A citation-based method for searching scientific literature

Early defects in human T-cell development severely affect distribution and maturation of thymic stromal cells: possible implications for the pathophysiology of Omenn syndrome.
Pietro Luigi Poliani, Fabio Facchetti, Maria Ravanini, Andrew Richard Gennery, Anna Villa, Chaim M Roifman, Luigi D Notarangelo. Blood 2009
Times Cited: 96






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List of co-cited articles
1104 articles co-cited >1



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  Times     Co-cited
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AIRE deficiency in thymus of 2 patients with Omenn syndrome.
Patrizia Cavadini, William Vermi, Fabio Facchetti, Stefania Fontana, Seiho Nagafuchi, Evelina Mazzolari, Anna Sediva, Veronica Marrella, Anna Villa, Alain Fischer,[...]. J Clin Invest 2005
109
30
31

A hypomorphic R229Q Rag2 mouse mutant recapitulates human Omenn syndrome.
Veronica Marrella, Pietro Luigi Poliani, Anna Casati, Francesca Rucci, Laura Frascoli, Marie-Lise Gougeon, Brigitte Lemercier, Marita Bosticardo, Maria Ravanini, Manuela Battaglia,[...]. J Clin Invest 2007
78
22
28

Partial V(D)J recombination activity leads to Omenn syndrome.
A Villa, S Santagata, F Bozzi, S Giliani, A Frattini, L Imberti, L B Gatta, H D Ochs, K Schwarz, L D Notarangelo,[...]. Cell 1998
308
21
21

An immunodeficiency disease with RAG mutations and granulomas.
Catharina Schuetz, Kirsten Huck, Sonja Gudowius, Mosaad Megahed, Oliver Feyen, Bernd Hubner, Dominik T Schneider, Burkhard Manfras, Ulrich Pannicke, Rein Willemze,[...]. N Engl J Med 2008
147
20
20

Expansion of immunoglobulin-secreting cells and defects in B cell tolerance in Rag-dependent immunodeficiency.
Jolan E Walter, Francesca Rucci, Laura Patrizi, Mike Recher, Stephan Regenass, Tiziana Paganini, Marton Keszei, Itai Pessach, Philipp A Lang, Pietro Luigi Poliani,[...]. J Exp Med 2010
68
20
29

V(D)J recombination defects in lymphocytes due to RAG mutations: severe immunodeficiency with a spectrum of clinical presentations.
A Villa, C Sobacchi, L D Notarangelo, F Bozzi, M Abinun, T G Abrahamsen, P D Arkwright, M Baniyash, E G Brooks, M E Conley,[...]. Blood 2001
243
19
19

Projection of an immunological self shadow within the thymus by the aire protein.
Mark S Anderson, Emily S Venanzi, Ludger Klein, Zhibin Chen, Stuart P Berzins, Shannon J Turley, Harald von Boehmer, Roderick Bronson, Andrée Dierich, Christophe Benoist,[...]. Science 2002
1605
18
18

Defect of regulatory T cells in patients with Omenn syndrome.
Barbara Cassani, Pietro Luigi Poliani, Daniele Moratto, Cristina Sobacchi, Veronica Marrella, Laura Imperatori, Donatella Vairo, Alessandro Plebani, Silvia Giliani, Paolo Vezzoni,[...]. J Allergy Clin Immunol 2010
54
18
33

Homeostatic expansion of autoreactive immunoglobulin-secreting cells in the Rag2 mouse model of Omenn syndrome.
Barbara Cassani, Pietro Luigi Poliani, Veronica Marrella, Francesca Schena, Aisha V Sauer, Maria Ravanini, Dario Strina, Christian E Busse, Stephan Regenass, Hedda Wardemann,[...]. J Exp Med 2010
48
17
35

Hypomorphic Rag mutations can cause destructive midline granulomatous disease.
Suk See De Ravin, Edward W Cowen, Kol A Zarember, Narda L Whiting-Theobald, Douglas B Kuhns, Netanya G Sandler, Daniel C Douek, Stefania Pittaluga, Pietro L Poliani, Yu Nee Lee,[...]. Blood 2010
81
17
20

