
U
Conference
2024
Loss-of-function of the Zinc Finger Homeobox 4 (ZFHX4) gene causes a novel neurodevelopmental disorder
Maria del Rocio Pérez Baca
Maria Palomares
Michiel Vanhooydonck
Eva D'haene
Eva Z. Jacobs
Lies Vantomme
Fernando Santos-Simarro
Roser Lleuger-Pujol
Sixto García-Miñáur
Itsaso Losantos-García
et al.
U
Conference
2024
Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP)
Astrid Van den broecke
Alexander Decruyenaere
Nika Schuermans
Hannah Verdin
Jody Ghijsels
Anne Sieben
Bart Dermaut
Dimitri Hemelsoet
A1
Journal Article
in
JOURNAL OF NEUROLOGY
2024
2023
A Solve-RD ClinVar-based reanalysis of 1522 index cases from ERN-ITHACA reveals common pitfalls and misinterpretations in exome sequencing
Anne-Sophie Denommé-Pichon
Leslie Matalonga
Elke de Boer
Adam Jackson
Elisa Benetti
Siddharth Banka
Ange-Line Bruel
Andrea Ciolfi
Jill Clayton-Smith
Bruno Dallapiccola
et al.
A1
Journal Article
in
GENETICS IN MEDICINE
2023
C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD
Pedro Ervilha Pereira
Nika Schuermans
Antoon Meylemans
Pontus LeBlanc
Lauren Versluys
KE Copley
JD Rubien
C Altheimer
Myra Peetermans
Elke Debackere
et al.
A1
Journal Article
in
ACTA NEUROPATHOLOGICA
2023
Exome sequencing and multigene panel testing in 1,411 patients with adult-onset neurologic disorders
Nika Schuermans
Hannah Verdin
Jody Ghijsels
Madeleine Hellemans
Elke Debackere
Elke Bogaert
Sofie Symoens
Leslie Naesens
Elien Lecomte
David Crosiers
et al.
A1
Journal Article
in
NEUROLOGY-GENETICS
2023
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling
Nika Schuermans
Salima El Chehadeh
Dimitri Hemelsoet
Jérémie Gautheron
Marie-Christine Vantyghem
Sonia Nouioua
Meriem Tazir
Corinne Vigouroux
Martine Auclair
Elke Bogaert
et al.
A1
Journal Article
in
NATURE GENETICS
2023
Phospholipid modifier PLAAT3 links defective PPARγ-dependent signaling to lipodystrophy
Bart Dermaut
Nika Schuermans
A1
Journal Article
in
NATURE GENETICS
2023
SRSF1 haploinsufficiency is responsible for a syndromic developmental disorder associated with intellectual disability
Elke Bogaert
Aurore Garde
Thierry Gautier
Kathleen Rooney
Yannis Duffourd
Pontus LeBlanc
Emma Van Reempts
Frederic Tran Mau-Them
Ingrid M. Wentzensen
Kit Sing Au
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2023
Tau promotes oxidative stress-associated cycling neurons in S phase as a pro-survival mechanism : possible implication for Alzheimer's disease
M Denechaud
Sarah Geurs
T Comptdaer
S Bégard
A Garcia-Núñez
LA Pechereau
T Bouillet
Y Vermeiren
PP De Deyn
R Perbet
et al.
A1
Journal Article
in
PROGRESS IN NEUROBIOLOGY
2023
Twist exome capture allows for lower average sequence coverage in clinical exome sequencing
Burcu Yaldiz
Erdi Kucuk
Juliet Hampstead
Tom Hofste
Rolph Pfundt
Jordi Corominas Galbany
Tuula Rinne
Helger G. Yntema
Alexander Hoischen
Marcel Nelen
et al.
A1
Journal Article
in
HUMAN GENOMICS
2023
2022
A novel neurodevelopmental syndrome caused by loss-of-function of the Zinc Finger Homeobox 3 (ZFHX3) gene
Maria del Rocio Pérez Baca
Eva Jacobs
Lies Vantomme
Pontus LeBlanc
Elke Bogaert
Annelies Dheedene
Laurenz De Cock
Bart Dermaut
Aidin Foroutan
Jennifer Kerkhof
et al.
C3
Conference
2022
A structural variant of the C-terminal prion-like domain of TDP-43 causes vacuolar muscle degeneration
Pedro Ervilha Pereira
Nika Schuermans
Antoon Meylemans
Pontus LeBlanc
L Versluys
Elke Debackere
Olivier Vanakker
Sara Janssens
Jonathan Baets
K Verhoeven
et al.
C3
Conference
2022
Expanding the TDP-43 proteinopathy pathway from neurons to muscle : physiological and pathophysiological functions
Lauren Versluys
Pedro Ervilha Pereira
Nika Schuermans
Boel De Paepe
Jan De Bleecker
Elke Bogaert
Bart Dermaut
A1
Journal Article
in
FRONTIERS IN NEUROSCIENCE
2022
Lipodystrophy due to genetic deficiency of picornavirus host factor and obesity regulator PLAAT3
Nika Schuermans
Salima El Chehadeh
Dimitri Hemelsoet
Elke Bogaert
Elke Debackere
Pascale Hilbert
Nike Van Doninck
Marie-Caroline Taquet
Toon Rosseel
Griet De Clercq
et al.
C3
Conference
2022
Marked hypotonia : an additional feature of ANO3-related movement disorder
Patrick Santens
Arnout Bruggeman
Nika Schuermans
Hannah Verdin
Bart Dermaut
A1
Journal Article
in
EUROPEAN JOURNAL OF MEDICAL GENETICS
2022
Moyamoya disease emerging as an immune-related angiopathy
Caroline Asselman
Dimitri Hemelsoet
Denzel Eggermont
Bart Dermaut
Francis Impens
A1
Journal Article
in
TRENDS IN MOLECULAR MEDICINE
2022
Shortcutting the diagnostic odyssey : the multidisciplinary program for undiagnosed rare diseases in adults (UD-PrOZA)
Nika Schuermans
Dimitri Hemelsoet
Wim Terryn
Sanne Steyaert
Rudy Van Coster
Paul Coucke
Wouter Steyaert
Bert Callewaert
Elke Bogaert
Patrick Verloo
et al.
