Examination of the current top candidate genes for AD in a genome-wide association study. - Wikidata - wikimedia - TriplyDB

Examination of the current top candidate genes for AD in a genome-wide association study.

Examination of the current top candidate genes for AD in a genome-wide association study.

http://www.wikidata.org/entity/Q44031576

about

Investigation of 15 of the top candidate genes for late-onset Alzheimer's disease Genetics of late-onset Alzheimer's disease: update from the alzgene database and analysis of shared pathways Intermediate phenotypes identify divergent pathways to Alzheimer's disease DYRK1A genetic variants are not linked to Alzheimer's disease in a Spanish case-control cohort.Caspase-1 genetic variation is not associated with Alzheimer's disease risk Recent insights into the molecular genetics of dementia Genetics of Alzheimer disease in the pre- and post-GWAS era Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease.The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease.Assessment and familial aggregation of psychosis in Alzheimer's disease from the National Institute on Aging Late Onset Alzheimer's Disease Family Study The insertion/deletion (I/D) polymorphism in the Angiotensin-converting enzyme gene and cancer risk: a meta-analysis.The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE.Genome-wide analysis of genetic loci associated with Alzheimer disease.Association between GAB2 haplotype and higher glucose metabolism in Alzheimer's disease-affected brain regions in cognitively normal APOEε4 carriers.Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes.No association of psychosis in Alzheimer disease with neurodegenerative pathway genes.Linking protective GAB2 variants, increased cortical GAB2 expression and decreased Alzheimer's disease pathology Meta-analysis of the association between variants in SORL1 and Alzheimer disease.Genetics of Vascular Dementia.Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk.Association and expression analyses with single-nucleotide polymorphisms in TOMM40 in Alzheimer disease.Blood-based biomarkers for Alzheimer's disease: plasma Aβ40 and Aβ42, and genetic variants.Functional analysis of APOE locus genetic variation implicates regional enhancers in the regulation of both TOMM40 and APOE.Identification of novel loci for Alzheimer disease and replication of CLU, PICALM, and BIN1 in Caribbean Hispanic individuals.Genetic Variants Associated with Lipid Profiles in Chinese Patients with Type 2 Diabetes.Association of TOMM40 and SLC22A4 polymorphisms with ischemic stroke.Meta-analysis of the Association between Alzheimer Disease and Variants in GAB2, PICALM, and SORL1.Promising Genetic Biomarkers of Preclinical Alzheimer's Disease: The Influence of APOE and TOMM40 on Brain Integrity.Interleukin-1β Promoter Polymorphism Enhances the Risk of Sleep Disturbance in Alzheimer's Disease Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease.Opening Pandora's jar: a primer on the putative roles of CRMP2 in a panoply of neurodegenerative, sensory and motor neuron, and central disorders.Panel of Genetic Variations as a Potential Non-invasive Biomarker for Early Diagnosis of Alzheimer's Disease.Genome-wide haplotype association study identify TNFRSF1A, CASP7, LRP1B, CDH1 and TG genes associated with Alzheimer's disease in Caribbean Hispanic individuals The Role of the Renin-Angiotensin System in Amyloid Metabolism of Alzheimer's Disease The influence of APOE and TOMM40 polymorphisms on hippocampal volume and episodic memory in old age Impact of SORL1 single nucleotide polymorphisms on Alzheimer's disease cerebrospinal fluid markers Variants in PPP3R1 and MAPT are associated with more rapid functional decline in Alzheimer's disease: the Cache County Dementia Progression Study.Sortilin receptor 1 predicts longitudinal cognitive change.Impact of SORL1 genetic variations on MRI markers in non-demented elders.

