A citation-based method for searching scientific literature

Kajal Biswas, Ranabir Das, Blanche P Alter, Sergey G Kuznetsov, Stacey Stauffer, Susan L North, Sandra Burkett, Lawrence C Brody, Stefan Meyer, R Andrew Byrd, Shyam K Sharan. Blood 2011
Times Cited: 35







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



Times Cited
  Times     Co-cited
Similarity


Assessment of functional effects of unclassified genetic variants.
Fergus J Couch, Lene Juel Rasmussen, Robert Hofstra, Alvaro N A Monteiro, Marc S Greenblatt, Niels de Wind. Hum Mutat 2008
80
8

Functional assays for BRCA1 and BRCA2.
Marcelo A Carvalho, Fergus J Couch, Alvaro N A Monteiro. Int J Biochem Cell Biol 2007
41
8

Simple and highly efficient BAC recombineering using galK selection.
Søren Warming, Nina Costantino, Donald L Court, Nancy A Jenkins, Neal G Copeland. Nucleic Acids Res 2005
896
8

Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group.
Sean V Tavtigian, Marc S Greenblatt, David E Goldgar, Paolo Boffetta. Hum Mutat 2008
56
8

Listening to silence and understanding nonsense: exonic mutations that affect splicing.
Luca Cartegni, Shern L Chew, Adrian R Krainer. Nat Rev Genet 2002
8

Prediction and assessment of splicing alterations: implications for clinical testing.
Amanda B Spurdle, Fergus J Couch, Frans B L Hogervorst, Paolo Radice, Olga M Sinilnikova. Hum Mutat 2008
90
8


BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk.
Amanda B Spurdle, Phillip J Whiley, Bryony Thompson, Bingjian Feng, Sue Healey, Melissa A Brown, Christopher Pettigrew, Christi J Van Asperen, Margreet G E M Ausems, Anna A Kattentidt-Mouravieva,[...]. J Med Genet 2012
67
8

ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.
C Sue Richards, Sherri Bale, Daniel B Bellissimo, Soma Das, Wayne W Grody, Madhuri R Hegde, Elaine Lyon, Brian E Ward. Genet Med 2008
529
8

Comparative in vitro and in silico analyses of variants in splicing regions of BRCA1 and BRCA2 genes and characterization of novel pathogenic mutations.
Mara Colombo, Giovanna De Vecchi, Laura Caleca, Claudia Foglia, Carla B Ripamonti, Filomena Ficarazzi, Monica Barile, Liliana Varesco, Bernard Peissel, Siranoush Manoukian,[...]. PLoS One 2013
39
8

Intronic variants in BRCA1 and BRCA2 that affect RNA splicing can be reliably selected by splice-site prediction programs.
Maaike P G Vreeswijk, Jaennelle N Kraan, Heleen M van der Klift, Geraldine R Vink, Cees J Cornelisse, Juul T Wijnen, Egbert Bakker, Christi J van Asperen, Peter Devilee. Hum Mutat 2009
77
8

VACTERL-H Association and Fanconi Anemia.
B P Alter, P S Rosenberg. Mol Syndromol 2013
41
8

Rare mutations in XRCC2 increase the risk of breast cancer.
D J Park, F Lesueur, T Nguyen-Dumont, M Pertesi, F Odefrey, F Hammet, S L Neuhausen, E M John, I L Andrulis, M B Terry,[...]. Am J Hum Genet 2012
118
8

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
453
8

Germline Brca2 heterozygosity promotes Kras(G12D) -driven carcinogenesis in a murine model of familial pancreatic cancer.
Ferdinandos Skoulidis, Liam D Cassidy, Venkat Pisupati, Jon G Jonasson, Hordur Bjarnason, Jorunn E Eyfjord, Florian A Karreth, Michael Lim, Lorraine M Barber, Susan A Clatworthy,[...]. Cancer Cell 2010
115
8

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
653
8

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
332
8

Inherited susceptibility to common cancers.
William D Foulkes. N Engl J Med 2008
314
8

A cross-linker-sensitive myeloid leukemia cell line from a 2-year-old boy with severe Fanconi anemia and biallelic FANCD1/BRCA2 mutations.
Stefan Meyer, William D Fergusson, Anneke B Oostra, Annette L Medhurst, Quinten Waisfisz, Johan P de Winter, Fei Chen, Trevor F Carr, Jill Clayton-Smith, Tara Clancy,[...]. Genes Chromosomes Cancer 2005
18
16

Fanconi anemia and its diagnosis.
Arleen D Auerbach. Mutat Res 2009
327
8

Hepatoblastoma in a 4-year-old girl with Fanconi anaemia.
Sascha Kopic, Katharina Eirich, Beatrice Schuster, Helmut Hanenberg, Raymonda Varon-Mateeva, Olaf Rittinger, Günther Schimpl, Detlev Schindler, Neil Jones. Acta Paediatr 2011
14
21

Stabilization of RAD51 nucleoprotein filaments by the C-terminal region of BRCA2.
Fumiko Esashi, Vitold E Galkin, Xiong Yu, Edward H Egelman, Stephen C West. Nat Struct Mol Biol 2007
182
8

BRCA1 RING function is essential for tumor suppression but dispensable for therapy resistance.
Rinske Drost, Peter Bouwman, Sven Rottenberg, Ute Boon, Eva Schut, Sjoerd Klarenbeek, Christiaan Klijn, Ingrid van der Heijden, Hanneke van der Gulden, Ellen Wientjens,[...]. Cancer Cell 2011
158
8


PALB2 links BRCA1 and BRCA2 in the DNA-damage response.
Feng Zhang, Jianglin Ma, Jiaxue Wu, Lin Ye, Hong Cai, Bing Xia, Xiaochun Yu. Curr Biol 2009
330
8