A1
Journal Article
in
ORPHANET JOURNAL OF RARE DISEASES
2022
The Alzheimer susceptibility gene BIN1 induces isoform-dependent neurotoxicity through early endosome defects
Erwan Lambert
Orthis Saha
Bruna Soares Landeira
Ana Raquel Melo de Farias
Xavier Hermant
Arnaud Carrier
Alexandre Pelletier
Johanna Gadaut
Lindsay Davoine
Cloe Dupont
et al.
A1
Journal Article
in
ACTA NEUROPATHOLOGICA COMMUNICATIONS
2022
2021
Adult-onset congenital central hypoventilation syndrome due to PHOX2B mutation
Antoon Meylemans
Pieter Depuydt
Elfride De Baere
Katrien Hertegonne
Eric Derom
Bart Dermaut
Dimitri Hemelsoet
A1
Journal Article
in
ACTA NEUROLOGICA BELGICA
2021
Proteome profiling of RNF213 depleted cells reveals nitric oxide regulator DDAH1 antilisterial activity
Lia Martina
Caroline Asselman
Fabien Henri Thery
Katie Boucher
Louis Delhaye
Teresa Maia
Bart Dermaut
Sven Eyckerman
Francis Impens
A1
Journal Article
in
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY
2021
Ring finger protein 213 assembles into a sensor for ISGylated proteins with antimicrobial activity
Fabien Henri Thery
Lia Martina
Caroline Asselman
Heidi Repo
Y Zhang
Koen Sedeyn
Georgios Moschonas
C Bredow
QW Teo
J Zhang
et al.
A1
Journal Article
in
NATURE COMMUNICATIONS
2021
2020
Amyloid-β1–43 cerebrospinal fluid levels and the interpretation of APP, PSEN1 and PSEN2 mutations
Federica Perrone
Maria Bjerke
Elisabeth Hens
Anne Sieben
Maarten Timmers
Arne De Roeck
Rik Vandenberghe
Kristel Sleegers
Jean-Jacques Martin
Peter P. De Deyn
et al.
A1
Journal Article
in
ALZHEIMERS RESEARCH & THERAPY
2020
2019
Biotinidase deficiency: A treatable cause of opticospinal syndrome in young adults
Vincent Van Iseghem
Mathieu Sprengers
Julie De Zaeytijd
Sindic CJM
B Willekens
Bart Dermaut
Dimitri Hemelsoet
Guy Laureys
Editorial material
2019
2018
Common and rare TBK1 variants in early-onset Alzheimer disease in a European cohort
Jan Verheijen
Julie van der Zee
Ilse Gijselinck
Tobi Van den Bossche
Lubina Dillen
Bavo Heeman
Estrella Gómez-Tortosa
Albert Lladó
Raquel Sanchez-Valle
Caroline Graff
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2018
Future perspectives of genome-scale sequencing
Wouter Steyaert
Steven Callens
Paul Coucke
Bart Dermaut
Dimitri Hemelsoet
Wim Terryn
Bruce Poppe
A1
Journal Article
in
ACTA CLINICA BELGICA
2018
IRF2BPL is associated with neurological phenotypes
Paul C Marcogliese
Vandana Shashi
Rebecca C Spillmann
Nicholas Stong
Jill A Rosenfeld
Mary Kay Koenig
Julian A Martínez-Agosto
Matthew Herzog
Agnes H Chen
Patricia I Dickson
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2018
Male-specific epistasis between WWC1 and TLN2 genes is associated with Alzheimer's disease
Elena S Gusareva
Jean-Claude Twizere
Kristel Sleegers
Pierre Dourlen
Jose F Abisambra
Shelby Meier
Ryan Cloyd
Blaine Weiss
Bart Dermaut
Kyrylo Bessonov
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2018
Teenage-onset progressive myoclonic epilepsy due to a familial C9orf72 repeat expansion
Jelle van den Ameele
Ivana Jedlickova
Anna Pristoupilova
Anne Sieben
Sara Van Mossevelde
Chantal Ceuterick-de Groote
Helena Hůlková
Radoslav Matej
Alfred Meurs
Christine Van Broeckhoven
et al.
A1
Journal Article
in
NEUROLOGY
2018
2017
Developmental expression of 4-repeat-Tau induces neuronal aneuploidy in Drosophila tauopathy models
Nicolas Malmanche
Pierre Dourlen
Marc Gistelinck
Florie Demiautte
Nichole Link
Cloé Dupont
Lies Vanden Broeck
Elisabeth Werkmeister
Philippe Amouyel
Antonino Bongiovanni
et al.
A1
Journal Article
in
SCIENTIFIC REPORTS
2017
Functional screening of Alzheimer risk loci identifies PTK2B as an in vivo modulator and early marker of Tau pathology
P Dourlen
FJ Fernandez-Gomez
C Dupont
B Grenier-Boley
C Bellenguez
H Obriot
R Caillierez
Y Sottejeau
J Chapuis
A Bretteville
et al.
A1
Journal Article
in
MOLECULAR PSYCHIATRY
2017
TBK1 mutation spectrum in an extended European patient cohort with frontotemporal dementia and amyotrophic lateral sclerosis
Julie van der Zee
Ilse Gijselinck
Sara Van Mossevelde
Federica Perrone
Lubina Dillen
Bavo Heeman
Veerle Bäumer
Sebastiaan Engelborghs
Jan De Bleecker
Jonathan Baets
et al.
