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1

Mutational analysis of the MPZ, PMP22 and Cx32 genes in patients of Spanish ancestry with Charcot-Marie-Tooth disease and hereditary neuropathy with liability to pressure palsies

Sylvia Bort, E. Nelis, Vincent Timmerman, Teresa Sevilla, Antonio Cruz-Martínez, Francisco Martínez, José M. Millán, Javier Arpa, Juan J. Vílchez, Felix Prieto, Christine Van Broeckhoven, F. Palau

Journal:

Year:

1997

Language:

english

File:

PDF, 105 KB

english, 1997

2

Systematic genetic study of Alzheimer disease in Latin America: Mutation frequencies of the amyloid β precursor protein and presenilin genes in Colombia

Diana Arango, Marc Cruts, Orlando Torres, Hubert Backhovens, Martha L. Serrano, Elsa Villareal, Patricia Montañes, Diana Matallana, Carlos Cano, Christine Van Broeckhoven, Martine Jacquier

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 122 KB

english, 2001

3

Non-replication of the brain-derived neurotrophic factor (BDNF) association in bipolar affective disorder: A Belgian patient-control study

Pierre Oswald, Jurgen Del-Favero, Isabelle Massat, Daniel Souery, Stephan Claes, Christine Van Broeckhoven, Julien Mendlewicz

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 50 KB

english, 2004

4

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update

Karen Nuytemans, Jessie Theuns, Marc Cruts, Christine Van Broeckhoven

Journal:

Year:

2010

Language:

english

File:

PDF, 290 KB

english, 2010

5

TMEM106Ba Novel Risk Factor for Frontotemporal Lobar Degeneration

Julie van der Zee, Christine Van Broeckhoven

Journal:

Journal of Molecular Neuroscience

Year:

2011

Language:

english

File:

PDF, 122 KB

english, 2011

6

Molecular Pathways of Frontotemporal Lobar Degeneration

Sleegers, Kristel, Cruts, Marc, Van Broeckhoven, Christine

Journal:

Annual Review of Neuroscience

Year:

2010

Language:

english

File:

PDF, 432 KB

english, 2010

7

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

Journal:

Neuroscience Letters

Year:

2006

Language:

english

File:

PDF, 79 KB

english, 2006

8

Genetic insights in Alzheimer's disease

Karolien Bettens, Kristel Sleegers, Christine Van Broeckhoven

Journal:

The Lancet Neurology

Year:

2013

Language:

english

File:

PDF, 250 KB

english, 2013

9

Right-handers can be made to think like lefties

Van Langenhove, Tim, Engelborghs, Sebastiaan, Vandenberghe, Rik, Santens, Patrick, Cras, Patrick, Nuytten, Dirk, De Jonghe, Peter, De Deyn, Peter P., Cruts, Marc, Van Broeckhoven, Christine, van der Z

Journal:

Year:

2011

Language:

english

File:

PDF, 410 KB

english, 2011

10

CLINICAL RELEVANCE OF APOE GENOTYPING AND APOLIPOPROTEIN E-ɛ4 IMMUNOASSAYS IN ALZHEIMER'S DISEASE

Soetewey, Femke, Struyfs, Hanne, Stoops, Erik, Van Broeckhoven, Christine, Vanderstichele, Hugo, Engelborghs, Sebastiaan

Journal:

Alzheimer's & Dementia

Year:

2014

Language:

english

File:

PDF, 54 KB

english, 2014

11

Modifiers of GRN -Associated Frontotemporal Lobar Degeneration

Wauters, Eline, Van Mossevelde, Sara, Van der Zee, Julie, Cruts, Marc, Van Broeckhoven, Christine

Journal:

Trends in Molecular Medicine

Year:

2017

Language:

english

File:

PDF, 2.61 MB

english, 2017

12

Peripheral myelin protein 2 – a novel cluster of mutations causing Charcot-Marie-Tooth neuropathy

Palaima, Paulius, Chamova, Teodora, Jander, Sebastian, Mitev, Vanyo, Van Broeckhoven, Christine, Tournev, Ivailo, Peeters, Kristien, Jordanova, Albena

Journal:

Orphanet Journal of Rare Diseases

Year:

2019

Language:

english

File:

PDF, 1.14 MB

english, 2019

13

18F-FDG PET, the early phases and the delivery rate of 18F-AV45 PET as proxies of cerebral blood flow in Alzheimer's disease: Validation against 15O-H2O PET

