A citation-based method for searching scientific literature

Sergio Comincini, Federico Manai, Cristina Meazza, Sara Pagani, Carolina Martinelli, Noemi Pasqua, Gloria Pelizzo, Marco Biggiogera, Mauro Bozzola. Int J Mol Sci 2017
Times Cited: 19







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



Times Cited
  Times     Co-cited
Similarity


microRNA profiles in coeliac patients distinguish different clinical phenotypes and are modulated by gliadin peptides in primary duodenal fibroblasts.
Valentina Vaira, Leda Roncoroni, Donatella Barisani, Gabriella Gaudioso, Silvano Bosari, Gaetano Bulfamante, Luisa Doneda, Dario Conte, Carolina Tomba, Maria Teresa Bardella,[...]. Clin Sci (Lond) 2014
46
36

miRNAs affect the expression of innate and adaptive immunity proteins in celiac disease.
Serena Magni, Gaia Buoli Comani, Luca Elli, Samanta Vanessi, Elisa Ballarini, Gabriella Nicolini, Michela Rusconi, Mirco Castoldi, Raffaella Meneveri, Martina U Muckenthaler,[...]. Am J Gastroenterol 2014
37
36

MicroRNA-449a overexpression, reduced NOTCH1 signals and scarce goblet cells characterize the small intestine of celiac patients.
Marina Capuano, Laura Iaffaldano, Nadia Tinto, Donatella Montanaro, Valentina Capobianco, Valentina Izzo, Francesca Tucci, Giancarlo Troncone, Luigi Greco, Lucia Sacchetti. PLoS One 2011
66
36

miRNA-regulated gene expression differs in celiac disease patients according to the age of presentation.
Gaia Buoli Comani, Roberto Panceri, Marco Dinelli, Andrea Biondi, Clara Mancuso, Raffaella Meneveri, Donatella Barisani. Genes Nutr 2015
26
36

Genetic variation in the autophagy gene ULK1 and risk of Crohn's disease.
Liesbet Henckaerts, Isabelle Cleynen, Marko Brinar, Jestinah Mahachie John, Kristel Van Steen, Paul Rutgeerts, Séverine Vermeire. Inflamm Bowel Dis 2011
107
26

Recessive mutations in EPG5 cause Vici syndrome, a multisystem disorder with defective autophagy.
Thomas Cullup, Ay Lin Kho, Carlo Dionisi-Vici, Birgit Brandmeier, Frances Smith, Zoe Urry, Michael A Simpson, Shu Yau, Enrico Bertini, Verity McClelland,[...]. Nat Genet 2013
168
26

Exome sequencing reveals de novo WDR45 mutations causing a phenotypically distinct, X-linked dominant form of NBIA.
Tobias B Haack, Penelope Hogarth, Michael C Kruer, Allison Gregory, Thomas Wieland, Thomas Schwarzmayr, Elisabeth Graf, Lynn Sanford, Esther Meyer, Eleanna Kara,[...]. Am J Hum Genet 2012
236
26

Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease.
Gosia Trynka, Karen A Hunt, Nicholas A Bockett, Jihane Romanos, Vanisha Mistry, Agata Szperl, Sjoerd F Bakker, Maria Teresa Bardella, Leena Bhaw-Rosun, Gemma Castillejo,[...]. Nat Genet 2011
497
26

MicroRNAs control intestinal epithelial differentiation, architecture, and barrier function.
Lindsay B McKenna, Jonathan Schug, Anastassios Vourekas, Jaime B McKenna, Nuria C Bramswig, Joshua R Friedman, Klaus H Kaestner. Gastroenterology 2010
225
21

Loss of the autophagy protein Atg16L1 enhances endotoxin-induced IL-1beta production.
Tatsuya Saitoh, Naonobu Fujita, Myoung Ho Jang, Satoshi Uematsu, Bo-Gie Yang, Takashi Satoh, Hiroko Omori, Takeshi Noda, Naoki Yamamoto, Masaaki Komatsu,[...]. Nature 2008
21

