A citation-based method for searching scientific literature

Satoru Takafuji, Takeshi Mori, Noriyuki Nishimura, Nobuyuki Yamamoto, Suguru Uemura, Kandai Nozu, Kiminori Terui, Tsutomu Toki, Etsuro Ito, Hideki Muramatsu, Yoshiyuki Takahashi, Masafumi Matsuo, Tomohiko Yamamura, Kazumoto Iijima. Pediatr Hematol Oncol 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


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
263
50

The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
50

Diagnostics of Primary Immunodeficiencies through Next-Generation Sequencing.
Vera Gallo, Laura Dotta, Giuliana Giardino, Emilia Cirillo, Vassilios Lougaris, Roberta D'Assante, Alberto Prandini, Rita Consolini, Emily G Farrow, Isabelle Thiffault,[...]. Front Immunol 2016
44
50

Heterogeneity in the genetic basis of human complement C9 deficiency.
K Witzel-Schlömp, M J Hobart, B A Fernie, A Orren, R Würzner, C Rittner, T Kaufmann, P M Schneider. Immunogenetics 1998
13
50

FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 gene.
Maurizio Miano, Enrico Cappelli, Agnese Pezzulla, Roberta Venè, Alice Grossi, Paola Terranova, Elena Palmisani, Rosario Maggiore, Daniela Guardo, Tiziana Lanza,[...]. Br J Haematol 2019
19
50

Targeted NGS: A Cost-Effective Approach to Molecular Diagnosis of PIDs.
Jennifer L Stoddard, Julie E Niemela, Thomas A Fleisher, Sergio D Rosenzweig. Front Immunol 2014
67
50

Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency.
Qiang Pan-Hammarström, Ulrich Salzer, Likun Du, Janne Björkander, Charlotte Cunningham-Rundles, David L Nelson, Chiara Bacchelli, H Bobby Gaspar, Steven Offer, Timothy W Behrens,[...]. Nat Genet 2007
159
50

Association of variants in BAFF (rs9514828 and rs1041569) and BAFF-R (rs61756766) genes with the risk of chronic lymphocytic leukemia.
Monika Jasek, Agnieszka Bojarska-Junak, Marta Wagner, Maciej Sobczyński, Dariusz Wołowiec, Jacek Roliński, Lidia Karabon, Piotr Kuśnierczyk. Tumour Biol 2016
10
50

The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity.
Markus G Seidel, Gerhard Kindle, Benjamin Gathmann, Isabella Quinti, Matthew Buckland, Joris van Montfrans, Raphael Scheible, Stephan Rusch, Lukas M Gasteiger, Bodo Grimbacher,[...]. J Allergy Clin Immunol Pract 2019
188
50

Unbiased targeted next-generation sequencing molecular approach for primary immunodeficiency diseases.
Hamoud Al-Mousa, Mohamed Abouelhoda, Dorota M Monies, Nada Al-Tassan, Abdulaziz Al-Ghonaium, Bandar Al-Saud, Hasan Al-Dhekri, Rand Arnaout, Saleh Al-Muhsen, Nazema Ades,[...]. J Allergy Clin Immunol 2016
79
50

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes.
Jérôme Hadjadj, Nathalie Aladjidi, Helder Fernandes, Guy Leverger, Aude Magérus-Chatinet, Fabienne Mazerolles, Marie-Claude Stolzenberg, Sidonie Jacques, Capucine Picard, Jérémie Rosain,[...]. Blood 2019
65
50

Diagnostic interpretation of genetic studies in patients with primary immunodeficiency diseases: A working group report of the Primary Immunodeficiency Diseases Committee of the American Academy of Allergy, Asthma & Immunology.
Ivan K Chinn, Alice Y Chan, Karin Chen, Janet Chou, Morna J Dorsey, Joud Hajjar, Artemio M Jongco, Michael D Keller, Lisa J Kobrynski, Attila Kumanovics,[...]. J Allergy Clin Immunol 2020
33
50

Late-onset and long-lasting autoimmune neutropenia: an analysis from the Italian Neutropenia Registry.
Francesca Fioredda, Gioacchino Andrea Rotulo, Piero Farruggia, Francesca Dagliano, Marta Pillon, Angela Trizzino, Lucia Notarangelo, Laura Luti, Tiziana Lanza, Paola Terranova,[...]. Blood Adv 2020
8
50

Molecular Diagnosis of Inherited Immune Disorders.
Jocelyn R Farmer, Vinay S Mahajan. Clin Lab Med 2019
3
50

