Zobrazeno 1 - 10
of 416
pro vyhledávání: '"Michelle, Ward"'
Autor:
Alison Eyre, Janice Cohen, Sarah Funnell, Lynsey James, Sheena Guglani, Hounaida Abi Haidar, Lindy Samson, Michelle Ward, Radha Jetty, Megan Harrison, John S. Lyons, Leigh Fraser-Roberts, Susan Bennett, Douglas Archibald, Soha Khorsand, Tobey Audcent
Publikováno v:
BMC Pediatrics, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Complex social determinants of health may not be easily recognized by health care providers and pose a unique challenge in the vulnerable pediatric population where patients may not be able to advocate for themselves. The goal of
Externí odkaz:
https://doaj.org/article/8308f592b56f4940b61411da19cfa2ae
Autor:
Gareth S. Kindler, Alexander M. Kusmanoff, Stephen Kearney, Michelle Ward, Richard A. Fuller, Thomas J. Lloyd, Sarah A. Bekessy, Emily A. Gregg, Romola Stewart, James E. M. Watson
Publikováno v:
Conservation Science and Practice, Vol 6, Iss 9, Pp n/a-n/a (2024)
Abstract Many of the proposed solutions to the global biodiversity crisis rely on national governments to act. The conservation movement needs to motivate governments or face an ongoing extinction crisis. Here we explore how linking biodiversity to e
Externí odkaz:
https://doaj.org/article/5dc08518eaf94cb59f09864536cd54cc
Shifting baselines clarify the impact of contemporary logging on forest‐dependent threatened species
Autor:
Michelle Ward, Kita Ashman, David B. Lindenmayer, Sarah Legge, Gareth Kindler, Timothy Cadman, Rachel Fletcher, Nick Whiterod, Mark Lintermans, Philip Zylstra, Romola Stewart, Hannah Thomas, Stuart Blanch, James E. M. Watson
Publikováno v:
Conservation Science and Practice, Vol 6, Iss 9, Pp n/a-n/a (2024)
Abstract Despite the importance of protecting forests and woodlands to achieve global climate and biodiversity goals, logging impacts persist worldwide. Forestry advocates often downplay these impacts but rarely consider the cumulative threat defores
Externí odkaz:
https://doaj.org/article/ad2f16103be147f0bc45a9dfaa644fda
Publikováno v:
Conservation Science and Practice, Vol 6, Iss 9, Pp n/a-n/a (2024)
Abstract Climate and land‐use change pose unprecedented threats to ecosystems, economies, and communities worldwide. To help mitigate the climate crisis, restoration is a rapidly growing industry used to offset carbon emissions. The most common app
Externí odkaz:
https://doaj.org/article/a5e2e1a4e8714d46b4672d5b3bf594fb
Autor:
Vanessa S. Fear, Catherine A. Forbes, Nicole C. Shaw, Kathryn O. Farley, Jessica L. Mantegna, Jasmin P. Htun, Genevieve Syn, Helena Viola, Henrietta Cserne Szappanos, Livia Hool, Michelle Ward, Gareth Baynam, Timo Lassmann
Publikováno v:
Stem Cell Research & Therapy, Vol 14, Iss 1, Pp 1-14 (2023)
Abstract Background Genomic sequencing in congenital heart disease (CHD) patients often discovers novel genetic variants, which are classified as variants of uncertain significance (VUS). Functional analysis of each VUS is required in specialised lab
Externí odkaz:
https://doaj.org/article/49a28e30727a4fc5a4c6a4dea486bcd8
Autor:
Kirsten Boggs, Fiona Lynch, Michelle Ward, Sophie E. Bouffler, Samantha Ayres, Robin Forbes, Amanda Springer, Michelle G. de Silva, Elly Lynch, Lyndon Gallacher, Tenielle Davis, Ana Rakonjac, Kirsty Stallard, Gemma R. Brett, Zornitza Stark
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 101878- (2024)
Genetic counselors (GCs) face unique challenges in the acute care setting. Acute care environments—such as neonatal and pediatric intensive care units—are characterized by urgency, complexity, and rapid decision making. These settings require GCs
Externí odkaz:
https://doaj.org/article/3a03183441dc45e5a43a52ce0c2a1ac9
Autor:
Kathryn O. Farley, Catherine A. Forbes, Nicole C. Shaw, Emma Kuzminski, Michelle Ward, Gareth Baynam, Timo Lassmann, Vanessa S. Fear
Publikováno v:
HGG Advances, Vol 5, Iss 1, Pp 100257- (2024)
Summary: An estimated 3.5%–5.9% of the global population live with rare diseases, and approximately 80% of these diseases have a genetic cause. Rare genetic diseases are difficult to diagnose, with some affected individuals experiencing diagnostic
Externí odkaz:
https://doaj.org/article/05ebced0f70c428089b7189aa4addd42
Autor:
Vanessa S. Fear, Catherine A. Forbes, Denise Anderson, Sebastian Rauschert, Genevieve Syn, Nicole Shaw, Sarra Jamieson, Michelle Ward, Gareth Baynam, Timo Lassmann
Publikováno v:
Stem Cell Research & Therapy, Vol 13, Iss 1, Pp 1-15 (2022)
Abstract Background Over 400 million people worldwide are living with a rare disease. Next Generation Sequencing (NGS) identifies potential disease causative genetic variants. However, many are identified as variants of uncertain significance (VUS) a
Externí odkaz:
https://doaj.org/article/abeada057df24630a66a292be29cabef
Autor:
Michelle Ward, Josie Carwardine, Chuan J. Yong, James E. M. Watson, Jennifer Silcock, Gary S. Taylor, Mark Lintermans, Graeme R. Gillespie, Stephen T. Garnett, John Woinarski, Reid Tingley, Rod J. Fensham, Conrad J. Hoskin, Harry B. Hines, J. Dale Roberts, Mark J. Kennard, Mark S. Harvey, David G. Chapple, April E. Reside
Publikováno v:
Ecology and Evolution, Vol 11, Iss 17, Pp 11749-11761 (2021)
Abstract Australia is in the midst of an extinction crisis, having already lost 10% of terrestrial mammal fauna since European settlement and with hundreds of other species at high risk of extinction. The decline of the nation's biota is a result of
Externí odkaz:
https://doaj.org/article/437c95a9435c4166ad81d284d9f814fd
Autor:
Timo Lassmann, Richard W. Francis, Alexia Weeks, Dave Tang, Sarra E. Jamieson, Stephanie Broley, Hugh J. S. Dawkins, Lauren Dreyer, Jack Goldblatt, Tudor Groza, Benjamin Kamien, Cathy Kiraly-Borri, Fiona McKenzie, Lesley Murphy, Nicholas Pachter, Gargi Pathak, Cathryn Poulton, Amanda Samanek, Rachel Skoss, Jennie Slee, Sharron Townshend, Michelle Ward, Gareth S. Baynam, Jenefer M. Blackwell
Publikováno v:
npj Genomic Medicine, Vol 5, Iss 1, Pp 1-11 (2020)
Abstract Exome sequencing has enabled molecular diagnoses for rare disease patients but often with initial diagnostic rates of ~25−30%. Here we develop a robust computational pipeline to rank variants for reassessment of unsolved rare disease patie
Externí odkaz:
https://doaj.org/article/811cb355cf5b4897b431fd467c9f3752