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Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study

The lancet oncology, 2017-07, Vol.18 (7), p.958-971

2017

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Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum

Brain (London, England : 1878), 2013-05, Vol.136 (Pt 5), p.1578-1591

2013

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A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease

PloS one, 2016-01, Vol.11 (1), p.e0145500

2016

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Histological Changes in the Urothelium and Suburothelium of Human Overactive Bladder following Intradetrusor Injections of Botulinum Neurotoxin Type A for the Treatment of Neurogenic or Idiopathic Detrusor Overactivity

European urology, 2008-06, Vol.53 (6), p.1245-1253

2008

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Towards in vivo focal cortical dysplasia phenotyping using quantitative MRI

NeuroImage clinical, 2017-01, Vol.15, p.95-105

2017

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Medulloblastoma group 3 and 4 tumors comprise a clinically and biologically significant expression continuum reflecting human cerebellar development

Cell reports (Cambridge), 2022-08, Vol.40 (5), p.111162-111162, Article 111162

2022

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Genomic Deletions Correlate with Underexpression of Novel Candidate Genes at Six Loci in Pediatric Pilocytic Astrocytoma

Neoplasia (New York, N.Y.), 2008-08, Vol.10 (8), p.757,IN2-772,IN9

2008

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Pulmonary hypertension in a GTP-cyclohydrolase 1-deficient mouse

Circulation (New York, N.Y.), 2005-04, Vol.111 (16), p.2086-2090

2005

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A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations

Brain (London, England : 1878), 2012-08, Vol.135 (Pt 8), p.2506-2514

2012

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The ten-year evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion

Scientific reports, 2018-01, Vol.8 (1), p.1032-10, Article 1032

2018

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Diffusion-weighted post-mortem magnetic resonance imaging of the human fetal brain in situ

European journal of radiology, 2016-06, Vol.85 (6), p.1167-1173

2016

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Epigenetic genome-wide analysis identifies BEX1 as a candidate tumour suppressor gene in paediatric intracranial ependymoma

Cancer letters, 2014-04, Vol.346 (1), p.34-44

2014

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Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene

Neuromuscular disorders : NMD, 2013-05, Vol.23 (5), p.391-398

2013

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Migrating partial seizures of infancy: delineation of the clinical and genetic features in a national patient cohort

The Lancet (British edition), 2014-02, Vol.383, p.S14-S14

2014

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CYP1B1 -Related Anterior Segment Developmental Anomalies

Ophthalmology (Rochester, Minn.), 2011, Vol.118 (9), p.1865-1873

2011

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Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation study

The Lancet (British edition), 2013-07, Vol.382 (9888), p.223-233

2013

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Sub-phenotyping of juvenile dermatomyositis: can it assist clinical decisions?

Pediatric rheumatology online journal, 2014-09, Vol.12 (S1), p.O18-O18, Article O18

2014

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Genomic Deletions Correlate with Underexpression of Novel Candidate Genes at Six Loci in Pediatric Pilocytic Astrocytoma1

Neoplasia (New York, N.Y.), 2008-08, Vol.10 (8), p.757-772

2008

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Book review

Neuromuscular Disorders, 2014, Vol.24 (8), p.746-746

Jacques, Thomas S

2014

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Profiling malaria infection among under-five children in the Democratic Republic of Congo

PloS one, 2021-05, Vol.16 (5), p.e0250550

2021

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Psychedelics and the human receptorome

PloS one, 2010-02, Vol.5 (2), p.e9019-e9019

2010

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Dendritic cells release HLA-B-associated transcript-3 positive exosomes to regulate natural killer function

PloS one, 2008-10, Vol.3 (10), p.e3377-e3377

2008

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Dysregulation of ribosome biogenesis and translational capacity is associated with tumor progression of human breast cancer cells

PloS one, 2009-09, Vol.4 (9), p.e7147-e7147

2009

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Prenatal stress and child development: A scoping review of research in low- and middle-income countries

PloS one, 2018-12, Vol.13 (12), p.e0207235-e0207235

2018

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Novel molecular subgroups for clinical classification and outcome prediction in childhood medulloblastoma: a cohort study

Migrating partial seizures of infancy: expansion of the electroclinical, radiological and pathological disease spectrum

A Clinical, Neuropathological and Genetic Study of Homozygous A467T POLG-Related Mitochondrial Disease

Histological Changes in the Urothelium and Suburothelium of Human Overactive Bladder following Intradetrusor Injections of Botulinum Neurotoxin Type A for the Treatment of Neurogenic or Idiopathic Detrusor Overactivity

Towards in vivo focal cortical dysplasia phenotyping using quantitative MRI

Medulloblastoma group 3 and 4 tumors comprise a clinically and biologically significant expression continuum reflecting human cerebellar development

Genomic Deletions Correlate with Underexpression of Novel Candidate Genes at Six Loci in Pediatric Pilocytic Astrocytoma

Pulmonary hypertension in a GTP-cyclohydrolase 1-deficient mouse

A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations

The ten-year evolutionary trajectory of a highly recurrent paediatric high grade neuroepithelial tumour with MN1:BEND2 fusion

Diffusion-weighted post-mortem magnetic resonance imaging of the human fetal brain in situ

Epigenetic genome-wide analysis identifies BEX1 as a candidate tumour suppressor gene in paediatric intracranial ependymoma

Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene

Migrating partial seizures of infancy: delineation of the clinical and genetic features in a national patient cohort

CYP1B1 -Related Anterior Segment Developmental Anomalies

Post-mortem MRI versus conventional autopsy in fetuses and children: a prospective validation study

Sub-phenotyping of juvenile dermatomyositis: can it assist clinical decisions?

Genomic Deletions Correlate with Underexpression of Novel Candidate Genes at Six Loci in Pediatric Pilocytic Astrocytoma1

Book review

Profiling malaria infection among under-five children in the Democratic Republic of Congo

Epacadostat plus pembrolizumab versus placebo plus pembrolizumab in patients with unresectable or metastatic melanoma (ECHO-301/KEYNOTE-252): a phase 3, randomised, double-blind study

Psychedelics and the human receptorome

Dendritic cells release HLA-B-associated transcript-3 positive exosomes to regulate natural killer function

Dysregulation of ribosome biogenesis and translational capacity is associated with tumor progression of human breast cancer cells

Prenatal stress and child development: A scoping review of research in low- and middle-income countries

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