A citation-based method for searching scientific literature

Valentina Favalli, Giulia Tini, Emanuele Bonetti, Gianluca Vozza, Alessandro Guida, Sara Gandini, Pier Giuseppe Pelicci, Luca Mazzarella. Am J Hum Genet 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Accurate classification of BRCA1 variants with saturation genome editing.
Gregory M Findlay, Riza M Daza, Beth Martin, Melissa D Zhang, Anh P Leith, Molly Gasperini, Joseph D Janizek, Xingfan Huang, Lea M Starita, Jay Shendure. Nature 2018
242
100

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
100

A model to infer the pathogenic significance of CDH1 germline missense variants.
Gianpaolo Suriano, Susana Seixas, Jorge Rocha, Raquel Seruca. J Mol Med (Berl) 2006
52
50

Cell division orientation is coupled to cell-cell adhesion by the E-cadherin/LGN complex.
Martijn Gloerich, Julie M Bianchini, Kathleen A Siemers, Daniel J Cohen, W James Nelson. Nat Commun 2017
65
50

Matrigel: basement membrane matrix with biological activity.
Hynda K Kleinman, George R Martin. Semin Cancer Biol 2005
862
50

Geographical Distribution of E-cadherin Germline Mutations in the Context of Diffuse Gastric Cancer: A Systematic Review.
Giovanni Corso, Federica Corso, Federica Bellerba, Patrícia Carneiro, Susana Seixas, Antonio Cioffi, Carlo La Vecchia, Francesca Magnoni, Bernardo Bonanni, Paolo Veronesi,[...]. Cancers (Basel) 2021
4
50

E-cadherin missense mutations, associated with hereditary diffuse gastric cancer (HDGC) syndrome, display distinct invasive behaviors and genetic interactions with the Wnt and Notch pathways in Drosophila epithelia.
Paulo S Pereira, Alexandra Teixeira, Sofia Pinho, Paulo Ferreira, Joana Fernandes, Carla Oliveira, Raquel Seruca, Gianpaolo Suriano, Fernando Casares. Hum Mol Genet 2006
27
50


E-cadherin alterations in hereditary disorders with emphasis on hereditary diffuse gastric cancer.
Carla Oliveira, Hugo Pinheiro, Joana Figueiredo, Raquel Seruca, Fátima Carneiro. Prog Mol Biol Transl Sci 2013
29
50

Genetics and mechanisms of ovarian cancer: parallels between Drosophila and humans.
Alicia E Rosales-Nieves, Acaimo González-Reyes. Semin Cell Dev Biol 2014
11
50

Identification of CDH1 germline missense mutations associated with functional inactivation of the E-cadherin protein in young gastric cancer probands.
Gianpaolo Suriano, Carla Oliveira, Paulo Ferreira, José C Machado, Maria C Bordin, Olivier De Wever, Erik A Bruyneel, Nicole Moguilevsky, Nicola Grehan, Timothy R Porter,[...]. Hum Mol Genet 2003
142
50

The importance of E-cadherin binding partners to evaluate the pathogenicity of E-cadherin missense mutations associated to HDGC.
Joana Figueiredo, Ola Söderberg, Joana Simões-Correia, Karin Grannas, Gianpaolo Suriano, Raquel Seruca. Eur J Hum Genet 2013
52
50

Quantification of topological features in cell meshes to explore E-cadherin dysfunction.
Tânia Mestre, Joana Figueiredo, Ana Sofia Ribeiro, Joana Paredes, Raquel Seruca, João Miguel Sanches. Sci Rep 2016
13
50

E-cadherin destabilization accounts for the pathogenicity of missense mutations in hereditary diffuse gastric cancer.
Joana Simões-Correia, Joana Figueiredo, Rui Lopes, François Stricher, Carla Oliveira, Luis Serrano, Raquel Seruca. PLoS One 2012
42
50

Hereditary Gastric and Breast Cancer Syndromes Related to CDH1 Germline Mutation: A Multidisciplinary Clinical Review.
Giovanni Corso, Giacomo Montagna, Joana Figueiredo, Carlo La Vecchia, Uberto Fumagalli Romario, Maria Sofia Fernandes, Susana Seixas, Franco Roviello, Cristina Trovato, Elena Guerini-Rocco,[...]. Cancers (Basel) 2020
7
50

