Exome-wide rare variant analysis in familial essential tremor

Inflammation biomarker discovery in Parkinson’s disease and atypical parkinsonisms

(2020) Anna Santaella et al.   BMC Neurology

Essential tremor pathology: neurodegeneration and reorganization of neuronal connections

(2020) Elan D. Louis et al.   Nature Reviews Neurology

Genome-wide estimates of heritability and genetic correlations in essential tremor

(2019) Monica Diez-Fairen et al.   PARKINSONISM & RELATED DISORDERS

Whole genome sequencing and rare variant analysis in essential tremor families

(2019) Zagaa Odgerel et al.   PLoS One

Multiplex proteomics identifies novel CSF and plasma biomarkers of early Alzheimer’s disease

(2019) Christopher D. Whelan et al.   Acta Neuropathologica Communications

Expansion of GGC repeat in the human-specific NOTCH2NLC gene is associated with essential tremor

(2019) Qi-Ying Sun et al.   BRAIN

Brain circuits and neurochemical systems in essential tremor: insights into current and future pharmacotherapeutic approaches

(2017) Sara M Schaefer et al.   Expert Review of Neurotherapeutics

Consensus Statement on the classification of tremors. from the task force on tremor of the International Parkinson and Movement Disorder Society

(2017) Kailash P. Bhatia et al.   MOVEMENT DISORDERS

Brain circuits and neurochemical systems in essential tremor: insights into current and future pharmacotherapeutic approaches

(2017) Sara M Schaefer et al.   Expert Review of Neurotherapeutics

Genome-wide association study in essential tremor identifies three new loci

(2016) Stefanie H. Müller et al.   BRAIN

FUS-linked essential tremor associated with motor dysfunction in Drosophila

(2016) Murni Tio et al.   HUMAN GENETICS

Analysis of DNAJC13 mutations in French-Canadian/French cohort of Parkinson's disease

(2016) Jay P. Ross et al.   NEUROBIOLOGY OF AGING

A family study ofDRD3rs6280, SLC1A2rs3794087 andMAPTrs1052553 variants in essential tremor

(2016) Félix Javier Jiménez-Jiménez et al.   NEUROLOGICAL RESEARCH

SORT1 Mutation Resulting in Sortilin Deficiency and p75NTR Upregulation in a Family With Essential Tremor

(2015) Elena Sánchez et al.   ASN Neuro

Identification of candidate genes for familial early-onset essential tremor

(2015) Xinmin Liu et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Missense mutations inTENM4, a regulator of axon guidance and central myelination, cause essential tremor

(2015) Hyun Hor et al.   HUMAN MOLECULAR GENETICS

Friends or Foes: Matrix Metalloproteinases and Their Multifaceted Roles in Neurodegenerative Diseases

(2015) Marjana Brkic et al.   MEDIATORS OF INFLAMMATION

Familial Aggregation and Co-Aggregation of Essential Tremor and Parkinson's Disease

(2015) Elan D. Louis et al.   NEUROEPIDEMIOLOGY

Mitochondrial serine protease HTRA2 p.G399S in a kindred with essential tremor and Parkinson disease

(2014) Hilal Unal Gulsuner et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Macrophage Migration and Invasion Is Regulated by MMP10 Expression

(2013) Megan Y. Murray et al.   PLoS One

Exome Sequencing Identifies FUS Mutations as a Cause of Essential Tremor

(2012) Nancy D. Merner et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Teneurin-4 Is a Novel Regulator of Oligodendrocyte Differentiation and Myelination of Small-Diameter Axons in the CNS

(2012) N. Suzuki et al.   JOURNAL OF NEUROSCIENCE

Exome sequencing and the genetic basis of complex traits

(2012) Adam Kiezun et al.   NATURE GENETICS

Polymorphisms in the glial glutamate transporter SLC1A2 are associated with essential tremor

(2012) S. Thier et al.   NEUROLOGY

Multiplexed Immunoassay Panel Identifies Novel CSF Biomarkers for Alzheimer's Disease Diagnosis and Prognosis

(2011) Rebecca Craig-Schapiro et al.   PLoS One

Demographic history and rare allele sharing among human populations

(2011) S. Gravel et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

How common is the most common adult movement disorder? Update on the worldwide prevalence of essential tremor

(2010) Elan D. Louis et al.   MOVEMENT DISORDERS

Matrix Metalloproteinases Are Modifiers of Huntingtin Proteolysis and Toxicity in Huntington's Disease

(2010) John P. Miller et al.   NEURON

Vascular MMP-9/TIMP-2 and Neuronal MMP-10 Up-Regulation in Human Brain after Stroke: A Combined Laser Microdissection and Protein Array Study

(2009) Eloy Cuadrado et al.   JOURNAL OF PROTEOME RESEARCH

Variant in the sequence of the LINGO1 gene confers risk of essential tremor

(2009) Hreinn Stefansson et al.   NATURE GENETICS