Works matching AU Peloso, Gina M.


Results: 59
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    Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program.

    Published in:
    PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0267900
    By:
    • Huang, Rose D. L.;
    • Nguyen, Xuan-Mai T.;
    • Peloso, Gina M.;
    • Trinder, Mark;
    • Posner, Daniel C.;
    • Aragam, Krishna G.;
    • Ho, Yuk-Lam;
    • Lynch, Julie A.;
    • Damrauer, Scott M.;
    • Chang, Kyong-Mi;
    • Tsao, Philip S.;
    • Natarajan, Pradeep;
    • Assimes, Themistocles;
    • Gaziano, J. Michael;
    • Djousse, Luc;
    • Cho, Kelly;
    • Wilson, Peter W. F.;
    • Huffman, Jennifer E.;
    • O'Donnell, Christopher J.
    Publication type:
    Article
    6

    The role of common structural variants in Alzheimer's disease.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.092501
    By:
    • Lee, Songmi;
    • Xia, Rui;
    • English, Adam C;
    • Peloso, Gina M.;
    • Bis, Josh;
    • Lin, Honghuang;
    • Choi, Seung Hoan;
    • Heard‐Costa, Nancy;
    • DeStefano, Anita L.;
    • Sedlazeck, Fritz J;
    • Fornage, Myriam
    Publication type:
    Article
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    Whole Genome Sequencing Analysis of Cognitively Wellderly Individuals Identifies Potential Protective Genetic Variants for Alzheimer's Disease.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, p. 1, doi. 10.1002/alz.088478
    By:
    • Wang, Dongyu;
    • Choi, Seung Hoan;
    • Abbruzzese, Sabrina;
    • Rosser, Morgan A;
    • Bis, Joshua C;
    • Fornage, Myriam;
    • Boerwinkle, Eric;
    • Satizabal, Claudia L;
    • Psaty, Bruce M.;
    • Lopez, Oscar L.;
    • Mosley, Thomas H.;
    • Wang, Yanbing;
    • Dupuis, Josée;
    • DeStefano, Anita L.;
    • Seshadri, Sudha;
    • Peloso, Gina M.
    Publication type:
    Article
    8

    Key variants via the Alzheimer's Disease Sequencing Project whole genome sequence data.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 5, p. 3290, doi. 10.1002/alz.13705
    By:
    • Wang, Yanbing;
    • Sarnowski, Chloé;
    • Lin, Honghuang;
    • Pitsillides, Achilleas N.;
    • Heard‐Costa, Nancy L.;
    • Choi, Seung Hoan;
    • Wang, Dongyu;
    • Bis, Joshua C.;
    • Blue, Elizabeth E.;
    • Boerwinkle, Eric;
    • De Jager, Philip L.;
    • Fornage, Myriam;
    • Wijsman, Ellen M.;
    • Seshadri, Sudha;
    • Dupuis, Josée;
    • Peloso, Gina M.;
    • DeStefano, Anita L.
    Publication type:
    Article
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    Common variants at 30 loci contribute to polygenic dyslipidemia.

    Published in:
    Nature Genetics, 2009, v. 41, n. 1, p. 56, doi. 10.1038/ng.291
    By:
    • Kathiresan, Sekar;
    • Willer, Cristen J.;
    • Peloso, Gina M;
    • Demissie, Serkalem;
    • Musunuru, Kiran;
    • Schadt, Eric E.;
    • Kaplan, Lee;
    • Bennett, Derrick;
    • Li, Yun;
    • Tanaka, Toshiko;
    • Voight, Benjamin F.;
    • Bonnycastle, Lori L.;
    • Jackson, Anne U.;
    • Crawford, Gabriel;
    • Surti, Aarti;
    • Guiducci, Candace;
    • Burtt, Noel P.;
    • Parish, Sarah;
    • Clarke, Robert;
    • Zelenika, Diana
    Publication type:
    Article
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    Systematic Cell-Based Phenotyping of Missense Alleles Empowers Rare Variant Association Studies: A Case for LDLR and Myocardial Infarction.

