نتائج البحث - Melissa Smart
- يعرض 1 - 19 نتائج من 19
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Novel DNA methylation profiles associated with key gene regulation and transcription pathways in blood and placenta of growth-restricted neonates حسب Sara Hillman, Sarah Finer, Melissa Smart, Christopher Mathews, Robert Lowe, Vardhman K. Rakyan, G. A. Hitman, David Williams
منشور في 2014Artigo -
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Is famine exposure during developmental life in rural Bangladesh associated with a metabolic and epigenetic signature in young adulthood? A historical cohort study حسب Sarah Finer, Mohd S. Iqbal, Robert Lowe, B Ogunkolade, Sonia Pervin, Christopher Mathews, Melissa Smart, Dewan S Alam, G. A. Hitman
منشور في 2016Artigo -
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Leveraging DNA-Methylation Quantitative-Trait Loci to Characterize the Relationship between Methylomic Variation, Gene Expression, and Complex Traits حسب Eilís Hannon, T.J. Gorrie-Stone, Melissa Smart, Joe Burrage, Amanda Hughes, Yanchun Bao, Meena Kumari, Leonard C. Schalkwyk, Jonathan Mill
منشور في 2018Artigo -
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Maternal gestational diabetes is associated with genome-wide DNA methylation variation in placenta and cord blood of exposed offspring حسب Sarah Finer, Christopher Mathews, Rob Lowe, Melissa Smart, Sara Hillman, L. Foo, Ajay Sinha, David Williams, Vardhman K. Rakyan, G. A. Hitman
منشور في 2015Artigo -
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BORIS, a paralogue of the transcription factor, CTCF, is aberrantly expressed in breast tumours حسب Vivien D'Arcy, Naresh Pore, France Docquier, Ziedulla Abdullaev, Igor Chernukhin, G-X Kita, Sushma Rai, Melissa Smart, Dawn Farrar, Svetlana Pack, Victor V. Lobanenkov, Elena Klenova
منشور في 2008Artigo -
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Systematic underestimation of the epigenetic clock and age acceleration in older subjects حسب Louis Y. El Khoury, T.J. Gorrie-Stone, Melissa Smart, Amanda Hughes, Yanchun Bao, Alexandria Andrayas, Joe Burrage, Eilís Hannon, Meena Kumari, Jonathan Mill, Leonard C. Schalkwyk
منشور في 2019Artigo -
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Genome-wide analysis of health-related biomarkers in the UK Household Longitudinal Study reveals novel associations حسب Bram P. Prins, Karoline Kuchenbaecker, Yanchun Bao, Melissa Smart, Delilah Zabaneh, Ghazaleh Fatemifar, Jian’an Luan, Nicholas J. Wareham, Robert A. Scott, John R. B. Perry, Claudia Langenberg, Michaela Benzeval, Meena Kumari, Eleftheria Zeggini
منشور في 2017Artigo -
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Vitamin B12 insufficiency induces cholesterol biosynthesis by limiting s-adenosylmethionine and modulating the methylation of SREBF1 and LDLR genes حسب Antonysunil Adaikalakoteswari, Sarah Finer, Philip Voyias, Ciara McCarthy, Manu Vatish, Jonathan D. Moore, Melissa Smart, Nahla Mohammed Bawazeer, Nasser M. Al‐Daghri, Philip G. McTernan, Sudhesh Kumar, G. A. Hitman, Ponnusamy Saravanan, Gyanendra Tripathi
