A citation-based method for searching scientific literature

Heather K Lehman. Curr Allergy Asthma Rep 2015
Times Cited: 18







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



Times Cited
  Times     Co-cited
Similarity


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
523
27

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
357
27

Phenotype, penetrance, and treatment of 133 cytotoxic T-lymphocyte antigen 4-insufficient subjects.
Charlotte Schwab, Annemarie Gabrysch, Peter Olbrich, Virginia Patiño, Klaus Warnatz, Daniel Wolff, Akihiro Hoshino, Masao Kobayashi, Kohsuke Imai, Masatoshi Takagi,[...]. J Allergy Clin Immunol 2018
191
27


Morbidity and mortality in common variable immune deficiency over 4 decades.
Elena S Resnick, Erin L Moshier, James H Godbold, Charlotte Cunningham-Rundles. Blood 2012
429
16

Common variable immunodeficiency mimicking rheumatoid arthritis with Sjögren's syndrome.
Li-Hsin Lin, Chih-Neng Tsai, Ming-Fei Liu, Chrong-Reen Wang. J Microbiol Immunol Infect 2005
12
25

Autoimmunity in IgA deficiency: revisiting the role of IgA as a silent housekeeper.
Cristina M A Jacob, Antonio C Pastorino, Kristine Fahl, Magda Carneiro-Sampaio, Renato C Monteiro. J Clin Immunol 2008
95
16

Clinical spectrum of X-linked hyper-IgM syndrome.
J Levy, T Espanol-Boren, C Thomas, A Fischer, P Tovo, P Bordigoni, I Resnick, A Fasth, M Baer, L Gomez,[...]. J Pediatr 1997
444
16

Autoimmunity in common variable immunodeficiency.
Shradha Agarwal, Charlotte Cunningham-Rundles. Curr Allergy Asthma Rep 2009
111
16

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
308
16

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
162
16

Antiviral immune responses: triggers of or triggered by autoimmunity?
Christian Münz, Jan D Lünemann, Meghann Teague Getts, Stephen D Miller. Nat Rev Immunol 2009
308
16

Control of regulatory T cell development by the transcription factor Foxp3.
Shohei Hori, Takashi Nomura, Shimon Sakaguchi. Science 2003
16

Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015.
Capucine Picard, Waleed Al-Herz, Aziz Bousfiha, Jean-Laurent Casanova, Talal Chatila, Mary Ellen Conley, Charlotte Cunningham-Rundles, Amos Etzioni, Steven M Holland, Christoph Klein,[...]. J Clin Immunol 2015
403
16


Early-onset lymphoproliferation and autoimmunity caused by germline STAT3 gain-of-function mutations.
Joshua D Milner, Tiphanie P Vogel, Lisa Forbes, Chi A Ma, Asbjørg Stray-Pedersen, Julie E Niemela, Jonathan J Lyons, Karin R Engelhardt, Yu Zhang, Nermina Topcagic,[...]. Blood 2015
313
16

Immune deficiency and autoimmunity in patients with CTLA-4 (CD152) mutations.
N Verma, S O Burns, L S K Walker, D M Sansom. Clin Exp Immunol 2017
58
16

The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies.
Aziz Bousfiha, Leïla Jeddane, Capucine Picard, Fatima Ailal, H Bobby Gaspar, Waleed Al-Herz, Talal Chatila, Yanick J Crow, Charlotte Cunningham-Rundles, Amos Etzioni,[...]. J Clin Immunol 2018
284
16

Inborn Errors of Immunity With Immune Dysregulation: From Bench to Bedside.
Ottavia Maria Delmonte, Riccardo Castagnoli, Enrica Calzoni, Luigi Daniele Notarangelo. Front Pediatr 2019
40
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
495
16

The extended phenotype of LPS-responsive beige-like anchor protein (LRBA) deficiency.
Laura Gámez-Díaz, Dietrich August, Polina Stepensky, Shoshana Revel-Vilk, Markus G Seidel, Mitsuiki Noriko, Tomohiro Morio, Austen J J Worth, Jacob Blessing, Frank Van de Veerdonk,[...]. J Allergy Clin Immunol 2016
158
16

Clinical Aspects of STAT3 Gain-of-Function Germline Mutations: A Systematic Review.
Alexandre Fabre, Sarah Marchal, Vincent Barlogis, Bernard Mari, Pascal Barbry, Pierre-Simon Rohrlich, Lisa R Forbes, Tiphanie P Vogel, Lisa Giovannini-Chami. J Allergy Clin Immunol Pract 2019
76
16


Clinical picture and treatment of 2212 patients with common variable immunodeficiency.
Benjamin Gathmann, Nizar Mahlaoui, Laurence Gérard, Eric Oksenhendler, Klaus Warnatz, Ilka Schulze, Gerhard Kindle, Taco W Kuijpers, Rachel T van Beem, David Guzman,[...]. J Allergy Clin Immunol 2014
330
11

Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.
Asghar Aghamohammadi, Payam Mohammadinejad, Hassan Abolhassani, Babak Mirminachi, Masoud Movahedi, Mohammad Gharagozlou, Nima Parvaneh, Vaheid Zeiaee, Bahram Mirsaeed-Ghazi, Zahra Chavoushzadeh,[...]. J Clin Immunol 2014
82
11

