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Min-Lee Yang
Min-Lee Yang
Bioinformatics PhD candidate, University of Michigan
Подтвержден адрес электронной почты в домене umich.edu
Название
Процитировано
Процитировано
Год
Genome-wide association study reveals multiple nasopharyngeal carcinoma-associated loci within the HLA region at chromosome 6p21. 3
KP Tse, WH Su, KP Chang, NM Tsang, CJ Yu, P Tang, LC See, C Hsueh, ...
The American Journal of Human Genetics 85 (2), 194-203, 2009
2062009
PHACTR1 Is a Genetic Susceptibility Locus for Fibromuscular Dysplasia Supporting Its Complex Genetic Pattern of Inheritance
NBN Soto Romuald Kiando, Nathan R. Tucker, Luis-Jaime Castro-Vega, Alexander ...
PLOS Genetics, 2016
1772016
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese
CS Tang, H Zhang, CYY Cheung, M Xu, JCY Ho, W Zhou, SS Cherny, ...
Nature communications 6 (1), 1-9, 2015
932015
Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations
SK Ganesh, DI Chasman, MG Larson, X Guo, G Verwoert, JC Bis, X Gu, ...
The American Journal of Human Genetics 95 (1), 49-65, 2014
922014
Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF‐β expression and connective tissue features
SK Ganesh, R Morissette, Z Xu, F Schoenhoff, BF Griswold, J Yang, ...
The FASEB Journal 28 (8), 3313-3324, 2014
882014
Chromosome 1q21. 2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction
J Saw, ML Yang, M Trinder, C Tcheandjieu, C Xu, A Starovoytov, I Birt, ...
Nature Communications 11 (1), 1-14, 2020
622020
A gender-specific association of CNV at 6p21. 3 with NPC susceptibility
KP Tse, WH Su, M Yang, HY Cheng, NM Tsang, KP Chang, SP Hao, ...
Human molecular genetics 20 (14), 2889-2896, 2011
572011
Loss-of-function mutations in YY1AP1 lead to grange syndrome and a fibromuscular dysplasia-like vascular disease
D Guo, XY Duan, ES Regalado, L Mellor-Crummey, CS Kwartler, D Kim, ...
The American Journal of Human Genetics 100 (1), 21-30, 2017
542017
Genome-wide Trans-ethnic Meta-analysis Identifies Seven Genetic Loci Influencing Erythrocyte Traits and a Role for RBPMS in Erythropoiesis
The American Journal of Human Genetics 100 (Issue 1), 2017
512017
Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits
N Pankratz, UM Schick, Y Zhou, W Zhou, TS Ahluwalia, ML Allende, ...
Nature genetics 48 (8), 867, 2016
412016
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases
A Georges, ML Yang, TE Berrandou, MK Bakker, O Dikilitas, SR Kiando, ...
Nature Communications 12 (1), 1-16, 2021
392021
Genomic estimates of aneuploid content in Glioblastoma Multiforme and improved classification
B Li, Y Senbabaoglu, W Peng, ML Yang, J Xu, JZ Li
Clinical Cancer Research 18 (20), 5595-5605, 2012
342012
A Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia
J Richer, HL Hill, Y Wang, ML Yang, KL Hunker, J Lane, S Blackburn, ...
Arteriosclerosis, Thrombosis, and Vascular Biology 40 (11), 2686-2699, 2020
322020
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits
A Choudhuri, E Trompouki, BJ Abraham, LM Colli, KH Kock, W Mallard, ...
Nature genetics 52 (12), 1333-1345, 2020
242020
Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia
A Georges, J Albuisson, T Berrandou, D Dupré, A Lorthioir, V D’Escamard, ...
Cardiovascular research 117 (4), 1154-1165, 2021
222021
Million Veteran Program
J Saw, ML Yang, M Trinder, C Tcheandjieu, C Xu, A Starovoytov, I Birt, ...
Chromosome 1q21 2, 0
15
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation
D Adlam, TE Berrandou, A Georges, CP Nelson, E Giannoulatou, J Henry, ...
Nature Genetics, 1-9, 2023
142023
Million Veteran Program. Chromosome 1q21. 2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction
J Saw, ML Yang, M Trinder, C Tcheandjieu, C Xu, A Starovoytov, I Birt, ...
Nat Commun 11 (1), 4432, 2020
122020
Spontaneous coronary artery dissection is infrequent in individuals with heritable thoracic aortic disease despite partially shared genetic susceptibility
AM Murad, HL Hill, Y Wang, M Ghannam, ML Yang, NL Pugh, FM Asch, ...
American Journal of Medical Genetics Part A, 2022
62022
Epidemiologic and Genetic Associations of Erythropoietin With Blood Pressure, Hypertension, and Coronary Artery Disease
P Sun, N Kumar, A Tin, J Zhao, MR Brown, Z Lin, ML Yang, Q Zheng, J Jia, ...
Hypertension 78 (5), 1555-1566, 2021
62021
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