منشور في 2015Artigo -
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Multivariate genome-wide analyses of the well-being spectrum حسب Bart M. L. Baselmans, Rick Jansen, Hill F. Ip, Jenny van Dongen, Abdel Abdellaoui, Margot P. van de Weijer, Yanchun Bao, Melissa Smart, Meena Kumari, Gonneke Willemsen, Jouke‐Jan Hottenga, Dorret I. Boomsma, Eco J. C. de Geus, Michel G. Nivard, Meike Bartels
منشور في 2019Revisão -
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The Relationship Between Plasma Angiopoietin-like Protein 4 Levels, Angiopoietin-like Protein 4 Genotype, and Coronary Heart Disease Risk حسب Melissa Smart, Marius R. Robciuc, Jackie A. Cooper, Matti Jauhiainen, Meena Kumari, Mika Kivimäki, Kay‐Tee Khaw, S. Matthijs Boekholdt, Nicholas J. Wareham, Tom R. Gaunt, Ian N. M. Day, Peter S. Braund, Christopher P. Nelson, Alistair S. Hall, Mark M. Iles, Steve E. Humphries, Christian Ehnholm, Philippa J. Talmud
منشور في 2010Revisão -
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Vitamin D and cognitive function: A Mendelian randomisation study حسب Jane Maddock, Ang Zhou, Alana Cavadino, Elżbieta Kuźma, Yanchun Bao, Melissa Smart, Kai-Uwe Saum, Ben Schöttker, Jorgen Engmann, Marie Kjærgaard, Ville Karhunen, Yiqiang Zhan, Terho Lehtimäki, Suvi P. Rovio, Liisa Byberg, Jari Lahti, Pedro Marques‐Vidal, Abhijit Sen, Laura Perna, Henrik Schirmer, Archana Singh‐Manoux, Juha Auvinen, Nina Hutri‐Kähönen, Mika Kähönen, Lena Kilander, Katri Räikkönen, Håkan Melhus, Erik Ingelsson, Idris Guessous, Katja Petrovic, Helena Schmidt, Reinhold Schmidt, Péter Vollenweider, Lars Lind, Johan G. Eriksson, Karl Michaëlsson, Olli T. Raitakari, Sara Hägg, Nancy L. Pedersen, Karl‐Heinz Herzig, Marjo‐Riitta Järvelin, Juha Veijola, Mika Kivimäki, Rolf Jorde, Hermann Brenner, Meena Kumari, Chris Power, David J. Llewellyn, Elina Hyppönen
منشور في 2017Revisão -
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Associations between common genetic variants and income provide insights about the socio-economic health gradient حسب Hyeokmoon Kweon, Casper A.P. Burik, Yuchen Ning, Rafael Ahlskog, Charley Xia, Erik Abner, Yanchun Bao, Laxmi Bhatta, Tariq Faquih, Maud de Feijter, Paul Fisher, Andrea Gelemanović, Alexandros Giannelis, Jouke‐Jan Hottenga, Bita Khalili, Yunsung Lee, Ruifang Li‐Gao, Jaan Masso, Ronny Myhre, Teemu Palviainen, Cornelius A. Rietveld, Alexander Teumer, Renske Verweij, Emily A. Willoughby, Esben Agerbo, Sven Bergmann, Dorret I. Boomsma, Anders D. Børglum, Ben Brumpton, Neil M Davies, Tõnu Esko, Scott D. Gordon, Georg Homuth, M. Arfan Ikram, Magnus Johannesson, Jaakko Kaprio, Michael P. Kidd, Zoltán Kutalik, Alex S. F. Kwong, James J. Lee, Annemarie I. Luik, Per Magnus, Pedro Marques‐Vidal, Nicholas G. Martin, Dennis O. Mook‐Kanamori, Preben Bo Mortensen, Sven Oskarsson, Emil M. Pedersen, Ozren Polašek, Frits R. Rosendaal, Melissa Smart, Harold Snieder, Peter J. van der Most, Péter Vollenweider, Henry Völzke, Gonneke Willemsen, Jonathan Beauchamp, Thomas A. DiPrete, Richard Karlsson Linnér, Qiongshi Lu, Tim Morris, Aysu Okbay, K. Paige Harden, Abdel Abdellaoui, W. David Hill, Ronald de Vlaming, Daniel J. Benjamin, Philipp Koellinger
