A citation-based method for searching scientific literature

Teodolinda Di Risi, Roberta Vinciguerra, Mariella Cuomo, Rosa Della Monica, Eleonora Riccio, Sirio Cocozza, Massimo Imbriaco, Giovanni Duro, Antonio Pisani, Lorenzo Chiariotti. Clin Epigenetics 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


APRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients.
Jean-Louis Guéant, Céline Chéry, Abderrahim Oussalah, Javad Nadaf, David Coelho, Thomas Josse, Justine Flayac, Aurélie Robert, Isabelle Koscinski, Isabelle Gastin,[...]. Nat Commun 2018
33
100


Optical coherence tomography morphology and evolution in cblC disease-related maculopathy in a case series of very young patients.
Giacomo M Bacci, Maria A Donati, Elisabetta Pasquini, Francis Munier, Catia Cavicchi, Amelia Morrone, Andrea Sodi, Vittoria Murro, Nuria Garcia Segarra, Claudio Defilippi,[...]. Acta Ophthalmol 2017
7
100

Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type.
Jordan P Lerner-Ellis, Jamie C Tirone, Peter D Pawelek, Carole Doré, Janet L Atkinson, David Watkins, Chantal F Morel, T Mary Fujiwara, Emily Moras, Angela R Hosack,[...]. Nat Genet 2006
232
100

Structure of MMACHC reveals an arginine-rich pocket and a domain-swapped dimer for its B12 processing function.
D Sean Froese, Tobias Krojer, Xuchu Wu, Roshi Shrestha, Wasim Kiyani, Frank von Delft, Roy A Gravel, Udo Oppermann, Wyatt W Yue. Biochemistry 2012
29
100


Two enzymes in one; two yeast peroxiredoxins display oxidative stress-dependent switching from a peroxidase to a molecular chaperone function.
Ho Hee Jang, Kyun Oh Lee, Yong Hun Chi, Bae Gyo Jung, Soo Kwon Park, Jin Ho Park, Jung Ro Lee, Seung Sik Lee, Jeong Chan Moon, Jeong Won Yun,[...]. Cell 2004
543
100

Regulation of reactive oxygen species, DNA damage, and c-Myc function by peroxiredoxin 1.
Rachel A Egler, Elaine Fernandes, Kristi Rothermund, Susan Sereika, Nadja de Souza-Pinto, Pawel Jaruga, Miral Dizdaroglu, Edward V Prochownik. Oncogene 2005
165
100

Exploiting epigenetics for the treatment of inborn errors of metabolism.
Martijn G S Rutten, Marianne G Rots, Maaike H Oosterveer. J Inherit Metab Dis 2020
6
100

Genetic architecture of vitamin B12 and folate levels uncovered applying deeply sequenced large datasets.
Niels Grarup, Patrick Sulem, Camilla H Sandholt, Gudmar Thorleifsson, Tarunveer S Ahluwalia, Valgerdur Steinthorsdottir, Helgi Bjarnason, Daniel F Gudbjartsson, Olafur T Magnusson, Thomas Sparsø,[...]. PLoS Genet 2013
66
100


Minfi: a flexible and comprehensive Bioconductor package for the analysis of Infinium DNA methylation microarrays.
Martin J Aryee, Andrew E Jaffe, Hector Corrada-Bravo, Christine Ladd-Acosta, Andrew P Feinberg, Kasper D Hansen, Rafael A Irizarry. Bioinformatics 2014
100

Epigenetic modification of the gene for the vitamin B(12) chaperone MMACHC can result in increased tumorigenicity and methionine dependence.
Amanda D Loewy, Kirsten M Niles, Natascia Anastasio, David Watkins, Josée Lavoie, Jordan P Lerner-Ellis, Tomi Pastinen, Jacquetta M Trasler, David S Rosenblatt. Mol Genet Metab 2009
15
100



Essential role for the peroxiredoxin Prdx1 in erythrocyte antioxidant defence and tumour suppression.
Carola A Neumann, Daniela S Krause, Christopher V Carman, Shampa Das, Devendra P Dubey, Jennifer L Abraham, Roderick T Bronson, Yuko Fujiwara, Stuart H Orkin, Richard A Van Etten. Nature 2003
568
100

Efficacy of early treatment in patients with cobalamin C disease identified by newborn screening: a 16-year experience.
Rebecca C Ahrens-Nicklas, Ashley M Whitaker, Paige Kaplan, Sanmati Cuddapah, Jessica Burfield, Jennifer Blair, Ligia Brochi, Marc Yudkoff, Can Ficicioglu. Genet Med 2017
8
100

