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



Times Cited
  Times     Co-cited
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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
11
50

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
218
50

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
171
50

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
66
50

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
468
40

Hematopoietic Stem Cell Transplantation for XIAP Deficiency in Japan.
Shintaro Ono, Tsubasa Okano, Akihiro Hoshino, Masakatsu Yanagimachi, Kazuko Hamamoto, Yozo Nakazawa, Toshihiko Imamura, Masaei Onuma, Hidetaka Niizuma, Yoji Sasahara,[...]. J Clin Immunol 2017
39
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
109
40

X-linked lymphoproliferative syndrome in mainland China: review of clinical, genetic, and immunological characteristic.
Tao Xu, Qin Zhao, Wenyan Li, Xuemei Chen, Xiuhong Xue, Zhi Chen, Xiao Du, Xiaoming Bai, Qian Zhao, Lina Zhou,[...]. Eur J Pediatr 2020
8
50

X-linked lymphoproliferative syndromes: brothers or distant cousins?
Alexandra H Filipovich, Kejian Zhang, Andrew L Snow, Rebecca A Marsh. Blood 2010
111
30

Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene.
A J Coffey, R A Brooksbank, O Brandau, T Oohashi, G R Howell, J M Bye, A P Cahn, J Durham, P Heath, P Wray,[...]. Nat Genet 1998
559
30

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
30

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
109
30

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
72
30

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
152
30


Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes.
Rebecca A Marsh, Kanchan Rao, Prakash Satwani, Kai Lehmberg, Ingo Müller, Dandan Li, Mi-Ok Kim, Alain Fischer, Sylvain Latour, Petr Sedlacek,[...]. Blood 2013
87
30

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.
Elizabeth A Worthey, Alan N Mayer, Grant D Syverson, Daniel Helbling, Benedetta B Bonacci, Brennan Decker, Jaime M Serpe, Trivikram Dasu, Michael R Tschannen, Regan L Veith,[...]. Genet Med 2011
481
30

Dysgammaglobulinemia Associated With Glu349del, a Hypomorphic XIAP Mutation.
N Nishida, X Yang, I Takasaki, K Imai, K Kato, Y Inoue, T Imamura, R Miyashita, F Kato, A Yamaide,[...]. J Investig Allergol Clin Immunol 2015
9
33


Two new families with X-linked inhibitor of apoptosis deficiency and a review of all 26 published cases.
Peter C Horn, Bernd H Belohradsky, Christian Urban, Daniela Weber-Mzell, Alfons Meindl, Volker Schuster. J Allergy Clin Immunol 2011
12
30

BIRC4 Mutation: An Important Rare Cause of Uveitis.
Matthew L Basiaga, Pamela F Weiss, Edward M Behrens. J Clin Rheumatol 2015
11
30

Successful stem cell transplant with antibody-based conditioning for XIAP deficiency with refractory hemophagocytic lymphohistiocytosis.
Austen J J Worth, Olga Nikolajeva, Robert Chiesa, Kanchan Rao, Paul Veys, Persis J Amrolia. Blood 2013
19
30

Symptomatic males and female carriers in a large Caucasian kindred with XIAP deficiency.
Magdalena Dziadzio, Sandra Ammann, Claire Canning, Fiona Boyle, Amel Hassan, Cathy Cale, Mamoun Elawad, Berthe Katrine Fiil, Mads Gyrd-Hansen, Ulrich Salzer,[...]. J Clin Immunol 2015
23
30

Different phenotypes of the same XIAP mutation in a family: A case of XIAP deficiency with juvenile idiopathic arthritis.
Mahsima Shabani, Anahita Razaghian, Hosein Alimadadi, Reza Shiari, Mohammad Shahrooei, Nima Parvaneh. Pediatr Blood Cancer 2019
5
60

Clinical phenotype and functional analysis of a rare XIAP/BIRC4 mutation.
S Vieth, S Ammann, K Schwarz, C Härtel, C Schultz, K Lehmberg, M Lauten. Klin Padiatr 2013
5
60

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
14
30

Successful Allogeneic Hematopoietic Stem Cell Transplantation in XIAP Deficiency Using Reduced-Intensity Conditioning.
Deepak Chellapandian, Joerg Krueger, Tal Schechter, Adam Gassas, Sheila Weitzman, Ahmed Naqvi, Muhammad Ali. Pediatr Blood Cancer 2016
11
30



The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency.
Martina Girardelli, Serena Arrigo, Arrigo Barabino, Claudia Loganes, Giuseppe Morreale, Sergio Crovella, Alberto Tommasini, Anna Monica Bianco. BMC Pediatr 2015
20
30

