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M

Min-Lee Yang

university of texas system
H指数:11
被引数:715

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Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation

自发性冠状动脉夹层的全基因组关联荟萃分析确定了与动脉完整性和组织介导的凝血相关的风险变异和基因

NATURE GENETICS
IF31.8
2023-05-2926
OAAI
Adlam, David; Berrandou, Takiy-Eddine N.; Georges, Adrien; Nelson, Christopher; Giannoulatou, Eleni; Henry, Josephine S.; Ma, Lijiang; Blencowe, Montgomery E.; Turley, Tamiel L.; Yang, Min-Lee; Chopade, Sandesh E.; Finan, Chris; Braund, Peter; Sadeg-Sayoud, Ines; Iismaa, Siiri; Kosel, Matthew; Zhou, Xiang; Hamby, Stephen R.; Cheng, Jenny; Liu, Lu; Tarr, Ingrid; Muller, David W. M.; d'Escamard, Valentina; King, Annette E.; Brunham, Liam R.; Baranowska-Clarke, Ania A.; Debette, Stephanie G.; Amouyel, Philippe; Olin, Jeffrey W.; Patil, Snehal; Hesselson, Stephanie E.; Junday, Keerat; Kanoni, Stavroula; Aragam, Krishna G.; Butterworth, Adam S.; Tweet, Marysia; Gulati, Rajiv; Combaret, Nicolas; Kadian-Dodov, Daniella; Kalman, Jonathan M.; Fatkin, Diane; Hingorani, Aroon D.; Saw, Jacqueline; Webb, Tom R.; Hayes, Sharonne N.; Yang, Xia; Ganesh, Santhi K.; Olson, Timothy M.; Kovacic, Jason C.; Graham, Robert M.; Samani, Nilesh J.; Bouatia-Naji, Nabila
Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture

纤维肌性发育不良和腹主动脉瘤是具有共同复杂遗传结构的双态性特异性疾病

CIRCULATION-GENOMIC AND PRECISION MEDICINE
IF5.5
2022-12-018
OA
Katz, Alexander E.; Yang, Min-Lee; Levin, Michael G.; Tcheandjieu, Catherine; Mathis, Michael; Hunker, Kristina; Blackburn, Susan; Eliason, Jonathan L.; Coleman, Dawn M.; Fendrikova-Mahlay, Natalia; Gornik, Heather L.; Karmakar, Monita; Hill, Hannah; Xu, Chang; Zawistowski, Matthew; Brummett, Chad M.; Zoellner, Sebastian; Zhou, Xiang; O'Donnell, Christopher J.; Douglas, Julie A.; Assimes, Themistocles L.; Tsao, Phillip S.; Li, Jun Z.; Damrauer, Scott M.; Stanley, James C.; Ganesh, Santhi K.
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases (vol 12, 6031, 2021)
NATURE COMMUNICATIONS
IF15.7
2022-04-200
OAAI
Georges, Adrien; Yang, Min-Lee; Berrandou, Takiy-Eddine; Bakker, Mark K.; Dikilitas, Ozan; Kiando, Soto Romuald; Ma, Lijiang; Satterfield, Benjamin A.; Sengupta, Sebanti; Yu, Mengyao; Deleuze, Jean-Francois; Dupre, Delia; Hunker, Kristina L.; Kyryachenko, Sergiy; Liu, Lu; Sayoud-Sadeg, Ines; Amar, Laurence; Brummett, Chad M.; Coleman, Dawn M.; d'Escamard, Valentina; de Leeuw, Peter; Fendrikova-Mahlay, Natalia; Kadian-Dodov, Daniella; Li, Jun Z.; Lorthioir, Aurelien; Pappaccogli, Marco; Prejbisz, Aleksander; Smigielski, Witold; Stanley, James C.; Zawistowski, Matthew; Zhou, Xiang; Zollner, Sebastian; Amouyel, Philippe; De Buyzere, Marc L.; Debette, Stephanie; Dobrowolski, Piotr; Drygas, Wojciech; Gornik, Heather L.; Olin, Jeffrey W.; Piwonski, Jerzy; Rietzschel, Ernst R.; Ruigrok, Ynte M.; Vikkula, Miikka; Warchol Celinska, Ewa; Januszewicz, Andrzej; Kullo, Iftikhar J.; Azizi, Michel; Jeunemaitre, Xavier; Persu, Alexandre; Kovacic, Jason C.; Ganesh, Santhi K.; Bouatia-Naji, Nabila
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases
NATURE COMMUNICATIONS
IF15.7
2021-10-1535
OAAI
Georges, Adrien; Yang, Min-Lee; Berrandou, Takiy-Eddine; Bakker, Mark K.; Dikilitas, Ozan; Kiando, Soto Romuald; Ma, Lijiang; Satterfield, Benjamin A.; Sengupta, Sebanti; Yu, Mengyao; Deleuze, Jean-Francois; Dupre, Delia; Hunker, Kristina L.; Kyryachenko, Sergiy; Liu, Lu; Sayoud-Sadeg, Ines; Amar, Laurence; Brummett, Chad M.; Coleman, Dawn M.; d'Escamard, Valentina; de Leeuw, Peter; Fendrikova-Mahlay, Natalia; Kadian-Dodov, Daniella; Li, Jun Z.; Lorthioir, Aurelien; Pappaccogli, Marco; Prejbisz, Aleksander; Smigielski, Witold; Stanley, James C.; Zawistowski, Matthew; Zhou, Xiang; Zoellner, Sebastian; Amouyel, Philippe; De Buyzere, Marc L.; Debette, Stephanie; Dobrowolski, Piotr; Drygas, Wojciech; Gornik, Heather L.; Olin, Jeffrey W.; Piwonski, Jerzy; Rietzschel, Ernst R.; Ruigrok, Ynte M.; Vikkula, Miikka; Celinska, Ewa Warchol; Januszewicz, Andrzej; Kullo, Iftikhar J.; Azizi, Michel; Jeunemaitre, Xavier; Persu, Alexandre; Kovacic, Jason C.; Ganesh, Santhi K.; Bouatia-Naji, Nabila
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traits
NATURE GENETICS
IF31.8
2020-11-2327
OAAI
Choudhuri, Avik; Trompouki, Eirini; Abraham, Brian J.; Colli, Leandro M.; Kock, Kian Hong; Mallard, William; Yang, Min-Lee; Vinjamur, Divya S.; Ghamari, Alireza; Sporrij, Audrey; Hoi, Karen; Hummel, Barbara; Boatman, Sonja; Chan, Victoria; Tseng, Sierra; Nandakumar, Satish K.; Yang, Song; Lichtig, Asher; Superdock, Michael; Grimes, Seraj N.; Bowman, Teresa V.; Zhou, Yi; Takahashi, Shinichiro; Joehanes, Roby; Cantor, Alan B.; Bauer, Daniel E.; Ganesh, Santhi K.; Rinn, John; Albert, Paul S.; Bulyk, Martha L.; Chanock, Stephen J.; Young, Richard A.; Zon, Leonard I.
A Novel Recurrent COL5A1 Genetic Variant Is Associated With a Dysplasia-Associated Arterial Disease Exhibiting Dissections and Fibromuscular Dysplasia

一种新的复发性COL5A1遗传变异与发育不良相关的动脉疾病相关，表现为解剖和纤维肌发育不良

ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY
IF7.4
2020-11-0135
OAAI
Richer, Julie; Hill, Hannah L.; Wang, Yu; Yang, Min-Lee; Hunker, Kristina L.; Lane, Jamie; Blackburn, Susan; Coleman, Dawn M.; Eliason, Jonathan; Sillon, Guillaume; D'Agostino, Maria-Daniela; Jetty, Prasad; Mongeon, Francois-Pierre; Laberge, Anne-Marie; Ryan, Stephen E.; Fendrikova-Mahlay, Natalia; Coutinho, Thais; Mathis, Michael R.; Zawistowski, Matthew; Hazen, Stanley L.; Katz, Alexander E.; Gornik, Heather L.; Brummett, Chad M.; Abecasis, Goncalo; Bergin, Ingrid L.; Stanley, James C.; Li, Jun Z.; Ganesh, Santhi K.
Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

