A citation-based method for searching scientific literature

Adam C Gunning, Verity Fryer, James Fasham, Andrew H Crosby, Sian Ellard, Emma L Baple, Caroline F Wright. J Med Genet 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants.
Nilah M Ioannidis, Joseph H Rothstein, Vikas Pejaver, Sumit Middha, Shannon K McDonnell, Saurabh Baheti, Anthony Musolf, Qing Li, Emily Holzinger, Danielle Karyadi,[...]. Am J Hum Genet 2016
556
75

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
50

The Ensembl Variant Effect Predictor.
William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016
50

Forkhead transcription factors: key players in health and disease.
Bérénice A Benayoun, Sandrine Caburet, Reiner A Veitia. Trends Genet 2011
185
25

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment.
Fadi F Hamdan, Hussein Daoud, Daniel Rochefort, Amélie Piton, Julie Gauthier, Mathieu Langlois, Gila Foomani, Sylvia Dobrzeniecka, Marie-Odile Krebs, Ridha Joober,[...]. Am J Hum Genet 2010
145
25

Structural and functional analyses of disease-causing missense mutations in the forkhead domain of FOXC1.
Ramsey A Saleem, Sharmila Banerjee-Basu, Fred B Berry, Andreas D Baxevanis, Michael A Walter. Hum Mol Genet 2003
69
25


Maximum allowed solvent accessibilites of residues in proteins.
Matthew Z Tien, Austin G Meyer, Dariya K Sydykova, Stephanie J Spielman, Claus O Wilke. PLoS One 2013
155
25

FOXG1 is responsible for the congenital variant of Rett syndrome.
Francesca Ariani, Giuseppe Hayek, Dalila Rondinella, Rosangela Artuso, Maria Antonietta Mencarelli, Ariele Spanhol-Rosseto, Marzia Pollazzon, Sabrina Buoni, Ottavia Spiga, Sara Ricciardi,[...]. Am J Hum Genet 2008
264
25

UniProt: the Universal Protein knowledgebase.
Rolf Apweiler, Amos Bairoch, Cathy H Wu, Winona C Barker, Brigitte Boeckmann, Serenella Ferro, Elisabeth Gasteiger, Hongzhan Huang, Rodrigo Lopez, Michele Magrane,[...]. Nucleic Acids Res 2004
25

MetaDome: Pathogenicity analysis of genetic variants through aggregation of homologous human protein domains.
Laurens Wiel, Coos Baakman, Daan Gilissen, Joris A Veltman, Gerrit Vriend, Christian Gilissen. Hum Mutat 2019
55
25

SWISS-MODEL: homology modelling of protein structures and complexes.
Andrew Waterhouse, Martino Bertoni, Stefan Bienert, Gabriel Studer, Gerardo Tauriello, Rafal Gumienny, Florian T Heer, Tjaart A P de Beer, Christine Rempfer, Lorenza Bordoli,[...]. Nucleic Acids Res 2018
25

Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
Denise Horn, Johannes Kapeller, Núria Rivera-Brugués, Ute Moog, Bettina Lorenz-Depiereux, Sebastian Eck, Maja Hempel, Janine Wagenstaller, Alex Gawthrope, Anthony P Monaco,[...]. Hum Mutat 2010
97
25


Regulation of FOXO Factors in Mammalian Cells.
Abigail K Brown, Ashley E Webb. Curr Top Dev Biol 2018
48
25


Forkhead Transcription Factors in Health and Disease.
Laetitia Herman, Anne-Laure Todeschini, Reiner A Veitia. Trends Genet 2021
6
25

Fox transcription factors: from development to disease.
Maria L Golson, Klaus H Kaestner. Development 2016
136
25


FOXC2 Disease Mutations Identified in Lymphedema Distichiasis Patients Impair Transcriptional Activity and Cell Proliferation.
Daniela Tavian, Sara Missaglia, Sandro Michelini, Paolo Enrico Maltese, Elena Manara, Alvaro Mordente, Matteo Bertelli. Int J Mol Sci 2020
4
25

Jalview Version 2--a multiple sequence alignment editor and analysis workbench.
Andrew M Waterhouse, James B Procter, David M A Martin, Michèle Clamp, Geoffrey J Barton. Bioinformatics 2009
25

Mutational probing of the forkhead domain of the transcription factor FOXL2 provides insights into the pathogenicity of naturally occurring mutations.
Anne-Laure Todeschini, Aurélie Dipietromaria, David L'hôte, Fatima Zohra Boucham, Adrien B Georges, P J Eswari Pandaranayaka, Sankaran Krishnaswamy, Isabelle Rivals, Claude Bazin, Reiner A Veitia. Hum Mol Genet 2011
15
25

Functional genetic analysis of mutations implicated in a human speech and language disorder.
Sonja C Vernes, Jérôme Nicod, Fanny M Elahi, Julie A Coventry, Niamh Kenny, Anne-Marie Coupe, Louise E Bird, Kay E Davies, Simon E Fisher. Hum Mol Genet 2006
113
25

Structure of the winged-helix protein hRFX1 reveals a new mode of DNA binding.
K S Gajiwala, H Chen, F Cornille, B P Roques, W Reith, B Mach, S K Burley. Nature 2000
245
25

The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
Peter D Stenson, Matthew Mort, Edward V Ball, Katy Evans, Matthew Hayden, Sally Heywood, Michelle Hussain, Andrew D Phillips, David N Cooper. Hum Genet 2017
637
25