    Published in:
    PLoS Genetics, 2015, v. 11, n. 2, p. 1, doi. 10.1371/journal.pgen.1004855
    By:
    • Thormaehlen, Aenne S.;
    • Schuberth, Christian;
    • Won, Hong-Hee;
    • Blattmann, Peter;
    • Joggerst-Thomalla, Brigitte;
    • Theiss, Susanne;
    • Asselta, Rosanna;
    • Duga, Stefano;
    • Merlini, Pier Angelica;
    • Ardissino, Diego;
    • Lander, Eric S.;
    • Gabriel, Stacey;
    • Rader, Daniel J.;
    • Peloso, Gina M.;
    • Pepperkok, Rainer;
    • Kathiresan, Sekar;
    • Runz, Heiko
    Publication type:
    Article
    16

    Machine learning‐based clustering identifies obesity subgroups with differential multi‐omics profiles and metabolic patterns.

    Published in:
    Obesity (19307381), 2024, v. 32, n. 11, p. 2024, doi. 10.1002/oby.24137
    By:
    • Anwar, Mohammad Y.;
    • Highland, Heather;
    • Buchanan, Victoria Lynn;
    • Graff, Mariaelisa;
    • Young, Kristin;
    • Taylor, Kent D.;
    • Tracy, Russell P.;
    • Durda, Peter;
    • Liu, Yongmei;
    • Johnson, Craig W.;
    • Aguet, Francois;
    • Ardlie, Kristin G.;
    • Gerszten, Robert E.;
    • Clish, Clary B.;
    • Lange, Leslie A.;
    • Ding, Jingzhong;
    • Goodarzi, Mark O.;
    • Chen, Yii‐Der Ida;
    • Peloso, Gina M.;
    • Guo, Xiuqing
    Publication type:
    Article
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    Meta-analysis of gene-level tests for rare variant association.

    Published in:
    Nature Genetics, 2014, v. 46, n. 2, p. 200, doi. 10.1038/ng.2852
    By:
    • Liu, Dajiang J;
    • Peloso, Gina M;
    • Zhan, Xiaowei;
    • Holmen, Oddgeir L;
    • Zawistowski, Matthew;
    • Feng, Shuang;
    • Nikpay, Majid;
    • Auer, Paul L;
    • Goel, Anuj;
    • Zhang, He;
    • Peters, Ulrike;
    • Farrall, Martin;
    • Orho-Melander, Marju;
    • Kooperberg, Charles;
    • McPherson, Ruth;
    • Watkins, Hugh;
    • Willer, Cristen J;
    • Hveem, Kristian;
    • Melander, Olle;
    • Kathiresan, Sekar
    Publication type:
    Article
    19

    Common variants associated with plasma triglycerides and risk for coronary artery disease.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1345, doi. 10.1038/ng.2795
    By:
    • Do, Ron;
    • Willer, Cristen J;
    • Schmidt, Ellen M;
    • Sengupta, Sebanti;
    • Gao, Chi;
    • Peloso, Gina M;
    • Gustafsson, Stefan;
    • Kanoni, Stavroula;
    • Ganna, Andrea;
    • Chen, Jin;
    • Buchkovich, Martin L;
    • Mora, Samia;
    • Beckmann, Jacques S;
    • Bragg-Gresham, Jennifer L;
    • Chang, Hsing-Yi;
    • Demirkan, Ayşe;
    • Den Hertog, Heleen M;
    • Donnelly, Louise A;
    • Ehret, Georg B;
    • Esko, Tõnu
    Publication type:
    Article
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    Discovery and refinement of loci associated with lipid levels.

