Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Scott Watkins"'
Autor:
Scott Watkins, Fatimah J. Chowdhury, Chloe Norman, Stephen J. Brett, Keith Couper, Laura Goodwin, Doug W. Gould, David AE. Harrison, Anower Hossain, Ranjit Lall, James Mason, Jerry P. Nolan, Henry Nwankwo, Gavin D. Perkins, Katie Samuel, Behnaz Schofield, Jasmeet Soar, Kath Starr, Matthew Thomas, Sarah Voss, Jonathan R. Benger
Publikováno v:
Resuscitation Plus, Vol 15, Iss , Pp 100430- (2023)
Survival from in-hospital cardiac arrest is approximately 18%, but for patients who require advanced airway management survival is lower. Those who do survive are often left with significant disability. Traditionally, resuscitation of cardiac arrest
Externí odkaz:
https://doaj.org/article/0fb0c1e5c70b4edf9e7c17ff68cd5b72
Publikováno v:
Genome Biology, Vol 23, Iss 1, Pp 1-19 (2022)
Abstract Background Short tandem repeats (STRs) compose approximately 3% of the genome, and mutations at STR loci have been linked to dozens of human diseases including amyotrophic lateral sclerosis, Friedreich ataxia, Huntington disease, and fragile
Externí odkaz:
https://doaj.org/article/34c99587bc204b03be3d81040f9fb3c0
Autor:
Shannon Hateley, Angelica Lopez-Izquierdo, Chuanchau J. Jou, Scott Cho, Joshua G. Schraiber, Shiya Song, Colin T. Maguire, Natalia Torres, Michael Riedel, Neil E. Bowles, Cammon B. Arrington, Brett J. Kennedy, Susan P. Etheridge, Shuping Lai, Chase Pribble, Lindsay Meyers, Derek Lundahl, Jake Byrnes, Julie M. Granka, Christopher A. Kauffman, Gordon Lemmon, Steven Boyden, W. Scott Watkins, Mary Anne Karren, Stacey Knight, J. Brent Muhlestein, John F. Carlquist, Jeffrey L. Anderson, Kenneth G. Chahine, Khushi U. Shah, Catherine A. Ball, Ivor J. Benjamin, Mark Yandell, Martin Tristani-Firouzi
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-10 (2021)
Many rare high-impact variants have been associated with disease, but the origins and functional impact are not always explored. Here, the authors trace the ancestry of a rare high impact atrial fibrillation allele in KCNQ1, and use iPSC-derived card
Externí odkaz:
https://doaj.org/article/fc7dba9c47974f5aa229e04e2b3a9d14
Autor:
W. Scott Watkins, E. Javier Hernandez, Sergiusz Wesolowski, Brent W. Bisgrove, Ryan T. Sunderland, Edwin Lin, Gordon Lemmon, Bradley L. Demarest, Thomas A. Miller, Daniel Bernstein, Martina Brueckner, Wendy K. Chung, Bruce D. Gelb, Elizabeth Goldmuntz, Jane W. Newburger, Christine E. Seidman, Yufeng Shen, H. Joseph Yost, Mark Yandell, Martin Tristani-Firouzi
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-12 (2019)
Large whole-exome sequencing studies have suggested that the genetic architecture of syndromic congenital heart disease (CHD) is different from sporadic forms. Here, Watkins et al. estimate the relative contribution of damaging recessive and de novo
Externí odkaz:
https://doaj.org/article/8135b5f4cd6b48d3b81b0a72c696e63e
Autor:
Jiun-Sheng Chen, Fulan Hu, Subra Kugathasan, Lynn B. Jorde, David Nix, Ann Rutherford, Lee Denson, W. Scott Watkins, Sampath Prahalad, Chad Huff, Stephen L. Guthery
Publikováno v:
G3: Genes, Genomes, Genetics, Vol 8, Iss 9, Pp 2881-2888 (2018)
Crohn’s disease is a complex genetic trait characterized by chronic relapsing intestinal inflammation. Genome wide association studies (GWAS) have identified more than 170 loci associated with the disease, accounting for ∼14% of the disease varia
Externí odkaz:
https://doaj.org/article/48f2ca51b33446928db7002199a09f51
Publikováno v:
Journal of Material Cycles and Waste Management. 24:2455-2469
Pharmaceuticals can enter the environment through disposal in toilets, sinks and general waste. In the UK, household medicines are correctly disposed of by returning them to a pharmacy. This study examined household patterns of medicine waste, storag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::694289edf28eddb5b11fcf91eb51451d
