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1

Left ventricular non-compaction with Ebstein anomaly attributed to a TPM1 mutation

Nijak, Aleksandra, Alaerts, Maaike, Kuiperi, Cuno, Corveleyn, Anniek, Suys, Bert, Paelinck, Bernard, Saenen, Johan, Van Craenenbroeck, Emeline, Van Laer, Lut, Loeys, Bart, Verstraeten, Aline

Journal:

European Journal of Medical Genetics

Année:

2017

Langue:

english

Fichier:

PDF, 799 KB

english, 2017

2

Mutation analysis of mitochondrial DNA 12SrRNA and tRNASer(UCN) genes in non-syndromic hearing loss patients

Annelies Konings, Guy Van Camp, Alain Goethals, Els Van Eyken, Ann Vandevelde, Jamila Ben Azza, Nils Peeters, Wim Wuyts, Hubert Smeets, Lut Van Laer

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 378 KB

english, 2008

3

Audiometric shape and presbycusis

Demeester, Kelly, van Wieringen, Astrid, Hendrickx, Jan-jaap, Topsakal, Vedat, Fransen, Erik, van Laer, Lut, Van Camp, Guy, Van de Heyning, Paul

Journal:

International Journal of Audiology

Année:

2009

Langue:

english

Fichier:

PDF, 272 KB

english, 2009

4

Identification of binding partners interacting with the α1-N-propeptide of type V collagen

Symoens, Sofie, Renard, Marjolijn, Bonod-Bidaud, Christelle, Syx, Delfien, Vaganay, Elisabeth, Malfait, Fransiska, Ricard-Blum, Sylvie, Kessler, Efrat, Van Laer, Lut, Coucke, Paul, Ruggiero, Florence,

Journal:

Biochemical Journal

Année:

2011

Langue:

english

Fichier:

PDF, 790 KB

english, 2011

5

Genetic Studies on Noise-Induced Hearing Loss: A Review

Konings, Annelies, Laer, Lut Van, Camp, Guy Van

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 441 KB

english, 2009

6

Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome

Meester, Josephina A. N., Verstraeten, Aline, Schepers, Dorien, Alaerts, Maaike, Van Laer, Lut, Loeys, Bart L.

Journal:

Annals of cardiothoracic surgery

Année:

2017

Langue:

english

Fichier:

PDF, 267 KB

english, 2017

7

Aortic aneurysm/dissection and osteogenesis imperfecta: Four new families and review of the literature

Balasubramanian, Meena, Verschueren, Aline, Kleevens, Simon, Luyckx, Ilse, Perik, Melanie, Schirwani, Schaida, Mortier, Geert, Morisaki, Hiroko, Rodrigus, Inez, Van Laer, Lut, Verstraeten, Aline, Loey

Journal:

Année:

2019

Langue:

english

Fichier:

PDF, 186 KB

english, 2019

8

Autosomal recessive nonsyndromic hearing loss

Sundstrom, Rachel A., van Laer, Lut, Van Camp, Guy, Smith, Richard J.H.

Journal:

American Journal of Medical Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 149 KB

english, 1999

9

Autosomal dominant nonsyndromic hearing impairment

Van Laer, Lut, McGuirt, Wyman T., Yang, Tao, Smith, Richard J.H., Van Camp, Guy

Journal:

American Journal of Medical Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 161 KB

english, 1999

10

GJB2 (connexin 26) mutations are not a major cause of hearing loss in the Indonesian population

Rikkert L. Snoeckx, Bulantrisna Djelantik, Lut Van Laer, Paul Van de Heyning, Guy Van Camp

Journal:

American Journal of Medical Genetics Part A

Année:

2005

Langue:

english

Fichier:

PDF, 66 KB

english, 2005

11

Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population

Haris Kokotas, Lut Van Laer, Maria Grigoriadou, Vassiliki Iliadou, John Economides, Stella Pomoni, Andreas Pampanos, Nikos Eleftheriades, Elisabeth Ferekidou, Stavros Korres, Aglaia Giannoulia-Karanta

Journal:

American Journal of Medical Genetics Part A

Année:

2008

Langue:

english

Fichier:

PDF, 88 KB

english, 2008

12

The contribution of genes involved in potassium-recycling in the inner ear to noise-induced hearing loss

