A citation-based method for searching scientific literature

Maurizio Pisanò, Valeria Mezzolla, Maria Maddalena Galante, Giovanni Alemanno, Corrado Manca, Vito Lorusso, Antonio Malvasi, Andrea Tinelli. Fam Cancer 2011
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


Searching for large genomic rearrangements of the BRCA1 gene in a Nigerian population.
Jing Zhang, James D Fackenthal, Dezheng Huo, Yonglan Zheng, Olufunmilayo I Olopade. Breast Cancer Res Treat 2010
18
40


BRCA1 and BRCA2 germline mutations in Moroccan breast/ovarian cancer families: novel mutations and unclassified variants.
Amal Tazzite, Hassan Jouhadi, Sellama Nadifi, Paolo Aretini, Elisabetta Falaschi, Anita Collavoli, Abdellatif Benider, Maria Adelaide Caligo. Gynecol Oncol 2012
38
20

G1738R is a BRCA1 founder mutation in Greek breast/ovarian cancer patients: evaluation of its pathogenicity and inferences on its genealogical history.
Theodore Anagnostopoulos, Maroulio Pertesi, Irene Konstantopoulou, Sofia Armaou, Smaragda Kamakari, George Nasioulas, Athanassios Athanasiou, Alex Dobrovic, Mary-Anne Young, David Goldgar,[...]. Breast Cancer Res Treat 2008
28
20

BRCA1 gene mutations frequency estimation by allele-specific real-time PCR of pooled genomic DNA samples.
Maksim S Anisimenko, Dmitriy V Mitrofanov, Olga B Chasovnikova, Mikhail I Voevoda, Sergey P Kovalenko. Breast 2013
3
33

BRCA1 germline mutations in Indian familial breast cancer.
Mani T Valarmathi, Agarwal A, Suryanarayana S V Deo, Nootan K Shukla, Satya N Das. Hum Mutat 2003
15
20

BRCA1 and BRCA2 mutations in Russian familial breast cancer.
Irina V Tereschenko, Victoria M Basham, Bruce A J Ponder, Paul D P Pharoah. Hum Mutat 2002
20
20

Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation.
M-W Seong, Si Cho, D-Y Noh, W Han, S-W Kim, C-M Park, H-W Park, S Y Kim, J Y Kim, S S Park. Clin Genet 2009
23
20

Evaluation of Cx26/GJB2 in German hearing impaired persons: mutation spectrum and detection of disequilibrium between M34T (c.101T>C) and -493del10.
Barbara Zoll, Lars Petersen, Katrin Lange, Peter Gabriel, Christiane Kiese-Himmel, Peter Rausch, Joachim Berger, Bastian Pasche, Moritz Meins, Manfred Gross,[...]. Hum Mutat 2003
29
20

The spectrum and incidence of BRCA1 pathogenic mutations in Slovak breast/ovarian cancer families.
M Konecny, M Vizvaryova, E Weismanova, D Ilencikova, I Mlkva, P Weismann, G Machackova, J Kausitz. Neoplasma 2007
4
25


Uptake of BRCA1 genetic testing in adult sisters and daughters of known mutation carriers in Norway.
Trine Levin Bodd, Jon Reichelt, Ketil Heimdal, Pal Moller. J Genet Couns 2003
21
20

Haplotype analysis of BRCA2 8765delAG mutation carriers in French Canadian and Yemenite Jewish hereditary breast cancer families.
A P Manning, D Abelovich, P Ghadirian, J A Lambert, D Frappier, D Provencher, A Robidoux, T Peretz, S A Narod, A M Mes-Masson,[...]. Hum Hered 2001
19
20

Novel sequence variants and a high frequency of recurrent polymorphisms in BRCA1 gene in Sri Lankan breast cancer patients and at risk individuals.
Wasanthi De Silva, Eric H Karunanayake, Kamani H Tennekoon, Marie Allen, Indrani Amarasinghe, Preethika Angunawala, Mohamed H Ziard. BMC Cancer 2008
13
20

The genetic epidemiology of breast cancer genes.
Deborah Thompson, Douglas Easton. J Mammary Gland Biol Neoplasia 2004
157
20

Application of multiplex PCR with histopathologic features for detection of familial breast cancer in formalin-fixed, paraffin-embedded histologic specimens.
H Rassi, M Houshmand, M Hashemi, K Majidzadeh, M H Hosseini Akbari, M Shafa Shariat Panahi. Tsitol Genet 2008
5
20


Hereditary breast and ovarian cancer in Cyprus: identification of a founder BRCA2 mutation.
Andreas Hadjisavvas, Elpida Charalambous, Adamos Adamou, Susan L Neuhausen, Christina G Christodoulou, Kyriacos Kyriacou. Cancer Genet Cytogenet 2004
17
20

