A citation-based method for searching scientific literature

Laurence E Cheng, Bittoo Kanwar, Haig Tcheurekdjian, James P Grenert, Mica Muskat, Melvin B Heyman, Joseph M McCune, Diane W Wara. Clin Immunol 2009
Times Cited: 48







List of co-cited articles
569 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
908
50

Infant colitis--it's in the genes.
Erik-Oliver Glocker, Natalie Frede, Mario Perro, Neil Sebire, Mamoun Elawad, Neil Shah, Bodo Grimbacher. Lancet 2010
180
37

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
272
37

Inflammatory skin and bowel disease linked to ADAM17 deletion.
Diana C Blaydon, Paolo Biancheri, Wei-Li Di, Vincent Plagnol, Rita M Cabral, Matthew A Brooke, David A van Heel, Franz Ruschendorf, Mark Toynbee, Amanda Walne,[...]. N Engl J Med 2011
211
31

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
112
29

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
326
29

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
158
27

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
738
25

The presentation and natural history of immunodeficiency caused by nuclear factor kappaB essential modulator mutation.
Jordan S Orange, Ashish Jain, Zuhair K Ballas, Lynda C Schneider, Raif S Geha, Francisco A Bonilla. J Allergy Clin Immunol 2004
127
25

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
25

Hypomorphic nuclear factor-kappaB essential modulator mutation database and reconstitution system identifies phenotypic and immunologic diversity.
Eric P Hanson, Linda Monaco-Shawver, Laura A Solt, Lisa A Madge, Pinaki P Banerjee, Michael J May, Jordan S Orange. J Allergy Clin Immunol 2008
145
22

Inflammatory bowel disease in CGD reproduces the clinicopathological features of Crohn's disease.
Daniel J B Marks, Kana Miyagi, Farooq Z Rahman, Marco Novelli, Stuart L Bloom, Anthony W Segal. Am J Gastroenterol 2009
161
22

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).
Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, Fabien Touzot, Nizar Mahlaoui, Fabian Hauck, Hirokazu Kanegane, Eduardo Lopez-Granados, Ester Mejstrikova, Isabelle Pellier,[...]. Blood 2011
213
22

Exome sequencing identifies novel compound heterozygous mutations of IL-10 receptor 1 in neonatal-onset Crohn's disease.
H Mao, W Yang, P P W Lee, M H-K Ho, J Yang, S Zeng, C-Y Chong, T-L Lee, W Tu, Y-L Lau. Genes Immun 2012
58
22

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
477
22

Defective IL10 signaling defining a subgroup of patients with inflammatory bowel disease.
Bernadette Begue, Julien Verdier, Frédéric Rieux-Laucat, Olivier Goulet, Alain Morali, Danielle Canioni, Jean-Pierre Hugot, Cécile Daussy, Virginie Verkarre, Bénédicte Pigneur,[...]. Am J Gastroenterol 2011
155
20

NADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2.
Aleixo M Muise, Wei Xu, Cong-Hui Guo, Thomas D Walters, Victorien M Wolters, Ramzi Fattouh, Grace Y Lam, Pingzhao Hu, Ryan Murchie, Mary Sherlock,[...]. Gut 2012
119
20

Colitis in chronic granulomatous disease.
M G Schäppi, V V Smith, D Goldblatt, K J Lindley, P J Milla. Arch Dis Child 2001
87
20

Autoimmunity in wiskott-Aldrich syndrome: an unsolved enigma.
Marco Catucci, Maria Carmina Castiello, Francesca Pala, Marita Bosticardo, Anna Villa. Front Immunol 2012
74
20

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
125
20

Whole-exome sequencing identifies tetratricopeptide repeat domain 7A (TTC7A) mutations for combined immunodeficiency with intestinal atresias.
Rui Chen, Silvia Giliani, Gaetana Lanzi, George I Mias, Silvia Lonardi, Kerry Dobbs, John Manis, Hogune Im, Jennifer E Gallagher, Douglas H Phanstiel,[...]. J Allergy Clin Immunol 2013
79
20

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
795
20

A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO).
J Zonana, M E Elder, L C Schneider, S J Orlow, C Moss, M Golabi, S K Shapira, P A Farndon, D W Wara, S A Emmal,[...]. Am J Hum Genet 2000
349
18

Successful treatment with infliximab for inflammatory colitis in a patient with X-linked anhidrotic ectodermal dysplasia with immunodeficiency.
Tomoyuki Mizukami, Megumi Obara, Ryuta Nishikomori, Tomoki Kawai, Yoshihiro Tahara, Naoki Sameshima, Kousuke Marutsuka, Hiroshi Nakase, Nobuhiro Kimura, Toshio Heike,[...]. J Clin Immunol 2012
26
34

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
87
18

Clinical, immunologic and genetic analysis of 29 patients with autosomal recessive hyper-IgM syndrome due to Activation-Induced Cytidine Deaminase deficiency.
Pierre Quartier, Jacinta Bustamante, Ozden Sanal, Alessandro Plebani, Marianne Debré, Anne Deville, Jiri Litzman, Jacov Levy, Jean-Paul Fermand, Peter Lane,[...]. Clin Immunol 2004
162
18


LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency.
Abdullah Alangari, Abdulrahman Alsultan, Nouran Adly, Michel J Massaad, Iram Shakir Kiani, Abdulrahman Aljebreen, Emad Raddaoui, Abdul-Kareem Almomen, Saleh Al-Muhsen, Raif S Geha,[...]. J Allergy Clin Immunol 2012
155
18

