Schizotypy: key feature of Klinefelter’s syndrome?

Por Verhoeven, Willem M A, Egger, Jos I M
Publicado em 2011

A Time Series Approach to Random Number Generation: Using Recurrence Quantification Analysis to Capture Executive Behavior

Por Oomens, Wouter, Maes, Joseph H. R., Hasselman, Fred, Egger, Jos I. M.
Publicado no Front Hum Neurosci (2015)

RandseqR: An R Package for Describing Performance on the Random Number Generation Task

Por Oomens, Wouter, Maes, Joseph H. R., Hasselman, Fred, Egger, Jos I. M.
Publicado no Front Psychol (2021)

Kallmann syndrome and paranoid schizophrenia: a rare combination

Por Verhoeven, Willem M A, Egger, Jos I M, Hovens, Johannes E, Hoefsloot, Lies
Publicado em 2013

Neuropsychological phenotype of a patient with a de novo 970 kb interstitial deletion in the distal 16p11.2 region

Por Egger, Jos I M, Verhoeven, Willem M A, Verbeeck, Wim, de Leeuw, Nicole
Publicado em 2014

Social cognitive training for adults with Noonan syndrome: a feasibility study

Por Roelofs, Renée L, Wingbermühle, Ellen, Kessels, Roy P C, Egger, Jos I M
Publicado no Neuropsychiatr Dis Treat (2019)

Unraveling Executive Functioning in Dual Diagnosis

Por Duijkers, Judith C. L. M., Vissers, Constance Th. W. M., Egger, Jos I. M.
Publicado no Front Psychol (2016)

Phelan-McDermid syndrome due to SHANK3 mutation in an intellectually disabled adult male: successful treatment with lithium

Por Egger, Jos I M, Verhoeven, Willem M A, Groenendijk-Reijenga, Renske, Kant, Sarina G
Publicado no BMJ Case Rep (2017)

Intellectual development in Noonan syndrome: a longitudinal study

Por Roelofs, Renée L., Janssen, Nikki, Wingbermühle, Ellen, Kessels, Roy P.C., Egger, Jos I.M.
Publicado no Brain Behav (2016)

Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene

Por Verhoeven, Willem M A, Egger, Jos I M, Janssen, Paddy K C, van Haeringen, Arie
Publicado no BMJ Case Rep (2020)

Inhibitory Control and Craving in Dual Disorders and Recurrent Substance Use. Preliminary Findings

Por Beerten-Duijkers, Judith C. L. M., Vissers, Constance Th. W. M., Rinck, Mike, Egger, Jos I. M.
Publicado no Front Psychiatry (2021)

The Interplay Between Attentional Strategies and Language Processing in High-functioning Adults with Autism Spectrum Disorder

Por Koolen, Sophieke, Vissers, Constance Th. W. M., Hendriks, Angelique W. C. J., Egger, Jos I. M., Verhoeven, Ludo
Publicado em 2011

Understanding and Remediating Social-Cognitive Dysfunctions in Patients with Serious Mental Illness Using Relational Frame Theory

Por Hendriks, Annemieke L., Barnes-Holmes, Yvonne, McEnteggart, Ciara, De Mey, Hubert R. A., Janssen, Gwenny T. L., Egger, Jos I. M.
Publicado no Front Psychol (2016)

Intellectual Profiles in KBG-Syndrome: A Wechsler Based Case-Control Study

Por van Dongen, Linde C. M., Wingbermühle, Ellen, Oomens, Wouter, Bos-Roubos, Anja G., Ockeloen, Charlotte W., Kleefstra, Tjitske, Egger, Jos I. M.
Publicado no Front Behav Neurosci (2017)

Personality and Psychopathology in Adults with Noonan Syndrome

Por Roelofs, Renée L., Wingbermühle, Ellen, van der Heijden, Paul T., Jonkers, Rosella, de Haan, Marieke, Kessels, Roy P. C., Egger, Jos I. M.
Publicado no J Clin Psychol Med Settings (2019)

Behavior and cognitive functioning in Witteveen–Kolk syndrome

Por van Dongen, Linde C. M., Wingbermühle, Ellen, Dingemans, Alexander J. M., Bos‐Roubos, Anja G., Vermeulen, Karlijn, Pop‐Purceleanu, Monica, Kleefstra, Tjitske, Egger, Jos I. M.
Publicado no Am J Med Genet A (2020)

Exploring the behavioral and cognitive phenotype of KBG syndrome

Por van Dongen, Linde C.M., Wingbermühle, Ellen, van der Veld, William M., Vermeulen, Karlijn, Bos‐Roubos, Anja G., Ockeloen, Charlotte W., Kleefstra, Tjitske, Egger, Jos I.M.
Publicado no Genes Brain Behav (2019)

A de novo CTNNB1 Novel Splice Variant in an Adult Female with Severe Intellectual Disability

Por Verhoeven, Willem M A, Egger, Jos I M, Jongbloed, Rob E, van Putten, Marloes Meijer, de Bruin-van Zandwijk, Marieke, Zwemer, Anne-Suus, Pfundt, Rolph, Willemsen, Marjolein H
Publicado no Int Med Case Rep J (2020)

EHMT1 mosaicism in apparently unaffected parents is associated with autism spectrum disorder and neurocognitive dysfunction

Por de Boer, Anneke, Vermeulen, Karlijn, Egger, Jos I. M., Janzing, Joost G. E., de Leeuw, Nicole, Veenstra-Knol, Hermine E., den Hollander, Nicolette S., van Bokhoven, Hans, Staal, Wouter, Kleefstra, Tjitske
Publicado no Mol Autism (2018)