A citation-based method for searching scientific literature

Qi Li, Cheng Hiang Lee, Lauren A Peters, Lucas A Mastropaolo, Cornelia Thoeni, Abdul Elkadri, Tobias Schwerd, Jun Zhu, Bin Zhang, Yongzhong Zhao, Ke Hao, Antonio Dinarzo, Gabriel Hoffman, Brian A Kidd, Ryan Murchie, Ziad Al Adham, Conghui Guo, Daniel Kotlarz, Ernest Cutz, Thomas D Walters, Dror S Shouval, Mark Curran, Radu Dobrin, Carrie Brodmerkel, Scott B Snapper, Christoph Klein, John H Brumell, Mingjing Hu, Ralph Nanan, Brigitte Snanter-Nanan, Melanie Wong, Francoise Le Deist, Elie Haddad, Chaim M Roifman, Colette Deslandres, Anne M Griffiths, Kevin J Gaskin, Holm H Uhlig, Eric E Schadt, Aleixo M Muise. Gastroenterology 2016
Times Cited: 52







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



Times Cited
  Times     Co-cited
Similarity


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
309
50

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
48

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
882
44

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
110
38

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
474
32

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
96
28


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
118
26

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
951
26

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
268
25

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
206
25

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
25

Genetics and pathogenesis of inflammatory bowel disease.
Bernard Khor, Agnès Gardet, Ramnik J Xavier. Nature 2011
23

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
757
21

Targeted gene panel sequencing in children with very early onset inflammatory bowel disease--evaluation and prospective analysis.
Jochen Kammermeier, Suzanne Drury, Chela T James, Robert Dziubak, Louise Ocaka, Mamoun Elawad, Philip Beales, Nicholas Lench, Holm H Uhlig, Chiara Bacchelli,[...]. J Med Genet 2014
56
21

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
J P Hugot, M Chamaillard, H Zouali, S Lesage, J P Cézard, J Belaiche, S Almer, C Tysk, C A O'Morain, M Gassull,[...]. Nature 2001
21

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
155
21

A Mendelian predisposition to B-cell lymphoma caused by IL-10R deficiency.
Bénédicte Neven, Emilie Mamessier, Julie Bruneau, Sophie Kaltenbach, Daniel Kotlarz, Felipe Suarez, Julien Masliah-Planchon, Katy Billot, Danielle Canioni, Pierre Frange,[...]. Blood 2013
71
19

Incidence, outcomes, and health services burden of very early onset inflammatory bowel disease.
Eric I Benchimol, David R Mack, Geoffrey C Nguyen, Scott B Snapper, Wenbin Li, Nassim Mojaverian, Pauline Quach, Aleixo M Muise. Gastroenterology 2014
137
19

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
79
19

Exome sequencing analysis reveals variants in primary immunodeficiency genes in patients with very early onset inflammatory bowel disease.
Judith R Kelsen, Noor Dawany, Christopher J Moran, Britt-Sabina Petersen, Mahdi Sarmady, Ariella Sasson, Helen Pauly-Hubbard, Alejandro Martinez, Kelly Maurer, Joanne Soong,[...]. Gastroenterology 2015
50
18

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
17

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
118
17

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
319
17

Interleukin-10 receptor mutations in children with neonatal-onset Crohn's disease and intractable ulcerating enterocolitis.
Jung Ok Shim, Solha Hwang, Hye Ran Yang, Jin Soo Moon, Ju Young Chang, Jae Sung Ko, Sung Sup Park, Gyeong-Hoon Kang, Woo Sun Kim, Jeong Kee Seo. Eur J Gastroenterol Hepatol 2013
39
20

Children with early-onset inflammatory bowel disease (IBD): analysis of a pediatric IBD consortium registry.
Melvin B Heyman, Barbara S Kirschner, Benjamin D Gold, George Ferry, Robert Baldassano, Stanley A Cohen, Harland S Winter, Patricia Fain, Chris King, Terry Smith,[...]. J Pediatr 2005
331
15

