A citation-based method for searching scientific literature

G L Fawcett, A Karina Eterovic. Adv Clin Chem 2017
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Advantages of RNA-seq compared to RNA microarrays for transcriptome profiling of anterior cruciate ligament tears.
Muhammad Farooq Rai, Eric D Tycksen, Linda J Sandell, Robert H Brophy. J Orthop Res 2018
23
50

Adult congenital heart disease: a 2008 overview.
Elisabeth Bédard, Darryl F Shore, Michael A Gatzoulis. Br Med Bull 2008
35
50


Genetics of congenital heart disease: the glass half empty.
Akl C Fahed, Bruce D Gelb, J G Seidman, Christine E Seidman. Circ Res 2013
310
50

Genetic analysis of Iranian family with hereditary cardiac arrhythmias by next generation sequencing.
Marzieh Asadi, Roger Foo, Mohammad Reza Samienasab, Ahmad Reza Salehi, Majid Kheirollahi, Hossein Khanahmad, Rasoul Salehi. Adv Biomed Res 2016
5
50

Genomic DNA pooling strategy for next-generation sequencing-based rare variant discovery in abdominal aortic aneurysm regions of interest-challenges and limitations.
Magdalena Harakalova, Isaäc J Nijman, Jelena Medic, Michal Mokry, Ivo Renkens, Jan D Blankensteijn, Wigard Kloosterman, Annette F Baas, Edwin Cuppen. J Cardiovasc Transl Res 2011
17
50

Impact of Next-Generation Sequencing (NGS) technology on cardiovascular disease research.
Fengping Xu, Qin Wang, Fangfang Zhang, Yinling Zhu, Qingquan Gu, Liping Wu, Lin Yang, Xu Yang. Cardiovasc Diagn Ther 2012
5
50

Clinical utility of genetic tests for inherited hypertrophic and dilated cardiomyopathies.
Maria Giovanna Colombo, Nicoletta Botto, Simona Vittorini, Umberto Paradossi, Maria Grazia Andreassi. Cardiovasc Ultrasound 2008
25
50

Familial hypertrophic cardiomyopathy: basic concepts and future molecular diagnostics.
Jessica E Rodríguez, Christopher R McCudden, Monte S Willis. Clin Biochem 2009
19
50

MicroRNA-208a is a regulator of cardiac hypertrophy and conduction in mice.
Thomas E Callis, Kumar Pandya, Hee Young Seok, Ru-Hang Tang, Mariko Tatsuguchi, Zhan-Peng Huang, Jian-Fu Chen, Zhongliang Deng, Bronwyn Gunn, Janelle Shumate,[...]. J Clin Invest 2009
588
50

A survey of best practices for RNA-seq data analysis.
Ana Conesa, Pedro Madrigal, Sonia Tarazona, David Gomez-Cabrero, Alejandra Cervera, Andrew McPherson, Michał Wojciech Szcześniak, Daniel J Gaffney, Laura L Elo, Xuegong Zhang,[...]. Genome Biol 2016
937
50

RNA-Seq and human complex diseases: recent accomplishments and future perspectives.
Valerio Costa, Marianna Aprile, Roberta Esposito, Alfredo Ciccodicola. Eur J Hum Genet 2013
120
50

Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome.
Catarina Allegue, Mònica Coll, Jesus Mates, Oscar Campuzano, Anna Iglesias, Beatriz Sobrino, Maria Brion, Jorge Amigo, Angel Carracedo, Pedro Brugada,[...]. PLoS One 2015
30
50

Bioinformatics for next generation sequencing.
Alex Bateman, John Quackenbush. Bioinformatics 2009
14
50

T-box transcription factor TBX20 mutations in Chinese patients with congenital heart disease.
Caixia Liu, Adong Shen, Xiaofeng Li, Weiwei Jiao, Xingen Zhang, Zhongzhi Li. Eur J Med Genet 2008
55
50