Ottoy, Julie, Verhaeghe, Jeroen, Niemantsverdriet, Ellis, De Roeck, Ellen, wyffels, Leonie, Ceyssens, Sarah, Van Broeckhoven, Christine, Engelborghs, Sebastiaan, Stroobants, Sigrid, Staelens, Steven

Journal:

Alzheimer's & Dementia

Year:

2019

File:

PDF, 1.53 MB

2019

14

Association study of bipolar disorder with candidate genes involved in catecholamine neurotransmission: DRD2, DRD3, DAT1, and TH genes

Souery, Daniel, Lipp, Olivier, Mahieu, Brigite, Mendelbaum, Karin, De Martelaer, Viviane, Broeckhoven, Christine Van, Mendlewicz, Julien

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 600 KB

english, 1996

15

ApoE genotype is a risk factor in nonpresenilin early-onset alzheimer's disease families

Houlden, Henry, Crook, Richard, Backhovens, Hubert, Prihar, Guy, Baker, Matt, Hutton, Mike, Rossor, Martin, Martin, Jean Jacques, Van Broeckhoven, Christine, Hardy, John

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 37 KB

english, 1998

16

Report of the chromosome 18 workshop

Van Broeckhoven, Christine, Verheyen, Geert, Ewald, A., Gershon, E.S., Hampson, R.M., Kaneva, R., Kelsoe, J.R., McMahon, F.J., Todd, R., Vorsanova, S.G., Wildenauer, D.B., Williams, N.M.

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 86 KB

english, 1999

17

WT1 MUTATION IN MALIGNANT MESOTHELIOMA AND WT1 IMMUNOREACTIVITY IN RELATION TOp53 AND GROWTH FACTOR RECEPTOR EXPRESSION, CELL-TYPE TRANSITION, AND PROGNOSIS

KUMAR-SINGH, SAMIR, SEGERS, KURT, RODECK, ULRICH, BACKHOVENS, HUBERT, BOGERS, JOHANNES, WEYLER, JOOST, VAN BROECKHOVEN, CHRISTINE, VAN MARCK, ERIC

Journal:

The Journal of Pathology

Year:

1997

Language:

english

File:

PDF, 1.71 MB

english, 1997

18

A de novo duplication in 17p11.2 and a novel mutation in the Po gene in two Déjérine—Sottas syndrome patients

Kaisa Silander, Päivi Meretoja, Eva Nelis, Vincent Timmerman, Christine Van Broeckhoven, Pertti Aula, Marja-Liisa Savontaus

Journal:

Year:

1996

Language:

english

File:

PDF, 742 KB

english, 1996

19

Mutation analysis of the connexin 32 (Cx32) gene in charcot-marie-tooth neuropathy type 1: Identification of five new mutations

Eva Nelis, Sandra Simokovic, Vincent Timmerman, Ann Löfgren, Hubert Backhovens, Peter De Jonghe, Jean-Jacques Martin, Christine Van Broeckhoven

Journal:

Year:

1997

Language:

english

File:

PDF, 171 KB

english, 1997

20

Presenilin mutations in Alzheimer's disease

Marc Cruts, Christine Van Broeckhoven

Journal:

Year:

1998

Language:

english

File:

PDF, 212 KB

english, 1998

21

Missense mutation in exon 11 (codon 378) of the presenilin-1 gene in a French family with early-onset Alzheimer's disease and transmission study by mismatch enhanced allele specific amplification

Roger Besançon, Alberta Lorenzi, Marc Cruts, Sandrine Radawiec, Franck Sturtz, Emmanuel Broussolle, Guy Chazot, Christine Van Broeckhoven, Geneviève Chamba, Antoon Vandenberghe

Journal:

Year:

1998

Language:

english

File:

PDF, 69 KB

english, 1998

22

Mutations in the peripheral myelin genes and associated genes in inherited peripheral neuropathies

Eva Nelis, Neva Haites, Christine Van Broeckhoven

Journal:

Year:

1999

Language:

english

File:

PDF, 569 KB

english, 1999

23

Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patients

Irina V. Mersiyanova, Sookhrat M. Ismailov, Alexandr V. Polyakov, Elena L. Dadali, Valeriy P. Fedotov, Eva Nelis, Ann Löfgren, Vincent Timmerman, Christine Van Broeckhoven, Oleg V. Evgrafov

Journal:

Year:

2000

Language:

english

File:

