Rezultati - Ruth March

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  1. 1
    Susceptibility Locus for IgA Deficiency and Common Variable Immunodeficiency in the HLA-DR3, -B8, -A1 Haplotypes

    Susceptibility Locus for IgA Deficiency and Common Variable Immunodeficiency in the HLA-DR3, -B8, -A1 Haplotypes od Harry W. Schroeder, Zeng-Bian Zhu, Ruth March, R. Duncan Campbell, S.M. Berney, Sergei A. Nedospasov, Regina L. Turetskaya, T. Prescott Atkinson, Rodney C.P. Go, Max D. Cooper, John E. Volanakis

    Izdano 1998
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  2. 2
    Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans

    Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans od Susanna Lemmelä, Eleanor M. Wigmore, Christian Benner, Aki S. Havulinna, Rachel M. Y. Ong, Tibor Kempf, Kai C. Wollert, Stefan Blankenberg, Tanja Zeller, James E. Peters, Veikko Salomaa, Maria Fritsch, Ruth March, Aarno Palotie, Mark J. Daly, Adam S. Butterworth, Mervi Alanne-Kinnunen, Dirk S. Paul, Athena Matakidou

    Izdano 2022
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  3. 3
    Author response: Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans

    Author response: Integrated analyses of growth differentiation factor-15 concentration and cardiometabolic diseases in humans od Susanna Lemmelä, Eleanor M. Wigmore, Christian Benner, Aki S. Havulinna, Rachel M. Y. Ong, Tibor Kempf, Kai C. Wollert, Stefan Blankenberg, Tanja Zeller, James E. Peters, Veikko Salomaa, Maria Fritsch, Ruth March, Aarno Palotie, Mark J. Daly, Adam S. Butterworth, Mervi Kinnunen, Dirk S. Paul, Athena Matakidou

    Izdano 2022
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  4. 4
    Exome-Based Rare-Variant Analyses in CKD

    Exome-Based Rare-Variant Analyses in CKD od Sophia Cameron‐Christie, Charles J. Wolock, Emily Groopman, Slavé Petrovski, Sitharthan Kamalakaran, Gundula Povysil, Dimitrios Vitsios, Mengqi Zhang, Jan Fleckner, Ruth March, Sahar Gelfman, Maddalena Marasà, Yifu Li, Simone Sanna‐Cherchi, Krzysztof Kiryluk, Andrew S. Allen, Bengt Fellström, Carolina Haefliger, Adam Platt, David B. Goldstein, Ali G. Gharavi

    Izdano 2019
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  5. 5
    Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification

    Multiomic Characterization of High-Grade Serous Ovarian Carcinoma Enables High-Resolution Patient Stratification od Robert L. Hollis, Alison Meynert, Caroline O. Michie, Tzyvia Rye, Michael Churchman, Amelia Hallas-Potts, Ian Croy, W. Glenn McCluggage, Alistair Williams, Clare Bartos, Yasushi Iida, Aikou Okamoto, Brian Dougherty, J. Carl Barrett, Ruth March, Athena Matakidou, Patricia Roxburgh, Colin A. Semple, D. Paul Harkin, Richard D. Kennedy, C. Simon Herrington, Charlie Gourley

    Izdano 2022
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  6. 6
    Structural Variants at the<i>BRCA1/2</i>Loci are a Common Source of Homologous Repair Deficiency in High-grade Serous Ovarian Carcinoma

    Structural Variants at the<i>BRCA1/2</i>Loci are a Common Source of Homologous Repair Deficiency in High-grade Serous Ovarian Carcinoma od Ailith Ewing, Alison Meynert, Michael Churchman, Graeme R. Grimes, Robert L. Hollis, C. Simon Herrington, Tzyvia Rye, Clare Bartos, Ian Croy, Michelle Ferguson, Mairi Lennie, Trevor McGoldrick, Neil McPhail, Nadeem Siddiqui, Suzanne Dowson, Rosalind Glasspool, Melanie Mackean, Fiona Nussey, Brian McDade, Darren Ennis, Lynn McMahon, Athena Matakidou, Brian Dougherty, Ruth March, J. Carl Barrett, Iain A. McNeish, Andrew V. Biankin, Patricia Roxburgh, Charlie Gourley, Colin A. Semple