De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.
James R Priest, Kazutoyo Osoegawa, Nebil Mohammed, Vivek Nanda, Ramendra Kundu, Kathleen Schultz, Edward J Lammer, Santhosh Girirajan, Todd Scheetz, Daryl Waggott,[...]. PLoS Genet 2016
60
50

Mutations in the gene for cardiac myosin-binding protein C and late-onset familial hypertrophic cardiomyopathy.
H Niimura, L L Bachinski, S Sangwatanaroj, H Watkins, A E Chudley, W McKenna, A Kristinsson, R Roberts, M Sole, B J Maron,[...]. N Engl J Med 1998
510
50

Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters.
K E Berge, H Tian, G A Graf, L Yu, N V Grishin, J Schultz, P Kwiterovich, B Shan, R Barnes, H H Hobbs. Science 2000
50

Missing heritability of common diseases and treatments outside the protein-coding exome.
Wolfgang Sadee, Katherine Hartmann, Michał Seweryn, Maciej Pietrzak, Samuel K Handelman, Grzegorz A Rempala. Hum Genet 2014
40
50

Next Generation Sequencing and Linkage Analysis for the Molecular Diagnosis of a Novel Overlapping Syndrome Characterized by Hypertrophic Cardiomyopathy and Typical Electrical Instability of Brugada Syndrome.
Ruggiero Mango, Andrea Luchetti, Raffaele Sangiuolo, Valentina Ferradini, Nicola Briglia, Emiliano Giardina, Fabrizio Ferrè, Manuela Helmer Citterich, Francesco Romeo, Giuseppe Novelli,[...]. Circ J 2016
17
50

Clinical utility gene card for: long-QT syndrome (types 1-13).
Britt-Maria Beckmann, Arthur A M Wilde, Stefan Kääb. Eur J Hum Genet 2013
8
50

The transcriptional landscape of the yeast genome defined by RNA sequencing.
Ugrappa Nagalakshmi, Zhong Wang, Karl Waern, Chong Shou, Debasish Raha, Mark Gerstein, Michael Snyder. Science 2008
50

SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing.
Muhammad Tariq, John W Belmont, Seema Lalani, Teresa Smolarek, Stephanie M Ware. Genome Biol 2011
42
50

Next-generation sequencing: from basic research to diagnostics.
Karl V Voelkerding, Shale A Dames, Jacob D Durtschi. Clin Chem 2009
375
50

Polygenic Versus Monogenic Causes of Hypercholesterolemia Ascertained Clinically.
Jian Wang, Jacqueline S Dron, Matthew R Ban, John F Robinson, Adam D McIntyre, Maher Alazzam, Pei Jun Zhao, Allison A Dilliott, Henian Cao, Murray W Huff,[...]. Arterioscler Thromb Vasc Biol 2016
116
50

A novel variant in RyR2 causes familiar catecholaminergic polymorphic ventricular tachycardia.
Cristina Bosch, Oscar Campuzano, Georgia Sarquella-Brugada, Sergi Cesar, Alexandra Perez-Serra, Monica Coll, Irene Mademont, Jesus Mates, Bernat Del Olmo, Anna Iglesias,[...]. Forensic Sci Int 2017
2
50

The genetics of dilated cardiomyopathy.
Lisa Dellefave, Elizabeth M McNally. Curr Opin Cardiol 2010
93
50

The resequencing imperative.
Eric J Topol, Kelly A Frazer. Nat Genet 2007
37
50

Obstacles and opportunities for the future of genomic medicine.
Benjamin D Solomon. Mol Genet Genomic Med 2014
9
50


The Benefits of Whole-Genome Sequencing Now and in the Future.
Alina Khromykh, Benjamin D Solomon. Mol Syndromol 2015
6
50



