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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

Brain (London, England : 1878), 2017-05, Vol.140 (5), p.1437-1446

2017

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Redox (phospho)lipidomics of signaling in inflammation and programmed cell death

Journal of leukocyte biology, 2019-07, Vol.106 (1), p.57-81

2019

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Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3115-3123

2006

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Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

Human molecular genetics, 2012-08, Vol.21 (15), p.3500-3512

2012

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A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

Brain (London, England : 1878), 2018-10, Vol.141 (10), p.2895-2907

2018

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A multi-disciplinary consensus statement concerning surgical approaches to low-grade, high-grade astrocytomas and diffuse intrinsic pontine gliomas in childhood (CPN Paris 2011) using the Delphi method

Neuro-oncology (Charlottesville, Va.), 2013-04, Vol.15 (4), p.462-468

2013

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Prion-like α-synuclein pathology in the brain of infants with Krabbe disease

Brain (London, England : 1878), 2022-05, Vol.145 (4), p.1257-1263

2022

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Does Drain Position and Duration Influence Outcomes in Patients Undergoing Burr-Hole Evacuation of Chronic Subdural Hematoma? Lessons from a UK Multicenter Prospective Cohort Study

Neurosurgery, 2019-10, Vol.85 (4), p.486-493

2019

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Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data

Human molecular genetics, 2014-09, Vol.23 (17), p.4710-4720

2014

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Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Human molecular genetics, 1998-01, Vol.7 (1), p.43-51

1998

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Risk of Estrogen Receptor–Positive and –Negative Breast Cancer and Single–Nucleotide Polymorphism 2q35-rs13387042

JNCI : Journal of the National Cancer Institute, 2009-07, Vol.101 (14), p.1012-1018

2009

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Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility

Human molecular genetics, 2008-08, Vol.17 (15), p.2274-2279

2008

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Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23

Human molecular genetics, 2009-07, Vol.18 (14), p.2693-2699

2009

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Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased Aβ42 Secretion

Human molecular genetics, 1999-08, Vol.8 (8), p.1529-1540

1999

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Gene-based association studies report genetic links for clinical subtypes of frontotemporal dementia

Redox (phospho)lipidomics of signaling in inflammation and programmed cell death

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

A multi-disciplinary consensus statement concerning surgical approaches to low-grade, high-grade astrocytomas and diffuse intrinsic pontine gliomas in childhood (CPN Paris 2011) using the Delphi method

Prion-like α-synuclein pathology in the brain of infants with Krabbe disease

Does Drain Position and Duration Influence Outcomes in Patients Undergoing Burr-Hole Evacuation of Chronic Subdural Hematoma? Lessons from a UK Multicenter Prospective Cohort Study

Estimation and partitioning of (co)heritability of inflammatory bowel disease from GWAS and immunochip data

Estimation of the Genetic Contribution of Presenilin-1 and -2 Mutations in a Population-Based Study of Presenile Alzheimer Disease

Risk of Estrogen Receptor–Positive and –Negative Breast Cancer and Single–Nucleotide Polymorphism 2q35-rs13387042

Re-evaluation of putative rheumatoid arthritis susceptibility genes in the post-genome wide association study era and hypothesis of a key pathway underlying susceptibility

Combined effects of three independent SNPs greatly increase the risk estimate for RA at 6q23

CPS position statement for prenatal counselling before a premature birth: Simple rules for complicated decisions

Aberrant Splicing in the Presenilin-1 Intron 4 Mutation Causes Presenile Alzheimer's Disease by Increased Aβ42 Secretion

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