    Published in:
    Nature Genetics, 2013, v. 45, n. 11, p. 1274, doi. 10.1038/ng.2797
    By:
    • Willer, Cristen J;
    • Schmidt, Ellen M;
    • Sengupta, Sebanti;
    • Peloso, Gina M;
    • Gustafsson, Stefan;
    • Kanoni, Stavroula;
    • Ganna, Andrea;
    • Chen, Jin;
    • Buchkovich, Martin L;
    • Mora, Samia;
    • Beckmann, Jacques S;
    • Bragg-Gresham, Jennifer L;
    • Chang, Hsing-Yi;
    • Demirkan, Ayşe;
    • Den Hertog, Heleen M;
    • Do, Ron;
    • Donnelly, Louise A;
    • Ehret, Georg B;
    • Esko, Tõnu;
    • Feitosa, Mary F
    Publication type:
    Article
    21

    Non-linear machine learning models incorporating SNPs and PRS improve polygenic prediction in diverse human populations.

    Published in:
    Communications Biology, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42003-022-03812-z
    By:
    • Elgart, Michael;
    • Lyons, Genevieve;
    • Romero-Brufau, Santiago;
    • Kurniansyah, Nuzulul;
    • Brody, Jennifer A.;
    • Guo, Xiuqing;
    • Lin, Henry J.;
    • Raffield, Laura;
    • Gao, Yan;
    • Chen, Han;
    • de Vries, Paul;
    • Lloyd-Jones, Donald M.;
    • Lange, Leslie A.;
    • Peloso, Gina M.;
    • Fornage, Myriam;
    • Rotter, Jerome I.;
    • Rich, Stephen S.;
    • Morrison, Alanna C.;
    • Psaty, Bruce M.;
    • Levy, Daniel
    Publication type:
    Article
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    Genetic Loci Associated With COVID-19 Positivity and Hospitalization in White, Black, and Hispanic Veterans of the VA Million Veteran Program.

    Published in:
    Frontiers in Genetics, 2022, v. 12, p. 1, doi. 10.3389/fgene.2021.777076
    By:
    • Peloso, Gina M.;
    • Tcheandjieu, Catherine;
    • McGeary, John E.;
    • Posner, Daniel C.;
    • Ho, Yuk-Lam;
    • Zhou, Jin J.;
    • Hilliard, Austin T.;
    • Joseph, Jacob;
    • O'Donnell, Christopher J.;
    • Efird, Jimmy T.;
    • Crawford, Dana C.;
    • Wu, Wen-Chih;
    • Arjomandi, Mehrdad;
    • Sun, Yan V.;
    • Assimes, Themistocles L;
    • Huffman, Jennifer E.
    Publication type:
    Article
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    Genome-wide association analysis and Mendelian randomization proteomics identify drug targets for heart failure.

    Published in:
    Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-39253-3
    By:
    • Rasooly, Danielle;
    • Peloso, Gina M.;
    • Pereira, Alexandre C.;
    • Dashti, Hesam;
    • Giambartolomei, Claudia;
    • Wheeler, Eleanor;
    • Aung, Nay;
    • Ferolito, Brian R.;
    • Pietzner, Maik;
    • Farber-Eger, Eric H.;
    • Wells, Quinn Stanton;
    • Kosik, Nicole M.;
    • Gaziano, Liam;
    • Posner, Daniel C.;
    • Bento, A. Patrícia;
    • Hui, Qin;
    • Liu, Chang;
    • Aragam, Krishna;
    • Wang, Zeyuan;
    • Charest, Brian
    Publication type:
    Article
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    Association of Sickle Cell Trait With Chronic Kidney Disease and Albuminuria in African Americans.

    Published in:
    JAMA: Journal of the American Medical Association, 2014, v. 312, n. 20, p. 2115, doi. 10.1001/jama.2014.15063
    By:
    • Naik, Rakhi P.;
    • Derebail, Vimal K.;
    • Grams, Morgan E.;
    • Franceschini, Nora;
    • Auer, Paul L.;
    • Peloso, Gina M.;
    • Young, Bessie A.;
    • Lettre, Guillaume;
    • Peralta, Carmen A.;
    • Katz, Ronit;
    • Hyacinth, Hyacinth I.;
    • Quarells, Rakale C.;
    • Grove, Megan L.;
    • Bick, Alexander G.;
    • Fontanillas, Pierre;
    • Rich, Stephen S.;
    • Smith, Joshua D.;
    • Boerwinkle, Eric;
    • Rosamond, Wayne D.;
    • Kaoru Ito
    Publication type:
    Article
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    Association of Low-Density Lipoprotein Cholesterol-Related Genetic Variants With Aortic Valve Calcium and Incident Aortic Stenosis.

