A citation-based method for searching scientific literature

Denice M Hodgson-Zingman, Margaret L Karst, Leonid V Zingman, Denise M Heublein, Dawood Darbar, Kathleen J Herron, Jeffrey D Ballew, Mariza de Andrade, John C Burnett, Timothy M Olson. N Engl J Med 2008
Times Cited: 206







List of co-cited articles
1474 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


KCNQ1 gain-of-function mutation in familial atrial fibrillation.
Yi-Han Chen, Shi-Jie Xu, Said Bendahhou, Xiao-Liang Wang, Ying Wang, Wen-Yuan Xu, Hong-Wei Jin, Hao Sun, Xiao-Yan Su, Qi-Nan Zhuang,[...]. Science 2003
691
42

Variants conferring risk of atrial fibrillation on chromosome 4q25.
Daniel F Gudbjartsson, David O Arnar, Anna Helgadottir, Solveig Gretarsdottir, Hilma Holm, Asgeir Sigurdsson, Adalbjorg Jonasdottir, Adam Baker, Gudmar Thorleifsson, Kristleifur Kristjansson,[...]. Nature 2007
613
35

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation.
Michael H Gollob, Douglas L Jones, Andrew D Krahn, Lynne Danis, Xiang-Qun Gong, Qing Shao, Xiaoqin Liu, John P Veinot, Anthony S L Tang, Alexandre F R Stewart,[...]. N Engl J Med 2006
355
33

Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
Patrick T Ellinor, Kathryn L Lunetta, Christine M Albert, Nicole L Glazer, Marylyn D Ritchie, Albert V Smith, Dan E Arking, Martina Müller-Nurasyid, Bouwe P Krijthe, Steven A Lubitz,[...]. Nat Genet 2012
412
30

Parental atrial fibrillation as a risk factor for atrial fibrillation in offspring.
Caroline S Fox, Helen Parise, Ralph B D'Agostino, Donald M Lloyd-Jones, Ramachandran S Vasan, Thomas J Wang, Daniel Levy, Philip A Wolf, Emelia J Benjamin. JAMA 2004
417
25

Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation.
Marylyn D Ritchie, Shane Rowan, Gayle Kucera, Tanya Stubblefield, Marcia Blair, Shannon Carter, Dan M Roden, Dawood Darbar. J Am Coll Cardiol 2012
68
36

Familial aggregation of atrial fibrillation in Iceland.
David O Arnar, Sverrir Thorvaldsson, Teri A Manolio, Gudmundur Thorgeirsson, Kristleifur Kristjansson, Hakon Hakonarson, Kari Stefansson. Eur Heart J 2006
210
23

Kv1.5 channelopathy due to KCNA5 loss-of-function mutation causes human atrial fibrillation.
Timothy M Olson, Alexey E Alekseev, Xiaoke K Liu, Sungjo Park, Leonid V Zingman, Martin Bienengraeber, Srinivasan Sattiraju, Jeffrey D Ballew, Arshad Jahangir, Andre Terzic. Hum Mol Genet 2006
325
23

Identification of a KCNE2 gain-of-function mutation in patients with familial atrial fibrillation.
Yiqing Yang, Min Xia, Qingfeng Jin, Saïd Bendahhou, Jingyi Shi, Yiping Chen, Bo Liang, Jie Lin, Yi Liu, Ban Liu,[...]. Am J Hum Genet 2004
290
23

Pitx2c and Nkx2-5 are required for the formation and identity of the pulmonary myocardium.
Mathilda T M Mommersteeg, Nigel A Brown, Owen W J Prall, Corrie de Gier-de Vries, Richard P Harvey, Antoon F M Moorman, Vincent M Christoffels. Circ Res 2007
259
23

Mutation in nuclear pore component NUP155 leads to atrial fibrillation and early sudden cardiac death.
Xianqin Zhang, Shenghan Chen, Shin Yoo, Susmita Chakrabarti, Teng Zhang, Tie Ke, Carlos Oberti, Sandro L Yong, Fang Fang, Lin Li,[...]. Cell 2008
177
22

Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation.
Dawood Darbar, Prince J Kannankeril, Brian S Donahue, Gayle Kucera, Tanya Stubblefield, Jonathan L Haines, Alfred L George, Dan M Roden. Circulation 2008
207
22

Familial aggregation in lone atrial fibrillation.
Patrick T Ellinor, Danita M Yoerger, Jeremy N Ruskin, Calum A MacRae. Hum Genet 2005
182
21

Common variants in KCNN3 are associated with lone atrial fibrillation.
Patrick T Ellinor, Kathryn L Lunetta, Nicole L Glazer, Arne Pfeufer, Alvaro Alonso, Mina K Chung, Moritz F Sinner, Paul I W de Bakker, Martina Mueller, Steven A Lubitz,[...]. Nat Genet 2010
342
21

Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation.
Robert L Abraham, Tao Yang, Marcia Blair, Dan M Roden, Dawood Darbar. J Mol Cell Cardiol 2010
62
33

Worldwide epidemiology of atrial fibrillation: a Global Burden of Disease 2010 Study.
Sumeet S Chugh, Rasmus Havmoeller, Kumar Narayanan, David Singh, Michiel Rienstra, Emelia J Benjamin, Richard F Gillum, Young-Hoon Kim, John H McAnulty, Zhi-Jie Zheng,[...]. Circulation 2014
21

A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.
Min Xia, Qingfeng Jin, Saïd Bendahhou, Yusong He, Marie-Madeleine Larroque, Yiping Chen, Qinshu Zhou, Yiqing Yang, Yi Liu, Ban Liu,[...]. Biochem Biophys Res Commun 2005
262
20

Familial atrial fibrillation is a genetically heterogeneous disorder.
Dawood Darbar, Kathleen J Herron, Jeffrey D Ballew, Arshad Jahangir, Bernard J Gersh, Win-K Shen, Stephen C Hammill, Douglas L Packer, Timothy M Olson. J Am Coll Cardiol 2003
231
20

Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
Emelia J Benjamin, Kenneth M Rice, Dan E Arking, Arne Pfeufer, Charlotte van Noord, Albert V Smith, Renate B Schnabel, Joshua C Bis, Eric Boerwinkle, Moritz F Sinner,[...]. Nat Genet 2009
275
19

Familial aggregation of atrial fibrillation: a study in Danish twins.
Ingrid Elisabeth Christophersen, Lasse Steen Ravn, Esben Budtz-Joergensen, Axel Skytthe, Stig Haunsoe, Jesper Hastrup Svendsen, Kaare Christensen. Circ Arrhythm Electrophysiol 2009
134
19

Paradigm of genetic mosaicism and lone atrial fibrillation: physiological characterization of a connexin 43-deletion mutant identified from atrial tissue.
Isabelle L Thibodeau, Ji Xu, Qiuju Li, Gele Liu, Khanh Lam, John P Veinot, David H Birnie, Douglas L Jones, Andrew D Krahn, Robert Lemery,[...]. Circulation 2010
111
18

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.
Morten S Olesen, Lei Yuan, Bo Liang, Anders G Holst, Nikolaj Nielsen, Jonas B Nielsen, Paula L Hedley, Michael Christiansen, Søren-Peter Olesen, Stig Haunsø,[...]. Circ Cardiovasc Genet 2012
92
19

PITX2c is expressed in the adult left atrium, and reducing Pitx2c expression promotes atrial fibrillation inducibility and complex changes in gene expression.
Paulus Kirchhof, Peter C Kahr, Sven Kaese, Ilaria Piccini, Ismail Vokshi, Hans-Heinrich Scheld, Heinrich Rotering, Lisa Fortmueller, Sandra Laakmann, Sander Verheule,[...]. Circ Cardiovasc Genet 2011
190
17