Hematopoietic Cell Transplantation in Patients With Primary Immune Regulatory Disorders (PIRD): A Primary Immune Deficiency Treatment Consortium (PIDTC) Survey.
Alice Y Chan, Jennifer W Leiding, Xuerong Liu, Brent R Logan, Lauri M Burroughs, Eric J Allenspach, Suzanne Skoda-Smith, Gulbu Uzel, Luigi D Notarangelo, Mary Slatter,[...]. Front Immunol 2020
26
50

Unusual Late-onset Enteropathy in a Patient With Lipopolysaccharide-responsive Beige-like Anchor Protein Deficiency.
Rosario Maggiore, Alice Grossi, Francesca Fioredda, Elena Palmisani, Paola Terranova, Enrico Cappelli, Tiziana Lanza, Filomena Pierri, Daniela Guardo, Michaela Calvillo,[...]. J Pediatr Hematol Oncol 2020
4
50

The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID).
Atil Bisgin, Ozge Sonmezler, Ibrahim Boga, Mustafa Yilmaz. Sci Rep 2021
1
100

Diagnostic Yield of Next Generation Sequencing in Genetically Undiagnosed Patients with Primary Immunodeficiencies: a Systematic Review.
Hemmo A F Yska, Kim Elsink, Taco W Kuijpers, Geert W J Frederix, Mariëlle E van Gijn, Joris M van Montfrans. J Clin Immunol 2019
34
50

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
454
50

Next generation sequencing panel in undifferentiated autoinflammatory diseases identifies patients with colchicine-responder recurrent fevers.
Riccardo Papa, Marta Rusmini, Stefano Volpi, Roberta Caorsi, Paolo Picco, Alice Grossi, Francesco Caroli, Francesca Bovis, Valeria Musso, Laura Obici,[...]. Rheumatology (Oxford) 2020
22
50

Exome sequencing in routine diagnostics: a generic test for 254 patients with primary immunodeficiencies.
Peer Arts, Annet Simons, Mofareh S AlZahrani, Elanur Yilmaz, Eman AlIdrissi, Koen J van Aerde, Njood Alenezi, Hamza A AlGhamdi, Hadeel A AlJubab, Abdulrahman A Al-Hussaini,[...]. Genome Med 2019
25
50

Autoimmunity and immunodeficiency.
Rodrigo Hoyos-Bachiloglu, Janet Chou. Curr Opin Rheumatol 2020
6
50


Use of Genetic Testing for Primary Immunodeficiency Patients.
Jennifer R Heimall, David Hagin, Joud Hajjar, Sarah E Henrickson, Hillary S Hernandez-Trujillo, Yuval Tan, Lisa Kobrynski, Kenneth Paris, Troy R Torgerson, James W Verbsky,[...]. J Clin Immunol 2018
51
50

Whole-exome sequencing-based discovery of STIM1 deficiency in a child with fatal classic Kaposi sarcoma.
Minji Byun, Avinash Abhyankar, Virginie Lelarge, Sabine Plancoulaine, Ayse Palanduz, Leyla Telhan, Bertrand Boisson, Capucine Picard, Scott Dewell, Connie Zhao,[...]. J Exp Med 2010
205
50

ADA2 deficiency: Clonal lymphoproliferation in a subset of patients.
Luca Trotta, Timi Martelius, Timo Siitonen, Timo Hautala, Sari Hämäläinen, Hanna Juntti, Mervi Taskinen, Mette Ilander, Emma Irene Andersson, Andrey Zavialov,[...]. J Allergy Clin Immunol 2018
47
50

Inborn errors of immunity-recent advances in research on the pathogenesis.
Motoi Yamashita, Kento Inoue, Tsubasa Okano, Tomohiro Morio. Inflamm Regen 2021
7
50

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
287
50

Genetic screening of children with marrow failure. The role of primary Immunodeficiencies.
Maurizio Miano, Alice Grossi, Gianluca Dell'Orso, Marina Lanciotti, Francesca Fioredda, Elena Palmisani, Tiziana Lanza, Daniela Guardo, Andrea Beccaria, Silvia Ravera,[...]. Am J Hematol 2021
7
50

Targeted next-generation sequencing: a novel diagnostic tool for primary immunodeficiencies.
Isaac J Nijman, Joris M van Montfrans, Marlous Hoogstraat, Marianne L Boes, Lisette van de Corput, Ellen D Renner, Patrick van Zon, Stef van Lieshout, Martin G Elferink, Mirjam van der Burg,[...]. J Allergy Clin Immunol 2014
99
50