A1
Journal Article
in
HUMAN MUTATION
2017
2016
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease
Jan Verheijen
Tobi Van den Bossche
Julie van der Zee
Sebastiaan Engelborghs
Raquel Sanchez-Valle
Albert Llado
Caroline Graff
Hakan Thonberg
Pau Pastor
Sara Ortega-Cubero
et al.
A1
Journal Article
in
ACTA NEUROPATHOLOGICA
2016
ADAM30 downregulates APP-linked defects through cathepsin D activation in Alzheimer's disease
Florent Letronne
Geoffroy Laumet
Anne-Marie Ayral
Julien Chapuis
Florie Demiautte
Mathias Laga
Michel E Vandenberghe
Nicolas Malmanche
Florence Leroux
Fanny Eysert
et al.
A1
Journal Article
in
EBIOMEDICINE
2016
Clinical features of TBKI carriers compared with C9orf72, GRN and non-mutation carriers in a Belgian cohort
Sara Van Mossevelde
Julie van der Zee
Ilse Gijselinck
Sebastiaan Engelborghs
Anne Sieben
Tim Van Langenhove
Jan De Bleecker
Jonathan Baets
Mathieu Vandenbulcke
Koen Van Laere
et al.
A1
Journal Article
in
BRAIN
2016
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia
Sarah Weckhuysen
Elise Marsan
Virginie Lambrecq
Cécile Marchal
Mélanie Morin-Brureau
Isabelle An-Gourfinkel
Michel Baulac
Martine Fohlen
Christine Kallay Zetchi
Margitta Seeck
et al.
A1
Journal Article
in
EPILEPSIA
2016
Phenotypic characteristics of Alzheimer patients carrying an ABCA7 mutation
Tobi Van den Bossche
Kristel Sleegers
Elise Cuyvers
Sebastiaan Engelborghs
Anne Sieben
Arne De Roeck
Caroline Van Cauwenberghe
Steven Vermeulen
Marleen Van den Broeck
Annelies Laureys
et al.
A1
Journal Article
in
NEUROLOGY
2016
The C9orf72 repeat size correlates with onset age of disease, DNA methylation and transcriptional downregulation of the promoter
I Gijselinck
S Van Mossevelde
J van der Zee
Anne Sieben
S Engelborghs
Jan De Bleecker
A Ivanoiu
O Deryck
D Edbauer
M Zhang
et al.
A1
Journal Article
in
MOLECULAR PSYCHIATRY
2016
2015
A 22-single nucleotide polymorphism Alzheimer's disease risk score correlates with family history, onset age, and cerebrospinal fluid Aβ42
Kristel Sleegers
Karolien Bettens
Arne De Roeck
Caroline Van Cauwenberghe
Elise Cuyvers
Jan Verheijen
Hanne Struyfs
Jasper Van Dongen
Steven Vermeulen
Sebastiaan Engelborghs
et al.
A1
Journal Article
in
ALZHEIMERS & DEMENTIA
2015
Functional complementation in Drosophila to predict the pathogenicity of TARDBP variants: evidence for a loss-of-function mechanism.
Lies Vanden Broeck
Gernot Kleinberger
Julien Chapuis
Marc Gistelinck
Philippe Amouyel
Christine Van Broeckhoven
Jean-Charles Lambert
Patrick Callaerts
Bart Dermaut
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2015
Investigating the role of filamin C in Belgian patients with frontotemporal dementia linked to GRN deficiency in FTLD-TDP brains
Jonathan Janssens
Stephanie Philtjens
Gernot Kleinberger
Sara Van Mossevelde
Julie van der Zee
Rita Cacace
Sebastiaan Engelborghs
Anne Sieben
Julia Banzhaf-Strathmann
Lubina Dillen
et al.
A1
Journal Article
in
ACTA NEUROPATHOLOGICA COMMUNICATIONS
2015
Loss of TBK1 is a frequent cause of frontotemporal dementia in a Belgian cohort
Ilse Gijselinck
Sara Van Mossevelde
Julie van der Zee
Anne Sieben
Stephanie Philtjens
Bavo Heeman
Sebastiaan Engelborghs
Mathieu Vandenbulcke
Greet De Baets
Veerle Baumer
et al.
A1
Journal Article
in
NEUROLOGY
2015
RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder
Patrick Santens
Tim Van Damme
Wouter Steyaert
Andy Willaert
Bernard Sablonnière
Anne De Paepe
Paul Coucke
Bart Dermaut
A1
Journal Article
in
NEUROLOGY
2015
Tau phosphorylation regulates the interaction between BIN1's SH3 domain and Tau's proline-rich domain
Yoann Sottejeau
Alexis Bretteville
François-Xavier Cantrelle
Nicolas Malmanche
Florie Demiaute
Tiago Mendes
Charlotte Delay
Harmony Alves Dos Alves
Amandine Flaig
Peter Davies
et al.
A1
Journal Article
in
ACTA NEUROPATHOLOGICA COMMUNICATIONS
2015
2014
Erfelijkheid
Bart Dermaut
Sandra Janssens
Ariane Van Tongerloo
Anne De Paepe
Bookchapter
in
Dementie op jonge leeftijd
2014
HDAC6 is a bruchpilot deacetylase that facilitates neurotransmitter release
Katarzyna Miskiewicz
Liya E Jose
Wondwossen M Yeshaw
Jorge S Valadas
Jef Swerts
Sebastian Munck
Fabian Feiguin
Bart Dermaut
Patrik Verstreken
A1
Journal Article
in
CELL REPORTS
2014
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
Elise Cuyvers
Karolien Bettens
Stéphanie Philtjens
Tim Van Langenhove
Ilse Gijselinck
Julie van der Zee
Sebastiaan Engelborghs
Mathieu Vandenbulcke
Jasper Van Dongen
Nathalie Geerts
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2014
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
Julie van der Zee
Tim Van Langenhove
Gabor G Kovacs
Lubina Dillen
William Deschamps
Sebastiaan Engelborghs
Radoslav Matěj
Mathieu Vandenbulcke
Anne Sieben
Bart Dermaut
et al.
