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1

Insights into the multifactorial causation of obesity by integrated genetic and epigenetic analysis

Diels, Sara, Vanden Berghe, Wim, Van Hul, Wim

Journal:

Obesity Reviews

Year:

2020

Language:

english

File:

PDF, 779 KB

english, 2020

2

The Effect of Low-Intensity Exercise Training on Fat Metabolism of Obese Women

Dorien P. van Aggel-Leijssen, Wim H. Saris, Anton J. Wagenmakers, Gabby B. Hul, Marleen A. van Baak

Journal:

Year:

2001

Language:

english

File:

PDF, 1.99 MB

english, 2001

3

Paget's Disease of Bone: Evidence for Complex Pathogenetic Interactions

Pui Yan Jenny Chung, Wim Van Hul

Journal:

Seminars in Arthritis and Rheumatism

Year:

2012

Language:

english

File:

PDF, 1.35 MB

english, 2012

4

Congenital skeletal abnormalities: an introduction to the radiological semiology

Filip M. Vanhoenacker, Wim Van Hul, Jan Gielen, Arthur M. De Schepper

Journal:

European Journal of Radiology

Year:

2001

Language:

english

File:

PDF, 1.13 MB

english, 2001

5

Long-term effects of low-intensity exercise training on fat metabolism in weight-reduced obese men

Dorien P. van Aggel-Leijssen, Wim H. Saris, Gabby B. Hul, Marleen A. van Baak

Journal:

Year:

2002

Language:

english

File:

PDF, 140 KB

english, 2002

6

A look behind the scenes: the risk and pathogenesis of primary osteoporosis

Hendrickx, Gretl, Boudin, Eveline, Van Hul, Wim

Journal:

Nature Reviews Rheumatology (formerly Nature Clinical Practice Rheumatology)

Year:

2015

Language:

english

File:

PDF, 490 KB

english, 2015

7

A novel frameshift mutation (1651ins5) in exon 10 of the CFTR gene can be misinterpreted as a ΔF508 mutation

Gino Delaere, Karel Stuer, Katrien Storm, Patrick J. Willems, Wim Van Hul

Journal:

Year:

1999

Language:

english

File:

PDF, 13 KB

english, 1999

8

Molecular basis of multiple exostoses: mutations in the EXT1 and EXT2 genes

Wim Wuyts, Wim Van Hul

Journal:

Year:

2000

Language:

english

File:

PDF, 232 KB

english, 2000

9

Multiple exostoses, mental retardation, hypertrichosis, and brain abnormalities in a boy with a de novo 8q24 submicroscopic interstitial deletion

Wim Wuyts, Dominique Roland, Hermann-Josef Lüdecke, Jan Wauters, Martine Foulon, Wim Van Hul, Lionel Van Maldergem

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 235 KB

english, 2002

10

Burning down DEFECT11

Wim Wuyts, Wim Van Hul, Oliver Bartsch, Andrew O.M. Wilkie, Peter Meinecke

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 41 KB

english, 2001

11

A novel mutation in the MSX2 gene in a family with foramina parietalia permagna (FPP)

Liesbeth Spruijt, Pieter Verdyck, Wim Van Hul, Wim Wuyts, Christine de Die-Smulders

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 94 KB

english, 2005

12

Exclusion of OGDH and BMP4 as candidate genes in two siblings with autosomal recessive DOOR syndrome

Yolande van Bever, Wendy Balemans, Els L.I.M. Duval, Ann Jespers, François Eyskens, Wim van Hul, Winnie Courtens

Journal:

American Journal of Medical Genetics Part A

Year:

2007

Language:

english

File:

PDF, 223 KB

english, 2007

13

First missense mutation in the SOST gene causing sclerosteosis by loss of sclerostin function

Elke Piters, Cavit Culha, Martiene Moester, Rutger Van Bezooijen, Dirk Adriaensen, Thomas Mueller, Stella Weidauer, Karen Jennes, Fenna de Freitas, Clemens Löwik, Jean-Pierre Timmermans, Wim Van Hul,

Journal:

Year:

2010

Language:

english

File:

PDF, 520 KB

english, 2010

14

Levels of serotonin, sclerostin, bone turnover markers as well as bone density and microarchitecture in patients with high-bone-mass phenotype due to a mutation in Lrp5

Morten Frost, Tom Andersen, Fatma Gossiel, Stinus Hansen, Jens Bollerslev, Wim van Hul, Richard Eastell, Moustapha Kassem, Kim Brixen

Journal:

Journal of Bone and Mineral Research

Year:

2011

Language:

english

File:

PDF, 216 KB

english, 2011

15

Identification of genetic modifiers of monogenic (bone) diseases: New tools available, but with limitations

Journal:

Journal of Bone and Mineral Research

Year:

