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PDGFRB mutants found in patients with familial infantile myofibromatosis or overgrowth syndrome are oncogenic and sensitive to imatinib

Oncogene, 2016-06, Vol.35 (25), p.3239-3248

2016

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Course and outcome of childhood epilepsy: A 15‐year follow‐up of the Dutch Study of Epilepsy in Childhood

Epilepsia (Copenhagen), 2010-07, Vol.51 (7), p.1189-1197

2010

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Course and prognosis of childhood epilepsy: 5-year follow-up of the Dutch study of epilepsy in childhood

Brain (London, England : 1878), 2004-08, Vol.127 (8), p.1774-1784

2004

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Mortality risks in new-onset childhood epilepsy

Pediatrics (Evanston), 2013-07, Vol.132 (1), p.124

2013

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Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy

Neurology, 2012-05, Vol.78 (19), p.1512

2012

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FastTree 2--approximately maximum-likelihood trees for large alignments

PloS one, 2010-03, Vol.5 (3), p.e9490-e9490

2010

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Enzyme replacement therapy in late-onset Pompe's disease: A three-year follow-up

Annals of neurology, 2004-04, Vol.55 (4), p.495-502

2004

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Sampling for microsatellite-based population genetic studies: 25 to 30 individuals per population is enough to accurately estimate allele frequencies

PloS one, 2012-09, Vol.7 (9), p.e45170-e45170

2012

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Bayesian analysis using a simple likelihood model outperforms parsimony for estimation of phylogeny from discrete morphological data

PloS one, 2014-10, Vol.9 (10), p.e109210-e109210

2014

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Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

Neurogenetics, 2013-02, Vol.14 (1), p.23-34

2013

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High-throughput sequencing of six bamboo chloroplast genomes: phylogenetic implications for temperate woody bamboos (Poaceae: Bambusoideae)

PloS one, 2011-05, Vol.6 (5), p.e20596-e20596

2011

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Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly

Journal of medical genetics, 2006-06, Vol.43 (6), p.490-495

2006

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Vidjil: A Web Platform for Analysis of High-Throughput Repertoire Sequencing

PloS one, 2016-11, Vol.11 (11), p.e0166126-e0166126

2016

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Landau‐Kleffner syndrome and CSWS syndrome: Treatment with intravenous immunoglobulins

Epilepsia (Copenhagen), 2009-08, Vol.50 (s7), p.55-58

2009

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jMOTU and Taxonerator: turning DNA Barcode sequences into annotated operational taxonomic units

PloS one, 2011-04, Vol.6 (4), p.e19259-e19259

2011

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Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease

Annals of neurology, 2005-04, Vol.57 (4), p.589-591

2005

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Long-term outcome in children with low grade tectal tumours and obstructive hydrocephalus

European journal of paediatric neurology, 2014-07, Vol.18 (4), p.469-474

2014

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The Early Prognosis of Epilepsy in Childhood: The Prediction of a Poor Outcome. The Dutch Study of Epilepsy in Childhood

Epilepsia (Copenhagen), 1999-06, Vol.40 (6), p.726-734

1999

Volltextzugriff (PDF)

Outcomes of antiretroviral therapy in Vietnam: results from a national evaluation

PloS one, 2013-02, Vol.8 (2), p.e55750-e55750

2013

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Molecular adaptation in Rubisco: Discriminating between convergent evolution and positive selection using mechanistic and classical codon models

PloS one, 2018-02, Vol.13 (2), p.e0192697-e0192697

2018

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Sequence imputation of HPV16 genomes for genetic association studies

PloS one, 2011-06, Vol.6 (6), p.e21375-e21375

2011

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Phylogenetic and molecular epidemiological studies reveal evidence of multiple past recombination events between infectious laryngotracheitis viruses

PloS one, 2013-02, Vol.8 (2), p.e55121-e55121

2013

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Evolutionary descent of prion genes from the ZIP family of metal ion transporters

PloS one, 2009-09, Vol.4 (9), p.e7208-e7208

2009

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Strong genome-wide selection early in the evolution of Prochlorococcus resulted in a reduced genome through the loss of a large number of small effect genes

PloS one, 2014-03, Vol.9 (3), p.e88837-e88837

2014

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A Kolmogorov-Smirnov test for the molecular clock based on Bayesian ensembles of phylogenies

PloS one, 2018-01, Vol.13 (1), p.e0190826

2018

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PDGFRB mutants found in patients with familial infantile myofibromatosis or overgrowth syndrome are oncogenic and sensitive to imatinib

Course and outcome of childhood epilepsy: A 15‐year follow‐up of the Dutch Study of Epilepsy in Childhood

Course and prognosis of childhood epilepsy: 5-year follow-up of the Dutch study of epilepsy in childhood

Mortality risks in new-onset childhood epilepsy

Cognitive outcome of patients with classic infantile Pompe disease receiving enzyme therapy

FastTree 2--approximately maximum-likelihood trees for large alignments

Enzyme replacement therapy in late-onset Pompe's disease: A three-year follow-up

Sampling for microsatellite-based population genetic studies: 25 to 30 individuals per population is enough to accurately estimate allele frequencies

Bayesian analysis using a simple likelihood model outperforms parsimony for estimation of phylogeny from discrete morphological data

Clinical and genetic aspects of PCDH19-related epilepsy syndromes and the possible role of PCDH19 mutations in males with autism spectrum disorders

High-throughput sequencing of six bamboo chloroplast genomes: phylogenetic implications for temperate woody bamboos (Poaceae: Bambusoideae)

Novel mutations in three families confirm a major role of COL4A1 in hereditary porencephaly

Vidjil: A Web Platform for Analysis of High-Throughput Repertoire Sequencing

Landau‐Kleffner syndrome and CSWS syndrome: Treatment with intravenous immunoglobulins

jMOTU and Taxonerator: turning DNA Barcode sequences into annotated operational taxonomic units

Early onset neuropathy in a compound form of Charcot-Marie-Tooth disease

Long-term outcome in children with low grade tectal tumours and obstructive hydrocephalus

The Early Prognosis of Epilepsy in Childhood: The Prediction of a Poor Outcome. The Dutch Study of Epilepsy in Childhood

Outcomes of antiretroviral therapy in Vietnam: results from a national evaluation

Molecular adaptation in Rubisco: Discriminating between convergent evolution and positive selection using mechanistic and classical codon models

Sequence imputation of HPV16 genomes for genetic association studies

Phylogenetic and molecular epidemiological studies reveal evidence of multiple past recombination events between infectious laryngotracheitis viruses

Evolutionary descent of prion genes from the ZIP family of metal ion transporters

Strong genome-wide selection early in the evolution of Prochlorococcus resulted in a reduced genome through the loss of a large number of small effect genes

A Kolmogorov-Smirnov test for the molecular clock based on Bayesian ensembles of phylogenies

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