A novel immunodeficiency associated with hypomorphic RAG1 mutations and CMV infection.
Jean-Pierre de Villartay, Annick Lim, Hamoud Al-Mousa, Sophie Dupont, Julie Déchanet-Merville, Edith Coumau-Gatbois, Marie-Lise Gougeon, Arnaud Lemainque, Céline Eidenschenk, Emmanuelle Jouanguy,[...]. J Clin Invest 2005
136
16
16

Hassall's corpuscles instruct dendritic cells to induce CD4+CD25+ regulatory T cells in human thymus.
Norihiko Watanabe, Yi-Hong Wang, Heung Kyu Lee, Tomoki Ito, Yui-Hsi Wang, Wei Cao, Yong-Jun Liu. Nature 2005
524
14
14

Intrathymic restriction and peripheral expansion of the T-cell repertoire in Omenn syndrome.
S Signorini, L Imberti, S Pirovano, A Villa, F Facchetti, M Ungari, F Bozzi, A Albertini, A G Ugazio, P Vezzoni,[...]. Blood 1999
68
14
20

A variant of SCID with specific immune responses and predominance of gamma delta T cells.
Stephan Ehl, Klaus Schwarz, Anselm Enders, Ulrich Duffner, Ulrich Pannicke, Joachim Kühr, Françoise Mascart, Annette Schmitt-Graeff, Charlotte Niemeyer, Paul Fisch. J Clin Invest 2005
109
14
14

Omenn syndrome: inflammation in leaky severe combined immunodeficiency.
Anna Villa, Luigi D Notarangelo, Chaim M Roifman. J Allergy Clin Immunol 2008
137
14
14

RAG mutations in human B cell-negative SCID.
K Schwarz, G H Gauss, L Ludwig, U Pannicke, Z Li, D Lindner, W Friedrich, R A Seger, T E Hansen-Hagge, S Desiderio,[...]. Science 1996
357
14
14

The tumor necrosis factor family receptors RANK and CD40 cooperatively establish the thymic medullary microenvironment and self-tolerance.
Taishin Akiyama, Yusuke Shimo, Hiromi Yanai, Junwen Qin, Daisuke Ohshima, Yuya Maruyama, Yukiko Asaumi, Juli Kitazawa, Hiroshi Takayanagi, Josef M Penninger,[...]. Immunity 2008
340
13
13

FAMILIAL RETICULOENDOTHELIOSIS WITH EOSINOPHILIA.
G S OMENN. N Engl J Med 1965
246
13
13

Journey through the thymus: stromal guides for T-cell development and selection.
Yousuke Takahama. Nat Rev Immunol 2006
442
12
12

A central role for central tolerance.
Bruno Kyewski, Ludger Klein. Annu Rev Immunol 2006
511
11
11

Identical mutations in RAG1 or RAG2 genes leading to defective V(D)J recombinase activity can cause either T-B-severe combined immune deficiency or Omenn syndrome.
B Corneo, D Moshous, T Güngör, N Wulffraat, P Philippet, F L Le Deist, A Fischer, J P de Villartay. Blood 2001
145
11
11

A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency.
Yu Nee Lee, Francesco Frugoni, Kerry Dobbs, Jolan E Walter, Silvia Giliani, Andrew R Gennery, Waleed Al-Herz, Elie Haddad, Francoise LeDeist, Jack H Bleesing,[...]. J Allergy Clin Immunol 2014
91
11
12

The cellular mechanism of Aire control of T cell tolerance.
Mark S Anderson, Emily S Venanzi, Zhibin Chen, Stuart P Berzins, Christophe Benoist, Diane Mathis. Immunity 2005
427
10
10

RAG-dependent primary immunodeficiencies.
Cristina Sobacchi, Veronica Marrella, Francesca Rucci, Paolo Vezzoni, Anna Villa. Hum Mutat 2006
85
10
11

