A citation-based method for searching scientific literature

Benjamin Stern, Thomas McGarrity, Maria Baker. Curr Treat Options Gastroenterol 2019
Times Cited: 1

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

Times Cited
  Times     Co-cited

Complexity of genome sequencing and reporting: Next generation sequencing (NGS) technologies and implementation of precision medicine in real life.
Stefania Morganti, Paolo Tarantino, Emanuela Ferraro, Paolo D'Amico, Giulia Viale, Dario Trapani, Bruno Achutti Duso, Giuseppe Curigliano. Crit Rev Oncol Hematol 2019

Translating cancer genomics into precision medicine with artificial intelligence: applications, challenges and future perspectives.
Jia Xu, Pengwei Yang, Shang Xue, Bhuvan Sharma, Marta Sanchez-Martin, Fang Wang, Kirk A Beaty, Elinor Dehan, Baiju Parikh. Hum Genet 2019

Lynch Syndrome: From Screening to Diagnosis to Treatment in the Era of Modern Molecular Oncology.
Stacey A Cohen, Colin C Pritchard, Gail P Jarvik. Annu Rev Genomics Hum Genet 2019

An Overview of DNA Analytical Methods.
Valerie A Arboleda, Rena R Xian. Methods Mol Biol 2019

The Ensembl Variant Effect Predictor.
William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010

Automated Workflow for Somatic and Germline Next Generation Sequencing Analysis in Routine Clinical Cancer Diagnostics.
Lucia Anna Muscarella, Federico Pio Fabrizio, Maria De Bonis, Maria Teresa Mancini, Teresa Balsamo, Paolo Graziano, Flavia Centra, Angelo Sparaneo, Domenico Trombetta, Antonio Bonfitto,[...]. Cancers (Basel) 2019

Multi-Gene Panel Testing of 23,179 Individuals for Hereditary Cancer Risk Identifies Pathogenic Variant Carriers Missed by Current Genetic Testing Guidelines.
Cynthia L Neben, Anjali D Zimmer, Will Stedden, Jeroen van den Akker, Robert O'Connor, Raymond C Chan, Elaine Chen, Zheng Tan, Annette Leon, Jack Ji,[...]. J Mol Diagn 2019

Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing.
Eric Samorodnitsky, Benjamin M Jewell, Raffi Hagopian, Jharna Miya, Michele R Wing, Ezra Lyon, Senthilkumar Damodaran, Darshna Bhatt, Julie W Reeser, Jharna Datta,[...]. Hum Mutat 2015

Workload measurement for molecular genetics laboratory: A survey study.
Enrico Tagliafico, Isabella Bernardis, Marina Grasso, Maria Rosaria D'Apice, Cristina Lapucci, Annalisa Botta, Daniela Francesca Giachino, Maria Marinelli, Paola Primignani, Silvia Russo,[...]. PLoS One 2018

Long walk to genomics: History and current approaches to genome sequencing and assembly.
Alice Maria Giani, Guido Roberto Gallo, Luca Gianfranceschi, Giulio Formenti. Comput Struct Biotechnol J 2019

Sanger Confirmation Is Required to Achieve Optimal Sensitivity and Specificity in Next-Generation Sequencing Panel Testing.
Wenbo Mu, Hsiao-Mei Lu, Jefferey Chen, Shuwei Li, Aaron M Elliott. J Mol Diagn 2016

A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers.
Michael A Quail, Miriam Smith, Paul Coupland, Thomas D Otto, Simon R Harris, Thomas R Connor, Anna Bertoni, Harold P Swerdlow, Yong Gu. BMC Genomics 2012

Validation of copy number variation analysis for next-generation sequencing diagnostics.
Jamie M Ellingford, Christopher Campbell, Stephanie Barton, Sanjeev Bhaskar, Saurabh Gupta, Rachel L Taylor, Panagiotis I Sergouniotis, Bradley Horn, Janine A Lamb, Michel Michaelides,[...]. Eur J Hum Genet 2017

Overview of Target Enrichment Strategies.
Iwanka Kozarewa, Javier Armisen, Andrew F Gardner, Barton E Slatko, C L Hendrickson. Curr Protoc Mol Biol 2015

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

Library preparation for next generation sequencing: A review of automation strategies.
J F Hess, T A Kohl, M Kotrová, K Rönsch, T Paprotka, V Mohr, T Hutzenlaub, M Brüggemann, R Zengerle, S Niemann,[...]. Biotechnol Adv 2020

Key questions about the future of laboratory medicine in the next decade of the 21st century: A report from the IFCC-Emerging Technologies Division.
Ronda F Greaves, Sergio Bernardini, Maurizio Ferrari, Paolo Fortina, Bernard Gouget, Damien Gruson, Tim Lang, Tze Ping Loh, Howard A Morris, Jason Y Park,[...]. Clin Chim Acta 2019

Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing.
Lisa R Susswein, Megan L Marshall, Rachel Nusbaum, Kristen J Vogel Postula, Scott M Weissman, Lauren Yackowski, Erica M Vaccari, Jeffrey Bissonnette, Jessica K Booker, M Laura Cremona,[...]. Genet Med 2016

Opportunities and challenges of whole-genome and -exome sequencing.
Britt-Sabina Petersen, Broder Fredrich, Marc P Hoeppner, David Ellinghaus, Andre Franke. BMC Genet 2017

Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients.
Beth Crawford, Sophie B Adams, Taylor Sittler, Jeroen van den Akker, Salina Chan, Ofri Leitner, Lauren Ryan, Elad Gil, Laura van 't Veer. Breast Cancer Res Treat 2017

Molecular genetic testing and the future of clinical genomics.
Sara Huston Katsanis, Nicholas Katsanis. Nat Rev Genet 2013

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.