    Izdano 2021
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  7. 7
    Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases

    Characterising the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases od Jonathan Mitchell, Niedzica Camacho, Patrick R. Shea, Konrad H. Stopsack, Joseph Vijai, Oliver S. Burren, Ryan S. Dhindsa, Abhishek Nag, Jacob E. Berchuck, Amanda O’Neill, Ali Abbasi, Anthony W. Zoghbi, Jesús Alegre-Díaz, Pablo Kuri‐Morales, Jaime Berúmen, Roberto Tapia‐Conyer, Jonathan Emberson, Jason Torres, Rory Collins, Quanli Wang, David B. Goldstein, Athena Matakidou, Carolina Haefliger, Lauren Anderson-Dring, Ruth March, Vaidehi Jobanputra, Brian Dougherty, Keren Carss, Slavé Petrovski, Philip W. Kantoff, Kenneth Offit, Lorelei A. Mucci, Mark M. Pomerantz, Margarete A. Fabre

    Izdano 2024
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  8. 8
    Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases

    Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases od Jonathan Mitchell, Niedzica Camacho, Patrick R. Shea, Konrad H. Stopsack, Joseph Vijai, Oliver S. Burren, Ryan S. Dhindsa, Abhishek Nag, Jacob E. Berchuck, Amanda O’Neill, Ali Abbasi, Anthony W. Zoghbi, Jesús Alegre-Díaz, Pablo Kuri‐Morales, Jaime Berúmen, Roberto Tapia‐Conyer, Jonathan Emberson, Jason Torres, Rory Collins, Quanli Wang, David B. Goldstein, Athena Matakidou, Carolina Haefliger, Lauren Anderson-Dring, Ruth March, Vaidehi Jobanputra, Brian Dougherty, Keren Carss, Slavé Petrovski, Philip W. Kantoff, Kenneth Offit, Lorelei A. Mucci, Mark M. Pomerantz, Margarete A. Fabre

    Izdano 2025
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  9. 9
    Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences

    Genetic architecture of telomere length in 462,666 UK Biobank whole-genome sequences od Oliver S. Burren, Ryan S. Dhindsa, Sri V. V. Deevi, Sean Wen, Abhishek Nag, Jonathan Mitchell, Fengyuan Hu, Douglas P. Loesch, Katherine R. Smith, Neetu Razdan, Henric Olsson, Adam Platt, Dimitrios Vitsios, Qiang Wu, Rasmus Ågren, Lauren Anderson-Dring, Santosh S. Atanur, David H. Baker, Maria G. Belvisi, Mohammad Bohlooly‐Y, Lisa Buvall, Sophia Cameron‐Christie, E. Suzanne Cohen, Regina Fritsche Danielson, Shikta Das, Andrew Davis, Guillermo del Angel, Wei Ding, Brian Dougherty, Zammy Fairhurst-Hunter, Manik Garg, Benjamin Georgi, Carmen Guerrero Rangel, Andrew R. Harper, Carolina Haefliger, Mårten Hammar, Richard N. Hanna, Pernille Hansen, Jennifer Harrow, Ian Henry, Sonja Hess, Ben Hollis, Jiang Xiao, Kousik Kundu, Zhongwu Lai, Mark Lal, Glenda Lassi, Yupu Liang, Margarida Lopes, Eagle Lou, Kieren Lythgow, Stewart MacArthur, Meeta Maisuria-Armer, Ruth March, Carla Martins, Dorota Matelska, Karyn Mégy, Robert Menzies, Erik Michaëlsson, Fiona K. Middleton, Bill Mowrey, Daniel Muthas, Sean M. O’Dell, Erin Oerton, Yoichiro Ohne, Henric Olsson, Amanda O’Neill, Kristoffer Ostridge, Dirk S. Paul, Bram P. Prins, Benjamin Pullman, William Rae, Arwa Bin Raies, Anna Reznichenko, Xavier Romero Ros, Hitesh J. Sanganee, Ben S. Sidders, Mike Snowden, Stasa Stankovic, Helen Stevens, Ioanna Tachmazidou, Haeyam Taiy, Lifeng Tian, Christina Underwood, Coralie Viollet, Anna Walentinsson, Lily Wang, Qing‐Dong Wang, Eleanor Wheeler, Ahmet Zehir, Zoe Zou, Veryan Codd, Christopher P. Nelson, Nilesh J. Samani, Ruth March, Sebastian Wasilewski, Keren Carss, Margarete A. Fabre, Quanli Wang, Menelas N. Pangalos

