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


TNF-alpha and IFN-gamma are overexpressed in the bone marrow of Fanconi anemia patients and TNF-alpha suppresses erythropoiesis in vitro.
Carlo Dufour, Anna Corcione, Johanna Svahn, Riccardo Haupt, Vincenzo Poggi, Albert Nandor Béka'ssy, Rosanna Scimè, Angela Pistorio, Vito Pistoia. Blood 2003
172
2

TGF-β Inhibition Rescues Hematopoietic Stem Cell Defects and Bone Marrow Failure in Fanconi Anemia.
Haojian Zhang, David E Kozono, Kevin W O'Connor, Sofia Vidal-Cardenas, Alix Rousseau, Abigail Hamilton, Lisa Moreau, Emily F Gaudiano, Joel Greenberger, Grover Bagby,[...]. Cell Stem Cell 2016
79
2

PALB2 connects BRCA1 and BRCA2 in the G2/M checkpoint response.
Srilatha Simhadri, Gabriele Vincelli, Yanying Huo, Sarah Misenko, Tzeh Keong Foo, Johanna Ahlskog, Claus S Sørensen, Gregory G Oakley, Shridar Ganesan, Samuel F Bunting,[...]. Oncogene 2019
17
5



Breast cancer-associated missense mutants of the PALB2 WD40 domain, which directly binds RAD51C, RAD51 and BRCA2, disrupt DNA repair.
J-Y Park, T R Singh, N Nassar, F Zhang, M Freund, H Hanenberg, A R Meetei, P R Andreassen. Oncogene 2014
83
2

BRCA1 and BRCA2 mutations account for a large proportion of ovarian carcinoma cases.
Tuya Pal, Jenny Permuth-Wey, Judith A Betts, Jeffrey P Krischer, James Fiorica, Hector Arango, James LaPolla, Mitchell Hoffman, Martin A Martino, Katie Wakeley,[...]. Cancer 2005
498
2

Major clinical research advances in gynecologic cancer in 2014.
Dong Hoon Suh, Kyung Hun Lee, Kidong Kim, Sokbom Kang, Jae Weon Kim. J Gynecol Oncol 2015
24
4

Genetic Testing to Guide Risk-Stratified Screens for Breast Cancer.
Ava Willoughby, Paul R Andreassen, Amanda Ewart Toland. J Pers Med 2019
13
7

Epigenetic regulation of DNA repair genes and implications for tumor therapy.
Markus Christmann, Bernd Kaina. Mutat Res Rev Mutat Res 2019
20
5

A second DNA binding site in human BRCA2 promotes homologous recombination.
Catharina von Nicolai, Åsa Ehlén, Charlotte Martin, Xiaodong Zhang, Aura Carreira. Nat Commun 2016
26
3

CRISPR/Cas9 for cancer research and therapy.
Tianzuo Zhan, Niklas Rindtorff, Johannes Betge, Matthias P Ebert, Michael Boutros. Semin Cancer Biol 2019
87
2


Recombination mediator and Rad51 targeting activities of a human BRCA2 polypeptide.
Joseph San Filippo, Peter Chi, Michael G Sehorn, Julia Etchin, Lumir Krejci, Patrick Sung. J Biol Chem 2006
100
2

Signatures of mutational processes in human cancer.
Ludmil B Alexandrov, Serena Nik-Zainal, David C Wedge, Samuel A J R Aparicio, Sam Behjati, Andrew V Biankin, Graham R Bignell, Niccolò Bolli, Ake Borg, Anne-Lise Børresen-Dale,[...]. Nature 2013
2


Myelodysplastic Syndrome, Acute Myeloid Leukemia, and Cancer Surveillance in Fanconi Anemia.
Sharon A Savage, Michael F Walsh. Hematol Oncol Clin North Am 2018
18
5

Functional interaction of monoubiquitinated FANCD2 and BRCA2/FANCD1 in chromatin.
XiaoZhe Wang, Paul R Andreassen, Alan D D'Andrea. Mol Cell Biol 2004
255
2

Contribution of epigenetic alteration of BRCA1 and BRCA2 genes in breast carcinomas in Tunisian patients.
R Ben Gacem, M Hachana, S Ziadi, K Amara, F Ksia, M Mokni, M Trimeche. Cancer Epidemiol 2012
21
4


