Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method. - Wikidata - wikimedia - TriplyDB

Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method.

Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method.

http://www.wikidata.org/entity/Q33721033

about

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update Structure of the human Parkin ligase domain in an autoinhibited state Predicting Disease Onset from Mutation Status Using Proband and Relative Data with Applications to Huntington's Disease.Efficient distribution estimation for data with unobserved sub-population identifiers.Nonparametric estimation for censored mixture data with application to the Cooperative Huntington's Observational Research Trial.Efficient Estimation of Nonparametric Genetic Risk Function with Censored Data.Estimation of genotype relative risks from pedigree data by retrospective likelihoods Comparison of Parkinson risk in Ashkenazi Jewish patients with Gaucher disease and GBA heterozygotes.COMBINING ISOTONIC REGRESSION AND EM ALGORITHM TO PREDICT GENETIC RISK UNDER MONOTONICITY CONSTRAINT The relation between depression and parkin genotype: the CORE-PD study.Age-specific penetrance of LRRK2 G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium.Predictors of parkin mutations in early-onset Parkinson disease: the consortium on risk for early-onset Parkinson disease study.Neuropsychological Profile of Parkin Mutation Carriers with and without Parkinson Disease: The CORE-PD Study.Genetic insights into sporadic Parkinson's disease pathogenesis.Nonparametric modeling and analysis of association between Huntington's disease onset and CAG repeats Mitochondrial contribution to Parkinson's disease pathogenesis.Second mutation in PARK2 is absent in patients with sporadic Parkinson's disease and heterozygous exonic deletions/duplications in parkin gene.Impact of different ionization states of phosphorylated Serine-65 on ubiquitin structure and interactions.Phenotype of the 202 adenine deletion in the parkin gene: 40 years of follow-up.PARK2 copy number aberrations in two children presenting with autism spectrum disorder: further support of an association and possible evidence for a new microdeletion/microduplication syndrome.Heterozygote carriers for CNVs inPARK2are at increased risk of Parkinson's disease

P2860

Q22252904-4D9088E3-BC41-49DF-BB56-0D1940D3FA45 Q27678455-36BE3088-B427-408B-A184-B483FD56B29F Q30597292-09CFFBBF-6D97-41A5-A11A-574E8FC93931 Q30651247-11459E0B-0F59-46F4-A39C-87BD44CA68CE Q30747024-DEA16F41-DB26-4161-AE4D-B8978120CEF5 Q30998396-2F470ED0-4650-4587-8E4C-82C3912B73E5 Q33521055-14A05390-4C47-47D2-89BA-EE1548C4DA5F Q33849233-B30A5FC7-9CAB-493A-BC20-997C5A6DFF93 Q34510437-CB2B9FD4-51BC-4F15-83EF-3C6B34DF1E1D Q35566358-629C459A-B765-4F4A-A5BE-792C465A0643 Q35850713-A25BB0BC-B28D-4941-A5DC-440B26A77CA5 Q35898027-0BF85AAD-AA94-4533-B46F-8E46576E195F Q36005602-E9C8F543-08D9-440E-A00F-CEA19CB17F9A Q37583402-213D52B1-C062-44B0-B232-7480B7425F80 Q37626486-70FF68D5-F731-43DA-B7E7-7786B7C9A2C8 Q37891820-15925256-D48C-4939-8B51-449BB70ECF15 Q39230378-A6A5AFAE-376F-4DA5-9118-AD20A44CDBFB Q49436375-30BE44B0-9AD3-4CDB-838F-715E0F6B14C5 Q50264707-2726EA6D-1F60-4539-9576-B7CBB4ED3E15 Q50312477-B6931B53-A89D-43B0-972B-F02BE587B70B Q57309405-EA4847E4-6F6B-4299-9BBC-09985FA78F60

P2860

Risk of Parkinson disease in carriers of parkin mutations: estimation using the kin-cohort method.

http://www.wikidata.org/entity/Q33721033

description

2008 nî lūn-bûn

@nan

2008 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

2008年の論文

@ja

2008年論文

@yue

2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

Risk of Parkinson disease in c ...... n using the kin-cohort method.

@ast

Risk of Parkinson disease in c ...... n using the kin-cohort method.

@en

type

label

Risk of Parkinson disease in c ...... n using the kin-cohort method.

@ast

Risk of Parkinson disease in c ...... n using the kin-cohort method.

@en

prefLabel

Risk of Parkinson disease in c ...... n using the kin-cohort method.

@ast

Risk of Parkinson disease in c ...... n using the kin-cohort method.

