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Gene expression profile, pathways, and transcriptional system regulation in indolent systemic mastocytosis

Allergy (Copenhagen), 2011-02, Vol.66 (2), p.229-237

2011

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Genetic testing for asthma

The European respiratory journal, 2008-09, Vol.32 (3), p.775-782

2008

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Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing

Scientific reports, 2017-05, Vol.7 (1), p.1838-11, Article 1838

2017

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Susceptibility to Buruli ulcer is associated with the SLC11A1 (NRAMP1) D543N polymorphism

Genes and immunity, 2006-04, Vol.7 (3), p.185-189

2006

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Association with HLA class I in Epstein-Barr-virus-positive and with HLA class III in Epstein-Barr-virus-negative Hodgkin's lymphoma

The Lancet (British edition), 2005-06, Vol.365 (9478), p.2216-2224

2005

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An extensive screen of the HLA region reveals an independent association of HLA class I and class II with susceptibility for systemic lupus erythematosus

Scandinavian journal of rheumatology, 2009, Vol.38 (4), p.256-262

2009

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Haplotype sharing test maps genes for familial cardiomyopathies

Clinical genetics, 2011-05, Vol.79 (5), p.459-467

2011

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Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility

Journal of medical genetics, 2002-04, Vol.39 (4), p.225-242

2002

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Susceptibility to development of Mycobacterium ulcerans disease: review of possible risk factors

Tropical medicine & international health, 2001-07, Vol.6 (7), p.554-562

2001

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Interleukin‐10 and Fas polymorphisms and susceptibility for (pre)neoplastic cervical disease

International journal of gynecological cancer, 2005-11, Vol.15 (s3), p.282-290

2005

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Analysis of the entire HLA region in susceptibility for cervical cancer: a comprehensive study

Journal of medical genetics, 2005-08, Vol.42 (8), p.e49-e49

2005

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CARD15 in inflammatory bowel disease and Crohn's disease phenotypes: An association study and pooled analysis

Digestive and liver disease, 2006-11, Vol.38 (11), p.834-845

2006

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Immunohistochemical changes induced by repeated footshock stress: revelations of gender-based differences

Neurobiology of disease, 2003-12, Vol.14 (3), p.602-618

2003

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Genetic susceptibility to Hodgkin's lymphoma associated with the human leukocyte antigen region

European journal of haematology, 2005-07, Vol.75 (s66), p.34-41

2005

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Long term prognosis of patients with cystic fibrosis in relation to early detection by neonatal screening and treatment in a cystic fibrosis centre

Thorax, 1995-07, Vol.50 (7), p.712-718

1995

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The probability that similar haplotypes are identical by descent

Annals of human genetics, 2002-05, Vol.66 (3), p.195-209

2002

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IBD and genetics: new developments

Scandinavian journal of gastroenterology, 2003-01, Vol.38 (239), p.63-68

2003

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Recurrence risk for germinal mosaics revisited

Journal of medical genetics, 1995-02, Vol.32 (2), p.102-104

1995

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Minimal volume of amniotic fluid for reliable prenatal cytogenetic diagnosis

Prenatal diagnosis, 2002-02, Vol.22 (2), p.164-165

2002

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Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations

Human genetics, 1996-09, Vol.98 (3), p.304-309

1996

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Parallel genome analysis by two-dimensional DNA typing

Nature (London), 1993-09, Vol.365 (6445), p.469-471

1993

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A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing

European journal of cancer (1990), 1997-12, Vol.33 (14), p.2390-2392

1997

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No recurrent structural abnormalities apart from i(12p) in primary germ cell tumors of the adult testis

Genes chromosomes & cancer, 1995-10, Vol.14 (2), p.133-144

1995

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Genetic Association Studies in Complex Disease: Disentangling Additional Predisposing Loci from Associated Neutral Loci Using a Constrained ‐ Permutation Approach

Annals of human genetics, 2005-01, Vol.69 (1), p.90-101

2005

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Cytogenetic analysis of ten human seminomas

Cancer research (Chicago, Ill.), 1989-01, Vol.49 (2), p.439-443

1989

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Gene expression profile, pathways, and transcriptional system regulation in indolent systemic mastocytosis

Genetic testing for asthma

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing

Susceptibility to Buruli ulcer is associated with the SLC11A1 (NRAMP1) D543N polymorphism

Association with HLA class I in Epstein-Barr-virus-positive and with HLA class III in Epstein-Barr-virus-negative Hodgkin's lymphoma

An extensive screen of the HLA region reveals an independent association of HLA class I and class II with susceptibility for systemic lupus erythematosus

Haplotype sharing test maps genes for familial cardiomyopathies

Genes other than BRCA1 and BRCA2 involved in breast cancer susceptibility

Susceptibility to development of Mycobacterium ulcerans disease: review of possible risk factors

Interleukin‐10 and Fas polymorphisms and susceptibility for (pre)neoplastic cervical disease

Analysis of the entire HLA region in susceptibility for cervical cancer: a comprehensive study

CARD15 in inflammatory bowel disease and Crohn's disease phenotypes: An association study and pooled analysis

Immunohistochemical changes induced by repeated footshock stress: revelations of gender-based differences

Genetic susceptibility to Hodgkin's lymphoma associated with the human leukocyte antigen region

Long term prognosis of patients with cystic fibrosis in relation to early detection by neonatal screening and treatment in a cystic fibrosis centre

The probability that similar haplotypes are identical by descent

IBD and genetics: new developments

Recurrence risk for germinal mosaics revisited

Minimal volume of amniotic fluid for reliable prenatal cytogenetic diagnosis

Haplotype identity between individuals who share a CFTR mutation allele "identical by descent": demonstration of the usefulness of the haplotype-sharing concept for gene mapping in real populations

Parallel genome analysis by two-dimensional DNA typing

A BRCA1 founder mutation, identified with haplotype analysis, allowing genotype/phenotype determination and predictive testing

No recurrent structural abnormalities apart from i(12p) in primary germ cell tumors of the adult testis

Genetic Association Studies in Complex Disease: Disentangling Additional Predisposing Loci from Associated Neutral Loci Using a Constrained ‐ Permutation Approach

Cytogenetic analysis of ten human seminomas

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