Compensatory functions and interdependency of the DNA-binding domain of BRCA2 with the BRCA1-PALB2-BRCA2 complex.
Muthana Al Abo, Donniphat Dejsuphong, Kouji Hirota, Yasukazu Yonetani, Mitsuyoshi Yamazoe, Hitoshi Kurumizaka, Shunichi Takeda. Cancer Res 2014
14
7

The BRCA2 gene product functionally interacts with p53 and RAD51.
L Y Marmorstein, T Ouchi, S A Aaronson. Proc Natl Acad Sci U S A 1998
215
2

Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations.
A Moran, C O'Hara, S Khan, L Shack, E Woodward, E R Maher, F Lalloo, D G R Evans. Fam Cancer 2012
163
2

Cloning, chromosomal mapping and expression pattern of the mouse Brca2 gene.
F Connor, A Smith, R Wooster, M Stratton, A Dixon, E Campbell, T M Tait, T Freeman, A Ashworth. Hum Mol Genet 1997
52
2

Insights into ssDNA recognition by the OB fold from a structural and thermodynamic study of Sulfolobus SSB protein.
Iain D Kerr, Ross I M Wadsworth, Liza Cubeddu, Wulf Blankenfeldt, James H Naismith, Malcolm F White. EMBO J 2003
100
2

Investigation of DNA damage response and apoptotic gene methylation pattern in sporadic breast tumors using high throughput quantitative DNA methylation analysis technology.
Ranjana Pal, Niloo Srivastava, Rupali Chopra, Sailesh Gochhait, Pawan Gupta, Neeraj Prakash, Gaurav Agarwal, Rameshwar N K Bamezai. Mol Cancer 2010
25
4

Epigenetic inactivation of the chromosomal stability control genes BRCA1, BRCA2, and XRCC5 in non-small cell lung cancer.
Ming-Ni Lee, Ruo-Chia Tseng, Han-Shui Hsu, Jia-Yang Chen, Ching Tzao, William L Ho, Yi-Ching Wang. Clin Cancer Res 2007
82
2

CRISPR-Cas: biology, mechanisms and relevance.
Frank Hille, Emmanuelle Charpentier. Philos Trans R Soc Lond B Biol Sci 2016
115
2

siRNA depletion of BRCA1, but not BRCA2, causes increased genome instability in Fanconi anemia cells.
Donald Bruun, Alexandra Folias, Yassmine Akkari, Yumi Cox, Susan Olson, Robb Moses. DNA Repair (Amst) 2003
45
2


Fanconi anaemia and cancer: an intricate relationship.
Grzegorz Nalepa, D Wade Clapp. Nat Rev Cancer 2018
121
2

Chapter 9. Studying nonsense-mediated mRNA decay in mammalian cells.
Daiki Matsuda, Hanae Sato, Lynne E Maquat. Methods Enzymol 2008
11
9

A RAD51 assay feasible in routine tumor samples calls PARP inhibitor response beyond BRCA mutation.
Marta Castroviejo-Bermejo, Cristina Cruz, Alba Llop-Guevara, Sara Gutiérrez-Enríquez, Mandy Ducy, Yasir Hussein Ibrahim, Albert Gris-Oliver, Benedetta Pellegrino, Alejandra Bruna, Marta Guzmán,[...]. EMBO Mol Med 2018
69
2

Mosaicism in Fanconi anemia: concise review and evaluation of published cases with focus on clinical course of blood count normalization.
Eileen Nicoletti, Gayatri Rao, Juan A Bueren, Paula Río, Susana Navarro, Jordi Surrallés, Grace Choi, Jonathan D Schwartz. Ann Hematol 2020
9
11

Diagnosis of Fanconi anemia in patients with bone marrow failure.
Fernando O Pinto, Thierry Leblanc, Delphine Chamousset, Gwenaelle Le Roux, Benoit Brethon, Bruno Cassinat, Jérôme Larghero, Jean-Pierre de Villartay, Dominique Stoppa-Lyonnet, André Baruchel,[...]. Haematologica 2009
55
2

The Fanconi Anemia Pathway Maintains Genome Stability by Coordinating Replication and Transcription.
Rebekka A Schwab, Jadwiga Nieminuszczy, Fenil Shah, Jamie Langton, David Lopez Martinez, Chih-Chao Liang, Martin A Cohn, Richard J Gibbons, Andrew J Deans, Wojciech Niedzwiedz. Mol Cell 2015
191
2

