Search

Author/Creator Lichtner, Peter Journal Circulation

1. Analysis for Genetic Modifiers of Disease Severity in Patients With Long-QT Syndrome Type 2. (June 2015)

Authors:
Kolder, Iris C.R.M.; Tanck, Michael W.T.; Postema, Pieter G.; Barc, Julien; Sinner, Moritz F.; Zumhagen, Sven; Husemann, Anja; Stallmeyer, Birgit; Koopmann, Tamara T.; Hofman, Nynke; Pfeufer, Arne; Lichtner, Peter; Meitinger, Thomas; Beckmann, Britt M.; Myerburg, Robert J.; Bishopric, Nanette H.;...
Journal:
Circulation
Issue:
Volume 8:Number 3(2015)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

2. Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?. (August 2016)

Authors:
Crotti, Lia; Lahtinen, Annukka M.; Spazzolini, Carla; Mastantuono, Elisa; Monti, Maria Cristina; Morassutto, Caterina; Parati, Gianfranco; Heradien, Marshall; Goosen, Althea; Lichtner, Peter; Meitinger, Thomas; Brink, Paul A.; Kontula, Kimmo; Swan, Heikki; Schwartz, Peter J.
Journal:
Circulation
Issue:
Volume 9:Number 4(2016)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

3. Response by Crotti et al to Letter Regarding Article, "Genetic Modifiers for the Long-QT Syndrome: How Important Is the Role of Variants in the 3′ Untranslated Region of KCNQ1?". (December 2016)

Authors:
Crotti, Lia; Lahtinen, Annukka M.; Spazzolini, Carla; Mastantuono, Elisa; Cristina Monti, Maria; Morassutto, Caterina; Parati, Gianfranco; Heradien, Marshall; Goosen, Althea; Lichtner, Peter; Meitinger, Thomas; Brink, Paul A.; Kontula, Kimmo; Swan, Heikki; Schwartz, Peter J.
Journal:
Circulation
Issue:
Volume 9:Number 6(2016)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

4. SCN5A Mutation Type and a Genetic Risk Score Associate Variably With Brugada Syndrome Phenotype in SCN5A Families. (December 2020)

Authors:
Wijeyeratne, Yanushi D.; Tanck, Michael W.; Mizusawa, Yuka; Batchvarov, Velislav; Barc, Julien; Crotti, Lia; Bos, J. Martijn; Tester, David J.; Muir, Alison; Veltmann, Christian; Ohno, Seiko; Page, Stephen P.; Galvin, Joseph; Tadros, Rafik; Muggenthaler, Martina; Raju, Hariharan; Denjoy, Isabelle...
Journal:
Circulation
Issue:
Volume 13:Number 6(2020)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

5. Sudden Cardiac Arrest and Rare Genetic Variants in the Community. (April 2016)

Authors:
Milano, Annalisa; Blom, Marieke T.; Lodder, Elisabeth M.; van Hoeijen, Daniel A.; Barc, Julien; Koopmann, Tamara T.; Bardai, Abdennasser; Beekman, Leander; Lichtner, Peter; van den Berg, Maarten P.; Wilde, Arthur A.M.; Bezzina, Connie R.; Tan, Hanno L.
Journal:
Circulation
Issue:
Volume 9:Number 2(2016)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

6. Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome. Issue 4 (28th July 2020)

Authors:
Lahrouchi, Najim; Tadros, Rafik; Crotti, Lia; Mizusawa, Yuka; Postema, Pieter G.; Beekman, Leander; Walsh, Roddy; Hasegawa, Kanae; Barc, Julien; Ernsting, Marko; Turkowski, Kari L.; Mazzanti, Andrea; Beckmann, Britt M.; Shimamoto, Keiko; Diamant, Ulla-Britt; Wijeyeratne, Yanushi D.; Kucho, Yu; Ro...
Journal:
Circulation
Issue:
Volume 142:Issue 4(2020)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