1971 - Fellow of John Simon Guggenheim Memorial Foundation
Genetics, Genome-wide association study, Parkinson's disease, Pathology and Single-nucleotide polymorphism are his primary areas of study. His Genetics research is multidisciplinary, relying on both Parkin and Age of onset. Nicholas W. Wood has included themes like Odds ratio, Immunology, LRRK2, Meta-analysis and Imputation in his Genome-wide association study study.
Parkinson's disease is a subfield of Disease that Nicholas W. Wood explores. His Pathology study combines topics in areas such as Internal medicine and Central nervous system disease. His work carried out in the field of Single-nucleotide polymorphism brings together such families of science as Genetic variation and Human genome.
Nicholas W. Wood spends much of his time researching Genetics, Parkinson's disease, Pathology, Disease and Internal medicine. Gene, Locus, Genome-wide association study, Haplotype and Single-nucleotide polymorphism are the core of his Genetics study. Many of his studies involve connections with topics such as Genetic association and Genome-wide association study.
Nicholas W. Wood has included themes like Neuroscience and Age of onset in his Parkinson's disease study. In most of his Disease studies, his work intersects topics such as Bioinformatics. His Internal medicine study combines topics in areas such as Endocrinology and Oncology.
The scientist’s investigation covers issues in Genetics, Disease, Parkinson's disease, Internal medicine and Genome-wide association study. Many of his studies on Genetics involve topics that are commonly interrelated, such as Ataxia. Nicholas W. Wood has researched Disease in several fields, including Clinical trial, Cognition, Immunology and Cohort.
As part of one scientific family, he deals mainly with the area of Parkinson's disease, narrowing it down to issues related to the Glucocerebrosidase, and often Dementia. His study in Internal medicine is interdisciplinary in nature, drawing from both Physical therapy and Oncology. His research in Genome-wide association study intersects with topics in Bipolar disorder, Amyotrophic lateral sclerosis, Genetic association and Candidate gene.
Nicholas W. Wood mostly deals with Genetics, Genome-wide association study, Disease, Internal medicine and Parkinson's disease. He regularly links together related areas like Bioinformatics in his Genetics studies. The study incorporates disciplines such as Bipolar disorder, Amyotrophic lateral sclerosis, Genetic association and Locus in addition to Genome-wide association study.
The Locus study which covers Multiple comparisons problem that intersects with Atrophy. His work is dedicated to discovering how Disease, Immunology are connected with Haploinsufficiency and Infectious disease and other disciplines. His Parkinson's disease research incorporates themes from Glucocerebrosidase, Prospective cohort study, Cohort study and Mendelian inheritance.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Hereditary Early-Onset Parkinson's Disease Caused by Mutations in PINK1
Eriza Maria Valente;Patrick M. Abou-Sleiman;Viviana Caputo;Miratul M K Muqit.
Second consensus statement on the diagnosis of multiple system atrophy
S. Gilman;G. K. Wenning;P. A. Low;D. J. Brooks.
Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease
Coro Paisán-Ruı́z;Shushant Jain;E.Whitney Evans;William P. Gilks.
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Stephen Sawcer;Garrett Hellenthal;Matti Pirinen;Chris C. A. Spencer.
Association between Early-Onset Parkinson's Disease and Mutations in the Parkin Gene
CB Lucking;A Durr;Bonifati;J Vaughan.
The New England Journal of Medicine (2000)
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Javier Simón-Sánchez;Claudia Schulte;Jose M Bras;Jose M Bras;Manu Sharma.
Nature Genetics (2009)
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
Daniel G Healy;Mario Falchi;Sean S O'Sullivan;Vincenzo Bonifati.
Lancet Neurology (2008)
Expanding insights of mitochondrial dysfunction in Parkinson's disease
Patrick M. Abou-Sleiman;Miratul M. K. Muqit;Nicholas W. Wood.
Nature Reviews Neuroscience (2006)
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansion
Gilles David;Nacer Abbas;Giovanni Stevanin;Alexandra Dürr.
Nature Genetics (1997)
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
Michael A. Nalls;Vincent Plagnol;Dena G. Hernandez;Dena G. Hernandez;Manu Sharma;Manu Sharma.
The Lancet (2011)
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