A citation-based method for searching scientific literature

Gulsah Cecener, Leila Sabour Takanlou, Maryam Sabour Takanlou, Unal Egeli, Gamze Guney Eskiler, Secil Aksoy, Ufuk Unal, Havva Tezcan, Isil Ezgi Eryilmaz, Mustafa Sehsuvar Gokgoz, Berrin Tunca, Erdem Cubukcu, Turkkan Evrensel, Sibel Cetintas, Ismet Tasdelen. Cancer Genet 2020
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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

Consensus for genes to be included on cancer panel tests offered by UK genetics services: guidelines of the UK Cancer Genetics Group.
Amy Taylor, Angela F Brady, Ian M Frayling, Helen Hanson, Marc Tischkowitz, Clare Turnbull, Lucy Side. J Med Genet 2018
43
50

Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results.
Mary Pritzlaff, Pia Summerour, Rachel McFarland, Shuwei Li, Patrick Reineke, Jill S Dolinsky, David E Goldgar, Hermela Shimelis, Fergus J Couch, Elizabeth C Chao,[...]. Breast Cancer Res Treat 2017
58
50

Increased yield of actionable mutations using multi-gene panels to assess hereditary cancer susceptibility in an ethnically diverse clinical cohort.
Charité Ricker, Julie O Culver, Katrina Lowstuter, Duveen Sturgeon, Julia D Sturgeon, Christopher R Chanock, William J Gauderman, Kevin J McDonnell, Gregory E Idos, Stephen B Gruber. Cancer Genet 2016
43
50

Variant classification changes over time in BRCA1 and BRCA2.
Chloe Mighton, George S Charames, Marina Wang, Kathleen-Rose Zakoor, Andrew Wong, Salma Shickh, Nicholas Watkins, Matthew S Lebo, Yvonne Bombard, Jordan Lerner-Ellis. Genet Med 2019
11
50

Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care.
Ella R Thompson, Simone M Rowley, Na Li, Simone McInerny, Lisa Devereux, Michelle W Wong-Brown, Alison H Trainer, Gillian Mitchell, Rodney J Scott, Paul A James,[...]. J Clin Oncol 2016
110
50

Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.
Freddie Bray, Jacques Ferlay, Isabelle Soerjomataram, Rebecca L Siegel, Lindsey A Torre, Ahmedin Jemal. CA Cancer J Clin 2018
50


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
247
50

Prevalence and predictors of BRCA1 and BRCA2 mutations in a population-based study of breast cancer in white and black American women ages 35 to 64 years.
Kathleen E Malone, Janet R Daling, David R Doody, Li Hsu, Leslie Bernstein, Ralph J Coates, Polly A Marchbanks, Michael S Simon, Jill A McDonald, Sandra A Norman,[...]. Cancer Res 2006
204
50

The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk.
Thomas P Slavin, Kara N Maxwell, Jenna Lilyquist, Joseph Vijai, Susan L Neuhausen, Steven N Hart, Vignesh Ravichandran, Tinu Thomas, Ann Maria, Danylo Villano,[...]. NPJ Breast Cancer 2017
68
50

Identification of novel BRCA founder mutations in Middle Eastern breast cancer patients using capture and Sanger sequencing analysis.
Rong Bu, Abdul K Siraj, Khadija A S Al-Obaisi, Shaham Beg, Mohsen Al Hazmi, Dahish Ajarim, Asma Tulbah, Fouad Al-Dayel, Khawla S Al-Kuraya. Int J Cancer 2016
29
50

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
32
50

Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients.
Holly LaDuca, A J Stuenkel, Jill S Dolinsky, Steven Keiles, Stephany Tandy, Tina Pesaran, Elaine Chen, Chia-Ling Gau, Erika Palmaer, Kamelia Shoaepour,[...]. Genet Med 2014
208
50

A CHEK2 genetic variant contributing to a substantial fraction of familial breast cancer.
Pia Vahteristo, Jirina Bartkova, Hannaleena Eerola, Kirsi Syrjäkoski, Salla Ojala, Outi Kilpivaara, Anitta Tamminen, Juha Kononen, Kristiina Aittomäki, Päivi Heikkilä,[...]. Am J Hum Genet 2002
328
50


A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients.
Holly LaDuca, Eric C Polley, Amal Yussuf, Lily Hoang, Stephanie Gutierrez, Steven N Hart, Siddhartha Yadav, Chunling Hu, Jie Na, David E Goldgar,[...]. Genet Med 2020
53
50

Gene panel sequencing in familial breast/ovarian cancer patients identifies multiple novel mutations also in genes others than BRCA1/2.
Cornelia Kraus, Juliane Hoyer, Georgia Vasileiou, Marius Wunderle, Michael P Lux, Peter A Fasching, Mandy Krumbiegel, Steffen Uebe, Miriam Reuter, Matthias W Beckmann,[...]. Int J Cancer 2017
59
50

Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis.
Carlos J Gallego, Brian H Shirts, Caroline S Bennette, Greg Guzauskas, Laura M Amendola, Martha Horike-Pyne, Fuki M Hisama, Colin C Pritchard, William M Grady, Wylie Burke,[...]. J Clin Oncol 2015
87
50

Clinical Actionability of Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Risk Assessment.
Andrea Desmond, Allison W Kurian, Michele Gabree, Meredith A Mills, Michael J Anderson, Yuya Kobayashi, Nora Horick, Shan Yang, Kristen M Shannon, Nadine Tung,[...]. JAMA Oncol 2015
197
50

Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer.
Fergus J Couch, Hermela Shimelis, Chunling Hu, Steven N Hart, Eric C Polley, Jie Na, Emily Hallberg, Raymond Moore, Abigail Thomas, Jenna Lilyquist,[...]. JAMA Oncol 2017
269
50

Association of Mismatch Repair Mutation With Age at Cancer Onset in Lynch Syndrome: Implications for Stratified Surveillance Strategies.
Neil A J Ryan, Julie Morris, Kate Green, Fiona Lalloo, Emma R Woodward, James Hill, Emma J Crosbie, D Gareth Evans. JAMA Oncol 2017
59
50

Large genomic deletions and duplications in the BRCA1 gene identified by a novel quantitative method.
Frans B L Hogervorst, Petra M Nederlof, Johan J P Gille, Cathal J McElgunn, Maartje Grippeling, Roelof Pruntel, Rein Regnerus, Tibor van Welsem, Resie van Spaendonk, Fred H Menko,[...]. Cancer Res 2003
255
50

Genomic rearrangements account for more than one-third of the BRCA1 mutations in northern Italian breast/ovarian cancer families.
Marco Montagna, Maurizia Dalla Palma, Chiara Menin, Simona Agata, Arcangela De Nicolo, Luigi Chieco-Bianchi, Emma D'Andrea. Hum Mol Genet 2003
150
50


Hereditary Cancer Syndromes-A Primer on Diagnosis and Management: Part 1: Breast-Ovarian Cancer Syndromes.
N Jewel Samadder, Karthik V Giridhar, Noemi Baffy, Douglas Riegert-Johnson, Fergus J Couch. Mayo Clin Proc 2019
16
50

Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations.
Georgios N Tsaousis, Eirini Papadopoulou, Angela Apessos, Konstantinos Agiannitopoulos, Georgia Pepe, Stavroula Kampouri, Nikolaos Diamantopoulos, Theofanis Floros, Rodoniki Iosifidou, Ourania Katopodi,[...]. BMC Cancer 2019
20
50

Use of the MLPA assay in the molecular diagnosis of gene copy number alterations in human genetic diseases.
Liborio Stuppia, Ivana Antonucci, Giandomenico Palka, Valentina Gatta. Int J Mol Sci 2012
100
50

Germline Mutations in Cancer Susceptibility Genes in a Large Series of Unselected Breast Cancer Patients.
Jie Sun, Hua Meng, Lu Yao, Meng Lv, Jian Bai, Jianguang Zhang, Lientu Wang, Tao Ouyang, Jinfeng Li, Tianfeng Wang,[...]. Clin Cancer Res 2017
77
50

The impact of hereditary cancer gene panels on clinical care and lessons learned.
Volkan Okur, Wendy K Chung. Cold Spring Harb Mol Case Stud 2017
19
50

Hereditary Cancer Syndromes-A Primer on Diagnosis and Management, Part 2: Gastrointestinal Cancer Syndromes.
N Jewel Samadder, Noemi Baffy, Karthik V Giridhar, Fergus J Couch, Douglas Riegert-Johnson. Mayo Clin Proc 2019
13
50


Beyond BRCA: new hereditary breast cancer susceptibility genes.
P Economopoulou, G Dimitriadis, A Psyrri. Cancer Treat Rev 2015
90
50

Molecular genetics analysis of hereditary breast and ovarian cancer patients in India.
Nagasamy Soumittra, Balaiah Meenakumari, Tithi Parija, Veluswami Sridevi, Karunakaran N Nancy, Rajaraman Swaminathan, Kamalalayam R Rajalekshmy, Urmila Majhi, Thangarajan Rajkumar. Hered Cancer Clin Pract 2009
11
50

BRCA1 polymorphisms and breast cancer epidemiology in the Western New York exposures and breast cancer (WEB) study.
Luisel J Ricks-Santi, Jing Nie, Catalin Marian, Heather M Ochs-Balcom, Maurizio Trevisan, Stephen B Edge, Yasmine Kanaan, Jo L Freudenheim, Peter G Shields. Genet Epidemiol 2013
9
50

