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1

ATYPICAL LANGUAGE CHARACTERISTICS AND TRAJECTORIES IN CHILDREN WITH 22Q11.2 DELETION SYNDROME

Den Heuvel, Ellen Van, Manders, Eric, Swillen, Ann, Zink, Inge

Journal:

Journal of Communication Disorders

Year:

2018

Language:

english

File:

PDF, 1.25 MB

english, 2018

2

PTEN mutation in a family with Cowden syndrome and autism

Aleide Goffin, Lies H. Hoefsloot, Ermanno Bosgoed, Ann Swillen, Jean-Pierre Fryns

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 107 KB

english, 2001

3

22q11.2 deletion syndrome

McDonald-McGinn, Donna M., Sullivan, Kathleen E., Marino, Bruno, Philip, Nicole, Swillen, Ann, Vorstman, Jacob A. S., Zackai, Elaine H., Emanuel, Beverly S., Vermeesch, Joris R., Morrow, Bernice E., S

Journal:

Nature Reviews Disease Primers

Year:

2015

Language:

english

File:

PDF, 3.62 MB

english, 2015

4

2-D Versus 3-D Cross-Correlation-Based Radial and Circumferential Strain Estimation Using Multiplane 2-D Ultrafast Ultrasound in a 3-D Atherosclerotic Carotid Artery Model

Fekkes, Stein, Swillens, Abigail E. S., Hansen, Hendrik H. G., Saris, Anne E. C. M., Nillesen, Maartje M., Iannaccone, Francesco, Segers, Patrick, de Korte, Chris L.

Journal:

IEEE Transactions on Ultrasonics Ferroelectrics and Frequency Control

Year:

2016

Language:

english

File:

PDF, 1.92 MB

english, 2016

5

Retraction Notice to: Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements

Demaerel, Wolfram, Hestand, Matthew S., Vergaelen, Elfi, Swillen, Ann, López-Sánchez, Marcos, Pérez-Jurado, Luis A., McDonald-McGinn, Donna M., Zackai, Elaine, Emanuel, Beverly S., Morrow, Bernice E.,

Journal:

The American Journal of Human Genetics

Year:

2018

Language:

english

File:

PDF, 97 KB

english, 2018

6

Autism and genetics: High incidence of specific genetic syndromes in 21 autistic adolescents and adults living in two residential homes in Belgium

Swillen, Ann, Hellemans, Hans, Steyaert, Jean, Fryns, Jean-Pierre

Journal:

American Journal of Medical Genetics

Year:

1996

File:

PDF, 212 KB

1996

7

Familial deletions of chromosome 22q11: The Leuven experience

Swillen, Ann, Devriendt, Koen, Vantrappen, Greet, Vogels, Annick, Rommel, Nathalie, Fryns, Jean-Pierre, Eyskens, Benedicte, Gewillig, Marc, Dumoulin, Monique

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 30 KB

english, 1998

8

Polyhydramnios as a prenatal symptom of the DiGeorge/velo-cardio-facial syndrome

Koenraad Devriendt, Dominique Van Schoubroeck, Benedicte Eyskens, Greet Vantrappen, Ann Swillen, Marc Gewillig, Monique Dumoulin, Philippe Moerman, Kamiel Vandenberghe, Jean-Pierre Fryns

Journal:

Prenatal Diagnosis

Year:

1998

Language:

english

File:

PDF, 37 KB

english, 1998

9

Neurodevelopmental changes with age in Ullrich-Turner syndrome

Ann Swillen, Jean-Pierre Fryns

Journal:

American Journal of Medical Genetics Part A

Year:

1996

Language:

english

File:

PDF, 112 KB

english, 1996

10

Middle and inner ear malformations in velocardiofacial syndrome

Koenraad Devriendt, Ann Swillen, Isabelle Schatteman, Marc Lemmerling, Ingeborg Dhooge

Journal:

American Journal of Medical Genetics Part A

Year:

2004

Language:

english

File:

PDF, 54 KB

english, 2004

11

Pulmonary atresia/ventricular septal defect associated with facial port-wine stain and retinal vascular abnormality: A new constellation or deletion in chromosome 22q11.2?

