Ghent University Academic Bibliography

Mark

journalArticle
A1
open access

Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care

Ivan Ivanovski, Olivera Djuric, Stefano Giuseppe Caraffi, Daniela Santodirocco, Marzia Pollazzon, Simonetta Rosato, Duccio Maria Cordelli, Ebtesam Abdalla, Patrizia Accorsi, Margaret P Adam, et al.

(2018) GENETICS IN MEDICINE. 20(9). p.965-975

Mark

journalArticle
A1
open access

Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications

Kate Wolfe, Andrew McQuillin, Viola Alesi, Elise Boudry Labis, Peter Cutajar, Bruno Dallapiccola, Maria Lisa Dentici, Anne Dieux-Coeslier, Benedicte Duban-Bedu, Tina Duelund Hjortshøj, et al.

(2018) AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 177(4). p.397-405

Mark

Integrating community service learning in undergraduate dental education : a controlled trial in a residential facility for people with intellectual disabilities

Inès Phlypo (UGent) , Jannick De Tobel (UGent) , Luc Marks (UGent) , Luc De Visschere (UGent) and Sebastiaan Koole (UGent)

(2018) SPECIAL CARE IN DENTISTRY. 38(4). p.201-207

Mark

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Claire Redin, Harrison Brand, Ryan L Collins, Tammy Kammin, Elyse Mitchell, Jennelle C Hodge, Carrie Hanscom, Vamsee Pillalamarri, Catarina M Seabra, Mary-Alice Abbott, et al.

(2017) NATURE GENETICS. 49(1). p.36-45

Mark

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Markus Wolff, Katrine M Johannesen, Ulrike BS Hedrich, Silvia Masnada, Guido Rubboli, Elena Gardella, Gaetan Lesca, Dorothée Ville, Mathieu Milh, Laurent Villard, et al.

(2017) BRAIN. 140(5). p.1316-1336

Mark

Confirmation of an ARID2 defect in SWI/SNF-related intellectual disability

Ruben Van Paemel (UGent) , Pauline De Bruyne (UGent) , Saskia van der Straaten (UGent) , Marleen D'Hondt (UGent) , Urlien Fränkel, Annelies Dheedene (UGent) , Björn Menten (UGent) and Bert Callewaert (UGent)

(2017) AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 173(11). p.3104-3108

Mark

journalArticle
A1
open access

Quality of life in parents of young adults with ASD : EpiTED cohort

Cecile Rattaz, Cecile Michelon, Herbert Roeyers (UGent) and Amaria Baghdadli

(2017) JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS. 47(9). p.2826-2837

Mark

Scale of emotional development-Short

Tanja Sappok, Brian F Barrett, Stijn Vandevelde (UGent) , Manuel Heinrich, Leen Poppe, Paula Sterkenburg, Jolanda Vonk, Juergen Kolb, Claudia Claes, Thomas Bergmann, et al.

(2016) RESEARCH IN DEVELOPMENTAL DISABILITIES . 59. p.166-175

Mark

dissertation

Oral health of athletes with intellectual disability from Europe and Eurasia

Carla Fernandez (UGent)

(2016)

Mark

7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly

Keiko Shimojima, Satoshi Narai, Masami Togawa, Tomotsune Doumoto, Noriko Sangu, Olivier Vanakker (UGent) , Anne De Paepe (UGent) , Matthew Edwards, John Whitehall, Sally Brescianini, et al.

(2016) EUROPEAN JOURNAL OF MEDICAL GENETICS. 59(10). p.502-506

Academic Bibliography

Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care

Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications

Integrating community service learning in undergraduate dental education : a controlled trial in a residential facility for people with intellectual disabilities

The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

Confirmation of an ARID2 defect in SWI/SNF-related intellectual disability

Quality of life in parents of young adults with ASD : EpiTED cohort

Scale of emotional development-Short

Oral health of athletes with intellectual disability from Europe and Eurasia

7p22.1 microdeletions involving ACTB associated with developmental delay, short stature, and microcephaly

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