A citation-based method for searching scientific literature

Diana Micleaa, Camelia Al-Khzouza, Sergiu Osan, Simona Bucerzan, Victoria Cret, Radu Anghel Popp, Maria Puiu, Adela Chirita-Emandi, Cristian Zimbru, Cristina Ghervan. J Pediatr Endocrinol Metab 2019
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Frequencies of BRCA1 and BRCA2 mutations among 1,342 unselected patients with invasive ovarian cancer.
Shiyu Zhang, Robert Royer, Song Li, John R McLaughlin, Barry Rosen, Harvey A Risch, Isabel Fan, Linda Bradley, Patricia A Shaw, Steven A Narod. Gynecol Oncol 2011
239
100

Cancer Risks in Patients Treated With Growth Hormone in Childhood: The SAGhE European Cohort Study.
Anthony J Swerdlow, Rosie Cooke, Dominique Beckers, Birgit Borgström, Gary Butler, Jean-Claude Carel, Stefano Cianfarani, Peter Clayton, Joël Coste, Annalisa Deodati,[...]. J Clin Endocrinol Metab 2017
56
100

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
7
100

Paediatric Anti-Müllerian Hormone measurement: Male and female reference intervals established using the automated Beckman Coulter Access AMH assay.
Helen Jopling, Allen Yates, Nicholas Burgoyne, Katharine Hayden, Christopher Chaloner, Lesley Tetlow. Endocrinol Diabetes Metab 2018
6
100

Spectrum and characterisation of BRCA1 and BRCA2 deleterious mutations in high-risk Czech patients with breast and/or ovarian cancer.
Eva Machackova, Lenka Foretova, Mirka Lukesova, Petra Vasickova, Marie Navratilova, Ilse Coene, Hana Pavlu, Veronika Kosinova, Jitka Kuklova, Kathleen Claes. BMC Cancer 2008
45
100

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
191
100

BRCA1 tumour suppression occurs via heterochromatin-mediated silencing.
Quan Zhu, Gerald M Pao, Alexis M Huynh, Hoonkyo Suh, Nina Tonnu, Petra M Nederlof, Fred H Gage, Inder M Verma. Nature 2011
288
100

Fanconi anemia: a single center experience of a large cohort.
Selman Kesici, Şule Ünal, Barış Kuşkonmaz, Selin Aytaç, Mualla Çetin, Fatma Gümrük. Turk J Pediatr 2019
3
100

Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.
Ake Borg, Robert W Haile, Kathleen E Malone, Marinela Capanu, Ahn Diep, Therese Törngren, Sharon Teraoka, Colin B Begg, Duncan C Thomas, Patrick Concannon,[...]. Hum Mutat 2010
75
100

Biallelic deleterious BRCA1 mutations in a woman with early-onset ovarian cancer.
Susan M Domchek, Jiangbo Tang, Jill Stopfer, Dana R Lilli, Nancy Hamel, Marc Tischkowitz, Alvaro N A Monteiro, Troy E Messick, Jacquelyn Powers, Alexandria Yonker,[...]. Cancer Discov 2013
88
100

Chromosome instability syndromes.
A Malcolm R Taylor, Cynthia Rothblum-Oviatt, Nathan A Ellis, Ian D Hickson, Stefan Meyer, Thomas O Crawford, Agata Smogorzewska, Barbara Pietrucha, Corry Weemaes, Grant S Stewart. Nat Rev Dis Primers 2019
34
100

Homozygous loss of function BRCA1 variant causing a Fanconi-anemia-like phenotype, a clinical report and review of previous patients.
Bruna L Freire, Thais K Homma, Mariana F A Funari, Antônio M Lerario, Aline M Leal, Elvira D R P Velloso, Alexsandra C Malaquias, Alexander A L Jorge. Eur J Med Genet 2018
20
100

Mechanism for survival of homozygous nonsense mutations in the tumor suppressor gene BRCA1.
Aaron Seo, Orna Steinberg-Shemer, Sule Unal, Silvia Casadei, Tom Walsh, Fatma Gumruk, Stavit Shalev, Akiko Shimamura, Nurten Ayse Akarsu, Hannah Tamary,[...]. Proc Natl Acad Sci U S A 2018
15
100

The Fanconi Anemia Pathway in Cancer.
Joshi Niraj, Anniina Färkkilä, Alan D D'Andrea. Annu Rev Cancer Biol 2019
103
100

Serum IGF-1 and IGFBP-3 levels in healthy children between 0 and 6 years of age.
Bilgin Yüksel, M Nuri Özbek, Neslihan Önenli Mungan, Feyza Darendeliler, Bahar Budan, Aysun Bideci, Ergün Çetinkaya, Merih Berberoğlu, Olcay Evliyaoğlu, Ediz Yeşilkaya,[...]. J Clin Res Pediatr Endocrinol 2011
22
100

Challenges in reporting pathogenic/potentially pathogenic variants in 94 cancer predisposing genes - in pediatric patients screened with NGS panels.
Adela Chirita-Emandi, Nicoleta Andreescu, Cristian G Zimbru, Paul Tutac, Smaranda Arghirescu, Margit Serban, Maria Puiu. Sci Rep 2020
5
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.