A citation-based method for searching scientific literature

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, Geng Wang, Hu-Ji Xu, Yan-Jie Hao, Zhuo-Li Zhang, Wei-Hua Yue, Huoru Zhang, Ming-Hui Zhao, Hong Zhang. Arthritis Rheumatol 2018
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


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
156
50

Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
John B Harley, Marta E Alarcón-Riquelme, Lindsey A Criswell, Chaim O Jacob, Robert P Kimberly, Kathy L Moser, Betty P Tsao, Timothy J Vyse, Carl D Langefeld, Swapan K Nath,[...]. Nat Genet 2008
982
42

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
42

A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus.
Vesela Gateva, Johanna K Sandling, Geoff Hom, Kimberly E Taylor, Sharon A Chung, Xin Sun, Ward Ortmann, Roman Kosoy, Ricardo C Ferreira, Gunnel Nordmark,[...]. Nat Genet 2009
617
35

Genome-wide association study in a Chinese Han population identifies nine new susceptibility loci for systemic lupus erythematosus.
Jian-Wen Han, Hou-Feng Zheng, Yong Cui, Liang-Dan Sun, Dong-Qing Ye, Zhi Hu, Jin-Hua Xu, Zhi-Ming Cai, Wei Huang, Guo-Ping Zhao,[...]. Nat Genet 2009
708
35

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
239
28

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
312
28

Detecting Genetic Associations between ATG5 and Lupus Nephritis by trans-eQTL.
Yue-Miao Zhang, Fa-Juan Cheng, Xu-Jie Zhou, Yuan-Yuan Qi, Ping Hou, Ming-Hui Zhao, Hong Zhang. J Immunol Res 2015
13
30

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
28

Noncanonical autophagy inhibits the autoinflammatory, lupus-like response to dying cells.
Jennifer Martinez, Larissa D Cunha, Sunmin Park, Mao Yang, Qun Lu, Robert Orchard, Quan-Zhen Li, Mei Yan, Laura Janke, Cliff Guy,[...]. Nature 2016
271
28

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
33

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
28

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
15
28

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
38
28

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
252
28

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
140
28

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
36

Identification of Autophagy-Related Genes and Their Regulatory miRNAs Associated with Celiac Disease in Children.
Sergio Comincini, Federico Manai, Cristina Meazza, Sara Pagani, Carolina Martinelli, Noemi Pasqua, Gloria Pelizzo, Marco Biggiogera, Mauro Bozzola. Int J Mol Sci 2017
22
28

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
28

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
108
28

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
40

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
57
28

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
28

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
28

Macroautophagy is deregulated in murine and human lupus T lymphocytes.
Frédéric Gros, Johan Arnold, Nicolas Page, Marion Décossas, Anne-Sophie Korganow, Thierry Martin, Sylviane Muller. Autophagy 2012
114
28

Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians.
Wanling Yang, Huayang Tang, Yan Zhang, Xianfa Tang, Jing Zhang, Liangdan Sun, Jing Yang, Yong Cui, Lu Zhang, Nattiya Hirankarn,[...]. Am J Hum Genet 2013
134
28

High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry.
Celi Sun, Julio E Molineros, Loren L Looger, Xu-Jie Zhou, Kwangwoo Kim, Yukinori Okada, Jianyang Ma, Yuan-Yuan Qi, Xana Kim-Howard, Prasenjeet Motghare,[...]. Nat Genet 2016
149
28

Autophagy is activated in systemic lupus erythematosus and required for plasmablast development.
Alexander J Clarke, Ursula Ellinghaus, Andrea Cortini, Amanda Stranks, Anna Katharina Simon, Marina Botto, Timothy J Vyse. Ann Rheum Dis 2015
153
28

Cargo recognition and degradation by selective autophagy.
Damián Gatica, Vikramjit Lahiri, Daniel J Klionsky. Nat Cell Biol 2018
507
28

Molecular definitions of autophagy and related processes.
Lorenzo Galluzzi, Eric H Baehrecke, Andrea Ballabio, Patricia Boya, José Manuel Bravo-San Pedro, Francesco Cecconi, Augustine M Choi, Charleen T Chu, Patrice Codogno, Maria Isabel Colombo,[...]. EMBO J 2017
846
28


WIPI3 and WIPI4 β-propellers are scaffolds for LKB1-AMPK-TSC signalling circuits in the control of autophagy.
Daniela Bakula, Amelie J Müller, Theresia Zuleger, Zsuzsanna Takacs, Mirita Franz-Wachtel, Ann-Katrin Thost, Daniel Brigger, Mario P Tschan, Tancred Frickey, Horst Robenek,[...]. Nat Commun 2017
105
21

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
21

Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of bone.
Omar M E Albagha, Micaela R Visconti, Nerea Alonso, Anne L Langston, Tim Cundy, Rosemary Dargie, Malcolm G Dunlop, William D Fraser, Michael J Hooper, Gianluca Isaia,[...]. Nat Genet 2010
185
21

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
116
21

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
21

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
47
21

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
21

A novel and functional variant within the ATG5 gene promoter in sporadic Parkinson's disease.
Dongfeng Chen, Cuiping Zhu, Xuenan Wang, Xungang Feng, Shuchao Pang, Wenhui Huang, Robert G Hawley, Bo Yan. Neurosci Lett 2013
31
21

Absence of the Autophagy Adaptor SQSTM1/p62 Causes Childhood-Onset Neurodegeneration with Ataxia, Dystonia, and Gaze Palsy.
Tobias B Haack, Erika Ignatius, Javier Calvo-Garrido, Arcangela Iuso, Pirjo Isohanni, Camilla Maffezzini, Tuula Lönnqvist, Anu Suomalainen, Matteo Gorza, Laura S Kremer,[...]. Am J Hum Genet 2016
65
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
103
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
21

Analysis of the C19orf12 and WDR45 genes in patients with neurodegeneration with brain iron accumulation.
Anne Tschentscher, Gabriele Dekomien, Sophia Ross, Kirsten Cremer, Guido M Kukuk, Jörg T Epplen, Sabine Hoffjan. J Neurol Sci 2015
20
21

Role of autophagy in immunity and autoimmunity, with a special focus on systemic lupus erythematosus.
Marina Pierdominici, Marta Vomero, Cristiana Barbati, Tania Colasanti, Angela Maselli, Davide Vacirca, Antonello Giovannetti, Walter Malorni, Elena Ortona. FASEB J 2012
101
21

Effect of genetic variants of OPTN in the pathophysiology of Paget's disease of bone.
Iris A L Silva, Natércia Conceição, Édith Gagnon, Helena Caiado, Jacques P Brown, Fernando Gianfrancesco, Laëtitia Michou, M Leonor Cancela. Biochim Biophys Acta Mol Basis Dis 2018
10
30

Significance of optineurin mutations in glaucoma and other diseases.
Yuriko Minegishi, Mao Nakayama, Daisuke Iejima, Kazuhide Kawase, Takeshi Iwata. Prog Retin Eye Res 2016
55
21

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
21

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

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
171
21

Ubiquitin-Dependent And Independent Signals In Selective Autophagy.
Aliaksandr Khaminets, Christian Behl, Ivan Dikic. Trends Cell Biol 2016
430
21


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.