A citation-based method for searching scientific literature

Ciyu Yang, Angela G Arnold, Magan Trottier, Yukio Sonoda, Nadeem R Abu-Rustum, Oliver Zivanovic, Mark E Robson, Zsofia K Stadler, Michael F Walsh, David M Hyman, Kenneth Offit, Liying Zhang. Breast Cancer Res Treat 2016
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Breast-cancer risk in families with mutations in PALB2.
Antonis C Antoniou, Silvia Casadei, Tuomas Heikkinen, Daniel Barrowdale, Katri Pylkäs, Jonathan Roberts, Andrew Lee, Deepak Subramanian, Kim De Leeneer, Florentia Fostira,[...]. N Engl J Med 2014
520
41

Fanconi anemia is associated with a defect in the BRCA2 partner PALB2.
Bing Xia, Josephine C Dorsman, Najim Ameziane, Yne de Vries, Martin A Rooimans, Qing Sheng, Gerard Pals, Abdellatif Errami, Eliane Gluckman, Julian Llera,[...]. Nat Genet 2007
345
33

Germline Mutations in the BRIP1, BARD1, PALB2, and NBN Genes in Women With Ovarian Cancer.
Susan J Ramus, Honglin Song, Ed Dicks, Jonathan P Tyrer, Adam N Rosenthal, Maria P Intermaggio, Lindsay Fraser, Aleksandra Gentry-Maharaj, Jane Hayward, Susan Philpott,[...]. J Natl Cancer Inst 2015
245
25

Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2.
Bing Xia, Qing Sheng, Koji Nakanishi, Akihiro Ohashi, Jianmin Wu, Nicole Christ, Xinggang Liu, Maria Jasin, Fergus J Couch, David M Livingston. Mol Cell 2006
579
25

PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene.
Nazneen Rahman, Sheila Seal, Deborah Thompson, Patrick Kelly, Anthony Renwick, Anna Elliott, Sarah Reid, Katarina Spanova, Rita Barfoot, Tasnim Chagtai,[...]. Nat Genet 2007
677
25

A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1.
Y Miki, J Swensen, D Shattuck-Eidens, P A Futreal, K Harshman, S Tavtigian, Q Liu, C Cochran, L M Bennett, W Ding. Science 1994
25

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
25

A recurrent mutation in PALB2 in Finnish cancer families.
Hannele Erkko, Bing Xia, Jenni Nikkilä, Johanna Schleutker, Kirsi Syrjäkoski, Arto Mannermaa, Anne Kallioniemi, Katri Pylkäs, Sanna-Maria Karppinen, Katrin Rapakko,[...]. Nature 2007
325
25

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families.
Xin Yang, Goska Leslie, Alicja Doroszuk, Sandra Schneider, Jamie Allen, Brennan Decker, Alison M Dunning, James Redman, James Scarth, Inga Plaskocinska,[...]. J Clin Oncol 2020
159
25

DNA breakpoint assay reveals a majority of gross duplications occur in tandem reducing VUS classifications in breast cancer predisposition genes.
Marcy E Richardson, Hansook Chong, Wenbo Mu, Blair R Conner, Vickie Hsuan, Sara Willett, Stephanie Lam, Pei Tsai, Tina Pesaran, Adam C Chamberlin,[...]. Genet Med 2019
11
27

Human genomic deletions mediated by recombination between Alu elements.
Shurjo K Sen, Kyudong Han, Jianxin Wang, Jungnam Lee, Hui Wang, Pauline A Callinan, Matthew Dyer, Richard Cordaux, Ping Liang, Mark A Batzer. Am J Hum Genet 2006
215
16

PALB2/FANCN: recombining cancer and Fanconi anemia.
Marc Tischkowitz, Bing Xia. Cancer Res 2010
129
16

Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls.
Ella R Thompson, Kylie L Gorringe, Simone M Rowley, Michelle W Wong-Brown, Simone McInerny, Na Li, Alison H Trainer, Lisa Devereux, Maria A Doyle, Jason Li,[...]. Breast Cancer Res 2015
26
16

Frequency of mutations in individuals with breast cancer referred for BRCA1 and BRCA2 testing using next-generation sequencing with a 25-gene panel.
Nadine Tung, Chiara Battelli, Brian Allen, Rajesh Kaldate, Satish Bhatnagar, Karla Bowles, Kirsten Timms, Judy E Garber, Christina Herold, Leif Ellisen,[...]. Cancer 2015
294
16

Biallelic mutations in PALB2 cause Fanconi anemia subtype FA-N and predispose to childhood cancer.
Sarah Reid, Detlev Schindler, Helmut Hanenberg, Karen Barker, Sandra Hanks, Reinhard Kalb, Kornelia Neveling, Patrick Kelly, Sheila Seal, Marcel Freund,[...]. Nat Genet 2007
446
16