Lut Van Laer, Per-Inge Carlsson, Natacha Ottschytsch, Marie-Louise Bondeson, Annelies Konings, Ann Vandevelde, Nele Dieltjens, Erik Fransen, Dirk Snyders, Erik Borg, Adam Raes, Guy Van Camp

Journal:

Année:

2006

Langue:

english

Fichier:

PDF, 255 KB

english, 2006

13

Musculocontractural Ehlers-Danlos Syndrome (former EDS type VIB) and adducted thumb clubfoot syndrome (ATCS) represent a single clinical entity caused by mutations in the dermatan-4-sulfotransferase 1 encoding CHST14 gene

Fransiska Malfait, Delfien Syx, Philip Vlummens, Sofie Symoens, Sheela Nampoothiri, Trinh Hermanns-Lê, Lut Van Laer, Anne De Paepe

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 402 KB

english, 2010

14

Applying massive parallel sequencing to molecular diagnosis of Marfan and Loeys-Dietz syndromes

Machteld Baetens, Lut Van Laer, Kim De Leeneer, Jan Hellemans, Joachim De Schrijver, Hendrik Van De Voorde, Marjolijn Renard, Hal Dietz, Ronald V. Lacro, Björn Menten, Wim Van Criekinge, Julie De Back

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 294 KB

english, 2011

15

Evaluation of host genetic and viral factors as surrogate markers for HTLV-1-associated myelopathy/tropical spastic paraparesis in Peruvian HTLV-1-infected patients

Michael Talledo, Giovanni López, Jeroen R. Huyghe, Kristien Verdonck, Vanessa Adaui, Elsa González, Iván Best, Daniel Clark, Guido Vanham, Eduardo Gotuzzo, Guy Van Camp, Lut Van Laer

Journal:

Journal of Medical Virology

Année:

2010

Langue:

english

Fichier:

PDF, 125 KB

english, 2010

16

Possible implication of NFKB1A and NKG2D genes in susceptibility to HTLV-1-associated myelopathy/tropical spastic paraparesis in Peruvian patients infected with HTLV-1

Michael Talledo, Giovanni López, Jeroen R. Huyghe, Kristien Verdonck, Elsa González, Daniel Clark, Guido Vanham, Eduardo Gotuzzo, Guy Van Camp, Lut Van Laer

Journal:

Journal of Medical Virology

Année:

2012

Langue:

english

Fichier:

PDF, 154 KB

english, 2012

17

HLA-G 14 bp insertion/deletion polymorphism is not associated to proviral load levels and presence of HAM/TSP in Peruvian HTLV-1 infected individuals

Sandra Morales, Jason Rosado, Giovanni López, Jeroen Huyghe, Kristien Verdonck, Elsa González, Martin Tipismana, Daniel Clark, Guido Vanham, Eduardo Gotuzzo, Guy Van Camp, Lut Van laer, Michael Talled

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 128 KB

english, 2011

18

Host genetic factors associated to proviral load in Peruvian HTLV-1 infected

Michael Talledo, Giovanni López, Jeroen R Huyghe, Kristien Verdonck, Elsa González, Martin Tipismana, Daniel Clark, Guido Vanham, Eduardo Gotuzzo, Guy Van Camp, Lut Van Laer

Journal:

Année:

2011

Langue:

english

Fichier:

PDF, 128 KB

english, 2011

19

GJB2deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation

Akihiro Ohtsuka, Isamu Yuge, Shinobu Kimura, Atsushi Namba, Satoko Abe, Lut Van Laer, Guy Van Camp, Shin-ichi Usami

Journal:

Année:

2003

Langue:

english

Fichier:

PDF, 243 KB

english, 2003

20

Human hereditary hearing impairment: mouse models can help to solve the puzzle

Karen Vrijens, Lut Van Laer, Guy Van Camp

Journal:

Année:

2008

Langue:

english

Fichier:

PDF, 1.01 MB

english, 2008

21

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)

Delfien Syx, Fransiska Malfait, Lut Van Laer, Jan Hellemans, Trinh Hermanns-Lê, Andy Willaert, Abdelmajid Benmansour, Anne De Paepe, Alain Verloes

Journal:

Année:

2010

Langue:

english

Fichier:

PDF, 574 KB

english, 2010

22

Physical mapping of the HOXA1 gene and the hnRPA2B1 gene in a YAC contig from human chromosome 7p14-p15