Koen Devriendt, Ann Swillen, Ingeborg Stalmans, Ingele Casteels

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 52 KB

english, 2005

12

Mathematical learning disabilities in children with 22q11.2 deletion syndrome: A review

Bert De Smedt, Ann Swillen, Lieven Verschaffel, Pol Ghesquière

Journal:

Development Diabilities Research Reviews

Year:

2009

Language:

english

File:

PDF, 150 KB

english, 2009

13

Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/digeorge/22q11.2 deletion syndrome patients

Tingwei Guo, Donna McDonald-McGinn, Anna Blonska, Alan Shanske, Anne S. Bassett, Eva Chow, Mark Bowser, Molly Sheridan, Frits Beemer, Koen Devriendt, Ann Swillen, Jeroen Breckpot, Maria C. Digilio, Br

Journal:

Year:

2011

Language:

english

File:

PDF, 611 KB

english, 2011

14

COMT Val158met genotype and striatal D2/3 receptor binding in adults with 22q11 deletion syndrome

Erik Boot, Jan Booij, Janneke R. Zinkstok, Frank Baas, Ann Swillen, Michael J. Owen, Declan G. Murphy, Kieran C. Murphy, Don H. Linszen, Thérèse A. Van Amelsvoort

Journal:

Year:

2011

Language:

english

File:

PDF, 69 KB

english, 2011

15

Velocardiofacial syndrome presenting as distal arthrogryposis

Koen Devriendt, Ann Swillen, Marc Gewillig, Jean-Pierre Fryns, Pierre Moens, Luc Smet

Journal:

European Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 219 KB

english, 2004

16

Ocular findings in children with a microdeletion in chromosome 22q11.2

Ingele Casteels, Patricia Casaer, Marc Gewillig, Ann Swillen, Koenraad Devriendt

Journal:

European Journal of Pediatrics

Year:

2008

Language:

english

File:

PDF, 94 KB

english, 2008

17

Laterality Preference and Cognition: Cross-Syndrome Comparison of Patients with Trisomy 21 (Down), del7q11.23 (Williams–Beuren) and del22q11.2 (DiGeorge or Velo-Cardio-Facial) Syndromes

Michèle Carlier, Aude Gérard Desplanches, Nicole Philip, Silvia Stefanini, Stefano Vicari, Virginia Volterra, Christine Deruelle, Gene Fisch, Anne Lise Doyen, Anne Swillen

Journal:

Behavior Genetics

Year:

2011

Language:

english

File:

PDF, 342 KB

english, 2011

18

Deletion in chromosome region 22q11 in a child with CHARGE association

Koen Devriendt, Ann Swillen, Jean-Pierre Fryns

Journal:

Clinical Genetics

Year:

1998

Language:

english

File:

PDF, 1.38 MB

english, 1998

19

Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defect

Ann Swillen, Hilde Feys, Tamara Adriaens, Loes Nelissen, Luc Mertens, Marc Gewillig, Koen Devriendt, Jean-Pierre Fryns

Journal:

Developmental Medicine & Child Neurology

Year:

2005

Language:

english

File:

PDF, 117 KB

english, 2005

20

Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)

Katrijn Van Aken, Bert De Smedt, Annelies Van Roie, Marc Gewillig, Koen Devriendt, Jean-Pierre Fryns, Johan Simons, Ann Swillen

Journal:

Developmental Medicine & Child Neurology

Year:

2007

Language:

english

File:

PDF, 97 KB

english, 2007

21

VEGF: A modifier of the del22q11 (DiGeorge) syndrome?

