A citation-based method for searching scientific literature

Daniel Kotlarz, Benjamin Marquardt, Tuva Barøy, Way S Lee, Liza Konnikova, Sebastian Hollizeck, Thomas Magg, Anna S Lehle, Christoph Walz, Ingo Borggraefe, Fabian Hauck, Philip Bufler, Raffaele Conca, Sarah M Wall, Eva M Schumacher, Doriana Misceo, Eirik Frengen, Beint S Bentsen, Holm H Uhlig, Karl-Peter Hopfner, Aleixo M Muise, Scott B Snapper, Petter Strømme, Christoph Klein. Nat Genet 2018
Times Cited: 62







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



Times Cited
  Times     Co-cited
Similarity


Inflammatory bowel disease and mutations affecting the interleukin-10 receptor.
Erik-Oliver Glocker, Daniel Kotlarz, Kaan Boztug, E Michael Gertz, Alejandro A Schäffer, Fatih Noyan, Mario Perro, Jana Diestelhorst, Anna Allroth, Dhaarini Murugan,[...]. N Engl J Med 2009
934
22

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.
Luke Jostins, Stephan Ripke, Rinse K Weersma, Richard H Duerr, Dermot P McGovern, Ken Y Hui, James C Lee, L Philip Schumm, Yashoda Sharma, Carl A Anderson,[...]. Nature 2012
19

Human ALPI deficiency causes inflammatory bowel disease and highlights a key mechanism of gut homeostasis.
Marianna Parlato, Fabienne Charbit-Henrion, Jie Pan, Claudio Romano, Rémi Duclaux-Loras, Marie-Helene Le Du, Neil Warner, Paola Francalanci, Julie Bruneau, Marc Bras,[...]. EMBO Mol Med 2018
31
35

The diagnostic approach to monogenic very early onset inflammatory bowel disease.
Holm H Uhlig, Tobias Schwerd, Sibylle Koletzko, Neil Shah, Jochen Kammermeier, Abdul Elkadri, Jodie Ouahed, David C Wilson, Simon P Travis, Dan Turner,[...]. Gastroenterology 2014
352
16

Variants in TRIM22 That Affect NOD2 Signaling Are Associated With Very-Early-Onset Inflammatory Bowel Disease.
Qi Li, Cheng Hiang Lee, Lauren A Peters, Lucas A Mastropaolo, Cornelia Thoeni, Abdul Elkadri, Tobias Schwerd, Jun Zhu, Bin Zhang, Yongzhong Zhao,[...]. Gastroenterology 2016
65
16

Interleukin 1β Mediates Intestinal Inflammation in Mice and Patients With Interleukin 10 Receptor Deficiency.
Dror S Shouval, Amlan Biswas, Yu Hui Kang, Alexandra E Griffith, Liza Konnikova, Ivan D Mascanfroni, Naresh S Redhu, Sandra M Frei, Michael Field, Andria L Doty,[...]. Gastroenterology 2016
104
14

AUTOIMMUNE DISEASE. Patients with LRBA deficiency show CTLA4 loss and immune dysregulation responsive to abatacept therapy.
Bernice Lo, Kejian Zhang, Wei Lu, Lixin Zheng, Qian Zhang, Chrysi Kanellopoulou, Yu Zhang, Zhiduo Liu, Jill M Fritz, Rebecca Marsh,[...]. Science 2015
353
14

CD25 deficiency causes an immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like syndrome, and defective IL-10 expression from CD4 lymphocytes.
Amy A Caudy, Sreelatha T Reddy, Talal Chatila, John P Atkinson, James W Verbsky. J Allergy Clin Immunol 2007
257
12

The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.
C L Bennett, J Christie, F Ramsdell, M E Brunkow, P J Ferguson, L Whitesell, T E Kelly, F T Saulsbury, P F Chance, H D Ochs. Nat Genet 2001
12

Human RIPK1 deficiency causes combined immunodeficiency and inflammatory bowel diseases.
Yue Li, Marita Führer, Ehsan Bahrami, Piotr Socha, Maja Klaudel-Dreszler, Amira Bouzidi, Yanshan Liu, Anna S Lehle, Thomas Magg, Sebastian Hollizeck,[...]. Proc Natl Acad Sci U S A 2019
77
12