Review of 54 patients with complete DiGeorge anomaly enrolled in protocols for thymus transplantation: outcome of 44 consecutive transplants.
M Louise Markert, Blythe H Devlin, Marilyn J Alexieff, Jie Li, Elizabeth A McCarthy, Stephanie E Gupton, Ivan K Chinn, Laura P Hale, Thomas B Kepler, Min He,[...]. Blood 2007
140
10
10

Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly.
Dietke Buck, Laurent Malivert, Régina de Chasseval, Anne Barraud, Marie-Claude Fondanèche, Ozden Sanal, Alessandro Plebani, Jean-Louis Stéphan, Markus Hufnagel, Françoise le Deist,[...]. Cell 2006
512
10
10

Mutations in CHD7 in patients with CHARGE syndrome cause T-B + natural killer cell + severe combined immune deficiency and may cause Omenn-like syndrome.
A R Gennery, M A Slatter, J Rice, L H Hoefsloot, D Barge, A McLean-Tooke, T Montgomery, J A Goodship, A D Burt, T J Flood,[...]. Clin Exp Immunol 2008
71
10
14

An autoimmune disease, APECED, caused by mutations in a novel gene featuring two PHD-type zinc-finger domains.
. Nat Genet 1997
836
10
10

Idiopathic CD4+ T lymphopenia without autoimmunity or granulomatous disease in the slipstream of RAG mutations.
Taco W Kuijpers, Hanna Ijspeert, Ester M M van Leeuwen, Machiel H Jansen, Mette D Hazenberg, Kees C Weijer, Rene A W van Lier, Mirjam van der Burg. Blood 2011
77
10
12

The cytokine RANKL produced by positively selected thymocytes fosters medullary thymic epithelial cells that express autoimmune regulator.
Yu Hikosaka, Takeshi Nitta, Izumi Ohigashi, Kouta Yano, Naozumi Ishimaru, Yoshio Hayashi, Mitsuru Matsumoto, Koichi Matsuo, Josef M Penninger, Hiroshi Takayanagi,[...]. Immunity 2008
308
9
9

Autoantigen-specific interactions with CD4+ thymocytes control mature medullary thymic epithelial cell cellularity.
Magali Irla, Stéphanie Hugues, Jason Gill, Takeshi Nitta, Yu Hikosaka, Ifor R Williams, François-Xavier Hubert, Hamish S Scott, Yousuke Takahama, Georg A Holländer,[...]. Immunity 2008
181
9
9

Omenn syndrome due to ARTEMIS mutations.
Markus Ege, Yunmei Ma, Burkhard Manfras, Krzysztof Kalwak, Haihui Lu, Michael R Lieber, Klaus Schwarz, Ulrich Pannicke. Blood 2005
144
9
9

A DNA-PKcs mutation in a radiosensitive T-B- SCID patient inhibits Artemis activation and nonhomologous end-joining.
Mirjam van der Burg, Hanna Ijspeert, Nicole S Verkaik, Tuba Turul, Wouter W Wiegant, Keiko Morotomi-Yano, Pierre-Olivier Mari, Ilhan Tezcan, David J Chen, Malgorzata Z Zdzienicka,[...]. J Clin Invest 2009
181
9
9

Gene therapy for immunodeficiency due to adenosine deaminase deficiency.
Alessandro Aiuti, Federica Cattaneo, Stefania Galimberti, Ulrike Benninghoff, Barbara Cassani, Luciano Callegaro, Samantha Scaramuzza, Grazia Andolfi, Massimiliano Mirolo, Immacolata Brigida,[...]. N Engl J Med 2009
669
9
9

Highly restricted human T cell repertoire in peripheral blood and tissue-infiltrating lymphocytes in Omenn's syndrome.
F Rieux-Laucat, P Bahadoran, N Brousse, F Selz, A Fischer, F Le Deist, J P De Villartay. J Clin Invest 1998
59
9
15

Omenn syndrome is associated with mutations in DNA ligase IV.
Eyal Grunebaum, Andrea Bates, Chaim M Roifman. J Allergy Clin Immunol 2008
72
9
12

