About: Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population

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About: Genome-wide association study identifies candidate genes for Parkinson's disease in an Ashkenazi Jewish population Goto Sponge NotDistinct Permalink

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description	artículu científicu espublizáu en 2011 (ast) наукова стаття, опублікована в серпні 2011 (uk) 2011 թվականի օգոստոսին հրատարակված գիտական հոդված (hy) 2011 թուականի Օգոստոսին հրատարակուած գիտական յօդուած (hyw) مقالة علمية (نشرت في 3-8-2011) (ar) wetenschappelijk artikel (gepubliceerd op 2011/08/03) (nl) scientific journal article (en) im August 2011 veröffentlichter wissenschaftlicher Artikel (de)
publication date	wds:Q28943392-42976749-1C9B-4256-B176-01D69A947A35
publication date	2011-08-03 00:00:00Z (xsd:dateTime)
exact match	wds:Q28943392-197FFCEB-24B5-4829-A235-F61C33BE694F
exact match	https://scigraph.springernature.com/pub.10.1186/1471-2350-12-104
cites work	wds:Q28943392-00FDCFD9-4138-4F40-B84A-78598E26E663 wds:Q28943392-052C3413-8B0C-4F87-8928-DAC864FB6225 wds:Q28943392-056759A0-BC55-40A3-893B-8AD3C458A481 wds:Q28943392-06A2E6FB-6BFF-455A-9612-6E3F32A53DD8 wds:Q28943392-0778C393-BE57-4EE1-A5EC-56A8E3D0019C wds:Q28943392-117DC456-B468-424C-B2BF-0942B34D7FE2 wds:Q28943392-13C6F5B8-B485-4899-8866-9126CE5A5614 wds:Q28943392-244661F9-4311-4C60-8363-A5B1CFEE2A17 wds:Q28943392-35252ED1-2FB5-43FC-B0BD-8ED8EB46C308 wds:Q28943392-361DE880-127C-4D97-8256-3FBD1DC1068E wds:Q28943392-39FDC926-9EB6-4244-8F33-EA7199C2080D wds:Q28943392-40F5320C-25C7-4015-95A9-E3A3E6C0D836 wds:Q28943392-4891FB06-2D1F-4AAB-A8D1-CAAF8BEE3F13 wds:Q28943392-49C40A25-9CCE-4DE6-B6B5-34F7D726B182 wds:Q28943392-537C354C-EB94-47D3-83DA-070AEF3E93E1 wds:Q28943392-560CBFD6-3F43-4492-AD2B-EDD6C83488A9 wds:Q28943392-63503C89-0B33-487B-9E55-76EDB06EA14D wds:Q28943392-63EA0134-70CF-437B-99A0-22C0FB79AA19 wds:Q28943392-66BFF95C-DB31-4276-AAE1-B6CA79BEB7BE wds:Q28943392-6D1B954A-F9DA-4FCB-BC3C-CC477D77D14E wds:Q28943392-7A968C69-8AFC-45A2-A1BC-3BD3A28E3038 wds:Q28943392-7BE3169B-B67C-4251-B4EC-D8A6ED42C7AC wds:Q28943392-8662B4CC-55A8-4149-B52F-DD0DA077C207 wds:Q28943392-91E4E720-B0AD-4E1C-89CD-D7660FB959A7 wds:Q28943392-A7067598-5D79-40FF-A7AB-8385C25914B1 wds:Q28943392-B45BEAFE-2D37-4CBE-83CF-08AAFFF7EDA1 wds:Q28943392-B48AB623-1EE9-4D34-A543-FE6FC166D201 wds:Q28943392-BAB645E0-9087-4B71-9ED9-1EE4F49BA5EC wds:Q28943392-C196050C-DD55-4E81-A1CF-85B145EA8ECC wds:Q28943392-CD1932C8-4880-4A11-9BF4-80DD5E82D187 wds:Q28943392-D9673F18-10F3-4982-AEEB-7D215EBA3590 wds:Q28943392-DE7DB84A-973B-48B5-A662-66E846EFD693 wds:Q28943392-E9277E61-7686-4285-AB0F-3602EE22A6EA wds:Q28943392-F7590062-4D92-4B21-B918-D05405A1B7D6 wds:Q28943392-F87682EA-425E-49E0-93F3-1433D6BA33DD wds:Q28943392-FA2F8045-DB42-4888-92F9-EC9510572194 wds:Q28943392-FD1101DF-8AF5-43F8-B8D2-B8F9511E4819 wds:Q28943392-FDE22786-F14D-4B97-BA1B-B34280D405A4
cites work	Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies Fourteen novel human members of mitochondrial solute carrier family 25 (SLC25) widely expressed in the central nervous system. Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data Genomewide association study for susceptibility genes contributing to familial Parkinson disease Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population Uncoupling protein 2 in the brain: distribution and function The mitochondrial transporter family (SLC25): physiological and pathological implications PLINK: a tool set for whole-genome association and population-based linkage analyses Mutation in the alpha-synuclein gene identified in families with Parkinson's disease Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism Hereditary early-onset Parkinson's disease caused by mutations in PINK1 Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease Genomewide association study for onset age in Parkinson disease Frequency of LRRK2 mutations in early- and late-onset Parkinson disease. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update SNAP: a web-based tool for identification and annotation of proxy SNPs using HapMap A common inversion under selection in Europeans Interaction of dopamine D1 receptor with N-ethylmaleimide-sensitive factor is important for the membrane localization of the receptor WGAViewer: software for genomic annotation of whole genome association studies Mutations in the glucocerebrosidase gene are associated with early-onset Parkinson disease High-resolution whole-genome association study of Parkinson disease. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism Genome-wide association study reveals genetic risk underlying Parkinson's disease Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease Genetic variability at the PARK16 locus LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. Familial aggregation of early- and late-onset Parkinson's disease Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry A genetic profile of contemporary Jewish populations. Parkinson's disease Dimerization of dopamine D1 and D3 receptors in the regulation of striatal function. A network of G-protein signaling pathways control neuronal activity in C. elegans Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries. NSF--fusion and beyond
author name string	wds:Q28943392-17D9A8D9-493D-401C-A288-B82E5ADC894D wds:Q28943392-325E4CDE-4182-4AD1-A9F3-00A07E841340 wds:Q28943392-71A34BBA-EB61-4E64-9050-95283A6E50BA wds:Q28943392-7EB82C27-95AC-4A95-9216-C728CC446D79 wds:Q28943392-98C52D04-B90E-4435-AA62-817DCB4E14A3
OpenCitations bibliographic resource ID	wds:Q28943392-FAD1736B-D23E-453A-A1CC-C693551D5D04
OpenCitations bibliographic resource ID	https://w3id.org/oc/corpus/br/3719277
author name string	Xinmin Liu Rong Cheng Howard Andrews Andrew Browne

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