Ann Swillen

Summary

Affiliation: Katholieke Universiteit Leuven
Country: Belgium

Publications

  1. ncbi request reprint Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defect
    Ann Swillen
    Department of Human Genetics, University Hospital Gasthuisberg, University of Leuven, Herestraat 49, 3000 Leuven, Belgium
    Dev Med Child Neurol 47:797-802. 2005
  2. doi request reprint Basic number processing and difficulties in single-digit arithmetic: evidence from Velo-Cardio-Facial Syndrome
    Bert De Smedt
    Centre for Disability, Special Needs Education, and Child Care, University of Leuven, Belgium
    Cortex 45:177-88. 2009
  3. ncbi request reprint Ocular findings in children with a microdeletion in chromosome 22q11.2
    Ingele Casteels
    Department of Ophthalmology, University Hospitals Leuven St Rafael, Leuven, Belgium
    Eur J Pediatr 167:751-5. 2008
  4. ncbi request reprint Interstitial 6q deletion: clinical and array CGH characterisation of a new patient
    Cedric Le Caignec
    Centre for Human Genetics, University Hospital Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium
    Eur J Med Genet 48:339-45. 2005
  5. ncbi request reprint Velocardiofacial syndrome presenting as distal arthrogryposis
    Koen Devriendt
    Centre for Human Genetics, University Hospital Leuven, Herestraat 49, 3000 Leuven, Belgium
    Eur J Pediatr 163:329-30. 2004
  6. doi request reprint Numerical magnitude processing impairments in genetic syndromes: a cross-syndrome comparison of Turner and 22q11.2 deletion syndromes
    Carmen Brankaer
    Parenting and Special Education Research Unit, Faculty of Psychology and Educational Sciences, University of Leuven, Belgium
    Dev Sci . 2016
  7. ncbi request reprint Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome
    Peter Stiers
    Department of Pediatrics, K U Leuven, Medical School, Herestraat 49, B 3000 Leuven, Belgium
    Child Neuropsychol 11:87-108. 2005
  8. ncbi request reprint 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
    Am J Med Genet A 132:340-1. 2005
  9. ncbi request reprint Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)
    Katrijn Van Aken
    Faculty of Kinesiology and Rehabilitation Sciences, Katholieke Universiteit Leuven, Leuven, Belgium
    Dev Med Child Neurol 49:210-3. 2007
  10. ncbi request reprint Middle and inner ear malformations in velocardiofacial syndrome
    Koenraad Devriendt
    Am J Med Genet A 131:225-6. 2004

Collaborators

  • Bert De Smedt
  • Koen Devriendt
  • Marc Gewillig
  • Carmen Brankaer
  • Bart Boets
  • Lieven Lagae
  • Bert Reynvoet
  • Luc De Smet
  • Katrijn Van Aken
  • Adriana C Gittenberger-de Groot
  • P Stiers
  • Jian Wang
  • S J Conway
  • Didier Lacombe
  • Ingele Casteels
  • Gregory Raux
  • Cedric Le Caignec
  • Joris R Vermeesch
  • Jean Pierre Fryns
  • Gabriel Stefan Gebhardt
  • Ingeborg Stalmans
  • Patricia Casaer
  • Sylvie Manouvrier-Hanu
  • Pierre Sarda
  • Marie Christine Nolen
  • Bernadette Hecketsweiler
  • Valérie Drouin-Garraud
  • Thierry Frebourg
  • Nicole Philip
  • Emilie Bumsel
  • Solenn Legallic
  • Carole Fantini
  • Caroline Demily
  • Janneke Zinkstok
  • Delphine Heron
  • Florence Thibaut
  • Cyril Coizet
  • Alexandra Afenjar
  • Didier Hannequin
  • Dominique Campion
  • Marie Lemarchand
  • Gaelle Opolczynski
  • Michele Carlier
  • Georges Marie M Brévière
  • Annick Vogels
  • Gabriella Di Rosa
  • Jacqueline Bou
  • Anne Philippe
  • Giuseppina Pustorino
  • Yves Alembik
  • Valérie Layet
  • Aude Gérard-Desplanches
  • Michel Petit
  • Therese Van Amelsvoort
  • Elvire Van Asche
  • Sandra Jansen
  • Peter Scambler
  • Robert Vlietinck
  • Stephane Plaisance
  • Christa Maes
  • Mieke Dewerchin
  • Thurid Boetel
  • Sunit Maity
  • Peter Hellings
  • Peter Carmeliet
  • Daniel G M Molin
  • Lieve Moons
  • Veerle Compernolle
  • Paige Kneer
  • Maren von der Ohe
  • Elly Pijkels
  • Diether Lambrechts
  • Maartin Haardt
  • Camila V Esguerra
  • Geert Carmeliet
  • Bernice Morrow
  • Beverly Emanuel
  • Reinhilde Thoelen
  • Deborah A Driscol
  • Frederik De Smet
  • Annett Behn-Krappa
  • Desire Collen

