| 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 | 206 | 2009 |
| 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 | 177 | 2016 |
| 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 | 93 | 2015 |
| 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 | 92 | 2014 |
| 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 | 89 | 2014 |
| 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 | 62 | 2020 |
| 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 | 57 | 2011 |
| 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 | 55 | 2017 |
| 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 | 51 | 2017 |
| 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 | 41 | 2021 |
| 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 | 41 | 2016 |
| 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 | 34 | 2012 |
| 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 | 32 | 2020 |
| 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 | 26 | 2020 |
| 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 | 22 | 2021 |
| 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 | 14 | 2023 |
| 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 | 12 | 2020 |
| 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 | 6 | 2022 |
| 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 | 6 | 2021 |