A novel SCN5A gain-of-function mutation M1875T associated with familial atrial fibrillation.
Takeru Makiyama, Masaharu Akao, Satoshi Shizuta, Takahiro Doi, Kei Nishiyama, Yuko Oka, Seiko Ohno, Yukiko Nishio, Keiko Tsuji, Hideki Itoh,[...]. J Am Coll Cardiol 2008
124
17

Identification of a genetic locus for familial atrial fibrillation.
R Brugada, T Tapscott, G Z Czernuszewicz, A J Marian, A Iglesias, L Mont, J Brugada, J Girona, A Domingo, L L Bachinski,[...]. N Engl J Med 1997
380
17

Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.
Hiroshi Watanabe, Dawood Darbar, Daniel W Kaiser, Kim Jiramongkolchai, Sameer Chopra, Brian S Donahue, Prince J Kannankeril, Dan M Roden. Circ Arrhythm Electrophysiol 2009
142
17

Chromosome 4q25 variants and atrial fibrillation recurrence after catheter ablation.
Daniela Husser, Volker Adams, Christopher Piorkowski, Gerhard Hindricks, Andreas Bollmann. J Am Coll Cardiol 2010
147
17

Stretch-sensitive KCNQ1 mutation A link between genetic and environmental factors in the pathogenesis of atrial fibrillation?
Robyn Otway, Jamie I Vandenberg, Guanglan Guo, Anthony Varghese, M Leticia Castro, Jian Liu, JingTing Zhao, Jane A Bursill, Ken R Wyse, Haley Crotty,[...]. J Am Coll Cardiol 2007
101
16

PITX2 insufficiency leads to atrial electrical and structural remodeling linked to arrhythmogenesis.
Ana Chinchilla, Houria Daimi, Estefanía Lozano-Velasco, Jorge N Dominguez, Ricardo Caballero, Eva Delpón, Juan Tamargo, Juan Cinca, Leif Hove-Madsen, Amelia E Aranega,[...]. Circ Cardiovasc Genet 2011
161
16

Association between familial atrial fibrillation and risk of new-onset atrial fibrillation.
Steven A Lubitz, Xiaoyan Yin, João D Fontes, Jared W Magnani, Michiel Rienstra, Manju Pai, Mark L Villalon, Ramachandran S Vasan, Michael J Pencina, Daniel Levy,[...]. JAMA 2010
194
16

Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation.
Moritz F Sinner, Nathan R Tucker, Kathryn L Lunetta, Kouichi Ozaki, J Gustav Smith, Stella Trompet, Joshua C Bis, Honghuang Lin, Mina K Chung, Jonas B Nielsen,[...]. Circulation 2014
128
16

Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.
Timothy M Olson, Virginia V Michels, Jeffrey D Ballew, Sandra P Reyna, Margaret L Karst, Kathleen J Herron, Steven C Horton, Richard J Rodeheffer, Jeffrey L Anderson. JAMA 2005
362
15

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation.
Lasse S Ravn, Yoshiyasu Aizawa, Guido D Pollevick, Jacob Hofman-Bang, Jonathan M Cordeiro, Ulrik Dixen, Gorm Jensen, Yuesheng Wu, Elena Burashnikov, Stig Haunso,[...]. Heart Rhythm 2008
92
16

Spontaneous initiation of atrial fibrillation by ectopic beats originating in the pulmonary veins.
M Haïssaguerre, P Jaïs, D C Shah, A Takahashi, M Hocini, G Quiniou, S Garrigue, A Le Mouroux, P Le Métayer, J Clémenty. N Engl J Med 1998
15

Impact of atrial fibrillation on the risk of death: the Framingham Heart Study.
E J Benjamin, P A Wolf, R B D'Agostino, H Silbershatz, W B Kannel, D Levy. Circulation 1998
15

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.
Morten S Olesen, Thomas Jespersen, Jonas B Nielsen, Bo Liang, Daniel V Møller, Paula Hedley, Michael Christiansen, András Varró, Søren-Peter Olesen, Stig Haunsø,[...]. Cardiovasc Res 2011
81
17