Mutations in tetratricopeptide repeat domain 7A result in a severe form of very early onset inflammatory bowel disease.
Yaron Avitzur, Conghui Guo, Lucas A Mastropaolo, Ehsan Bahrami, Hannah Chen, Zhen Zhao, Abdul Elkadri, Sandeep Dhillon, Ryan Murchie, Ramzi Fattouh,[...]. Gastroenterology 2014
120
11

Worldwide incidence and prevalence of inflammatory bowel disease in the 21st century: a systematic review of population-based studies.
Siew C Ng, Hai Yun Shi, Nima Hamidi, Fox E Underwood, Whitney Tang, Eric I Benchimol, Remo Panaccione, Subrata Ghosh, Justin C Y Wu, Francis K L Chan,[...]. Lancet 2017
11

Impaired antibacterial autophagy links granulomatous intestinal inflammation in Niemann-Pick disease type C1 and XIAP deficiency with NOD2 variants in Crohn's disease.
Tobias Schwerd, Sumeet Pandey, Huei-Ting Yang, Katrin Bagola, Elisabeth Jameson, Jonathan Jung, Robin H Lachmann, Neil Shah, Smita Y Patel, Claire Booth,[...]. Gut 2017
88
11

Biallelic RIPK1 mutations in humans cause severe immunodeficiency, arthritis, and intestinal inflammation.
Delphine Cuchet-Lourenço, Davide Eletto, Changxin Wu, Vincent Plagnol, Olivier Papapietro, James Curtis, Lourdes Ceron-Gutierrez, Chris M Bacon, Scott Hackett, Badr Alsaleem,[...]. Science 2018
113
11

Intestinal Inflammation and Dysregulated Immunity in Patients With Inherited Caspase-8 Deficiency.
Anna S Lehle, Henner F Farin, Benjamin Marquardt, Birgitta E Michels, Thomas Magg, Yue Li, Yanshan Liu, Maryam Ghalandary, Katja Lammens, Sebastian Hollizeck,[...]. Gastroenterology 2019
61
11

Targeted disruption of the mouse transforming growth factor-beta 1 gene results in multifocal inflammatory disease.
M M Shull, I Ormsby, A B Kier, S Pawlowski, R J Diebold, M Yin, R Allen, C Sidman, G Proetzel, D Calvin. Nature 1992
11

Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.
Federica Barzaghi, Laura Cristina Amaya Hernandez, Benedicte Neven, Silvia Ricci, Zeynep Yesim Kucuk, Jack J Bleesing, Zohreh Nademi, Mary Anne Slatter, Erlinda Rose Ulloa, Anna Shcherbina,[...]. J Allergy Clin Immunol 2018
128
11

Variants in nicotinamide adenine dinucleotide phosphate oxidase complex components determine susceptibility to very early onset inflammatory bowel disease.
Sandeep S Dhillon, Ramzi Fattouh, Abdul Elkadri, Wei Xu, Ryan Murchie, Thomas Walters, Conghui Guo, David Mack, Hien Q Huynh, Shairaz Baksh,[...]. Gastroenterology 2014
84
9

Immune dysregulation in human subjects with heterozygous germline mutations in CTLA4.
Hye Sun Kuehn, Weiming Ouyang, Bernice Lo, Elissa K Deenick, Julie E Niemela, Danielle T Avery, Jean-Nicolas Schickel, Dat Q Tran, Jennifer Stoddard, Yu Zhang,[...]. Science 2014
518
9

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.
Elizabeth A Worthey, Alan N Mayer, Grant D Syverson, Daniel Helbling, Benedetta B Bonacci, Brennan Decker, Jaime M Serpe, Trivikram Dasu, Michael R Tschannen, Regan L Veith,[...]. Genet Med 2011
483
9

SKIV2L mutations cause syndromic diarrhea, or trichohepatoenteric syndrome.
Alexandre Fabre, Bernard Charroux, Christine Martinez-Vinson, Bertrand Roquelaure, Egritas Odul, Ersin Sayar, Hilary Smith, Virginie Colomb, Nicolas Andre, Jean-Pierre Hugot,[...]. Am J Hum Genet 2012
92
9

Familial diarrhea syndrome caused by an activating GUCY2C mutation.
Torunn Fiskerstrand, Najla Arshad, Bjørn Ivar Haukanes, Rune Rose Tronstad, Khanh Do-Cong Pham, Stefan Johansson, Bjarte Håvik, Siv L Tønder, Shawn E Levy, Damien Brackman,[...]. N Engl J Med 2012
126
9