Lut Van Laer, Guy Van Camp, Eric D. Green, Egbert H. Huizing, Patrick J. Willems

Journal:

Année:

1997

Langue:

english

Fichier:

PDF, 51 KB

english, 1997

23

A novelDFNA5mutation does not cause hearing loss in an Iranian family

Lut Van Laer, Nicole C. Meyer, Mahdi Malekpour, Yasser Riazalhosseini, Mahdi Moghannibashi, Kimia Kahrizi, Ann Vandevelde, Fatemeh Alasti, Hossein Najmabadi, Guy Van Camp, Richard J. H. Smith

Journal:

Journal of Human Genetics

Année:

2007

Langue:

english

Fichier:

PDF, 223 KB

english, 2007

24

Occupational Noise, Smoking, and a High Body Mass Index are Risk Factors for Age-related Hearing Impairment and Moderate Alcohol Consumption is Protective: A European Population-based Multicenter Study

Erik Fransen, Vedat Topsakal, Jan-Jaap Hendrickx, Lut Van Laer, Jeroen R. Huyghe, Els Van Eyken, Nele Lemkens, Samuli Hannula, Elina Mäki-Torkko, Mona Jensen, Kelly Demeester, Anke Tropitzsch, Amanda

Journal:

Journal of the Association for Research in Otolaryngology

Année:

2008

Langue:

english

Fichier:

PDF, 211 KB

english, 2008

25

Analysis of Gene Polymorphisms Associated with K+ Ion Circulation in the Inner Ear of Patients Susceptible and Resistant to Noise-induced Hearing Loss

Malgorzata Pawelczyk, Lut Van Laer, Erik Fransen, Elzbieta Rajkowska, Annelies Konings, Per-Inge Carlsson, Erik Borg, Guy Van Camp, Mariola Sliwinska-Kowalska

Journal:

Annals of Human Genetics

Année:

2009

Langue:

english

Fichier:

PDF, 294 KB

english, 2009

26

10.1038/2503

Laer, Lut Van, Huizing, Egbert H., Verstreken, Margriet, Zuijlen, Diederick van, Wauters, Jan G., Bossuyt, Paul J., Van de Heyning, Paul, McGuirt, Wyman T., Smith, Richard J.H., Willems, Patrick J., L

Journal:

Nature Genetics

Année:

1998

Langue:

english

Fichier:

PDF, 139 KB

english, 1998

27

Variations in HSP70 genes associated with noise-induced hearing loss in two independent populations

Van Laer, Lut, Michel, Sophie, Pawelczyk, Malgorzata, Carlsson, Per-Inge, Bondeson, Marie-Louise, Rajkowska, Elzbieta, Dudarewicz, Adam, Vandevelde, Ann, Fransen, Erik, Konings, Annelies

Journal:

European Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 139 KB

english, 2008

28

A genome-wide association study for age-related hearing impairment in the Saami

Van Laer, Lut, Huyghe, Jeroen R, Hannula, Samuli, Van Eyken, Els, Stephan, Dietrich A, Mäki-Torkko, Elina, Aikio, Pekka, Fransen, Erik, Lysholm-Bernacchi, Alana, Sorri, Martti

Journal:

European Journal of Human Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 398 KB

english, 2010

29

A genome-wide analysis of population structure in the Finnish Saami with implications for genetic association studies

Huyghe, Jeroen R, Fransen, Erik, Hannula, Samuli, Van Laer, Lut, Van Eyken, Els, Mäki-Torkko, Elina, Aikio, Pekka, Sorri, Martti, Huentelman, Matthew J, Camp, Guy Van

Journal:

European Journal of Human Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 476 KB

english, 2010

30

The DFNA5 gene, responsible for hearing loss and involved in cancer, encodes a novel apoptosis-inducing protein

de Beeck, Ken Op, Van Camp, Guy, Thys, Sofie, Cools, Nathalie, Callebaut, Isabelle, Vrijens, Karen, Van Nassauw, Luc, Van Tendeloo, Viggo FI, Timmermans, Jean Pierre, Van Laer, Lut

Journal:

European Journal of Human Genetics

Année:

2011

Langue:

english

Fichier:

PDF, 738 KB

english, 2011

31

Mutations in the human α-tectorin gene cause autosomal dominant non-syndromic hearing impairment

