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1

The effect of resistance training, detraining and retraining on muscle strength and power, myofibre size, satellite cells and myonuclei in older men

Blocquiaux, Sara, Gorski, Tatiane, Van Roie, Evelien, Ramaekers, Monique, Van Thienen, Ruud, Nielens, Henri, Delecluse, Christophe, De Bock, Katrien, Thomis, Martine

Journal:

Experimental Gerontology

Year:

2020

File:

PDF, 1.78 MB

2020

2

Sport participation and stress among women and men

Melinda Asztalos, Katrien Wijndaele, Ilse De Bourdeaudhuij, Renaat Philippaerts, Lynn Matton, Nathalie Duvigneaud, Martine Thomis, Johan Lefevre, Greet Cardon

Journal:

Psychology of Sport and Exercise

Year:

2012

Language:

english

File:

PDF, 342 KB

english, 2012

3

Genome-wide linkage scan for resistance to muscle fatigue

M. A. Thomis, G. De Mars, A. Windelinckx, M. W. Peeters, W. Huygens, J. Aerssens, G. P. Beunen

Journal:

Scandinavian Journal of Medicine & Science in Sports

Year:

2011

Language:

english

File:

PDF, 202 KB

english, 2011

4

A further mutation of the FGFR2 tyrosine kinase domain in mild Crouzon syndrome

de Ravel, Thomy J L, Taylor, Indira B, Van Oostveldt, Alex J T, Fryns, Jean-Pierre, Wilkie, Andrew O M

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 130 KB

english, 2004

5

Specific associations between types of physical activity and components of mental health

Melinda Asztalos, Katrien Wijndaele, Ilse De Bourdeaudhuij, Renaat Philippaerts, Lynn Matton, Nathalie Duvigneaud, Martine Thomis, William Duquet, Johan Lefevre, Greet Cardon

Journal:

Journal of Science and Medicine in Sport

Year:

2009

Language:

english

File:

PDF, 761 KB

english, 2009

6

High Frequency Of Submicroscopic Chromosomal Deletions in Patients with Idiopathic Congenital Eye Malformations

Irina Balikova, Thomy de Ravel, Carmen Ayuso, Bernard Thienpont, Ingele Casteels, Cristina Villaverde, Koenraad Devriendt, Jean-Pierre Fryns, Joris Robert Vermeesch

Journal:

American Journal of Ophthalmology

Year:

2011

Language:

english

File:

PDF, 2.92 MB

english, 2011

7

Novel and recurrentPITX3mutations in Belgian families with autosomal dominant congenital cataract and anterior segment dysgenesis have similar phenotypic and functional characteristics

Verdin, Hannah, Sorokina, Elena A, Meire, Françoise, Casteels, Ingele, de Ravel, Thomy, Semina, Elena V, De Baere, Elfride

Journal:

Orphanet Journal of Rare Diseases

Year:

2014

Language:

english

File:

PDF, 2.66 MB

english, 2014

8

Design of a high-field twin aperture superconducting dipole model

Leroy, D., Perin, R., de Rijk, G., Thomi, W.

Journal:

IEEE Transactions on Magnetics

Year:

1988

Language:

english

File:

PDF, 436 KB

english, 1988

9

Identification and prioritization of NUAK1 and PPP1CC as positional candidate loci for skeletal muscle strength phenotypes

Windelinckx, A., De Mars, G., Huygens, W., Peeters, M. W., Vincent, B., Wijmenga, C., Lambrechts, D., Aerssens, J., Vlietinck, R., Beunen, G., Thomis, M. A. I.

Journal:

Physiological Genomics

Year:

2011

Language:

english

File:

PDF, 813 KB

english, 2011

10

No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome

Schlögel, Matthieu J, Mendola, Antonella, Fastré, Elodie, Vasudevan, Pradeep, Devriendt, Koen, de Ravel, Thomy JL, Van Esch, Hilde, Casteels, Ingele, Arroyo Carrera, Ignacio, Cristofoli, Francesca, Fi

Journal:

Orphanet Journal of Rare Diseases

Year:

2015

Language:

english

File:

PDF, 1.61 MB

english, 2015

11

Predicting fetoplacental chromosomal mosaicism during non-invasive prenatal testing

