A citation-based method for searching scientific literature

I Kobayashi, R Shiari, M Yamada, N Kawamura, M Okano, A Yara, A Iguchi, N Ishikawa, T Ariga, Y Sakiyama, H D Ochs, K Kobayashi. J Med Genet 2001
Times Cited: 84







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



Times Cited
  Times     Co-cited
Similarity


The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3.
C L Bennett, J Christie, F Ramsdell, M E Brunkow, P J Ferguson, L Whitesell, T E Kelly, F T Saulsbury, P F Chance, H D Ochs. Nat Genet 2001
80

X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.
R S Wildin, F Ramsdell, J Peake, F Faravelli, J L Casanova, N Buist, E Levy-Lahad, M Mazzella, O Goulet, L Perroni,[...]. Nat Genet 2001
66


JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome.
T A Chatila, F Blaeser, N Ho, H M Lederman, C Voulgaropoulos, C Helms, A M Bowcock. J Clin Invest 2000
625
53

Foxp3 programs the development and function of CD4+CD25+ regulatory T cells.
Jason D Fontenot, Marc A Gavin, Alexander Y Rudensky. Nat Immunol 2003
52

Control of regulatory T cell development by the transcription factor Foxp3.
Shohei Hori, Takashi Nomura, Shimon Sakaguchi. Science 2003
50

Disruption of a new forkhead/winged-helix protein, scurfin, results in the fatal lymphoproliferative disorder of the scurfy mouse.
M E Brunkow, E W Jeffery, K A Hjerrild, B Paeper, L B Clark, S A Yasayko, J E Wilkinson, D Galas, S F Ziegler, F Ramsdell. Nat Genet 2001
47


Treatment of the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) by allogeneic bone marrow transplantation.
O Baud, O Goulet, D Canioni, F Le Deist, I Radford, D Rieu, S Dupuis-Girod, N Cerf-Bensussan, M Cavazzana-Calvo, N Brousse,[...]. N Engl J Med 2001
160
35

An essential role for Scurfin in CD4+CD25+ T regulatory cells.
Roli Khattri, Tom Cox, Sue-Ann Yasayko, Fred Ramsdell. Nat Immunol 2003
35

A rare polyadenylation signal mutation of the FOXP3 gene (AAUAAA-->AAUGAA) leads to the IPEX syndrome.
C L Bennett, M E Brunkow, F Ramsdell, K C O'Briant, Q Zhu, R L Fuleihan, A O Shigeoka, H D Ochs, P F Chance. Immunogenetics 2001
167
34

Defective regulatory and effector T cell functions in patients with FOXP3 mutations.
Rosa Bacchetta, Laura Passerini, Eleonora Gambineri, Minyue Dai, Sarah E Allan, Lucia Perroni, Franca Dagna-Bricarelli, Claudia Sartirana, Susanne Matthes-Martin, Anita Lawitschka,[...]. J Clin Invest 2006
350
33

Successful bone marrow transplantation for IPEX syndrome after reduced-intensity conditioning.
Aarati Rao, Naynesh Kamani, Alexandra Filipovich, Susan Molleran Lee, Stella M Davies, Jignesh Dalal, Shalini Shenoy. Blood 2007
109
30


Mutational analysis of the FOXP3 gene and evidence for genetic heterogeneity in the immunodysregulation, polyendocrinopathy, enteropathy syndrome.
Catherine J Owen, Claire E Jennings, Helen Imrie, Alain Lachaux, Nicola A Bridges, Tim D Cheetham, Simon H S Pearce. J Clin Endocrinol Metab 2003
85
26

Scurfin (FOXP3) acts as a repressor of transcription and regulates T cell activation.
L A Schubert, E Jeffery, Y Zhang, F Ramsdell, S F Ziegler. J Biol Chem 2001
407
25

Dermatologic and immunologic findings in the immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
David S Nieves, Richard P Phipps, Stephen J Pollock, Hans D Ochs, Qili Zhu, Glynis A Scott, Charlotte K Ryan, Ichiro Kobayashi, Thomas M Rossi, Lowell A Goldsmith. Arch Dermatol 2004
82
25

Clinical and molecular profile of a new series of patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome: inconsistent correlation between forkhead box protein 3 expression and disease severity.
Eleonora Gambineri, Lucia Perroni, Laura Passerini, Lucia Bianchi, Claudio Doglioni, Franco Meschi, Riccardo Bonfanti, Yves Sznajer, Alberto Tommasini, Anita Lawitschka,[...]. J Allergy Clin Immunol 2008
144
25

X-Linked syndrome of polyendocrinopathy, immune dysfunction, and diarrhea maps to Xp11.23-Xq13.3.
C L Bennett, R Yoshioka, H Kiyosawa, D F Barker, P R Fain, A O Shigeoka, P F Chance. Am J Hum Genet 2000
59
32

Induction of FoxP3 and acquisition of T regulatory activity by stimulated human CD4+CD25- T cells.
Mindi R Walker, Deborah J Kasprowicz, Vivian H Gersuk, Angele Benard, Megan Van Landeghen, Jane H Buckner, Steven F Ziegler. J Clin Invest 2003
964
22

Single-cell analysis of normal and FOXP3-mutant human T cells: FOXP3 expression without regulatory T cell development.
Marc A Gavin, Troy R Torgerson, Evan Houston, Paul DeRoos, William Y Ho, Asbjørg Stray-Pedersen, Elizabeth L Ocheltree, Philip D Greenberg, Hans D Ochs, Alexander Y Rudensky. Proc Natl Acad Sci U S A 2006
606
22