A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease.
Y Ogura, D K Bonen, N Inohara, D L Nicolae, F F Chen, R Ramos, H Britton, T Moran, R Karaliuskas, R H Duerr,[...]. Nature 2001
9

NOX1 loss-of-function genetic variants in patients with inflammatory bowel disease.
T Schwerd, R V Bryant, S Pandey, M Capitani, L Meran, J-B Cazier, J Jung, K Mondal, M Parkes, C G Mathew,[...]. Mucosal Immunol 2018
46
13

TTC7A mutations disrupt intestinal epithelial apicobasal polarity.
Amélie E Bigorgne, Henner F Farin, Roxane Lemoine, Nizar Mahlaoui, Nathalie Lambert, Marine Gil, Ansgar Schulz, Pierre Philippet, Patrick Schlesser, Tore G Abrahamsen,[...]. J Clin Invest 2014
106
9

Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory disease.
Walter H A Kahr, Fred G Pluthero, Abdul Elkadri, Neil Warner, Marko Drobac, Chang Hua Chen, Richard W Lo, Ling Li, Ren Li, Qi Li,[...]. Nat Commun 2017
112
9

Genome-wide association study implicates immune activation of multiple integrin genes in inflammatory bowel disease.
Katrina M de Lange, Loukas Moutsianas, James C Lee, Christopher A Lamb, Yang Luo, Nicholas A Kennedy, Luke Jostins, Daniel L Rice, Javier Gutierrez-Achury, Sun-Gou Ji,[...]. Nat Genet 2017
441
9


Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations.
Jimmy Z Liu, Suzanne van Sommeren, Hailiang Huang, Siew C Ng, Rudi Alberts, Atsushi Takahashi, Stephan Ripke, James C Lee, Luke Jostins, Tejas Shah,[...]. Nat Genet 2015
9

Autosomal dominant immune dysregulation syndrome in humans with CTLA4 mutations.
Desirée Schubert, Claudia Bode, Rupert Kenefeck, Tie Zheng Hou, James B Wing, Alan Kennedy, Alla Bulashevska, Britt-Sabina Petersen, Alejandro A Schäffer, Björn A Grüning,[...]. Nat Med 2014
492
9

Regulatory T cell-derived interleukin-10 limits inflammation at environmental interfaces.
Yuri P Rubtsov, Jeffrey P Rasmussen, Emil Y Chi, Jason Fontenot, Luca Castelli, Xin Ye, Piper Treuting, Lisa Siewe, Axel Roers, William R Henderson,[...]. Immunity 2008
9

Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse.
M E Brunkow, E W Jeffery, K A Hjerrild, B Paeper, L B Clark, S A Yasayko, J E Wilkinson, D Galas, S F Ziegler, F Ramsdell. Nat Genet 2001
9

Human interleukin-2 receptor β mutations associated with defects in immunity and peripheral tolerance.
Zinan Zhang, Florian Gothe, Perrine Pennamen, John R James, David McDonald, Carlos P Mata, Yorgo Modis, Anas M Alazami, Meghan Acres, Wolfram Haller,[...]. J Exp Med 2019
38
15

Identification of Variants in Genes Associated with Single-gene Inflammatory Bowel Disease by Whole-exome Sequencing.
James J Ashton, Gaia Andreoletti, Tracy Coelho, Rachel Haggarty, Akshay Batra, Nadeem A Afzal, R Mark Beattie, Sarah Ennis. Inflamm Bowel Dis 2016
27
18

Epithelial NEMO links innate immunity to chronic intestinal inflammation.
Arianna Nenci, Christoph Becker, Andy Wullaert, Ralph Gareus, Geert van Loo, Silvio Danese, Marion Huth, Alexei Nikolaev, Clemens Neufert, Blair Madison,[...]. Nature 2007
761
8

Reduced sodium/proton exchanger NHE3 activity causes congenital sodium diarrhea.
Andreas R Janecke, Peter Heinz-Erian, Jianyi Yin, Britt-Sabina Petersen, Andre Franke, Silvia Lechner, Irene Fuchs, Serge Melancon, Holm H Uhlig, Simon Travis,[...]. Hum Mol Genet 2015
72
8

