A citation-based method for searching scientific literature


List of co-cited articles
1365 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1.
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, Marcin Szynkiewicz, Gabriella M A Forte, Hannah L Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman,[...]. Am J Med Genet A 2015
306
51

Aicardi-Goutières syndrome and the type I interferonopathies.
Yanick J Crow, Nicolas Manel. Nat Rev Immunol 2015
470
43

Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling.
Gillian I Rice, Yoandris Del Toro Duany, Emma M Jenkinson, Gabriella Ma Forte, Beverley H Anderson, Giada Ariaudo, Brigitte Bader-Meunier, Eileen M Baildam, Roberta Battini, Michael W Beresford,[...]. Nat Genet 2014
358
39

Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection.
Yanick J Crow, Andrea Leitch, Bruce E Hayward, Anna Garner, Rekha Parmar, Elen Griffith, Manir Ali, Colin Semple, Jean Aicardi, Riyana Babul-Hirji,[...]. Nat Genet 2006
490
38

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus.
Yanick J Crow, Bruce E Hayward, Rekha Parmar, Peter Robins, Andrea Leitch, Manir Ali, Deborah N Black, Hans van Bokhoven, Han G Brunner, Ben C Hamel,[...]. Nat Genet 2006
581
34

Mutations involved in Aicardi-Goutières syndrome implicate SAMHD1 as regulator of the innate immune response.
Gillian I Rice, Jacquelyn Bond, Aruna Asipu, Rebecca L Brunette, Iain W Manfield, Ian M Carr, Jonathan C Fuller, Richard M Jackson, Teresa Lamb, Tracy A Briggs,[...]. Nat Genet 2009
489
34

Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study.
Gillian I Rice, Gabriella M A Forte, Marcin Szynkiewicz, Diana S Chase, Alec Aeby, Mohamed S Abdel-Hamid, Sam Ackroyd, Rebecca Allcock, Kathryn M Bailey, Umberto Balottin,[...]. Lancet Neurol 2013
239
34

Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature.
Gillian I Rice, Paul R Kasher, Gabriella M A Forte, Niamh M Mannion, Sam M Greenwood, Marcin Szynkiewicz, Jonathan E Dickerson, Sanjeev S Bhaskar, Massimiliano Zampini, Tracy A Briggs,[...]. Nat Genet 2012
484
33

Trex1 prevents cell-intrinsic initiation of autoimmunity.
Daniel B Stetson, Joan S Ko, Thierry Heidmann, Ruslan Medzhitov. Cell 2008
832
30

Activated STING in a vascular and pulmonary syndrome.
Y Liu, A A Jesus, B Marrero, D Yang, S E Ramsey, G A Montealegre Sanchez, K Tenbrock, H Wittkowski, O Y Jones, H S Kuehn,[...]. N Engl J Med 2014
666
25

Clinical and molecular phenotype of Aicardi-Goutieres syndrome.
Gillian Rice, Teresa Patrick, Rekha Parmar, Claire F Taylor, Alec Aeby, Jean Aicardi, Rafael Artuch, Simon Attard Montalto, Carlos A Bacino, Bruno Barroso,[...]. Am J Hum Genet 2007
275
25

Intrathecal synthesis of interferon-alpha in infants with progressive familial encephalopathy.
P Lebon, J Badoual, G Ponsot, F Goutières, F Hémeury-Cukier, J Aicardi. J Neurol Sci 1988
158
24


Reverse-Transcriptase Inhibitors in the Aicardi–Goutières Syndrome
Gillian I Rice, Candice Meyzer, Naïm Bouazza, Marie Hully, Nathalie Boddaert, Michaela Semeraro, Leo A H Zeef, Flore Rozenberg, Vincent Bondet, Darragh Duffy,[...]. N Engl J Med 2018
59
30


Activation of cyclic GMP-AMP synthase by self-DNA causes autoimmune diseases.
Daxing Gao, Tuo Li, Xiao-Dong Li, Xiang Chen, Quan-Zhen Li, Mary Wight-Carter, Zhijian J Chen. Proc Natl Acad Sci U S A 2015
321
16

Ribonuclease H2 mutations induce a cGAS/STING-dependent innate immune response.
Karen J Mackenzie, Paula Carroll, Laura Lettice, Žygimantė Tarnauskaitė, Kaalak Reddy, Flora Dix, Ailsa Revuelta, Erika Abbondati, Rachel E Rigby, Björn Rabe,[...]. EMBO J 2016
135
16

RNase H2 catalytic core Aicardi-Goutières syndrome-related mutant invokes cGAS-STING innate immune-sensing pathway in mice.
Vladislav Pokatayev, Naushaba Hasin, Hyongi Chon, Susana M Cerritelli, Kiran Sakhuja, Jerrold M Ward, H Douglas Morris, Nan Yan, Robert J Crouch. J Exp Med 2016
127
16

