A citation-based method for searching scientific literature

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
Times Cited: 152







List of co-cited articles
1056 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


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
64

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
47

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
40

HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.
Jan-Inge Henter, Annacarin Horne, Maurizio Aricó, R Maarten Egeler, Alexandra H Filipovich, Shinsaku Imashuku, Stephan Ladisch, Ken McClain, David Webb, Jacek Winiarski,[...]. Pediatr Blood Cancer 2007
35

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
256
30

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
28

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
161
28

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
29

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
36

XIAP mediates NOD signaling via interaction with RIP2.
Andreas Krieg, Ricardo G Correa, Jason B Garrison, Gaëlle Le Negrate, Kate Welsh, Ziwei Huang, Wolfram T Knoefel, John C Reed. Proc Natl Acad Sci U S A 2009
215
23

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
31

X-linked lymphoproliferative syndromes: brothers or distant cousins?
Alexandra H Filipovich, Kejian Zhang, Andrew L Snow, Rebecca A Marsh. Blood 2010
111
22

Perforin gene defects in familial hemophagocytic lymphohistiocytosis.
S E Stepp, R Dufourcq-Lagelouse, F Le Deist, S Bhawan, S Certain, P A Mathew, J I Henter, M Bennett, A Fischer, G de Saint Basile,[...]. Science 1999
855
22

Sustained elevation of serum interleukin-18 and its association with hemophagocytic lymphohistiocytosis in XIAP deficiency.
Taizo Wada, Hirokazu Kanegane, Kazuhide Ohta, Fumiyo Katoh, Toshihiko Imamura, Yozo Nakazawa, Ritsuko Miyashita, Junichi Hara, Kazuko Hamamoto, Xi Yang,[...]. Cytokine 2014
71
30

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
21

The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM.
J Sayos, C Wu, M Morra, N Wang, X Zhang, D Allen, S van Schaik, L Notarangelo, R Geha, M G Roncarolo,[...]. Nature 1998
716
20

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
20

Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).
Jérôme Feldmann, Isabelle Callebaut, Graça Raposo, Stéphanie Certain, Delphine Bacq, Cécile Dumont, Nathalie Lambert, Marie Ouachée-Chardin, Gaëlle Chedeville, Hannah Tamary,[...]. Cell 2003
624
20

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
19

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
19

An activating NLRC4 inflammasome mutation causes autoinflammation with recurrent macrophage activation syndrome.
Scott W Canna, Adriana A de Jesus, Sushanth Gouni, Stephen R Brooks, Bernadette Marrero, Yin Liu, Michael A DiMattia, Kristien J M Zaal, Gina A Montealegre Sanchez, Hanna Kim,[...]. Nat Genet 2014
382
19

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
61
29

Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH.
Kejian Zhang, Michael B Jordan, Rebecca A Marsh, Judith A Johnson, Diane Kissell, Jarek Meller, Joyce Villanueva, Kimberly A Risma, Qian Wei, Peter S Klein,[...]. Blood 2011
241
17

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11.
Udo zur Stadt, Susanne Schmidt, Brigitte Kasper, Karin Beutel, A Sarper Diler, Jan-Inge Henter, Hartmut Kabisch, Reinhard Schneppenheim, Peter Nürnberg, Gritta Janka,[...]. Hum Mol Genet 2005
373
17

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
285
17

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
345
16

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
16

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11.
Udo zur Stadt, Jan Rohr, Wenke Seifert, Florian Koch, Samantha Grieve, Julia Pagel, Julia Strauss, Brigitte Kasper, Gudrun Nürnberg, Christian Becker,[...]. Am J Hum Genet 2009
264
16

XIAP regulates cytosol-specific innate immunity to Listeria infection.
Laura D Bauler, Colin S Duckett, Mary X D O'Riordan. PLoS Pathog 2008
80
17

A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes.
Yenan T Bryceson, Daniela Pende, Andrea Maul-Pavicic, Kimberly C Gilmour, Heike Ufheil, Thomas Vraetz, Samuel C Chiang, Stefania Marcenaro, Raffaella Meazza, Ilka Bondzio,[...]. Blood 2012
179
14


Girls homozygous for an IL-2-inducible T cell kinase mutation that leads to protein deficiency develop fatal EBV-associated lymphoproliferation.
Kirsten Huck, Oliver Feyen, Tim Niehues, Franz Rüschendorf, Norbert Hübner, Hans-Jürgen Laws, Tanja Telieps, Stefan Knapp, Hans-Heinrich Wacker, Alfons Meindl,[...]. J Clin Invest 2009
188
13

Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.
G Ménasché, E Pastural, J Feldmann, S Certain, F Ersoy, S Dupuis, N Wulffraat, D Bianchi, A Fischer, F Le Deist,[...]. Nat Genet 2000
652
13

XIAP deficiency syndrome in humans.
Sylvain Latour, Claire Aguilar. Semin Cell Dev Biol 2015
68
19

X-linked IAP is a direct inhibitor of cell-death proteases.
Q L Deveraux, R Takahashi, G S Salvesen, J C Reed. Nature 1997
12

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
248
12

XIAP deficiency is a mendelian cause of late-onset IBD.
Carsten Speckmann, Stephan Ehl. Gut 2014
34
35

Second messenger role for Mg2+ revealed by human T-cell immunodeficiency.
Feng-Yen Li, Benjamin Chaigne-Delalande, Chrysi Kanellopoulou, Jeremiah C Davis, Helen F Matthews, Daniel C Douek, Jeffrey I Cohen, Gulbu Uzel, Helen C Su, Michael J Lenardo. Nature 2011
320
12

Identification of the homologous beige and Chediak-Higashi syndrome genes.
M D Barbosa, Q A Nguyen, V T Tchernev, J A Ashley, J C Detter, S M Blaydes, S J Brandt, D Chotai, C Hodgman, R C Solari,[...]. Nature 1996
379
12


Immunotherapy of familial hemophagocytic lymphohistiocytosis with antithymocyte globulins: a single-center retrospective report of 38 patients.
Nizar Mahlaoui, Marie Ouachée-Chardin, Geneviève de Saint Basile, Bénédicte Neven, Capucine Picard, Stéphane Blanche, Alain Fischer. Pediatrics 2007
147
12

cIAPs and XIAP regulate myelopoiesis through cytokine production in an RIPK1- and RIPK3-dependent manner.
W Wei-Lynn Wong, James E Vince, Najoua Lalaoui, Kate E Lawlor, Diep Chau, Aleksandra Bankovacki, Holly Anderton, Donald Metcalf, Lorraine O'Reilly, Philipp J Jost,[...]. Blood 2014
116
12

XIAP as a ubiquitin ligase in cellular signaling.
S Galbán, C S Duckett. Cell Death Differ 2010
162
12

Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
J P Hugot, M Chamaillard, H Zouali, S Lesage, J P Cézard, J Belaiche, S Almer, C Tysk, C A O'Morain, M Gassull,[...]. Nature 2001
11

Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells.
Marjorie Côte, Mickaël M Ménager, Agathe Burgess, Nizar Mahlaoui, Capucine Picard, Catherine Schaffner, Fahad Al-Manjomi, Musa Al-Harbi, Abdullah Alangari, Françoise Le Deist,[...]. J Clin Invest 2009
246
11

IAPs limit activation of RIP kinases by TNF receptor 1 during development.
Maryline Moulin, Holly Anderton, Anne K Voss, Tim Thomas, Wendy Wei-Lynn Wong, Aleksandra Bankovacki, Rebecca Feltham, Diep Chau, Wendy D Cook, John Silke,[...]. EMBO J 2012
148
11

Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases.
R M Linka, S L Risse, K Bienemann, M Werner, Y Linka, F Krux, C Synaeve, R Deenen, S Ginzel, R Dvorsky,[...]. Leukemia 2012
84
13

Combined immunodeficiency with life-threatening EBV-associated lymphoproliferative disorder in patients lacking functional CD27.
Elisabeth Salzer, Svenja Daschkey, Sharon Choo, Michael Gombert, Elisangela Santos-Valente, Sebastian Ginzel, Martina Schwendinger, Oskar A Haas, Gerhard Fritsch, Winfried F Pickl,[...]. Haematologica 2013
112
11

Salvage therapy of refractory hemophagocytic lymphohistiocytosis with alemtuzumab.
Rebecca A Marsh, Carl E Allen, Kenneth L McClain, Joanna L Weinstein, Julie Kanter, Jodi Skiles, Nadine D Lee, Shakila P Khan, Julia Lawrence, Jun Q Mo,[...]. Pediatr Blood Cancer 2013
159
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.