J
Jackie Crawford
Researcher at Boston Children's Hospital
Publications - 36
Citations - 1887
Jackie Crawford is an academic researcher from Boston Children's Hospital. The author has contributed to research in topics: Sudden death & Long QT syndrome. The author has an hindex of 18, co-authored 35 publications receiving 1550 citations. Previous affiliations of Jackie Crawford include Auckland City Hospital & University of Auckland.
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Journal ArticleDOI
A Prospective Study of Sudden Cardiac Death among Children and Young Adults
Richard D. Bagnall,Robert G. Weintraub,Jodie Ingles,Jodie Ingles,Johan Duflou,Johan Duflou,Laura Yeates,Laura Yeates,Lien Lam,Andrew M. Davis,T. Thompson,V. Connell,Jennie Wallace,Charles Naylor,Jackie Crawford,Donald R. Love,Lavinia Hallam,Jodi White,Christopher Lawrence,Matthew J Lynch,Natalie Morgan,Paul A. James,Desirée du Sart,Rajesh Puranik,Rajesh Puranik,Neil E. I. Langlois,Jitendra K. Vohra,Ingrid Winship,John Atherton,Julie McGaughran,Jonathan R. Skinner,Christopher Semsarian,Christopher Semsarian +32 more
TL;DR: The addition of genetic testing to autopsy investigation substantially increased the identification of a possible cause of sudden cardiac death among children and young adults.
Journal ArticleDOI
Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome
Najim Lahrouchi,Hariharan Raju,Elisabeth M. Lodder,Efstathios Papatheodorou,James S. Ware,Michael Papadakis,Rafik Tadros,Della Cole,Jonathan R. Skinner,Jackie Crawford,Donald R. Love,Chee Jian Pua,Bee Y. Soh,Jaydutt D. Bhalshankar,Risha Govind,Jacob Tfelt-Hansen,Bo Gregers Winkel,Christian van der Werf,Yanushi D. Wijeyeratne,Greg Mellor,Jan Till,Marta C. Cohen,Maria Tome-Esteban,Sanjay Sharma,Arthur A.M. Wilde,Stuart A. Cook,Connie R. Bezzina,Mary N. Sheppard,Elijah R. Behr +28 more
TL;DR: Molecular autopsy for electrical disorder and cardiomyopathy genes, using ACMG guidelines for variant classification, identified a modest but realistic yield in SADS, which highlighted the predominant role of catecholaminergic polymorphic ventricular tachycardia and long QT syndrome, as well as the minimal yield from other genes.
Journal ArticleDOI
Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds
Jonathan R. Skinner,Jackie Crawford,Warren Smith,Andrew Aitken,David Heaven,Cary-Anne Evans,Ian Hayes,Katherine Neas,Simon Stables,Timothy Koelmeyer,Lloyd Denmark,Jane C. Vuletic,Fraser Maxwell,Kate White,Tao Yang,Dan M. Roden,Trond P. Leren,Andrew N. Shelling,Donald R. Love +18 more
TL;DR: Most community SUDY occurs at rest or during light activity, and a diagnostic rate of 15% supports the transition of LQT genetic autopsy, combined with family investigation, into routine medical practice.
Journal ArticleDOI
Misdiagnosis of long QT syndrome as epilepsy at first presentation
Judith M. MacCormick,Hugh McAlister,Jackie Crawford,John K. French,Ian Crozier,Andrew N. Shelling,Carey-Anne Eddy,Mark I. Rees,Mark I. Rees,Jonathan R. Skinner +9 more
TL;DR: In this paper, the authors evaluated a series of patients with genetically confirmed long QT syndrome to establish the frequency of delayed recognition and examined causes and potential consequences of diagnostic delay, and concluded that patients labeled as epileptic experience a particularly long diagnostic delay.
Journal ArticleDOI
Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome
Carey-Anne Eddy,Carey-Anne Eddy,Judith M. MacCormick,Seo-Kyung Chung,Seo-Kyung Chung,Jackie Crawford,Donald R. Love,Mark I. Rees,Mark I. Rees,Mark I. Rees,Jonathan R. Skinner,Andrew N. Shelling,Andrew N. Shelling +12 more
TL;DR: It is demonstrated that more than 10% of patients with LQ TS and a negative current generation genetic test have large gene deletions or duplications among the major known LQTS susceptibility genes.