Novel genetic variants of inborn errors of immunity.
Farida Almarzooqi, Abdul-Kader Souid, Ranjit Vijayan, Suleiman Al-Hammadi. PLoS One 2021
3
50

Inborn Errors of Immunity With Immune Dysregulation: From Bench to Bedside.
Ottavia Maria Delmonte, Riccardo Castagnoli, Enrica Calzoni, Luigi Daniele Notarangelo. Front Pediatr 2019
41
50

Deficiency of ADA2 mimicking autoimmune lymphoproliferative syndrome in the absence of livedo reticularis and vasculitis.
Abdulrahman Alsultan, Enas Basher, Jubran Alqanatish, Reem Mohammed, Majid Alfadhel. Pediatr Blood Cancer 2018
32
50


Impaired receptor editing and heterozygous RAG2 mutation in a patient with systemic lupus erythematosus and erosive arthritis.
Jolan E Walter, Mindy S Lo, Katalin Kis-Toth, Irit Tirosh, Francesco Frugoni, Yu Nee Lee, Krisztian Csomos, Karin Chen, Shiv Pillai, Jonathan Dunham,[...]. J Allergy Clin Immunol 2015
19
50

TACI mutation in common variable immunodeficiency and IgA deficiency.
Rima Rachid, Emanuela Castigli, Raif S Geha, Francisco A Bonilla. Curr Allergy Asthma Rep 2006
30
50

Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes.
Paul Dunn, Cassie L Albury, Neven Maksemous, Miles C Benton, Heidi G Sutherland, Robert A Smith, Larisa M Haupt, Lyn R Griffiths. Front Genet 2018
52
50

Thrombotic thrombocytopenic purpura and defective apoptosis due to CASP8/10 mutations: the role of mycophenolate mofetil.
F Fioredda, E Cappelli, A Mariani, A Beccaria, E Palmisani, A Grossi, I Ceccherini, R Venè, C Micalizzi, M Calvillo,[...]. Blood Adv 2019
2
50

Corrigendum: Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies.
Cristina Cifaldi, Immacolata Brigida, Federica Barzaghi, Matteo Zoccolillo, Valentina Ferradini, Davide Petricone, Maria Pia Cicalese, Dejan Lazarevic, Davide Cittaro, Maryam Omrani,[...]. Front Immunol 2019
7
50

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
176
50


Next-generation sequencing and its initial applications for molecular diagnosis of systemic auto-inflammatory diseases.
Marta Rusmini, Silvia Federici, Francesco Caroli, Alice Grossi, Maurizia Baldi, Laura Obici, Antonella Insalaco, Alberto Tommasini, Roberta Caorsi, Eleonora Gallo,[...]. Ann Rheum Dis 2016
44
50

Innate Mechanisms in Selective IgA Deficiency.
Jingyan Zhang, Dèlenn van Oostrom, JianXi Li, Huub F J Savelkoul. Front Immunol 2021
5
50

Adult-onset manifestation of idiopathic T-cell lymphopenia due to a heterozygous RAG1 mutation.
Roshini S Abraham, Mike Recher, Silvia Giliani, Jolan E Walter, Yu Nee Lee, Francesco Frugoni, Daniel E Maddox, Salman Kirmani, Luigi D Notarangelo. J Allergy Clin Immunol 2013
24
50

Uses of Next-Generation Sequencing Technologies for the Diagnosis of Primary Immunodeficiencies.
Michael Seleman, Rodrigo Hoyos-Bachiloglu, Raif S Geha, Janet Chou. Front Immunol 2017
44
50

ADA2 deficiency due to a novel structural variation in 22q11.1.
Alice Grossi, Roberto Cusano, Marta Rusmini, Federica Penco, Francesca Schena, Rosa A Podda, Roberta Caorsi, Marco Gattorno, Paolo Uva, Isabella Ceccherini. Clin Genet 2019
8
50

Hematopoietic stem cell transplantation in Omenn syndrome: a single-center experience.
E Mazzolari, D Moshous, C Forino, D De Martiis, C Offer, A Lanfranchi, S Giliani, L Imberti, S Pasic, A G Ugazio,[...]. Bone Marrow Transplant 2005
27
50

Primary immunodeficiency.
Christine McCusker, Julia Upton, Richard Warrington. Allergy Asthma Clin Immunol 2018
60
50

TACI mutations and impaired B-cell function in subjects with CVID and healthy heterozygotes.
Monica Martinez-Gallo, Lin Radigan, María Belén Almejún, Natalia Martínez-Pomar, Núria Matamoros, Charlotte Cunningham-Rundles. J Allergy Clin Immunol 2013
59
50


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.