Search Results - Omid Sadeghi‐Alavijeh
- Showing 1 - 9 results of 9
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Prevalence Estimates of Predicted Pathogenic COL4A3–COL4A5 Variants in a Population Sequencing Database and Their Implications for Alport Syndrome by Joel T. Gibson, Rachel Fieldhouse, Melanie Chan, Omid Sadeghi‐Alavijeh, Leslie Burnett, Valerio Izzi, Anton V. Persikov, Daniel P. Gale, Helen Storey, Judy Savige
Published 2021Artigo -
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Evaluation of a digitally-enabled care pathway for acute kidney injury management in hospital emergency admissions by Alistair Connell, Hugh Montgomery, Peter Martin, Claire Nightingale, Omid Sadeghi‐Alavijeh, Dominic King, Alan Karthikesalingam, Cían Hughes, Trevor Back, Kareem Ayoub, Mustafa Suleyman, Gareth Jones, Jennifer Cross, Sarah Stanley, Mary Emerson, Charles Merrick, Geraint Rees, Chris Laing, Rosalind Raine
Published 2019Artigo -
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Large-Scale Whole-Genome Sequencing Reveals the Genetic Architecture of Primary Membranoproliferative GN and C3 Glomerulopathy by Adam P. Levine, Melanie Chan, Omid Sadeghi‐Alavijeh, Edwin Wong, H. Terence Cook, Sofie Ashford, Keren Carss, Martin Christian, Matthew Hall, Claire L. Harris, Paul McAlinden, Kevin J. Marchbank, Stephen D. Marks, Heather Maxwell, Karyn Mégy, Christopher J. Penkett, Monika Mozere, Kathleen Stirrups, Salih Tuna, Julie Wessels, Deborah Whitehorn, Sally Johnson, Daniel P. Gale
Published 2020Artigo -
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Rare variants in the sodium-dependent phosphate transporter gene SLC34A3 explain missing heritability of urinary stone disease by Omid Sadeghi‐Alavijeh, Melanie Chan, Shabbir H. Moochhala, Sarah Howles, Daniel P. Gale, Detlef Böckenhauer, John C. Ambrose, Prabhu Arumugam, R. Bevers, Marta Bleda, F. Boardman-Pretty, C. R. Boustred, Helen Brittain, Mark J. Caulfield, G. C. Chan, Greg Elgar, Tom Fowler, Adam Giess, Angela Hamblin, Bingyang Shi, Tim Hubbard, R. Jackson, J. Louise Jones, Dalia Kasperavičiūtė, Melis Kayikci, Athanasios Kousathanas, L. Lahnstein, S. E. A. Leigh, I. U. S. Leong, Javier F. Lopez, F. Maleady-Crowe, Meriel McEntagart, Federico Minneci, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Peter O’Donovan, Chris A. Odhams, Christine Patch, Mariana Buongermino Pereira, D. Perez-Gil, J. Pullinger, T. Rahim, Augusto Rendon, Tim Rogers, K. Savage, Kushmita Sawant, Richard H. Scott, Afshan Siddiq, A. Sieghart, Samuel C. Smith, Alona Sosinsky, Alexander Stuckey, M. Tanguy, Ana Lisa Taylor Tavares, Ellen Thomas, Simon R. Thompson, Arianna Tucci, M. J. Welland, Eleanor Williams, Katarzyna Witkowska, S. M. Wood
Published 2023Artigo -
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Rare disease gene association discovery in the 100,000 Genomes Project by Valentina Cipriani, Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr, Katherine A. Benson, Marta Bértoli, Detlef Böckenhauer, Michael R. Bowl, Kate Burley, Li Chan, Patrick F. Chinnery, Peter J. Conlon, Marcos Abreu Costa, Alice E. Davidson, Sally J. Dawson, Elhussein A. Elhassan, Sarah E. Flanagan, Marta Futema, Daniel P. Gale, Sonia García-Ruiz, M. Cecilia Gonzalez Corcia, Helen Griffin, Sophie Hambleton, Amy R. Hicks, Henry Houlden, Richard S. Houlston, Sarah Howles, Robert