Fiji: an open-source platform for biological-image analysis.
Johannes Schindelin, Ignacio Arganda-Carreras, Erwin Frise, Verena Kaynig, Mark Longair, Tobias Pietzsch, Stephan Preibisch, Curtis Rueden, Stephan Saalfeld, Benjamin Schmid,[...]. Nat Methods 2012
50

Isolation and characterization of type IV procollagen, laminin, and heparan sulfate proteoglycan from the EHS sarcoma.
H K Kleinman, M L McGarvey, L A Liotta, P G Robey, K Tryggvason, G R Martin. Biochemistry 1982
50

Identification of germline mutations in the cancer predisposing gene CDH1 in patients with orofacial clefts.
Ingrid P Vogelaar, Joana Figueiredo, Iris A L M van Rooij, Joana Simões-Correia, Rachel S van der Post, Soraia Melo, Raquel Seruca, Carine E L Carels, Marjolijn J L Ligtenberg, Nicoline Hoogerbrugge. Hum Mol Genet 2013
36
50

Hereditary Diffuse Gastric Cancer Syndrome: CDH1 Mutations and Beyond.
Samantha Hansford, Pardeep Kaurah, Hector Li-Chang, Michelle Woo, Janine Senz, Hugo Pinheiro, Kasmintan A Schrader, David F Schaeffer, Karey Shumansky, George Zogopoulos,[...]. JAMA Oncol 2015
311
50

Geometric compensation applied to image analysis of cell populations with morphological variability: a new role for a classical concept.
Joana Figueiredo, Isabel Rodrigues, João Ribeiro, Maria Sofia Fernandes, Soraia Melo, Bárbara Sousa, Joana Paredes, Raquel Seruca, João M Sanches. Sci Rep 2018
3
50



Blepharocheilodontic syndrome is a CDH1 pathway-related disorder due to mutations in CDH1 and CTNND1.
Jamal Ghoumid, Morgane Stichelbout, Anne-Sophie Jourdain, Frederic Frenois, Sophie Lejeune-Dumoulin, Marie-Pierre Alex-Cordier, Marine Lebrun, Pierre Guerreschi, Veronique Duquennoy-Martinot, Matthieu Vinchon,[...]. Genet Med 2017
24
50

E-cadherin germline mutations in familial gastric cancer.
P Guilford, J Hopkins, J Harraway, M McLeod, N McLeod, P Harawira, H Taite, R Scoular, A Miller, A E Reeve. Nature 1998
50

E-cadherin germline mutation carriers: clinical management and genetic implications.
Giovanni Corso, Joana Figueiredo, Roberto Biffi, Chiara Trentin, Bernardo Bonanni, Irene Feroce, Davide Serrano, Enrico Cassano, Bruno Annibale, Soraia Melo,[...]. Cancer Metastasis Rev 2014
32
50

Predicting the Functional Impact of CDH1 Missense Mutations in Hereditary Diffuse Gastric Cancer.
Soraia Melo, Joana Figueiredo, Maria Sofia Fernandes, Margarida Gonçalves, Eurico Morais-de-Sá, João Miguel Sanches, Raquel Seruca. Int J Mol Sci 2017
26
50

Endoplasmic reticulum quality control: a new mechanism of E-cadherin regulation and its implication in cancer.
Joana Simões-Correia, Joana Figueiredo, Carla Oliveira, Jolanda van Hengel, Raquel Seruca, Frans van Roy, Gianpaolo Suriano. Hum Mol Genet 2008
44
50

Polarity proteins in oncogenesis.
Maria Fomicheva, Erica M Tross, Ian G Macara. Curr Opin Cell Biol 2020
13
50

Germline E-cadherin gene (CDH1) mutations predispose to familial gastric cancer and colorectal cancer.
F M Richards, S A McKee, M H Rajpar, T R Cole, D G Evans, J A Jankowski, C McKeown, D S Sanders, E R Maher. Hum Mol Genet 1999
256
50

Germline E-cadherin mutations in familial lobular breast cancer.
S Masciari, N Larsson, J Senz, N Boyd, P Kaurah, M J Kandel, L N Harris, H C Pinheiro, A Troussard, P Miron,[...]. J Med Genet 2007
116
50


Phenotypic heterogeneity of hereditary diffuse gastric cancer: report of a family with early-onset disease.
Irene Gullo, Vitor Devezas, Manuela Baptista, Luzia Garrido, Sérgio Castedo, Rui Morais, Xiaogang Wen, Elisabete Rios, Jorge Pinheiro, Inês Pinto-Ribeiro,[...]. Gastrointest Endosc 2018
21
50