Linking Histopathology and Family History in Breast Cancer.
M Atri, P Mehdipour, M Javidroozi, SS Hosseini-Asl, E Jafarimojarrad. Asian Pac J Cancer Prev 2002
5
20

BRCA1 and BRCA2 mutations among breast cancer patients from the Philippines.
Maria Lourdes De Leon Matsuda, Alexander Liede, Elaine Kwan, Cynthia A Mapua, Eva Maria C Cutiongco, Alex Tan, Ake Borg, Steven A Narod. Int J Cancer 2002
65
20

BRCA1 germline mutations and tumor characteristics in Chinese women with familial or early-onset breast cancer.
Weiqiu Chen, Kaifeng Pan, Tao Ouyang, Jinfeng Li, Tianfeng Wang, Zhaoqing Fan, Tie Fan, Benyao Lin, Youyong Lu, Weicheng You,[...]. Breast Cancer Res Treat 2009
33
20

Incidence and outcome of BRCA mutations in unselected patients with triple receptor-negative breast cancer.
Ana M Gonzalez-Angulo, Kirsten M Timms, Shuying Liu, Huiqin Chen, Jennifer K Litton, Jennifer Potter, Jerry S Lanchbury, Katherine Stemke-Hale, Bryan T Hennessy, Banu K Arun,[...]. Clin Cancer Res 2011
342
20


Identification of a novel mutations BRCA1*c.80 + 3del4 and BRCA2*c.6589delA in Slovak HBOC families.
Michal Konecny, Miriam Vizvaryova, Katarina Zavodna, Regina Behulova, Maria Gerykova Bujalkova, Tomas Krivulcik, Frantisek Cisarik, Juraj Kausitz, Eva Weismanova. Breast Cancer Res Treat 2010
2
50


BRCA1 and BRCA2 in breast cancer families from Wales: moderate mutation frequency and two recurrent mutations in BRCA1.
J M Lancaster, M E Carney, J Gray, J Myring, C Gumbs, J Sampson, D Wheeler, E France, R Wiseman, P Harper,[...]. Br J Cancer 1998
10
20

Mutation analysis of BRIP1/BACH1 in BRCA1/BRCA2 negative Chinese women with early onset breast cancer or affected relatives.
A-Yong Cao, Juan Huang, Zhen Hu, Wen-Feng Li, Zhong-Liang Ma, Li-Li Tang, Bin Zhang, Feng-Xi Su, Jie Zhou, Gen-Hong Di,[...]. Breast Cancer Res Treat 2009
28
20

Geographical distribution of Slovenian BRCA1/2 families according to family origin: implications for genetic screening.
M Krajc, V Zadnik, S Novaković, V Stegel, E Teugels, N Bešič, M Hočevar, A Vakselj, J De Grève, J Zgajnar. Clin Genet 2014
10
20

Significant contribution of large BRCA1 gene rearrangements in 120 French breast and ovarian cancer families.
Sophie Gad, Virginie Caux-Moncoutier, Sabine Pagès-Berhouet, Marion Gauthier-Villars, Isabelle Coupier, Pascal Pujol, Marc Frénay, Brigitte Gilbert, Christine Maugard, Yves-Jean Bignon,[...]. Oncogene 2002
76
20

The R71G BRCA1 is a founder Spanish mutation and leads to aberrant splicing of the transcript.
A Vega, B Campos, B Bressac-De-Paillerets, P M Bond, N Janin, F S Douglas, M Domènech, M Baena, C Pericay, C Alonso,[...]. Hum Mutat 2001
71
20

Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predisposition.
E Rouleau, B Jesson, A Briaux, C Nogues, V Chabaud, L Demange, J Sokolowska, F Coulet, E Barouk-Simonet, Y J Bignon,[...]. Breast Cancer Res Treat 2012
18
20


Complete genomic sequence and analysis of 117 kb of human DNA containing the gene BRCA1.
T M Smith, M K Lee, C I Szabo, N Jerome, M McEuen, M Taylor, L Hood, M C King. Genome Res 1996
223
20

Li-Fraumeni-like syndrome associated with a large BRCA1 intragenic deletion.
Amanda Gonçalves Silva, Ingrid Petroni Ewald, Marina Sapienza, Manuela Pinheiro, Ana Peixoto, Amanda França de Nóbrega, Dirce M Carraro, Manuel R Teixeira, Patricia Ashton-Prolla, Maria Isabel W Achatz,[...]. BMC Cancer 2012
12
20

BRCA1-related breast cancer in Austrian breast and ovarian cancer families: specific BRCA1 mutations and pathological characteristics.
T M Wagner, R A Möslinger, D Muhr, G Langbauer, K Hirtenlehner, H Concin, W Doeller, A Haid, A H Lang, P Mayer,[...]. Int J Cancer 1998
79
20

