216 related articles for article (PubMed ID: 37479695)
1. The STROMICS genome study: deep whole-genome sequencing and analysis of 10K Chinese patients with ischemic stroke reveal complex genetic and phenotypic interplay.
Cheng S; Xu Z; Bian S; Chen X; Shi Y; Li Y; Duan Y; Liu Y; Lin J; Jiang Y; Jing J; Li Z; Wang Y; Meng X; Liu Y; Fang M; Jin X; Xu X; Wang J; Wang C; Li H; Liu S; Wang Y
Cell Discov; 2023 Jul; 9(1):75. PubMed ID: 37479695
[TBL] [Abstract][Full Text] [Related]
2. Whole Genome Analyses of Chinese Population and De Novo Assembly of A Northern Han Genome.
Du Z; Ma L; Qu H; Chen W; Zhang B; Lu X; Zhai W; Sheng X; Sun Y; Li W; Lei M; Qi Q; Yuan N; Shi S; Zeng J; Wang J; Yang Y; Liu Q; Hong Y; Dong L; Zhang Z; Zou D; Wang Y; Song S; Liu F; Fang X; Chen H; Liu X; Xiao J; Zeng C
Genomics Proteomics Bioinformatics; 2019 Jun; 17(3):229-247. PubMed ID: 31494266
[TBL] [Abstract][Full Text] [Related]
3. NOTCH3 variants and risk of ischemic stroke.
Ross OA; Soto-Ortolaza AI; Heckman MG; Verbeeck C; Serie DJ; Rayaprolu S; Rich SS; Nalls MA; Singleton A; Guerreiro R; Kinsella E; Wszolek ZK; Brott TG; Brown RD; Worrall BB; Meschia JF
PLoS One; 2013; 8(9):e75035. PubMed ID: 24086431
[TBL] [Abstract][Full Text] [Related]
4. Pleiotropy informed adaptive association test of multiple traits using genome-wide association study summary data.
Masotti M; Guo B; Wu B
Biometrics; 2019 Dec; 75(4):1076-1085. PubMed ID: 31021400
[TBL] [Abstract][Full Text] [Related]
5. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project.
Auer PL; Nalls M; Meschia JF; Worrall BB; Longstreth WT; Seshadri S; Kooperberg C; Burger KM; Carlson CS; Carty CL; Chen WM; Cupples LA; DeStefano AL; Fornage M; Hardy J; Hsu L; Jackson RD; Jarvik GP; Kim DS; Lakshminarayan K; Lange LA; Manichaikul A; Quinlan AR; Singleton AB; Thornton TA; Nickerson DA; Peters U; Rich SS;
JAMA Neurol; 2015 Jul; 72(7):781-8. PubMed ID: 25961151
[TBL] [Abstract][Full Text] [Related]
6.
Lee YC; Chung CP; Chang MH; Wang SJ; Liao YC
Neurology; 2020 Jan; 94(1):e87-e96. PubMed ID: 31792094
[TBL] [Abstract][Full Text] [Related]
7. Deep whole-genome sequencing of 90 Han Chinese genomes.
Lan T; Lin H; Zhu W; Laurent TCAM; Yang M; Liu X; Wang J; Wang J; Yang H; Xu X; Guo X
Gigascience; 2017 Sep; 6(9):1-7. PubMed ID: 28938720
[TBL] [Abstract][Full Text] [Related]
8. Broad phenotype of cysteine-altering
Rutten JW; Hack RJ; Duering M; Gravesteijn G; Dauwerse JG; Overzier M; van den Akker EB; Slagboom E; Holstege H; Nho K; Saykin A; Dichgans M; Malik R; Lesnik Oberstein SAJ
Neurology; 2020 Sep; 95(13):e1835-e1843. PubMed ID: 32732295
[TBL] [Abstract][Full Text] [Related]
9. Whole genome sequencing of 10K patients with acute ischaemic stroke or transient ischaemic attack: design, methods and baseline patient characteristics.
Cheng S; Xu Z; Liu Y; Lin J; Jiang Y; Wang Y; Meng X; Wang A; Huang X; Wang Z; Chen G; Wu S; Jia Z; Chen Y; Qiu X; Wu J; Song B; Ji W; An Z; Xue W; Zhao L; Geng Y; Li H; Li H; Wang Y
Stroke Vasc Neurol; 2021 Jun; 6(2):291-297. PubMed ID: 33443231
[TBL] [Abstract][Full Text] [Related]
10. Cysteine-Altering
Hack RJ; Rutten JW; Person TN; Li J; Khan A; Griessenauer CJ; ; Abedi V; Lesnik Oberstein SAJ; Zand R
Stroke; 2020 Dec; 51(12):3562-3569. PubMed ID: 33161844
[TBL] [Abstract][Full Text] [Related]
11. Exome-based gene panel analysis in a cohort of acute juvenile ischemic stroke patients:relevance of NOTCH3 and GLA variants.
