A citation-based method for searching scientific literature

Elisabeth Salzer, Aydan Kansu, Heiko Sic, Peter Májek, Aydan Ikincioğullari, Figen E Dogu, Nina Kathrin Prengemann, Elisangela Santos-Valente, Winfried F Pickl, Ivan Bilic, Sol A Ban, Zarife Kuloğlu, Arzu Meltem Demir, Arzu Ensari, Jacques Colinge, Marta Rizzi, Hermann Eibel, Kaan Boztug. J Allergy Clin Immunol 2014
Times Cited: 81







List of co-cited articles
1241 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndrome.
Daniel Kotlarz, Natalia Ziętara, Gulbu Uzel, Thomas Weidemann, Christian J Braun, Jana Diestelhorst, Peter M Krawitz, Peter N Robinson, Jochen Hecht, Jacek Puchałka,[...]. J Exp Med 2013
128
55

B cell-intrinsic signaling through IL-21 receptor and STAT3 is required for establishing long-lived antibody responses in humans.
Danielle T Avery, Elissa K Deenick, Cindy S Ma, Santi Suryani, Nicholas Simpson, Gary Y Chew, Tyani D Chan, Umamainthan Palendira, Jacinta Bustamante, Stéphanie Boisson-Dupuis,[...]. J Exp Med 2010
266
28

Human IL-21 and IL-21R deficiencies: two novel entities of primary immunodeficiency.
Daniel Kotlarz, Natalia Ziętara, Joshua D Milner, Christoph Klein. Curr Opin Pediatr 2014
43
44

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
490
20

Naive and memory human B cells have distinct requirements for STAT3 activation to differentiate into antibody-secreting plasma cells.
Elissa K Deenick, Danielle T Avery, Anna Chan, Lucinda J Berglund, Megan L Ives, Leen Moens, Jennifer L Stoddard, Jacinta Bustamante, Stephanie Boisson-Dupuis, Miyuki Tsumura,[...]. J Exp Med 2013
111
20

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
19

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
19

Interleukin-21: a double-edged sword with therapeutic potential.
Rosanne Spolski, Warren J Leonard. Nat Rev Drug Discov 2014
284
19

Extending the clinical and immunological phenotype of human interleukin-21 receptor deficiency.
Polina Stepensky, Baerbel Keller, Omar Abuzaitoun, Avraham Shaag, Barak Yaacov, Susanne Unger, Maximilian Seidl, Marta Rizzi, Michael Weintraub, Orly Elpeleg,[...]. Haematologica 2015
27
59

Combined immunodeficiency with CD4 lymphopenia and sclerosing cholangitis caused by a novel loss-of-function mutation affecting IL21R.
Baran Erman, Ivan Bilic, Tatjana Hirschmugl, Elisabeth Salzer, Deniz Çagdas, Saliha Esenboga, Zuhal Akcoren, Ozden Sanal, Ilhan Tezcan, Kaan Boztug. Haematologica 2015
30
53

Interleukin 21 and its receptor are involved in NK cell expansion and regulation of lymphocyte function.
J Parrish-Novak, S R Dillon, A Nelson, A Hammond, C Sprecher, J A Gross, J Johnston, K Madden, W Xu, J West,[...]. Nature 2000
901
18

A critical role for IL-21 in regulating immunoglobulin production.
Katsutoshi Ozaki, Rosanne Spolski, Carl G Feng, Chen-Feng Qi, Jun Cheng, Alan Sher, Herbert C Morse, Chengyu Liu, Pamela L Schwartzberg, Warren J Leonard. Science 2002
731
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
17

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
17

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
17

The good, the bad and the ugly - TFH cells in human health and disease.
Stuart G Tangye, Cindy S Ma, Robert Brink, Elissa K Deenick. Nat Rev Immunol 2013
356
17

Cytokine-mediated regulation of human B cell differentiation into Ig-secreting cells: predominant role of IL-21 produced by CXCR5+ T follicular helper cells.
Vanessa L Bryant, Cindy S Ma, Danielle T Avery, Ying Li, Kim L Good, Lynn M Corcoran, Rene de Waal Malefyt, Stuart G Tangye. J Immunol 2007
358
17

