Convergent effects of a functional C3 variant on brain atrophy, demyelination, and cognitive impairment in multiple sclerosis

Novel genetic loci associated with hippocampal volume

(2017) Derrek P. Hibar et al.   Nature Communications

Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation

(2016) Hansen Lui et al.   CELL

Novel MRI and PET markers of neuroinflammation in multiple sclerosis

(2016) Marloes Hagens et al.   CURRENT OPINION IN NEUROLOGY

Channelopathy-relatedSCN10Agene variants predict cerebellar dysfunction in multiple sclerosis

(2016) Tina Roostaei et al.   NEUROLOGY

Novel allele-dependent role for APOE in controlling the rate of synapse pruning by astrocytes

(2016) Won-Suk Chung et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Complement C1q-C3-associated synaptic changes in multiple sclerosis hippocampus

(2015) Iliana Michailidou et al.   ANNALS OF NEUROLOGY

Complement C3-Deficient Mice Fail to Display Age-Related Hippocampal Decline

(2015) Q. Shi et al.   JOURNAL OF NEUROSCIENCE

Common genetic variants influence human subcortical brain structures

(2015) Derrek P. Hibar et al.   NATURE

Nonconventional MRI and microstructural cerebral changes in multiple sclerosis

(2015) Christian Enzinger et al.   Nature Reviews Neurology

Multi-level block permutation

(2015) Anderson M. Winkler et al.   NEUROIMAGE

Complement Component C3 and Butyrylcholinesterase Activity Are Associated with Neurodegeneration and Clinical Disability in Multiple Sclerosis

(2015) Shahin Aeinehband et al.   PLoS One

A Revised Mechanism for the Activation of Complement C3 to C3b

(2014) Elizabeth Rodriguez et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

Microglial priming in neurodegenerative disease

(2014) V. Hugh Perry et al.   Nature Reviews Neurology

Complement activation in multiple sclerosis plaques: an immunohistochemical analysis

(2014) Gillian Ingram et al.   Acta Neuropathologica Communications

Validity and Reliability of a Persian Translation of the Minimal Assessment of Cognitive Function in Multiple Sclerosis (MACFIMS)

(2012) Arman Eshaghi et al.   CLINICAL NEUROPSYCHOLOGIST

The investigation of allele and genotype frequencies of human C3 (rs2230199) in south Iranian population

(2012) Najmeh Bazyar et al.   MOLECULAR BIOLOGY REPORTS

Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner

(2012) Dorothy P. Schafer et al.   NEURON

Genetic Studies of Age-related Macular Degeneration

(2012) Rinki Ratna Priya et al.   OPHTHALMOLOGY

C3-dependent mechanism of microglial priming relevant to multiple sclerosis

(2012) V. Ramaglia et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease risk

(2011) M. Heurich et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Complement regulator factor H as a serum biomarker of multiple sclerosis disease state

(2010) Gillian Ingram et al.   BRAIN

Immunoglobulins and complement in postmortem multiple sclerosis tissue

(2009) Michael H. Barnett et al.   ANNALS OF NEUROLOGY

Demyelination, Inflammation, and Neurodegeneration in Multiple Sclerosis Deep Gray Matter

(2009) Marco Vercellino et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Substantial Archaeocortical Atrophy and Neuronal Loss in Multiple Sclerosis

(2008) Dimitrios Papadopoulos et al.   BRAIN PATHOLOGY

A study of diffusion tensor imaging by tissue-specific, smoothing-compensated voxel-based analysis

(2008) Jee Eun Lee et al.   NEUROIMAGE

Threshold-free cluster enhancement: Addressing problems of smoothing, threshold dependence and localisation in cluster inference

(2008) S SMITH et al.   NEUROIMAGE