A citation-based method for searching scientific literature

Tao Xu, Qin Zhao, Wenyan Li, Xuemei Chen, Xiuhong Xue, Zhi Chen, Xiao Du, Xiaoming Bai, Qian Zhao, Lina Zhou, Xuemei Tang, Xi Yang, Hirokazu Kanegane, Xiaodong Zhao. Eur J Pediatr 2020
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity


X-linked lymphoproliferative disease due to SAP/SH2D1A deficiency: a multicenter study on the manifestations, management and outcome of the disease.
Claire Booth, Kimberly C Gilmour, Paul Veys, Andrew R Gennery, Mary A Slatter, Helen Chapel, Paul T Heath, Colin G Steward, Owen Smith, Anna O'Meara,[...]. Blood 2011
165
60

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
106
40

Clinical and genetic characteristics of XIAP deficiency in Japan.
Xi Yang, Hirokazu Kanegane, Naonori Nishida, Toshihiko Imamura, Kazuko Hamamoto, Ritsuko Miyashita, Kohsuke Imai, Shigeaki Nonoyama, Kazunori Sanayama, Akiko Yamaide,[...]. J Clin Immunol 2012
64
40

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
67
40

Consequences of Identifying XIAP Deficiency in an Adult Patient With Inflammatory Bowel Disease.
Maria Quaranta, Rachel Wilson, Eva Gonçalves Serra, Sumeet Pandey, Tobias Schwerd, Kimberly Gilmour, Paul Klenerman, Fiona Powrie, Satish Keshav, Simon P L Travis,[...]. Gastroenterology 2018
13
40

Inhibitor of apoptosis proteins limit RIP3 kinase-dependent interleukin-1 activation.
James E Vince, W Wei-Lynn Wong, Ian Gentle, Kate E Lawlor, Ramanjaneyulu Allam, Lorraine O'Reilly, Kylie Mason, Olaf Gross, Stephen Ma, Greta Guarda,[...]. Immunity 2012
339
40

XIAP deficiency: a unique primary immunodeficiency best classified as X-linked familial hemophagocytic lymphohistiocytosis and not as X-linked lymphoproliferative disease.
Rebecca A Marsh, Lisa Madden, Brenda J Kitchen, Rajen Mody, Brad McClimon, Michael B Jordan, Jack J Bleesing, Kejian Zhang, Alexandra H Filipovich. Blood 2010
148
40

TAK1 is a ubiquitin-dependent kinase of MKK and IKK.
C Wang, L Deng, M Hong, G R Akkaraju, J Inoue , Z J Chen. Nature 2001
40

Advances in understanding the pathogenesis of HLH.
G Naheed Usmani, Bruce A Woda, Peter E Newburger. Br J Haematol 2013
131
40

XIAP deficiency syndrome in humans.
Sylvain Latour, Claire Aguilar. Semin Cell Dev Biol 2015
63
40

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency).
Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, Fabien Touzot, Nizar Mahlaoui, Fabian Hauck, Hirokazu Kanegane, Eduardo Lopez-Granados, Ester Mejstrikova, Isabelle Pellier,[...]. Blood 2011
213
40

X-linked IAP is a direct inhibitor of cell-death proteases.
Q L Deveraux, R Takahashi, G S Salvesen, J C Reed. Nature 1997
40

X-linked lymphoproliferative syndromes: brothers or distant cousins?
Alexandra H Filipovich, Kejian Zhang, Andrew L Snow, Rebecca A Marsh. Blood 2010
106
40

Cellular inhibitors of apoptosis cIAP1 and cIAP2 are required for innate immunity signaling by the pattern recognition receptors NOD1 and NOD2.
Mathieu J M Bertrand, Karine Doiron, Katherine Labbé, Robert G Korneluk, Philip A Barker, Maya Saleh. Immunity 2009
245
40

A critical role of RICK/RIP2 polyubiquitination in Nod-induced NF-kappaB activation.
Mizuho Hasegawa, Yukari Fujimoto, Peter C Lucas, Hiroyasu Nakano, Koichi Fukase, Gabriel Núñez, Naohiro Inohara. EMBO J 2008
360
40

XIAP restricts TNF- and RIP3-dependent cell death and inflammasome activation.
Monica Yabal, Nicole Müller, Heiko Adler, Nathalie Knies, Christina J Groß, Rune Busk Damgaard, Hirokazu Kanegane, Marc Ringelhan, Thomas Kaufmann, Mathias Heikenwälder,[...]. Cell Rep 2014
156
40

