Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Christina Honeywell"'
Autor:
Natasha Macchio, Martin Stepan, Gianluigi Pilu, Zohar Nachum, Tullio Ghi, Courtney Kiss, Susan Crocker, Gabriel Quiroz, Federica Bellussi, Shawna Morrison, Giuliana Simonazzi, Anita J. Moon-Grady, Daniel Martínez, Amy J.M. McNaughton, Darrell L. Cass, Enav Yefet, F. Correa, Stéphanie Friszer, Timothy M. Crombleholme, Gregory A.L. Davies, Hubert Ducou Le Pointe, Alberto Galindo, Jean-Marie Jouannic, Anne-Gaël Cordier, Max B. Mitchell, Yanwei Xi, Naama Schwartz, Juan Manuel Carretero, Helene Perras, Flora Basson, Bienvenido Puerto, Satz Mengensatzproduktion, Mireille Cloutier, Michael Brudno, Noémie Girard, A. Mendoza, Emilie Creede, Catherine Garel, Alison Hamilton, Christina Honeywell, Ahmed I. Marwan, Olga Gómez, Ross Welch, F. Viñals, Mary E. Norton, Regina M. Reynolds, Gregory J. Anger, Alexandra Benachi, Mar Bennasar, Stephen P. Emery, Enrique García-Torres, Aly Youssef, Mahesh Choolani, Enery Gómez-Montes, Pilar Ruiz, Fatima Crispi, Michael R. Harrison, Christine M. Armour, Paul Bussière, Jaroslav Stranik, I. Cataneo, Marian Kacerovsky, Druckerei Stückle, Mark I. Evans, Joshua A. Copel, Ginevra Salsi, Ignacio Herraiz, Ahmet Baschat, Baptiste Morel, Bo Jacobsson, Xudong Liu, Benjamin Viaris de Lesegno, Kuojen Tsao, Aryan Arbabi, Francois I. Luks, Henry L. Galan, Greg Ryan, Ivana Musilova, Danna Hull, Francisco A. Guerra, Matthew Green, D. Escribano, Tillie Chiu, Jan Deprest, Bettina F. Cuneo, Johannes C. von Alvensleben, Tomas Bestvina, Josep M. Martinez, Eduard Gratacós, Catherine Egoroff, Olga Kuzmin, Claire Goldsmith, Eléonore Blondiaux
Publikováno v:
Fetal Diagnosis and Therapy. 42:I-IV
Autor:
Shawna Morrison, Xudong Liu, Helene Perras, Michael Brudno, Danna Hull, Susan Crocker, Claire Goldsmith, Christina Honeywell, Tillie Chiu, Gregory A.L. Davies, Aryan Arbabi, Yanwei Xi, Amy J.M. McNaughton, Christine M. Armour, Natasha Macchio, Courtney Kiss, Emilie Creede, Mireille Cloutier, Alison Hamilton, Gregory J. Anger
Publikováno v:
Fetal diagnosis and therapy. 42(4)
Objective: To develop an alternate noninvasive prenatal testing method for the assessment of trisomy 21 (T21) using a targeted semiconductor sequencing approach. Methods: A customized AmpliSeq panel was designed with 1,067 primer pairs targeting spec
Publikováno v:
Circulation: Arrhythmia and Electrophysiology. 6:939-945
Background— International guidelines recommend restriction of activities for many children and adolescents with inherited arrhythmia syndromes to moderate activity ( Methods and Results— Participants wore the Actiheart for ≤7 days on 2 occasion
Autor:
Kym M. Boycott, Chandree L. Beaulieu, Jacek Majewski, Yanwei Xi, Dapeng Zhang, L. Aravind, Christina Honeywell, Taila Hartley, Silvia M. Vidal, Jeremy Schwartzentruber, Michael H. Gollob, Jennifer Marton, Robert M. Gow, Martine Tétreault
Publikováno v:
International Journal of Cardiology. 185:114-116
Whole exome sequencing identifies the TNNI3K gene as a cause of familial conduction system disease and congenital junctional ectopic tachycardia☆ Yanwei Xi , Christina Honeywell , Dapeng Zhang , Jeremy Schwartzentruber , Chandree L. Beaulieu , Mart
Publikováno v:
Academic Forensic Pathology. 3:183-190
Sudden cardiac death is a tragic result of a number of cardiovascular diseases. While the majority of sudden cardiac death cases are in older individuals with coronary artery disease, victims also include younger people (those less than 40 years old)
Autor:
Christina Honeywell, Owen Middleton, Erin Demo, Frank Miller, J. Keith Pinckard, Jeff Jentzen, Carl C Stacy, R. Ross Reichard, Samantha Baxter, Heather MacLeod, Julie Rutberg
Publikováno v:
Academic Forensic Pathology. 3:191-194
Sudden unexpected death is typically diagnosed in infants, children, teenagers, and young adults following completion of an autopsy that fails to identify a cause of death or when autopsy suggests a potentially genetic cause of death in an individual
Publikováno v:
Journal of Community Genetics. 4:233-242
Family communication of genetic risk information is a complex process. Currently, there are no evidence-based interventions to help genetics professionals facilitate the process of disclosure within families. This study was designed to create a frame
Autor:
Robert M. Gow, Jonathan R. Silva, Ronald J. Kanter, Geoffrey S. Pitt, Hong-Gang Wang, Wandi Zhu, Christina Honeywell
Background Inherited autosomal dominant mutations in cardiac sodium channels (Na V 1.5) cause various arrhythmias, such as long QT syndrome and Brugada syndrome. Although dozens of mutations throughout the protein have been reported, there are few re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40c3c4abf74e59782dc8aade1355105e
https://europepmc.org/articles/PMC4789166/
https://europepmc.org/articles/PMC4789166/
Autor:
Kimberly Gall, Tim Ramsay, Makda H. Araia, Pranesh Chakraborty, Brenda Wilson, Jennifer Milburn, Christina Honeywell, Beth K. Potter
Publikováno v:
Genetics in Medicine
Purpose: Effective parental education about newborn blood-spot screening may facilitate prompt follow-up, reduce psychosocial harms, and promote trust in screening programs. However, little is known about the aspects of education delivery and content
Autor:
Christina Honeywell, Judith Allanson, Stuart Douglas, Bob Argiropoulos, Jean McGowan-Jordan, M. Elizabeth McCready, Andrea L. Blumenthal
Publikováno v:
American Journal of Medical Genetics Part A. :1262-1268
Pericentric chromosome inversions are often associated with infertility, recurrent pregnancy loss, and an increased risk for offspring with congenital anomalies. We report on a chromosome 1 inversion between 1p36.21 and 1q42.13, one of the largest de