Phased whole-genome genetic risk in a family quartet using a major allele reference sequence.
Frederick E Dewey, Rong Chen, Sergio P Cordero, Kelly E Ormond, Colleen Caleshu, Konrad J Karczewski, Michelle Whirl-Carrillo, Matthew T Wheeler, Joel T Dudley, Jake K Byrnes,[...]. PLoS Genet 2011
99
50

Targeted next-generation sequencing identifies pathogenic variants in familial congenital heart disease.
Gillian M Blue, Edwin P Kirk, Eleni Giannoulatou, Sally L Dunwoodie, Joshua W K Ho, Desiree C K Hilton, Susan M White, Gary F Sholler, Richard P Harvey, David S Winlaw. J Am Coll Cardiol 2014
54
50

Deep mRNA sequencing for in vivo functional analysis of cardiac transcriptional regulators: application to Galphaq.
Scot J Matkovich, Yan Zhang, Derek J Van Booven, Gerald W Dorn. Circ Res 2010
68
50

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death.
Charles Antzelevitch, Guido D Pollevick, Jonathan M Cordeiro, Oscar Casis, Michael C Sanguinetti, Yoshiyasu Aizawa, Alejandra Guerchicoff, Ryan Pfeiffer, Antonio Oliva, Bernd Wollnik,[...]. Circulation 2007
590
50

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).
Michael J Ackerman, Silvia G Priori, Stephan Willems, Charles Berul, Ramon Brugada, Hugh Calkins, A John Camm, Patrick T Ellinor, Michael Gollob, Robert Hamilton,[...]. Heart Rhythm 2011
619
50


The sequence of sequencers: The history of sequencing DNA.
James M Heather, Benjamin Chain. Genomics 2016
264
50


Brugada syndrome.
Ramon Brugada, Oscar Campuzano, Georgia Sarquella-Brugada, Josep Brugada, Pedro Brugada. Methodist Debakey Cardiovasc J 2014
65
50

A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia.
Dalya Marks, Margaret Thorogood, H Andrew W Neil, Steve E Humphries. Atherosclerosis 2003
384
50

Yield of genetic screening in inherited cardiac channelopathies: how to prioritize access to genetic testing.
Rong Bai, Carlo Napolitano, Raffaella Bloise, Nicola Monteforte, Silvia G Priori. Circ Arrhythm Electrophysiol 2009
94
50

Rapid detection of gene mutations responsible for non-syndromic aortic aneurysm and dissection using two different methods: resequencing microarray technology and next-generation sequencing.
Haruya Sakai, Shinichi Suzuki, Takeshi Mizuguchi, Kiyotaka Imoto, Yuki Yamashita, Hiroshi Doi, Masakazu Kikuchi, Yoshinori Tsurusaki, Hirotomo Saitsu, Noriko Miyake,[...]. Hum Genet 2012
16
50

Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease.
Stephanie LaHaye, Don Corsmeier, Madhumita Basu, Jessica L Bowman, Sara Fitzgerald-Butt, Gloria Zender, Kevin Bosse, Kim L McBride, Peter White, Vidu Garg. Circ Cardiovasc Genet 2016
39
50


Molecular basis of a linkage peak: exome sequencing and family-based analysis identify a rare genetic variant in the ADIPOQ gene in the IRAS Family Study.
Donald W Bowden, S Sandy An, Nicholette D Palmer, W Mark Brown, Jill M Norris, Stephen M Haffner, Gregory A Hawkins, Xiuqing Guo, Jerome I Rotter, Y-D Ida Chen,[...]. Hum Mol Genet 2010
65
50

A common variant on chromosome 9p21 affects the risk of myocardial infarction.
Anna Helgadottir, Gudmar Thorleifsson, Andrei Manolescu, Solveig Gretarsdottir, Thorarinn Blondal, Aslaug Jonasdottir, Adalbjorg Jonasdottir, Asgeir Sigurdsson, Adam Baker, Arnar Palsson,[...]. Science 2007
50

Technology: The $1,000 genome.
Erika Check Hayden. Nature 2014
207
50


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.