Characteristics of inflammatory bowel disease with onset during the first year of life.
Frank M Ruemmele, Maurice G El Khoury, Cécile Talbotec, Chantal Maurage, Jean-François Mougenot, Jacques Schmitz, Olivier Goulet. J Pediatr Gastroenterol Nutr 2006
73
15

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
159
15

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
56
15

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
81
15


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
153
15

The age of gene discovery in very early onset inflammatory bowel disease.
Aleixo M Muise, Scott B Snapper, Subra Kugathasan. Gastroenterology 2012
57
15

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
153
15

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
62
15

Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy.
Daniel Kotlarz, Benjamin Marquardt, Tuva Barøy, Way S Lee, Liza Konnikova, Sebastian Hollizeck, Thomas Magg, Anna S Lehle, Christoph Walz, Ingo Borggraefe,[...]. Nat Genet 2018
51
15

Phenotype and disease course of early-onset pediatric inflammatory bowel disease.
Marina Aloi, Paolo Lionetti, Arrigo Barabino, Graziella Guariso, Stefano Costa, Massimo Fontana, Claudio Romano, Giuliano Lombardi, Erasmo Miele, Patrizia Alvisi,[...]. Inflamm Bowel Dis 2014
71
13

XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome.
Stéphanie Rigaud, Marie-Claude Fondanèche, Nathalie Lambert, Benoit Pasquier, Véronique Mateo, Pauline Soulas, Lionel Galicier, Françoise Le Deist, Frédéric Rieux-Laucat, Patrick Revy,[...]. Nature 2006
447
13


A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report.
Judith R Kelsen, Noor Dawany, Alejandro Martinez, Christopher M Grochowski, Kelly Maurer, Eric Rappaport, David A Piccoli, Robert N Baldassano, Petar Mamula, Kathleen E Sullivan,[...]. BMC Gastroenterol 2015
28
25

X-linked inhibitor of apoptosis (XIAP) deficiency: the spectrum of presenting manifestations beyond hemophagocytic lymphohistiocytosis.
C Speckmann, K Lehmberg, M H Albert, R B Damgaard, M Fritsch, M Gyrd-Hansen, A Rensing-Ehl, T Vraetz, B Grimbacher, U Salzer,[...]. Clin Immunol 2013
100
13

Characterization of Crohn disease in X-linked inhibitor of apoptosis-deficient male patients and female symptomatic carriers.
Claire Aguilar, Christelle Lenoir, Nathalie Lambert, Bernadette Bègue, Nicole Brousse, Danielle Canioni, Dominique Berrebi, Maryline Roy, Stéphane Gérart, Helen Chapel,[...]. J Allergy Clin Immunol 2014
63
13

IBD and IBD mimicking enterocolitis in children younger than 2 years of age.
Z Cannioto, I Berti, S Martelossi, I Bruno, N Giurici, S Crovella, A Ventura. Eur J Pediatr 2009
69
13

Colitis in chronic granulomatous disease.
M G Schäppi, V V Smith, D Goldblatt, K J Lindley, P J Milla. Arch Dis Child 2001
86
13

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
82
13

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
262
13

Complications of tumor necrosis factor-α blockade in chronic granulomatous disease-related colitis.
Gulbu Uzel, Jordan S Orange, Nina Poliak, Beatriz E Marciano, Theo Heller, Steven M Holland. Clin Infect Dis 2010
98
13

Life-threatening NLRC4-associated hyperinflammation successfully treated with IL-18 inhibition.
Scott W Canna, Charlotte Girard, Louise Malle, Adriana de Jesus, Neil Romberg, Judith Kelsen, Lea F Surrey, Pierre Russo, Andrew Sleight, Eduardo Schiffrin,[...]. J Allergy Clin Immunol 2017
136
13

IL-1 receptor blockade restores autophagy and reduces inflammation in chronic granulomatous disease in mice and in humans.
Antonella de Luca, Sanne P Smeekens, Andrea Casagrande, Rossana Iannitti, Kara L Conway, Mark S Gresnigt, Jakob Begun, Theo S Plantinga, Leo A B Joosten, Jos W M van der Meer,[...]. Proc Natl Acad Sci U S A 2014
205
13

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
95
13


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.