A citation-based method for searching scientific literature

Maria Valeria Esposito, Giuseppina Minopoli, Luciana Esposito, Valeria D'Argenio, Federica Di Maggio, Emanuele Sasso, Massimiliano D'Aiuto, Nicola Zambrano, Francesco Salvatore. Cancers (Basel) 2019
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


High-throughput functional evaluation of BRCA2 variants of unknown significance.
Masachika Ikegami, Shinji Kohsaka, Toshihide Ueno, Yukihide Momozawa, Satoshi Inoue, Kenji Tamura, Akihiko Shimomura, Noriko Hosoya, Hiroshi Kobayashi, Sakae Tanaka,[...]. Nat Commun 2020
13
66

Germline and somatic mutations in homologous recombination genes predict platinum response and survival in ovarian, fallopian tube, and peritoneal carcinomas.
Kathryn P Pennington, Tom Walsh, Maria I Harrell, Ming K Lee, Christopher C Pennil, Mara H Rendi, Anne Thornton, Barbara M Norquist, Silvia Casadei, Alexander S Nord,[...]. Clin Cancer Res 2014
489
66

A cancer-associated BRCA2 mutation reveals masked nuclear export signals controlling localization.
Anand D Jeyasekharan, Yang Liu, Hiroyoshi Hattori, Venkat Pisupati, Asta Bjork Jonsdottir, Eeson Rajendra, Miyoung Lee, Elayanambi Sundaramoorthy, Simon Schlachter, Clemens F Kaminski,[...]. Nat Struct Mol Biol 2013
61
66

Significance of sarcomere gene mutations analysis in the end-stage phase of hypertrophic cardiomyopathy.
Elena Biagini, Iacopo Olivotto, Maria Iascone, Maria I Parodi, Francesca Girolami, Giulia Frisso, Camillo Autore, Giuseppe Limongelli, Massimiliano Cecconi, Barry J Maron,[...]. Am J Cardiol 2014
48
33

Compound and digenic heterozygosity contributes to arrhythmogenic right ventricular cardiomyopathy.
Tianhong Xu, Zhao Yang, Matteo Vatta, Alessandra Rampazzo, Giorgia Beffagna, Kalliopi Pilichou, Steven E Scherer, Jeffrey Saffitz, Joshua Kravitz, Wojciech Zareba,[...]. J Am Coll Cardiol 2010
223
33

Impact of genotype on clinical course in arrhythmogenic right ventricular dysplasia/cardiomyopathy-associated mutation carriers.
Aditya Bhonsale, Judith A Groeneweg, Cynthia A James, Dennis Dooijes, Crystal Tichnell, Jan D H Jongbloed, Brittney Murray, Anneline S J M te Riele, Maarten P van den Berg, Hennie Bikker,[...]. Eur Heart J 2015
198
33

Arrhythmogenic right ventricular cardiomyopathy: An update.
G Thiene, C Basso. Cardiovasc Pathol 2001
59
33

Perspectives on pre-participation cardiovascular screening in young competitive athletes: U SPORTS.
Carlee Cater, Mackenzie MacDonald, Daniel Lithwick, Kamal Sidhu, Saul Isserow, James McKinney. Phys Sportsmed 2018
1
100

Diagnosis of arrhythmogenic right ventricular cardiomyopathy/dysplasia: proposed modification of the Task Force Criteria.
Frank I Marcus, William J McKenna, Duane Sherrill, Cristina Basso, Barbara Bauce, David A Bluemke, Hugh Calkins, Domenico Corrado, Moniek G P J Cox, James P Daubert,[...]. Eur Heart J 2010
719
33

Trends in sudden cardiovascular death in young competitive athletes after implementation of a preparticipation screening program.
Domenico Corrado, Cristina Basso, Andrea Pavei, Pierantonio Michieli, Maurizio Schiavon, Gaetano Thiene. JAMA 2006
889
33


Harms and benefits of screening young people to prevent sudden cardiac death.
Hans Van Brabandt, Anja Desomer, Sophie Gerkens, Mattias Neyt. BMJ 2016
27
33