Associations of CDH1 germline variant location and cancer phenotype in families with hereditary diffuse gastric cancer (HDGC).
Winifred Lo, Bin Zhu, Arvind Sabesan, Ho-Hsiang Wu, Astin Powers, Rebecca A Sorber, Sarangan Ravichandran, Ina Chen, Lucas A McDuffie, Humair S Quadri,[...]. J Med Genet 2019
14
50

The E-cadherin gene (CDH1) variants T340A and L599V in gastric and colorectal cancer patients in Korea.
H C Kim, J M Wheeler, J C Kim, M Ilyas, N E Beck, B S Kim, K C Park, W F Bodmer. Gut 2000
50
50


Quantification of mutant E-cadherin using bioimaging analysis of in situ fluorescence microscopy. A new approach to CDH1 missense variants.
João Miguel Sanches, Joana Figueiredo, Martina Fonseca, Cecília Durães, Soraia Melo, Sofia Esménio, Raquel Seruca. Eur J Hum Genet 2015
20
50

A method and server for predicting damaging missense mutations.
Ivan A Adzhubei, Steffen Schmidt, Leonid Peshkin, Vasily E Ramensky, Anna Gerasimova, Peer Bork, Alexey S Kondrashov, Shamil R Sunyaev. Nat Methods 2010
50

Hereditary lobular breast cancer with an emphasis on E-cadherin genetic defect.
Giovanni Corso, Joana Figueiredo, Carlo La Vecchia, Paolo Veronesi, Gabriella Pravettoni, Debora Macis, Rachid Karam, Roberto Lo Gullo, Elena Provenzano, Antonio Toesca,[...]. J Med Genet 2018
29
50

Hereditary diffuse gastric cancer: updated clinical practice guidelines.
Vanessa R Blair, Maybelle McLeod, Fátima Carneiro, Daniel G Coit, Johanna L D'Addario, Jolanda M van Dieren, Kirsty L Harris, Nicoline Hoogerbrugge, Carla Oliveira, Rachel S van der Post,[...]. Lancet Oncol 2020
49
50

Pathological features of total gastrectomy specimens from asymptomatic hereditary diffuse gastric cancer patients and implications for clinical management.
João P Rocha, Irene Gullo, Xiaogang Wen, Vítor Devezas, Manuela Baptista, Carla Oliveira, Fátima Carneiro. Histopathology 2018
22
50

Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants.
Kristy Lee, Kate Krempely, Maegan E Roberts, Michael J Anderson, Fatima Carneiro, Elizabeth Chao, Katherine Dixon, Joana Figueiredo, Rajarshi Ghosh, David Huntsman,[...]. Hum Mutat 2018
53
50

E-cadherin mutations and cell motility: a genotype-phenotype correlation.
Ana Rita Mateus, Joana Simões-Correia, Joana Figueiredo, Stefan Heindl, Catarina Castro Alves, Gianpaolo Suriano, Birgit Luber, Raquel Seruca. Exp Cell Res 2009
46
50

Familial gastric cancer: genetic susceptibility, pathology, and implications for management.
Carla Oliveira, Hugo Pinheiro, Joana Figueiredo, Raquel Seruca, Fátima Carneiro. Lancet Oncol 2015
170
50

A graphical interface for the FoldX forcefield.
Joost Van Durme, Javier Delgado, Francois Stricher, Luis Serrano, Joost Schymkowitz, Frederic Rousseau. Bioinformatics 2011
183
50



Clinical spectrum and pleiotropic nature of CDH1 germline mutations.
Joana Figueiredo, Soraia Melo, Patrícia Carneiro, Ana Margarida Moreira, Maria Sofia Fernandes, Ana Sofia Ribeiro, Parry Guilford, Joana Paredes, Raquel Seruca. J Med Genet 2019
33
50


Rare and common variants: twenty arguments.
Greg Gibson. Nat Rev Genet 2012
691
50

An entire exon 3 germ-line rearrangement in the BRCA2 gene: pathogenic relevance of exon 3 deletion in breast cancer predisposition.
Danièle Muller, Etienne Rouleau, Inès Schultz, Sandrine Caputo, Cédrick Lefol, Ivan Bièche, Olivier Caron, Catherine Noguès, Jean Marc Limacher, Liliane Demange,[...]. BMC Med Genet 2011
18
50


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.