Risk-factors Associated With Poor Outcomes in VEO-IBD Secondary to XIAP Deficiency: A Case Report and Literature Review.
Asama Lekbua, Jodie Ouahed, Amy E O'Connell, Stacy A Kahn, Jeffrey D Goldsmith, Toshihiko Imamura, Christine N Duncan, Judith R Kelsen, Elizabeth Worthey, Scott B Snapper,[...]. J Pediatr Gastroenterol Nutr 2019
11
30

X-linked Inhibitor of Apoptosis Complicated by Granulomatous Lymphocytic Interstitial Lung Disease (GLILD) and Granulomatous Hepatitis.
Cathal L Steele, Matthew Doré, Sandra Ammann, Maurice Loughrey, Angeles Montero, Siobhan O Burns, Emma C Morris, Bobby Gaspar, Kimberly Gilmour, Shahnaz Bibi,[...]. J Clin Immunol 2016
16
30


Successful treatment of idiopathic colitis related to XIAP deficiency with allo-HSCT using reduced-intensity conditioning.
Yusuke Tsuma, Toshihiko Imamura, Eisuke Ichise, Kenichi Sakamoto, Kazutaka Ouchi, Shinya Osone, Hiroyuki Ishida, Taizo Wada, Hajime Hosoi. Pediatr Transplant 2015
20
30

A de novo whole gene deletion of XIAP detected by exome sequencing analysis in very early onset inflammatory bowel disease: a case report.
Judith R Kelsen, Noor Dawany, Alejandro Martinez, Christopher M Grochowski, Kelly Maurer, Eric Rappaport, David A Piccoli, Robert N Baldassano, Petar Mamula, Kathleen E Sullivan,[...]. BMC Gastroenterol 2015
32
30

XIAP deficiency syndrome in humans.
Sylvain Latour, Claire Aguilar. Semin Cell Dev Biol 2015
68
30


Allogeneic stem cell transplantation in X-linked lymphoproliferative disease: two cases in one family and review of the literature.
A C Lankester, L F A Visser, N G Hartwig, R G M Bredius, H B Gaspar, M van der Burg, M J D van Tol, T G Gross, R M Egeler. Bone Marrow Transplant 2005
33
20

Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease.
J Sumegi, D Huang, A Lanyi, J D Davis, T A Seemayer, A Maeda, G Klein, M Seri, H Wakiguchi, D T Purtilo,[...]. Blood 2000
179
20

Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome.
K E Nichols, D P Harkin, S Levitz, M Krainer, K A Kolquist, C Genovese, A Bernard, M Ferguson, L Zuo, E Snyder,[...]. Proc Natl Acad Sci U S A 1998
401
20

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
22
20

Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene.
M Arico, S Imashuku, R Clementi, S Hibi, T Teramura, C Danesino, D A Haber, K E Nichols. Blood 2001
116
20

[X-linked inhibitor of apoptosis deficiency manifested as Crohn's disease: a case report and literature review].
L J Xu, Y Y Luo, J D Yu, J G Lou, Y H Fang, J Chen. Zhonghua Er Ke Za Zhi 2018
2
100

X-linked lymphoproliferative disease: twenty-five years after the discovery.
T A Seemayer, T G Gross, R M Egeler, S J Pirruccello, J R Davis, C M Kelly, M Okano, A Lanyi, J Sumegi. Pediatr Res 1995
228
20

Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.
Huang Zhizhuo, Xu Junmei, Shen Yuelin, Qin Qiang, Liu Chunyan, Xie Zhengde, Shen Kunling. Pediatr Blood Cancer 2012
35
20

Diagnosing XLP1 in patients with hemophagocytic lymphohistiocytosis.
Raffaella Meazza, Claudia Tuberosa, Valentina Cetica, Michela Falco, Silvia Parolini, Sam Grieve, Gillian M Griffiths, Elena Sieni, Stefania Marcenaro, Concetta Micalizzi,[...]. J Allergy Clin Immunol 2014
11
20

Lymphocytic vasculitis involving the central nervous system occurs in patients with X-linked lymphoproliferative disease in the absence of Epstein-Barr virus infection.
Kawsar R Talaat, Jennifer A Rothman, Jeffrey I Cohen, Mariarita Santi, John K Choi, Miguel Guzman, Robert Zimmerman, Sudha Nallasamy, Alexander Brucker, Martha Quezado,[...]. Pediatr Blood Cancer 2009
23
20


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
106
20

IFNɣ Block, Treosulfan Conditioning and αβ T Cell Deplete PBSCT for XIAP-Deficient HLH.
Ciara O'Rafferty, Mark Velangi, Sarah Lawson, Prashant Hiwarkar, Jayashree Motwani. J Clin Immunol 2017
4
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.