BRCA1 and BRCA2 mutations in Danish families with hereditary breast and/or ovarian cancer.
Mads Thomassen, Thomas V O Hansen, Ake Borg, Henriette Theilmann Lianee, Friedrik Wikman, Inge Søkilde Pedersen, Marie Luise Bisgaard, Finn C Nielsen, Torben A Kruse, Anne-Marie Gerdes. Acta Oncol 2008
36
20

Similar contributions of BRCA1 and BRCA2 germline mutations to early-onset breast cancer in Germany.
Ute Hamann, Xuan Liu, Nikola Bungardt, Hans Ulrich Ulmer, Gunther Bastert, Hans-Peter Sinn. Eur J Hum Genet 2003
20
20

Molecular and genealogical characterization of the R1443X BRCA1 mutation in high-risk French-Canadian breast/ovarian cancer families.
Hélène Vézina, Francine Durocher, Martine Dumont, Louis Houde, Csilla Szabo, Martine Tranchant, Jocelyne Chiquette, Marie Plante, Rachel Laframboise, Jean Lépine,[...]. Hum Genet 2005
43
20

Contribution of BRCA1 and BRCA2 germline mutations to the incidence of early-onset breast cancer in Cyprus.
M Loizidou, Y Marcou, V Anastasiadou, R Newbold, A Hadjisavvas, K Kyriacou. Clin Genet 2007
33
20

Full-exon pyrosequencing screening of BRCA germline mutations in Mexican women with inherited breast and ovarian cancer.
Felipe Vaca-Paniagua, Rosa María Alvarez-Gomez, Verónica Fragoso-Ontiveros, Silvia Vidal-Millan, Luis Alonso Herrera, David Cantú, Enrique Bargallo-Rocha, Alejandro Mohar, César López-Camarillo, Carlos Pérez-Plasencia. PLoS One 2012
31
20

Mutations P51U and G122E in retinal transcription factor NRL associated with autosomal dominant and sporadic retinitis pigmentosa.
M Martinez-Gimeno, M Maseras, M Baiget, M Beneito, G Antiñolo, C Ayuso, M Carballo. Hum Mutat 2001
34
20

Ashkenazi founder BRCA1/BRCA2 mutations in Slovak hereditary breast and/or ovarian cancer families.
S Cierniková, M Tomka, M Kovác, V Stevurková, V Zajac. Neoplasma 2006
13
20

Glyceraldehyde-3-phosphate dehydrogenase interacts with proapoptotic kinase mst1 to promote cardiomyocyte apoptosis.
Bei You, Shengdong Huang, Qing Qin, Bing Yi, Yang Yuan, Zhiyun Xu, Jianxin Sun. PLoS One 2013
73
20

Promoter methylation of the PTEN gene is a common molecular change in breast cancer.
Jose M García, Javier Silva, Cristina Peña, Vanesa Garcia, Rufo Rodríguez, Miguel A Cruz, Blanca Cantos, Mariano Provencio, Pilar España, Felix Bonilla. Genes Chromosomes Cancer 2004
165
20

BRCA1 mutations and polymorphisms in a hospital-based consecutive series of breast cancer patients from Apulia, Italy.
S Tommasi, A Crapolicchio, R Lacalamita, M Bruno, A Monaco, S Petroni, F Schittulli, S Longo, M Digennaro, D Calistri,[...]. Mutat Res 2005
49
20

De novo Alu element insertions targeted to a sequence common to the BRCA1 and BRCA2 genes.
Erik Teugels, Sylvia De Brakeleer, Guido Goelen, Willy Lissens, Erica Sermijn, Jacques De Grève. Hum Mutat 2005
61
20

Four novel mutations in APOB causing heterozygous and homozygous familial hypobetalipoproteinemia.
A J Whitfield, A D Marais, K Robertson, P H R Barrett, F M van Bockxmeer, J R Burnett. Hum Mutat 2003
15
20

Identification of germline 185delAG BRCA1 mutations in non-Jewish Americans of Spanish ancestry from the San Luis Valley, Colorado.
Lisa G Mullineaux, Teresa M Castellano, Jeffrey Shaw, Lisen Axell, Marie E Wood, Sami Diab, Catherine Klein, Mark Sitarik, Amie M Deffenbaugh, Sharon L Graw. Cancer 2003
42
20

Germline BRCA1 mutations in Iranian women with breast cancer.
A Ghaderi, A Talei, S Farjadian, A Mosalaei, M Doroudchi, H Kimura. Cancer Lett 2001
18
20

Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer.
S Håkansson, O Johannsson, U Johansson, G Sellberg, N Loman, A M Gerdes, E Holmberg, N Dahl, N Pandis, U Kristoffersson,[...]. Am J Hum Genet 1997
154
20


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.