Detail Information

Publications13

  1. ncbi request reprint Early motor development in young children with 22q.11 deletion syndrome and a conotruncal heart defect
    Ann Swillen
    Department of Human Genetics, University Hospital Gasthuisberg, University of Leuven, Herestraat 49, 3000 Leuven, Belgium
    Dev Med Child Neurol 47:797-802. 2005
    ..These data reveal a significant motor delay in many young children with del22q.11, which is not caused by the presence of a congenital heart defect or by behavioural features...
  2. doi request reprint Basic number processing and difficulties in single-digit arithmetic: evidence from Velo-Cardio-Facial Syndrome
    Bert De Smedt
    Centre for Disability, Special Needs Education, and Child Care, University of Leuven, Belgium
    Cortex 45:177-88. 2009
    ..s model (2003). Most importantly, the correlational analyses showed that basic number processing skills directly accounted for single-digit arithmetic performance and strategy use in the children of the present study...
  3. ncbi request reprint Ocular findings in children with a microdeletion in chromosome 22q11.2
    Ingele Casteels
    Department of Ophthalmology, University Hospitals Leuven St Rafael, Leuven, Belgium
    Eur J Pediatr 167:751-5. 2008
    ..2. Ophthalmological examination at a young age and refractive correction in those children is warranted. On the other hand, ocular findings can give a clue to the diagnosis of del 22q11.2...
  4. ncbi request reprint Interstitial 6q deletion: clinical and array CGH characterisation of a new patient
    Cedric Le Caignec
    Centre for Human Genetics, University Hospital Gasthuisberg, Herestraat 49, 3000 Leuven, Belgium
    Eur J Med Genet 48:339-45. 2005
    ....
  5. ncbi request reprint Velocardiofacial syndrome presenting as distal arthrogryposis
    Koen Devriendt
    Centre for Human Genetics, University Hospital Leuven, Herestraat 49, 3000 Leuven, Belgium
    Eur J Pediatr 163:329-30. 2004
  6. doi request reprint Numerical magnitude processing impairments in genetic syndromes: a cross-syndrome comparison of Turner and 22q11.2 deletion syndromes
    Carmen Brankaer
    Parenting and Special Education Research Unit, Faculty of Psychology and Educational Sciences, University of Leuven, Belgium
    Dev Sci . 2016
    ....
  7. ncbi request reprint Atypical neuropsychological profile in a boy with 22q11.2 Deletion Syndrome
    Peter Stiers
    Department of Pediatrics, K U Leuven, Medical School, Herestraat 49, B 3000 Leuven, Belgium
    Child Neuropsychol 11:87-108. 2005
    ..At least in this boy the microdeletion seems to have interfered with the development and functioning of particular neural subsystems, while the structure and functioning of other subsystems was left intact...
  8. ncbi request reprint 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
    Am J Med Genet A 132:340-1. 2005
  9. ncbi request reprint Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome)
    Katrijn Van Aken
    Faculty of Kinesiology and Rehabilitation Sciences, Katholieke Universiteit Leuven, Leuven, Belgium
    Dev Med Child Neurol 49:210-3. 2007
    ..To conclude, primary school children with a del22q11 syndrome showed a significant deficit in motor performance compared with a control group. A significant effect of IQ on motor performance in del22q11 was found...
  10. ncbi request reprint Middle and inner ear malformations in velocardiofacial syndrome
    Koenraad Devriendt
    Am J Med Genet A 131:225-6. 2004
  11. ncbi request reprint Involvement of hyperprolinemia in cognitive and psychiatric features of the 22q11 deletion syndrome
    Gregory Raux
    Department of Genetics and Inserm U614, IFRMP, Faculty of Medicine, Rouen, France
    Hum Mol Genet 16:83-91. 2007
    ....
  12. ncbi request reprint No evidence for a parental inversion polymorphism predisposing to rearrangements at 22q11.2 in the DiGeorge/Velocardiofacial syndrome
    Gabriel Stefan Gebhardt
    Eur J Hum Genet 11:109-11. 2003
  13. ncbi request reprint VEGF: a modifier of the del22q11 (DiGeorge) syndrome?
    Ingeborg Stalmans
    The Center for Transgene Technology and Gene Therapy, Flanders Interuniversity Institute for Biotechnology, Katholieke Universiteit Leuven, Leuven, Belgium
    Nat Med 9:173-82. 2003
    ..These genetic data in mouse, fish and human indicate that VEGF is a modifier of cardiovascular birth defects in the del22q11 syndrome...