Correlation of ventricular arrhythmias with genotype in arrhythmogenic right ventricular cardiomyopathy.
Jingru Bao, Jizheng Wang, Yan Yao, Yilu Wang, Xiaohan Fan, Kai Sun, Ding Sheng He, Frank I Marcus, Shu Zhang, Rutai Hui,[...]. Circ Cardiovasc Genet 2013
39
33

Clinical Presentation, Long-Term Follow-Up, and Outcomes of 1001 Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Patients and Family Members.
Judith A Groeneweg, Aditya Bhonsale, Cynthia A James, Anneline S te Riele, Dennis Dooijes, Crystal Tichnell, Brittney Murray, Ans C P Wiesfeld, Abhishek C Sawant, Bina Kassamali,[...]. Circ Cardiovasc Genet 2015
222
33


Novel plakophilin2 mutation: three-generation family with arrhythmogenic right ventricular cardiomyopathy.
Meriam Åström Aneq, Christina Fluur, Malin Rehnberg, Peter Söderkvist, Jan Engvall, Eva Nylander, Cecilia Gunnarsson. Scand Cardiovasc J 2012
5
33

Syncope Due to Ventricular Arrhythmia Triggered by Electronic Gaming.
Claire M Lawley, Jonathan R Skinner, Christian Turner. N Engl J Med 2019
3
33

Clinical Genetic Testing for the Cardiomyopathies and Arrhythmias: A Systematic Framework for Establishing Clinical Validity and Addressing Genotypic and Phenotypic Heterogeneity.
John Garcia, Jackie Tahiliani, Nicole Marie Johnson, Sienna Aguilar, Daniel Beltran, Amy Daly, Emily Decker, Eden Haverfield, Blanca Herrera, Laura Murillo,[...]. Front Cardiovasc Med 2016
13
33

Vigorous physical activity impairs myocardial function in patients with arrhythmogenic right ventricular cardiomyopathy and in mutation positive family members.
Jørg Saberniak, Nina E Hasselberg, Rasmus Borgquist, Pyotr G Platonov, Sebastian I Sarvari, Hans-Jørgen Smith, Margareth Ribe, Anders G Holst, Thor Edvardsen, Kristina H Haugaa. Eur J Heart Fail 2014
125
33

DANN: a deep learning approach for annotating the pathogenicity of genetic variants.
Daniel Quang, Yifei Chen, Xiaohui Xie. Bioinformatics 2015
376
33

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy.
Brenda Gerull, Arnd Heuser, Thomas Wichter, Matthias Paul, Craig T Basson, Deborah A McDermott, Bruce B Lerman, Steve M Markowitz, Patrick T Ellinor, Calum A MacRae,[...]. Nat Genet 2004
534
33

Clinical Diagnosis, Imaging, and Genetics of Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia: JACC State-of-the-Art Review.
Estelle Gandjbakhch, Alban Redheuil, Françoise Pousset, Philippe Charron, Robert Frank. J Am Coll Cardiol 2018
74
33

Role of Genetic Testing in Inherited Cardiovascular Disease: A Review.
Allison L Cirino, Stephanie Harris, Neal K Lakdawala, Michelle Michels, Iacopo Olivotto, Sharlene M Day, Dominic J Abrams, Philippe Charron, Colleen Caleshu, Christopher Semsarian,[...]. JAMA Cardiol 2017
43
33

Compound and digenic heterozygosity predicts lifetime arrhythmic outcome and sudden cardiac death in desmosomal gene-related arrhythmogenic right ventricular cardiomyopathy.
Ilaria Rigato, Barbara Bauce, Alessandra Rampazzo, Alessandro Zorzi, Kalliopi Pilichou, Elisa Mazzotti, Federico Migliore, Martina Perazzolo Marra, Alessandra Lorenzon, Marzia De Bortoli,[...]. Circ Cardiovasc Genet 2013
143
33

