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Julie Rutberg

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J D Roberts; J P van Tintelen; A C P Wiesfeld; D Dooijes; Julie Rutberg; Robert M Gow; J C Herkert; S M Nikkel; Michael H Gollob
Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy.
Michael H Gollob; Louis Blier; Ramon Brugada; Jean Champagne; Vijay Chauhan; Sean P Connors; Martin Gardner; Martin S Green; Robert M Gow; Robert Murray Hamilton; Louise Harris; Jeffrey S Healey; Kathleen Hodgkinson; Christina Honeywell; Michael Kantoch; Joel Kirsh; Andrew Krahn; Michelle Mullen; Ratika Parkash; Damian Redfearn; Julie Rutberg; Shubhayan Sanatani; Anna Woo
Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper.
Jason D Roberts; John P Veinot; Julie Rutberg; Michael H Gollob
Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy.

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2013: J D Roberts; J P van Tintelen; A C P Wiesfeld; D Dooijes; Julie Rutberg; Robert M Gow; J C Herkert; S M Nikkel; Michael H Gollob
Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy.
Clinical genetics 2013;83(5):452-6.
2011: Michael H Gollob; Louis Blier; Ramon Brugada; Jean Champagne; Vijay Chauhan; Sean P Connors; Martin Gardner; Martin S Green; Robert M Gow; Robert Murray Hamilton; Louise Harris; Jeffrey S Healey; Kathleen Hodgkinson; Christina Honeywell; Michael Kantoch; Joel Kirsh; Andrew Krahn; Michelle Mullen; Ratika Parkash; Damian Redfearn; Julie Rutberg; Shubhayan Sanatani; Anna Woo
Recommendations for the use of genetic testing in the clinical evaluation of inherited cardiac arrhythmias associated with sudden cardiac death: Canadian Cardiovascular Society/Canadian Heart Rhythm Society joint position paper.
The Canadian journal of cardiology 2011;27(2):232-45.
2010: Jason D Roberts; John P Veinot; Julie Rutberg; Michael H Gollob
Inherited cardiomyopathies mimicking arrhythmogenic right ventricular cardiomyopathy.
Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology 2010;19(5):316-20.
2009: Philip S Wells; Martha L Louzada; Monica Taljaard; David R Anderson; Susan R Kahn; Nicole J Langlois; Julie Rutberg; Michael J Kovacs; Marc A Rodger
A pilot study to assess the feasibility of a multicenter cluster randomized trial for the management of asymptomatic persons with a thrombophilia.
Journal of genetic counseling 2009;18(5):475-82.
2009: Qiuju Li; Hai Huang; Gele Liu; Khanh Lam; Julie Rutberg; Martin S Green; David H Birnie; Robert Lemery; Mohamed Chahine; Michael H Gollob
Gain-of-function mutation of Nav1.5 in atrial fibrillation enhances cellular excitability and lowers the threshold for action potential firing.
Biochemical and biophysical research communications 2009;380(1):132-7.
2008: J Heshka; C Palleschi; Brenda J Wilson; J Brehaut; Julie Rutberg; Holly Etchegary; N Langlois; Marc A Rodger; Philip S Wells
Cognitive and behavioural effects of genetic testing for thrombophilia.
Journal of genetic counseling 2008;17(3):288-96.
2007: Julie Rutberg; Martin S Green; Robert M Gow; Michael T Geraghty; Christina Honeywell; John Ewen; David H Birnie; Anthony Tang; Robert Lemery; Michael H Gollob
Molecular autopsy in the sudden cardiac death of a young woman: a first Canadian report.
The Canadian journal of cardiology 2007;23(11):904-6.
2004: Harikrishna Tandri; David A Bluemke; Victor A Ferrari; Chandra Bomma; Khurram Nasir; Julie Rutberg; Crystal Tichnell; Cynthia James; João A C Lima; Hugh Calkins
Findings on magnetic resonance imaging of idiopathic right ventricular outflow tachycardia.
The American journal of cardiology 2004;94(11):1441-5.
2004: Ernesto Castillo; Harikrishna Tandri; E Rene Rodriguez; Khurram Nasir; Julie Rutberg; Hugh Calkins; João A C Lima; David A Bluemke
Arrhythmogenic right ventricular dysplasia: ex vivo and in vivo fat detection with black-blood MR imaging.
Radiology 2004;232(1):38-48.
2004: Ariel Roguin; Chandra Bomma; Khurram Nasir; Harikrishna Tandri; Crystal Tichnell; Cynthia James; Julie Rutberg; Jane Crosson; Philip J Spevak; Ronald D Berger; Henry Halperin; Hugh Calkins
Implantable cardioverter-defibrillators in patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Journal of the American College of Cardiology 2004;43(10):1843-52.
