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
Times Cited: 152
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
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
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
Jana Pachlopnik Schmid, Danielle Canioni, Despina Moshous, Fabien Touzot, Nizar Mahlaoui, Fabian Hauck, Hirokazu Kanegane, Eduardo Lopez-Granados, Ester Mejstrikova, Isabelle Pellier,[...]. Blood 2011
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
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
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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
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
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
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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
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
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
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
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
Rebecca A Marsh, Kanchan Rao, Prakash Satwani, Kai Lehmberg, Ingo Müller, Dandan Li, Mi-Ok Kim, Alain Fischer, Sylvain Latour, Petr Sedlacek,[...]. Blood 2013
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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
Xi Yang, Hirokazu Kanegane, Naonori Nishida, Toshihiko Imamura, Kazuko Hamamoto, Ritsuko Miyashita, Kohsuke Imai, Shigeaki Nonoyama, Kazunori Sanayama, Akiko Yamaide,[...]. J Clin Immunol 2012
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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
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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
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
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X-linked lymphoproliferative syndromes: brothers or distant cousins?
Alexandra H Filipovich, Kejian Zhang, Andrew L Snow, Rebecca A Marsh. Blood 2010
Alexandra H Filipovich, Kejian Zhang, Andrew L Snow, Rebecca A Marsh. Blood 2010
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Perforin gene defects in familial hemophagocytic lymphohistiocytosis.
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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
Taizo Wada, Hirokazu Kanegane, Kazuhide Ohta, Fumiyo Katoh, Toshihiko Imamura, Yozo Nakazawa, Ritsuko Miyashita, Junichi Hara, Kazuko Hamamoto, Xi Yang,[...]. Cytokine 2014
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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
Yvonne Zeissig, Britt-Sabina Petersen, Snezana Milutinovic, Esther Bosse, Gabriele Mayr, Kenneth Peuker, Jelka Hartwig, Andreas Keller, Martina Kohl, Martin W Laass,[...]. Gut 2015
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The X-linked lymphoproliferative-disease gene product SAP regulates signals induced through the co-receptor SLAM.
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Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene.
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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
Jérôme Feldmann, Isabelle Callebaut, Graça Raposo, Stéphanie Certain, Delphine Bacq, Cécile Dumont, Nathalie Lambert, Marie Ouachée-Chardin, Gaëlle Chedeville, Hannah Tamary,[...]. Cell 2003
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
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
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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
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
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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
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
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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
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
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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
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
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
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
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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
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
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
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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
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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
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XIAP regulates cytosol-specific innate immunity to Listeria infection.
Laura D Bauler, Colin S Duckett, Mary X D O'Riordan. PLoS Pathog 2008
Laura D Bauler, Colin S Duckett, Mary X D O'Riordan. PLoS Pathog 2008
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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
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
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An animal model of hemophagocytic lymphohistiocytosis (HLH): CD8+ T cells and interferon gamma are essential for the disorder.
Michael B Jordan, David Hildeman, John Kappler, Philippa Marrack. Blood 2004
Michael B Jordan, David Hildeman, John Kappler, Philippa Marrack. Blood 2004
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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
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
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Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.
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X-linked IAP is a direct inhibitor of cell-death proteases.
Q L Deveraux, R Takahashi, G S Salvesen, J C Reed. Nature 1997
Q L Deveraux, R Takahashi, G S Salvesen, J C Reed. Nature 1997
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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
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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
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Identification of the homologous beige and Chediak-Higashi syndrome genes.
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X-linked lymphoproliferative disease. 2B4 molecules displaying inhibitory rather than activating function are responsible for the inability of natural killer cells to kill Epstein-Barr virus-infected cells.
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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
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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
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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease.
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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
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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
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Loss-of-function mutations within the IL-2 inducible kinase ITK in patients with EBV-associated lymphoproliferative diseases.
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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
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
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Salvage therapy of refractory hemophagocytic lymphohistiocytosis with alemtuzumab.
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X-linked inhibitor of apoptosis protein deficiency: more than an X-linked lymphoproliferative syndrome.
Claire Aguilar, Sylvain Latour. J Clin Immunol 2015
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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.