B-cell activating factor receptor deficiency is associated with an adult-onset antibody deficiency syndrome in humans.
Klaus Warnatz, Ulrich Salzer, Marta Rizzi, Beate Fischer, Sylvia Gutenberger, Joachim Böhm, Anne-Kathrin Kienzler, Qiang Pan-Hammarström, Lennart Hammarström, Mirzokhid Rakhmanov,[...]. Proc Natl Acad Sci U S A 2009
246
17

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
16

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
293
16

Functional STAT3 deficiency compromises the generation of human T follicular helper cells.
Cindy S Ma, Danielle T Avery, Anna Chan, Marcel Batten, Jacinta Bustamante, Stephanie Boisson-Dupuis, Peter D Arkwright, Alexandra Y Kreins, Diana Averbuch, Dan Engelhard,[...]. Blood 2012
221
16

IL-21 induces differentiation of human naive and memory B cells into antibody-secreting plasma cells.
Rachel Ettinger, Gary P Sims, Anna-Marie Fairhurst, Rachel Robbins, Yong Sing da Silva, Rosanne Spolski, Warren J Leonard, Peter E Lipsky. J Immunol 2005
459
16

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
464
16

Dominant-negative mutations in the DNA-binding domain of STAT3 cause hyper-IgE syndrome.
Yoshiyuki Minegishi, Masako Saito, Shigeru Tsuchiya, Ikuya Tsuge, Hidetoshi Takada, Toshiro Hara, Nobuaki Kawamura, Tadashi Ariga, Srdjan Pasic, Oliver Stojkovic,[...]. Nature 2007
679
16

STAT3 mutations in the hyper-IgE syndrome.
Steven M Holland, Frank R DeLeo, Houda Z Elloumi, Amy P Hsu, Gulbu Uzel, Nina Brodsky, Alexandra F Freeman, Andrew Demidowich, Joie Davis, Maria L Turner,[...]. N Engl J Med 2007
784
16

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
14

CD81 gene defect in humans disrupts CD19 complex formation and leads to antibody deficiency.
Menno C van Zelm, Julie Smet, Brigitte Adams, Françoise Mascart, Liliane Schandené, Françoise Janssen, Alina Ferster, Chiung-Chi Kuo, Shoshana Levy, Jacques J M van Dongen,[...]. J Clin Invest 2010
250
14

An antibody-deficiency syndrome due to mutations in the CD19 gene.
Menno C van Zelm, Ismail Reisli, Mirjam van der Burg, Diana Castaño, Carel J M van Noesel, Maarten J D van Tol, Cristina Woellner, Bodo Grimbacher, Pablo J Patiño, Jacques J M van Dongen,[...]. N Engl J Med 2006
373
14

Genetic CD21 deficiency is associated with hypogammaglobulinemia.
Jens Thiel, Lucas Kimmig, Ulrich Salzer, Magdalena Grudzien, Dirk Lebrecht, Tina Hagena, Ruth Draeger, Nadine Voelxen, Astrid Bergbreiter, Stephanie Jennings,[...]. J Allergy Clin Immunol 2012
121
14

Phosphoinositide 3-kinase δ gene mutation predisposes to respiratory infection and airway damage.
Ivan Angulo, Oscar Vadas, Fabien Garçon, Edward Banham-Hall, Vincent Plagnol, Timothy R Leahy, Helen Baxendale, Tanya Coulter, James Curtis, Changxin Wu,[...]. Science 2013
360
14

Gain-of-function human STAT1 mutations impair IL-17 immunity and underlie chronic mucocutaneous candidiasis.
Luyan Liu, Satoshi Okada, Xiao-Fei Kong, Alexandra Y Kreins, Sophie Cypowyj, Avinash Abhyankar, Julie Toubiana, Yuval Itan, Magali Audry, Patrick Nitschke,[...]. J Exp Med 2011
495
14

Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies.
Cindy S Ma, Natalie Wong, Geetha Rao, Danielle T Avery, James Torpy, Thomas Hambridge, Jacinta Bustamante, Satoshi Okada, Jennifer L Stoddard, Elissa K Deenick,[...]. J Allergy Clin Immunol 2015
121
14

Dominant-activating germline mutations in the gene encoding the PI(3)K catalytic subunit p110δ result in T cell senescence and human immunodeficiency.
Carrie L Lucas, Hye Sun Kuehn, Fang Zhao, Julie E Niemela, Elissa K Deenick, Umaimainthan Palendira, Danielle T Avery, Leen Moens, Jennifer L Cannons, Matthew Biancalana,[...]. Nat Immunol 2014
377
13

