Хайлтын үр дүнгүүд - Garan Jones
- 5-н 1 - 5 үр дүнгүүдийг харуулж байна
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Common conditions associated with hereditary haemochromatosis genetic variants: cohort study in UK Biobank -н Luke C. Pilling, Jone Tamosauskaite, Garan Jones, Andrew R. Wood, Lindsay Jones, Chai-Ling Kuo, George A. Kuchel, Luigi Ferrucci, David Melzer
Хэвлэсэн 2019Artigo -
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Dominant ER Stress–Inducing <i>WFS1</i> Mutations Underlie a Genetic Syndrome of Neonatal/Infancy-Onset Diabetes, Congenital Sensorineural Deafness, and Congenital Cataracts -н Elisa De Franco, Sarah E. Flanagan, Takuya Yagi, Damien Abreu, Jana Mahadevan, Matthew B. Johnson, Garan Jones, Fernanda Acosta, Mphele Mulaudzi, Ngee Lek, Vera Oh, Oliver Petz, Richard Caswell, Sian Ellard, Fumihiko Urano, Andrew T. Hattersley
Хэвлэсэн 2017Artigo -
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Diagnosis of lethal or prenatal‐onset autosomal recessive disorders by parental exome sequencing -н Karen Stals, Matthew N. Wakeling, Júlia Baptista, Richard Caswell, Andrew Parrish, Julia Rankin, Carolyn Tysoe, Garan Jones, Adam C. Gunning, Hana Lango Allen, Lisa Bradley, Angela F. Brady, Helena Carley, Jenny Carmichael, Bruce Castle, Deirdre Cilliers, Helen Cox, Charu Deshpande, Abhijit Dixit, Jacqueline Eason, Frances Elmslie, Andrew E. Fry, Alan Fryer, Muriel Holder, Tessa Homfray, Emma Kivuva, Victoria McKay, Ruth Newbury‐Ecob, Michael Parker, Ravi Savarirayan, Claire Searle, Nora Shannon, Deborah Shears, Sarah Smithson, Ellen Thomas, Peter D. Turnpenny, Vinod Varghese, Pradeep Vasudevan, Emma Wakeling, Emma L. Baple, Sian Ellard
Хэвлэсэн 2017Artigo -
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Genome-wide meta-analysis of muscle weakness identifies 15 susceptibility loci in older men and women -н Garan Jones, Katerina Trajanoska, Adam J. Santanasto, Najada Stringa, Chia‐Ling Kuo, Janice L. Atkins, Joshua R. Lewis, ThuyVy Duong, Shengjun Hong, Mary L. Biggs, Jian’an Luan, Chloé Sarnowski, Kathryn L. Lunetta, Toshiko Tanaka, Mary K. Wojczynski, Ryan Cvejkus, Maria Nethander, Sahar Ghasemi, Jingyun Yang, M. Carola Zillikens, Stefan Walter, Kamil Sicinski, Érika Kague, Cheryl L. Ackert‐Bicknell, Dan E. Arking, B. Gwen Windham, Eric Boerwinkle, Megan L. Grove, Misa Graff, Dominik Spira, Ilja Demuth, Nathalie van der Velde, C.P.G.M. de Groot, Bruce M. Psaty, Michelle C. Odden, Alison E. Fohner, Claudia Langenberg, Nicholas J. Wareham, Stefania Bandinelli, Natasja M. van Schoor, Martijn Huisman, Qihua Tan, Joseph M. Zmuda, Dan Mellström, Magnus K. Karlsson, David A. Bennett, Aron S. Buchman, Philip L. De Jager, André G. Uitterlinden, Uwe Völker, Thomas Kocher, Alexander Teumer, Leocadio Rodríguez‐Mañas, Francisco J. García‐García, José Antonio Carranza Carnicero, Pamela Herd, Lars Bertram, Claes Ohlsson, Joanne M. Murabito, David Melzer, George A. Kuchel, Luigi Ferrucci, David Karasik, Fernando Rivadeneira, Douglas P. Kiel, Luke C. Pilling
Хэвлэсэн 2021Revisão
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Gene
Genetics
Medicine
Internal medicine
Computational biology
Exome sequencing
Genome
Genotype
Mutation
Anatomy
Audiology
Bacteria
Biobank
Bioinformatics
Carrier testing
Cataracts
Cohort
Cohort study
Compound heterozygosity
Demography
Diabetes mellitus
Endocrinology
Etiology
Evolutionary biology
Exome
Fetus
Genetic counseling
Genetic testing
Genetic variants