منشور في 2025Artigo -
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Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals حسب James J. Lee, Robbee Wedow, Aysu Okbay, Edward Kong, Omeed Maghzian, Meghan Zacher, Tuan Anh Nguyen-Viet, Peter N. Bowers, Julia Sidorenko, Richard Karlsson Linnér, Mark Alan Fontana, Tushar Kundu, Chan Wook Lee, Hui Li, Ruoxi Li, Rebecca Royer, Pascal Timshel, Raymond K. Walters, Emily A. Willoughby, Loïc Yengo, Maris Alver, Yanchun Bao, David W. Clark, Felix R. Day, Nicholas A. Furlotte, Peter K. Joshi, Kathryn E. Kemper, Aaron Kleinman, Claudia Langenberg, Reedik Mägi, Joey W. Trampush, Shefali S. Verma, Yang Wu, Max Lam, Jing Hua Zhao, Zhili Zheng, Jason D. Boardman, Harry Campbell, Jeremy Freese, Kathleen Mullan Harris, Caroline Hayward, Pamela Herd, Meena Kumari, Todd Lencz, Jian’an Luan, Anil K. Malhotra, Andres Metspalu, Lili Milani, Ken K. Ong, John R. B. Perry, David J. Porteous, Marylyn D. Ritchie, Melissa Smart, Blair H. Smith, Joyce Y. Tung, Nicholas J. Wareham, James F. Wilson, Jonathan Beauchamp, Dalton Conley, Tõnu Esko, Steven F. Lehrer, Patrik K. E. Magnusson, Sven Oskarsson, Tune H. Pers, Matthew R. Robinson, Kevin Thom, Chelsea Watson, Christopher F. Chabris, Michelle N. Meyer, David Laibson, Jian Yang, Magnus Johannesson, Philipp Koellinger, Patrick Turley, Peter M. Visscher, Daniel J. Benjamin, David Cesarini
منشور في 2018Revisão -
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences حسب Richard Karlsson Linnér, Pietro Biroli, Edward Kong, S. Fleur W. Meddens, Robbee Wedow, Mark Alan Fontana, Maël P. Lebreton, Stephen P. Tino, Abdel Abdellaoui, Anke R. Hammerschlag, Michel G. Nivard, Aysu Okbay, Cornelius A. Rietveld, Pascal Timshel, Maciej Trzaskowski, Ronald de Vlaming, Christian Zünd, Yanchun Bao, Laura Buzdugan, Ann H. Caplin, Chia‐Yen Chen, Peter Eibich, Pierre Fontanillas, Juan R. González, Peter K. Joshi, Ville Karhunen, Aaron Kleinman, Remy Z. Levin, Christina M. Lill, Gerardus A. Meddens, Gerard Muntané, Sandra Sanchez‐Roige, Frank J.A. van Rooij, Erdogan Taskesen, Yang Wu, Futao Zhang, Adam Auton, Jason D. Boardman, David W. Clark, Andrew Conlin, Conor Dolan, Urs Fischbacher, Patrick J. F. Groenen, Kathleen Mullan Harris, Gregor Hasler, Albert Hofman, M. Arfan Ikram, Sonia Jain, Robert Karlsson, Ronald C. Kessler, Maarten Kooyman, James MacKillop, Minna Männikkö, Carlos Morcillo-Suárez, Matthew B. McQueen, Klaus M. Schmidt, Melissa Smart, Matthias Sutter, Roy Thurik, André G. Uitterlinden, Jon White, Harriet de Wit, Jian Yang, Lars Bertram, Dorret I. Boomsma, Tõnu Esko, Ernst Fehr, David A. Hinds, Magnus Johannesson, Meena Kumari, David Laibson, Patrik K. E. Magnusson, Michelle N. Meyer, Arcadi Navarro, Abraham A. Palmer, Tune H. Pers, Daniëlle Posthuma, Daniel Schunk, Murray B. Stein, Rauli Svento, Henning Tiemeier, Paul R. H. J. Timmers, Patrick Turley, Robert J. Ursano, Gert G. Wagner, James F. Wilson, Jacob Gratten, James J. Lee, David Cesarini, Daniel J. Benjamin, Philipp Koellinger, Jonathan Beauchamp
