View of healthcare professionals on ultra-rapid genome sequencing and its implementation in clinical routine for critically ill children

被引：0

作者：

Caillot, Claire ^{[1
]}

Javouhey, Etienne ^{[2
]}

Hays, Stephane ^{[3
]}

Gouy, Evan ^{[1
]}

Monin, Pauline ^{[1
]}

Lesca, Gaetan ^{[1
,4
]}

Sanlaville, Damien ^{[1
,4
]}

Chatron, Nicolas ^{[1
,4
]}

机构：

[1] Hosp Civils Lyon, Serv Genet, Lyon, France

[2] Hospices Civils Lyon, Serv Durgences & Reanimat Pediat, Hop Femme Mere Enfant, Lyon, France

[3] Hospices Civils Lyon, Serv Neonatol & Reanimat Neonatale, Hop Croix Rousse, Lyon, France

[4] Univ Lyon 1, Inst Neuromyogene,UMR 5310, Lab Physiopathol & Genet Neurone & Muscle,CNRS, Equipe Metabolisme Energet & Developpement Neuro, Lyon, France

来源：

EUROPEAN JOURNAL OF HUMAN GENETICS | 2024年 / 32卷

关键词：

D O I：

暂无

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

P23.046.D

引用

页码：1818 / 1818

页数：1

共 26 条

[1] Clinical application of 24-hour ultra-rapid genome sequencing in a critically ill neonate
Zhang, Ping
Zhang, Rong
Zhang, Lan
Lu, Yulan
Wang, Huijun
Zhou, Wenhao
Wu, Bingbing
GENETICS IN MEDICINE, 2022, 24 (03) : S255 - S255
[2] Rapid decisions: A qualitative analysis of health professionals' experiences using ultra-rapid genomic sequencing in critically ill children
Arkell, Katie
Gyngell, Christopher
Stark, Zornitza
Vears, Danya
EUROPEAN JOURNAL OF HUMAN GENETICS, 2023, 31 : 689 - 689
[3] Rapid Whole Genome Sequencing for Critically Ill Children With Cardiomyopathy
van der Zwaag, Paul A.
Herkert, Johanna C.
Sarvaas, Gideon J. du Marchie
Bartelds, Beatrijs
van Diemen, Cleo C.
de Koning, Tom J.
Jongbloed, Jan D.
Sikkema-Raddatz, Birgit
Franke, Lude
Sinke, Richard J.
van Langen, Irene M.
Wijmenga, Cisca
Kerstjens-Frederikse, Wilhelmina S.
CIRCULATION, 2016, 134
[4] Is faster better? An economic evaluation of rapid and ultra-rapid genomic testing in critically ill infants and children
Goranitis, Ilias
Wu, You
Lunke, Sebastian
White, Susan M.
Tan, Tiong Y.
Yeung, Alison
Hunter, Matthew F.
Martyn, Melissa
Gaff, Clara
Stark, Zornitza
GENETICS IN MEDICINE, 2022, 24 (05) : 1037 - 1044
[5] Implementation of Rapid Genome Sequencing for Critically Ill Infants With Complex Congenital Heart Disease
Hays, Thomas
Hernan, Rebecca
Disco, Michele
Griffin, Emily L.
Goldshtrom, Nimrod
Vargas, Diana
Krishnamurthy, Ganga
Bomback, Miles
Rehman, Atteeq U.
Wilson, Amanda T.
Guha, Saurav
Phadke, Shruti
Okur, Volkan
Robinson, Dino
Felice, Vanessa
Abhyankar, Avinash
Jobanputra, Vaidehi
Chung, Wendy K.
CIRCULATION-GENOMIC AND PRECISION MEDICINE, 2023, 16 (05): : 415 - 420
[6] Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Lunke, Sebastian
Eggers, Stefanie
Wilson, Meredith
Patel, Chirag
Barnett, Christopher P.
Pinner, Jason
Sandaradura, Sarah A.
Buckley, Michael F.
Krzesinski, Emma I.
de Silva, Michelle G.
Brett, Gemma R.
Boggs, Kirsten
Mowat, David
Kirk, Edwin P.
Ades, Lesley C.
Akesson, Lauren S.
Amor, David J.
Ayres, Samantha
Baxendale, Anne
Borrie, Sarah
Bray, Alessandra
Brown, Natasha J.
Chan, Cheng Yee
Chong, Belinda
Cliffe, Corrina
Delatycki, Martin B.
Edwards, Matthew
Elakis, George
Fahey, Michael C.
Fennell, Andrew
Fowles, Lindsay
Gallacher, Lyndon
Higgins, Megan
Howell, Katherine B.
Hunt, Lauren
Hunter, Matthew F.
Jones, Kristi J.
King, Sarah
Kumble, Smitha
Lang, Sarah
Le Moing, Maelle
Ma, Alan
Phelan, Dean
Quinn, Michael C. J.
Richards, Anna
Richmond, Christopher M.
Riseley, Jessica
Rodgers, Jonathan
Sachdev, Rani
Sadedin, Simon
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2020, 323 (24): : 2503 - 2511
[7] Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Lunke, Sebastian
Eggers, Stefanie
Wilson, Meredith
Patel, Chirag
Barnett, Christopher P.
Pinner, Jason
Sandaradura, Sarah A.
Buckley, Michael F.
Krzesinski, Emma I.
de Silva, Michelle G.
Brett, Gemma R.
Boggs, Kirsten
Mowat, David
Kirk, Edwin P.
Ades, Lesley C.
Akesson, Lauren S.
Amor, David J.
Ayres, Samantha
Baxendale, Anne
Borrie, Sarah
Bray, Alessandra
Brown, Natasha J.
Chan, Cheng Yee
Chong, Belinda
Cliffe, Corrina
Delatycki, Martin B.
Edwards, Matthew
Elakis, George
Fahey, Michael C.
Fennell, Andrew
Fowles, Lindsay
Gallacher, Lyndon
Higgins, Megan
Howell, Katherine B.
Hunt, Lauren
Hunter, Matthew F.
Jones, Kristi J.
King, Sarah
Kumble, Smitha
Lang, Sarah
Le Moing, Maelle
Ma, Alan
Phelan, Dean
Quinn, Michael C. J.
Richards, Anna
Richmond, Christopher M.
Riseley, Jessica
Rodgers, Jonathan
Sachdev, Rani
Sadedin, Simon
OBSTETRICAL & GYNECOLOGICAL SURVEY, 2020, 75 (11) : 662 - 664
[8] Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level
Stephanie Best
Helen Brown
Sebastian Lunke
Chirag Patel
Jason Pinner
Christopher P. Barnett
Meredith Wilson
Sarah A. Sandaradura
Belinda McClaren
Gemma R. Brett
Jeffrey Braithwaite
Zornitza Stark
npj Genomic Medicine, 6
[9] Learning from scaling up ultra-rapid genomic testing for critically ill children to a national level
Best, Stephanie
Brown, Helen
Lunke, Sebastian
Patel, Chirag
Pinner, Jason
Barnett, Christopher P.
Wilson, Meredith
Sandaradura, Sarah A.
McClaren, Belinda
Brett, Gemma R.
Braithwaite, Jeffrey
Stark, Zornitza
NPJ GENOMIC MEDICINE, 2021, 6 (01)
[10] Rapid whole-genome sequencing in critically Ill children: shifting from unease to evidence, education, and equitable implementation
Franck, Linda S.
Dimmock, David
Hobbs, Charlotte
Kingsmore, Stephen F.
JOURNAL OF PEDIATRICS, 2021, 238 : 343 - 343

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