染色体1 q2l.2和其他基因座会影响自发性冠状动脉夹层和心肌梗死的风险

NATURE COMMUNICATIONS
IF15.7
2020-09-0468
OAAI
Saw, Jacqueline; Yang, Min-Lee; Trinder, Mark; Tcheandjieu, Catherine; Xu, Chang; Starovoytov, Andrew; Birt, Isabelle; Mathis, Michael R.; Hunker, Kristina L.; Schmidt, Ellen M.; Jackson, Linda; Fendrikova-Mahlay, Natalia; Zawistowski, Matthew; Brummett, Chad M.; Zoellner, Sebastian; Katz, Alexander; Coleman, Dawn M.; Swan, Kirby; O'Donnell, Christopher J.; Assimes, Themistocles L.; Zhou, Xiang; Li, Jun Z.; Gornik, Heather L.; Assimes, Themistocles L.; Stanley, James C.; Brunham, Liam R.; Ganesh, Santhi K.
Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2017-01-0149
OAAI
Guo, Dong-chuan; Duan, Xue-Yan; Regalado, Ellen S.; Mellor-Crummey, Lauren; Kwartler, Callie S.; Kim, Dong; Lieberman, Kenneth; de Vries, Bert B. A.; Pfundt, Rolph; Schinzel, Albert; Kotzot, Dieter; Shen, Xuetong; Yang, Min-Lee; Bamshad, Michael J.; Nickerson, Deborah A.; Gornik, Heather L.; Ganesh, Santhi K.; Braverman, Alan C.; Grange, Dorothy K.; Milewicz, Dianna M.
Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits
NATURE GENETICS
IF31.8
2016-07-1135
OAAI
Pankratz, Nathan; Schick, Ursula M.; Zhou, Yi; Zhou, Wei; Ahluwalia, Tarunveer Singh; Allende, Maria Laura; Auer, Paul L.; Bork-Jensen, Jette; Brody, Jennifer A.; Chen, Ming-Huei; Clavo, Vinna; Eicher, John D.; Grarup, Niels; Hagedorn, Elliott J.; Hu, Bella; Hunker, Kristina; Johnson, Andrew D.; Leusink, Maarten; Lu, Yingchang; Lyytikainen, Leo-Pekka; Manichaikul, Ani; Marioni, Riccardo E.; Nalls, Mike A.; Pazoki, Raha; Smith, Albert Vernon; van Rooij, Frank J. A.; Yang, Min-Lee; Zhang, Xiaoling; Zhang, Yan; Asselbergs, Folkert W.; Boerwinkle, Eric; Borecki, Ingrid B.; Bottinger, Erwin P.; Cushman, Mary; de Bakker, Paul I. W.; Deary, Ian J.; Dong, Liguang; Feitosa, Mary F.; Floyd, James S.; Franceschini, Nora; Franco, Oscar H.; Garcia, Melissa E.; Grove, Megan L.; Gudnason, Vilmundur; Hansen, Torben; Harris, Tamara B.; Hofman, Albert; Jackson, Rebecca D.; Jia, Jia; Kahonen, Mika; Launer, Lenore J.; Lehtimaki, Terho; Liewald, David C.; Linneberg, Allan; Liu, Yongmei; Loos, Ruth J. F.; Nguyen, Vy M.; Numans, Mattijs E.; Pedersen, Oluf; Psaty, Bruce M.; Raitakari, Olli T.; Rich, Stephen S.; Rivadeneira, Fernando; Di Sant, Amanda M. Rosa; Rotter, Jerome I.; Starr, John M.; Taylor, Kent D.; Thuesen, Betina Heinsbaek; Tracy, Russell P.; Uitterlinden, Andre G.; Wang, Jiansong; Wang, Judy; Dehghan, Abbas; Huo, Yong; Cupples, L. Adrienne; Wilson, James G.; Proia, Richard L.; Zon, Leonard I.; O'Donnell, Christopher J.; Reiner, Alex P.; Ganesh, Santhi K.
Exome-wide association analysis reveals novel coding sequence variants associated with lipid traits in Chinese
NATURE COMMUNICATIONS
IF15.7
2015-12-2280
OAAI