JAK1/2 inhibition with baricitinib in the treatment of autoinflammatory interferonopathies.
Gina A Montealegre Sanchez, Adam Reinhardt, Suzanne Ramsey, Helmut Wittkowski, Philip J Hashkes, Yackov Berkun, Susanne Schalm, Sara Murias, Jason A Dare, Diane Brown,[...]. J Clin Invest 2018
225
16

Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome.
Marije E C Meuwissen, Rachel Schot, Sofija Buta, Grétel Oudesluijs, Sigrid Tinschert, Scott D Speer, Zhi Li, Leontine van Unen, Daphne Heijsman, Tobias Goldmann,[...]. J Exp Med 2016
146
15

Cyclic GMP-AMP synthase is a cytosolic DNA sensor that activates the type I interferon pathway.
Lijun Sun, Jiaxi Wu, Fenghe Du, Xiang Chen, Zhijian J Chen. Science 2013
15

Gene-targeted mice lacking the Trex1 (DNase III) 3'-->5' DNA exonuclease develop inflammatory myocarditis.
Masashi Morita, Gordon Stamp, Peter Robins, Anna Dulic, Ian Rosewell, Geza Hrivnak, Graham Daly, Tomas Lindahl, Deborah E Barnes. Mol Cell Biol 2004
254
15


Modeling of TREX1-Dependent Autoimmune Disease using Human Stem Cells Highlights L1 Accumulation as a Source of Neuroinflammation.
Charles A Thomas, Leon Tejwani, Cleber A Trujillo, Priscilla D Negraes, Roberto H Herai, Pinar Mesci, Angela Macia, Yanick J Crow, Alysson R Muotri. Cell Stem Cell 2017
134
15

Aicardi-Goutières syndrome is caused by IFIH1 mutations.
Hirotsugu Oda, Kenji Nakagawa, Junya Abe, Tomonari Awaya, Masahide Funabiki, Atsushi Hijikata, Ryuta Nishikomori, Makoto Funatsuka, Yusei Ohshima, Yuji Sugawara,[...]. Am J Hum Genet 2014
126
15

RNA editing by ADAR1 prevents MDA5 sensing of endogenous dsRNA as nonself.
Brian J Liddicoat, Robert Piskol, Alistair M Chalk, Gokul Ramaswami, Miyoko Higuchi, Jochen C Hartner, Jin Billy Li, Peter H Seeburg, Carl R Walkley. Science 2015
387
14

Tartrate-resistant acid phosphatase deficiency causes a bone dysplasia with autoimmunity and a type I interferon expression signature.
Tracy A Briggs, Gillian I Rice, Sarah Daly, Jill Urquhart, Hannah Gornall, Brigitte Bader-Meunier, Kannan Baskar, Shankar Baskar, Veronique Baudouin, Michael W Beresford,[...]. Nat Genet 2011
156
14

Heterozygous mutations in TREX1 cause familial chilblain lupus and dominant Aicardi-Goutieres syndrome.
Gillian Rice, William G Newman, John Dean, Teresa Patrick, Rekha Parmar, Kim Flintoff, Peter Robins, Scott Harvey, Thomas Hollis, Ann O'Hara,[...]. Am J Hum Genet 2007
253
14

Mammalian RNase H2 removes ribonucleotides from DNA to maintain genome integrity.
Bjoern Hiller, Martin Achleitner, Silke Glage, Ronald Naumann, Rayk Behrendt, Axel Roers. J Exp Med 2012
157
14


Cutting Edge: cGAS Is Required for Lethal Autoimmune Disease in the Trex1-Deficient Mouse Model of Aicardi-Goutières Syndrome.
Elizabeth E Gray, Piper M Treuting, Joshua J Woodward, Daniel B Stetson. J Immunol 2015
191
13

An autoimmune disease prevented by anti-retroviral drugs.
Gabriele B Beck-Engeser, Dan Eilat, Matthias Wabl. Retrovirology 2011
85
15

Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity.
Yin Liu, Yuval Ramot, Antonio Torrelo, Amy S Paller, Nuo Si, Sofia Babay, Peter W Kim, Afzal Sheikh, Chyi-Chia Richard Lee, Yongqing Chen,[...]. Arthritis Rheum 2012
245
13

Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.
Min Ae Lee-Kirsch, Maolian Gong, Dipanjan Chowdhury, Lydia Senenko, Kerstin Engel, Young-Ae Lee, Udesh de Silva, Suzanna L Bailey, Torsten Witte, Timothy J Vyse,[...]. Nat Genet 2007
453
13

Enzymatic removal of ribonucleotides from DNA is essential for mammalian genome integrity and development.
Martin A M Reijns, Björn Rabe, Rachel E Rigby, Pleasantine Mill, Katy R Astell, Laura A Lettice, Shelagh Boyle, Andrea Leitch, Margaret Keighren, Fiona Kilanowski,[...]. Cell 2012
301
13