Brison, Nathalie, Neofytou, Maria, Dehaspe, Luc, Bayindir, Baran, Van Den Bogaert, Kris, Dardour, Leila, Peeters, Hilde, Van Esch, Hilde, Van Buggenhout, Griet, Vogels, Annick, de Ravel, Thomy, Legius

Journal:

Prenatal Diagnosis

Year:

2018

Language:

english

File:

PDF, 1.03 MB

english, 2018

12

Manual lymph drainage may not have a preventive effect on the development of breast cancer-related lymphoedema in the long term: a randomised trial

Devoogdt, Nele, Geraerts, Inge, Van Kampen, Marijke, De Vrieze, Tessa, Vos, Lore, Neven, Patrick, Vergote, Ignace, Christiaens, Marie-Rose, Thomis, Sarah, De Groef, An

Journal:

Journal of Physiotherapy

Year:

2018

Language:

english

File:

PDF, 487 KB

english, 2018

13

What is the best method to determine excessive arm volume in patients with breast cancer–related lymphoedema in clinical practice? Reliability, time efficiency and clinical feasibility of five different methods

De Vrieze, Tessa, Gebruers, Nick, Tjalma, Wiebren AA, Nevelsteen, Ines, Thomis, Sarah, De Groef, An, Dams, Lore, Van der Gucht, Elien, Belgrado, Jean-Paul, Vandermeeren, Liesbeth, Devoogdt, Nele

Journal:

Clinical Rehabilitation

Year:

2019

File:

PDF, 96 KB

2019

14

Lethal neonatal mandibuloacral dysplasia

Seftel, Matthew D., Wright, Colleen A., Po, Patrick Li Wan, de Ravel, Thomy J.L.

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 279 KB

english, 1996

15

Tetra-amelia and splenogonadal fusion in Roberts syndrome

de Ravel, Thomy J. L., Seftel, Matthew D., Wright, Colleen A.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 258 KB

english, 1997

16

Trisomy 18 with total cranio-rachischisis and thoraco-abdominoschisis

Susan J. F. Donaldson, Colleen A. Wright, Thomy J. L. de Ravel

Journal:

Prenatal Diagnosis

Year:

1999

Language:

english

File:

PDF, 181 KB

english, 1999

17

Novel mutations and polymorphisms in the Fanconi anemia group C gene

Rachel A. Gibson, Neil V. Morgan, Laura H. Goldstein, Ian C. Pearson, Ian P. Kesterton, Nicola J. Foot, Stander Jansen, Charmaine Havenga, Thomas Pearson, Thomy J. de Ravel, Richard J. Cohn, Isabel M.

Journal:

Year:

1996

Language:

english

File:

PDF, 982 KB

english, 1996

18

Possible isochromosome 22 leading to trisomy 22

Bridget F. Manasse, Wilma M. Pfaffenzeller, Nursen Gurtunca, Thomy J.L. de Ravel

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 542 KB

english, 2000

19

Maternal origin of extra haploid set of chromosomes in third trimester triploid fetuses

Erin Dietzsch, Michele Ramsay, Arnold L. Christianson, Bertram D. Henderson, Dr. Thomy J. L. de Ravel

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 463 KB

english, 1995

20

“Opitz C syndrome and pseudohypoaldosteronism” is caused by a chromosome 4q deletion

Thomy de Ravel, Irina Balikova, Jozef Van Driessche, Joris Vermeesch, Jean-Pierre Fryns

Journal:

American Journal of Medical Genetics Part A

Year:

2009

Language:

english

File:

PDF, 82 KB

english, 2009

21

Tumor spectrum in children with Noonan syndrome and SOS1 or RAF1 mutations

Ellen Denayer, Koen Devriendt, Thomy de Ravel, Griet Van Buggenhout, Eric Smeets, Inge Francois, Yves Sznajer, Margarita Craen, George Leventopoulos, Léon Mutesa, Willy Vandecasseye, Guy Massa, Hulya

Journal:

Genes, Chromosomes and Cancer

Year:

2010

Language:

english

File:

PDF, 185 KB

english, 2010

22

Atypical neurofibromas in neurofibromatosis type 1 are premalignant tumors

Eline Beert, Hilde Brems, Bruno Daniëls, Ivo De Wever, Frank Van Calenbergh, Joseph Schoenaers, Maria Debiec-Rychter, Olivier Gevaert, Thomas De Raedt, Annick Van Den Bruel, Thomy de Ravel, Karen Cich

Journal:

Genes, Chromosomes and Cancer

Year:

2011

Language:

english

File:

PDF, 1.17 MB

english, 2011

23

Subtelomeric imbalances in phenotypically normal individuals

Irina Balikova, Björn Menten, Thomy de Ravel, Cédric Le Caignec, Bernard Thienpont, Montse Urbina, Martine Doco-Fenzy, Marjan de Rademaeker, Geert Mortier, Frank Kooy, Janneke van Den Ende, Koen Devri

Journal:

Year:

2007

Language:

english

File:

PDF, 327 KB

english, 2007

24

Mutation analysis in Costello syndrome: functional and structural characterization of the HRAS p.Lys117Arg mutation

Ellen Denayer, Annabel Parret, Magdalena Chmara, Suzanne Schubbert, Annick Vogels, Koen Devriendt, Jean-Pierre Frijns, Vladimir Rybin, Thomy J. de Ravel, Kevin Shannon, Jan Cools, Klaus Scheffzek, Eri

Journal:

Year:

2008

Language:

english

File:

PDF, 344 KB

english, 2008

25

Post-zygotic origin of isochromosome 12p

Dr Thomy J. L. de Ravel, Kathelijn Keymolen, Elvire van Assche, Ingrid Wittevronghel, Philippe Moerman, Ivo Salden, Gert Matthijs, Jean-Pierre Fryns, Joris R. Vermeesch

Journal:

Prenatal Diagnosis

Year:

2004

Language:

english

File:

PDF, 133 KB

english, 2004

26

Polymorphisms in the vitamin D receptor gene are associated with muscle strength in men and women

A. Windelinckx, G. De Mars, G. Beunen, J. Aerssens, C. Delecluse, J. Lefevre, M. A. I. Thomis

Journal:

Osteoporosis International

Year:

2007

Language:

english

File:

PDF, 190 KB

english, 2007

27

What’s new in karyotyping? The move towards array comparative genomic hybridisation (CGH)

Thomy J. L. de Ravel, Koen Devriendt, Jean-Pierre Fryns, Joris R. Vermeesch

Journal:

European Journal of Pediatrics

Year:

2007

Language:

english

File:

PDF, 301 KB

english, 2007

28

High resolution mapping ofOCA2intragenic rearrangements and identification of a founder effect associated with a deletion in Polish albino patients

Caroline Rooryck, Fanny Morice-Picard, Eulalie Lasseaux, Dorothée Cailley, Hélène Dollfus, Sabine Defoort-Dhellemme, Bénédicte Duban-Bedu, Thomy J. L. de Ravel, Alain Taieb, Didier Lacombe, Benoît Arv

Journal:

Year:

2011

Language:

english

File:

PDF, 750 KB

english, 2011

29

Revisiting the phenotype associated withFOXG1mutations: two novel cases of congenital Rett variant

Nadia Bahi-Buisson, Juliette Nectoux, Benoit Girard, Hilde Van Esch, Thomy De Ravel, Nathalie Boddaert, Perrine Plouin, Marlene Rio, Yann Fichou, Jamel Chelly, Thierry Bienvenu

Journal:

Year:

2010

Language:

english

File:

PDF, 485 KB

english, 2010

30

The spectrum of hand and foot malformations in patients with Greig cephalopolysyndactyly

Philippe Debeer, Koen Devriendt, Luc De Smet, Thomy deRavel, Antonio Gonzalez-Meneses, Karl-Heinz Grzeschik, Jean-Pierre Fryns

Journal:

Journal of Children's Orthopaedics

Year:

2007

Language:

english

File:

PDF, 339 KB

english, 2007

31

Is PPARα intron 7 G/C polymorphism associated with muscle strength characteristics in nonathletic young men?