Stalmans, Ingeborg, Lambrechts, Diether, De smet, Frederik, Jansen, Sandra, Wang, Jian, Maity, Sunit, Kneer, Paige, von der Ohe, Maren, Swillen, Ann, Maes, Christa

Journal:

Nature Medicine

Year:

2003

Language:

english

File:

PDF, 1.57 MB

english, 2003

22

No evidence for a parental inversion polymorphism predisposing to rearrangements at 22q11.2 in the DiGeorge/Velocardiofacial syndrome

Gebhardt, G Stefan, Devriendt, Koenraad, Thoelen, Reinhilde, Swillen, Ann, Pijkels, Elly, Gewillig, Marc, Fryns, Jean-Pierre, Vermeesch, Joris R

Journal:

European Journal of Human Genetics

Year:

2003

Language:

english

File:

PDF, 110 KB

english, 2003

23

Characterization of the interaction constants for the binding of two unlabelled ligands to the sites of a receptor

Stéphane Swillens, Anne Gourdin, Olivier Delahaut

Journal:

Naunyn-Schmiedeberg's Archives of Pharmacology

Year:

1989

Language:

english

File:

PDF, 1023 KB

english, 1989

24

Practical Guidelines for Managing Patients with 22q11.2 Deletion Syndrome

Anne S. Bassett, Donna M. McDonald-McGinn, Koen Devriendt, Maria Cristina Digilio, Paula Goldenberg, Alex Habel, Bruno Marino, Solveig Oskarsdottir, Nicole Philip, Kathleen Sullivan, Ann Swillen, Jaco

Journal:

The Journal of Pediatrics

Year:

2011

Language:

english

File:

PDF, 325 KB

english, 2011

25

The Coffin-Siris syndrome: data on mental development, language, behavior and social skills in 12 children

Ann Swillen, Nausikaa Glorieux, Marijke Peeters, Jean-Pierre Fryns

Journal:

Clinical Genetics

Year:

1995

Language:

english

File:

PDF, 594 KB

english, 1995

26

Cerebellar Hypoplasia in a Patient with Velo-Cardio-Facial Syndrome

Koenraad Devriendt, Marie-Noëlle Van Thienen, Ann Swillen, Jean-Pierre Fryns

Journal:

Developmental Medicine & Child Neurology

Year:

1996

Language:

english

File:

PDF, 505 KB

english, 1996

27

Basic number processing and difficulties in single-digit arithmetic: Evidence from Velo-Cardio-Facial Syndrome

Bert De Smedt, Bert Reynvoet, Ann Swillen, Lieven Verschaffel, Bart Boets, Pol Ghesquière

Journal:

Year:

2009

Language:

english

File:

PDF, 281 KB

english, 2009

28

Interstitial 6q deletion: clinical and array CGH characterisation of a new patient

Cédric Le Caignec, Ann Swillen, Elvire Van Asche, Jean-Pierre Fryns, Joris R. Vermeesch

Journal:

European Journal of Medical Genetics

Year:

2005

Language:

english

File:

PDF, 221 KB

english, 2005

29

Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls

Katrijn Van Aken, Ann Swillen, Marc Beirinckx, Luc Janssens, Karen Caeyenberghs, Bouwien Smits-Engelsman

Journal:

Research in Developmental Disabilities

Year:

2010

Language:

english

File:

PDF, 452 KB

english, 2010

30

Kinematic movement strategies in primary school children with 22q11.2 Deletion Syndrome compared to age- and IQ-matched controls during visuo-manual tracking

Katrijn Van Aken, Ann Swillen, Marc Beirinckx, Luc Janssens, Karen Caeyenberghs, Bouwien Smits-Engelsman

Journal:

Research in Developmental Disabilities

Year:

2010

Language:

english

File:

PDF, 260 KB

english, 2010

31

Social phenotypes in genetic syndromes

Ann Swillen, Thomy de Ravel, Chris Oliver

Journal:

Journal of Intellectual Disability Research

Year:

2012

Language:

english

File:

PDF, 82 KB

english, 2012

32

Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients

Herman, Sean B., Guo, Tingwei, McGinn, Donna M. McDonald, Blonska, Anna, Shanske, Alan L., Bassett, Anne S., Chow, Eva W.C., Bowser, Mark, Sheridan, Molly, Beemer, Frits, Devriendt, Koen, Swillen, Ann