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
458
40

A new functional assay for the diagnosis of X-linked inhibitor of apoptosis (XIAP) deficiency.
S Ammann, R Elling, M Gyrd-Hansen, G Dückers, R Bredius, S O Burns, J D M Edgar, A Worth, H Brandau, K Warnatz,[...]. Clin Exp Immunol 2014
57
40

The ubiquitin ligase XIAP recruits LUBAC for NOD2 signaling in inflammation and innate immunity.
Rune Busk Damgaard, Ueli Nachbur, Monica Yabal, Wendy Wei-Lynn Wong, Berthe Katrine Fiil, Mischa Kastirr, Eva Rieser, James Arthur Rickard, Aleksandra Bankovacki, Christian Peschel,[...]. Mol Cell 2012
249
40

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
40

Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation.
Neil Romberg, Khatoun Al Moussawi, Carol Nelson-Williams, Amy L Stiegler, Erin Loring, Murim Choi, John Overton, Eric Meffre, Mustafa K Khokha, Anita J Huttner,[...]. Nat Genet 2014
277
40

Disease-causing mutations in the XIAP BIR2 domain impair NOD2-dependent immune signalling.
Rune Busk Damgaard, Berthe Katrine Fiil, Carsten Speckmann, Monica Yabal, Udo zur Stadt, Simon Bekker-Jensen, Philipp J Jost, Stephan Ehl, Niels Mailand, Mads Gyrd-Hansen. EMBO Mol Med 2013
102
40

Clinical features and outcome of X-linked lymphoproliferative syndrome type 1 (SAP deficiency) in Japan identified by the combination of flow cytometric assay and genetic analysis.
Hirokazu Kanegane, Xi Yang, Meina Zhao, Kazumi Yamato, Masami Inoue, Kazuko Hamamoto, Chie Kobayashi, Ako Hosono, Yoshikiyo Ito, Yozo Nakazawa,[...]. Pediatr Allergy Immunol 2012
21
40

Clinical and genetic features of 5 Chinese patients with X-linked lymphoproliferative syndrome.
J Sun, W Ying, D Liu, X Hui, Y Yu, J Wang, X Wang. Scand J Immunol 2013
10
40


Non-Hodgkin lymphoma and pre-existing conditions: spectrum, clinical characteristics and outcome in 213 children and adolescents.
Andishe Attarbaschi, Elisa Carraro, Oussama Abla, Shlomit Barzilai-Birenboim, Simon Bomken, Laurence Brugieres, Eva Bubanska, Birgit Burkhardt, Alan K S Chiang, Monika Csoka,[...]. Haematologica 2016
27
20

Prevalence and morbidity of primary immunodeficiency diseases, United States 2001-2007.
Lisa Kobrynski, Rachel Waltenburg Powell, Scott Bowen. J Clin Immunol 2014
58
20

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
393
20

Radiation therapy and adjuvant chemotherapy in a patient with a malignant glioneuronal tumor and underlying ataxia telangiectasia: a case report and review of the literature.
Mariko D DeWire, Chris Beltran, Frederick A Boop, Kathleen J Helton, David W Ellison, Peter J McKinnon, Amar Gajjar, Atmaram S Pai Panandiker. J Clin Oncol 2013
10
20

Non-Hodgkin lymphoma (NHL) in children with Nijmegen Breakage syndrome (NBS).
Bozenna Dembowska-Baginska, Danuta Perek, Agnieszka Brozyna, Anna Wakulinska, Dorota Olczak-Kowalczyk, Malgorzata Gladkowska-Dura, Wieslawa Grajkowska, Krystyna H Chrzanowska. Pediatr Blood Cancer 2009
45
20

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
249
20

Promising therapy results for lymphoid malignancies in children with chromosomal breakage syndromes (Ataxia teleangiectasia or Nijmegen-breakage syndrome): a retrospective survey.
Klaus Bienemann, Birgit Burkhardt, Simon Modlich, Ulrike Meyer, Anja Möricke, Kirsten Bienemann, Christine Mauz-Körholz, Gabriele Escherich, Martin Zimmermann, Dieter Körholz,[...]. Br J Haematol 2011
33
20

Common Variable Immunodeficiency: Epidemiology, Pathogenesis, Clinical Manifestations, Diagnosis, Classification, and Management.
R Yazdani, S Habibi, L Sharifi, G Azizi, H Abolhassani, P Olbrich, A Aghamohammadi. J Investig Allergol Clin Immunol 2020
16
20

Recommendations for Childhood Cancer Screening and Surveillance in DNA Repair Disorders.
Michael F Walsh, Vivian Y Chang, Wendy K Kohlmann, Hamish S Scott, Christopher Cunniff, Franck Bourdeaut, Jan J Molenaar, Christopher C Porter, John T Sandlund, Sharon E Plon,[...]. Clin Cancer Res 2017
46
20