EPCAM deletion carriers constitute a unique subgroup of Lynch syndrome patients.
Marjolijn J L Ligtenberg, Roland P Kuiper, Ad Geurts van Kessel, Nicoline Hoogerbrugge. Fam Cancer 2013
70
100

Peroxiredoxin 1 - an antioxidant enzyme in cancer.
Chenbo Ding, Xiaobo Fan, Guoqiu Wu. J Cell Mol Med 2017
85
100

The role of epigenetics in lysosomal storage disorders: Uncharted territory.
Shahzeb Hassan, Ellen Sidransky, Nahid Tayebi. Mol Genet Metab 2017
24
100

Defining the criteria for identifying constitutional epimutations.
Mathew A Sloane, Robyn L Ward, Luke B Hesson. Clin Epigenetics 2016
14
100


CoNVaDING: Single Exon Variation Detection in Targeted NGS Data.
Lennart F Johansson, Freerk van Dijk, Eddy N de Boer, Krista K van Dijk-Bos, Jan D H Jongbloed, Annemieke H van der Hout, Helga Westers, Richard J Sinke, Morris A Swertz, Rolf H Sijmons,[...]. Hum Mutat 2016
49
100


Transcription of antisense RNA leading to gene silencing and methylation as a novel cause of human genetic disease.
Cristina Tufarelli, Jackie A Sloane Stanley, David Garrick, Jackie A Sharpe, Helena Ayyub, William G Wood, Douglas R Higgs. Nat Genet 2003
392
100


A human somatic cell culture system for modelling gene silencing by transcriptional interference.
Theresa Kühnel, Helena Sophie Barbara Heinz, Nadja Utz, Tanja Božić, Bernhard Horsthemke, Laura Steenpass. Heliyon 2020
1
100

Newborn screening for homocystinurias and methylation disorders: systematic review and proposed guidelines.
Martina Huemer, Viktor Kožich, Piero Rinaldo, Matthias R Baumgartner, Begoña Merinero, Elisabetta Pasquini, Antonia Ribes, Henk J Blom. J Inherit Metab Dis 2015
55
100

Transcriptional interference--a crash course.
Keith E Shearwin, Benjamin P Callen, J Barry Egan. Trends Genet 2005
373
100


DNA methylation and body-mass index: a genome-wide analysis.
Katherine J Dick, Christopher P Nelson, Loukia Tsaprouni, Johanna K Sandling, Dylan Aïssi, Simone Wahl, Eshwar Meduri, Pierre-Emmanuel Morange, France Gagnon, Harald Grallert,[...]. Lancet 2014
483
100


Multiple sclerosis and intracellular cobalamin defect (MMACHC/PRDX1) comorbidity in a young male.
Luca Pollini, Manuela Tolve, Francesca Nardecchia, Serena Galosi, Claudia Carducci, Emanuele di Carlo, Carla Carducci, Vincenzo Leuzzi. Mol Genet Metab Rep 2020
2
100

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase.
P Frosst, H J Blom, R Milos, P Goyette, C A Sheppard, R G Matthews, G J Boers, M den Heijer, L A Kluijtmans, L P van den Heuvel. Nat Genet 1995
100

Guidelines for diagnosis and management of the cobalamin-related remethylation disorders cblC, cblD, cblE, cblF, cblG, cblJ and MTHFR deficiency.
Martina Huemer, Daria Diodato, Bernd Schwahn, Manuel Schiff, Anabela Bandeira, Jean-Francois Benoist, Alberto Burlina, Roberto Cerone, Maria L Couce, Angeles Garcia-Cazorla,[...]. J Inherit Metab Dis 2017
88
100

Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations.
Jordan P Lerner-Ellis, Natascia Anastasio, Junhui Liu, David Coelho, Terttu Suormala, Martin Stucki, Amanda D Loewy, Scott Gurd, Elin Grundberg, Chantal F Morel,[...]. Hum Mutat 2009
118
100

The role of peroxiredoxin 1 in redox sensing and transducing.
Elizabeth C Ledgerwood, James W A Marshall, Johannes F Weijman. Arch Biochem Biophys 2017
23
100

Peroxiredoxin 1 Protects Telomeres from Oxidative Damage and Preserves Telomeric DNA for Extension by Telomerase.
Eric Aeby, Wareed Ahmed, Sophie Redon, Viesturs Simanis, Joachim Lingner. Cell Rep 2016
58
100


Combined methylmalonic acidemia and homocystinuria, cblC type. I. Clinical presentations, diagnosis and management.
Nuria Carrillo-Carrasco, Randy J Chandler, Charles P Venditti. J Inherit Metab Dis 2012
102
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.