Homeostatically proliferating CD4 T cells are involved in the pathogenesis of an Omenn syndrome murine model.
Khie Khiong, Masaaki Murakami, Chika Kitabayashi, Naoko Ueda, Shin-ichiro Sawa, Akemi Sakamoto, Brian L Kotzin, Stephen J Rozzo, Katsuhiko Ishihara, Marileila Verella-Garcia,[...]. J Clin Invest 2007
57
9
15

Thymus microenvironment in human primary immunodeficiency diseases.
Pietro Luigi Poliani, William Vermi, Fabio Facchetti. Curr Opin Allergy Clin Immunol 2009
16
9
56

Positional cloning of the APECED gene.
K Nagamine, P Peterson, H S Scott, J Kudoh, S Minoshima, M Heino, K J Krohn, M D Lalioti, P E Mullis, S E Antonarakis,[...]. Nat Genet 1997
923
9
9

Transplantation of hematopoietic stem cells and long-term survival for primary immunodeficiencies in Europe: entering a new century, do we do better?
Andrew R Gennery, Mary A Slatter, Laure Grandin, Pierre Taupin, Andrew J Cant, Paul Veys, Persis J Amrolia, H Bobby Gaspar, E Graham Davies, Wilhelm Friedrich,[...]. J Allergy Clin Immunol 2010
276
9
9

Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome).
G de Saint-Basile, F Le Deist, J P de Villartay, N Cerf-Bensussan, O Journet, N Brousse, C Griscelli, A Fischer. J Clin Invest 1991
125
9
9

Abnormalities of thymic stroma may contribute to immune dysregulation in murine models of leaky severe combined immunodeficiency.
Francesca Rucci, Pietro Luigi Poliani, Stefano Caraffi, Tiziana Paganini, Elena Fontana, Silvia Giliani, Frederick W Alt, Luigi Daniele Notarangelo. Front Immunol 2011
22
9
40

Anti-CD3ε mAb improves thymic architecture and prevents autoimmune manifestations in a mouse model of Omenn syndrome: therapeutic implications.
Veronica Marrella, Pietro L Poliani, Elena Fontana, Anna Casati, Virginia Maina, Barbara Cassani, Francesca Ficara, Manuela Cominelli, Francesca Schena, Marianna Paulis,[...]. Blood 2012
19
9
47

Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience.
William T Shearer, Elizabeth Dunn, Luigi D Notarangelo, Christopher C Dvorak, Jennifer M Puck, Brent R Logan, Linda M Griffith, Donald B Kohn, Richard J O'Reilly, Thomas A Fleisher,[...]. J Allergy Clin Immunol 2014
170
9
9

Exposing the human nude phenotype.
J Frank, C Pignata, A A Panteleyev, D M Prowse, H Baden, L Weiner, L Gaetaniello, W Ahmad, N Pozzi, P B Cserhalmi-Friedman,[...]. Nature 1999
185
8
8

Aire.
Diane Mathis, Christophe Benoist. Annu Rev Immunol 2009
425
8
8

Unravelling the association of partial T-cell immunodeficiency and immune dysregulation.
Adrian Liston, Anselm Enders, Owen M Siggs. Nat Rev Immunol 2008
92
8
8

The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency.
Lawrence R Shiow, David W Roadcap, Kenneth Paris, Susan R Watson, Irina L Grigorova, Tonya Lebet, Jinping An, Ying Xu, Craig N Jenne, Niko Föger,[...]. Nat Immunol 2008
164
8
8

Leaky severe combined immunodeficiency and aberrant DNA rearrangements due to a hypomorphic RAG1 mutation.
William Giblin, Monalisa Chatterji, Gerwin Westfield, Tehmina Masud, Brian Theisen, Hwei-Ling Cheng, Jeffrey DeVido, Frederick W Alt, David O Ferguson, David G Schatz,[...]. Blood 2009
37
8
21

Reduced central tolerance in Omenn syndrome leads to immature self-reactive oligoclonal T cells.
Raz Somech, Amos J Simon, Atar Lev, Ilan Dalal, Zvi Spirer, Itamar Goldstein, Meital Nagar, Ninette Amariglio, Gideon Rechavi, Chaim M Roifman. J Allergy Clin Immunol 2009
35
8
22


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.

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