Verhoeven, Kristien, Laer, Lut Van, Kirschhofer, Karin, Legan, P. Kevin, Hughes, David C., Schatteman, Isabelle, Verstreken, Margriet, Hauwe, Peter Van, Coucke, Paul, Chen, Achih

Journal:

Nature Genetics

Année:

1998

Fichier:

PDF, 585 KB

1998

32

Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

Delmaghani, Sedigheh, del Castillo, Francisco J, Michel, Vincent, Leibovici, Michel, Aghaie, Asadollah, Ron, Uri, Van Laer, Lut, Ben-Tal, Nir, Van Camp, Guy, Weil, Dominique

Journal:

Nature Genetics

Année:

2006

Langue:

english

Fichier:

PDF, 638 KB

english, 2006

33

Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene

Verhoeven, Kristien, Ensink, Robbert JH, Tiranti, Valeria, Huygen, Patrick LM, Johnson, David F, Schatteman, Isabelle, Van Laer, Lut, Verstreken, Margriet, Van de Heyning, Paul, Fischel-Ghodsian, Nath

Journal:

European Journal of Human Genetics

Année:

1999

Langue:

english

Fichier:

PDF, 145 KB

english, 1999

34

Is DFNA5 a susceptibility gene for age-related hearing impairment?

Van Laer, Lut, DeStefano, Anita L, Myers, Richard H, Flothmann, Kris, Thys, Sofie, Fransen, Erik, Gates, George A, Van Camp, Guy, Baldwin, Clinton T

Journal:

European Journal of Human Genetics

Année:

2002

Langue:

english

Fichier:

PDF, 84 KB

english, 2002

35

TheWFS1gene, responsible for low frequency sensorineural hearing loss and Wolfram syndrome, is expressed in a variety of inner ear cells

Kim Cryns,Sofie Thys,Lut Van Laer,Yoshitomo Oka…

Journal:

Histochemistry and Cell Biology

Année:

2003

Langue:

english

Fichier:

PDF, 532 KB

english, 2003

36

Genome-wide SNP-Based Linkage Scan Identifies a Locus on 8q24 for an Age-Related Hearing Impairment Trait

Jeroen R. Huyghe, Lut Van Laer, Jan-Jaap Hendrickx, Erik Fransen, Kelly Demeester, Vedat Topsakal, Sylvia Kunst, Minna Manninen, Mona Jensen, Amanda Bonaconsa, Manuela Mazzoli, Manuela Baur, Samuli Ha

Journal:

The American Journal of Human Genetics

Année:

2008

Langue:

english

Fichier:

PDF, 495 KB

english, 2008

37

Ozzy, a Jag1 vestibular mouse mutant, displays characteristics of Alagille syndrome

Karen Vrijens, Sofie Thys, Marcel T. De Jeu, Andrei A. Postnov, Markus Pfister, Luk Cox, An Zwijsen, Viviane Van Hoof, Marcus Mueller, Nora M. De Clerck, Chris I. De Zeeuw, Guy Van Camp, Lut Van Laer

Journal:

Neurobiology of Disease

Année:

2006

Langue:

english

Fichier:

PDF, 927 KB

english, 2006

38

Age-related hearing impairment (ARHI): environmental risk factors and genetic prospects

Erik Fransen, Nele Lemkens, Lut Van Laer, Guy Van Camp

Journal:

Experimental Gerontology

Année:

2003

Langue:

english

Fichier:

PDF, 241 KB

english, 2003

39

Identification of a new connexin gene GJA11 (Cx59) using degenerate PCR primers

Paul J. Coucke, Lut Van Laer, Johan Meyers, Peter Van Hauwe, Natacha Ottschytsch, Jan G. Wauters, Philip Kelley, Patrick J. Willems, Guy Van Camp

Journal:

Année:

2000

Langue:

english

Fichier:

PDF, 553 KB

english, 2000

40

Educational paper

Laer, Lut, Proost, Dorien, Loeys, Bart L.

