A citation-based method for searching scientific literature

Catherine Rehder, Lora J H Bean, David Bick, Elizabeth Chao, Wendy Chung, Soma Das, Julianne O'Daniel, Heidi Rehm, Vandana Shashi, Lisa M Vincent. Genet Med 2021
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


Diagnostic gene sequencing panels: from design to report-a technical standard of the American College of Medical Genetics and Genomics (ACMG).
Lora J H Bean, Birgit Funke, Colleen M Carlston, Jennifer L Gannon, Sibel Kantarci, Bryan L Krock, Shulin Zhang, Pinar Bayrak-Toydemir. Genet Med 2020
23
37

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
37


Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
292
25

Determining the frequency of de novo germline mutations in DNA mismatch repair genes.
Aung Ko Win, Mark A Jenkins, Daniel D Buchanan, Mark Clendenning, Joanne P Young, Graham G Giles, Jack Goldblatt, Barbara A Leggett, John L Hopper, Stephen N Thibodeau,[...]. J Med Genet 2011
28
12

Lynch syndrome and MYH-associated polyposis: review and testing strategy.
McKinsey Goodenberger, Noralane M Lindor. J Clin Gastroenterol 2011
37
12

Constitutive deficiency in DNA mismatch repair.
K E A Felton, D M Gilchrist, S E Andrew. Clin Genet 2007
72
12

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
12

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
12

MUTYH Associated Polyposis (MAP).
M L M Poulsen, M L Bisgaard. Curr Genomics 2008
54
12

Constitutive deficiency in DNA mismatch repair: is it time for Lynch III?
K E A Felton, D M Gilchrist, S E Andrew. Clin Genet 2007
35
12

Testing guidelines for hereditary non-polyposis colorectal cancer.
Asad Umar, John I Risinger, Ernest T Hawk, J Carl Barrett. Nat Rev Cancer 2004
114
12


Distinct CpG island methylation profiles and BRAF mutation status in serrated and adenomatous colorectal polyps.
Yong Ho Kim, Sanjay Kakar, Lisa Cun, Guoren Deng, Young S Kim. Int J Cancer 2008
102
12

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
12

Comparison between universal molecular screening for Lynch syndrome and revised Bethesda guidelines in a large population-based cohort of patients with colorectal cancer.
Lucía Pérez-Carbonell, Clara Ruiz-Ponte, Carla Guarinos, Cristina Alenda, Artemio Payá, Alejandro Brea, Cecilia M Egoavil, Adela Castillejo, Victor M Barberá, Xavier Bessa,[...]. Gut 2012
134
12

MLH1 and MSH2 constitutional mutations in colorectal cancer families not meeting the standard criteria for hereditary nonpolyposis colorectal cancer.
M Genuardi, M Anti, E Capozzi, F Leonardi, M Fornasarig, E Novella, A Bellacosa, A Valenti, G B Gasbarrini, L Roncucci,[...]. Int J Cancer 1998
47
12

BRAF mutation is frequently present in sporadic colorectal cancer with methylated hMLH1, but not in hereditary nonpolyposis colorectal cancer.
Guoren Deng, Ian Bell, Suzanne Crawley, James Gum, Jonathan P Terdiman, Brian A Allen, Brindusa Truta, Marvin H Sleisenger, Young S Kim. Clin Cancer Res 2004
302
12

Heterozygous mutations in PMS2 cause hereditary nonpolyposis colorectal carcinoma (Lynch syndrome).
Yvonne M C Hendriks, Shantie Jagmohan-Changur, Heleen M van der Klift, Hans Morreau, Marjo van Puijenbroek, Carli Tops, Theo van Os, Anja Wagner, Margreet G F M Ausems, Encarna Gomez,[...]. Gastroenterology 2006
97
12

Association of low-risk MSH3 and MSH2 variant alleles with Lynch syndrome: probability of synergistic effects.
Francesca Duraturo, Raffaella Liccardo, Angela Cavallo, Marina De Rosa, Michela Grosso, Paola Izzo. Int J Cancer 2011
38
12

Precision and performance characteristics of bisulfite conversion and real-time PCR (MethyLight) for quantitative DNA methylation analysis.
Shuji Ogino, Takako Kawasaki, Mohan Brahmandam, Mami Cantor, Gregory J Kirkner, Donna Spiegelman, G Mike Makrigiorgos, Daniel J Weisenberger, Peter W Laird, Massimo Loda,[...]. J Mol Diagn 2006
324
12

Promoter hypermethylation of mismatch repair gene hMLH1 predicts the clinical response of malignant astrocytomas to nitrosourea.
Takao Fukushima, Yoichi Katayama, Takao Watanabe, Atsuo Yoshino, Akiyoshi Ogino, Takashi Ohta, Chiaki Komine. Clin Cancer Res 2005
22
12

Identification of cancer patients with Lynch syndrome: clinically significant discordances and problems in tissue-based mismatch repair testing.
Angela N Bartley, Rajyalakshmi Luthra, Devki S Saraiya, Diana L Urbauer, Russell R Broaddus. Cancer Prev Res (Phila) 2012
76
12

Germline Genetic Features of Young Individuals With Colorectal Cancer.
Elena M Stoffel, Erika Koeppe, Jessica Everett, Peter Ulintz, Mark Kiel, Jenae Osborne, Linford Williams, Kristen Hanson, Stephen B Gruber, Laura S Rozek. Gastroenterology 2018
109
12

Mutations of two PMS homologues in hereditary nonpolyposis colon cancer.
N C Nicolaides, N Papadopoulos, B Liu, Y F Wei, K C Carter, S M Ruben, C A Rosen, W A Haseltine, R D Fleischmann, C M Fraser. Nature 1994
12

