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迟发型阿兹海默病
迟发型阿兹海默病
发起讨论
迟发型阿兹海默病
40 个讨论
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阿兹海默风险什么时候再更新，有和我一样1.82倍的吗？
暴躁的ABCC4基因
• 最后回复
[已注销]
•
2019-01-31 12:49
3567
8
• 来自相关小组
判断阿茨海默病的APOE分型
守望的距离
• 最后回复
社区小助手
•
2019-01-04 14:32
3252
2
• 来自相关小组
SNPedia里面跟老年痴呆有关的位点没有全部包括进来，例如RS2075650
wq
• 最后回复
•
2018-11-10 03:54
4991
2
• 来自相关小组
6.32倍，大概比百分之多少人风险大？
运球的11号染色体
• 最后回复
siauhoo
•
2018-10-03 16:59
3130
2
• 来自相关小组
2.31倍
糜鉴
• 最后回复
horinee
•
2018-09-17 15:48
2704
2
• 来自相关小组
你们的阿兹海默发病预测年龄都是多少？
看海的COBL基因
• 最后回复
珂学发展观
•
2018-06-08 00:35
4362
14
• 来自相关小组
阿兹海默症
调皮的TOX基因
• 最后回复
zhengqiang
•
2018-05-15 09:56
2900
1
• 来自相关小组
【社区活动】关爱阿兹海默，参与活动赢取限量T恤和检测优惠啦！
lily
• 最后回复
wushantao
•
2018-05-02 10:05
4488
9
• 来自相关小组
大家觉得阿兹海默风险的项目更新后准吗
坚韧的PRKG1基因
• 最后回复
kumotan
•
2018-01-16 11:18
2806
3
• 来自相关小组
这两个数据矛盾吗
四点半宋丹丹
• 最后回复
•
2017-12-22 16:18
2817
2
• 来自相关小组
我想问下这个病和数据的关系
Ceribon
• 最后回复
Orion_yin
•
2017-12-12 18:18
2913
8
• 来自相关小组
更新之后的数据好像准了
木桌
• 最后回复
•
2017-11-01 02:03
3463
4
• 来自相关小组
五分之一的得病率？
囧囧的PSD3基因
• 最后回复
妹不萌
•
2017-09-16 12:14
3229
5
• 来自相关小组
测完父母的基因之后又看了下自己的基因，发现更新的项目里有阿兹海默高危，正好提点小意见
nnlory
• 最后回复
生气的TENM3基因
•
2017-09-15 02:36
3569
6
• 来自相关小组
更新了？我的老年痴呆概率降低为0.47了
Oliver
• 最后回复
jankinc
•
2017-09-11 10:03
3154
3
• 来自相关小组
高于99%的人，4.78倍，有没有和我一样的？
wegenecarmen
• 最后回复
很好的1号染色体
•
2017-08-01 20:35
3690
5
• 来自相关小组
得老年痴呆的风险大于94%的人
wxy55639
• 最后回复
yaoxt
•
2017-05-11 10:26
3227
2
• 来自相关小组
有什么能够延缓老年痴呆的的游戏？
费力科思
• 最后回复
Chipmunk
•
2017-03-06 15:26
5656
9
• 来自相关小组
我的测试里没有阿尔兹海默症的概率？请回答
田客
• 最后回复
luehr
•
2017-03-04 18:47
3077
1
• 来自相关小组
今天发现汇丰银行合作的保险公司的重疾险包括了阿尔兹海默症～～
费力科思
• 最后回复
asaki
•
2017-01-26 11:40
4296
7
• 来自相关小组
发起讨论
迟发型阿兹海默病
40 个讨论
相关基因
SLC24A4
位点：RS10498633
CELF1
位点：RS10838725
CD2AP
位点：RS10948363
SORL1
位点：RS11218343
位点：RS11218350
位点：RS1699103
位点：RS1784931
位点：RS1792113
位点：RS726601
EPHA1-AS1
位点：RS11771145
PLD3
位点：RS145999145
ZCWPW1
位点：RS1476679
FERMT2
位点：RS17125944
MEF2C-AS1
位点：RS190982
PTK2B
位点：RS28834970
PSEN2
位点：RS28936379
位点：RS63750048
INPP5D
位点：RS35349669
APOE
位点：RS429358
位点：RS7412
GRN
位点：RS5848
CETP
位点：RS5882
PSEN1
位点：RS63749824
位点：RS63749885
位点：RS63749891
位点：RS63750218
位点：RS63750526
位点：RS63750577
位点：RS63750590
位点：RS63750599
位点：RS63750815
位点：RS63750886
位点：RS63750900
位点：RS63751037
位点：RS63751141
位点：RS63751144
位点：RS63751163
位点：RS63751223
位点：RS63751229
位点：RS63751235
位点：RS63751320
CR1
位点：RS6656401
DISC1
位点：RS6675281
GAB2
位点：RS7101429
CASS4
位点：RS7274581
TREM2
位点：RS75932628
位点：RS143332484
DNM2
位点：RS892086
ABCA2
位点：RS908832
CLU
位点：RS9331896
KCNJ15
位点：RS928771
CNTNAP2
位点：RS802571
PICALM
位点：RS11234495
SPI1
位点：RS3740688
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Association between SORL1 and Alzheimer disease in a genome-wide study
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Rare coding variants in Phospholipase D3 (PLD3) confer risk for Alzheimer's disease
ZCWPW1 is associated with late-onset Alzheimer's disease in Han Chinese: a replication study and meta-analyses.
Association between SORL1 and Alzheimer disease in a genome-wide study
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Association between SORL1 and Alzheimer disease in a genome-wide study
Association between SORL1 and Alzheimer disease in a genome-wide study
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene.