@en

P1433

Q33721033-DBDEEF6C-DA4F-4608-AB90-939F5AE7FCF0

P1476

Q33721033-AF7208E2-B5E3-48FF-A1C0-88810D28AF32

P2093

Q33721033-05CB7F7F-0B8D-45A9-927E-74046DF87020

Q33721033-308999B4-8549-47D7-9AC8-C7D9901814C3

Q33721033-36C11ACF-1457-480A-8549-93977E0DDC62

Q33721033-3C838BCF-B127-438C-BB88-D1032C8E8415

Q33721033-606BE3AF-519F-474A-84D8-1885181D6054

Q33721033-63E65CE3-F959-4AB8-A178-D95FB9B25CDE

Q33721033-AD4AE257-3E0B-4052-A999-588DE8819C68

Q33721033-AFFB7B2A-CAF7-41AD-A30C-741E72428ABB

Q33721033-C3C854F0-4234-42AE-812E-C05251C26040

Q33721033-ED120E69-D1B0-4570-8BE5-1C649153650E

P2860

Q33721033-021A40C5-5AE5-4122-940F-31DD71B10724

Q33721033-078EA018-A974-400E-AEA7-C1A8D2EC99C2

Q33721033-109D208C-07C4-4775-B6A9-DCA65F0B0AE6

Q33721033-180D3035-29ED-4BDF-8790-AA472ADAED1F

Q33721033-2A2F2970-6E93-44FD-9434-44500D736ACE

Q33721033-3107C2E2-9C58-47A3-94BD-C0AFE77A0FB4

Q33721033-4821F98A-FB43-4CA9-B201-6ECAAB4BE86E

Q33721033-4A0D53D9-37BF-437D-9A02-3A64C1FECE06

Q33721033-6FBA9475-DC92-4636-A2A7-F35219B81D0A

Q33721033-707EE9F7-C473-4329-9DB1-281EE4D611E8

P304

Q33721033-CCFDE4F6-1CD6-4C95-8CBE-8E4003E0A963

P31

Q33721033-91AD265E-75C1-4969-8DCB-29CF1E3CAA27

P356

Q33721033-7BCA84D7-5F9D-4A8D-93CC-99E3BAF697FA

P433

Q33721033-03F7C5AE-1994-497F-A18B-BB3C6E19DD19

P478

Q33721033-C003DA6F-5D53-4037-B32F-031F4767C368

P50

Q33721033-181FDC70-89F5-42E4-895C-A57CECD1FA1E

Q33721033-788B3463-B1A2-445B-B5D0-719CC7DDD444

P577

Q33721033-9888F148-84D7-4D4E-B50D-C50AF9214EFE

P5875

Q33721033-C041519F-17A3-4F68-BAD0-DB3376264707

P698

Q33721033-ACB110D2-73EE-47BB-A940-DED11467AE1E

P921

Q33721033-2AB38437-880F-4922-949D-3F0D3C033AD5

P932

Q33721033-8380AC0E-F0D9-4CBD-9E2D-959C90F41A32

P356

ARCHNEUR.65.4.467

P1433

P1476

Risk of Parkinson disease in c ...... n using the kin-cohort method.

@en

P2093

Blair Ford

http://www.w3.org/2001/XMLSchema#string

Cheryl Waters

http://www.w3.org/2001/XMLSchema#string

Daniel Rabinowitz

http://www.w3.org/2001/XMLSchema#string

Helen Mejia-Santana

http://www.w3.org/2001/XMLSchema#string

Howard Andrews

http://www.w3.org/2001/XMLSchema#string

Juliette Harris

http://www.w3.org/2001/XMLSchema#string

Karen Marder

http://www.w3.org/2001/XMLSchema#string

Lorraine N Clark

http://www.w3.org/2001/XMLSchema#string

Lucien J Cote

http://www.w3.org/2001/XMLSchema#string

Ruth Ottman

http://www.w3.org/2001/XMLSchema#string

P2860

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

Association between early-onset Parkinson's disease and mutations in the parkin gene

The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews

Accuracy of family history data on Parkinson's disease.

How much phenotypic variation can be attributed to parkin genotype?

Complex relationship between Parkin mutations and Parkinson disease.

Parkinson's disease: piecing together a genetic jigsaw.

Distribution, type, and origin of Parkin mutations: review and case studies.

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.

P304

467-474

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1001/ARCHNEUR.65.4.467

http://www.w3.org/2001/XMLSchema#string

P433

4

http://www.w3.org/2001/XMLSchema#string

P478

65

http://www.w3.org/2001/XMLSchema#string

P50

P577

2008-04-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

5440128

http://www.w3.org/2001/XMLSchema#string

P698

18413468

http://www.w3.org/2001/XMLSchema#string

P921

Parkinson's disease

P932

2836931

http://www.w3.org/2001/XMLSchema#string