2011

Language:

english

File:

PDF, 48 KB

english, 2011

16

The Binding Between Sclerostin and LRP5 is Altered by DKK1 and by High-Bone MassLRP5Mutations

Wendy Balemans, Elke Piters, Erna Cleiren, Minrong Ai, Liesbeth Van Wesenbeeck, Matthew L. Warman, Wim Van Hul

Journal:

Calcified Tissue International

Year:

2008

Language:

english

File:

PDF, 379 KB

english, 2008

17

Common Genetic Variation in theDKK1Gene is Associated with Hip Axis Length but not with Bone Mineral Density and Bone Turnover Markers in Young Adult Men: Results from the Odense Androgen Study

Elke Piters, Wendy Balemans, Torben Leo Nielsen, Marianne Andersen, Eveline Boudin, Kim Brixen, Wim Van Hul

Journal:

Calcified Tissue International

Year:

2010

Language:

english

File:

PDF, 267 KB

english, 2010

18

Association Study of Polymorphisms in theSOSTGene Region and Parameters of Bone Strength and Body Composition in Both Young and Elderly Men: Data from the Odense Androgen Study

Elke Piters, Fenna de Freitas, Torben Leo Nielsen, Marianne Andersen, Kim Brixen, Wim Van Hul

Journal:

Calcified Tissue International

Year:

2012

Language:

english

File:

PDF, 228 KB

english, 2012

19

Association ofSIRT1gene variation with visceral obesity

Armand V. Peeters, Sigri Beckers, An Verrijken, Ilse Mertens, Peter Roevens, Pieter J. Peeters, Wim Van Hul, Luc F. Van Gaal

Journal:

Year:

2008

Language:

english

File:

PDF, 299 KB

english, 2008

20

Clinical and molecular studies of EXT1/EXT2 in Bulgaria

Malina Kirilova Stancheva-Ivanova, Wim Wuyts, Els van Hul, Briguita Ivanova Radeva, Radoslava Vasileva Vazharova, Todor Petrov Sokolov, Borislav Yordanov Vladimirov, Margarita Dimitrova Apostolova, Iv

Journal:

Journal of Inherited Metabolic Disease

Year:

2011

Language:

english

File:

PDF, 179 KB

english, 2011

21

Osteopetrosis: from Animal Models to Human Conditions

Bram Perdu, Wim Van Hul, Liesbeth Van Wesenbeeck

Journal:

Clinical Reviews in Bone and Mineral Metabolism

Year:

2008

Language:

english

File:

PDF, 325 KB

english, 2008

22

The G1422A variant of the cannabinoid receptor gene (CNR1) is associated with abdominal adiposity in obese men

Armand Peeters, Sigri Beckers, Ilse Mertens, Wim Van Hul, Luc Van Gaal

Journal:

Endocrine (Springer)

Year:

2007

Language:

english

File:

PDF, 131 KB

english, 2007

23

Possible role forENPP1polymorphism in obesity but not forINSIG2andPLINvariants

Armand Peeters, Sigri Beckers, An Verrijken, Ilse Mertens, Luc Van Gaal, Wim Van Hul

Journal:

Endocrine (Springer)

Year:

2009

Language:

english

File:

PDF, 228 KB

english, 2009

24

Common melanocortin-3 receptor variants are not associated with obesity, although rs3746619 does influence weight in obese individuals

Doreen Zegers, Sigri Beckers, Ilse L. Mertens, Luc F. Van Gaal, Wim Van Hul

Journal:

Endocrine (Springer)

Year:

2010

Language:

english

File:

PDF, 195 KB

english, 2010

25

Common variants in the gene for the serotonin receptor 6 (HTR6) do not contribute to obesity

Armand V. Peeters, Sigri Beckers, An Verrijken, Peter Roevens, Pieter J. Peeters, Luc F. van Gaal, Wim van Hul

Journal:

Journal of Genetics

Year:

2010

Language:

english

File:

PDF, 149 KB

english, 2010

26

Exclusion de la région p21 du chromosome 1 dans une variante phénotypique d’ostéopétrose autosomique dominante de type II (ADO II)

Olivier Bénichou, Els Van Hul, Wim Van Hul, Marie-Chrisine de Vernejoul

Journal:

Revue du Rhumatisme

Year:

2001

File:

PDF, 262 KB

2001

27

Association Study and Mutation Analysis of Adiponectin Shows Association of Variants in APM1 with Complex Obesity in Women

Sigri Beckers, Armand V. Peeters, Fenna De Freitas, Ilse L. Mertens, Stijn L. Verhulst, Dominique Haentjens, Kristine N. Desager, Luc F. Van Gaal, Wim Van Hul

Journal:

Annals of Human Genetics

Year:

2009

Language:

english

File:

