A citation-based method for searching scientific literature

John Michael O Ranola, Rachel Pearlman, Heather Hampel, Brian H Shirts. Fam Cancer 2019
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Improving performance of multigene panels for genomic analysis of cancer predisposition.
Brian H Shirts, Silvia Casadei, Angela L Jacobson, Ming K Lee, Suleyman Gulsuner, Robin L Bennett, Margaret Miller, Sarah A Hall, Heather Hampel, Fuki M Hisama,[...]. Genet Med 2016
54
100

Barriers to Lynch Syndrome Testing and Preoperative Result Availability in Early-onset Colorectal Cancer: A National Physician Survey Study.
Alan Noll, Parth J Parekh, Meijiao Zhou, Thomas K Weber, Dennis Ahnen, Xiao-Cheng Wu, Jordan J Karlitz. Clin Transl Gastroenterol 2018
16
100

Two-stain immunohistochemical screening for Lynch syndrome in colorectal cancer may fail to detect mismatch repair deficiency.
Rachel Pearlman, Michael Markow, Deborah Knight, Wei Chen, Christina A Arnold, Colin C Pritchard, Heather Hampel, Wendy L Frankel. Mod Pathol 2018
27
100

Tumour MLH1 promoter region methylation testing is an effective prescreen for Lynch Syndrome (HNPCC).
K Newton, N M Jorgensen, A J Wallace, D D Buchanan, F Lalloo, R F T McMahon, J Hill, D G Evans. J Med Genet 2014
37
100

Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Matthew B Yurgelun, Matthew H Kulke, Charles S Fuchs, Brian A Allen, Hajime Uno, Jason L Hornick, Chinedu I Ukaegbu, Lauren K Brais, Philip G McNamara, Robert J Mayer,[...]. J Clin Oncol 2017
183
100

Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Mark Clendenning, Kaisa Sotamaa, Thomas Prior, Judith A Westman,[...]. J Clin Oncol 2008
547
100

Prevalence and Spectrum of Germline Cancer Susceptibility Gene Mutations Among Patients With Early-Onset Colorectal Cancer.
Rachel Pearlman, Wendy L Frankel, Benjamin Swanson, Weiqiang Zhao, Ahmet Yilmaz, Kristin Miller, Jason Bacher, Christopher Bigley, Lori Nelsen, Paul J Goodfellow,[...]. JAMA Oncol 2017
283
100

Colon and endometrial cancers with mismatch repair deficiency can arise from somatic, rather than germline, mutations.
Sigurdis Haraldsdottir, Heather Hampel, Jerneja Tomsic, Wendy L Frankel, Rachel Pearlman, Albert de la Chapelle, Colin C Pritchard. Gastroenterology 2014
234
100

Impact of a Cancer Gene Variant Reclassification Program Over a 20-Year Period.
Lisa Esterling, Ranjula Wijayatunge, Krystal Brown, Brian Morris, Elisha Hughes, Dmitry Pruss, Susan Manley, Karla R Bowles, Theodora S Ross. JCO Precis Oncol 2020
10
100

Immunohistochemistry as first-line screening for detecting colorectal cancer patients at risk for hereditary nonpolyposis colorectal cancer syndrome: a 2-antibody panel may be as predictive as a 4-antibody panel.
Jinru Shia, Laura H Tang, Efsevia Vakiani, Jose G Guillem, Zsofia K Stadler, Robert A Soslow, Nora Katabi, Martin R Weiser, Philip B Paty, Larissa K Temple,[...]. Am J Surg Pathol 2009
118
100

Accurate and exact CNV identification from targeted high-throughput sequence data.
Alex S Nord, Ming Lee, Mary-Claire King, Tom Walsh. BMC Genomics 2011
140
100

Reflex immunohistochemistry and microsatellite instability testing of colorectal tumors for Lynch syndrome among US cancer programs and follow-up of abnormal results.
Laura C Beamer, Marcia L Grant, Carin R Espenschied, Kathleen R Blazer, Heather L Hampel, Jeffrey N Weitzel, Deborah J MacDonald. J Clin Oncol 2012
147
100

MSH6 immunohistochemical heterogeneity in colorectal cancer: comparative sequencing from different tumor areas.
Wei Chen, Rachel Pearlman, Heather Hampel, Colin C Pritchard, Michael Markow, Christina Arnold, Deborah Knight, Wendy L Frankel. Hum Pathol 2020
8
100

Unexpected expression of mismatch repair protein is more commonly seen with pathogenic missense than with other mutations in Lynch syndrome.
Wei Chen, Heather Hampel, Rachel Pearlman, Dan Jones, Weiqiang Zhao, Mohammed Alsomali, Deborah Knight, Wendy L Frankel. Hum Pathol 2020
3
100

Assessment of Tumor Sequencing as a Replacement for Lynch Syndrome Screening and Current Molecular Tests for Patients With Colorectal Cancer.
Heather Hampel, Rachel Pearlman, Mallory Beightol, Weiqiang Zhao, Daniel Jones, Wendy L Frankel, Paul J Goodfellow, Ahmet Yilmaz, Kristin Miller, Jason Bacher,[...]. JAMA Oncol 2018
78
100