De novo mutations in the autophagy gene WDR45 cause static encephalopathy of childhood with neurodegeneration in adulthood.
Hirotomo Saitsu, Taki Nishimura, Kazuhiro Muramatsu, Hirofumi Kodera, Satoko Kumada, Kenji Sugai, Emi Kasai-Yoshida, Noriko Sawaura, Hiroya Nishida, Ai Hoshino,[...]. Nat Genet 2013
306
21

Mutation in TECPR2 reveals a role for autophagy in hereditary spastic paraparesis.
Danit Oz-Levi, Bruria Ben-Zeev, Elizabeth K Ruzzo, Yuki Hitomi, Amir Gelman, Kimberly Pelak, Yair Anikster, Haike Reznik-Wolf, Ifat Bar-Joseph, Tsviya Olender,[...]. Am J Hum Genet 2012
101
21

A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1.
Jochen Hampe, Andre Franke, Philip Rosenstiel, Andreas Till, Markus Teuber, Klaus Huse, Mario Albrecht, Gabriele Mayr, Francisco M De La Vega, Jason Briggs,[...]. Nat Genet 2007
21

A Rare Variant (rs933717) at FBXO31-MAP1LC3B in Chinese Is Associated With Systemic Lupus Erythematosus.
Yuan-Yuan Qi, Xu-Jie Zhou, Swapan K Nath, Celi Sun, Yan-Na Wang, Ping Hou, Rong Mu, Chun Li, Jian-Ping Guo, Zhan-Guo Li,[...]. Arthritis Rheumatol 2018
14
28

Association between variants of PRDM1 and NDP52 and Crohn's disease, based on exome sequencing and functional studies.
David Ellinghaus, Hu Zhang, Sebastian Zeissig, Simone Lipinski, Andreas Till, Tao Jiang, Björn Stade, Yana Bromberg, Eva Ellinghaus, Andreas Keller,[...]. Gastroenterology 2013
116
15

Fanconi Anemia Proteins Function in Mitophagy and Immunity.
Rhea Sumpter, Shyam Sirasanagandla, Álvaro F Fernández, Yongjie Wei, Xiaonan Dong, Luis Franco, Zhongju Zou, Christophe Marchal, Ming Yeh Lee, D Wade Clapp,[...]. Cell 2016
160
15

The ubiquitin kinase PINK1 recruits autophagy receptors to induce mitophagy.
Michael Lazarou, Danielle A Sliter, Lesley A Kane, Shireen A Sarraf, Chunxin Wang, Jonathon L Burman, Dionisia P Sideris, Adam I Fogel, Richard J Youle. Nature 2015
15


Autophagy in infection, inflammation and immunity.
Vojo Deretic, Tatsuya Saitoh, Shizuo Akira. Nat Rev Immunol 2013
15

Refined mapping of autoimmune disease associated genetic variants with gene expression suggests an important role for non-coding RNAs.
Isis Ricaño-Ponce, Daria V Zhernakova, Patrick Deelen, Oscar Luo, Xingwang Li, Aaron Isaacs, Juha Karjalainen, Jennifer Di Tommaso, Zuzanna Agnieszka Borek, Maria M Zorro,[...]. J Autoimmun 2016
42
15

Autophagy and Neurodegeneration: Pathogenic Mechanisms and Therapeutic Opportunities.
Fiona M Menzies, Angeleen Fleming, Andrea Caricasole, Carla F Bento, Stephen P Andrews, Avraham Ashkenazi, Jens Füllgrabe, Anne Jackson, Maria Jimenez Sanchez, Cansu Karabiyik,[...]. Neuron 2017
578
15

Systematic analysis of chromatin interactions at disease associated loci links novel candidate genes to inflammatory bowel disease.
Claartje A Meddens, Magdalena Harakalova, Noortje A M van den Dungen, Hassan Foroughi Asl, Hemme J Hijma, Edwin P J G Cuppen, Johan L M Björkegren, Folkert W Asselbergs, Edward E S Nieuwenhuis, Michal Mokry. Genome Biol 2016
29
15

Immunoreactivities of p62, an ubiqutin-binding protein, in the spinal anterior horn cells of patients with amyotrophic lateral sclerosis.
Yuji Mizuno, Masakuni Amari, Masamitsu Takatama, Hitoshi Aizawa, Ban Mihara, Koichi Okamoto. J Neurol Sci 2006
115
15

