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The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease

American journal of human genetics, 2003-12, Vol.73 (6), p.1438-1443

2003

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Risk of malignancy in 22q11.2 deletion syndrome

Clinical case reports, 2017-04, Vol.5 (4), p.486-490

2017

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Major affective disorders and schizophrenia: a common molecular signature?

Human mutation, 2006-09, Vol.27 (9), p.833-853

2006

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Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

Nature genetics, 2004-08, Vol.36 (8), p.783-784

2004

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Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles

European journal of human genetics : EJHG, 2024-01, Vol.32 (1), p.31-36

2024

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Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges

European journal of medical genetics, 2014-03, Vol.57 (4), p.151-156

2014

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Can clinical characteristics be criteria to perform chromosomal microarray analysis in children and adolescents with autism spectrum disorders?

Minerva Pediatrics, 2018-06, Vol.70 (3), p.225

2018

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Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder

Human molecular genetics, 2008-01, Vol.17 (1), p.87-97

2008

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Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population

Psychiatric genetics, 2004-12, Vol.14 (4), p.233-234

2004

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Response to Zhang et al (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major Depression. Neuron 45, 11-16

Neuron (Cambridge, Mass.), 2005-12, Vol.48 (5), p.704; author reply 705-705

2005

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Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16

Neuron (Cambridge, Mass.), 2005-12, Vol.48 (5), p.702-703

2005

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Response to Loss-of-Function Mutation in Tryptophan Hydroxylase-2 Identified in Unipolar Major Depression. Neuron 45, 11–16

Neuron (Cambridge, Mass.), 2005-12, Vol.48 (5), p.704-704

2005

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No allelic association or interaction of three known functional polymorphisms with bipolar disorder in a northern Swedish isolated population

Psychiatric genetics, 2006-10, Vol.16 (5), p.209-212

2006

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Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16

Neuron (Cambridge, Mass.), 2005-12, Vol.48 (5), p.704-704

2005

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Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in bipolar disorder

Psychiatric genetics, 2007-10, Vol.17 (5), p.304-307

2007

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Radiation Dose Homogeneity in an EORTC Multicenter Trial on Breast Irradiation

Acta oncologica, 1999, Vol.38 (13), p.19-27

Ptaszynski, Walter Van den Bogaert, Jean-Claude Horiot, Philip Poortmans, Alain Fourquet, Henk Struikmans, Harry Bartelink, Marianne Pierart, Laurence Collette, Emmanuel van der Schueren, Ann-Marie

1999

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Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population

Archives of general psychiatry, 2006-10, Vol.63 (10), p.1103

2006

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Risk of malignancy in 22q11.2 deletion syndrome

Clinical case reports, 2017, Vol.5 (4), p.486-490

2017

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IgA rheumatoid factor in rheumatoid arthritis

Clinical chemistry and laboratory medicine, 2022-09, Vol.60 (10), p.1617-1626

2022

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Standardisation of ACPA tests: evaluation of a new candidate reference preparation

Annals of the rheumatic diseases, 2022-06, Vol.81 (10), p.1379-1384

2022

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How do people living with chronic conditions and their informal caregivers experience primary care? A phenomenological‐hermeneutical study

Journal of clinical nursing, 2023-02, Vol.32 (3-4), p.422-437

2023

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Metastases of primary mixed no-special type and lobular breast cancer display an exclusive lobular histology

Breast (Edinburgh), 2024-06, Vol.75, p.103732-103732, Article 103732

2024

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The DTNBP1 (Dysbindin) Gene Contributes to Schizophrenia, Depending on Family History of the Disease

Risk of malignancy in 22q11.2 deletion syndrome

Major affective disorders and schizophrenia: a common molecular signature?

Lack of support for a genetic association of the XBP1 promoter polymorphism with bipolar disorder in probands of European origin

Population screening for 15q11-q13 duplications: corroboration of the difference in impact between maternally and paternally inherited alleles

Prenatally detected copy number variants in a national cohort: A postnatal follow‐up study

Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges

The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations

Can clinical characteristics be criteria to perform chromosomal microarray analysis in children and adolescents with autism spectrum disorders?

Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5′-region are associated with bipolar affective disorder

Systematic screening for mutations in the human N-methyl-D-aspartate receptor 1 gene in schizophrenic patients from the German population

Response to Zhang et al (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major Depression. Neuron 45, 11-16

Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16

Response to Loss-of-Function Mutation in Tryptophan Hydroxylase-2 Identified in Unipolar Major Depression. Neuron 45, 11–16

No allelic association or interaction of three known functional polymorphisms with bipolar disorder in a northern Swedish isolated population

Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16

Single nucleotide polymorphism analysis of corticotropin-releasing factor-binding protein gene in bipolar disorder

Radiation Dose Homogeneity in an EORTC Multicenter Trial on Breast Irradiation

Association of brain-specific tryptophan hydroxylase, TPH2, with unipolar and bipolar disorder in a Northern Swedish, isolated population

Risk of malignancy in 22q11.2 deletion syndrome

The BElgian PREnatal MicroArray (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations

IgA rheumatoid factor in rheumatoid arthritis

Standardisation of ACPA tests: evaluation of a new candidate reference preparation

How do people living with chronic conditions and their informal caregivers experience primary care? A phenomenological‐hermeneutical study

Metastases of primary mixed no-special type and lobular breast cancer display an exclusive lobular histology

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