Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation

Por Ritchie, Marylyn D, Rowan, Shane, Kucera, Gayle, Stubblefield, Tanya, Blair, Marcia, Roden, Dan M, Darbar, Dawood
Publicado em 2012

Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation

Por Weeke, Peter, Parvez, Babar, Blair, Marcia, Short, Laura, Ingram, Christie, Kucera, Gayle, Stubblefield, Tanya, Roden, Dan M.
Publicado em 2013

Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation

Por Parvez, Babar, Vaglio, Joseph, Rowan, Shane, Muhammad, Raafia, Kucera, Gayle, Stubblefield, Tanya, Carter, Shannon, Roden, Dan, Darbar, Dawood
Publicado em 2012

Cardiac Sodium Channel (SCN5A) Variants Associated with Atrial Fibrillation

Por Darbar, Dawood, Kannankeril, Prince J, Donahue, Brian S, Kucera, Gayle, Stubblefield, Tanya, Haines, Jonathan, George, Alfred L, Roden, Dan M
Publicado em 2008

QT variability during initial exposure to sotalol: experience based on a large electronic medical record

Por Weeke, Peter, Delaney, Jessica, Mosley, Jonathan D., Wells, Quinn, Van Driest, Sara, Norris, Kris, Kucera, Gayle, Stubblefield, Tanya, Roden, Dan M.
Publicado em 2013

Whole-exome sequencing in familial atrial fibrillation

Por Weeke, Peter, Muhammad, Raafia, Delaney, Jessica T., Shaffer, Christian, Mosley, Jonathan D., Blair, Marcia, Short, Laura, Stubblefield, Tanya, Roden, Dan M., Darbar, Dawood
Publicado em 2014

A Common Variant on Chromosome 4q25 is Associated With Prolonged PR Interval in Subjects With and Without Atrial Fibrillation

Por Kolek, Matthew J., Parvez, Babar, Muhammad, Raafia, Shoemaker, M. Benjamin, Blair, Marcia A., Stubblefield, Tanya, Kucera, Gayle A., Denny, Joshua C., Roden, Dan M., Darbar, Dawood
Publicado em 2013

Relation of Morbid Obesity and Female Gender to Risk of Procedural Complications in Patients Undergoing Atrial Fibrillation Ablation

Por Shoemaker, M Benjamin, Muhammad, Raafia, Farrell, Maureen, Parvez, Babar, White, Brenda W., Streur, Megan, Stubblefield, Tanya, Rytlewski, Jason, Parvathaneni, Sunthosh, Nagarakanti, Rangadham, Roden, Dan M, Saavedra, Pablo, Ellis, Christopher, Whalen, S. Patrick, Darbar, Dawood
Publicado em 2012

Common Atrial Fibrillation Risk Alleles at 4q25 Predict Recurrence after Catheter-based Atrial Fibrillation Ablation

Por Shoemaker, M. Benjamin, Muhammad, Raafia, Parvez, Babar, White, Brenda W., Streur, Megan, Song, Yanna, Stubblefield, Tanya, Kucera, Gayle, Blair, Marcia, Rytlewski, Jason, Parvathaneni, Sunthosh, Nagarakanti, Rangadham, Saavedra, Pablo, Ellis, Christopher, Whalen, S. Patrick, Roden, Dan M, Darbar, Dawood
Publicado em 2012

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke

Por Gudbjartsson, Daniel F., Holm, Hilma, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Walters, G. Bragi, Thorgeirsson, Gudmundur, Gulcher, Jeffrey, Mathiesen, Ellisiv, Njølstad, Inger, Nyrnes, Audhild, Wilsgaard, Tom, Hald, Erin, Hveem, Kristian, Stoltenberg, Camilla, Kucera, Gayle, Stubblefield, Tanya, Carter, Shannon, Roden, Dan, Ng, Maggie C.Y., Baum, Larry, So, Wing Yee, Wong, Ka Sing, Chan, Juliana C. N., Gieger, Christian, Wichmann, H-Erich, Gschwendtner, Andreas, Dichgans, Martin, Kuhlenbäumer, Gregor, Berger, Klaus, Ringelstein, E. Bernd, Bevan, Steve, Markus, Hugh, Kostulas, Konstantinos, Hillert, Jan, Sveinbjörnsdóttir, Sigurlaug, Valdimarsson, Einar M., Løchen, Maja-Lisa, Ma, Ronald C. W., Darbar, Dawood, Kong, Augustine, Arnar, David O., Thorsteinsdottir, Unnur, Stefansson, Kari
Publicado em 2009