Phenotypic and Genotypic Characterisation of Inflammatory Bowel Disease Presenting Before the Age of 2 years.
Jochen Kammermeier, Robert Dziubak, Matilde Pescarin, Suzanne Drury, Heather Godwin, Kate Reeve, Sibongile Chadokufa, Bonita Huggett, Sara Sider, Chela James,[...]. J Crohns Colitis 2017
77
8

Pediatric modification of the Montreal classification for inflammatory bowel disease: the Paris classification.
Arie Levine, Anne Griffiths, James Markowitz, David C Wilson, Dan Turner, Richard K Russell, John Fell, Frank M Ruemmele, Thomas Walters, Mary Sherlock,[...]. Inflamm Bowel Dis 2011
845
8

Mongersen, an oral SMAD7 antisense oligonucleotide, and Crohn's disease.
Giovanni Monteleone, Markus F Neurath, Sandro Ardizzone, Antonio Di Sabatino, Massimo C Fantini, Fabiana Castiglione, Maria L Scribano, Alessandro Armuzzi, Flavio Caprioli, Giacomo C Sturniolo,[...]. N Engl J Med 2015
285
8

Clinical and immunological manifestations of patients with atypical severe combined immunodeficiency.
Kerstin Felgentreff, Ruy Perez-Becker, Carsten Speckmann, Klaus Schwarz, Krzysztof Kalwak, Gasper Markelj, Tadej Avcin, Waseem Qasim, E G Davies, Tim Niehues,[...]. Clin Immunol 2011
103
8

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity.
Gabriela Lopez-Herrera, Giacomo Tampella, Qiang Pan-Hammarström, Peer Herholz, Claudia M Trujillo-Vargas, Kanchan Phadwal, Anna Katharina Simon, Michel Moutschen, Amos Etzioni, Adi Mory,[...]. Am J Hum Genet 2012
304
8

From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation.
Rosa Bacchetta, Federica Barzaghi, Maria-Grazia Roncarolo. Ann N Y Acad Sci 2018
162
8

Transforming growth factor beta 1 null mutation in mice causes excessive inflammatory response and early death.
A B Kulkarni, C G Huh, D Becker, A Geiser, M Lyght, K C Flanders, A B Roberts, M B Sporn, J M Ward, S Karlsson. Proc Natl Acad Sci U S A 1993
8

Loss of interleukin-10 signaling and infantile inflammatory bowel disease: implications for diagnosis and therapy.
Daniel Kotlarz, Rita Beier, Dhaarini Murugan, Jana Diestelhorst, Ole Jensen, Kaan Boztug, Dietmar Pfeifer, Hans Kreipe, Eva-Doreen Pfister, Ulrich Baumann,[...]. Gastroenterology 2012
284
8

Clinical outcome in IL-10- and IL-10 receptor-deficient patients with or without hematopoietic stem cell transplantation.
Karin R Engelhardt, Neil Shah, Intan Faizura-Yeop, Dilara F Kocacik Uygun, Natalie Frede, Aleixo M Muise, Eyal Shteyer, Serkan Filiz, Ronnie Chee, Mamoun Elawad,[...]. J Allergy Clin Immunol 2013
164
8

Loss of TGF-beta 1 leads to increased neuronal cell death and microgliosis in mouse brain.
Thomas C Brionne, Ina Tesseur, Eliezer Masliah, Tony Wyss-Coray. Neuron 2003
263
8

Dual T cell- and B cell-intrinsic deficiency in humans with biallelic RLTPR mutations.
Yi Wang, Cindy S Ma, Yun Ling, Aziz Bousfiha, Yildiz Camcioglu, Serge Jacquot, Kathryn Payne, Elena Crestani, Romain Roncagalli, Aziz Belkadi,[...]. J Exp Med 2016
69
8

A human immunodeficiency syndrome caused by mutations in CARMIL2.
T Schober, T Magg, M Laschinger, M Rohlfs, N D Linhares, J Puchalka, T Weisser, K Fehlner, J Mautner, C Walz,[...]. Nat Commun 2017
68
8

Contextual determinants of TGFβ action in development, immunity and cancer.
Charles J David, Joan Massagué. Nat Rev Mol Cell Biol 2018
334
8

Immunoregulation by members of the TGFβ superfamily.
WanJun Chen, Peter Ten Dijke. Nat Rev Immunol 2016
191
8


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.