P2860

Q24628049-096B9884-30B6-4716-B660-0CD0AF00634B Q24629875-8A5480EA-375B-4A65-80A0-CD13364CD520 Q28751409-32E8D5CD-6483-4A47-8023-5B85E00E7B24 Q30967631-112DB7BB-1252-4971-81D7-0C9A78EBB2A5 Q33534445-D22FEE7C-1C3C-4C9C-84B8-1F2FBD1CA20D Q33830518-B4A121EC-0CAF-4546-BCB8-F84BF773AF5C Q33867876-145E5E14-BA21-4460-BFEE-5E040922C607 Q33879307-8A9B6C34-2AF7-469E-9BCA-B1EA4A6EB571 Q33986970-8765C91D-0849-4CE6-9BF1-685B4032D5E4 Q34030692-A8997450-4FFE-4909-8946-821DFB8333F6 Q34094498-46A39C3F-C5B6-43BF-A18A-D395C105C95A Q34123651-C27926FE-E7E9-49A6-9C09-33B8151E0823 Q34339530-E078048A-2362-4BEF-9587-06AE25A2B69F Q34440468-393A21E4-434D-49E7-A5BE-B7977E9089E8 Q34544940-E13F48B8-6884-497B-992C-CB6A2D802B15 Q34624775-524CB8CA-9593-4F3D-8330-6420097D1513 Q34728992-573EBFD7-80F7-4E00-87C3-9ED30D00AD49 Q34749829-0EAE263C-5D52-432F-AD1E-B657F57FA24C Q34913294-B8EECE2E-8BEA-4819-9116-D47256E1F9E8 Q35094704-53E922FC-247C-42AE-B53D-7E6BF9468054 Q35232774-0ADBDA83-1342-4E45-B398-7C29FD0CB307 Q35484526-D4A33FEF-6DD5-40E7-9410-3233C53CB79D Q35601036-112FBA9D-0AB2-48B1-A376-50499658422F Q35696751-C42F87A3-4A79-4AA3-9A57-D0D86CF937B3 Q35712611-3BCE18B0-0CF3-4C7E-9588-FF655D6AF3BA Q35739715-9AE06DE1-ABA6-41B3-AE48-901AD5B033E0 Q35803446-15066426-3DB3-4D3A-90E8-CD348C90B703 Q35854065-DA11DFED-734A-4EBE-846A-BB6481D21482 Q35895780-A6A10BEB-481D-4709-8FC6-97AA6B79B7D5 Q35944099-A3D226A3-E71A-45D2-8D4B-EBC978A8478C Q36036376-D7E1B1EA-D8A8-43E3-A2BD-5A491B6A8124 Q36517220-56C251E7-7FBD-4B1E-9AE2-2F18A20033AD Q36600561-7BDF852D-E87B-4536-9AD1-D01AE9C726E2 Q36618909-28A4BA5D-3A69-4BED-98BB-DD6027075746 Q36721915-DD069234-0906-4B12-83AC-078AE7FFD514 Q36864568-6EDD5C8B-C4AB-4469-9D8B-3D63D0133D8B Q36966070-3610B094-7A0B-42A0-B192-D9F1031DBFD7 Q37258203-BEE0291E-F8E6-42E6-8319-8414F1B96F6C Q37340530-B35786C8-9C4C-4C40-9377-DA6FB0E8A410 Q37362490-0F554DE5-4450-4A15-B85C-61C22C7770F1

P2860

Examination of the current top candidate genes for AD in a genome-wide association study.

http://www.wikidata.org/entity/Q44031576

description

2009 nî lūn-bûn

@nan

2009年の論文

@ja

2009年学术文章

@wuu

2009年学术文章

@zh-cn

2009年学术文章

@zh-hans

2009年学术文章

@zh-my

2009年学术文章

@zh-sg

2009年學術文章

@yue

2009年學術文章

@zh

2009年學術文章

@zh-hant

name

Examination of the current top candidate genes for AD in a genome-wide association study.

@en

Examination of the current top candidate genes for AD in a genome-wide association study.

@nl

type

label

Examination of the current top candidate genes for AD in a genome-wide association study.

@en

Examination of the current top candidate genes for AD in a genome-wide association study.

@nl

prefLabel

Examination of the current top candidate genes for AD in a genome-wide association study.

@en

Examination of the current top candidate genes for AD in a genome-wide association study.