Genomic structures and population histories of linguistically distinct tribal groups of India.
S Roychoudhury, S Roy, A Basu, R Banerjee, H Vishwanathan, M V Usha Rani, S K Sil, M Mitra, P P Majumder. Hum Genet 2001
78
50

Screening for BRCA1 and BRCA2 mutations among French-Canadian breast cancer cases attending an outpatient clinic in Montreal.
P Ghadirian, A Robidoux, E Nassif, G Martin, C Potvin, E Patocskai, R Younan, N Larouche, A Venne, S Zhang,[...]. Clin Genet 2014
11
50

The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to Ashkenazim.
R B Bar-Sade, A Kruglikova, B Modan, E Gak, G Hirsh-Yechezkel, L Theodor, I Novikov, R Gershoni-Baruch, S Risel, M Z Papa,[...]. Hum Mol Genet 1998
104
50

Screening of over 1000 Indian patients with breast and/or ovarian cancer with a multi-gene panel: prevalence of BRCA1/2 and non-BRCA mutations.
Jaya Singh, Nishita Thota, Suhasini Singh, Shila Padhi, Puja Mohan, Shivani Deshwal, Soumit Sur, Mithua Ghosh, Amit Agarwal, Ramesh Sarin,[...]. Breast Cancer Res Treat 2018
20
50

BRCA1 mutations in South African breast and/or ovarian cancer families: evidence of a novel founder mutation in Afrikaner families.
Michelle D Reeves, Tali M Yawitch, Nerina C van der Merwe, Hester J van den Berg, Greta Dreyer, Elizabeth J van Rensburg. Int J Cancer 2004
34
50

Germline BRCA1 mutation analysis in Indian breast/ovarian cancer families.
B Vinod Kumar, Smita Lakhotia, Ravindran Ankathil, Jayaprakash Madhavan, P G Jayaprakash, M Krishnan Nair, Kumaravel Somasundaram. Cancer Biol Ther 2002
27
50

Recent admixture in an Indian population of African ancestry.
Ankita Narang, Pankaj Jha, Vimal Rawat, Arijit Mukhopadhyay, Debasis Dash, Analabha Basu, Mitali Mukerji. Am J Hum Genet 2011
17
50

Novel inherited mutations and variable expressivity of BRCA1 alleles, including the founder mutation 185delAG in Ashkenazi Jewish families.
L S Friedman, C I Szabo, E A Ostermeyer, P Dowd, L Butler, T Park, M K Lee, E L Goode, S E Rowell, M C King. Am J Hum Genet 1995
157
50

Novel de novo BRCA2 mutation in a patient with a family history of breast cancer.
Thomas V O Hansen, Marie Luise Bisgaard, Lars Jønson, Anders Albrechtsen, Bettina Filtenborg-Barnkob, Hans Eiberg, Bent Ejlertsen, Finn C Nielsen. BMC Med Genet 2008
30
50

Detection of high frequency of mutations in a breast and/or ovarian cancer cohort: implications of embracing a multi-gene panel in molecular diagnosis in India.
Ashraf U Mannan, Jaya Singh, Ravikiran Lakshmikeshava, Nishita Thota, Suhasini Singh, T S Sowmya, Avshesh Mishra, Aditi Sinha, Shivani Deshwal, Megha R Soni,[...]. J Hum Genet 2016
36
50

Novel germline mutations in the BRCA1 and BRCA2 genes in Indian breast and breast-ovarian cancer families.
Mani T Valarmathi, Meenakshi Sawhney, Suryanarayana S V Deo, Nootan K Shukla, Satya N Das. Hum Mutat 2004
37
50

Contribution of germline BRCA1 and BRCA2 sequence alterations to breast cancer in Northern India.
Sunita Saxena, Anurupa Chakraborty, Mishi Kaushal, Sanjeev Kotwal, Dinesh Bhatanager, Ravindar S Mohil, Chintamani Chintamani, Anil K Aggarwal, Veena K Sharma, Prakash C Sharma,[...]. BMC Med Genet 2006
58
50

Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer.
J P Struewing, L C Brody, M R Erdos, R G Kase, T R Giambarresi, S A Smith, F S Collins, M A Tucker. Am J Hum Genet 1995
143
50

Comprehensive spectrum of BRCA1 and BRCA2 deleterious mutations in breast cancer in Asian countries.
Ava Kwong, Vivian Y Shin, John C W Ho, Eunyoung Kang, Seigo Nakamura, Soo-Hwang Teo, Ann S G Lee, Jen-Hwei Sng, Ophira M Ginsburg, Allison W Kurian,[...]. J Med Genet 2016
40
50

Reconstruction of major maternal and paternal lineages of the Cape Muslim population.
Shafieka Isaacs, Tasneem Geduld-Ullah, Mongi Benjeddou. Genet Mol Biol 2013
1
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.