منشور في 2019Revisão -
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Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences<sup>1</sup> حسب Richard Karlsson Linnér, Pietro Biroli, Edward Kong, S. Fleur W. Meddens, Robbee Wedow, Mark Alan Fontana, Maël P. Lebreton, Abdel Abdellaoui, Anke R. Hammerschlag, Michel G. Nivard, Aysu Okbay, Cornelius A. Rietveld, Pascal Timshel, Stephen P. Tino, Maciej Trzaskowski, Ronald de Vlaming, Christian Zünd, Yanchun Bao, Laura Buzdugan, Ann H. Caplin, Chia‐Yen Chen, Peter Eibich, Pierre Fontanillas, Juan R Gonzalez, Peter K. Joshi, Ville Karhunen, Aaron Kleinman, Remy Z. Levin, Christina M. Lill, Gerardus A. Meddens, Gerard Muntané, Sandra Sanchez‐Roige, Frank J.A. van Rooij, Erdogan Taskesen, Yang Wu, Futao Zhang, Adam Auton, Jason D. Boardman, David W. Clark, Andrew Conlin, Conor Dolan, Urs Fischbacher, Patrick J. F. Groenen, Kathleen Mullan Harris, Gregor Hasler, Albert Hofman, M. Arfan Ikram, Sonia Jain, Robert Karlsson, Ronald C. Kessler, Maarten Kooyman, James MacKillop, Minna Männikkö, Carlos Morcillo-Suárez, Matthew B. McQueen, Klaus M. Schmidt, Melissa Smart, Matthias Sutter, Roy Thurik, André G. Uitterlinden, Jon White, Harriet de Wit, Jian Yang, Lars Bertram, Dorret I. Boomsma, Tõnu Esko, Ernst Fehr, David A. Hinds, Magnus Johannesson, Meena Kumari, David Laibson, Patrik K. E. Magnusson, Michelle N. Meyer, Arcadi Navarro, Abraham A. Palmer, Tune H. Pers, Daniëlle Posthuma, Daniel Schunk, Murray B. Stein, Rauli Svento, Henning Tiemeier, Paul R. H. J. Timmers, Patrick Turley, Robert J. Ursano, Gert G. Wagner, James F. Wilson, Jacob Gratten, James J. Lee, David Cesarini, Daniel J. Benjamin, Philipp Koellinger, Jonathan Beauchamp
منشور في 2018Pré-impressão -
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Associations of autozygosity with a broad range of human phenotypes حسب David W. Clark, Yukinori Okada, Kristjan H. S. Moore, Dan Mason, Nicola Pirastu, Ilaria Gandin, Hannele Mattsson, Catriona L. K. Barnes, Kuang Lin, Jing Hua Zhao, Patrick Deelen, Rebecca Rohde, Claudia Schurmann, Xiuqing Guo, Franco Giulianini, Weihua Zhang, Carolina Medina‐Gómez, Robert Karlsson, Yanchun Bao, Traci M. Bartz, Clemens Baumbach, Ginevra Biino, Matthew J. Bixley, Marco Brumat, Jin Fang Chai, Tanguy Corre, Diana L. Cousminer, Annelot M. Dekker, David Eccles, Kristel R. van Eijk, Christian Fuchsberger, He Gao, Marine Germain, Scott D. Gordon, Hugoline G. de Haan, Sarah E. Harris, Edith Hofer, Alicia Huerta-Chagoya, Catherine Igartua, Iris E. Jansen, Yucheng Jia, Tim Kacprowski, Torgny Karlsson, Marcus E. Kleber, Shengchao Alfred Li, Ruifang Li‐Gao, Anubha Mahajan, Koichi Matsuda, Karina Meidtner, Weihua Meng, May E. Montasser, Peter J. van der Most, Matthias Munz, Teresa Nutile, Teemu Palviainen, Gauri Prasad, Rashmi B. Prasad, Tallapragada