A citation-based method for searching scientific literature

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, Elisha D O Roberson, Helen Matthews, James W Verbsky, Trivikram Dasu, Alexander Vargas-Hernandez, Nidhy Varghese, Kenneth L McClain, Lina B Karam, Karen Nahmod, George Makedonas, Emily M Mace, Hanne S Sorte, Gøri Perminow, V Koneti Rao, Michael P O'Connell, Susan Price, Helen C Su, Morgan Butrick, Joshua McElwee, Jason D Hughes, Joseph Willet, David Swan, Yaobo Xu, Mauro Santibanez-Koref, Voytek Slowik, Darrell L Dinwiddie, Christina E Ciaccio, Carol J Saunders, Seth Septer, Stephen F Kingsmore, Andrew J White, Andrew J Cant, Sophie Hambleton, Megan A Cooper. Blood 2015
Times Cited: 282







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



Times Cited
  Times     Co-cited
Similarity


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
281
42

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
151
37

Jakinibs for the treatment of immune dysregulation in patients with gain-of-function signal transducer and activator of transcription 1 (STAT1) or STAT3 mutations.
Lisa R Forbes, Tiphanie P Vogel, Megan A Cooper, Johana Castro-Wagner, Edith Schussler, Katja G Weinacht, Ashley S Plant, Helen C Su, Eric J Allenspach, Mary Slatter,[...]. J Allergy Clin Immunol 2018
79
36

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
61
45

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
154
26

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
445
23

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
324
23

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
235
20

Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee.
Stuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, Talal Chatila, Charlotte Cunningham-Rundles, Amos Etzioni, Jose Luis Franco, Steven M Holland, Christoph Klein, Tomohiro Morio,[...]. J Clin Immunol 2020
286
20

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
475
19

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
772
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
139
14

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
671
13

The Ying and Yang of STAT3 in Human Disease.
Tiphanie P Vogel, Joshua D Milner, Megan A Cooper. J Clin Immunol 2015
82
15

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
486
13

STAT3 gain-of-function mutations associated with autoimmune lymphoproliferative syndrome like disease deregulate lymphocyte apoptosis and can be targeted by BH3 mimetic compounds.
Schafiq Nabhani, Cyrill Schipp, Hagit Miskin, Carina Levin, Sergey Postovsky, Tal Dujovny, Ariel Koren, Dan Harlev, Anne-Marie Bis, Franziska Auer,[...]. Clin Immunol 2017
28
42

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
288
11

Partial growth hormone insensitivity and dysregulatory immune disease associated with de novo germline activating STAT3 mutations.
Mariana Gutiérrez, Paula Scaglia, Ana Keselman, Lucía Martucci, Liliana Karabatas, Sabina Domené, Ayelen Martin, Patricia Pennisi, Miguel Blanco, Nora Sanguineti,[...]. Mol Cell Endocrinol 2018
22
50

Genetic Diagnosis Using Whole Exome Sequencing in Common Variable Immunodeficiency.
Patrick Maffucci, Charles A Filion, Bertrand Boisson, Yuval Itan, Lei Shang, Jean-Laurent Casanova, Charlotte Cunningham-Rundles. Front Immunol 2016
136
11

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
368
11

Abatacept alleviates severe autoimmune symptoms in a patient carrying a de novo variant in CTLA-4.
Sangmoon Lee, Jin Soo Moon, Cho-Rong Lee, Hye-Eun Kim, Sun-Mi Baek, Solha Hwang, Gyeong Hoon Kang, Jeong Kee Seo, Choong Ho Shin, Hyoung Jin Kang,[...]. J Allergy Clin Immunol 2016
74
13

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
10

Short Stature in a Boy with Multiple Early-Onset Autoimmune Conditions due to a STAT3 Activating Mutation: Could Intracellular Growth Hormone Signalling Be Compromised?
.
Hana Sediva, Petra Dusatkova, Veronika Kanderova, Barbora Obermannova, Jana Kayserova, Lucie Sramkova, Dana Zemkova, Lenka Elblova, Michal Svaton, Radana Zachova,[...]. Horm Res Paediatr 2017
19
52

Clinical spectrum and features of activated phosphoinositide 3-kinase δ syndrome: A large patient cohort study.
Tanya I Coulter, Anita Chandra, Chris M Bacon, Judith Babar, James Curtis, Nick Screaton, John R Goodlad, George Farmer, Cathal Laurence Steele, Timothy Ronan Leahy,[...]. J Allergy Clin Immunol 2017
190
10

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
148
10

Ruxolitinib reverses dysregulated T helper cell responses and controls autoimmunity caused by a novel signal transducer and activator of transcription 1 (STAT1) gain-of-function mutation.
Katja G Weinacht, Louis-Marie Charbonnier, Fayhan Alroqi, Ashley Plant, Qi Qiao, Hao Wu, Clement Ma, Troy R Torgerson, Sergio D Rosenzweig, Thomas A Fleisher,[...]. J Allergy Clin Immunol 2017
79
12

Distinct molecular response patterns of activating STAT3 mutations associate with penetrance of lymphoproliferation and autoimmunity.
Sabine Jägle, Maximilian Heeg, Sarah Grün, Anne Rensing-Ehl, Maria Elena Maccari, Christian Klemann, Neil Jones, Kai Lehmberg, Claudia Bettoni, Klaus Warnatz,[...]. Clin Immunol 2020
16
62

Revised diagnostic criteria and classification for the autoimmune lymphoproliferative syndrome (ALPS): report from the 2009 NIH International Workshop.
Joao B Oliveira, Jack J Bleesing, Umberto Dianzani, Thomas A Fleisher, Elaine S Jaffe, Michael J Lenardo, Frederic Rieux-Laucat, Richard M Siegel, Helen C Su, David T Teachey,[...]. Blood 2010
243
9