DSS1 is required for the stability of BRCA2.
J Li, C Zou, Y Bai, D E Wazer, V Band, Q Gao. Oncogene 2006
87
8

Truncated BRCA2 is cytoplasmic: implications for cancer-linked mutations.
B H Spain, C J Larson, L S Shihabuddin, F H Gage, I M Verma. Proc Natl Acad Sci U S A 1999
108
8

PALB2 functionally connects the breast cancer susceptibility proteins BRCA1 and BRCA2.
Fan Zhang, Qiang Fan, Keqin Ren, Paul R Andreassen. Mol Cancer Res 2009
186
8

Nuclear localization signals of the BRCA2 protein.
K Yano, K Morotomi, H Saito, M Kato, F Matsuo, Y Miki. Biochem Biophys Res Commun 2000
43
8


BRCA2 is required for ionizing radiation-induced assembly of Rad51 complex in vivo.
S S Yuan, S Y Lee, G Chen, M Song, G E Tomlinson, E Y Lee. Cancer Res 1999
326
8

Tumorigenesis and a DNA repair defect in mice with a truncating Brca2 mutation.
F Connor, D Bertwistle, P J Mee, G M Ross, S Swift, E Grigorieva, V L Tybulewicz, A Ashworth. Nat Genet 1997
345
8


Fanconi anaemia and the repair of Watson and Crick DNA crosslinks.
Molly C Kottemann, Agata Smogorzewska. Nature 2013
385
8

Identification of a RING protein that can interact in vivo with the BRCA1 gene product.
L C Wu, Z W Wang, J T Tsan, M A Spillman, A Phung, X L Xu, M C Yang, L Y Hwang, A M Bowcock, R Baer. Nat Genet 1996
561
8

Cooperation of breast cancer proteins PALB2 and piccolo BRCA2 in stimulating homologous recombination.
Rémi Buisson, Anne-Marie Dion-Côté, Yan Coulombe, Hélène Launay, Hong Cai, Alicja Z Stasiak, Andrzej Stasiak, Bing Xia, Jean-Yves Masson. Nat Struct Mol Biol 2010
202
8


Biallelic mutations in BRCA1 cause a new Fanconi anemia subtype.
Sarah L Sawyer, Lei Tian, Marketta Kähkönen, Jeremy Schwartzentruber, Martin Kircher, Jacek Majewski, David A Dyment, A Micheil Innes, Kym M Boycott, Lisa A Moreau,[...]. Cancer Discov 2015
194
8

Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing.
Tom Walsh, Silvia Casadei, Ming K Lee, Christopher C Pennil, Alex S Nord, Anne M Thornton, Wendy Roeb, Kathy J Agnew, Sunday M Stray, Anneka Wickramanayake,[...]. Proc Natl Acad Sci U S A 2011
569
8

Resistance to therapy caused by intragenic deletion in BRCA2.
Stacey L Edwards, Rachel Brough, Christopher J Lord, Rachael Natrajan, Radost Vatcheva, Douglas A Levine, Jeff Boyd, Jorge S Reis-Filho, Alan Ashworth. Nature 2008
656
8

Plasticity of BRCA2 function in homologous recombination: genetic interactions of the PALB2 and DNA binding domains.
Nicolas Siaud, Maria A Barbera, Akinori Egashira, Isabel Lam, Nicole Christ, Katharina Schlacher, Bing Xia, Maria Jasin. PLoS Genet 2011
47
8

53BP1 inhibits homologous recombination in Brca1-deficient cells by blocking resection of DNA breaks.
Samuel F Bunting, Elsa Callén, Nancy Wong, Hua-Tang Chen, Federica Polato, Amanda Gunn, Anne Bothmer, Niklas Feldhahn, Oscar Fernandez-Capetillo, Liu Cao,[...]. Cell 2010
8

CDK-dependent phosphorylation of BRCA2 as a regulatory mechanism for recombinational repair.
Fumiko Esashi, Nicole Christ, Julian Gannon, Yilun Liu, Tim Hunt, Maria Jasin, Stephen C West. Nature 2005
320
8

Stabilization of stalled DNA replication forks by the BRCA2 breast cancer susceptibility protein.
Mikhail Lomonosov, Shubha Anand, Mahesh Sangrithi, Rachel Davies, Ashok R Venkitaraman. Genes Dev 2003
182
8


The BRCA2 genetic variant IVS7 + 2T-->G is a mutation.
M T Pyne, A R Brothman, B Ward, D Pruss, B C Hendrickson, T Scholl. J Hum Genet 2000
19
15

A Dominant Mutation in Human RAD51 Reveals Its Function in DNA Interstrand Crosslink Repair Independent of Homologous Recombination.
Anderson T Wang, Taeho Kim, John E Wagner, Brooke A Conti, Francis P Lach, Athena L Huang, Henrik Molina, Erica M Sanborn, Heather Zierhut, Belinda K Cornes,[...]. Mol Cell 2015
156
8

BRCA2 prevents R-loop accumulation and associates with TREX-2 mRNA export factor PCID2.
Vaibhav Bhatia, Sonia I Barroso, María L García-Rubio, Emanuela Tumini, Emilia Herrera-Moyano, Andrés Aguilera. Nature 2014
280
8

Comprehensive annotation of splice junctions supports pervasive alternative splicing at the BRCA1 locus: a report from the ENIGMA consortium.
Mara Colombo, Marinus J Blok, Phillip Whiley, Marta Santamariña, Sara Gutiérrez-Enríquez, Atocha Romero, Pilar Garre, Alexandra Becker, Lindsay Denise Smith, Giovanna De Vecchi,[...]. Hum Mol Genet 2014
58
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.