A1
Journal Article
in
ACTA NEUROPATHOLOGICA
2014
2013
Explorative genetic study of UBQLN2 and PFN1 in an extended Flanders-Belgian cohort of frontotemporal lobar degeneration patients
Lubina Dillen
Tim Van Langenhove
Sebastiaan Engelborghs
Mathieu Vandenbulcke
Stayko Sarafov
Ivailo Tournev
Celine Merlin
Patrick Cras
Rik Vandenberghe
Peter P De Deyn
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2013
Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology
J Chapuis
F Hansmannel
M Gistelinck
A Mounier
C Van Cauwenberghe
KV Kolen
F Geller
Y Sottejeau
D Harold
P Dourlen
et al.
A1
Journal Article
in
MOLECULAR PSYCHIATRY
2013
Loss and gain of Drosophila TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration by loss-of-function phenotypes
Danielle C Diaper
Yoshitsugu Adachi
Ben Sutcliffe
Dickon M Humphrey
Christopher JH Elliott
Alan Stepto
Zoe N Ludlow
Lies Vanden Broeck
Patrick Callaerts
Bart Dermaut
et al.
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
2013
TDP-43 loss-of-function causes neuronal loss due to defective steroid receptor-mediated gene program switching in Drosophila
Lies Vanden Broeck
Marina Naval-Sánchez
Yoshitsugu Adachi
Danielle Diaper
Pierre Dourlen
Julien Chapuis
Gernot Kleinberger
Marc Gistelinck
Christine Van Broeckhoven
Jean-Charles Lambert
et al.
A1
Journal Article
in
CELL REPORTS
2013
TDP-43-mediated neurodegeneration : towards a loss-of-function hypothesis?
Lies Vanden Broeck
Patrick Callaerts
Bart Dermaut
A1
Journal Article
in
TRENDS IN MOLECULAR MEDICINE
2013
2012
Both loss and gain of TDP-43 impair synaptic efficacy and motor control leading to age-related neurodegeneration in Drosophila
DC Diaper
Y Adachi
B Sutcliffe
DM Humphrey
C Elliott
T Fielding
M Burki
ZN Ludlow
L Vanden Broeck
P Callaerts
et al.
C3
Conference
2012
Drosophila models of tauopathies : what have we learned?
Marc Gistelinck
Jean-Charles Lambert
Patrick Callaerts
Bart Dermaut
Pierre Dourlen
A2
Journal Article
in
INTERNATIONAL JOURNAL OF ALZHEIMER'S DISEASE
2012
TDP-43 neurotoxicity by failed steroid receptor-dependent transcriptional program switching
L Vanden Broeck
Naval M Sanchez
Y Adachi
D Diaper
P Dourlen
M Gistelinck
F Hirth
S Aerts
P Callaerts
Bart Dermaut
C3
Conference
2012
The nuclear receptor Hr46 protects against tau toxicity by activation of S6K
M Gistelinck
L Vanden Broeck
P Callaerts
Bart Dermaut
C3
Conference
2012
2010
Progressive myoclonic epilepsy as an adult-onset manifestation of Leigh syndrome due to m.14487T > C
Bart Dermaut
S Seneca
L Dom
K Smets
L Ceulemans
Joél Smet
Boel De Paepe
S Tousseyn
S Weckhuysen
M Gewillig
et al.
A1
Journal Article
in
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
2010
The characterization of drosophila vesicular excitatory amino acid transporter
Takaaki Miyaji
Bram Laridon
Bart Dermaut
Haruka Ouchi
Patrick Callaerts
Yoshinori Moriyama
Koen Norga
C3
Conference
2010
2009
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
Ilse Gijselinck
Kristel Sleegers
Sebastiaan Engelborghs
Wim Robberecht
Jean-Jacques Martin
Rik Vandenberghe
Raf Sciot
Bart Dermaut
Dirk Goossens
Julie van der Zee
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2009
Vagus nerve stimulation for refractory status epilepticus
Veerle De Herdt
Liesbeth Waterschoot
Kristl Vonck
Bart Dermaut
Heleen Verhelst
Rudy Van Coster
Annick De Jaeger
Dirk Van Roost
Paul Boon
A1
Journal Article
in
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
2009
2008
CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro
Julie van der Zee
Hazel Urwin
Sebastiaan Engelborghs
Marc Bruyland
Rik Vandenberghe
Bart Dermaut
Tim De Pooter
Karin Peeters
Patrick Santens
Peter P De Deyn
et al.
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
2008
2007
Alzheimer and Parkinson diagnoses in progranulin null mutation carriers in an extended founder family
Nathalie Brouwers
Karen Nuytemans
Julie van der Zee
Ilse Gijselinck
Sebastiaan Engelborghs
Jessie Theuns
Samir Kumar-Singh
Barbara A Pickut
Philippe Pals
Bart Dermaut
et al.
A1
Journal Article
in
ARCHIVES OF NEUROLOGY
2007
Follow-up of a patient treated with vagus nerve stimulation for refractory status epilepticus
Kristl Vonck
Veerle De Herdt
Helene Verhelst
Bart Dermaut
Isabelle Dewaele
Liesbeth Waterschoot
Evelien Carrette
ANNIK DE JAEGER
Rudy Van Coster
Dirk Van Roost
et al.