Kleta, Iris Lekkerkerker, Siying Lin, Petra Lišková, Hannah M. Mitchison, Heba Morsy, Andrew Mumford, William G. Newman, Ruxandra Neatu, Edel A. O’Toole, Albert Ong, Alistair T. Pagnamenta, Shamima Rahman, Neil Rajan, Peter N. Robinson, Mina Ryten, Omid Sadeghi‐Alavijeh, John A. Sayer, Claire L. Shovlin, Jenny C. Taylor, Omri Teltsh, Ian Tomlinson, Arianna Tucci, Clare Turnbull, Albertien M. van Eerde, James S. Ware, Laura Watts, Andrew R. Webster, Sarah K. Westbury, Sean L. Zheng, Mark J. Caulfield, Damian Smedley
Published 2025Artigo -
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Genotype–phenotype correlations for COL4A3–COL4A5 variants resulting in Gly substitutions in Alport syndrome by Joel T. Gibson, Mary Huang, Marina Shenelli Croos Dabrera, Krushnam Shukla, H. Rothe, Pascale Hilbert, Constantinos Deltas, Helen Storey, Beata S. Lipska‐Ziętkiewicz, Melanie Chan, Omid Sadeghi‐Alavijeh, Daniel P. Gale, J. C. Ambrose, P. Arumugam, E. L. Baple, Marta Bleda, F. Boardman-Pretty, J. M. Boissiere, C. R. Boustred, Helen Brittain, Mark J. Caulfield, G. C. Chan, C. E. H. Craig, Louise C. Daugherty, Anna de Burca, A. Devereau, Greg Elgar, R. E. Foulger, Tom Fowler, Pedro Furió‐Tarí, A. Giess, J. M. Hackett, Dina Halai, Angela Hamblin, S. A. Henderson, J. E. Holman, Tim Hubbard, Kristina Ibáñez, R. Jackson, L. J. Jones, D. Kasperaviciute, Melis Kayikci, A. Kousathanas, L. Lahnstein, Kim Lawson, S. E. A. Leigh, Ivone Leong, F. J. Lopez, F. Maleady-Crowe, Joanne Mason, Ellen M. McDonagh, Loukas Moutsianas, Michael Mueller, Nirupa Murugaesu, Anna C. Need, Chris A. Odhams, Andrea Orioli, Christine Patch, D. Perez-Gil, Mariana Buongermino Pereira, Dimitris Polychronopoulos, J. Pullinger, T. Rahim, Augusto Rendon, Pablo Riesgo-Ferreiro, T. Rogers, Mina Ryten, K. Savage, K. Sawant, Richard H. Scott, A. Siddiq, A. Sieghart, D. Smedley, K. R. Smith, S. C. Smith, Alona Sosinsky, W. Spooner, H. E. Stevens, Alexander Stuckey, Razia Sultana Mohammad, M. Tanguy, Elaine Thomas, S. R. Thompson, Carolyn Tregidgo, Arianna Tucci, Edward E. Walsh, S. A. Watters, M. J. Welland, Eric O. Williams, Kate Witkowska, S. M. Wood, Magdalena Zarowiecki, Agnė Čerkauskaitė, Judy Savige
Published 2022Artigo -
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Cosmic Kidney Disease: The Effects of Spaceflight and Galactic Cosmic Radiation on Renal Structure and Function by Stephen B. Walsh, Keith Siew, Fatemeh Afsari, Maneera Al-Jaber, Noah Allen, Mohammed Al‐Maadheed, Selin Altınok, Shehbeel Arif, Nourdine Bah, Sergio E. Baranzini, Peter Barker, Afshin Beheshti, Elizabeth A. Blaber, Samuel Border, Valery Boyko, Jessica Broni-Tabi, Keith Burling, Robert G. Campbell, Margareth Cheng-Campbell, Chris Cheshire, Lorianna M. Colón, Sylvain V. Costes, Laura Cubitt, Viola D’Ambrosio, Lovorka Degoricija, Amelia J. Eisch, Hossein Fazelinia, Nichola Figg, Rebecca Finch, Jonathan Foox, Alison J. French, Jonathan M. Galazka, Samrawit Gebre, Peter Gordon, Alessandra Grillo, Nadia Houerbi, Hossein Valipour Kahrood, Fathi Karouia, Frederico Kiffer, JangKeun Kim, Aleksandra S. Klosinska, Angela Kubik, Han-Chung Lee, Yinghui Li, Zhongwang Li, Nicholas Lucarelli, Steven Lynham, Anthony L. Marullo, Christopher E. Mason, Irina Matei, Cem Meydan, Sayat Mimar, Vidya Mohamed‐Ali, Masafumi Muratani, Ahmed M. Naglah, Charlotte Nelson, Kevin Nestler, Jérôme Nicod, Kevin