Autoimmune lymphoproliferative syndrome: an update and review of the literature.
Shaili Shah, Eveline Wu, V Koneti Rao, Teresa K Tarrant. Curr Allergy Asthma Rep 2014
42
20

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
334
20

Recommendations for Surveillance for Children with Leukemia-Predisposing Conditions.
Christopher C Porter, Todd E Druley, Ayelet Erez, Roland P Kuiper, Kenan Onel, Joshua D Schiffman, Kami Wolfe Schneider, Sarah R Scollon, Hamish S Scott, Louise C Strong,[...]. Clin Cancer Res 2017
44
20

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
140
20

Functional analysis of naturally occurring DCLRE1C mutations and correlation with the clinical phenotype of ARTEMIS deficiency.
Kerstin Felgentreff, Yu Nee Lee, Francesco Frugoni, Likun Du, Mirjam van der Burg, Silvia Giliani, Ilhan Tezcan, Ismail Reisli, Ester Mejstrikova, Jean-Pierre de Villartay,[...]. J Allergy Clin Immunol 2015
39
20

Outcomes after Allogeneic Transplant in Patients with Wiskott-Aldrich Syndrome.
Alexander Ngwube, I Celine Hanson, Jordan Orange, Nicholas L Rider, Filiz Seeborg, William Shearer, Lenora Noroski, Sarah Nicholas, Lisa Forbes, Kathryn Leung,[...]. Biol Blood Marrow Transplant 2018
11
20

Cancer in primary immunodeficiency diseases: Cancer incidence in the United States Immune Deficiency Network Registry.
Paul C Mayor, Kevin H Eng, Kelly L Singel, Scott I Abrams, Kunle Odunsi, Kirsten B Moysich, Ramsay Fuleihan, Elizabeth Garabedian, Patricia Lugar, Hans D Ochs,[...]. J Allergy Clin Immunol 2018
82
20

Nijmegen breakage syndrome (NBS).
Krystyna H Chrzanowska, Hanna Gregorek, Bożenna Dembowska-Bagińska, Maria A Kalina, Martin Digweed. Orphanet J Rare Dis 2012
129
20

Primary immunodeficiencies in the Netherlands: national patient data demonstrate the increased risk of malignancy.
B M Jonkman-Berk, J M van den Berg, I J M Ten Berge, R G M Bredius, G J Driessen, V A S H Dalm, J T van Dissel, M van Deuren, P M Ellerbroek, M van der Flier,[...]. Clin Immunol 2015
45
20

Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim.
J German, D Bloom, E Passarge, K Fried, R M Goodman, I Katzenellenbogen, Z Laron, C Legum, S Levin, Wahrman. Am J Hum Genet 1977
61
20

Ataxia telangiectasia: a review.
Cynthia Rothblum-Oviatt, Jennifer Wright, Maureen A Lefton-Greif, Sharon A McGrath-Morrow, Thomas O Crawford, Howard M Lederman. Orphanet J Rare Dis 2016
206
20

Heritable GATA2 mutations associated with familial myelodysplastic syndrome and acute myeloid leukemia.
Christopher N Hahn, Chan-Eng Chong, Catherine L Carmichael, Ella J Wilkins, Peter J Brautigan, Xiao-Chun Li, Milena Babic, Ming Lin, Amandine Carmagnac, Young K Lee,[...]. Nat Genet 2011
360
20

Review: Diagnosing Common Variable Immunodeficiency Disorder in the Era of Genome Sequencing.
Rohan Ameratunga, Klaus Lehnert, See-Tarn Woon, David Gillis, Vanessa L Bryant, Charlotte A Slade, Richard Steele. Clin Rev Allergy Immunol 2018
42
20

CVID-Associated Tumors: Czech Nationwide Study Focused on Epidemiology, Immunology, and Genetic Background in a Cohort of Patients With CVID.
Pavlina Kralickova, Tomas Milota, Jiri Litzman, Ivana Malkusova, Dalibor Jilek, Jitka Petanova, Jana Vydlakova, Alena Zimulova, Eva Fronkova, Michael Svaton,[...]. Front Immunol 2019
19
20

Increased risk of hematologic malignancies in primary immunodeficiency disorders: opportunities for immunotherapy.
Dorit Verhoeven, Arie Jan Stoppelenburg, Friederike Meyer-Wentrup, Marianne Boes. Clin Immunol 2018
14
20

Carrier frequency of the Bloom syndrome blmAsh mutation in the Ashkenazi Jewish population.
L Li, C Eng, R J Desnick, J German, N A Ellis. Mol Genet Metab 1998
62
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.