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Author/Creator Vogels, Annick

1. Accuracy and Clinical Value of Maternal Incidental Findings During Noninvasive Prenatal Testing for Fetal Aneuploidies. Issue 8 (August 2017)

Authors:
Brison, Nathalie; van den Bogaert, Kris; Dehaspe, Luc; van den Oever, Jessica M. E.; Janssens, Katrien; Blaumeiser, Bettina; Peeters, Hilde; van Esch, Hilde; van Buggenhout, Griet; Vogels, Annick; de Ravel, Thomy; Legius, Eric; Devriendt, Koen; Vermeesch, Joris R.
Journal:
Obstetrical & gynecological survey
Issue:
Volume 72:Issue 8(2017)
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Record Type:
Journal Article
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3. Increased Dosage of RAB39B Affects Neuronal Development and Could Explain the Cognitive Impairment in Male Patients with Distal Xq28 Copy Number Gains. Issue 3 (13th January 2014)

Authors:
Vanmarsenille, Lieselot; Giannandrea, Maila; Fieremans, Nathalie; Verbeeck, Jelle; Belet, Stefanie; Raynaud, Martine; Vogels, Annick; Männik, Katrin; Õunap, Katrin; Jacqueline, Vigneron; Briault, Sylvain; Van, Hilde; D'Adamo, Patrizia; Froyen, Guy
Journal:
Human mutation
Issue:
Volume 35:Issue 3(2014:Mar.)
Page Start:
377
Record Type:
Journal Article
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4. Low prevalence of substance use in people with 22q11.2 deletion syndrome. (November 2019)

Authors:
Vingerhoets, Claudia; van Oudenaren, Mathilde J.F.; Bloemen, Oswald J.N.; Boot, Erik; van Duin, Esther D.A.; Evers, Laurens J.M.; Fiksinski, Ania M.; Breetvelt, Elemi J.; Palmer, Lisa D.; Vergaelen, Elfi; Vogels, Annick; Meijer, Carin; Booij, Jan; de Haan, Liewe; Swillen, Ann; Vorstman, Jacob A.S...
Journal:
British journal of psychiatry
Issue:
Volume 215:Number 5(2019)
Page Start:
661
Record Type:
Journal Article
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6. Neurodevelopmental risk copy number variants in adults with intellectual disabilities and comorbid psychiatric disorders. (25th April 2018)

Authors:
Thygesen, Johan H.; Wolfe, Kate; McQuillin, Andrew; Viñas-Jornet, Marina; Baena, Neus; Brison, Nathalie; D'Haenens, Greet; Esteba-Castillo, Susanna; Gabau, Elisabeth; Ribas-Vidal, Núria; Ruiz, Anna; Vermeesch, Joris; Weyts, Eddy; Novell, Ramon; Buggenhout, Griet Van; Strydom, André; Bass, Nick; G...
Journal:
British journal of psychiatry
Issue:
Volume 212:Number 5(2018)
Page Start:
287
Record Type:
Journal Article
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7. Predicting fetoplacental chromosomal mosaicism during non‐invasive prenatal testing. (19th February 2018)

Authors:
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, Eric; Devriendt, Koen; Vermeesch, Joris R.
Journal:
Prenatal diagnosis
Issue:
Volume 38:Number 4(2018)
Page Start:
258
Record Type:
Journal Article
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9. The clinical relevance of intragenic NRXN1 deletions. Issue 5 (13th January 2020)

Authors:
Cosemans, Nele; Vandenhove, Laura; Vogels, Annick; Devriendt, Koenraad; Van Esch, Hilde; Van Buggenhout, Griet; Olivié, Hilde; de Ravel, Thomy; Ortibus, Els; Legius, Eric; Aerssens, Peter; Breckpot, Jeroen; R. Vermeesch, Joris; Shen, Sanbing; Fitzgerald, Jacqueline; Gallagher, Louise; Peeters, Hilde
Journal:
Journal of medical genetics
Issue:
Volume 57:Issue 5(2020)
Page Start:
347
Record Type:
Journal Article
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10. Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2. (5th June 2018)

Authors:
Boot, Erik; Butcher, Nancy J.; Udow, Sean; Marras, Connie; Mok, Kin Y.; Kaneko, Satoshi; Barrett, Matthew J.; Prontera, Paolo; Berman, Brian D.; Masellis, Mario; Dufournet, Boris; Nguyen, Karine; Charles, Perrine; Mutez, Eugénie; Danaila, Teodor; Jacquette, Aurélia; Colin, Olivier; Drapier, Sophi...
Journal:
Neurology
Issue:
Volume 90:Number 23(2018)
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Record Type:
Journal Article
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