Divya Sri Priyanka, Federica Rizzi, Erika Salvi, Bishwa R. Sapkota, Daniel Shriner, Line Skotte, Melissa Smart, Albert V. Smith, Ashley van der Spek, Cassandra N. Spracklen, Rona J. Strawbridge, Salman M. Tajuddin, Stella Trompet, Constance Turman, Niek Verweij, Clara Viberti, Lihua Wang, Helen R. Warren, Robyn E. Wootton, Lisa R. Yanek, Jie Yao, Noha A. Yousri, Wei Zhao, Adebowale Adeyemo, Saima Afaq, Carlos A. Aguilar‐Salinas, Masato Akiyama, Matthew L. Albert, Matthew Allison, Maris Alver, Tin Aung, Fereidoun Azizi, Amy R. Bentley, Heiner Boeing, Eric Boerwinkle, Judith B. Borja, Gert J. de Borst, Erwin P. Böttinger, Linda Broer, Harry Campbell, Stephen J. Chanock, Miao-Li Chee, Guanjie Chen
منشور في 2019Revisão -
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Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation حسب Josine L. Min, Gibran Hemani, Eilís Hannon, Koen F. Dekkers, Juan Castillo‐Fernandez, René Luijk, Elena Carnero‐Montoro, Daniel J. Lawson, Kimberley Burrows, Matthew Suderman, Andrew D. Bretherick, Tom G. Richardson, Johanna Klughammer, Valentina Iotchkova, Gemma C. Sharp, Ahmad Al Khleifat, Aleksey Shatunov, Alfredo Iacoangeli, Wendy L. McArdle, Karen Ho, Ashish Kumar, Cilla Söderhäll, Carolina Soriano‐Tárraga, Eva Giralt‐Steinhauer, Nabila Kazmi, Dan Mason, Allan F. McRae, David L. Corcoran, Karen Sugden, Silva Kasela, Alexia Cardona, Felix R. Day, Giovanni Cugliari, Clara Viberti, Simonetta Guarrera, Michael C. Lerro, Richa Gupta, Sailalitha Bollepalli, Pooja R. Mandaviya, Yanni Zeng, Toni‐Kim Clarke, Rosie M. Walker, Vanessa Schmoll, Darina Czamara, Carlos Ruiz-Arenas, Faisal I. Rezwan, Riccardo E. Marioni, Tian Lin, Yvonne Awaloff, Marine Germain, Dylan Aïssi, Ramona Zwamborn, Kristel van Eijk, Annelot M. Dekker, Jenny van Dongen, Jouke‐Jan Hottenga, Gonneke Willemsen, Cheng‐Jian Xu, Guillermo Barturen, Francesc Català‐Moll, Martin Kerick, Carol A. Wang, Phillip E. Melton, Hannah R. Elliott, Jean Shin, Manon Bernard, İdil Yet, Melissa Smart, T.J. Gorrie-Stone, Chris Shaw, Ammar Al‐Chalabi, Susan M. Ring, Göran Pershagen, Erik Melén, Jordi Jiménez‐Conde, Jaume Roquer, Debbie A. Lawlor, John Wright, Nicholas G. Martin, Grant W. Montgomery, Terrie E. Moffitt, Richie Poulton, Tõnu Esko, Lili Milani, Andres Metspalu, John R. B. Perry, Ken K. Ong, Nicholas J. Wareham, Giuseppe Matullo, Carlotta Sacerdote, Salvatore Panico, Avshalom Caspi, Louise Arseneault, France Gagnon, Miina Ollikainen, Jaakko Kaprio, Janine F. Felix, Fernando Rivadeneira, Henning Tiemeier, Marinus H. van IJzendoorn
منشور في 2021Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Gene
Genetics
Medicine
Genotype
DNA methylation
Gene expression
Single-nucleotide polymorphism
Genome-wide association study
Internal medicine
Genetic association
Bioinformatics
Epigenetics
Methylation
Pregnancy
Biochemistry
Computational biology
Demography
Evolutionary biology
Genome
Offspring
Sociology
Andrology
Computer science
Confounding
Cord blood
Developmental psychology
Endocrinology
Fetus
Genetic variants