A cryptic paracentric inversion of MSH2 exons 2-6 causes Lynch syndrome.
Qing Liu, Luke B Hesson, Andrea C Nunez, Deborah Packham, Rachel Williams, Robyn L Ward, Mathew A Sloane. Carcinogenesis 2016
20
12

Designing and Implementing NGS Tests for Inherited Disorders: A Practical Framework with Step-by-Step Guidance for Clinical Laboratories.
Avni Santani, Birgitte B Simen, Marian Briggs, Matthew Lebo, Jason D Merker, Marina Nikiforova, Patricia Vasalos, Karl Voelkerding, John Pfeifer, Birgit Funke. J Mol Diagn 2019
7
14

MSH6 and PMS2 mutation positive Australian Lynch syndrome families: novel mutations, cancer risk and age of diagnosis of colorectal cancer.
Bente A Talseth-Palmer, Mary McPhillips, Claire Groombridge, Allan Spigelman, Rodney J Scott. Hered Cancer Clin Pract 2010
22
12

Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics.
Monika Morak, Verena Steinke-Lange, Trisari Massdorf, Anna Benet-Pages, Melanie Locher, Andreas Laner, Katrin Kayser, Stefan Aretz, Elke Holinski-Feder. Fam Cancer 2020
8
12

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
12


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
12

Alu element insertion in the MLH1 exon 6 coding sequence as a mutation predisposing to Lynch syndrome.
Jérôme Solassol, Marion Larrieux, Julie Leclerc, Vincent Ducros, Carole Corsini, Jean Chiésa, Pascal Pujol, Jean-Marc Rey. Hum Mutat 2019
5
20

Cancer risk in Lynch Syndrome.
Emma Barrow, James Hill, D Gareth Evans. Fam Cancer 2013
108
12


Molecular origins of cancer: Molecular basis of colorectal cancer.
Sanford D Markowitz, Monica M Bertagnolli. N Engl J Med 2009
12


Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability.
Asad Umar, C Richard Boland, Jonathan P Terdiman, Sapna Syngal, Albert de la Chapelle, Josef Rüschoff, Richard Fishel, Noralane M Lindor, Lawrence J Burgart, Richard Hamelin,[...]. J Natl Cancer Inst 2004
12

Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework.
Bryce A Seifert, Jennifer L McGlaughon, Sarah A Jackson, Deborah I Ritter, Maegan E Roberts, Ryan J Schmidt, Bryony A Thompson, Sharisse Jimenez, Mackenzie Trapp, Kristy Lee,[...]. Genet Med 2019
10
12

Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.
Valérie Bonadona, Bernard Bonaïti, Sylviane Olschwang, Sophie Grandjouan, Laetitia Huiart, Michel Longy, Rosine Guimbaud, Bruno Buecher, Yves-Jean Bignon, Olivier Caron,[...]. JAMA 2011
593
12

PMS2 mutations in HNPCC.
B E Hayward, M De Vos, E Sheridan, D T Bonthron. Clin Genet 2004
9
12

A homozygous mutation in MSH6 causes Turcot syndrome.
Madhuri R Hegde, Belinda Chong, Maria E Blazo, Lip Hon E Chin, Patricia A Ward, Murali M Chintagumpala, John Y Kim, Sharon E Plon, C Sue Richards. Clin Cancer Res 2005
50
12


Prevalence of the Y165C, G382D and 1395delGGA germline mutations of the MYH gene in Italian patients with adenomatous polyposis coli and colorectal adenomas.
Viviana Gismondi, Maurizio Meta, Luigina Bonelli, Paolo Radice, Paola Sala, Lucio Bertario, Alessandra Viel, Mara Fornasarig, Arrigo Arrigoni, Mattia Gentile,[...]. Int J Cancer 2004
124
12

A missense mutation in both hMSH2 and APC in an Ashkenazi Jewish HNPCC kindred: implications for clinical screening.
Z Q Yuan, N Wong, W D Foulkes, L Alpert, F Manganaro, C Andreutti-Zaugg, R Iggo, K Anthony, E Hsieh, M Redston,[...]. J Med Genet 1999
23
12

Frequency of deletions of EPCAM (TACSTD1) in MSH2-associated Lynch syndrome cases.
Kandelaria Rumilla, Karen V Schowalter, Noralane M Lindor, Brittany C Thomas, Kara A Mensink, Steven Gallinger, Spring Holter, Polly A Newcomb, John D Potter, Mark A Jenkins,[...]. J Mol Diagn 2011
58
12

Incorporation of somatic BRAF mutation testing into an algorithm for the investigation of hereditary non-polyposis colorectal cancer.
M B Loughrey, P M Waring, A Tan, M Trivett, S Kovalenko, V Beshay, M-A Young, G McArthur, A Boussioutas, A Dobrovic. Fam Cancer 2007
127
12

DNA mismatch repair deficiency in sporadic colorectal cancer and Lynch syndrome.
George Poulogiannis, Ian M Frayling, Mark J Arends. Histopathology 2010
135
12

MSH6 and MUTYH deficiency is a frequent event in early-onset colorectal cancer.
María Dolores Giráldez, Francesc Balaguer, Luis Bujanda, Miriam Cuatrecasas, Jenifer Muñoz, Virginia Alonso-Espinaco, Mikel Larzabal, Anna Petit, Victoria Gonzalo, Teresa Ocaña,[...]. Clin Cancer Res 2010
59
12

A 60-year tale of spots, maps, and genes.
Victor A McKusick. Annu Rev Genomics Hum Genet 2006
23
12


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.