Härtl J; Hartberger J; Wunderlich S; Cordts I; Bafligil C; Sturm M; ; Westphal D; Haack T; Hemmer B; Ikenberg BD; Deschauer M
J Neurol; 2023 Mar; 270(3):1501-1511. PubMed ID: 36411388
[TBL] [Abstract][Full Text] [Related]
12. Genetic spectrum of NOTCH3 and clinical phenotype of CADASIL patients in different populations.
Ni W; Zhang Y; Zhang L; Xie JJ; Li HF; Wu ZY
CNS Neurosci Ther; 2022 Nov; 28(11):1779-1789. PubMed ID: 35822697
[TBL] [Abstract][Full Text] [Related]
13. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
[TBL] [Abstract][Full Text] [Related]
14. Rare
Liu JY; Yao M; Dai Y; Han F; Zhai FF; Zhang DD; Zhou LX; Ni J; Zhang SY; Cui LY; Zhu YC
Stroke; 2021 Dec; 52(12):3918-3925. PubMed ID: 34404235
[TBL] [Abstract][Full Text] [Related]
15. Whole-exome sequencing analyses in a Saudi Ischemic Stroke Cohort reveal association signals, and shows polygenic risk scores are related to Modified Rankin Scale Risk.
Alkhamis FA; Alabdali MM; Alsulaiman AA; Alamri AS; Alali R; Akhtar MS; Alsalman SA; Cyrus C; Albakr AI; Alduhalan AS; Gandla D; Al-Romaih K; Abouelhoda M; Loza BL; Keating B; Al-Ali AK
Funct Integr Genomics; 2023 Mar; 23(2):102. PubMed ID: 36973604
[TBL] [Abstract][Full Text] [Related]
16. Large-Scale Targeted Sequencing Study of Ischemic Stroke in the Han Chinese Population.
Shi M; Kelly TN; Zhu Z; Li C; Shen C; Sun Y; Wang A; Shan G; Bu X; Guo D; Zhao J; Xu T; Peng H; Xu T; Zhong C; Sun X; Chen J; Zhang Y; He J
J Am Heart Assoc; 2022 Oct; 11(19):e025245. PubMed ID: 36193932
[TBL] [Abstract][Full Text] [Related]
17. Three-tiered EGFr domain risk stratification for individualized NOTCH3-small vessel disease prediction.
Hack RJ; Gravesteijn G; Cerfontaine MN; Santcroos MA; Gatti L; Kopczak A; Bersano A; Duering M; Rutten JW; Lesnik Oberstein SAJ
Brain; 2023 Jul; 146(7):2913-2927. PubMed ID: 36535904
[TBL] [Abstract][Full Text] [Related]
18. Tagging SNPs in the MTHFR gene and risk of ischemic stroke in a Chinese population.
Zhou BS; Bu GY; Li M; Chang BG; Zhou YP
Int J Mol Sci; 2014 May; 15(5):8931-40. PubMed ID: 24853127
[TBL] [Abstract][Full Text] [Related]
19. Genetic polymorphisms of methylenetetrahydrofolate reductase C677T and risk of ischemic stroke in a southern Chinese Hakka population.
Hou J; Zeng X; Xie Y; Wu H; Zhao P
Medicine (Baltimore); 2018 Dec; 97(51):e13645. PubMed ID: 30572478
[TBL] [Abstract][Full Text] [Related]
20. Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets.
Grarup N; Sulem P; Sandholt CH; Thorleifsson G; Ahluwalia TS; Steinthorsdottir V; Bjarnason H; Gudbjartsson DF; Magnusson OT; Sparsø T; Albrechtsen A; Kong A; Masson G; Tian G; Cao H; Nie C; Kristiansen K; Husemoen LL; Thuesen B; Li Y; Nielsen R; Linneberg A; Olafsson I; Eyjolfsson GI; Jørgensen T; Wang J; Hansen T; Thorsteinsdottir U; Stefánsson K; Pedersen O
PLoS Genet; 2013 Jun; 9(6):e1003530. PubMed ID: 23754956
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