Journal:

European Journal of Pediatrics

Année:

2013

Langue:

english

Fichier:

PDF, 277 KB

english, 2013

41

Characterization of the murine Dfna5 promoter and regulatory regions

Karen Vrijens, Guy Van Camp, Lut Van Laer

Journal:

Année:

2009

Langue:

english

Fichier:

PDF, 987 KB

english, 2009

42

The influence of genetic variation in oxidative stress genes on human noise susceptibility

Per-Inge Carlsson, Lut Van Laer, Erik Borg, Marie-Louise Bondeson, Melissa Thys, Erik Fransen, Guy Van Camp

Journal:

Hearing Research

Année:

2005

Langue:

english

Fichier:

PDF, 312 KB

english, 2005

43

Heritability of audiometric shape parameters and familial aggregation of presbycusis in an elderly Flemish population

Kelly Demeester, Astrid van Wieringen, Jan-jaap Hendrickx, Vedat Topsakal, Jeroen Huyghe, Erik Fransen, Lut Van Laer, Guy Van Camp, Paul Van de Heyning

Journal:

Hearing Research

Année:

2010

Langue:

english

Fichier:

PDF, 517 KB

english, 2010

44

Role of killer cell immunoglobulin-like receptor gene content and human leukocyte antigen–C group in susceptibility to human T-lymphotropic virus 1–associated myelopathy/tropical spastic paraparesis in Peru

Michael Talledo, Giovanni López, Jeroen R. Huyghe, Kristien Verdonck, Elsa González, Daniel Clark, David Senitzer, Guido Vanham, Eduardo Gotuzzo, Guy Van Camp, Lut Van Laer

Journal:

Human Immunology

Année:

2010

Langue:

english

Fichier:

PDF, 247 KB

english, 2010

45

Mice lacking Dfna5 show a diverging number of cochlear fourth row outer hair cells

Lut Van Laer, Markus Pfister, Sofie Thys, Karen Vrijens, Marcus Mueller, Lieve Umans, Lutgarde Serneels, Luc Van Nassauw, Frank Kooy, Richard J.H. Smith, Jean-Pierre Timmermans, Fred Van Leuven, Guy V

Journal:

Neurobiology of Disease

Année:

2005

Langue:

english

Fichier:

PDF, 704 KB

english, 2005

46

A yeast model for the study of human DFNA5, a gene mutated in nonsyndromic hearing impairment

Juraj Gregan, Lut Van Laer, Louis D. Lieto, Guy Van Camp, Stephen E. Kearsey

Journal:

Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Année:

2003

Langue:

english

Fichier:

PDF, 854 KB

english, 2003

47

Genome-wide SNP analysis reveals no gain in power for association studies of common variants in the Finnish Saami

Huyghe, Jeroen R, Fransen, Erik, Hannula, Samuli, Van Laer, Lut, Van Eyken, Els, Mäki-Torkko, Elina, Lysholm-Bernacchi, Alana, Aikio, Pekka, Stephan, Dietrich A, Sorri, Martti, Huentelman, Matthew J,

Journal:

European Journal of Human Genetics

Année:

2010

Langue:

english

Fichier:

PDF, 513 KB

english, 2010

48

Thoracic Aortic Aneurysm in Infancy in Aneurysms-Osteoarthritis Syndrome Due to a Novel SMAD 3 Mutation: Further Delineation of the Phenotype

Wischmeijer, Anita, Van Laer, Lut, Tortora, Giada, Bolar, Nikhita Ajit, Van Camp, Guy, Fransen, Erik, Peeters, Nils, di Bartolomeo, Roberto, Pacini, Davide, Gargiulo, Gaetano, Turci, Simone, Bonvicini

Journal:

American Journal of Medical Genetics Part A

Année:

2013

Langue:

english

Fichier:

PDF, 2.63 MB

english, 2013

49

Severe aortopathy due to fibulin-4 deficiency: molecular insights, surgical strategy, and a review of the literature

Hebson, Camden, Coleman, Karlene, Clabby, Martha, Sallee, Denver, Shankar, Suma, Loeys, Bart, Laer, Lut, Kogon, Brian

Journal:

European Journal of Pediatrics

Année:

2014

Langue:

english

Fichier:

PDF, 159 KB

english, 2014

50

Mutation in the type II collagen gene (COL2AI) as a cause of primary osteoarthritis associated with mild spondyloepiphyseal involvement

Rukavina, Iva, Mortier, Geert, Van Laer, Lut, Frković, Marijan, Đapić, Tomislav, Jelušić, Marija

Journal:

Seminars in Arthritis and Rheumatism

Année:

2014

Langue:

english

Fichier:

PDF, 614 KB

english, 2014