2023 - Research.com Genetics in United States Leader Award
As part of his studies on Disease, Andrew B. Singleton often connects relevant areas like Dementia. Andrew B. Singleton brings together Dementia and Dementia with Lewy bodies to produce work in his papers. In his study, he carries out multidisciplinary Dementia with Lewy bodies and Lewy body research. Andrew B. Singleton merges Lewy body with Neurodegeneration in his study. He undertakes multidisciplinary studies into Neurodegeneration and Parkinson's disease in his work. He incorporates Parkinson's disease and Alpha-synuclein in his studies. His Alpha-synuclein study frequently links to other fields, such as Disease. His work often combines Gene and Human genetics studies. He integrates Genetics and Computational biology in his studies.
Haplotype and Allele frequency are inherently bound to his Allele studies. In his work, Andrew B. Singleton performs multidisciplinary research in Haplotype and Allele. His multidisciplinary approach integrates Gene and Locus (genetics) in his work. Andrew B. Singleton performs integrative study on Locus (genetics) and Genotype. Borrowing concepts from Genotyping, he weaves in ideas under Genotype. In his works, he performs multidisciplinary study on Genetics and Genotyping. As part of his studies on Disease, he frequently links adjacent subjects like Neurodegeneration. His Pathology study often links to related topics such as Dementia with Lewy bodies. Andrew B. Singleton undertakes interdisciplinary study in the fields of Dementia with Lewy bodies and Lewy body through his works.
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α-Synuclein Locus Triplication Causes Parkinson's Disease
A. B. Singleton;M. Farrer;J. Johnson;A. Singleton.
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Alan E. Renton;Elisa Majounie;Adrian James Waite;Javier Simón-Sánchez;Javier Simón-Sánchez.
Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease
Denise Harold;Richard Abraham;Paul Hollingworth;Rebecca Sims.
Nature Genetics (2009)
Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease (Nature Genetics (2009) 41 (1088-1093))
D Harold;R Abraham;P Hollingworth;R Sims.
Nature Genetics (2013)
Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease
Coro Paisán-Ruı́z;Shushant Jain;E.Whitney Evans;William P. Gilks.
TREM2 Variants in Alzheimer's Disease
Rita Guerreiro;Rita Guerreiro;Aleksandra Wojtas;Jose Bras;Minerva Carrasquillo.
The New England Journal of Medicine (2013)
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
Josée Dupuis;Josée Dupuis;Claudia Langenberg;Inga Prokopenko;Richa Saxena;Richa Saxena.
Nature Genetics (2010)
Diagnosis and management of dementia with Lewy bodies Fourth consensus report of the DLB Consortium
Ian G. McKeith;Bradley F. Boeve;Dennis W. DIckson;Glenda Halliday.
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk (vol 42, pg 105, 2010)
J Dupuis;C Langenberg;I Prokopenko;R Saxena.
Nature Genetics (2010)
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
Georg B. Ehret;Georg B. Ehret;Georg B. Ehret;Patricia B. Munroe;Kenneth M. Rice;Murielle Bochud.
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