PDF, 242 KB

english, 2009

28

10.1038/12699

Warman, Matthew L., Hurvitz, Jennifer R., Suwairi, Wafaa M., Van Hul, Wim, El-Shanti, Hatem, Superti-Furga, Andrea, Roudier, Jean, Holderbaum, Daniel, Pauli, Richard M., Herd, J. Kenneth, Hul, Els Van

Journal:

Nature Genetics

Year:

1999

Language:

english

File:

PDF, 318 KB

english, 1999

29

10.1038/71667

Hughes, Anne E., Ralston, Stuart H., Marken, John, Bell, Christine, MacPherson, Heather, Wallace, Richard G.H., van Hul, Wim, Whyte, Michael P., Nakatsuka, Kyoshi, Hovy, Louis, Anderson, Dirk M.

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 385 KB

english, 2000

30

10.1038/81563

Van Hul, Wim, Janssens, Katrien, Gershoni-Baruch, Ruth, Guañabens, Nuria, Migone, Nicola, Ralston, Stuart, Bonduelle, Maryse, Lissens, Willy, Van Maldergem, Lionel, Vanhoenacker, Filip, Verbruggen, Le

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 293 KB

english, 2000

31

Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene

Hendriks, Lydia, van Duijn, Cornelia M., Cras, Patrick, Cruts, Marc, Van Hul, Wim, van Harskamp, Frans, Warren, Andrew, McInnis, Melvin G., Antonarakis, Stylianos E., Martin, Jean-Jacques

Journal:

Nature Genetics

Year:

1992

File:

PDF, 403 KB

1992

32

The Effects of Increasing Serum Calcitriol on Energy and Fat Metabolism and Gene Expression

Niels Boon, Gabby B. J. Hul, Audrey Sicard, Eveline Kole, Elisa R. Van, Den Berg, Nathalie Viguerie, Dominique Langin, Wim H. M. Saris

Journal:

Year:

2006

Language:

english

File:

PDF, 152 KB

english, 2006

33

Analysis of Genetic Variations in the Resistin Gene Shows No Associations With Obesity in Women

Sigri Beckers, Armand V. Peeters, Fenna de Freitas, Ilse L. Mertens, Jan-Jaap Hendrickx, Luc F. Van Gaal, Wim Van Hul

Journal:

Year:

2008

Language:

english

File:

PDF, 125 KB

english, 2008

34

Skeletal Muscle Fatty Acid Handling in Insulin Resistant Men

Anneke M.J. van Hees, Anneke Jans, Gabby B. Hul, Helen M. Roche, Wim H.M. Saris, Ellen E. Blaak

Journal:

Year:

2011

Language:

english

File:

PDF, 422 KB

english, 2011

35

Molecular and clinical examination of an Italian DEFECT 11 family

Wuyts, Wim, Gennaro, Giancarlo Di, Bianco, Federico, Wauters, Jan, Morocutti, Cristoforo, Pierelli, Francesco, Bossuyt, Paul, Van Hul, Wim, Casali, Carlo

Journal:

European Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 293 KB

english, 1999

36

Clinical and molecular analysis of nine families with Adams–Oliver syndrome

Verdyck, Pieter, Holder-Espinasse, Muriel, Hul, Wim Van, Wuyts, Wim

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 138 KB

english, 2003

37

Proximal 11p deletion syndrome (P11pDS): additional evaluation of the clinical and molecular aspects

Wuyts, Wim, Waeber, Gerard, Meinecke, Peter, Schüler, Herdit, Goecke, Timm O, Hul, Wim Van, Bartsch, Oliver

Journal:

European Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 175 KB

english, 2004

38

LRP5 and Wnt Signaling: A Union Made for Bone

Mark L Johnson, Kimberley Harnish, Roel Nusse, Wim Van Hul

Journal:

Journal of Bone and Mineral Research

Year:

2004

Language:

english

File:

PDF, 159 KB

english, 2004

39

An Autosomal Dominant High Bone Mass Phenotype in Association With Craniosynostosis in an Extended Family Is Caused by an LRP5 Missense Mutation

Mei Lan Kwee, Wendy Balemans, Erna Cleiren, Johan JP Gille, Frits Van Der Blij, Jan M Sepers, Wim Van Hul

Journal:

Journal of Bone and Mineral Research

Year:

2005

Language:

english

File:

PDF, 493 KB

english, 2005

40

Missense Mutations in LRP5 Are Not a Common Cause of Idiopathic Osteoporosis in Adult Men

Patricia Crabbe, Wendy Balemans, Andy Willaert, Inge Van Pottelbergh, Erna Cleiren, Paul J Coucke, Minrong Ai, Stefan Goemaere, Wim Van Hul, Anne De Paepe, Jean-Marc Kaufman

Journal:

Journal of Bone and Mineral Research

Year:

2005

Language:

english

File:

PDF, 375 KB

english, 2005

41

Polymorphisms of the CLCN7 Gene Are Associated With BMD in Women

Ulrika Pettersson, Omar ME Albagha, Max Mirolo, Anna Taranta, Annalisa Frattini, Fiona EA McGuigan, Paolo Vezzoni, Anna Teti, Wim Van Hul, David M Reid, Anna Villa, Stuart H Ralston

Journal:

Journal of Bone and Mineral Research

Year:

2005

Language:

english

File:

PDF, 102 KB

english, 2005

42

Novel LRP5 Missense Mutation in a Patient With a High Bone Mass Phenotype Results in Decreased DKK1-Mediated Inhibition of Wnt Signaling*

Wendy Balemans, Jean-Pierre Devogelaer, Erna Cleiren, Elke Piters, Emanuelle Caussin, Wim Van Hul

Journal:

Journal of Bone and Mineral Research

Year:

2007

Language:

english

File:

PDF, 1.87 MB

english, 2007

43

A New Heterozygous Mutation (R714C) of the Osteopetrosis Gene, Pleckstrin Homolog Domain Containing Family M (With Run Domain) Member 1 (PLEKHM1), Impairs Vesicular Acidification and Increases TRACP Secretion in Osteoclasts

Andrea Del Fattore, Rachele Fornari, Liesbeth Van Wesenbeeck, Fenna de Freitas, Jean-Pierre Timmermans, Barbara Peruzzi, Alfredo Cappariello, Nadia Rucci, Giovanni Spera, Miep H Helfrich, Wim Van Hul,

Journal:

Journal of Bone and Mineral Research

Year:

2008

Language:

english

File:

PDF, 2.87 MB

english, 2008

44

A new familial sclerosing bone dysplasia

Eliane Chouery, Alessandra Pangrazio, Annalisa Frattini, Anna Villa, Liesbeth Van Wesenbeeck, Elke Piters, Wim Van Hul, Fraser P Coxon, Tabitha Schouten, Miep Helfrich, Gérard Lefranc, André Mégarbané

Journal:

Journal of Bone and Mineral Research

Year:

2010

Language:

english

File:

PDF, 236 KB

english, 2010

45

Paget's Disease of Bone: Evidence for a Susceptibility Locus on Chromosome 18q and for Genetic Heterogeneity

Sonya I. Haslam, Wim Van Hul, Antonio Morales-Piga, Wendy Balemans, J. L. San-Millan, Kiyoshi Nakatsuka, Patrick Willems, Neva E. Haites, Stuart H. Ralston

Journal:

Journal of Bone and Mineral Research

Year:

1998

Language:

english

File:

PDF, 183 KB

english, 1998

46

Localization of the Gene Causing Autosomal Dominant Osteopetrosis Type I to Chromosome 11q12-13

Els Van Hul, Jeppe Gram, Jens Bollerslev, Liesbeth Van Wesenbeeck, Danny Mathysen, Poul Erik Andersen, Filip Vanhoenacker, Wim Van Hul

Journal:

Journal of Bone and Mineral Research

Year:

2002

Language:

english

File:

PDF, 3.64 MB

english, 2002

47

Localization of the Gene Causing the Osteopetrotic Phenotype in the Incisors Absent (Ia) Rat on Chromosome 10q32.1

Liesbeth van Wesenbeeck, Paul R Odgren, Carole A Mackay, Wim Van Hul

Journal:

Journal of Bone and Mineral Research

Year:

2004

Language:

english

File:

PDF, 194 KB

english, 2004

48

Physical mapping of chromosome 21 DNA markers in Alzheimer's disease region using somatic cell hybrids

Guy Van Camp, Wim Van Hul, Hubert Backhovens, Piet Stinissen, Anita Wehnert, David Patterson, Antoon Vandenberghe, Christine Van Broeckhoven

Journal:

Somatic Cell and Molecular Genetics

Year:

1990

Language:

english

File:

PDF, 843 KB

english, 1990

49

Recurrent Sclerosing Dysplasia of Bone: Report of a Case

Martin Druce Batstone, Gary Walton, Anthony Lynham, Frank Monsour, Wendy Balemans, Wim Van Hul

Journal:

Journal of Oral and Maxillofacial Surgery

Year:

2008

Language:

english

File:

PDF, 309 KB

english, 2008

50

Exclusion of the chromosomal 1p21 region in a large pedigree with a phenotypic variant of type II autosomal dominant osteopetrosis

Olivier David Bénichou, Els Van Hul, Wim Van Hul, Marie-Christine de Vernejoul

Journal:

Joint Bone Spine

Year:

2001

Language:

english

File:

PDF, 243 KB

english, 2001