The United Kingdom Primary Immune Deficiency (UKPID) Registry: report of the first 4 years' activity 2008-2012.
J D M Edgar, M Buckland, D Guzman, N P Conlon, V Knerr, C Bangs, V Reiser, Z Panahloo, S Workman, M Slatter,[...]. Clin Exp Immunol 2014
68
11

Common variable immunodeficiency and autoimmunity--an inconvenient truth.
Xiao Xiao, Qi Miao, Christopher Chang, M Eric Gershwin, Xiong Ma. Autoimmun Rev 2014
40
11

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
697
11

Concerted action of wild-type and mutant TNF receptors enhances inflammation in TNF receptor 1-associated periodic fever syndrome.
Anna Simon, Heiyoung Park, Ravikanth Maddipati, Adrian A Lobito, Ariel C Bulua, Adrianna J Jackson, Jae Jin Chae, Rachel Ettinger, Heleen D de Koning, Anthony C Cruz,[...]. Proc Natl Acad Sci U S A 2010
123
11


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
248
11

TNFRSF1A mutations and autoinflammatory syndromes.
J Galon, I Aksentijevich, M F McDermott, J J O'Shea, D L Kastner. Curr Opin Immunol 2000
188
11


Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.
Julie Toubiana, Satoshi Okada, Julia Hiller, Matias Oleastro, Macarena Lagos Gomez, Juan Carlos Aldave Becerra, Marie Ouachée-Chardin, Fanny Fouyssac, Katta Mohan Girisha, Amos Etzioni,[...]. Blood 2016
268
11

Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome).
K E Sullivan, D M McDonald-McGinn, D A Driscoll, C M Zmijewski, A S Ellabban, L Reed, B S Emanuel, E H Zackai, B H Athreya, G Keenan. Arthritis Rheum 1997
76
11

Common variable immunodeficiency disorders: division into distinct clinical phenotypes.
Helen Chapel, Mary Lucas, Martin Lee, Janne Bjorkander, David Webster, Bodo Grimbacher, Claire Fieschi, Vojtech Thon, Mohammad R Abedi, Lennart Hammarstrom. Blood 2008
510
11

From infection to autoimmunity.
D Fairweather, Z Kaya, G R Shellam, C M Lawson, N R Rose. J Autoimmun 2001
206
11

Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked-like disorder caused by loss-of-function mutations in LRBA.
Louis-Marie Charbonnier, Erin Janssen, Janet Chou, Toshiro K Ohsumi, Sevgi Keles, Joyce T Hsu, Michel J Massaad, Maria Garcia-Lloret, Rima Hanna-Wakim, Ghassan Dbaibo,[...]. J Allergy Clin Immunol 2015
154
11

Severe combined immunodeficiency--an update.
Emilia Cirillo, Giuliana Giardino, Vera Gallo, Roberta D'Assante, Fiorentino Grasso, Roberta Romano, Cristina Di Lillo, Giovanni Galasso, Claudio Pignata. Ann N Y Acad Sci 2015
46
11

Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features.
Vassilios Lougaris, Raffaele Badolato, Simona Ferrari, Alessandro Plebani. Immunol Rev 2005
103
11

Common variable immunodeficiency in systemic lupus erythematosus.
Mónica Fernández-Castro, Susana Mellor-Pita, María Jesús Citores, Pilar Muñoz, Pablo Tutor-Ureta, Lucia Silva, Juan Antonio Vargas, Miguel Yebra-Bango, José Luis Andreu. Semin Arthritis Rheum 2007
42
11

LRBA gene deletion in a patient presenting with autoimmunity without hypogammaglobulinemia.
Siobhan O Burns, Helen L Zenner, Vincent Plagnol, James Curtis, Kin Mok, Michael Eisenhut, Dinakantha Kumararatne, Rainer Doffinger, Adrian J Thrasher, Sergey Nejentsev. J Allergy Clin Immunol 2012
72
11


Atypical manifestation of LRBA deficiency with predominant IBD-like phenotype.
Nina Kathrin Serwas, Aydan Kansu, Elisangela Santos-Valente, Zarife Kuloğlu, Arzu Demir, Aytaç Yaman, Laura Yaneth Gamez Diaz, Reha Artan, Ersin Sayar, Arzu Ensari,[...]. Inflamm Bowel Dis 2015
52
11

Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes.
Ulrich Salzer, Chiara Bacchelli, Sylvie Buckridge, Qiang Pan-Hammarström, Stephanie Jennings, Vassilis Lougaris, Astrid Bergbreiter, Tina Hagena, Jennifer Birmelin, Alessandro Plebani,[...]. Blood 2009
175
11

Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3.
Emma M Haapaniemi, Meri Kaustio, Hanna L M Rajala, Arjan J van Adrichem, Leena Kainulainen, Virpi Glumoff, Rainer Doffinger, Heikki Kuusanmäki, Tarja Heiskanen-Kosma, Luca Trotta,[...]. Blood 2015
164
11


Autoimmunity in Wiskott-Aldrich syndrome.
Shepherd H Schurman, Fabio Candotti. Curr Opin Rheumatol 2003
75
11

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
165
11

Lymphoproliferative disorders with early lethality in mice deficient in Ctla-4.
P Waterhouse, J M Penninger, E Timms, A Wakeham, A Shahinian, K P Lee, C B Thompson, H Griesser, T W Mak. Science 1995
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.