A. Bremer

Sixteen New Cases Contributing to the Characterization of Patients with Distal 22q11.2 Microduplications

B. V. van Bon, E. Bongers, D. Newbury, 2011, Molecular Syndromology.

Dravet syndrome – considerable delay in making the diagnosis

K. Nakken, M. Lossius, A. Bremer, 2012, Acta neurologica Scandinavica.

[Dravet syndrome as a cause of epilepsy and learning disability].

E. Brodtkorb, K. Nakken, K. Selmer, 2012, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

Molecular Mechanisms Generating and Stabilizing Terminal 22q13 Deletions in 44 Subjects with Phelan/McDermid Syndrome

M. Fichera, C. Romano, R. Borgatti, 2011, PLoS genetics.

Characterisation of hairy cell leukaemia by tiling resolution array‐based comparative Genome hybridisation: a series of 13 cases and review of the literature

A. Nordgren, H. Kluin-Nelemans, D. Grandér, 2010, European journal of haematology.

Rare copy number variants are common in young children with autism spectrum disorder

C. Gillberg, E. Fernell, B. Anderlid, 2015, Acta paediatrica.

Unraveling genetic mechanisms in autism spectrum disorders

A. Bremer, 2011 .

Copy number variation characteristics in subpopulations of patients with autism spectrum disorders

C. Gillberg, A. Nordgren, E. Fernell, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mutation screening of melatonin-related genes in patients with autism spectrum disorders

M. Landén, L. Jonsson, J. Melke, 2010, BMC Medical Genomics.

An interstitial deletion of 7.1Mb in chromosome band 6p22.3 associated with developmental delay and dysmorphic features including heart defects, short neck, and eye abnormalities.

J. Schoumans, M. Nordenskjöld, B. Anderlid, 2009, European journal of medical genetics.

Screening for copy number alterations in loci associated with autism spectrum disorders by two‐color multiplex ligation‐dependent probe amplification

J. Schoumans, M. Nordenskjöld, K. Brøndum‐Nielsen, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A complete digital karyotype of the B-cell leukemia REH cell line resolved by long-read sequencing

L. Feuk, A. Ameur, I. Bunikis, 2023, bioRxiv.

[Vagal nerve stimulation in children with drug-resistant epilepsy].

G. K. Røste, A. Eriksson, K. Nakken, 2006, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.

Rare copy number variants are common in young children with autism spectrum disorder

C. Gillberg, E. Fernell, B. Anderlid, 2015, Acta paediatrica.

Characterisation of hairy cell leukaemia by tiling resolution array‐based comparative Genome hybridisation: a series of 13 cases and review of the literature

A. Nordgren, H. Kluin-Nelemans, D. Grandér, 2010, European journal of haematology.