@nl

P1433

Q44031576-052EB19A-2E3C-4B93-B7F6-D1CF3DF698DA

P1476

Q44031576-19D6F523-2E1A-4E6A-9F26-C1CF3AFB089B

P2093

Q44031576-2345F3B4-C023-427B-9AF8-33D81233DFF0

Q44031576-29E86EF9-6C09-4455-B9B9-39E47280D26E

Q44031576-3EA36DD2-8532-473B-A865-5D6CE5D129D1

Q44031576-409F92BF-2773-4452-9DA9-4981F30C5F07

Q44031576-44827E2C-7658-4BA6-B1C2-AA11F599DC26

Q44031576-50F75F73-91BA-47E9-A8DC-1DFA1505D9F6

Q44031576-780C4AED-CDE1-475A-A5ED-D77CC42E0473

Q44031576-92B72A5C-6257-4520-930B-AED0CEDDC298

Q44031576-DD0D38D6-6C4A-42C4-94DF-F38FCC6D15BB

Q44031576-EECCD944-4017-4EF0-8DAE-9C5EAD588709

P2860

Q44031576-0090886B-2B2C-40B2-8857-E57AF0478F06

Q44031576-0554D61B-9A56-4C33-AB54-1225CEB8AC32

Q44031576-0C6DDF3D-1901-420B-A933-CFB5011ACE4B

Q44031576-0C7EAA24-94B8-4640-8C40-FA7D68A485FD

Q44031576-1D01C7A8-6267-49B4-999A-391F773384E0

Q44031576-27F97C67-CE65-4C6E-BE43-1040E974218B

Q44031576-28908ECF-C3FA-48CF-99F1-98ACAA8773B6

Q44031576-2CA2BAB1-21FD-400D-B9C5-6229D5184AA6

Q44031576-31E808BB-9E6A-47FA-98E4-8752C1086624

Q44031576-388EDDC1-CCE2-4CC9-BD37-C5E23EF4FBDD

P2888

Q44031576-5F3A0679-5789-4C22-A40A-C23FC69EEA30

P304

Q44031576-68E06EAA-D7FD-4298-B16B-718EAF824F63

P31

Q44031576-1D5AD178-B7C7-4992-9421-D1A10AEE9DE8

P356

Q44031576-4361CCAB-16E2-414B-A886-C555E50D21B5

P407

Q44031576-E717CB91-21E8-47F9-922E-6AADA269DFF1

P433

Q44031576-9C4386F5-E0E9-4A81-BEF9-468355A1A0EF

P478

Q44031576-FC5AC9F5-DE7A-41E3-BE8D-164E694C5CF5

P50

Q44031576-41B6D695-F7CE-4899-BEB6-9AC99175D4A6

P577

Q44031576-0D9E9B6C-14CC-4995-BE67-7DFE9FE9204E

P5875

Q44031576-908D9CC0-7E20-4DB7-9238-87367D3F8BCB

P6179

Q44031576-6EE6F152-91B9-4161-8791-9079B267F003

P698

Q44031576-1D4EFED8-6433-42BB-978C-1518BBE2D036

P921

Q44031576-DEA7A5F0-4F23-40EE-B4B7-D7173E86D43D

P356

P1433

Molecular Psychiatry

P1476

Examination of the current top candidate genes for AD in a genome-wide association study.

@en

P2093

A Kurz

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

C Riehle

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

H Förstl

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

K A Kuhn

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

M Krawczak

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

M Riemenschneider

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

P Friedrich

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

S H R Wurst

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

S Nikolaus

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

S Schreiber

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

P2860

Promoter polymorphism in PCK1 (phosphoenolpyruvate carboxykinase gene) associated with type 2 diabetes mellitus

Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease

A novel mutation in AlphaA-crystallin (CRYAA) caused autosomal dominant congenital cataract in a large Chinese family

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers

The neuronal sortilin-related receptor SORL1 is genetically associated with Alzheimer disease

A haplotype map of the human genome

Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.

“Mini-mental state”

The structure of haplotype blocks in the human genome

Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families

P2888

P304

756-766

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

P31

scholarly article

P356

10.1038/MP.2008.141

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

P407

P433

7

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

P478

15

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

P50

P577

2009-01-06T00:00:00Z

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

P5875

23760191

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

P6179

1013602583

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

P698

19125160

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

P921

genome-wide association study