Diagnosis of fanconi anemia: chromosomal breakage analysis.
Anneke B Oostra, Aggie W M Nieuwint, Hans Joenje, Johan P de Winter. Anemia 2012
61
2

Is BRCA2 involved in early onset colorectal cancer risk?
Mathilde Gay-Bellile, Maud Privat, Alexandra Martins, Sandrine M Caputo, Céline Pebrel-Richard, Mathias Cavaillé, Sandrine Viala, Carole Corsini, Michael Rodrigues, Nicolas Barnich,[...]. Clin Genet 2020
3
33

RAD51 foci as a functional biomarker of homologous recombination repair and PARP inhibitor resistance in germline BRCA-mutated breast cancer.
C Cruz, M Castroviejo-Bermejo, S Gutiérrez-Enríquez, A Llop-Guevara, Y H Ibrahim, A Gris-Oliver, S Bonache, B Morancho, A Bruna, O M Rueda,[...]. Ann Oncol 2018
123
2

BRCA1- and BRCA2-specific in silico tools for variant interpretation in the CAGI 5 ENIGMA challenge.
Natàlia Padilla, Alejandro Moles-Fernández, Casandra Riera, Gemma Montalban, Selen Özkan, Lars Ootes, Sandra Bonache, Orland Díez, Sara Gutiérrez-Enríquez, Xavier de la Cruz. Hum Mutat 2019
5
20

Optimised molecular genetic diagnostics of Fanconi anaemia by whole exome sequencing and functional studies.
Massimo Bogliolo, Roser Pujol, Miriam Aza-Carmona, Núria Muñoz-Subirana, Benjamin Rodriguez-Santiago, José Antonio Casado, Paula Rio, Christopher Bauser, Judith Reina-Castillón, Marcos Lopez-Sanchez,[...]. J Med Genet 2020
10
10

Decapping protein EDC4 regulates DNA repair and phenocopies BRCA1.
Gonzalo Hernández, María José Ramírez, Jordi Minguillón, Paco Quiles, Gorka Ruiz de Garibay, Miriam Aza-Carmona, Massimo Bogliolo, Roser Pujol, Rosario Prados-Carvajal, Juana Fernández,[...]. Nat Commun 2018
24
4

Chromosome fragility in patients with Fanconi anaemia: diagnostic implications and clinical impact.
Maria Castella, Roser Pujol, Elsa Callén, Maria J Ramírez, José A Casado, Maria Talavera, Teresa Ferro, Arturo Muñoz, Julián Sevilla, Luis Madero,[...]. J Med Genet 2011
36
2

Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes.
Jo Vandesompele, Katleen De Preter, Filip Pattyn, Bruce Poppe, Nadine Van Roy, Anne De Paepe, Frank Speleman. Genome Biol 2002
2

Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort.
Sebastian M Waszak, Paul A Northcott, Ivo Buchhalter, Giles W Robinson, Christian Sutter, Susanne Groebner, Kerstin B Grund, Laurence Brugières, David T W Jones, Kristian W Pajtler,[...]. Lancet Oncol 2018
131
2

Exome sequencing of osteosarcoma reveals mutation signatures reminiscent of BRCA deficiency.
Michal Kovac, Claudia Blattmann, Sebastian Ribi, Jan Smida, Nikola S Mueller, Florian Engert, Francesc Castro-Giner, Joachim Weischenfeldt, Monika Kovacova, Andreas Krieg,[...]. Nat Commun 2015
152
2

RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies.
Antonis C Antoniou, Olga M Sinilnikova, Jacques Simard, Mélanie Léoné, Martine Dumont, Susan L Neuhausen, Jeffery P Struewing, Dominique Stoppa-Lyonnet, Laure Barjhoux, David J Hughes,[...]. Am J Hum Genet 2007
192
2


The tumor suppressor gene Brca1 is required for embryonic cellular proliferation in the mouse.
R Hakem, J L de la Pompa, C Sirard, R Mo, M Woo, A Hakem, A Wakeham, J Potter, A Reitmair, F Billia,[...]. Cell 1996
547
2

Biallelic germline BRCA1 mutations in a patient with early onset breast cancer, mild Fanconi anemia-like phenotype, and no chromosome fragility.
Katharina Keupp, Stephanie Hampp, Annette Hübbel, Monika Maringa, Sarah Kostezka, Kerstin Rhiem, Anke Waha, Barbara Wappenschmidt, Roser Pujol, Jordi Surrallés,[...]. Mol Genet Genomic Med 2019
8
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.