Association of Egr-1 and autophagy-related gene polymorphism in men with chronic obstructive pulmonary disease.
Chiung-Zuei Chen, Chih-Ying Ou, Ru-Hsueh Wang, Cheng-Hung Lee, Chien-Chung Lin, Han-Yu Chang, Tzuen-Ren Hsiue. J Formos Med Assoc 2015
17
17

Variants in the autophagy-related gene IRGM confer susceptibility to non-alcoholic fatty liver disease by modulating lipophagy.
Yu-Cheng Lin, Pi-Feng Chang, Hsueh-Fang Lin, Kevin Liu, Mei-Hwei Chang, Yen-Hsuan Ni. J Hepatol 2016
45
15

Genetic analysis of the ATG7 gene promoter in sporadic Parkinson's disease.
Dongfeng Chen, Shuchao Pang, Xungang Feng, Wenhui Huang, Robert G Hawley, Bo Yan. Neurosci Lett 2013
30
15

Genetic association, mRNA and protein expression analysis identify ATG4C as a susceptibility gene for Kashin-Beck disease.
C Wu, Y Wen, X Guo, T Yang, H Shen, X Chen, Q Tian, L Tan, H-W Deng, F Zhang. Osteoarthritis Cartilage 2017
12
25

Rare variants in SQSTM1 and VCP genes and risk of sporadic inclusion body myositis.
Qiang Gang, Conceição Bettencourt, Pedro M Machado, Stefen Brady, Janice L Holton, Alan M Pittman, Deborah Hughes, Estelle Healy, Matthew Parton, David Hilton-Jones,[...]. Neurobiol Aging 2016
30
15

Variants of autophagy-related gene 5 are associated with neuromyelitis optica in the Southern Han Chinese population.
Ping-Ping Cai, Hong-Xia Wang, Jing-Cong Zhuang, Qi-Bing Liu, Gui-Xian Zhao, Zhen-Xin Li, Zhi-Ying Wu. Autoimmunity 2014
14
21

Polymorphisms in autophagy genes are associated with paget disease of bone.
Ricardo Usategui-Martín, Judith García-Aparicio, Luis Corral-Gudino, Ismael Calero-Paniagua, Javier Del Pino-Montes, Rogelio González Sarmiento. PLoS One 2015
26
15

Significance of optineurin mutations in glaucoma and other diseases.
Yuriko Minegishi, Mao Nakayama, Daisuke Iejima, Kazuhide Kawase, Takeshi Iwata. Prog Retin Eye Res 2016
53
15

Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45.
Gemma L Carvill, Aijie Liu, Simone Mandelstam, Amy Schneider, Amy Lacroix, Matthew Zemel, Jacinta M McMahon, Luis Bello-Espinosa, Mark Mackay, Geoffrey Wallace,[...]. Epilepsia 2018
36
15

WDR45 mutations in Rett (-like) syndrome and developmental delay: Case report and an appraisal of the literature.
Sabine Hoffjan, Aysegül Ibisler, Anne Tschentscher, Gabriele Dekomien, Carla Bidinost, Alberto L Rosa. Mol Cell Probes 2016
29
15

The T300A Crohn's disease risk polymorphism impairs function of the WD40 domain of ATG16L1.
Emilio Boada-Romero, Inmaculada Serramito-Gómez, María P Sacristán, David L Boone, Ramnik J Xavier, Felipe X Pimentel-Muiños. Nat Commun 2016
44
15

Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease.
Lynne J Hocking, Gavin J A Lucas, Anna Daroszewska, Jon Mangion, Mark Olavesen, Tim Cundy, Geoff C Nicholson, Lynley Ward, Simon T Bennett, Wim Wuyts,[...]. Hum Mol Genet 2002
251
15

Immunochip analysis identifies multiple susceptibility loci for systemic sclerosis.
Maureen D Mayes, Lara Bossini-Castillo, Olga Gorlova, José Ezequiel Martin, Xiaodong Zhou, Wei V Chen, Shervin Assassi, Jun Ying, Filemon K Tan, Frank C Arnett,[...]. Am J Hum Genet 2014
137
15

