genome-wide association study

  • Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy
    Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy
    Adam P. Levine, Melanie M.Y. Chan, Omid Sadeghi-Alavijeh, Edwin K.S. Wong, H. Terence Cook, Sofie Ashford, Keren Carss, Martin T. Christian, Matthew Hall, Claire Louise Harris, Paul McAlinden, Kevin J. Marchbank, Stephen D. Marks, Heather Maxwell, Karyn Megy, Christopher J. Penkett, Monika Mozere, Kathleen E. Stirrups, Salih Tuna, Julie Wessels, Deborah Whitehorn, MPGN/DDD/C3 Glomerulopathy Rare Disease Group, NIHR BioResource, Sally A. Johnson and Daniel P. Gale
    JASN January 2020, ASN.2019040433; DOI: https://doi.org/10.1681/ASN.2019040433
  • Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome
    Transethnic, Genome-Wide Analysis Reveals Immune-Related Risk Alleles and Phenotypic Correlates in Pediatric Steroid-Sensitive Nephrotic Syndrome
    Hanna Debiec, Claire Dossier, Eric Letouzé, Christopher E. Gillies, Marina Vivarelli, Rosemary K. Putler, Elisabet Ars, Evelyne Jacqz-Aigrain, Valery Elie, Manuela Colucci, Stéphanie Debette, Philippe Amouyel, Siham C. Elalaoui, Abdelaziz Sefiani, Valérie Dubois, Tabassome Simon, Matthias Kretzler, Jose Ballarin, Francesco Emma, Matthew G. Sampson, Georges Deschênes and Pierre Ronco
    JASN July 2018, 29 (7) 2000-2013; DOI: https://doi.org/10.1681/ASN.2017111185
  • Genetic Variants Associated with Circulating Parathyroid Hormone
    Cassianne Robinson-Cohen, Pamela L. Lutsey, Marcus E. Kleber, Carrie M. Nielson, Braxton D. Mitchell, Joshua C. Bis, Karen M. Eny, Laura Portas, Joel Eriksson, Mattias Lorentzon, Daniel L. Koller, Yuri Milaneschi, Alexander Teumer, Stefan Pilz, Maria Nethander, Elizabeth Selvin, Weihong Tang, Lu-Chen Weng, Hoi Suen Wong, Dongbing Lai, Munro Peacock, Anke Hannemann, Uwe Völker, Georg Homuth, Matthias Nauk, Federico Murgia, Jack W. Pattee, Eric Orwoll, Joseph M. Zmuda, Jose Antonio Riancho, Myles Wolf, Frances Williams, Brenda Penninx, Michael J. Econs, Kathleen A. Ryan, Claes Ohlsson, Andrew D. Paterson, Bruce M. Psaty, David S. Siscovick, Jerome I. Rotter, Mario Pirastu, Elizabeth Streeten, Winfried März, Caroline Fox, Josef Coresh, Henri Wallaschofski, James S. Pankow, Ian H. de Boer and Bryan Kestenbaum
    JASN May 2017, 28 (5) 1553-1565; DOI: https://doi.org/10.1681/ASN.2016010069
  • The Genetic Landscape of Renal Complications in Type 1 Diabetes
    Niina Sandholm, Natalie Van Zuydam, Emma Ahlqvist, Thorhildur Juliusdottir, Harshal A. Deshmukh, N. William Rayner, Barbara Di Camillo, Carol Forsblom, Joao Fadista, Daniel Ziemek, Rany M. Salem, Linda T. Hiraki, Marcus Pezzolesi, David Trégouët, Emma Dahlström, Erkka Valo, Nikolay Oskolkov, Claes Ladenvall, M. Loredana Marcovecchio, Jason Cooper, Francesco Sambo, Alberto Malovini, Marco Manfrini, Amy Jayne McKnight, Maria Lajer, Valma Harjutsalo, Daniel Gordin, Maija Parkkonen, The FinnDiane Study Group, Jaakko Tuomilehto, Valeriya Lyssenko, Paul M. McKeigue, Stephen S. Rich, Mary Julia Brosnan, Eric Fauman, Riccardo Bellazzi, Peter Rossing, Samy Hadjadj, Andrzej Krolewski, Andrew D. Paterson, The DCCT/EDIC Study Group, Jose C. Florez, Joel N. Hirschhorn, Alexander P. Maxwell, GENIE Consortium, David Dunger, Claudio Cobelli, Helen M. Colhoun, Leif Groop, Mark I. McCarthy and Per-Henrik Groop
    JASN February 2017, 28 (2) 557-574; DOI: https://doi.org/10.1681/ASN.2016020231