PDF, 255 KB

english, 2000

24

Course of objective memory impairment in non-demented subjects attending a memory clinic and predictors of outcome

Pieter Jelle Visser, Frans R. J. Verhey, Rudolf W. H. M. Ponds, Marc Cruts, Christine L. Van Broeckhoven, Jellemer Jolles

Journal:

International Journal of Geriatric Psychiatry

Year:

2000

Language:

english

File:

PDF, 118 KB

english, 2000

25

Efficient generation of stably electrotransfected human hematopoietic cell lines without drug selection by consecutive FACsorting

Viggo F. I. Van Tendeloo, Peter Ponsaerts, Christine Van Broeckhoven, Zwi N. Berneman, Dirk R. Van Bockstaele

Journal:

Cytometry Part A

Year:

2000

Language:

english

File:

PDF, 126 KB

english, 2000

26

Further evidence that neurofilament light chain gene mutations can cause Charcot-Marie-Tooth disease type 2E

Peter De Jonghe, Irina Mersivanova, Eva Nelis, Jurgen Del Favero, Jean-Jacques Martin, Christine Van Broeckhoven, Oleg Evgrafov, Vincent Timmerman

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 7.87 MB

english, 2001

27

Gene-based SNP genetic association study of the corticotropin-releasing hormone receptor-2 (CRHR2) in major depression

Sandra M. Villafuerte, Jurgen Del-Favero, Rolf Adolfsson, Daniel Souery, Isabelle Massat, Julien Mendlewicz, Christine Van Broeckhoven, Stephan Claes

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 94 KB

english, 2002

28

Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms

Piet Stinissen, Bernadette Van Roy, Guy Van Camp, Hubert Backhovens, Peter Partoens, Anita Wehnert, Heidi Verniers, Jan Dumon, Antoon Vandenberghe, Dr. Christine Van Broeckhoven

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 400 KB

english, 1990

29

Expanded RED products and loci containing CAG/CTG repeats on chromosome 17 (ERDA1) and chromosome 18 (CTG18.1) in trans-generational pairs with bipolar affective disorder

Julien Mendlewicz, Daniel Souery, Jurgen Del-Favero, Isabelle Massat, Kerstin Lindblad, Christer Engström, Dirk Van den Bossche, Rolf Adolfsson, Martin Schalling, Christine Van Broeckhoven

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2004

Language:

english

File:

PDF, 68 KB

english, 2004

30

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

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 67 KB

english, 2003

31

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 M. B. Breteler, Albert Hofman, Christine van Broeckhoven, Cornelia M. van Duijn

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 73 KB

english, 2003

32

Reply

Bart Dermaut, Esther Croes, Cornelia van Duijn, Christine Van Broeckhoven

Journal:

Annals of Neurology

Year:

2003

Language:

english

File:

PDF, 79 KB

english, 2003

33

Endocytic disturbances distinguish among subtypes of alzheimer's disease and related disorders

Anne Cataldo, G. William Rebeck, Bernadino Ghetti, Christine Hulette, Carol Lippa, Christine Van Broeckhoven, Cornelia Van Duijn, Patrick Cras, Nenad Bogdanovic, Thomas Bird, Corrinne Peterhoff, Ralph

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 12.19 MB

english, 2001

34

Ataxin-7 aggregation and ubiquitination in infantile SCA7 with 180 CAG repeats

Olaf Ansorge, Paola Giunti, Andrej Michalik, Christine Van Broeckhoven, Brian Harding, Nicholas Wood, Francesco Scaravilli

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 212 KB

english, 2004

35

α-Synuclein promoter confers susceptibility to Parkinson's disease

Philippe Pals, Sarah Lincoln, Jonathan Manning, Michael Heckman, Lisa Skipper, Mary Hulihan, Marleen Van den Broeck, Tim De Pooter, Patrick Cras, Julia Crook, Christine Van Broeckhoven, Matt J. Farrer

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 164 KB

english, 2004

36

Reply

Kristel Sleegers, Nathalie Brouwers, Christine Van Broeckhoven

Journal:

Annals of Neurology

Year:

2010

Language:

english

File:

PDF, 57 KB

english, 2010

37

The apolipoprotein E ε4 allele does not influence the clinical expression of the amyloid precursor protein gene codon 693 or 692 mutations

Dr. Joost Haan, Christine Van Broeckhoven, Cornelia M. Van Duijn, Els Voorhoeve, Frans van Harskamp, John C. van Swieten, Marion L. C. Maat-Schieman, Raymund A. C. Roos, Egbert Bakker