Autophagy in health and disease: a double-edged sword.
Takahiro Shintani, Daniel J Klionsky. Science 2004
15

Novel and functional ATG12 gene variants in sporadic Parkinson's disease.
Yuequn Li, Jian Huang, Shuchao Pang, Haihua Wang, Aimei Zhang, Robert G Hawley, Bo Yan. Neurosci Lett 2017
11
27

Association of ATG5 Gene Polymorphisms With Behçet's Disease and ATG10 Gene Polymorphisms With VKH Syndrome in a Chinese Han Population.
Minming Zheng, Hongsong Yu, Lijun Zhang, Hua Li, Yunjia Liu, Aize Kijlstra, Peizeng Yang. Invest Ophthalmol Vis Sci 2015
18
16

Identification of a novel 21bp-insertion variant within the LC3B gene promoter in sporadic Parkinson's disease.
Jing Xu, Yan Yang, Shuchao Pang, Wenhui Huang, Xianyun Qin, Robert G Hawley, Bo Yan. Transl Res 2013
5
60

A phenotype of atypical apraxia of speech in a family carrying SQSTM1 mutation.
Claire Boutoleau-Bretonnière, Agnès Camuzat, Isabelle Le Ber, Kawtar Bouya-Ahmed, Rita Guerreiro, Anne-Laure Deruet, Christelle Evrard, José Bras, Estelle Lamy, Elisabeth Auffray-Calvier,[...]. J Alzheimers Dis 2015
10
30

Genetic association of PRDM1-ATG5 intergenic region and autophagy with systemic lupus erythematosus in a Chinese population.
Xu-jie Zhou, Xiao-lan Lu, Ji-cheng Lv, Hai-zhen Yang, Lian-xiang Qin, Ming-hui Zhao, Yin Su, Zhan-guo Li, Hong Zhang. Ann Rheum Dis 2011
153
15

SQSTM1 splice site mutation in distal myopathy with rimmed vacuoles.
Robert C Bucelli, Khalid Arhzaouy, Alan Pestronk, Sara K Pittman, Luisa Rojas, Carolyn M Sue, Anni Evilä, Peter Hackman, Bjarne Udd, Matthew B Harms,[...]. Neurology 2015
56
15

Genetic variants in autophagy-related genes and granuloma formation in a cohort of surgically treated Crohn's disease patients.
Marko Brinar, Séverine Vermeire, Isabelle Cleynen, Bart Lemmens, Xavier Sagaert, Liesbet Henckaerts, Gert Van Assche, Karel Geboes, Paul Rutgeerts, Gert De Hertogh. J Crohns Colitis 2012
25
15

Mutation in ATG5 reduces autophagy and leads to ataxia with developmental delay.
Myungjin Kim, Erin Sandford, Damian Gatica, Yu Qiu, Xu Liu, Yumei Zheng, Brenda A Schulman, Jishu Xu, Ian Semple, Seung-Hyun Ro,[...]. Elife 2016
109
15

Multiple common variants for celiac disease influencing immune gene expression.
Patrick C A Dubois, Gosia Trynka, Lude Franke, Karen A Hunt, Jihane Romanos, Alessandra Curtotti, Alexandra Zhernakova, Graham A R Heap, Róza Adány, Arpo Aromaa,[...]. Nat Genet 2010
647
15

Defective autophagy in spastizin mutated patients with hereditary spastic paraparesis type 15.
Chiara Vantaggiato, Claudia Crimella, Giovanni Airoldi, Roman Polishchuk, Sara Bonato, Erika Brighina, Marina Scarlato, Olimpia Musumeci, Antonio Toscano, Andrea Martinuzzi,[...]. Brain 2013
53
15

Primary LAMP-2 deficiency causes X-linked vacuolar cardiomyopathy and myopathy (Danon disease).
I Nishino, J Fu, K Tanji, T Yamada, S Shimojo, T Koori, M Mora, J E Riggs, S J Oh, Y Koga,[...]. Nature 2000
630
15

Autophagy: renovation of cells and tissues.
Noboru Mizushima, Masaaki Komatsu. Cell 2011
15



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.