A citation-based method for searching scientific literature

Encarna B Gómez García, Jan C Oosterwijk, Maarten Timmermans, Christi J van Asperen, Frans B L Hogervorst, Nicoline Hoogerbrugge, Rogier Oldenburg, Senno Verhoef, Charlotte J Dommering, Margreet G E M Ausems, Theo A M van Os, Annemarie H van der Hout, Marjolijn Ligtenberg, Ans van den Ouweland, Rob B van der Luijt, Juul T Wijnen, Jan J P Gille, Patrick J Lindsey, Peter Devilee, Marinus J Blok, Maaike P G Vreeswijk. Breast Cancer Res 2009
Times Cited: 41



A Osorio, R L Milne, E Honrado, A Barroso, O Diez, R Salazar, M de la Hoya, A Vega, J Benítez. Hum Mutat 2007
Times Cited: 35




List of shared articles



Times cited

ENIGMA--evidence-based network for the interpretation of germline mutant alleles: an international initiative to evaluate risk and clinical significance associated with sequence variation in BRCA1 and BRCA2 genes.
Amanda B Spurdle, Sue Healey, Andrew Devereau, Frans B L Hogervorst, Alvaro N A Monteiro, Katherine L Nathanson, Paolo Radice, Dominique Stoppa-Lyonnet, Sean Tavtigian, Barbara Wappenschmidt,[...]. Hum Mutat 2012
181

The BRCA1 variant p.Ser36Tyr abrogates BRCA1 protein function and potentially confers a moderate risk of breast cancer.
Charita M Christou, Andreas Hadjisavvas, Maria Kyratzi, Christina Flouri, Ioanna Neophytou, Violetta Anastasiadou, Maria A Loizidou, Kyriacos Kyriacou. PLoS One 2014
2

A Danish national effort of BRCA1/2 variant classification.
Inge Søkilde Pedersen, Ane Y Schmidt, Birgitte Bertelsen, Anja Ernst, Christian Liebst Toft Andersen, Torben Kruse, Maria Rossing, Mads Thomassen. Acta Oncol 2018
2


A simple method for co-segregation analysis to evaluate the pathogenicity of unclassified variants; BRCA1 and BRCA2 as an example.
Leila Mohammadi, Maaike P Vreeswijk, Rogier Oldenburg, Ans van den Ouweland, Jan C Oosterwijk, Annemarie H van der Hout, Nicoline Hoogerbrugge, Marjolijn Ligtenberg, Margreet G Ausems, Rob B van der Luijt,[...]. BMC Cancer 2009
44

Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicity.
Logan C Walker, Phillip J Whiley, Fergus J Couch, Daniel J Farrugia, Sue Healey, Diana M Eccles, Feng Lin, Samantha A Butler, Sheila A Goff, Bryony A Thompson,[...]. Hum Mutat 2010
46

Phenotype-genotype correlation in familial breast cancer.
Ana Cristina Vargas, Jorge S Reis-Filho, Sunil R Lakhani. J Mammary Gland Biol Neoplasia 2011
24

A missense variant within BRCA1 exon 23 causing exon skipping.
Etienne Rouleau, Cédrick Lefol, Virginie Moncoutier, Laurent Castera, Claude Houdayer, Sandrine Caputo, Ivan Bièche, Monique Buisson, Sylvie Mazoyer, Dominique Stoppa-Lyonnet,[...]. Cancer Genet Cytogenet 2010
11

Characterization of BRCA1 ring finger variants of uncertain significance.
Kevin Sweet, Leigha Senter, Robert Pilarski, Lai Wei, Amanda Ewart Toland. Breast Cancer Res Treat 2010
20