Journal:

American Journal of Medical Genetics Part A

Year:

2012

Language:

english

File:

PDF, 1009 KB

english, 2012

33

Presenting symptoms in adults with the 22q11 deletion syndrome

Vogels, Annick, Schevenels, Sara, Cayenberghs, Richard, Weyts, Eddy, Van Buggenhout, Griet, Swillen, Ann, Van Esch, Hilde, de Ravel, Thomy, Corveleyn, Pieter, Devriendt, Koen

Journal:

European Journal of Medical Genetics

Year:

2014

Language:

english

File:

PDF, 235 KB

english, 2014

34

On the use of DNA fingerprints for linkage studies in cattle

Georges, Michel, Lathrop, Mark, Hilbert, Pascale, Marcotte, Anne, Schwers, Anne, Swillens, Stephane, Vassart, Gilbert, Hanset, Roger

Journal:

Year:

1990

Language:

english

File:

PDF, 4.71 MB

english, 1990

35

[IEEE 2012 IEEE International Ultrasonics Symposium - Dresden, Germany (2012.10.7-2012.10.10)] 2012 IEEE International Ultrasonics Symposium - Shunt quantification in congenital heart disease based on two-dimensional speckle tracking

Fadnes, Solveig, Nyrnes, Siri Ann, Swillens, Abigail, Torp, Hans, Lovstakken, Lasse

Year:

2012

Language:

english

File:

PDF, 1.97 MB

english, 2012

36

[IEEE 2014 IEEE International Ultrasonics Symposium (IUS) - Chicago, IL, USA (2014.9.3-2014.9.6)] 2014 IEEE International Ultrasonics Symposium - Semi-3D strain imaging of an atherosclerotic carotid artery by multi-cross-sectional radial strain estimations using simulated multi-angle plane wave ultrasound

Fekkes, Stein, Swillens, Abigail E.S., Hansen, Hendrik H.G., Saris, Anne E.C.M., Nillesen, Maartje M., Iannaccone, Francesco, Segers, Patrick, de Korte, Chris L.

Year:

2014

Language:

english

File:

PDF, 944 KB

english, 2014

37

Atypical Neuropsychological Profile in a Boy with 22q11.2 Deletion Syndrome Keywords:

Stiers, Peter, Swillen, Ann, De Smedt, Bert, Lagae, Lieven, Devriendt, Koen, D'Agostino, Emiliano, Sunaert, Stefan, Fryns, andJean-Pierre

Journal:

Child Neuropsychology

Year:

2005

Language:

english

File:

PDF, 192 KB

english, 2005

38

Neuropsychological, Learning and Psychosocial Profile of Primary School Aged Children with the Velo-Cardio-Facial Syndrome (22q11 Deletion): Evidence for a Nonverbal Learning Disability?

Vandeputte, Leen, Cracco, Joris, Maes, Bea, Ghesqui�re, Pol, Devriendt, Koen, Fryns, Jean-Pierre, Swillen, Ann

Journal:

Child Neuropsychology

Year:

1999

Language:

english

File:

PDF, 120 KB

english, 1999

39

The influence of aortic dimensions on calculated wall shear stress in the mouse aortic arch

Trachet, Bram, Swillens, Abigail, Van Loo, Denis, Casteleyn, Christophe, De Paepe, Anne, Loeys, Bart, Segers, Patrick

Journal:

Computer Methods in Biomechanics & Biomedical Engineering

Year:

2009

Language:

english

File:

PDF, 955 KB

english, 2009

40

Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

Mlynarski, Elisabeth E., Sheridan, Molly B., Xie, Michael, Guo, Tingwei, Racedo, Silvia E., McDonald-McGinn, Donna M., Gai, Xiaowu, Chow, Eva W.C., Vorstman, Jacob, Swillen, Ann, Devriendt, Koen, Brec

