يعرض 1 - 10 نتائج من 39 نتيجة بحث عن '"Ming-Huei Chen"', وقت الاستعلام: 1.08s تنقيح النتائج
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    المصدر: Am J Hum Genet

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    المساهمون: Bordeaux population health (BPH), Université de Bordeaux (UB)-Institut de Santé Publique, d'Épidémiologie et de Développement (ISPED)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre recherche en CardioVasculaire et Nutrition = Center for CardioVascular and Nutrition research (C2VN), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE)

    المصدر: American Journal of Human Genetics
    American Journal of Human Genetics, Elsevier (Cell Press), In press, 107 (2), pp.211-221. ⟨10.1016/j.ajhg.2020.06.008⟩
    American Journal of Human Genetics, In press, 107 (2), pp.211-221. ⟨10.1016/j.ajhg.2020.06.008⟩
    Am J Hum Genet
    Rodriguez, B A T, Bhan, A, Beswick, A, Elwood, P C, Niiranen, T J, Salomaa, V, Trégouët, D-A, Morange, P-E, Civelek, M, Ben-Shlomo, Y, Schlaeger, T, Chen, M-H & Johnson, A D 2020, ' A Platelet Function Modulator of Thrombin Activation Is Causally Linked to Cardiovascular Disease and Affects PAR4 Receptor Signaling ', American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2020.06.008Test

    وصف الملف: application/pdf

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    المصدر: Human molecular genetics, vol 26, iss 11

    وصف الملف: application/pdf

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    المساهمون: Epidemiology, Internal Medicine

    المصدر: Nature genetics
    Pankratz, N, Schick, U M, Zhou, Y, Zhou, W, Ahluwalia, T S, Allende, M L, Auer, P L, Bork-Jensen, J, Brody, J A, Chen, M H, Clavo, V, Eicher, J D, Grarup, N, Hagedorn, E J, Hu, B, Hunker, K, Johnson, A D, Leusink, M, Lu, Y, Lyytikainen, L P, Manichaikul, A, Marioni, R, Nalls, M A, Pazoki, R, Smith, A V, Van Rooij, F J A, Yang, M L, Zhang, X, Zhang, Y, Asselbergs, F W, Boerwinkle, E, Borecki, I B, Bottinger, E P, Cushman, M, De Bakker, P I W, Deary, I, Dong, L, Feitosa, M F, Floyd, J S, Franceschini, N, Franco, O H, Garcia, M E, Grove, M L, Gudnason, V, Hansen, T, Harris, T B, Hofman, A, Jackson, R D, Jia, J, Kahonen, M, Launer, L J, Lehtimaki, T, Liewald, D, Linneberg, A, Liu, Y, Loos, R J F, Nguyen, V M, Numans, M E, Pedersen, O, Psaty, B M, Raitakari, O T, Rich, S S, Rivadeneira, F, Di Sant, A M R, Rotter, J I, Starr, J, Taylor, K D, Thuesen, B H, Tracy, R P, Uitterlinden, A G, Wang, J, Wang, J, Dehghan, A, Huo, Y, Adrienne Cupples, L, Wilson, J G, Proia, R L, Zon, L I, O'Donnell, C J, Reiner, A P & Ganesh, S K 2016, ' Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits ', Nature Genetics, vol. 48, no. 8, pp. 867-876 . https://doi.org/10.1038/ng.3607Test
    Nature Genetics, 48(8), 867. Nature Publishing Group
    Nature Genetics, 48(8), 867-876. Nature Publishing Group
    Nature Genetics, 48(8), 867

    وصف الملف: image/pdf; application/vnd.openxmlformats-officedocument.wordprocessingml.document