C3
Conference
2007
Mutations other than null mutations producing a pathogenic loss of progranulin in frontotemporal dementia
Julie van der Zee
Isabelle Le Ber
Sebastian Maurer-Stroh
Sebastiaan Engelborghs
Ilse Gijselinck
Agnès Camuzat
Nathalie Brouwers
Rik Vandenberghe
Kristel Sleegers
Didier Hannequin
et al.
A1
Journal Article
in
HUMAN MUTATION
2007
Neuronal inclusion protein TDP-43 has no primary genetic role in FTD and ALS
Ilse Gijselinck
Kristel Sleegers
Sebastiaan Engelborghs
Wim Robberecht
Jean-Jacques Martin
Rik Vandenberghe
Raf Sciot
Bart Dermaut
Dirk Goossens
Julie van der Zee
et al.
P1
Conference
2007
2006
A Belgian ancestral haplotype harbours a highly prevalent mutation for 17q21-linked tau-negative FTLD
J VAN DER ZEE
R RADEMAKERS
S ENGELBORGHS
I GIJSELINCK
V BOGAERTS
R VANDENBERGHE
Patrick Santens
J CAEKEBEKE
T DE POOTER
K PEETERS
et al.
A1
Journal Article
in
BRAIN
2006
Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family
Daniel Pirici
Rik Vandenberghe
Rosa Rademakers
Bart Dermaut
Marc Cruts
Krist'l Vennekens
Ivy Cuijt
Ursula Lubke
Chantal Ceuterick
Jean-Jacques Martin
et al.
A1
Journal Article
in
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY
2006
Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementia
Sebastiaan Engelborghs
Bart Dermaut
Peter Mariën
Anoek Symons
Ellen Vloeberghs
Karen Maertens
Nore Somers
Johan Goeman
Rosa Rademakers
Marleen Van den Broeck
et al.
A1
Journal Article
in
NEUROBIOLOGY OF AGING
2006
Mean age-of-onset of familial Alzheimer disease caused by presenilin mutations correlates with both increased Aβ42 and decreased Aβ40
Samir Kumar-Singh
Jessie Theuns
Bianca Van Broeck
Daniel Pirici
Krist'l Vennekens
Ellen Corsmit
Marc Cruts
Bart Dermaut
Rong Wang
Christine Van Broeckhoven
A1
Journal Article
in
HUMAN MUTATION
2006
Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21
M CRUTS
I GIJSELINCK
J VAN DER ZEE
S ENGELBORGHS
H WILS
D PIRICI
R RADEMAKERS
R VANDENBERGHE
Bart Dermaut
JJ MARTIN
et al.
A1
Journal Article
in
NATURE
2006
The UBQLN1 polymorphism, UBQ-8i, at 9q22 is not associated with Alzheimer's disease with onset before 70 years
Nathalie Brouwers
Kristel Sleegers
Sebastiaan Engelborghs
Veerle Bogaerts
Cornelia M van Duijn
Peter Paul De Deyn
Christine Van Broeckhoven
Bart Dermaut
A1
Journal Article
in
NEUROSCIENCE LETTERS
2006
2005
Aberrant lysosomal carbohydrate storage accompanies endocytic defects and neurodegeneration in Drosophila benchwarmer
Bart Dermaut
Koenraad K Norga
Artur Kania
Patrik Verstreken
Hongling Pan
Yi Zhou
Patrick Callaerts
Hugo J Bellen
A1
Journal Article
in
JOURNAL OF CELL BIOLOGY
2005
Genomic architecture of human 17q21 linked to frontotemporal dementia uncovers a highly homologous family of low-copy repeats in the tau region
Marc Cruts
Rosa Rademakers
Ilse Gijselinck
Julie van der Zee
Bart Dermaut
Tim de Pooter
Peter de Rijk
Jurgen Del-Favero
Christine van Broeckhoven
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
2005
Linkage and association studies identify a novel locus for Alzheimer disease at 7q36 in a Dutch population-based sample
Rosa Rademakers
Marc Cruts
Kristel Sleegers
Bart Dermaut
Jessie Theuns
Yurii Aulchenko
Stefan Weckx
Tim De Pooter
Marleen Van den Broeck
Ellen Corsmit
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2005
Tau is central in the genetic Alzheimer-frontotemporal dementia spectrum
Bart Dermaut
Samir Kumar-Singh
Rosa Rademakers
Jessie Theuns
Marc Cruts
Christine Van Broeckhoven
A1
Journal Article
in
TRENDS IN GENETICS
2005
2004
A novel presenilin 1 mutation (gly183val) is associated with Pick's disease in the absence of β-amyloid plaques
Bart Dermaut
Samir Kumar-Singh
Sebastiaan Engelborghs
Jessie Theuns
Rosa Rademakers
Karin Peeters
Stephan Claes
Marc Cruts
Jean-Jacques Martin
Peter De Deyn
et al.
C3
Conference
2004
A novel presenilin 1 mutation associated with Pick's disease but not β-amyloid plaques
Bart Dermaut
Samir Kumar-Singh
Sebastian Engelborghs
Jessie Theuns
Rosa Rademakers
Jos Saerens
Barbara A Pickut
Karin Peeters
Marleen van den Broeck
Krist'l Vennekens
et al.
A1
Journal Article
in
ANNALS OF NEUROLOGY
2004
Dose dependent effect of APOE ε4 on behavioral symptoms in frontal lobe dementia patients
Sebastiaan Engelborghs
Bart Dermaut
Peter Mariën
Anoek Symons
Ellen Vloeberghs
Karen Maertens
Nore Somers
Jos Goeman
Roos Rademakers
Marleen Van Den Broeck
et al.