S. Broos, A. Windelinckx, G. De Mars, W. Huygens, M. W. Peeters, J. Aerssens, R. Vlietinck, G. P. Beunen, M. A. Thomis

Journal:

Scandinavian Journal of Medicine & Science in Sports

Year:

2012

Language:

english

File:

PDF, 238 KB

english, 2012

32

Prediction of creatinine clearance from serum creatinine concentration based on lean body mass

Hallynck, Thierry, Soep, Hans H, Thomis, Jozef, Boelaert, Johann, Daneels, Roger, Fillastre, Jean P, De Rosa, Franco, Rubinstein, Ethan, Hatala, Milan, Spousta, Josef

Journal:

Clinical Pharmacology & Therapeutics

Year:

1981

Language:

english

File:

PDF, 744 KB

english, 1981

33

A syndrome of short stature, microcephaly and speech delay is associated with duplications reciprocal to the common Sotos syndrome deletion

Franco, Luis M, de Ravel, Thomy, Graham, Brett H, Frenkel, Stephanie M, Van Driessche, Jozef, Stankiewicz, Pawel, Lupski, James R, Vermeesch, Joris R, Cheung, Sau Wai

Journal:

European Journal of Human Genetics

Year:

2009

Language:

english

File:

PDF, 357 KB

english, 2009

34

Duplications of noncoding elements 5′ of SOX9 are associated with brachydactyly-anonychia

Kurth, Ingo, Klopocki, Eva, Stricker, Sigmar, van Oosterwijk, Jolieke, Vanek, Sebastian, Altmann, Jens, Santos, Heliosa G, van Harssel, Jeske J T, de Ravel, Thomy, Wilkie, Andrew O M

Journal:

Nature Genetics

Year:

2009

Language:

english

File:

PDF, 204 KB

english, 2009

35

Partial duplications of the ATRX gene cause the ATR-X syndrome

Thienpont, Bernard, de Ravel, Thomy, Van Esch, Hilde, Van Schoubroeck, Dominique, Moerman, Philippe, Vermeesch, Joris Robert, Fryns, Jean-Pierre, Froyen, Guy, Lacoste, Caroline, Badens, Catherine

Journal:

European Journal of Human Genetics

Year:

2007

Language:

english

File:

PDF, 140 KB

english, 2007

36

Human variome project country nodes: Documenting genetic information within a country

George P. Patrinos, Timothy D. Smith, Heather Howard, Fahd Al-Mulla, Lotfi Chouchane, Andreas Hadjisavvas, Sherifa A. Hamed, Xi-Tao Li, Makia Marafie, Rajkumar S. Ramesar, Feliciano J. Ramos, Thomy de

Journal:

Year:

2012

Language:

english

File:

PDF, 175 KB

english, 2012

37

Fetal pyelectasis and corkscrew-shaped ureters: an association observed in postmortem fetal imaging studies of osteochondrodysplasia and trisomy 21

Kenneth Carels, Luc De Catte, Philippe Moerman, Thomy de Ravel, Raymond Oyen, Jan Deprest, Filip Claus

Journal:

Prenatal Diagnosis

Year:

2012

Language:

english

File:

PDF, 76 KB

english, 2012

38

Deletion and Point Mutations of PTHLH Cause Brachydactyly Type E

Eva Klopocki, Bianca P. Hennig, Katarina Dathe, Randi Koll, Thomy de Ravel, Emiel Baten, Eveline Blom, Yves Gillerot, Johannes F.W. Weigel, Gabriele Krüger, Olaf Hiort, Petra Seemann, Stefan Mundlos

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 492 KB

english, 2010

39

Reliability, equivalence and respondent preference of computerized versus paper-and-pencil mental health questionnaires

K. Wijndaele, L. Matton, N. Duvigneaud, J. Lefevre, W. Duquet, M. Thomis, I. De Bourdeaudhuij, R. Philippaerts

Journal:

Computers in Human Behavior

Year:

2007

Language:

english

File:

PDF, 151 KB

english, 2007

40

Array Comparative Genomic Hybridization as a Diagnostic Tool for Syndromic Heart Defects

Jeroen Breckpot, Bernard Thienpont, Hilde Peeters, Thomy de Ravel, Amihood Singer, Maissa Rayyan, Karel Allegaert, Christine Vanhole, Benedicte Eyskens, Joris Robert Vermeesch, Marc Gewillig, Koenraad