Genetic analysis in a family affected by sick sinus syndrome may reduce the sudden death risk in a young aspiring competitive athlete.
Nicola Detta, Giulia Frisso, Giuseppe Limongelli, Michele Marzullo, Raffaele Calabrò, Francesco Salvatore. Int J Cardiol 2014
16
33

DNA sequence capture and next-generation sequencing for the molecular diagnosis of genetic cardiomyopathies.
Valeria D'Argenio, Giulia Frisso, Vincenza Precone, Angelo Boccia, Antonella Fienga, Giuseppe Pacileo, Giuseppe Limongelli, Giovanni Paolella, Raffaele Calabrò, Francesco Salvatore. J Mol Diagn 2014
32
33

Does sports activity enhance the risk of sudden death in adolescents and young adults?
Domenico Corrado, Cristina Basso, Giulio Rizzoli, Maurizio Schiavon, Gaetano Thiene. J Am Coll Cardiol 2003
732
33

Association of competitive and recreational sport participation with cardiac events in patients with arrhythmogenic right ventricular cardiomyopathy: results from the North American multidisciplinary study of arrhythmogenic right ventricular cardiomyopathy.
Anne-Christine Ruwald, Frank Marcus, N A Mark Estes, Mark Link, Scott McNitt, Bronislava Polonsky, Hugh Calkins, Jeffrey A Towbin, Arthur J Moss, Wojciech Zareba. Eur Heart J 2015
141
33

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013.
Silvia G Priori, Arthur A Wilde, Minoru Horie, Yongkeun Cho, Elijah R Behr, Charles Berul, Nico Blom, Josep Brugada, Chern-En Chiang, Heikki Huikuri,[...]. Heart Rhythm 2013
995
33

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
33

Arrhythmogenic right ventricular cardiomyopathy: evaluation of the current diagnostic criteria and differential diagnosis.
Domenico Corrado, Peter J van Tintelen, William J McKenna, Richard N W Hauer, Aris Anastastakis, Angeliki Asimaki, Cristina Basso, Barbara Bauce, Corinna Brunckhorst, Chiara Bucciarelli-Ducci,[...]. Eur Heart J 2020
74
33

A novel PKP2 mutation and intrafamilial phenotypic variability in ARVC/D.
Nejat Mahdieh, Sedigheh Saedi, Mahdieh Soveizi, Bahareh Rabbani, Nasim Najafi, Majid Maleki. Med J Islam Repub Iran 2018
2
50



2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary.
Jeffrey A Towbin, William J McKenna, Dominic J Abrams, Michael J Ackerman, Hugh Calkins, Francisco C C Darrieux, James P Daubert, Christian de Chillou, Eugene C DePasquale, Milind Y Desai,[...]. Heart Rhythm 2019
58
33

A child cohort study from southern Italy enlarges the genetic spectrum of hypertrophic cardiomyopathy.
G Frisso, G Limongelli, G Pacileo, A Del Giudice, L Forgione, P Calabrò, M Iacomino, N Detta, L M Di Fonzo, V Maddaloni,[...]. Clin Genet 2009
26
33

Familial evaluation in arrhythmogenic right ventricular cardiomyopathy: impact of genetics and revised task force criteria.
Giovanni Quarta, Alison Muir, Antonios Pantazis, Petros Syrris, Katja Gehmlich, Pablo Garcia-Pavia, Deirdre Ward, Srijita Sen-Chowdhry, Perry M Elliott, William J McKenna. Circulation 2011
159
33

Risk of sports: do we need a pre-participation screening for competitive and leisure athletes?
Domenico Corrado, Christian Schmied, Cristina Basso, Mats Borjesson, Maurizio Schiavon, Antonio Pelliccia, Luc Vanhees, Gaetano Thiene. Eur Heart J 2011
117
33

BRCA1 and Its Network of Interacting Partners.
Charita M Christou, Kyriacos Kyriacou. Biology (Basel) 2013
23
33