C3
Conference
2004
Genetic testing has no place as a routine diagnostic test in sporadic and familial cases of Alzheimer's disease
Tischa JM van der Cammen
Esther A Croes
Bart Dermaut
Marie-Claire de Jager
Marc Cruts
Christine Van Broeckhoven
Cornelia M van Duijn
A1
Journal Article
in
JOURNAL OF THE AMERICAN GERIATRICS SOCIETY
2004
Mutation analysis of candidate genes for chromosome 17-linked tau-negative FTD
R Rademakers
Bart Dermaut
M Van den Broeck
T De Pooter
CM van Duijn
C Van Broeckhoven
M Cruts
C3
Conference
2004
Neuropathological and biochemical characterization of a familial FTD patient carrying PS1 GLY183VAL
S Kumar-Singh
J Theuns
N Sergeant
Bart Dermaut
K Vennekens
A Ghestem
A Delacourte
PP De Deyn
C Van Broeckhoven
C3
Conference
2004
Octapeptide repeat insertions in the prion protein gene and early onset dementia
EA Croes
J Theuns
JJ Houwing-Duistermaat
Bart Dermaut
K Sleegers
G Roks
M Van den Broeck
B van Harten
JC van Swieten
M Cruts
et al.
A1
Journal Article
in
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
2004
Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease
Esther A Croes
Behrooz Z Alizadeh
Aida M Bertoli-Avella
Tessa Rademaker
Jeannette Vergeer-Drop
Bart Dermaut
Jeanine J Houwing-Duistermaat
Dorothee PWM Wientjens
Albert Hofman
Christine Van Broeckhoven
et al.
A1
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2004
Possible association of nicastrin polymorphisms and Alzheimer disease in the Finnish population
S Helisalmi
Bart Dermaut
M Hiltunen
A Mannermaa
M Van den Broeck
M Lehtovirta
AM Koivisto
S Iivonen
M Cruts
H Soininen
et al.
A1
Journal Article
in
NEUROLOGY
2004
The molecular genetics of early-onset Alzheimer's disease
C Van Broeckhoven
R Rademakers
Bart Dermaut
S Kumar-Singh
C van Duijn
M Cruts
C3
Conference
2004
2003
A straightforward approach to evaluate false positive associations in studies of gene interaction
CM Van Duijn
JJ Hottenga
G Roks
Bart Dermaut
C Van Broeckhoven
C3
Conference
2003
Absence of association between codon 129/219 polymorphisms of the prion protein gene and Alzheimer's disease in Japan: reply
Bart Dermaut
Esther A Croes
Cornelia M van Duijn
Christine Van Broeckhoven
A1
Journal Article
in
ANNALS OF NEUROLOGY
2003
Digenic progressive external ophthalmoplegiain a sporadic patient: recessive mutationsin POLG and C10orf2/Twinkle
Gert Van Goethem
Ann Löfgren
Bart Dermaut
Chantal Ceuterick
Jean-Jacques Martin
Christine Van Broeckhoven
A1
Journal Article
in
HUMAN MUTATION
2003
Early cognitive decline is associated with prion protein codon 129 polymorphism
Esther A Croes
Bart Dermaut
Jeanine J Houwing-Duistermaat
Marleen Van den Broeck
Marc Cruts
Monique MB Breteler
Albert Hofman
Christine van Broeckhoven
Cornelia M van Duijn
A1
Journal Article
in
ANNALS OF NEUROLOGY
2003
Effect of APOE genotype on behavioral and psychological signs and symptoms of dementia
S Engelborghs
Bart Dermaut
R D'Hooge
A Symons
F Clement
P Marien
J Goeman
BA Pickut
M Van den Broeck
S Serneels
et al.
C3
Conference
2003
Novel APP mutation V715A associated with presenile Alzheimer's disease in a German family
Marc Cruts
Bart Dermaut
Rosa Rademakers
Marleen Van den Broeck
Florian Stögbauer
Christine Van Broeckhoven
A1
Journal Article
in
JOURNAL OF NEUROLOGY
2003
Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy
Gert Van Goethem
Marianne Schwartz
Ann Löfgren
Bart Dermaut
Christine Van Broeckhoven
John Vissing
A1
Journal Article
in
EUROPEAN JOURNAL OF HUMAN GENETICS
2003
PRNP Val129 homozygosity increases risk for early-onset Alzheimer's disease
Bart Dermaut
Esther A Croes
Rosa Rademakers
Marleen Van den Broeck
Marc Cruts
Albert Hofman
Cornelia M van Duijn
Christine Van Broeckhoven
A1
Journal Article
in
ANNALS OF NEUROLOGY
2003
Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects
S Engelborghs
Bart Dermaut
J Goeman
J Saerens
P Marien
BA Pickut
M Van den Broeck
S Serneels
M Cruts
C Van Broeckhoven
et al.
A1
Journal Article
in
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
2003
Recessive POLG mutations presenting with sensory and ataxic neuropathy in compound heterozygote patients with progressive external ophthalmoplegia
G Van Goethem
JJ Martin
Bart Dermaut
A Löfgren
A Wibail
D Ververken
P Tack
I Dehaene
M Van Zandijcke
M Moonen
et al.