Journal:

The Journal of Pediatrics

Year:

2010

Language:

english

File:

PDF, 257 KB

english, 2010

41

An unbalanced translocation 46,XX,+der(18)t(18;21)(q12.2;q11.2)mat,-21 associated with maternal isodisomy 18pter→18q12.2

Thomy J.L de Ravel, Gert Matthijs, Jean-Pierre Fryns

Journal:

Annales de Génétique

Year:

2001

Language:

english

File:

PDF, 138 KB

english, 2001

42

O4: Detection of structural low-grade mosaicism by array CGH

Bernard Thienpont, Nicole Maas, Björn Menten, Karen Buysse, Jo Vandesompele, Cindy Melotte, Thomy de Ravel, Steven Van Vooren, Irina G. Balikova, Liesbeth Backx, Sandra Janssen, Anne De Paepe, Bart De

Journal:

European Journal of Medical Genetics

Year:

2005

Language:

english

File:

PDF, 49 KB

english, 2005

43

Follow-up of adult males with chromosome 18p deletion

Thomy J.L. de Ravel, Paul Thiry, Jean-Pierre Fryns

Journal:

European Journal of Medical Genetics

Year:

2005

Language:

english

File:

PDF, 161 KB

english, 2005

44

O3: Array CGH findings in a large series of 150 patients with idiopathic mental retardation and congenital anomalies: unexpected findings and implications for future routine diagnostic screening

Björn Menten, Karen Buysse, Nicole Maas, Bernard Thienpont, Jo Vandesompele, Cindy Melotte, Thomy de Ravel, Steven Van Vooren, Irina Balikova, Liesbeth Backx, Sandra Janssens, Anne De Paepe, Bart De M

Journal:

European Journal of Medical Genetics

Year:

2005

Language:

english

File:

PDF, 47 KB

english, 2005

45

Trisomy of chromosome 16p13.3 due to an unbalanced insertional translocation into chromosome 22p13

Thomy de Ravel, Peter Aerssens, Joris R. Vermeesch, Jean-Pierre Fryns

Journal:

European Journal of Medical Genetics

Year:

2005

Language:

english

File:

PDF, 142 KB

english, 2005

46

The genetic basis of inherited anomalies of the teeth. Part 2: Syndromes with significant dental involvement

Isabelle Bailleul-Forestier, Ariane Berdal, Frans Vinckier, Thomy de Ravel, Jean Pierre Fryns, Alain Verloes

Journal:

European Journal of Medical Genetics

Year:

2008

Language:

english

File:

PDF, 1.71 MB

english, 2008

47

Another patient with a de novo deletion further delineates the 2q33.1 microdeletion syndrome

Thomy J. de Ravel, Irina Balikova, Paul Thiry, Joris R. Vermeesch, Jean-Pierre Frijns

Journal:

European Journal of Medical Genetics

Year:

2009

Language:

english

File:

PDF, 183 KB

english, 2009

48

Early detection of chromosome 9q22.32q31.1 microdeletion and the nevoid basal cell carcinoma syndrome

Thomy J.L. de Ravel, Liliane Ameye, Katleen Ballon, Martine Borghgraef, Joris R. Vermeesch, Koen Devriendt

Journal:

European Journal of Medical Genetics

Year:

2009

Language:

english

File:

PDF, 155 KB

english, 2009

49

PPP2R2C, a gene disrupted in autosomal dominant intellectual disability

Liesbeth Backx, Joris Vermeesch, Elly Pijkels, Thomy de Ravel, Eve Seuntjens, Hilde Van Esch

Journal:

European Journal of Medical Genetics

Year:

2010

Language:

english

File:

PDF, 544 KB

english, 2010

50

Association between leisure time physical activity and stress, social support and coping: A cluster-analytical approach

Katrien Wijndaele, Lynn Matton, Nathalie Duvigneaud, Johan Lefevre, Ilse De Bourdeaudhuij, William Duquet, Martine Thomis, Renaat M. Philippaerts

Journal:

Psychology of Sport and Exercise

Year:

2007

Language:

english

File:

PDF, 217 KB

english, 2007

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