    Published in:
    JAMA: Journal of the American Medical Association, 2014, v. 312, n. 17, p. 1764, doi. 10.1001/jama.2014.13959
    By:
    • Smith, J. Gustav;
    • Luk, Kevin;
    • Schulz, Christina-Alexandra;
    • Engert, James C.;
    • Do, Ron;
    • Hindy, George;
    • Rukh, Gull;
    • Dufresne, Line;
    • Almgren, Peter;
    • Owens, David S.;
    • Harris, Tamara B.;
    • Peloso, Gina M.;
    • Kerr, Kathleen F.;
    • Wong, Quenna;
    • Smith, Albert V.;
    • Budoff, Matthew J.;
    • Rotter, Jerome I.;
    • Cupples, L. Adrienne;
    • Rich, Stephen;
    • Kathiresan, Sekar
    Publication type:
    Article
    28

    Additive Effect of Polymorphisms in the IL-6, LTA, and TNF-α Genes and Plasma Fatty Acid Level Modulate Risk for the Metabolic Syndrome and Its Components.

    Published in:
    Journal of Clinical Endocrinology & Metabolism, 2010, v. 95, n. 3, p. 1386, doi. 10.1210/jc.2009-1081
    By:
    • Phillips, Catherine M.;
    • Goumidi, Louisa;
    • Bertrais, Sandrine;
    • Ferguson, Jane F.;
    • Field, Martyn R.;
    • Kelly, Enda D.;
    • Mehegan, John;
    • Peloso, Gina M.;
    • Cupples, L. Adrienne;
    • Jian Shen;
    • Ordovas, Jose M.;
    • McManus, Ross;
    • Hercberg, Serge;
    • Portugal, Henri;
    • Lairon, Denis;
    • Planells, Richard;
    • Roche, Helen M.
    Publication type:
    Article
    29

    Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels.

    Published in:
    Nature Communications, 2015, v. 6, n. 3, p. 1, doi. 10.1038/ncomms7065
    By:
    • van Leeuwen, Elisabeth M.;
    • Karssen, Lennart C.;
    • Deelen, Joris;
    • Isaacs, Aaron;
    • Medina-Gomez, Carolina;
    • Mbarek, Hamdi;
    • Kanterakis, Alexandros;
    • Trompet, Stella;
    • Postmus, Iris;
    • Verweij, Niek;
    • van Enckevort, David J.;
    • Huffman, Jennifer E.;
    • White, Charles C.;
    • Feitosa, Mary F.;
    • Bartz, Traci M.;
    • Manichaikul, Ani;
    • Joshi, Peter K.;
    • Peloso, Gina M.;
    • Deelen, Patrick;
    • van Dijk, Freerk
    Publication type:
    Article
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    Expression quantitative trait methylation analysis elucidates gene regulatory effects of DNA methylation: the Framingham Heart Study.

    Published in:
    Scientific Reports, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41598-023-39936-3
    By:
    • Keshawarz, Amena;
    • Bui, Helena;
    • Joehanes, Roby;
    • Ma, Jiantao;
    • Liu, Chunyu;
    • Huan, Tianxiao;
    • Hwang, Shih-Jen;
    • Tejada, Brandon;
    • Sooda, Meera;
    • Courchesne, Paul;
    • Munson, Peter J.;
    • Demirkale, Cumhur Y.;
    • Yao, Chen;
    • Heard-Costa, Nancy L.;
    • Pitsillides, Achilleas N.;
    • Lin, Honghuang;
    • Liu, Ching-Ti;
    • Wang, Yuxuan;
    • Peloso, Gina M.;
    • Lundin, Jessica
    Publication type:
    Article
    32

    Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05975-y
    By:
    • Zekavat, Seyedeh M.;
    • Ruotsalainen, Sanni;
    • Handsaker, Robert E.;
    • Alver, Maris;
    • Bloom, Jonathan;
    • Poterba, Timothy;
    • Seed, Cotton;
    • Ernst, Jason;
    • Chaffin, Mark;
    • Engreitz, Jesse;
    • Peloso, Gina M.;
    • Manichaikul, Ani;
    • Yang, Chaojie;
    • Ryan, Kathleen A.;
    • Fu, Mao;
    • Johnson, W. Craig;
    • Tsai, Michael;
    • Budoff, Matthew;
    • Vasan, Ramachandran S.;
    • Cupples, L. Adrienne
    Publication type:
    Article
    33

    Deep-coverage whole genome sequences and blood lipids among 16,324 individuals.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-05747-8
    By:
    • Natarajan, Pradeep;
    • Peloso, Gina M.;
    • Zekavat, Seyedeh Maryam;
    • Montasser, May;
    • Ganna, Andrea;
    • Chaffin, Mark;
    • Khera, Amit V.;
    • Zhou, Wei;
    • Bloom, Jonathan M.;
    • Engreitz, Jesse M.;
    • Ernst, Jason;
    • O’Connell, Jeffrey R.;
    • Ruotsalainen, Sanni E.;
    • Alver, Maris;
    • Manichaikul, Ani;
    • Johnson, W. Craig;
    • Perry, James A.;
    • Poterba, Timothy;
    • Seed, Cotton;
    • Surakka, Ida L.
    Publication type:
    Article
    34

    Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-018-04668-w
    By:
    • Zekavat, Seyedeh M.;
    • Ruotsalainen, Sanni;
    • Handsaker, Robert E.;
    • Alver, Maris;
    • Bloom, Jonathan;
    • Poterba, Timothy;
    • Seed, Cotton;
    • Ernst, Jason;
    • Chaffin, Mark;
    • Engreitz, Jesse;
    • Peloso, Gina M.;
    • Manichaikul, Ani;
    • Yang, Chaojie;
    • Ryan, Kathleen A.;
    • Fu, Mao;
    • Johnson, W. Craig;
    • Tsai, Michael;
    • Budoff, Matthew;
    • Ramachandran, Vasan S.;
    • Cupples, L. Adrienne
    Publication type:
    Article
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    Genetic variants in CETP increase risk of intracerebral hemorrhage.

    Published in:
    2016
    By:
    • Anderson, Christopher D.;
    • Falcone, Guido J.;
    • Phuah, Chia‐Ling;
    • Radmanesh, Farid;
    • Brouwers, H. Bart;
    • Battey, Thomas W. K.;
    • Biffi, Alessandro;
    • Peloso, Gina M.;
    • Liu, Dajiang J.;
    • Ayres, Alison M.;
    • Goldstein, Joshua N.;
    • Viswanathan, Anand;
    • Greenberg, Steven M.;
    • Selim, Magdy;
    • Meschia, James F.;
    • Brown, Devin L.;
    • Worrall, Bradford B.;
    • Silliman, Scott L.;
    • Tirschwell, David L.;
    • Flaherty, Matthew L.
    Publication type:
    journal article
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    A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study.

    Published in:
    BMC Medical Genetics, 2007, v. 8, p. S17, doi. 10.1186/1471-2350-8-S1-S17
    By:
    • Kathiresan, Sekar;
    • Manning, Alisa K.;
    • Demissie, Serkalem;
    • D'Agostino, Ralph B.;
    • Surti, Aarti;
    • Guiducci, Candace;
    • Gianniny, Lauren;
    • Burtt, Nöel P.;
    • Melander, Olle;
    • Orho-Melander, Marju;
    • Arnett, Donna K.;
    • Peloso, Gina M.;
    • Ordovas, Jose M.;
    • Cupples, L. Adrienne
    Publication type:
    Article
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    Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries.