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    المؤلفون: Anne-Claire Vergnaud, Nauder Faraday, Tim Kacprowski, Lisa R. Yanek, Oscar H. Franco, Yongmei Liu, Andreas Greinacher, Gina M. Peloso, Cristen J. Willer, Leslie A. Lange, Eric S. Torstenson, Reedik Mägi, Jeanette Erdmann, Ethan M. Lange, Deborah A. Nickerson, Henry Völzke, David R. Crosslin, Gunnar Engström, Albert V. Smith, André G. Uitterlinden, Salman M. Tajuddin, W. David Hill, Diane M. Becker, Paul Elliot, Caterina Vacchi-Suzzi, Linda M. Polfus, Traci M. Bartz, Nathalie Chami, Abbas Dehghan, Mike A. Nalls, John D. Eicher, Leo-Pekka Lyytikäinen, Evelin Mihailov, Uwe Völker, Caroline Hayward, Ioanna Tzoulaki, Myriam Fornage, Marju Orho-Melander, Mary Cushman, Lars Wallentin, Terho Lehtimäki, Ayush Giri, Laura M. Raffield, Lewis C. Becker, Yingchang Lu, Emma Raitoharju, Sekar Kathiresan, Simon de Denus, Ruth J. F. Loos, James S. Floyd, Dawn M. Waterworth, James G. Wilson, Nathan Pankratz, Lenore J. Launer, Andrew D. Johnson, Andrew J. Slater, Jean-Claude Tardif, Raha Pazoki, Evangelos Evangelou, Kenneth Rice, Harvey D. White, Marie-Pierre Dubé, Frank J. A. van Rooij, Akihiro Nomura, Tamara B. Harris, Vilmundur Gudnason, Gonçalo R. Abecasis, Alan B. Zonderman, Guillaume Lettre, Todd L. Edwards, Amber A. Burt, Ani Manichaikul, Heribert Schunkert, Ming-Huei Chen, Ian J. Deary, Michelle L. O'Donoghue, Jennifer A. Brody, Russell P. Tracy, Tõnu Esko, Mika Kähönen, Panos Deloukas, Eric Boerwinkle, Rasika A. Mathias, Dajiang J. Liu, Jin Li, Santhi K. Ganesh, David C. Liewald, Paul L. Auer, Digna R. Velez Edwards, Erwin P. Bottinger, Nina Mononen, Claudia Schurmann, Michele K. Evans, John M. Starr, Thomas Thiele, Jussi Hernesniemi, Jerome I. Rotter, Rakale C. Quarells, He Gao, Kjell Nikus, Stephen S. Rich, Heather M. Highland, Bruce M. Psaty, Ursula M. Schick, Andres Metspalu, Melissa A. Richard, Neil A. Zakai, Olle Melander, John D. Rioux, Olli T. Raitakari, Alexander P. Reiner, Joel N. Hirschhorn, Nilesh J. Samani

    المساهمون: Epidemiology, Internal Medicine, Home Office, National Institute for Health Research, Medical Research Council (MRC)

    المصدر: American Journal of Human Genetics, 99(1), 40-55. Cell Press
    Eicher, J D, Chami, N, Kacprowski, T, Nomura, A, Chen, M-H, Yanek, L R, Tajuddin, S M, Schick, U M, Slater, A J, Pankratz, N, Polfus, L, Schurmann, C, Giri, A, Brody, J A, Lange, L A, Manichaikul, A, Hill, W D, Pazoki, R, Elliot, P, Evangelou, E, Tzoulaki, I, Gao, H, Vergnaud, A-C, Mathias, R A, Becker, D M, Becker, L C, Burt, A, Crosslin, D R, Lyytikäinen, L-P, Nikus, K, Hernesniemi, J, Kähönen, M, Raitoharju, E, Mononen, N, Raitakari, O T, Lehtimäki, T, Cushman, M, Zakai, N A, Nickerson, D A, Raffield, L M, Quarells, R, Willer, C J, Peloso, G M, Abecasis, G R, Liu, D J, Deloukas, P, Starr, J M, Liewald, D C M & Hayward, C & Deary, I J 2016, ' Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals ', American Journal of Human Genetics, vol. 99, no. 1, pp. 40-55 . https://doi.org/10.1016/j.ajhg.2016.05.005Test
    The American Journal of Human Genetics

    وصف الملف: application/vnd.openxmlformats-officedocument.wordprocessingml.document

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    المساهمون: Home Office, National Institute for Health Research, Imperial College Healthcare NHS Trust- BRC Funding, Medical Research Council (MRC)

    المصدر: PLoS Genetics, Vol 13, Iss 8, p e1006925 (2017)
    PLoS Genetics