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
9

STAT3 Gain of Function: A New Kid on the Block in Interstitial Lung Diseases.
Alexandre Fabre, Sarah Marchal, Lisa Renee Forbes, Tiphanie Phillips Vogel, Vincent Barlogis, Valérie Triolo, Pierre-Simon Rohrlich, Etienne Bérard, Diane Frankel, Damien Ambrosetti,[...]. Am J Respir Crit Care Med 2018
16
56

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
350
9

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry.
Maria Elena Maccari, Hassan Abolhassani, Asghar Aghamohammadi, Alessandro Aiuti, Olga Aleinikova, Catherine Bangs, Safa Baris, Federica Barzaghi, Helen Baxendale, Matthew Buckland,[...]. Front Immunol 2018
73
12

STAT1 mutations in autosomal dominant chronic mucocutaneous candidiasis.
Frank L van de Veerdonk, Theo S Plantinga, Alexander Hoischen, Sanne P Smeekens, Leo A B Joosten, Christian Gilissen, Peer Arts, Diana C Rosentul, Andrew J Carmichael, Chantal A A Smits-van der Graaf,[...]. N Engl J Med 2011
398
9

Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification.
Aziz Bousfiha, Leila Jeddane, Capucine Picard, Waleed Al-Herz, Fatima Ailal, Talal Chatila, Charlotte Cunningham-Rundles, Amos Etzioni, Jose Luis Franco, Steven M Holland,[...]. J Clin Immunol 2020
150
9

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
105
8

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
812
8

Tocilizumab Promotes Regulatory T-cell Alleviation in STAT3 Gain-of-function-associated Multi-organ Autoimmune Syndrome.
Tawfik Khoury, Vered Molho-Pessach, Yuval Ramot, Abu Rmeileh Ayman, Orly Elpeleg, Neville Berkman, Abraham Zlotogorski, Yaron Ilan. Clin Ther 2017
17
47

Spectrum of Phenotypes Associated with Mutations in LRBA.
Omar K Alkhairy, Hassan Abolhassani, Nima Rezaei, Mingyan Fang, Kasper Krogh Andersen, Zahra Chavoshzadeh, Iraj Mohammadzadeh, Mariam A El-Rajab, Michel Massaad, Janet Chou,[...]. J Clin Immunol 2016
112
8

Effective "activated PI3Kδ syndrome"-targeted therapy with the PI3Kδ inhibitor leniolisib.
V Koneti Rao, Sharon Webster, Virgil A S H Dalm, Anna Šedivá, P Martin van Hagen, Steven Holland, Sergio D Rosenzweig, Andreas D Christ, Birgitte Sloth, Maciej Cabanski,[...]. Blood 2017
123
8

Efficacy of Ruxolitinib Therapy in a Patient With Severe Enterocolitis Associated With a STAT3 Gain-of-Function Mutation.
Marianna Parlato, Fabienne Charbit-Henrion, Elie Abi Nader, Bernadette Begue, Nicolas Guegan, Julie Bruneau, Shérine Khater, Elizabeth Macintyre, Capucine Picard, Rieux-Laucat Frédéric,[...]. Gastroenterology 2019
13
61

Human IL2RA null mutation mediates immunodeficiency with lymphoproliferation and autoimmunity.
Kevin Goudy, Didem Aydin, Federica Barzaghi, Eleonora Gambineri, Marina Vignoli, Sara Ciullini Mannurita, Claudio Doglioni, Maurilio Ponzoni, Maria Pia Cicalese, Andrea Assanelli,[...]. Clin Immunol 2013
101
8

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
251
7

International Consensus Document (ICON): Common Variable Immunodeficiency Disorders.
Francisco A Bonilla, Isil Barlan, Helen Chapel, Beatriz T Costa-Carvalho, Charlotte Cunningham-Rundles, M Teresa de la Morena, Francisco J Espinosa-Rosales, Lennart Hammarström, Shigeaki Nonoyama, Isabella Quinti,[...]. J Allergy Clin Immunol Pract 2016
313
7

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
887
7

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
176
7

International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity.
Capucine Picard, H Bobby Gaspar, Waleed Al-Herz, Aziz Bousfiha, Jean-Laurent Casanova, Talal Chatila, Yanick J Crow, Charlotte Cunningham-Rundles, Amos Etzioni, Jose Luis Franco,[...]. J Clin Immunol 2018
402
7

JAK1 gain-of-function causes an autosomal dominant immune dysregulatory and hypereosinophilic syndrome.
Kate L Del Bel, Robert J Ragotte, Aabida Saferali, Susan Lee, Suzanne M Vercauteren, Sara A Mostafavi, Richard A Schreiber, Julie S Prendiville, Min S Phang, Jessica Halparin,[...]. J Allergy Clin Immunol 2017
45
15

Hematopoietic stem cell transplantation for CTLA4 deficiency.
Mary A Slatter, Karin R Engelhardt, Lauri M Burroughs, Peter D Arkwright, Zohreh Nademi, Suzanne Skoda-Smith, David Hagin, Alan Kennedy, Dawn Barge, Terence Flood,[...]. J Allergy Clin Immunol 2016
54
12

The STAT5b Pathway Defect and Autoimmunity.
Takahiro Kanai, Jennifer Jenks, Kari Christine Nadeau. Front Immunol 2012
63
11

Signal transducer and activator of transcription 3: a year in review.
Lisa R Forbes, Josh Milner, Elie Haddad. Curr Opin Hematol 2016
34
20


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.