GATA4 loss-of-function mutations in familial atrial fibrillation.
Yi-Qing Yang, Mao-Ya Wang, Xian-Ling Zhang, Hong-Wei Tan, Hai-Feng Shi, Wei-Feng Jiang, Xin-Hua Wang, Wei-Yi Fang, Xu Liu. Clin Chim Acta 2011
53
26


KCNE3 mutation V17M identified in a patient with lone atrial fibrillation.
Alicia Lundby, Lasse Steen Ravn, Jesper Hastrup Svendsen, Stig Hauns, Søren-Peter Olesen, Nicole Schmitt. Cell Physiol Biochem 2008
65
21


Secular trends in incidence of atrial fibrillation in Olmsted County, Minnesota, 1980 to 2000, and implications on the projections for future prevalence.
Yoko Miyasaka, Marion E Barnes, Bernard J Gersh, Stephen S Cha, Kent R Bailey, Walter P Abhayaratna, James B Seward, Teresa S M Tsang. Circulation 2006
14

A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
Daniel F Gudbjartsson, Hilma Holm, Solveig Gretarsdottir, Gudmar Thorleifsson, G Bragi Walters, Gudmundur Thorgeirsson, Jeffrey Gulcher, Ellisiv B Mathiesen, Inger Njølstad, Audhild Nyrnes,[...]. Nat Genet 2009
317
14

Symptomatic response to antiarrhythmic drug therapy is modulated by a common single nucleotide polymorphism in atrial fibrillation.
Babar Parvez, Joseph Vaglio, Shane Rowan, Raafia Muhammad, Gayle Kucera, Tanya Stubblefield, Shannon Carter, Dan Roden, Dawood Darbar. J Am Coll Cardiol 2012
92
15

Development of a risk score for atrial fibrillation (Framingham Heart Study): a community-based cohort study.
Renate B Schnabel, Lisa M Sullivan, Daniel Levy, Michael J Pencina, Joseph M Massaro, Ralph B D'Agostino, Christopher Newton-Cheh, Jennifer F Yamamoto, Jared W Magnani, Thomas M Tadros,[...]. Lancet 2009
686
14

Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillation.
Saumya Das, Seiko Makino, Yonathan F Melman, Marisa A Shea, Sanjeev B Goyal, Anthony Rosenzweig, Calum A Macrae, Patrick T Ellinor. Heart Rhythm 2009
68
19

Autosomal recessive atrial dilated cardiomyopathy with standstill evolution associated with mutation of Natriuretic Peptide Precursor A.
Marcello Disertori, Silvia Quintarelli, Maurizia Grasso, Andrea Pilotto, Nupoor Narula, Valentina Favalli, Camilla Canclini, Marta Diegoli, Silvia Mazzola, Massimiliano Marini,[...]. Circ Cardiovasc Genet 2013
32
40

Novel germline GJA5/connexin40 mutations associated with lone atrial fibrillation impair gap junctional intercellular communication.
Yiguo Sun, Yi-Qing Yang, Xiang-Qun Gong, Xin-Hua Wang, Ruo-Gu Li, Hong-Wei Tan, Xu Liu, Wei-Yi Fang, Donglin Bai. Hum Mutat 2013
48
27

Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.
Pengyun Wang, Qinbo Yang, Xiaofen Wu, Yanzong Yang, Lisong Shi, Chuchu Wang, Gang Wu, Yunlong Xia, Bo Yang, Rongfeng Zhang,[...]. Biochem Biophys Res Commun 2010
59
22

Identification of NPPA variants associated with atrial fibrillation in a Chinese GeneID population.
Xiang Ren, Chengqi Xu, Chengxiong Zhan, Yanzong Yang, Lisong Shi, Fan Wang, Chuchu Wang, Yunlong Xia, Bo Yang, Gang Wu,[...]. Clin Chim Acta 2010
46
28

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.
Ri-Tai Huang, Song Xue, Ying-Jia Xu, Min Zhou, Yi-Qing Yang. Int J Mol Med 2013
48
27


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.