M. O’Shaughnessy, Lorraine Christine De Oliveira, Leah Oswalt, Eliah Overbey, Vaksha Patel, Laura Pătraș, San-Huei Lai Polo, María Rodríguez‐López, Samuel G. Rodriques, Candice Roufosse, Omid Sadeghi‐Alavijeh, Rebekah Sanchez‐Hodge, Lauren Sanders, Anindya Sankar, Pinaki Sarder, Jonathan C. Schisler, Ralf B. Schittenhelm, Annalise Schweickart, Ryan T. Scott, Dai Shiba, Terry C.C. Lim Kam Sian, Wilian A. Silveira, Hubert Slawinski, Scott M. Smith, Daniel M. Snell, Julio Sosa, Joel R. Steele, Marshall Tabetah, Erwin Tanuwidjaya, Akira Uruno, Michael Vaughan, Simon Walker‐Samuel, Elizabeth R Wan, Masayuki Yamamoto, Xiaoping Yang, Yasmin Yasmin, Sanghee Yun, Haijian Zhang, Zhongquan Dai, Jasminka Zimmermann, Sara R. Zwart, Eduardo Almeida
Published 2023Pré-impressão -
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Cosmic kidney disease: an integrated pan-omic, physiological and morphological study into spaceflight-induced renal dysfunction by Keith Siew, Kevin Nestler, Charlotte Nelson, Viola D’Ambrosio, Chutong Zhong, Zhongwang Li, Alessandra Grillo, Elizabeth R Wan, Vaksha Patel, Eliah Overbey, JangKeun Kim, Sanghee Yun, Michael Vaughan, Chris Cheshire, Laura Cubitt, Jessica Broni-Tabi, Maneera Al-Jaber, Valery Boyko, Cem Meydan, Peter Barker, Shehbeel Arif, Fatemeh Afsari, Noah Allen, Mohammed Al‐Maadheed, Selin Altınok, Nourdine Bah, Samuel Border, Amanda Brown, Keith Burling, Margareth Cheng-Campbell, Lorianna M. Colón, Lovorka Degoricija, Nichola Figg, Rebecca Finch, Jonathan Foox, Pouya Faridi, Alison J. French, Samrawit Gebre, Peter Gordon, Nadia Houerbi, Hossein Valipour Kahrood, Frederico Kiffer, Aleksandra S. Klosinska, Angela Kubik, Han-Chung Lee, Yinghui Li, Nicholas Lucarelli, Anthony L. Marullo, Irina Matei, Colleen McCann, Sayat Mimar, Ahmed M. Naglah, Jérôme Nicod, Kevin M. O’Shaughnessy, Lorraine Christine De Oliveira, Leah Oswalt, Laura Pătraș, San-Huei Lai Polo, María Rodríguez‐López, Candice Roufosse, Omid Sadeghi‐Alavijeh, Rebekah Sanchez‐Hodge, Anindya S. Paul, Ralf B. Schittenhelm, Annalise Schweickart, Ryan T. Scott, Terry C.C. Lim Kam Sian, Willian A. da Silveira, Hubert Slawinski, Daniel M. Snell, Julio Sosa, Amanda Saravia-Butler, Marshall Tabetah, Erwin Tanuwidjaya, Simon Walker‐Samuel, Xiaoping Yang, Yasmin Yasmin, Haijian Zhang, Jasminka Godovac‐Zimmermann, Pinaki Sarder, Lauren Sanders, Sylvain V. Costes, Robert A. A. Campbell, Fathi Karouia, Vidya Mohamed-Alis, Samuel G. Rodriques, Steven Lynham, Joel R. Steele, Sergio E. Baranzini, Hossein Fazelinia, Zhongquan Dai, Akira Uruno, Dai Shiba, Masayuki Yamamoto, Eduardo Almeida, Elizabeth A. Blaber, Jonathan C. Schisler, Amelia J. Eisch, Masafumi Muratani, Sara R. Zwart
Published 2024Artigo
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Medicine
Biology
Gene
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Genetics
Internal medicine
Endocrinology
Genotype
Glomerulonephritis
Acute kidney injury
Alport syndrome
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Compound heterozygosity
Computational biology
Creatinine
Disease
Emergency medicine
Environmental health
Genetic association
Genome
Genome-wide association study
Intensive care medicine
Kidney disease
Mendelian inheritance
Nephron
Physics
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Renal replacement therapy
Single-nucleotide polymorphism
Spaceflight