    Published in:
    2020
    By:
    • Zekavat, Seyedeh M.;
    • Ruotsalainen, Sanni;
    • Handsaker, Robert E.;
    • Alver, Maris;
    • Bloom, Jonathan;
    • Poterba, Timothy;
    • Seed, Cotton;
    • Ernst, Jason;
    • Chaffin, Mark;
    • Engreitz, Jesse;
    • Peloso, Gina M.;
    • Manichaikul, Ani;
    • Yang, Chaojie;
    • Ryan, Kathleen A.;
    • Fu, Mao;
    • Johnson, W. Craig;
    • Tsai, Michael;
    • Budoff, Matthew;
    • Vasan, Ramachandran S.;
    • Cupples, L. Adrienne
    Publication type:
    Correction Notice
    42

    Best Practices and Joint Calling of the HumanExome BeadChip: The CHARGE Consortium.

    Published in:
    PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0068095
    By:
    • Grove, Megan L.;
    • Yu, Bing;
    • Cochran, Barbara J.;
    • Haritunians, Talin;
    • Bis, Joshua C.;
    • Taylor, Kent D.;
    • Hansen, Mark;
    • Borecki, Ingrid B.;
    • Cupples, L. Adrienne;
    • Fornage, Myriam;
    • Gudnason, Vilmundur;
    • Harris, Tamara B.;
    • Kathiresan, Sekar;
    • Kraaij, Robert;
    • Launer, Lenore J.;
    • Levy, Daniel;
    • Liu, Yongmei;
    • Mosley, Thomas;
    • Peloso, Gina M.;
    • Psaty, Bruce M.
    Publication type:
    Article
    43

    Biological, clinical and population relevance of 95 loci for blood lipids.

    Published in:
    Nature, 2010, v. 466, n. 7307, p. 707, doi. 10.1038/nature09270
    By:
    • Teslovich, Tanya M.;
    • Musunuru, Kiran;
    • Smith, Albert V.;
    • Edmondson, Andrew C.;
    • Stylianou, Ioannis M.;
    • Koseki, Masahiro;
    • Pirruccello, James P.;
    • Ripatti, Samuli;
    • Chasman, Daniel I.;
    • Willer, Cristen J.;
    • Johansen, Christopher T.;
    • Fouchier, Sigrid W.;
    • Isaacs, Aaron;
    • Peloso, Gina M.;
    • Barbalic, Maja;
    • Ricketts, Sally L.;
    • Bis, Joshua C.;
    • Aulchenko, Yurii S.;
    • Thorleifsson, Gudmar;
    • Feitosa, Mary F.
    Publication type:
    Article
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    Functional Annotations‐Informed Whole Genome Sequence Analysis Identifies Novel Rare Variants for AD in the Alzheimer's Disease Sequencing Project.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2022, v. 18, n. 4, p. 1, doi. 10.1002/alz.063968
    By:
    • Lee, Songmi;
    • Shi, Bin;
    • Peloso, Gina M;
    • Wang, Yanbing;
    • Heard‐Costa, Nancy;
    • Lin, Honghuang;
    • Pitsillides, Achilleas N;
    • Sarnowski, Chloé;
    • Boerwinkle, Eric;
    • De Jager, Philip L;
    • Dupuis, Josée;
    • Seshadri, Sudha;
    • Wijsman, Ellen M;
    • DeStefano, Anita L.;
    • Fornage, Myriam
    Publication type:
    Article
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    Whole genome sequencing analysis of cognitively Wellderly individuals identifies potential protective genetic variants for Alzheimer's disease.

    Published in:
    Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2021, v. 17, n. 3, p. 1, doi. 10.1002/alz.054917
    By:
    • Peloso, Gina M;
    • Rosser, Morgan A;
    • Bis, Josh C;
    • Fornage, Myriam;
    • Boerwinkle, Eric;
    • Satizabal, Claudia L;
    • Psaty, Bruce M.;
    • Lopez, Oscar L.;
    • Mosley, Thomas H;
    • Wang, Yanbing;
    • Dupuis, Josée;
    • Destefano, Anita L.;
    • Seshadri, Sudha
    Publication type:
    Article