Using Somatic Mutations from Tumors to Classify Variants in Mismatch Repair Genes.
Brian H Shirts, Eric Q Konnick, Sarah Upham, Tom Walsh, John Michael O Ranola, Angela L Jacobson, Mary-Claire King, Rachel Pearlman, Heather Hampel, Colin C Pritchard. Am J Hum Genet 2018
16
100

Clinical characteristics of patients with colorectal cancer with double somatic mismatch repair mutations compared with Lynch syndrome.
Rachel Pearlman, Sigurdis Haraldsdottir, Albert de la Chapelle, Jon G Jonasson, Sandya Liyanarachchi, Wendy L Frankel, Thorunn Rafnar, Kari Stefansson, Colin C Pritchard, Heather Hampel. J Med Genet 2019
27
100

PD-1 Blockade in Tumors with Mismatch-Repair Deficiency.
Dung T Le, Jennifer N Uram, Hao Wang, Bjarne R Bartlett, Holly Kemberling, Aleksandra D Eyring, Andrew D Skora, Brandon S Luber, Nilofer S Azad, Dan Laheru,[...]. N Engl J Med 2015
100

Development and analytical validation of a 25-gene next generation sequencing panel that includes the BRCA1 and BRCA2 genes to assess hereditary cancer risk.
Thaddeus Judkins, Benoît Leclair, Karla Bowles, Natalia Gutin, Jeff Trost, James McCulloch, Satish Bhatnagar, Adam Murray, Jonathan Craft, Bryan Wardell,[...]. BMC Cancer 2015
72
100

ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.
Colin C Pritchard, Christina Smith, Stephen J Salipante, Ming K Lee, Anne M Thornton, Alex S Nord, Cassandra Gulden, Sonia S Kupfer, Elizabeth M Swisher, Robin L Bennett,[...]. J Mol Diagn 2012
142
100

Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer.
Colin C Pritchard, Joaquin Mateo, Michael F Walsh, Navonil De Sarkar, Wassim Abida, Himisha Beltran, Andrea Garofalo, Roman Gulati, Suzanne Carreira, Rosalind Eeles,[...]. N Engl J Med 2016
699
100

Comparison of Universal Genetic Testing vs Guideline-Directed Targeted Testing for Patients With Hereditary Cancer Syndrome.
N Jewel Samadder, Douglas Riegert-Johnson, Lisa Boardman, Deborah Rhodes, Myra Wick, Scott Okuno, Katie L Kunze, Michael Golafshar, Pedro L S Uson, Luke Mountjoy,[...]. JAMA Oncol 2021
31
100

Association Between Inherited Germline Mutations in Cancer Predisposition Genes and Risk of Pancreatic Cancer.
Chunling Hu, Steven N Hart, Eric C Polley, Rohan Gnanaolivu, Hermela Shimelis, Kun Y Lee, Jenna Lilyquist, Jie Na, Raymond Moore, Samuel O Antwi,[...]. JAMA 2018
189
100

Mismatch Repair Deficiency Testing in Patients With Colorectal Cancer and Nonadherence to Testing Guidelines in Young Adults.
Talha Shaikh, Elizabeth A Handorf, Joshua E Meyer, Michael J Hall, Nestor F Esnaola. JAMA Oncol 2018
35
100

Guidelines on genetic evaluation and management of Lynch syndrome: a consensus statement by the US Multi-society Task Force on colorectal cancer.
Francis M Giardiello, John I Allen, Jennifer E Axilbund, C Richard Boland, Carol A Burke, Randall W Burt, James M Church, Jason A Dominitz, David A Johnson, Tonya Kaltenbach,[...]. Am J Gastroenterol 2014
269
100

EGAPP supplementary evidence review: DNA testing strategies aimed at reducing morbidity and mortality from Lynch syndrome.
Glenn E Palomaki, Monica R McClain, Stephanie Melillo, Heather L Hampel, Stephen N Thibodeau. Genet Med 2009
327
100

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
100

Hereditary cancer syndromes: utilizing DNA repair deficiency as therapeutic target.
Gaurav Goyal, Tiffany Fan, Peter Todd Silberstein. Fam Cancer 2016
15
100

A comprehensive laboratory-based program for classification of variants of uncertain significance in hereditary cancer genes.
J M Eggington, K R Bowles, K Moyes, S Manley, L Esterling, S Sizemore, E Rosenthal, A Theisen, J Saam, C Arnell,[...]. Clin Genet 2014
118
100

Comparing universal Lynch syndrome tumor-screening programs to evaluate associations between implementation strategies and patient follow-through.
Deborah Cragun, Rita D DeBate, Susan T Vadaparampil, Julie Baldwin, Heather Hampel, Tuya Pal. Genet Med 2014
46
100

Multigene Panel Testing Provides a New Perspective on Lynch Syndrome.
Carin R Espenschied, Holly LaDuca, Shuwei Li, Rachel McFarland, Chia-Ling Gau, Heather Hampel. J Clin Oncol 2017
77
100

Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Hidewaki Nakagawa, Kaisa Sotamaa, Thomas W Prior, Judith Westman,[...]. N Engl J Med 2005
923
100


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.