Resultados da pesquisa

Beyond Mendelian randomization: how to interpret evidence of shared genetic predictors Por Stephen Burgess, Adam S. Butterworth, John R. Thompson

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Disease-associated variants in different categories of disease located in distinct regulatory elements Por Meng Ma, Ru Ying, Ling-Shiang Chuang, Nai-Yun Hsu, Lisong Shi, Jörg Hakenberg, Wei‐Yi Cheng, Andrew Uzilov, Wei Ding, Benjamin S. Glicksberg, Rong Chen

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Genetics of Familial Amyotrophic Lateral Sclerosis Por Feneberg Emily, J. Joanna, Johnathan Cooper‐Knock, J. Pamela, Janine Kirby

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Genetics of cleft lip and cleft palate Por Elizabeth J. Leslie, Mary L. Marazita

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Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families Por Hanan E. Shamseldin, Maha Tulbah, Wesam Kurdi, Maha Nemer, Nada Alsahan, Elham Al Mardawi, Ola Khalifa, Amal Hashem, Ahmed M Kurdi, Zainab Babay, Dalal Bubshait, Niema Ibrahim, Firdous Abdulwahab, Zuhair Rahbeeni, Mais Hashem, Fowzan S. Alkuraya

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The epidemiology of retinitis pigmentosa in Denmark Por Marianne Haim

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The discovery of endogenous retroviruses Por Robin A. Weiss

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Molecular Pathogenesis of Renal Cell Carcinoma: A Review Por Israel Gomy, Wilson Arajo Silva

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Genetic basis of autoimmunity Por Alexander Marson, William Housley, David A. Hafler

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Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: a Mendelian randomisation analysis Por Daniel F. Freitag, Adam S. Butterworth, Peter Willeit, Joanna M. M. Howson, Stephen Burgess, Stephen Kaptoge, Robin Young, Weang-Kee Ho, Angela Wood, Michael Sweeting, Sarah Spackman, James R Staley, Anna Ramond, Eric L. Harshfield, Sune F. Nielsen, Peer Grande, Leslie A. Lange, Matthew J. Bown, Gregory T. Jones, Robert A. Scott, Steve Bevan, Eleonora Porcu, Gudmar Thorleifsson, Lingyao Zeng, Thorsten Kessler, Majid Nikpay, Ron Do, Weihua Zhang, Jemma C. Hopewell, Marcus E. Kleber, Graciela E. Delgado, Christopher P. Nelson, Anuj Goel, Joshua C. Bis, Abbas Dehghan, Symen Ligthart, Albert V. Smith, Liming Qu, Femke N. G. van ’t Hof, P. Bakker, Annette F. Baas, André van Rij, Gerard Tromp, Helena Kuivaniemi, Marylyn D. Ritchie, Shefali S. Verma, Dana C. Crawford, Jennifer Malinowski, Mariza de Andrade, Iftikhar J. Kullo, Peggy Peissig, Catherine A. McCarty, Erwin P. Böttinger, Omri Gottesman, David R. Crosslin, David Carrell, Laura J. Rasmussen‐Torvik, Jennifer A. Pacheco, Jie Huang, Nicholas J. Timpson, Johannes Kettunen, Mika Ala‐Korpela, Gary F. Mitchell, Afshin Parsa, Ian B. Wilkinson, Mathias Gorski, Yong Li, Nora Franceschini, Margaux F. Keller, Santhi K. Ganesh, Carl D. Langefeld, Lucie Bruijn, Matthew A. Brown, David M. Evans, Svetlana Baltic, Manuel A. R. Ferreira, Hansjörg Baurecht, Stephan Weidinger, Andre Franke, Steven A. Lubitz, Martina Müller‐Nurasyid, Janine F. Felix, Nicholas Smith, Marc Sudman, Susan D. Thompson, Eleftheria Zeggini, Kalliope Panoutsopoulou, Mike A. Nalls, Andrew Singleton, Constantin Polychronakos, Jonathan P. Bradfield, Hákon Hákonarson, Douglas F. Easton, Deborah J. Thompson, Ian Tomlinson, Malcolm G. Dunlop, Kari Hemminki, Gareth J. Morgan, Timothy Eisen, Hartmut Goldschmidt

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Hemoglobinopatias: hipótese da malária e efeito materno Por Antonio Sérgio Ramalho, Iara Duchovni-Silva

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Use of population isolates for mapping complex traits Por Leena Peltonen, Aarno Palotie, Kenneth Lange

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Gene with Quantitative Effect on Circulating Interferon Induced by Newcastle Disease Virus Por Edward De Maeyer, Jaqueline De Maeyer‐Guignard

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Clinical application of next-generation sequencing for Mendelian diseases Por Saumya Shekhar Jamuar, Ene‐Choo Tan

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Toward a Deeper Understanding of the Genetics of Bipolar Disorder Por Berit Kerner

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Molecular mapping in tropical maize (Zea mays L.) using microsatellite markers. 1. Map construction and localization of loci showing distorted segregation Por Sérgio Tadeu Sibov, Cláudio Lopes de Souza, Antônio Augusto Franco Garcia, Alexandre Garcia, ADELMO REZENDE SILVA, Claudete Aparecida Mangolin, Luciana Lasry Benchimol‐Reis, Anete Pereira de Souza

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Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations Por Javier T Granados-Riveron, Mark Pope, Frances Bu’Lock, Christopher Thornborough, Jacqueline Eason, Kerry Setchfield, Ami Ketley, Edwin P. Kirk, Diane Fatkin, Michael P. Feneley, Richard P. Harvey, J. David Brook

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Lipoprotein Subclass Profiling Reveals Pleiotropy in the Genetic Variants of Lipid Risk Factors for Coronary Heart Disease Por Peter Würtz, Antti J. Kangas, Pasi Soininen, Terho Lehtimäki, Mika Kähönen, Jorma Viikari, Olli T. Raitakari, Marjo‐Riitta Järvelin, George Davey Smith, Mika Ala‐Korpela

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Genetic and phenotypic characterization of capsule mutants of Cryptococcus neoformans Por E S Jacobson, D J Ayers, A. C. Harrell, Courtney Nicholas

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The Mechanism of Mendelian Heredity Por T. H. Morgan

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