A1
Journal Article
in
NEUROMUSCULAR DISORDERS
2003
Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in western Europe
R Rademakers
Bart Dermaut
K Peeters
M Cruts
P Heutink
A Goate
C Van Broeckhoven
A1
Journal Article
in
HUMAN MUTATION
2003
2002
Atypical clinical phenotype in a 2 octapeptide repeat insert mutation in the prion protein gene
E Croes
K Sleegers
G Roks
C van Duijn
J Theuns
Bart Dermaut
C Van Broeckhoven
J van Swieten
C3
Conference
2002
Behavioral and psychological signs and symptoms in patients with dementia of the Alzheimer type (DAT) and frontotemporal dementia (FTD): no effect of APOE genotype
S Engelborghs
Bart Dermaut
M Cruts
C Van Broeckhoven
PP De Deyn
C3
Conference
2002
Effect of the APOE-491A/T promoter polymorphism on apolipoprotein E levels and risk of Alzheimer disease: the Rotterdam study
G Roks
M Cruts
JJ Houwing-Duistermaat
Bart Dermaut
S Serneels
LM Havekes
A Hofman
MMB Breteler
C Van Broeckhoven
CM van Duijn
A1
Journal Article
in
AMERICAN JOURNAL OF MEDICAL GENETICS
2002
Familial dementia caused by MAPT R406W clinically resembles Alzheimer's disease
R Rademakers
Bart Dermaut
K Peeters
M Pellis
M Cruts
C Van Broeckhoven
C3
Conference
2002
Homozygosity of valine at PRNP codon 129 is associated with early onset Alzheimer's disease in a Dutch population based sample
Bart Dermaut
R Rademakers
M Van den Broeck
M Cruts
C Van Broeckhoven
E Croes
CM van Duijn
C3
Conference
2002
In vitro analysis of Alzheimer's disease-related presenilin 1 and 2 mutations: effect on beta-amyloid processing
J Theuns
S Kumar-Singh
Bart Dermaut
K Vennekens
E Corsmit
M Cruts
C Van Broeckhoven
CM van Duijn
C3
Conference
2002
Nicastrin significantly modifies risk for familial early-onset Alzheimer's disease in a Dutch population based sample
Bart Dermaut
J Theuns
M Van den Broeck
K Vennekens
E Corsmit
M Cruts
C Van Broeckhoven
K Sleegers
CM van Duijn
H Hasegawa
et al.
C3
Conference
2002
Novel German APP V715A mutation associated with presenile Alzheimer's disease
M Cruts
Bart Dermaut
S Kumar-Singh
R Rademakers
M Van den Broeck
C Van Broeckhoven
F Stögbauer
C3
Conference
2002
Systematic analysis of the effect of novel Alzheimer disease PS1/2 mutations on A beta secretion
J Theuns
S Kumar-Singh
Bart Dermaut
K Vennekens
E Corsmit
M Cruts
CM Van Duijn
C Van Broeckhoven
C3
Conference
2002
Tau negative frontal lobe dementia at 17q21 : significant finemapping of the candidate region to a 4.8 cM interval
R Rademakers
M Cruts
Bart Dermaut
K Sleegers
SM Rosso
M Van den Broeck
H Backhovens
J van Swieten
CM van Duijn
C Van Broeckhoven
A1
Journal Article
in
MOLECULAR PSYCHIATRY
2002
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cm interval
R Rademakers
M Cruts
Bart Dermaut
M Van den Broeck
H Backhovens
C Van Broeckhoven
K Sleegers
CM van Duijn
SM Rosso
J van Swieten
C3
Conference
2002
Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cm interval
M Cruts
R Rademakers
Bart Dermaut
K Sleegers
SM Rosso
M Van den Broeck
H Backhovens
J van Swieten
CM van Duijn
C Van Broeckhoven
C3
Conference
2002
Tau negative frontal lobe dementia at 17q21: significant finernapping of the candidate region to a 4.8cM interval
R Rademakers
M Cruts
Bart Dermaut
K Sleegers
SM Rosso
M Van den Broeck
H Backhovens
J van Swieten
CM van Duijn
C Van Broeckhoven
C3
Conference
2002
The gene encoding nicastrin, a major γ-secretase component, modifies risk for familial early-onset Alzheimer disease in a Dutch population-based sample
Bart Dermaut
Jessie Theuns
Kristel Sleegers
Hiroshi Hasegawa
Marleen Van den Broeck
Krist'l Vennekens
Ellen Corsmit
Peter St George-Hyslop
Marc Cruts
Cornelia M van Duijn
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2002
2001
Amyloid beta-secretase gene (BACE) is neither mutated nor associated with early-onset Alzheimers disease
M Cruts
Bart Dermaut
R Rademakers
G Roks
M Van den Broeck
G Munteanu
CM van Duijn
C Van Broeckhoven
C3
Conference
2001
Amyloid β secretase gene (BACE) is neither mutated in nor associated with early-onset Alzheimer's disease
Marc Cruts
Bart Dermaut
Rosa Rademakers
Gerwin Roks
Marleen Van den Broeck
Gabriela Munteanu
Cornelia M van Duijn
Christine Van Broeckhoven
A1
Journal Article
in
NEUROSCIENCE LETTERS
2001
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia
Hiroto Fujigasaki
Jean-Jacques Martin
Peter Paul De Deyn
Agnès Camuzat
Didier Deffond
Giovanni Stevanin
Bart Dermaut
Christine Van Broeckhoven
Alexandra Dürr
Alexis Brice
A1
Journal Article
in
BRAIN
2001
Cerebral amyloid angiopathy is a pathogenic lesion in Alzheimer's disease due to a novel presenilin 1 mutation
Bart Dermaut
S Kumar-Singh
C De Jonghe
M Cruts
A Löfgren
U Lübke
P Cras
R Dom
PP De Deyn
JJ Martin
et al.