DOMINO: Using Machine Learning to Predict Genes Associated with Dominant Disorders.
Mathieu Quinodoz, Beryl Royer-Bertrand, Katarina Cisarova, Silvio Alessandro Di Gioia, Andrea Superti-Furga, Carlo Rivolta. Am J Hum Genet 2017
44
25


SnapShot: forkhead transcription factors I.
Geetu Tuteja, Klaus H Kaestner. Cell 2007
83
25

MEF2C haploinsufficiency caused by either microdeletion of the 5q14.3 region or mutation is responsible for severe mental retardation with stereotypic movements, epilepsy and/or cerebral malformations.
N Le Meur, M Holder-Espinasse, S Jaillard, A Goldenberg, S Joriot, P Amati-Bonneau, A Guichet, M Barth, A Charollais, H Journel,[...]. J Med Genet 2010
140
25


Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase.
Bérénice A Benayoun, Adrien B Georges, David L'Hôte, Noora Andersson, Aurélie Dipietromaria, Anne-Laure Todeschini, Sandrine Caburet, Claude Bazin, Mikko Anttonen, Reiner A Veitia. Hum Mol Genet 2011
65
25

Assessing the efficiency of multiple sequence alignment programs.
Fabiano Sviatopolk-Mirsky Pais, Patrícia de Cássia Ruy, Guilherme Oliveira, Roney Santos Coimbra. Algorithms Mol Biol 2014
40
25

The emerging roles of forkhead box (Fox) proteins in cancer.
Stephen S Myatt, Eric W-F Lam. Nat Rev Cancer 2007
778
25

Transcription factor haploinsufficiency: when half a loaf is not enough.
J G Seidman, Christine Seidman. J Clin Invest 2002
138
25

SuSPect: enhanced prediction of single amino acid variant (SAV) phenotype using network features.
Christopher M Yates, Ioannis Filippis, Lawrence A Kelley, Michael J E Sternberg. J Mol Biol 2014
116
25

Forkhead transcription factors II.
Geetu Tuteja, Klaus H Kaestner. Cell 2007
78
25

ClinVar: public archive of relationships among sequence variation and human phenotype.
Melissa J Landrum, Jennifer M Lee, George R Riley, Wonhee Jang, Wendy S Rubinstein, Deanna M Church, Donna R Maglott. Nucleic Acids Res 2014
25

Fox's in development and disease.
Ordan J Lehmann, Jane C Sowden, Peter Carlsson, Tim Jordan, Shomi S Bhattacharya. Trends Genet 2003
274
25


Update of human and mouse forkhead box (FOX) gene families.
Brian C Jackson, Christopher Carpenter, Daniel W Nebert, Vasilis Vasiliou. Hum Genomics 2010
133
25

FOXC2 disease-mutations identified in lymphedema-distichiasis patients cause both loss and gain of protein function.
Daniela Tavian, Sara Missaglia, Paolo E Maltese, Sandro Michelini, Alessandro Fiorentino, Maurizio Ricci, Roberta Serrani, Michael A Walter, Matteo Bertelli. Oncotarget 2016
15
25

Transcription factor binding site analysis identifies FOXO transcription factors as regulators of the cutaneous wound healing process.
Karl Markus Roupé, Srinivas Veerla, Joshua Olson, Erica L Stone, Ole E Sørensen, Stephen M Hedrick, Victor Nizet. PLoS One 2014
19
25

Missense mutations in the forkhead domain of FOXL2 lead to subcellular mislocalization, protein aggregation and impaired transactivation.
Diane Beysen, Lara Moumné, Reiner Veitia, Hartmut Peters, Bart P Leroy, Anne De Paepe, Elfride De Baere. Hum Mol Genet 2008
62
25

The evolution of Fox genes and their role in development and disease.
Sridhar Hannenhalli, Klaus H Kaestner. Nat Rev Genet 2009
392
25

iStable 2.0: Predicting protein thermal stability changes by integrating various characteristic modules.
Chi-Wei Chen, Meng-Han Lin, Chi-Chou Liao, Hsung-Pin Chang, Yen-Wei Chu. Comput Struct Biotechnol J 2020
11
25

Towards a functional classification of pathogenic FOXL2 mutations using transactivation reporter systems.
Aurélie Dipietromaria, Bérénice A Benayoun, Anne-Laure Todeschini, Isabelle Rivals, Claude Bazin, Reiner A Veitia. Hum Mol Genet 2009
34
25


Stereotactically Injected Kv1.2 and CASPR2 Antisera Cause Differential Effects on CA1 Synaptic and Cellular Excitability, but Both Enhance the Vulnerability to Pro-epileptic Conditions.
Timo Kirschstein, Erika Sadkiewicz, Gerda Hund-Göschel, Juliane Becker, Xiati Guli, Steffen Müller, Marco Rohde, Dora-Charlotte Hübner, Hannes Brehme, Stephan Kolbaske,[...]. Front Synaptic Neurosci 2020
3
33

Incidence and phenotypes of childhood-onset genetic epilepsies: a prospective population-based national cohort.
Joseph D Symonds, Sameer M Zuberi, Kirsty Stewart, Ailsa McLellan, Mary O'Regan, Stewart MacLeod, Alice Jollands, Shelagh Joss, Martin Kirkpatrick, Andreas Brunklaus,[...]. Brain 2019
76
25

Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation.
Laura Canafoglia, Barbara Castellotti, Francesca Ragona, Elena Freri, Tiziana Granata, Luisa Chiapparini, Cinzia Gellera, Vidmer Scaioli, Silvana Franceschetti, Jacopo C DiFrancesco. Seizure 2019
6
25


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.