https://doi.org/10.1007/s10163-022-01494-7
https://doi.org/10.1007/s10163-022-01494-7
Autor:
Julie Feusier, David J. Witherspoon, W. Scott Watkins, Clément Goubert, Thomas A. Sasani, Lynn B. Jorde
Publikováno v:
Mobile DNA, Vol 8, Iss 1, Pp 1-10 (2017)
Abstract Background Polymorphic human Alu elements are excellent tools for assessing population structure, and new retrotransposition events can contribute to disease. Next-generation sequencing has greatly increased the potential to discover Alu ele
Externí odkaz:
https://doaj.org/article/046ccbb1e3264f1ba464b90929820dbd
Autor:
Navin Rustagi, Anbo Zhou, W. Scott Watkins, Erika Gedvilaite, Shuoguo Wang, Naveen Ramesh, Donna Muzny, Richard A. Gibbs, Lynn B. Jorde, Fuli Yu, Jinchuan Xing
Publikováno v:
BMC Genomics, Vol 18, Iss 1, Pp 1-12 (2017)
Abstract Background The cost of Whole Genome Sequencing (WGS) has decreased tremendously in recent years due to advances in next-generation sequencing technologies. Nevertheless, the cost of carrying out large-scale cohort studies using WGS is still
Externí odkaz:
https://doaj.org/article/082816d78c974cf38b2f17d92c98c203
Autor:
Annery G. Garcia-Marcinkiewicz, Lisa K. Lee, Bishr Haydar, John E. Fiadjoe, Clyde T. Matava, Pete G. Kovatsis, James Peyton, Mary L. Stein, Raymond Park, Brad M. Taicher, Thomas W. Templeton, Benjamin B. Bruins, Paul Stricker, Elizabeth K. Laverriere, Justin L. Lockman, Brian Struyk, Christopher Ward, Akira Nishisaki, Ramesh Kodavatiganti, Rodrigo J. Daly Guris, Luis Sequera-Ramos, Mark S. Teen, Ayodele Oke, Grace Hsu, Arul Lingappan, Chinyere Egbuta, Stephen Flynn, Lina Sarmiento, Tally Goldfarb, Edgar E. Kiss, Patrick N. Olomu, Peter Szmuk, Sam Mireles, Andrea Murray, Simon Whyte, Ranu Jain, Maria Matuszczak, Agnes Hunyady, Adrian Bosenberg, See Tham, Daniel Low, Christopher Holmes, Stefan Sabato, Nicholas Dalesio, Robert Greenberg, Angela Lucero, Paul Reynolds, Ian Lewis, Charles Schrock, Sydney Nykiel-Bailey, Elizabeth Starker, Judit Szolnoki, Melissa Brooks-Peterson, Somaletha Bhattacharya, Nicholas E. Burjek, Narasimhan Jagannathan, David Lardner, Scott Watkins, Christy Crockett, John Moore, Sara Robertson, Madhankumar Sathyamoorthy, Franklin Chiao, Jasmine Patel, Aarti Sharma, Piedad Echeverry Marin, Carolina Pérez-Pradilla, Neeta Singh, Britta S. von Ungern-Sternberg, David Sommerfield, Guelay Bilen-Rosas, Hilana Lewkowitz-Shpuntoff, Pilar Castro, N. Ricardo Riveros Perez, Jurgen C. de Graaff, Eduardo Vega, Alejandro González, Paola Ostermann, Kasia Rubin, Charles (Ted) Lord, Angela Lee, Eugenie Heitmiller, Songyos Valairucha, Priti Dalal, Thanh Tran, Ihab Ayad, Mohamed Rehman, Allison Fernandez, Lillian Zamora, Niroop Ravula, Sadiq Shaik
Publikováno v:
British Journal of Anaesthesia. Elsevier Ltd.
Background: Difficult facemask ventilation is perilous in children whose tracheas are difficult to intubate. We hypothesised that certain physical characteristics and anaesthetic factors are associated with difficult mask ventilation in paediatric pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::89d2617f1d6a9bb11c64454761035631
https://doi.org/10.1016/j.bja.2023.02.035
https://doi.org/10.1016/j.bja.2023.02.035
Autor:
Raquel M. Zimmerman, Edgar J. Hernandez, W. Scott Watkins, Nathan Blue, Martin Tristani-Firouzi, Mark Yandell, Benjamin A. Steinberg
Atrial fibrillation (AF) leads to significant morbidity and mortality, which is primarily related to stroke despite effective stroke prevention therapies. There remains a critical need for personalized, socially aware, equitable stroke risk predictio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da9906a5fa67ba36fa2eb8c8a3f1b8b9
https://doi.org/10.1101/2023.02.27.23286470
https://doi.org/10.1101/2023.02.27.23286470