PALB2 is an integral component of the BRCA complex required for homologous recombination repair.
Shirley M H Sy, Michael S Y Huen, Junjie Chen. Proc Natl Acad Sci U S A 2009
384
16

PALB2 regulates recombinational repair through chromatin association and oligomerization.
Shirley M-H Sy, Michael S Y Huen, Yongyou Zhu, Junjie Chen. J Biol Chem 2009
78
16

Genomic rearrangements in BRCA1 and BRCA2: A literature review.
Ingrid Petroni Ewald, Patricia Lisboa Izetti Ribeiro, Edenir Inêz Palmero, Silvia Liliana Cossio, Roberto Giugliani, Patricia Ashton-Prolla. Genet Mol Biol 2009
68
16


Evolution of the tumor suppressor BRCA1 locus in primates: implications for cancer predisposition.
Adam Pavlicek, Vladimir N Noskov, Natalay Kouprina, J Carl Barrett, Jerzy Jurka, Vladimir Larionov. Hum Mol Genet 2004
75
16

Detection of large rearrangements in a hereditary pan-cancer panel using next-generation sequencing.
Debora Mancini-DiNardo, Thaddeus Judkins, John Kidd, Ryan Bernhisel, Courtney Daniels, Krystal Brown, Kirsten Meek, Jonathan Craft, Jayson Holladay, Brian Morris,[...]. BMC Med Genomics 2019
9
22

Detection of Genomic Structural Variants from Next-Generation Sequencing Data.
Lorenzo Tattini, Romina D'Aurizio, Alberto Magi. Front Bioeng Biotechnol 2015
141
16

The human genome browser at UCSC.
W James Kent, Charles W Sugnet, Terrence S Furey, Krishna M Roskin, Tom H Pringle, Alan M Zahler, David Haussler. Genome Res 2002
16

A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Mark A DePristo, Eric Banks, Ryan Poplin, Kiran V Garimella, Jared R Maguire, Christopher Hartl, Anthony A Philippakis, Guillermo del Angel, Manuel A Rivas, Matt Hanna,[...]. Nat Genet 2011
16

Characterization and Genomic Localization of a SMAD4 Processed Pseudogene.
Christopher M Watson, Nick Camm, Laura A Crinnion, Agne Antanaviciute, Julian Adlard, Alexander F Markham, Ian M Carr, Ruth Charlton, David T Bonthron. J Mol Diagn 2017
5
40

Improved structural variant interpretation for hereditary cancer susceptibility using long-read sequencing.
My Linh Thibodeau, Kieran O'Neill, Katherine Dixon, Caralyn Reisle, Karen L Mungall, Martin Krzywinski, Yaoqing Shen, Howard J Lim, Dean Cheng, Kane Tse,[...]. Genet Med 2020
16
16

Identification of the breast cancer susceptibility gene BRCA2.
R Wooster, G Bignell, J Lancaster, S Swift, S Seal, J Mangion, N Collins, S Gregory, C Gumbs, G Micklem. Nature 1995
16

Germline mutations in RAD51D confer susceptibility to ovarian cancer.
Chey Loveday, Clare Turnbull, Emma Ramsay, Deborah Hughes, Elise Ruark, Jessica R Frankum, Georgina Bowden, Bolot Kalmyrzaev, Margaret Warren-Perry, Katie Snape,[...]. Nat Genet 2011
346
16

Frequency of Germline Mutations in 25 Cancer Susceptibility Genes in a Sequential Series of Patients With Breast Cancer.
Nadine Tung, Nancy U Lin, John Kidd, Brian A Allen, Nanda Singh, Richard J Wenstrup, Anne-Renee Hartman, Eric P Winer, Judy E Garber. J Clin Oncol 2016
298
16

Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancer.
Ana Blanco, Miguel de la Hoya, Judith Balmaña, Teresa Ramón y Cajal, Alex Teulé, María-Dolores Miramar, Eva Esteban, Mar Infante, Javier Benítez, Asunción Torres,[...]. Breast Cancer Res Treat 2012
39
16

Breast cancer.
Nadia Harbeck, Frédérique Penault-Llorca, Javier Cortes, Michael Gnant, Nehmat Houssami, Philip Poortmans, Kathryn Ruddy, Janice Tsang, Fatima Cardoso. Nat Rev Dis Primers 2019
805
16

Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene.
Alfons Meindl, Heide Hellebrand, Constanze Wiek, Verena Erven, Barbara Wappenschmidt, Dieter Niederacher, Marcel Freund, Peter Lichtner, Linda Hartmann, Heiner Schaal,[...]. Nat Genet 2010
485
16

Pathogenic Germline Variants in 10,389 Adult Cancers.
Kuan-Lin Huang, R Jay Mashl, Yige Wu, Deborah I Ritter, Jiayin Wang, Clara Oh, Marta Paczkowska, Sheila Reynolds, Matthew A Wyczalkowski, Ninad Oak,[...]. Cell 2018
372
16

The PALB2 gene is a strong candidate for clinical testing in BRCA1- and BRCA2-negative hereditary breast cancer.
Marketa Janatova, Zdenek Kleibl, Jana Stribrna, Ales Panczak, Kamila Vesela, Martina Zimovjanova, Petra Kleiblova, Pavel Dundr, Jana Soukupova, Petr Pohlreich. Cancer Epidemiol Biomarkers Prev 2013
36
16

[The French Genetic and Cancer Consortium guidelines for multigene panel analysis in hereditary breast and ovarian cancer predisposition].
Jessica Moretta, Pascaline Berthet, Valérie Bonadona, Olivier Caron, Odile Cohen-Haguenauer, Chrystelle Colas, Carole Corsini, Véronica Cusin, Antoine De Pauw, Capucine Delnatte,[...]. Bull Cancer 2018
24
16


An Alu-mediated 7.1 kb deletion of BRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10.
E M Rohlfs, N Puget, M L Graham, B L Weber, J E Garber, C Skrzynia, J L Halperin, G M Lenoir, L M Silverman, S Mazoyer. Genes Chromosomes Cancer 2000
64
8

Genomic investigation of alpha-synuclein multiplication and parkinsonism.
Owen A Ross, Adam T Braithwaite, Lisa M Skipper, Jennifer Kachergus, Mary M Hulihan, Frank A Middleton, Kenya Nishioka, Julia Fuchs, Thomas Gasser, Demetrius M Maraganore,[...]. Ann Neurol 2008
239
8

Alu repeats and human disease.
P L Deininger, M A Batzer. Mol Genet Metab 1999
643
8

Alu-mediated nonallelic homologous and nonhomologous recombination in the BMPR2 gene in heritable pulmonary arterial hypertension.
Masaharu Kataoka, Yuki Aimi, Ryoji Yanagisawa, Masae Ono, Akira Oka, Keiichi Fukuda, Hideaki Yoshino, Toru Satoh, Shinobu Gamou. Genet Med 2013
18
8

Distinctive patterns of age-dependent hypomethylation in interspersed repetitive sequences.
Pornrutsami Jintaridth, Apiwat Mutirangura. Physiol Genomics 2010
133
8

Discovery and characterization of Alu repeat sequences via precise local read assembly.
Julia H Wildschutte, Alayna Baron, Nicolette M Diroff, Jeffrey M Kidd. Nucleic Acids Res 2015
19
8



The (mis)use of overlap of confidence intervals to assess effect modification.
Mirjam J Knol, Wiebe R Pestman, Diederick E Grobbee. Eur J Epidemiol 2011
78
8

Hypomethylation of Alu elements in post-menopausal women with osteoporosis.
Pornrutsami Jintaridth, Rungsunn Tungtrongchitr, Sangchai Preutthipan, Apiwat Mutirangura. PLoS One 2013
48
8

Leukocyte telomere dynamics in the elderly.
Troels Steenstrup, Jacob V B Hjelmborg, Laust H Mortensen, Masayuki Kimura, Kaare Christensen, Abraham Aviv. Eur J Epidemiol 2013
23
8

The 5'-end transitional CpGs between the CpG islands and retroelements are hypomethylated in association with loss of heterozygosity in gastric cancers.
Young-Ho Kim, Seung-Jin Hong, Yu-Chae Jung, Sung-Ja Kim, Eun-Joo Seo, Sang-Wook Choi, Mun-Gan Rhyu. BMC Cancer 2006
12
8

Leukocytes of exceptionally old persons display ultra-short telomeres.
M Kimura, M Barbieri, J P Gardner, J Skurnick, X Cao, N van Riel, M R Rizzo, G Paoliso, A Aviv. Am J Physiol Regul Integr Comp Physiol 2007
38
8

Cellular aging of skeletal muscle: telomeric and free radical evidence that physical inactivity is responsible and not age.
Massimo Venturelli, Garrett R Morgan, Anthony J Donato, Van Reese, Renato Bottura, Cantor Tarperi, Chiara Milanese, Federico Schena, Carlo Reggiani, Fabio Naro,[...]. Clin Sci (Lond) 2014
28
8


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.