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Pleiotropy in the presence of allelic heterogeneity: alternative genetic models for the influence of APOE on serum LDL, CSF Aβ42, and Dementia
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
Association of a functional polymorphism in the cholesteryl ester transfer protein (CETP) gene with memory decline and incidence of dementia.
Extreme cerebrospinal fluid amyloid beta levels identify family with late-onset Alzheimer's disease presenilin 1 mutation.
The acylation stimulating protein-adipsin system.
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype.
A novel PSEN2 mutation associated with a peculiar phenotype.
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset.
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.
Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life.
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.
A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis.
A novel mutation (V89L) in the presenilin 1 gene in a family with early onset Alzheimer's disease and marked behavioural disturbances.
Two novel (M233T and R278T) presenilin-1 mutations in early-onset Alzheimer's disease pedigrees and preliminary evidence for association of presenilin-1 mutations with a novel phenotype.
Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene.
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families.
The presenilin 1 C92S mutation increases abeta 42 production.
A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease.
Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 gene.
Missense mutations in the chromosome 14 familial Alzheimer's disease presenilin 1 gene.
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families.
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease.
Two novel presenilin-1 mutations (Y256S and Q222H) are associated with early-onset Alzheimer's disease.
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Association of DISC1 Polymorphisms with Late-Onset Alzheimer's Disease in Northern Han Chinese.
GAB2 as an Alzheimer Disease Susceptibility Gene
Identifying genetic interactions associated with late-onset Alzheimer’s disease
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Pleiotropy in the presence of allelic heterogeneity: alternative genetic models for the influence of APOE on serum LDL, CSF Aβ42, and Dementia
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Dynamin 2 gene is a novel susceptibility gene for late-onset Alzheimer disease in non-APOE-epsilon4 carriers
Meta-Analyses of 8 Polymorphisms Associated with the Risk of the Alzheimer’s Disease
Review: The genetics of Alzheimer’s disease; putting flesh on the bones
Identification of genetic risk factors in the Chinese population implicates a role of immune system in Alzheimer’s disease pathogenesis
A genome-wide association study of late-onset Alzheimer's disease in a Japanese population.
Validating GWAS-Identified Risk Loci for Alzheimer's Disease in Han Chinese Populations.
Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing.
Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease
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姓氏祖源
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