A1
Journal Article
in
BRAIN
2001
Chromosome 17 linked dementia in the absence of tau mutations
R Rademakers
M Cruts
Bart Dermaut
G Roks
M Van den Broeck
CM Van Duijn
C Van Broeckhoven
C3
Conference
2001
Homozygosity of the prion Met129Val polymorphism increases risk of developing clinical early-onset but not late-onset Alzheimer's disease
Bart Dermaut
E Croes
M Cruts
M Van den Broeck
CM van Duijn
C Van Broeckhoven
C3
Conference
2001
Influence of the prion protein and the apolipoprotein E genotype on the Creutzfeldt-Jakob disease phenotype
Bart Van Everbroeck
Esther A Croes
Philippe Pals
Bart Dermaut
Gerard Jansen
Cornelia M van Duijn
Marc Cruts
Christine Van Broeckhoven
Jean-Jacques Martin
Patrick Cras
A1
Journal Article
in
NEUROSCIENCE LETTERS
2001
Mutated POLG associated with progressive external ophtalmoplegia characterised by multiple mtDNA deletions
G Van Goethem
Bart Dermaut
A Löfgren
JJ Martin
C Van Broeckhoven
C3
Conference
2001
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions
Gert Van Goethem
Bart Dermaut
Ann Löfgren
Jean-Jacques Martin
Christine Van Broeckhoven
A1
Journal Article
in
NATURE GENETICS
2001
The TNFRSF6 gene is not implicated in familial early-onset Alzheimer's disease
Jessie Theuns
Lars Feuk
Bart Dermaut
Jurgen Del-Favero
Gerwin Roks
Dirk Van den Bossche
Ellen Corsmit
Marleen Van den Broeck
Cornelia M van Duijn
Marc Cruts
et al.
A1
Journal Article
in
HUMAN GENETICS
2001
The cystatin C polymorphism is not associated with early onset Alzheimer's disease
G Roks
M Cruts
AJC Slooter
Bart Dermaut
A Hofman
C Van Broeckhoven
CM Van Duijn
A1
Journal Article
in
NEUROLOGY
2001
Variable expression of presenilin 1 is not a major determinant of risk for late-onset Alzheimer's disease
Bart Dermaut
G Roks
J Theuns
R Rademakers
JJ Houwing-Duistermaat
S Serneels
A Hofman
MMB Breteler
M Cruts
C Van Broeckhoven
et al.
A1
Journal Article
in
JOURNAL OF NEUROLOGY
2001
2000
Familial Creutzfeldt-Jakob disease in a patient carrying both a presenilin 1 missense substitution and a prion protein gene insertion
Bart Dermaut
Marc Cruts
Hubert Backhovens
Ursula Lubke
Bart Van Everbroeck
Raf Sciot
René Dom
Jean-Jacques Martin
Christine Van Broeckhoven
Patrick Cras
A1
Journal Article
in
JOURNAL OF NEUROLOGY
2000
Genetic testing should not be advocated as a diagnostic tool in familial forms of dementia
Esther A Croes
Bart Dermaut
Tischa JM van der Cammen
Christine van Broeckhoven
Cornelia M van Duijn
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
2000
Genetic variability in the regulatory region of presenilin 1 associated with risk for Alzheimer's disease and variable expression
Jessie Theuns
Jurgen Del-Favero
Bart Dermaut
Cornelia M van Duijn
Hubert Backhovens
Marleen Van den Broeck
Sally Serneels
Ellen Corsmit
Christine Van Broeckhoven
Marc Cruts
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
2000
The α2-macroglobulin gene in AD : a population-based study and meta-analysis
MN Koster
Bart Dermaut
M Cruts
JJ Houwing-Duistermaat
G Roks
J Tol
A Ott
A Hofman
G Munteanu
MMB Breteler
et al.
A1
Journal Article
in
NEUROLOGY
2000
1999
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimer's disease by increased Aβ42 secretion
Chris De Jonghe
Marc Cruts
Ekaterina A Rogaeva
Carolyn Tysoe
Andrew Singleton
Hugo Vanderstichele
Wendy Meschino
Bart Dermaut
Inge Vanderhoeven
Hubert Backhovens
et al.
A1
Journal Article
in
HUMAN MOLECULAR GENETICS
1999
Aberrant splicing in the presenilin-1 intron 4 mutation causes presenile Alzheimers disease by increased a beta 42 secretion
M Cruts
C De Jonghe
EA Rogaeva
C Tysoe
A Singleton
H Vanderstichele
W Meschino
Bart Dermaut
I Vanderhoeven
H Backhovens
et al.
C3
Conference
1999
Glu318gly in presenilin-1 is a neutral mutation in relation to dementia: the Rotterdam study
Bart Dermaut
M Cruts
AJC Slooter
S Van Gestel
C De Jonghe
H Backhovens
H Vanderstichele
E Vanmechelen
MMB Breteler
A Hofman
et al.
P1
Conference
1999
Mutation screening of the tau gene in patients with early-onset Alzheimer's disease
Gerwin Roks
Bart Dermaut
Peter Heutink
Ann Julliams
Hubert Backhovens
Marleen Van de Broeck
Sally Serneels
Albert Hofman
Christine Van Broeckhoven
Cornelia M van Duijn
et al.
A1
Journal Article
in
NEUROSCIENCE LETTERS
1999
Polymorphisms in the 5' regulatory region of presenilin 1 associated with an increased risk for early-onset Alzheimers disease
J Theuns
J Del-Favero
Bart Dermaut
CM van Duijn
H Backhovens
M Van den Broeck
S Serneels
C Van Broeckhoven
M Cruts
C3
Conference
1999
The Glu318Gly substitution in presenilin 1 is not causally related to Alzheimer disease
Bart Dermaut
Marc Cruts
Arjen JC Slooter
Sofie Van Gestel
Chris De Jonghe
Hugo Vanderstichele
Eugeen Vanmechelen
Monique M Breteler
Albert Hofman
Cornelia M van Duijn
et al.
A1
Journal Article
in
AMERICAN JOURNAL OF HUMAN GENETICS
1999
1997
Monosomy 22 in a mixed germ cell sex cord stromal tumor of the ovary
Franki Speleman
Bart Dermaut
Christian R De Potter
Mireille Van Gele
Nadine Van Roy
Anne De Paepe
Genevieve Laureys
A1
Journal Article
in
GENES CHROMOSOMES & CANCER
1997
1996
A putative tumor suppressor gene involved in Merkel cell carcinoma maps between p58 and D172
Franki Speleman
ML Geerts
Filomeen Haerynck
Bart Dermaut
Nadine Van Roy
C3
Conference
1996