Human ADAR1 Prevents Endogenous RNA from Triggering Translational Shutdown.
Hachung Chung, Jorg J A Calis, Xianfang Wu, Tony Sun, Yingpu Yu, Stephanie L Sarbanes, Viet Loan Dao Thi, Abigail R Shilvock, H-Heinrich Hoffmann, Brad R Rosenberg,[...]. Cell 2018
208
13

Early-onset stroke and vasculopathy associated with mutations in ADA2.
Qing Zhou, Dan Yang, Amanda K Ombrello, Andrey V Zavialov, Camilo Toro, Anton V Zavialov, Deborah L Stone, Jae Jin Chae, Sergio D Rosenzweig, Kevin Bishop,[...]. N Engl J Med 2014
405
12

Efficacy of the Janus kinase 1/2 inhibitor ruxolitinib in the treatment of vasculopathy associated with TMEM173-activating mutations in 3 children.
Marie-Louise Frémond, Mathieu Paul Rodero, Nadia Jeremiah, Alexandre Belot, Eric Jeziorski, Darragh Duffy, Didier Bessis, Guilhem Cros, Gillian I Rice, Bruno Charbit,[...]. J Allergy Clin Immunol 2016
128
12

Expanding the phenotypic spectrum of lupus erythematosus in Aicardi-Goutières syndrome.
Georgia Ramantani, Jürgen Kohlhase, Christoph Hertzberg, A Micheil Innes, Kerstin Engel, Susan Hunger, Wiktor Borozdin, Jean K Mah, Kristina Ungerath, Hartmut Walkenhorst,[...]. Arthritis Rheum 2010
131
12

Therapies in Aicardi-Goutières syndrome.
Y J Crow, A Vanderver, S Orcesi, T W Kuijpers, G I Rice. Clin Exp Immunol 2014
56
21

Structural and functional neuropathology in transgenic mice with CNS expression of IFN-alpha.
I L Campbell, T Krucker, S Steffensen, Y Akwa, H C Powell, T Lane, D J Carr, L H Gold, S J Henriksen, G R Siggins. Brain Res 1999
130
12

Detection of interferon alpha protein reveals differential levels and cellular sources in disease.
Mathieu P Rodero, Jérémie Decalf, Vincent Bondet, David Hunt, Gillian I Rice, Scott Werneke, Sarah L McGlasson, Marie-Alexandra Alyanakian, Brigitte Bader-Meunier, Christine Barnerias,[...]. J Exp Med 2017
171
12

Autoimmunity initiates in nonhematopoietic cells and progresses via lymphocytes in an interferon-dependent autoimmune disease.
Alevtina Gall, Piper Treuting, Keith B Elkon, Yueh-Ming Loo, Michael Gale, Glen N Barber, Daniel B Stetson. Immunity 2012
336
11

PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome.
Anil K Agarwal, Chao Xing, George N DeMartino, Dario Mizrachi, Maria Dolores Hernandez, Ana Berta Sousa, Laura Martínez de Villarreal, Heloísa G dos Santos, Abhimanyu Garg. Am J Hum Genet 2010
206
11

Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation.
Xianqin Zhang, Dusan Bogunovic, Béatrice Payelle-Brogard, Véronique Francois-Newton, Scott D Speer, Chao Yuan, Stefano Volpi, Zhi Li, Ozden Sanal, Davood Mansouri,[...]. Nature 2015
293
11

Cyclic GMP-AMP is an endogenous second messenger in innate immune signaling by cytosolic DNA.
Jiaxi Wu, Lijun Sun, Xiang Chen, Fenghe Du, Heping Shi, Chuo Chen, Zhijian J Chen. Science 2013
11

Type I interferon-mediated autoinflammation due to DNase II deficiency.
Mathieu P Rodero, Alessandra Tesser, Eva Bartok, Gillian I Rice, Erika Della Mina, Marine Depp, Benoit Beitz, Vincent Bondet, Nicolas Cagnard, Darragh Duffy,[...]. Nat Commun 2017
99
11

Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus.
Sulaiman M Al-Mayouf, Asma Sunker, Reem Abdwani, Safiya Al Abrawi, Fathiya Almurshedi, Nadia Alhashmi, Abdullah Al Sonbul, Wafaa Sewairi, Aliya Qari, Eiman Abdallah,[...]. Nat Genet 2011
237
10

The RNA-editing enzyme ADAR1 controls innate immune responses to RNA.
Niamh M Mannion, Sam M Greenwood, Robert Young, Sarah Cox, James Brindle, David Read, Christoffer Nellåker, Cornelia Vesely, Chris P Ponting, Paul J McLaughlin,[...]. Cell Rep 2014
326
10

Defective removal of ribonucleotides from DNA promotes systemic autoimmunity.
Claudia Günther, Barbara Kind, Martin A M Reijns, Nicole Berndt, Manuel Martinez-Bueno, Christine Wolf, Victoria Tüngler, Osvaldo Chara, Young Ae Lee, Norbert Hübner,[...]. J Clin Invest 2015
133
10


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.