    Izdano 2024
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  10. 10
    Diagnostic Utility of Exome Sequencing for Kidney Disease

    Diagnostic Utility of Exome Sequencing for Kidney Disease od Emily Groopman, Maddalena Marasà, Sophia Cameron‐Christie, Slavé Petrovski, Vimla S. Aggarwal, Hila Milo Rasouly, Yifu Li, Junying Zhang, Jordan G. Nestor, Priya Krithivasan, Wan Yee Lam, Adele Mitrotti, Stacy Piva, Byum Hee Kil, Debanjana Chatterjee, Rachel Reingold, Drew Bradbury, Michael DiVecchia, Holly Snyder, Xueru Mu, Karla Mehl, Olivia Balderes, David Fasel, Chunhua Weng, Jai Radhakrishnan, Pietro A. Canetta, Gerald B. Appel, Andrew S. Bomback, Wooin Ahn, Natalie Uy, Shumyle Alam, David Cohen, Russell J. Crew, Geoffrey K. Dube, Maya K. Rao, Sitharthan Kamalakaran, Brett Copeland, Zhong Ren, Joshua Bridgers, Colin D. Malone, Caroline M. Mebane, Neha Dagaonkar, Bengt Fellström, Carolina Haefliger, Sumit Mohan, Simone Sanna‐Cherchi, Krzysztof Kiryluk, Jan Fleckner, Ruth March, Adam Platt, David B. Goldstein, Ali G. Gharavi

    Izdano 2018
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  11. 11
    Rare variant contribution to human disease in 281,104 UK Biobank exomes

    Rare variant contribution to human disease in 281,104 UK Biobank exomes od Quanli Wang, Ryan S. Dhindsa, Keren Carss, Andrew R. Harper, Abhishek Nag, Ioanna Tachmazidou, Dimitrios Vitsios, Sri V. V. Deevi, Alex Mackay, Daniel Muthas, Michael Hühn, Susan J. Monkley, Henric Olsson, Bastian R. Angermann, Ronen Artzi, Carl Barrett, Maria G. Belvisi, Mohammad Bohlooly‐Y, Oliver S. Burren, Lisa Buvall, Benjamin Challis, Sophia Cameron‐Christie, E. Suzanne Cohen, Andrew Davis, Regina Fritsche Danielson, Brian Dougherty, Benjamin Georgi, Zara Ghazoui, Pernille Hansen, Fengyuan Hu, Magda Jeznach, Xiao Jiang, Chanchal Kumar, Zhongwu Lai, Glenda Lassi, Samuel H. Lewis, Bolan Linghu, Kieren Lythgow, Peter Maccallum, Carla Martins, Athena Matakidou, Erik Michaëlsson, Sven Moosmang, Sean M. O’Dell, Yoichiro Ohne, Joel Okae, Amanda O’Neill, Dirk S. Paul, Anna Reznichenko, Michael Snowden, Anna Walentinsson, Jorge Zeron, Menelas N. Pangalos, Sebastian Wasilewski, Katherine R. Smith, Ruth March, Adam Platt, Carolina Haefliger, Slavé Petrovski

    Izdano 2021
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  12. 12
    Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

    Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank od Joseph D. Szustakowski, Suganthi Balasubramanian, Erika Kvikstad, Shareef Khalid, Paola G. Bronson, Ariella Sasson, Emily H. M. Wong, Daren Liu, J. Wade Davis, Carolina Haefliger, A. Katrina Loomis, Rajesh Mikkilineni, Hyun Ji Noh, Samir Wadhawan, Xiaodong Bai, Alicia Hawes, Olga Krasheninina, Ricardo H. Ulloa, Alex E. Lopez, Erin N. Smith, Jeffrey F. Waring, Christopher D. Whelan, Ellen Tsai, John D. Overton, William Salerno, Howard J. Jacob, Sándor Szalma, Heiko Runz, Gregory Hinkle, Paul Nioi, Slavé Petrovski, Melissa Miller, Aris Baras, Lyndon J. Mitnaul, Jeffrey G. Reid, Oleg Moiseyenko, Carlos Garcia Rios, Saurabh Saha, Gonçalo R. Abecasis, Nilanjana Banerjee, Christina Beechert, Boris Boutkov, Michael Cantor, Giovanni Coppola, Aris N. Economides, Gisu Eom, Caitlin Forsythe, Erin D. Fuller, Zhenhua Gu, Lukas Habegger, Marcus B. Jones, Rouel Lanche, Michael Lattari, Michelle G. LeBlanc, Dadong Li, Luca A. Lotta, Kia Manoochehri, Adam J. Mansfield, Evan K. Maxwell, Jason Mighty, Mrunali Nafde, Sean O’Keeffe, Max Orelus, Maria Sotiropoulos Padilla, Razvan Panea, Tommy Polanco, Manasi Pradhan, Ayesha Rasool, Thomas D. Schleicher, Deepika Sharma, Alan R. Shuldiner, Jeffrey Staples, Cristopher V. Van Hout, Louis Widom, Sarah E. Wolf, Sally John, Chia‐Yen Chen, David Sexton, Varant Kupelian, Eric Marshall, T. Swan, Susan Eaton, Jimmy Z. Liu, Stephanie Loomis, Megan E. Jensen, Saranya Duraisamy, Jason Tetrault, David Merberg, Sunita Badola, Mark Reppell, Jason Grundstad, Xiuwen Zheng, Aimée M. Deaton, Margaret M. Parker, Lucas D. Ward, Alexander O. Flynn-Carroll, Caroline A. Austin, Ruth March, Menelas N. Pangalos, Adam Platt

    Izdano 2021
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  13. 13
    Rare variant associations with plasma protein levels in the UK Biobank

    Rare variant associations with plasma protein levels in the UK Biobank od Ryan S. Dhindsa, Oliver S. Burren, Benjamin B. Sun, Bram P. Prins, Dorota Matelska, Eleanor Wheeler, Jonathan Mitchell, Erin Oerton, Ventzislava A. Hristova, Katherine R. Smith, Keren Carss, Sebastian Wasilewski, Andrew R. Harper, Dirk S. Paul, Margarete A. Fabre, Heiko Runz, Coralie Viollet, Benjamin Challis, Adam Platt, Rasmus Ågren, Lauren Anderson-Dring, Santosh S. Atanur, David H. Baker, Carl Barrett, Maria G. Belvisi, Mohammad Bohlooly‐Y, Lisa Buvall, Niedzica Camacho, Lisa H. Cazares, Sophia Cameron‐Christie, Morris Chen, E. Suzanne Cohen, Regina Fritsche Danielson, Shikta Das, Andrew Davis, Sri Vishnu Vardhan Deevi, Wei Ding, Brian Dougherty, Zammy Fairhurst-Hunter, Manik Garg, Benjamin Georgi, Carmen Guerrero Rangel, Carolina Haefliger, Mårten Hammar, Richard N. Hanna, Pernille Hansen, Jennifer Harrow, Ian Henry, Sonja Hess, Ben Hollis, Fengyuan Hu, Xiao Jiang, Kousik Kundu, Zhongwu Lai, Mark Lal, Glenda Lassi, Yupu Liang, Margarida Lopes, Kieren Lythgow, Stewart MacArthur, Meeta Maisuria-Armer, Ruth March, Carla Martins, Karyn Mégy, Robert Menzies, Erik Michaëlsson, Fiona K. Middleton, Bill Mowrey, Daniel Muthas, Abhishek Nag, Sean M. O’Dell, Yoichiro Ohne, Henric Olsson, Amanda O’Neill, Kristoffer Ostridge, Benjamin Pullman, William Rae, Arwa Bin Raies, Anna Reznichenko, Xavier Romero Ros, Maria Ryaboshapkina, Hitesh J. Sanganee, Ben S. Sidders, Mike Snowden, Stasa Stankovic, Helen Stevens, Ioanna Tachmazidou, Haeyam Taiy, Lifeng Tian, Christina Underwood, Anna Walentinsson, Qing‐Dong Wang, Ahmet Zehir, Zoe Zou, Dimitrios Vitsios, Euan A. Ashley, Christopher D. Whelan, Menelas N. Pangalos, Quanli Wang, Slavé Petrovski

    Izdano 2023
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