Journal:

Annals of Neurology

Year:

1994

Language:

english

File:

PDF, 429 KB

english, 1994

38

The apolipoprotein E ε2 allele is associated with an increased risk of early-onset alzheimer's disease and a reduced survival

Cornelia M. van Duijn, Peter de Knijff, Anita Wehnert, Joke De Voecht, Juliana B. Bronzova, Louis M. Havekes, Albert Hofman, Dr Christine van Broeckhoven

Journal:

Annals of Neurology

Year:

1995

Language:

english

File:

PDF, 652 KB

english, 1995

39

Reply

C. M. van Duijn, Christine van Broeckhoven

Journal:

Annals of Neurology

Year:

1996

Language:

english

File:

PDF, 239 KB

english, 1996

40

Digenic progressive external ophthalmoplegia in a sporadic patient: Recessive mutations in POLG and C10orf2/Twinkle

Gert Van Goethem, Ann Löfgren, Bart Dermaut, Chantal Ceuterick, Jean-Jacques Martin, Christine Van Broeckhoven

Journal:

Year:

2003

Language:

english

File:

PDF, 73 KB

english, 2003

41

Identification of a 4 bp deletion (1560de14) in Po gene in a family with severe charcot-Marie-Tooth disease

Emilia Bellone, Paola Mandich, Rosella James, Eva Nelis, Laura Doria Lamba, Christine Van Broeckhoven, Franco Ajmar

Journal:

Year:

1996

Language:

english

File:

PDF, 195 KB

english, 1996

42

Genes and loci involved in febrile seizures and related epilepsy syndromes

Dominique Audenaert, Christine Van Broeckhoven, Peter De Jonghe

Journal:

Year:

2006

Language:

english

File:

PDF, 279 KB

english, 2006

43

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

Journal:

Year:

2006

Language:

english

File:

PDF, 425 KB

english, 2006

44

Major affective disorders and schizophrenia: a common molecular signature?

Ann Van Den Bogaert, Jurgen Del-Favero, Christine Van Broeckhoven

Journal:

Year:

2006

Language:

english

File:

PDF, 358 KB

english, 2006

45

Visualization of MAPT inversion on stretched chromosomes of tau-negative frontotemporal dementia patients

Ilse Gijselinck, Veerle Bogaerts, Rosa Rademakers, Julie van der Zee, Christine Van Broeckhoven, Marc Cruts

Journal:

Year:

2006

Language:

english

File:

PDF, 168 KB

english, 2006

46

SORL1 is genetically associated with increased risk for late-onset Alzheimer disease in the Belgian population

Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Peter P. De Deyn, Christine Van Broeckhoven, Kristel Sleegers

Journal:

Year:

2008

Language:

english

File:

PDF, 362 KB

english, 2008

47

Common variation in GRB-associated Binding Protein 2 (GAB2) and increased risk for Alzheimer dementia

Kristel Sleegers, Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Helen van Miegroet, Peter P De Deyn, Christine Van Broeckhoven

Journal:

Year:

2009

Language:

english

File:

PDF, 195 KB

english, 2009

48

No association between CALHM1 and risk for Alzheimer dementia in a Belgian population

Kristel Sleegers, Nathalie Brouwers, Karolien Bettens, Sebastiaan Engelborghs, Helen van Miegroet, Peter P De Deyn, Christine Van Broeckhoven

Journal:

Year:

2009

Language:

english

File:

PDF, 121 KB

english, 2009

49

APP and BACE1 miRNA genetic variability has no major role in risk for Alzheimer disease

Karolien Bettens, Nathalie Brouwers, Sebastiaan Engelborghs, Helen Van Miegroet, Peter P. De Deyn, Jessie Theuns, Kristel Sleegers, Christine Van Broeckhoven

Journal:

Year:

2009

Language:

english

File:

PDF, 247 KB

english, 2009

50

Genetic variant in the HSPB1 promoter region impairs the HSP27 stress response

Ines Dierick, Joy Irobi, Sophie Janssens, Jessie Theuns, Robin Lemmens, An Jacobs, Ellen Corsmit, Nicole Hersmus, Ludo Van Den Bosch, Wim Robberecht, Peter De Jonghe, Christine Van Broeckhoven, Vincen

Journal:

Year:

2007

Language:

english

File:

PDF, 289 KB

english, 2007

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