sameAs
Sequential use of transcriptional profiling, expression quantitative trait mapping, and gene association implicates MMP20 in human kidney agingDeletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humansA meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americansA genome-wide association study identifies protein quantitative trait loci (pQTLs)Analysis of IFT74 as a candidate gene for chromosome 9p-linked ALS-FTDAbundant quantitative trait loci exist for DNA methylation and gene expression in human brainTREM2 Variants in Alzheimer's DiseaseRare coding variants in the phospholipase D3 gene confer risk for Alzheimer's diseaseExome sequencing in Brown-Vialetto-van Laere syndromeA large study reveals no association between APOE and Parkinson's diseaseMeta-analysis of genome-wide association data identifies two loci influencing age at menarcheImputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studiesGenome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's diseaseDistinct DNA methylation changes highly correlated with chronological age in the human brainGenome-wide association analyses identify 18 new loci associated with serum urate concentrationsCCAAT-enhancer-binding protein-beta expression in vivo is associated with muscle strengthGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskNew loci associated with kidney function and chronic kidney diseaseA hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDGenome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrationsA nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial diseaseGenome-wide association studies in neurological disordersGenome-wide association study reveals genetic risk underlying Parkinson's diseaseA two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisCandidate gene polymorphisms for ischemic stroke.Multiple loci influence erythrocyte phenotypes in the CHARGE ConsortiumSplice mutation in the iron-sulfur cluster scaffold protein ISCU causes myopathy with exercise intoleranceGlucocerebrosidase mutations in clinical and pathologically proven Parkinson's diseaseLack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patientsThe genetics and neuropathology of Parkinson's diseaseCanine hereditary ataxia in old english sheepdogs and gordon setters is associated with a defect in the autophagy gene encoding RAB24Novel genetic loci underlying human intracranial volume identified through genome-wide associationalpha-Synuclein locus triplication causes Parkinson's diseaseMutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritanceArguing against the proposed definition changes of PDMutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosisLarge-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's diseaseExome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseAltered alpha-synuclein homeostasis causing Parkinson's disease: the potential roles of dardarin
P50
Q21092453-55E77BED-2246-407A-AC78-0A8C81EBABFAQ21092490-4B3C035E-DDBD-46D0-A7BD-BEDE32FC1830Q21144930-AC38FF64-0E72-437A-8F57-0E487AFE1D14Q21145048-9982C172-2685-4995-A04E-25536FE763E3Q21261387-F58D623E-C03D-427E-AD80-AEDB61AB0817Q21563315-E78C27DF-4787-47AC-B7CD-8DD82E018F9DQ22250873-F7196FB8-6307-4734-8A6B-A481515B3BB8Q24312938-1AE32B13-B362-4063-B0B9-08A304625E2DQ24596601-FA9EC089-0424-4BB8-922C-B40ACAEFD83CQ24598836-C52E4F1C-A579-4FA7-ACD6-346519DFB2D4Q24604815-DFD23FA6-9392-4A68-A75A-BFC8220602AAQ24606055-6B230CD9-B621-4A9C-9054-E6ABDC993891Q24612662-48A6F7A1-6521-41B9-87A1-A72EA9687451Q24616264-1B58D6CB-B4F3-4880-9D86-E59E19457796Q24620065-AD0E1BFF-ECDA-48FE-A240-928B038EDD2FQ24620519-E8F389EC-8370-4A1F-9EE5-E5A72AE484EAQ24630394-90973690-22F4-4BB8-BF47-75A071DEB149Q24630646-9D32F374-A6DE-4805-A574-E99ABECC9880Q24634583-02FCEFE5-BBED-4012-88CC-394D71820CCDQ24644637-F8E886EF-F3E6-459D-90B1-379833253A8CQ24645475-E79DFF61-AE6A-4D58-BAD7-F561FC09AD8BQ24646144-E185A821-C199-40FA-82F5-6DF887EC08D0Q24646654-1C95AF38-EBAD-4E8D-A63B-F4E9CF0F4478Q24648667-92FB2A4B-6652-423C-9452-4C18467F0C55Q24649888-51A4D3B0-F0E2-490E-8941-BEC914013CDAQ24655591-D3BF1000-BF6B-4470-BAAD-7A2D12CA5C32Q24656037-C1FE4E45-091B-4606-95A0-6F5CB7462516Q24656668-37DAC661-26C5-430A-96CD-F294828F12B3Q24810778-49BA931B-C1AC-4DFD-9A8F-A69A7C3835C1Q26859945-2338E3CC-6C3F-4405-8A69-FB98F73B8BD0Q27318512-C6D69E09-2A48-4CAE-BF36-3C53E20ABF06Q27653381-5982F8FD-55EF-4D18-9AE3-BD6351C5EE93Q27860533-b7f691e2-4ab4-950f-8f4a-41d05a5c187bQ27919715-C5A62AEE-B6E4-479E-8D62-2882FCE106BEQ28077356-E270B97E-2BB9-4745-9E7D-F14EF3430FE6Q28079237-6833B181-14E2-4012-AC41-89181F948771Q28237200-BB819FA9-87E6-472E-ABBB-0BD0FF3365FEQ28244731-E9DC721D-932B-4810-A695-5F7134E5C52FQ28254930-0B0A722B-A3D2-4F55-9FE9-6CE4346FFFDFQ28256424-F8871012-23AF-4715-8C92-DBC71FA08522
P50
description
British neuroscientist
@en
onderzoeker
@nl
name
Andrew B. Singleton
@nl
Andrew Singleton
@ast
Andrew Singleton
@ca
Andrew Singleton
@da
Andrew Singleton
@de
Andrew Singleton
@en
Andrew Singleton
@es
Andrew Singleton
@fr
Andrew Singleton
@hu
Andrew Singleton
@nb
type
label
Andrew B. Singleton
@nl
Andrew Singleton
@ast
Andrew Singleton
@ca
Andrew Singleton
@da
Andrew Singleton
@de
Andrew Singleton
@en
Andrew Singleton
@es
Andrew Singleton
@fr
Andrew Singleton
@hu
Andrew Singleton
@nb
altLabel
A B Singleton
@ast
A B Singleton
@en
A Singleton
@en
A. B. Singleton
@en
A. Singleton
@en
Andrew B Singleton
@en
Andrew B. Singleton
@en
Andrew Singleton
@en
Singleton A
@en
Singleton A. B.
@en
prefLabel
Andrew B. Singleton
@nl
Andrew Singleton
@ast
Andrew Singleton
@ca
Andrew Singleton
@da
Andrew Singleton
@de
Andrew Singleton
@en
Andrew Singleton
@es
Andrew Singleton
@fr
Andrew Singleton
@hu
Andrew Singleton
@nb
P106
P108
P1960
Pf_pMQkAAAAJ
P21
P31
P4012
P496
0000-0001-5606-700X
P569
1972-01-01T00:00:00Z
P6023
2119312569