2004: Chandra Bomma; Julie Rutberg; Harikrishna Tandri; Khurram Nasir; Ariel Roguin; Crystal Tichnell; Rene Rodriguez; Cynthia James; Edward K Kasper; Philip J Spevak; David A Bluemke; Hugh Calkins
Misdiagnosis of arrhythmogenic right ventricular dysplasia/cardiomyopathy.
Journal of cardiovascular electrophysiology 2004;15(3):300-6.
2003: Khurram Nasir; Harikrishna Tandri; Julie Rutberg; Crystal Tichnell; Philip J Spevak; Jane Crossan; Kenneth L Baughman; Edward K Kasper; Gordon F Tomaselli; Ronald D Berger; Hugh Calkins
Filtered QRS duration on signal-averaged electrocardiography predicts inducibility of ventricular tachycardia in arrhythmogenic right ventricle dysplasia.
Pacing and clinical electrophysiology : PACE 2003;26(10):1955-60.
2003: Khurram Nasir; Chandra Bomma; Faisal A Khan; Harikrishna Tandri; Crystal Tichnell; Cynthia James; Julie Rutberg; Ronald D Berger; Hugh Calkins
Utility of a combined signal-averaged electrocardiogram and QT dispersion algorithm in identifying arrhythmogenic right ventricular dysplasia in patients with tachycardia of right ventricular origin.
The American journal of cardiology 2003;92(1):105-9.
2003: Harikrishna Tandri; Hugh Calkins; Khurram Nasir; Chandra Bomma; Ernesto Castillo; Julie Rutberg; Crystal Tichnell; João A C Lima; David A Bluemke
Magnetic resonance imaging findings in patients meeting task force criteria for arrhythmogenic right ventricular dysplasia.
Journal of cardiovascular electrophysiology 2003;14(5):476-82.
2003: Khurram Nasir; Julie Rutberg; Harikrishna Tandri; Ronald D Berger; Gordon F Tomaselli; Hugh Calkins
Utility of SAECG in arrhythmogenic right ventricle dysplasia.
Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc 2003;8(2):112-20.
2002: Harikrishna Tandri; Julie Rutberg; David A Bluemke; Hugh Calkins
Magnetic resonance imaging of arrhythmogenic right ventricular dysplasia.
Journal of cardiovascular electrophysiology 2002;13(11):1180.
2001: Wendy R Kates; Courtney P Burnette; Ethylin Jabs; Julie Rutberg; Anne M Murphy; Grados Marco; Michael T Geraghty; Walter E Kaufmann; Godfrey D Pearlson
Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis.
Biological psychiatry 2001;49(8):677-84.
2000: Barbara K Goodman; Julie Rutberg; Wei-Wen Lin; Ann E Pulver; George H Thomas
Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome.
Journal of inherited metabolic disease 2000;23(8):847-8.
2000: Colyn B Cargile; Iain McIntosh; MV Clough; Julie Rutberg; Reza Yaghmai; Barbara K Goodman; Xiao-Ning Chen; Julie R Korenberg; George H Thomas; Michael T Geraghty
Delayed membranous ossification of the cranium associated with familial translocation (2;3)(p15;q12).
American journal of medical genetics 2000;92(5):328-35.
1999: S Sigurdardottir; Barbara K Goodman; Julie Rutberg; George H Thomas; Ethylin Jabs; Michael T Geraghty
Clinical, cytogenetic, and fluorescence in situ hybridization findings in two cases of "complete ring" syndrome.
American journal of medical genetics 1999;87(5):384-90.
1998: Barbara K Goodman; Lisa Shaffer; Julie Rutberg; M Leppert; KH Harum; S Gagos; J H Ray; M G Bialer; X Zhou; B A Pletcher; Stuart K Shapira; Michael T Geraghty
Inherited duplication Xq27-qter at Xp22.3 in severely affected males: molecular cytogenetic evaluation and clinical description in three unrelated families.
American journal of medical genetics 1998;80(4):377-84.
1997: Kimberly F Doheny; S A Rasmussen; Julie Rutberg; Gregg L Semenza; J Stamberg; M Schwartz; Denise A S Batista; Gail Stetten; George H Thomas
Segregation of a familial balanced (12;10) insertion resulting in Dup(10)(q21.2q22.1) and Del(10)(q21.2q22.1) in first cousins.
American journal of medical genetics 1997;69(2):188-93.