Journal:

The American Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 538 KB

english, 2015

41

3 generation pedigree with paternal transmission of the 22q11.2 deletion syndrome: Intrafamilial phenotypic variability

Vergaelen, Elfi, Swillen, Ann, Van Esch, Hilde, Claes, Stephan, Van Goethem, Gert, Devriendt, Koenraad

Journal:

European Journal of Medical Genetics

Year:

2015

Language:

english

File:

PDF, 672 KB

english, 2015

42

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

Mlynarski, Elisabeth E., Xie, Michael, Taylor, Deanne, Sheridan, Molly B., Guo, Tingwei, Racedo, Silvia E., McDonald-McGinn, Donna M., Chow, Eva W. C., Vorstman, Jacob, Swillen, Ann, Devriendt, Koen,

Journal:

Year:

2016

Language:

english

File:

PDF, 924 KB

english, 2016

43

Psychotic disorder associated with 22q11.2 duplication syndrome

Amelsvoort, Therese van, Denayer, Astrid, Boermans, Jacques, Swillen, Ann

Journal:

Psychiatry Research

Year:

2016

Language:

english

File:

PDF, 152 KB

english, 2016

44

[IEEE 2015 IEEE International Ultrasonics Symposium (IUS) - Taipei, Taiwan (2015.10.21-2015.10.24)] 2015 IEEE International Ultrasonics Symposium (IUS) - 2D versus 3D cross-correlation-based radial and circumferential strain imaging in a 3D atherosclerotic carotid artery model using ultrafast plane wave ultrasound

Fekkes, Stein, Swillens, Abigail E.S., Hansen, Hendrik H.G., Saris, Anne E.C.M., Nillesen, Maartje M., Iannaccone, Francesco, Segers, Patrick, de Korte, Chris L.

Year:

2015

Language:

english

File:

PDF, 1.10 MB

english, 2015

45

Developmental trajectories in 22q11.2 deletion syndrome

Swillen, Ann, McDonald-McGinn, Donna

Journal:

American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Year:

2015

Language:

english

File:

PDF, 863 KB

english, 2015

46

The importance of understanding cognitive trajectories

Journal:

Current Opinion in Psychiatry

Year:

2016

Language:

english

File:

PDF, 228 KB

english, 2016

47

Prevalence and Nature of Hearing Loss in 22q11.2 Deletion Syndrome

Van Eynde, Charlotte, Swillen, Ann, Lambeens, Elien, Verhaert, Nicolas, Desloovere, Christian, Luts, Heleen, Poorten, Vincent Vander, Devriendt, Koenraad, Hens, Greet

Journal:

Journal of Speech Language and Hearing Research

Year:

2016

Language:

english

File:

PDF, 295 KB

english, 2016

48

Malformations of the middle and inner ear on CT imaging in 22q11 deletion syndrome

Loos, Elke, Verhaert, Nicolas, Willaert, Annelore, Devriendt, Koenraad, Swillen, Ann, Hermans, Robert, Op de Beeck, Katya, Hens, Greet

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 462 KB

english, 2016

49

Referential communication abilities in children with 22q11.2 deletion syndrome

Van Den Heuvel, Ellen, ReuterskiöLd, Christina, Solot, Cynthia, Manders, Eric, Swillen, Ann, Zink, Inge

Journal:

International Journal of Speech-Language Pathology

Year:

2016

Language:

english

File:

PDF, 531 KB

english, 2016

50

[IEEE 2016 IEEE International Ultrasonics Symposium (IUS) - Tours, France (2016.9.18-2016.9.21)] 2016 IEEE International Ultrasonics Symposium (IUS) - Model-based estimation of intra-cardiac blood flow velocities using an unscented Kalman filter

Hogenes, Jakob, Wigen, Morten, Nyrnes, Siri Ann, Segers, Patrick, Swillens, Abigail, Lovstakken, Lasse

Year:

2016

Language:

english

File:

PDF, 2.39 MB

english, 2016

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