Human blood CXCR5(+)CD4(+) T cells are counterparts of T follicular cells and contain specific subsets that differentially support antibody secretion.
Rimpei Morita, Nathalie Schmitt, Salah-Eddine Bentebibel, Rajaram Ranganathan, Laure Bourdery, Gerard Zurawski, Emile Foucat, Melissa Dullaers, SangKon Oh, Natalie Sabzghabaei,[...]. Immunity 2011
983
13

Early commitment of naïve human CD4(+) T cells to the T follicular helper (T(FH)) cell lineage is induced by IL-12.
Cindy S Ma, Santi Suryani, Danielle T Avery, Anna Chan, Ralph Nanan, Brigitte Santner-Nanan, Elissa K Deenick, Stuart G Tangye. Immunol Cell Biol 2009
266
13

Regulation of B cell differentiation and plasma cell generation by IL-21, a novel inducer of Blimp-1 and Bcl-6.
Katsutoshi Ozaki, Rosanne Spolski, Rachel Ettinger, Hyoung-Pyo Kim, Gang Wang, Chen-Feng Qi, Patrick Hwu, Daniel J Shaffer, Shreeram Akilesh, Derry C Roopenian,[...]. J Immunol 2004
490
13

IL-21 regulates germinal center B cell differentiation and proliferation through a B cell-intrinsic mechanism.
Dimitra Zotos, Jonathan M Coquet, Yang Zhang, Amanda Light, Kathy D'Costa, Axel Kallies, Lynn M Corcoran, Dale I Godfrey, Kai-Michael Toellner, Mark J Smyth,[...]. J Exp Med 2010
519
13

Cutting edge: the common gamma-chain is an indispensable subunit of the IL-21 receptor complex.
H Asao, C Okuyama, S Kumaki, N Ishii, S Tsuchiya, D Foster, K Sugamura. J Immunol 2001
404
13

Essential autocrine regulation by IL-21 in the generation of inflammatory T cells.
Roza Nurieva, Xuexian O Yang, Gustavo Martinez, Yongliang Zhang, Athanasia D Panopoulos, Li Ma, Kimberly Schluns, Qiang Tian, Stephanie S Watowich, Anton M Jetten,[...]. Nature 2007
13

Germline mutations in NFKB2 implicate the noncanonical NF-κB pathway in the pathogenesis of common variable immunodeficiency.
Karin Chen, Emily M Coonrod, Attila Kumánovics, Zechariah F Franks, Jacob D Durtschi, Rebecca L Margraf, Wilfred Wu, Nahla M Heikal, Nancy H Augustine, Perry G Ridge,[...]. Am J Hum Genet 2013
140
13

Homozygous loss of ICOS is associated with adult-onset common variable immunodeficiency.
Bodo Grimbacher, Andreas Hutloff, Michael Schlesier, Erik Glocker, Klaus Warnatz, Ruth Dräger, Hermann Eibel, Beate Fischer, Alejandro A Schäffer, Hans W Mages,[...]. Nat Immunol 2003
513
13

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
12

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
12

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
12

Cloning of a type I cytokine receptor most related to the IL-2 receptor beta chain.
K Ozaki, K Kikly, D Michalovich, P R Young, W J Leonard. Proc Natl Acad Sci U S A 2000
250
12

Generation of T follicular helper cells is mediated by interleukin-21 but independent of T helper 1, 2, or 17 cell lineages.
Roza I Nurieva, Yeonseok Chung, Daehee Hwang, Xuexian O Yang, Hong Soon Kang, Li Ma, Yi-hong Wang, Stephanie S Watowich, Anton M Jetten, Qiang Tian,[...]. Immunity 2008
868
12

Activating germline mutations in STAT3 cause early-onset multi-organ autoimmune disease.
Sarah E Flanagan, Emma Haapaniemi, Mark A Russell, Richard Caswell, Hana Lango Allen, Elisa De Franco, Timothy J McDonald, Hanna Rajala, Anita Ramelius, John Barton,[...]. Nat Genet 2014
291
12

Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome.
Joshua D Milner, Jason M Brenchley, Arian Laurence, Alexandra F Freeman, Brenna J Hill, Kevin M Elias, Yuka Kanno, Christine Spalding, Houda Z Elloumi, Michelle L Paulson,[...]. Nature 2008
818
12

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
334
12

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
11


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.