Agammaglobulinemia and absent B lineage cells in a patient lacking the p85α subunit of PI3K.
Mary Ellen Conley, A Kerry Dobbs, Anita M Quintana, Amma Bosompem, Yong-Dong Wang, Elaine Coustan-Smith, Amber M Smith, Elena E Perez, Peter J Murray. J Exp Med 2012
138
18

A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiency.
Qing Zhou, Geun-Shik Lee, Jillian Brady, Shrimati Datta, Matilda Katan, Afzal Sheikh, Marta S Martins, Tom D Bunney, Brian H Santich, Susan Moir,[...]. Am J Hum Genet 2012
193
18

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
83
18


Hematopoietic stem cell transplantation in a CD3 gamma-deficient infant with inflammatory bowel disease.
Tuba Turul Ozgür, Gülten Türkkani Asal, D Cetinkaya, D Orhan, S S Kiliç, Y Usta, H Ozen, Ilhan Tezcan. Pediatr Transplant 2008
20
45

Dominant gain-of-function STAT1 mutations in FOXP3 wild-type immune dysregulation-polyendocrinopathy-enteropathy-X-linked-like syndrome.
Gulbu Uzel, Elizabeth P Sampaio, Monica G Lawrence, Amy P Hsu, Mary Hackett, Morna J Dorsey, Richard J Noel, James W Verbsky, Alexandra F Freeman, Erin Janssen,[...]. J Allergy Clin Immunol 2013
180
18

XIAP variants in male Crohn's disease.
Yvonne Zeissig, Britt-Sabina Petersen, Snezana Milutinovic, Esther Bosse, Gabriele Mayr, Kenneth Peuker, Jelka Hartwig, Andreas Keller, Martina Kohl, Martin W Laass,[...]. Gut 2015
101
18

X-linked anhidrotic ectodermal dysplasia with immunodeficiency is caused by impaired NF-kappaB signaling.
R Döffinger, A Smahi, C Bessia, F Geissmann, J Feinberg, A Durandy, C Bodemer, S Kenwrick, S Dupuis-Girod, S Blanche,[...]. Nat Genet 2001
579
16

Allogeneic transplantation successfully corrects immune defects, but not susceptibility to colitis, in a patient with nuclear factor-kappaB essential modulator deficiency.
Sung-Yun Pai, Ofer Levy, Haifa H Jabara, Jonathan N Glickman, Liat Stoler-Barak, Jessica Sachs, Samuel Nurko, Jordan S Orange, Raif S Geha. J Allergy Clin Immunol 2008
35
22


IL-10R polymorphisms are associated with very-early-onset ulcerative colitis.
Christopher J Moran, Thomas D Walters, Cong-Hui Guo, Subra Kugathasan, Christoph Klein, Dan Turner, Victorien M Wolters, Robert H Bandsma, Marialena Mouzaki, Mary Zachos,[...]. Inflamm Bowel Dis 2013
160
16

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
253
16

A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40 phox and selective defects in neutrophil NADPH oxidase activity.
Juan D Matute, Andres A Arias, Nicola A M Wright, Iwona Wrobel, Christopher C M Waterhouse, Xing Jun Li, Christophe C Marchal, Natalie D Stull, David B Lewis, MacGregor Steele,[...]. Blood 2009
265
16

Inflammatory bowel disease and T cell lymphopenia in G6PC3 deficiency.
Philippe Bégin, Natalie Patey, Pascal Mueller, Andrée Rasquin, Alain Sirard, Christoph Klein, Elie Haddad, Éric Drouin, Françoise Le Deist. J Clin Immunol 2013
30
26

Chronic inflammatory bowel disease as key manifestation of atypical ARTEMIS deficiency.
Jan Rohr, Ulrich Pannicke, Michaela Döring, Annette Schmitt-Graeff, Elisabeth Wiech, Andreas Busch, Carsten Speckmann, Ingo Müller, Peter Lang, Rupert Handgretinger,[...]. J Clin Immunol 2010
30
26

Exome sequencing identifies mutations in the gene TTC7A in French-Canadian cases with hereditary multiple intestinal atresia.
Mark E Samuels, Jacek Majewski, Najmeh Alirezaie, Isabel Fernandez, Ferran Casals, Natalie Patey, Hélène Decaluwe, Isabelle Gosselin, Elie Haddad, Alan Hodgkinson,[...]. J Med Genet 2013
68
16

Early-onset inflammatory bowel disease and common variable immunodeficiency-like disease caused by IL-21 deficiency.
Elisabeth Salzer, Aydan Kansu, Heiko Sic, Peter Májek, Aydan Ikincioğullari, Figen E Dogu, Nina Kathrin Prengemann, Elisangela Santos-Valente, Winfried F Pickl, Ivan Bilic,[...]. J Allergy Clin Immunol 2014
81
16


Interleukin-10-deficient mice develop chronic enterocolitis.
R Kühn, J Löhler, D Rennick, K Rajewsky, W Müller. Cell 1993
14


X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production.
Orchidée Filipe-Santos, Jacinta Bustamante, Margje H Haverkamp, Emilie Vinolo, Cheng-Lung Ku, Anne Puel, David M Frucht, Karin Christel, Horst von Bernuth, Emmanuelle Jouanguy,[...]. J Exp Med 2006
186
14

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.
A Smahi, G Courtois, P Vabres, S Yamaoka, S Heuertz, A Munnich, A Israël, N S Heiss, S M Klauck, P Kioschis,[...]. Nature 2000
500
14


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.