Replication Fork Reversal: Players and Guardians.
Annabel Quinet, Delphine Lemaçon, Alessandro Vindigni. Mol Cell 2017
106
33

Inherited Mutations in Women With Ovarian Carcinoma.
Barbara M Norquist, Maria I Harrell, Mark F Brady, Tom Walsh, Ming K Lee, Suleyman Gulsuner, Sarah S Bernards, Silvia Casadei, Qian Yi, Robert A Burger,[...]. JAMA Oncol 2016
338
33

Impact of amino acid substitutions at secondary structures in the BRCT domains of the tumor suppressor BRCA1: Implications for clinical annotation.
Vanessa C Fernandes, Volha A Golubeva, Giuliano Di Pietro, Cara Shields, Kwabena Amankwah, Thales C Nepomuceno, Giuliana de Gregoriis, Renata B V Abreu, Carly Harro, Thiago T Gomes,[...]. J Biol Chem 2019
13
33

Improved survival in women with BRCA-associated ovarian carcinoma.
Ilana Cass, Rae Lynn Baldwin, Taz Varkey, Roxana Moslehi, Steven A Narod, Beth Y Karlan. Cancer 2003
339
33

Long-term ovarian cancer survival associated with mutation in BRCA1 or BRCA2.
John R McLaughlin, Barry Rosen, Joel Moody, Tuya Pal, Isabel Fan, Patricia A Shaw, Harvey A Risch, Thomas A Sellers, Ping Sun, Steven A Narod. J Natl Cancer Inst 2013
93
33

Integrated analysis of germline and somatic variants in ovarian cancer.
Krishna L Kanchi, Kimberly J Johnson, Charles Lu, Michael D McLellan, Mark D M Leiserson, Michael C Wendl, Qunyuan Zhang, Daniel C Koboldt, Mingchao Xie, Cyriac Kandoth,[...]. Nat Commun 2014
176
33

Olaparib Versus Nonplatinum Chemotherapy in Patients With Platinum-Sensitive Relapsed Ovarian Cancer and a Germline BRCA1/2 Mutation (SOLO3): A Randomized Phase III Trial.
Richard T Penson, Ricardo Villalobos Valencia, David Cibula, Nicoletta Colombo, Charles A Leath, Mariusz Bidziński, Jae-Weon Kim, Joo Hyun Nam, Radoslaw Madry, Carlos Hernández,[...]. J Clin Oncol 2020
43
33

BRCA1-BARD1 promotes RAD51-mediated homologous DNA pairing.
Weixing Zhao, Justin B Steinfeld, Fengshan Liang, Xiaoyong Chen, David G Maranon, Chu Jian Ma, Youngho Kwon, Timsi Rao, Weibin Wang, Chen Sheng,[...]. Nature 2017
123
33

Improved survival for BRCA2-associated serous ovarian cancer compared with both BRCA-negative and BRCA1-associated serous ovarian cancer.
David M Hyman, Qin Zhou, Alexia Iasonos, Rachel N Grisham, Angela G Arnold, Mary F Phillips, Jasmine Bhatia, Douglas A Levine, Carol Aghajanian, Kenneth Offit,[...]. Cancer 2012
58
33

Similar response rates and survival with PARP inhibitors for patients with solid tumors harboring somatic versus Germline BRCA mutations: a Meta-analysis and systematic review.
Ghulam Rehman Mohyuddin, Muhammad Aziz, Alec Britt, Lee Wade, Weijing Sun, Joaquina Baranda, Raed Al-Rajabi, Anwaar Saeed, Anup Kasi. BMC Cancer 2020
12
33

ATR inhibition disrupts rewired homologous recombination and fork protection pathways in PARP inhibitor-resistant BRCA-deficient cancer cells.
Stephanie A Yazinski, Valentine Comaills, Rémi Buisson, Marie-Michelle Genois, Hai Dang Nguyen, Chu Kwen Ho, Tanya Todorova Kwan, Robert Morris, Sam Lauffer, André Nussenzweig,[...]. Genes Dev 2017
158
33


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.