Tang, Clara S.; Zhang, He; Cheung, Chloe Y. Y.; Xu, Ming; Ho, Jenny C. Y.; Zhou, Wei; Cherny, Stacey S.; Zhang, Yan; Holmen, Oddgeir; Au, Ka-Wing; Yu, Haiyi; Xu, Lin; Jia, Jia; Porsch, Robert M.; Sun, Lijie; Xu, Weixian; Zheng, Huiping; Wong, Lai-Yung; Mu, Yiming; Dou, Jingtao; Fong, Carol H. Y.; Wang, Shuyu; Hong, Xueyu; Dong, Liguang; Liao, Yanhua; Wang, Jiansong; Lam, Levina S. M.; Su, Xi; Yan, Hua; Yang, Min-Lee; Chen, Jin; Siu, Chung-Wah; Xie, Gaoqiang; Woo, Yu-Cho; Wu, Yangfeng; Tan, Kathryn C. B.; Hveem, Kristian; Cheung, Bernard M. Y.; Zoellner, Sebastian; Xu, Aimin; Chen, Eugene; Jiang, Chao Qiang; Zhang, Youyi; Lam, Tai-Hing; Ganesh, Santhi K.; Huo, Yong; Sham, Pak C.; Lam, Karen S. L.; Willer, Cristen J.; Tse, Hung-Fat; Gao, Wei
Effects of Long-Term Averaging of Quantitative Blood Pressure Traits on the Detection of Genetic Associations
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2014-07-0167
OAAI
Ganesh, Santhi K.; Chasman, Daniel I.; Larson, Martin G.; Guo, Xiuqing; Verwoert, Germain; Bis, Joshua C.; Gu, Xiangjun; Smith, Albert V.; Yang, Min-Lee; Zhang, Yan; Ehret, Georg; Rose, Lynda M.; Hwang, Shih-Jen; Papanicolau, George J.; Sijbrands, Eric J.; Rice, Kenneth; Eiriksdottir, Gudny; Pihur, Vasyl; Ridker, Paul M.; Vasan, Ramachandran S.; Newton-Cheh, Christopher; Raffel, Leslie J.; Amin, Najaf; Rotter, Jerome I.; Liu, Kiang; Launer, Lenore J.; Xu, Ming; Caulfield, Mark; Morrison, Alanna C.; Johnson, Andrew D.; Vaidya, Dhananjay; Dehghan, Abbas; Li, Guo; Bouchard, Claude; Harris, Tamara B.; Zhang, He; Boerwinkle, Eric; Siscovick, David S.; Gao, Wei; Uitterlinden, Andre G.; Rivadeneira, Fernando; Hofman, Albert; Willer, Cristen J.; Franco, Oscar H.; Huo, Yong; Witteman, Jacqueline C. M.; Munroe, Patricia B.; Gudnason, Vilmundur; Palmas, Walter; van Duijn, Cornelia; Fornage, Myriam; Levy, Daniel; Psaty, Bruce M.; Chakravarti, Aravinda
Clinical and biochemical profiles suggest fibromuscular dysplasia is a systemic disease with altered TGF-10.1096/fj.14-251207β expression and connective tissue features
FASEB JOURNAL
IF4.2
2014-04-1466
OAAI
Ganesh, Santhi K.; Morissette, Rachel; Xu, Zhi; Schoenhoff, Florian; Griswold, Benjamin F.; Yang, Jiandong; Tong, Lan; Yang, Min-Lee; Hunker, Kristina; Sloper, Leslie; Kuo, Shinie; Raza, Rafi; Milewicz, Dianna M.; Francomano, Clair A.; Dietz, Harry C.; Van Eyk, Jennifer; McDonnell, Nazli B.

研究方向

暂未获取到该数据
S
Santhi K. Ganesh
H 指数:62论文数:222被引数:1.8万
K
Kristina L. Hunker
H 指数:13论文数:38被引数:921
Xiang Zhou 封面图
Xiang Zhou
H 指数:61论文数:310被引数:1.9万
J
Jun Z. Li
H 指数:58论文数:226被引数:2.4万
D
Dawn M. Coleman
H 指数:36论文数:286被引数:4,426
C
Chad M. Brummett
H 指数:71论文数:414被引数:2.4万
张
张燕
H 指数:57论文数:753被引数:1.5万
M
Matthew Zawistowski
H 指数:31论文数:111被引数:5,251
J
James C. Stanley
H 指数:74论文数:441被引数:2.7万
N
Natalia Fendrikova-Mahlay
H 指数:9论文数:29被引数:820