FOXP3: of mice and men.
Steven F Ziegler. Annu Rev Immunol 2006
742
21

FOXP3 controls regulatory T cell function through cooperation with NFAT.
Yongqing Wu, Madhuri Borde, Vigo Heissmeyer, Markus Feuerer, Ariya D Lapan, James C Stroud, Darren L Bates, Liang Guo, Aidong Han, Steven F Ziegler,[...]. Cell 2006
815
21

Severe food allergy as a variant of IPEX syndrome caused by a deletion in a noncoding region of the FOXP3 gene.
Troy R Torgerson, Avriel Linane, Nicolette Moes, Stephanie Anover, Véronique Mateo, Frédéric Rieux-Laucat, Olivier Hermine, Shashi Vijay, Eleonora Gambineri, Nadine Cerf-Bensussan,[...]. Gastroenterology 2007
163
21

Manifestations and linkage analysis in X-linked autoimmunity-immunodeficiency syndrome.
P J Ferguson, S H Blanton, F T Saulsbury, M J McDuffie, V Lemahieu, J M Gastier, U Francke, S M Borowitz, J L Sutphen, T E Kelly. Am J Med Genet 2000
62
27

Successful use of the new immune-suppressor sirolimus in IPEX (immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome).
Lutz Bindl, Troy Torgerson, Lucia Perroni, Nelly Youssef, Hans D Ochs, Olivier Goulet, Frank M Ruemmele. J Pediatr 2005
74
22

Immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome: an unusual cause of proteinuria in infancy.
Asha Moudgil, Paige Perriello, Brett Loechelt, Ronald Przygodzki, Wendy Fitzerald, Naynesh Kamani. Pediatr Nephrol 2007
28
60

Mechanistic associations of a mild phenotype of immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome.
Fabrizio De Benedetti, Antonella Insalaco, Antonella Diamanti, Elisabetta Cortis, Flaminia Muratori, Andrea Lamioni, Rita Carsetti, Roberto Cusano, Rita De Vito, Lucia Perroni,[...]. Clin Gastroenterol Hepatol 2006
40
40

Clinical and molecular findings in IPEX syndrome.
A K Myers, L Perroni, C Costigan, W Reardon. Arch Dis Child 2006
34
47

Developmental changes of FOXP3-expressing CD4+CD25+ regulatory T cells and their impairment in patients with FOXP3 gene mutations.
Tatsuya Fuchizawa, Yuichi Adachi, Yasunori Ito, Hiroyuki Higashiyama, Hirokazu Kanegane, Takeshi Futatani, Ichiro Kobayashi, Yoshiro Kamachi, Tatsuo Sakamoto, Ikuya Tsuge,[...]. Clin Immunol 2007
41
39

Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.
Oscar Rubio-Cabezas, Jayne A L Minton, Richard Caswell, Julian P Shield, Dorothee Deiss, Zdenek Sumnik, Amely Cayssials, Mathias Herr, Anja Loew, Vaughan Lewis,[...]. Diabetes Care 2009
72
22

Minimal change nephrotic syndrome associated with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Yuya Hashimura, Kandai Nozu, Hirokazu Kanegane, Toshio Miyawaki, Akira Hayakawa, Norishige Yoshikawa, Koichi Nakanishi, Minoru Takemoto, Kazumoto Iijima, Masafumi Matsuo. Pediatr Nephrol 2009
53
30

Crucial role of FOXP3 in the development and function of human CD25+CD4+ regulatory T cells.
Haruhiko Yagi, Takashi Nomura, Kyoko Nakamura, Sayuri Yamazaki, Toshio Kitawaki, Shohei Hori, Michiyuki Maeda, Masafumi Onodera, Takashi Uchiyama, Shingo Fujii,[...]. Int Immunol 2004
623
17

The role of 2 FOXP3 isoforms in the generation of human CD4+ Tregs.
Sarah E Allan, Laura Passerini, Rosa Bacchetta, Natasha Crellin, Minyue Dai, Paul C Orban, Steven F Ziegler, Maria Grazia Roncarolo, Megan K Levings. J Clin Invest 2005
339
17

Analysis of FOXP3 reveals multiple domains required for its function as a transcriptional repressor.
Jared E Lopes, Troy R Torgerson, Lisa A Schubert, Stephanie D Anover, Elizabeth L Ocheltree, Hans D Ochs, Steven F Ziegler. J Immunol 2006
193
17

A 75-kD autoantigen recognized by sera from patients with X-linked autoimmune enteropathy associated with nephropathy.
I Kobayashi, K Imamura, M Yamada, M Okano, A Yara, S Ikema, N Ishikawa. Clin Exp Immunol 1998
62
22

X-linked immune dysregulation, neonatal insulin dependent diabetes, and intractable diarrhoea.
J E Peake, R B McCrossin, G Byrne, R Shepherd. Arch Dis Child Fetal Neonatal Ed 1996
43
32


A new case of IPEX receiving bone marrow transplantation.
E Mazzolari, C Forino, M Fontana, C D'Ippolito, A Lanfranchi, E Gambineri, H Ochs, R Badolato, L D Notarangelo. Bone Marrow Transplant 2005
47
29

A potential screening tool for IPEX syndrome.
Meredith Lee Heltzer, John K Choi, Hans D Ochs, Kathleen E Sullivan, Troy R Torgerson, Linda M Ernst. Pediatr Dev Pathol 2007
29
48

Cutaneous manifestations of immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) syndrome.
M Halabi-Tawil, F M Ruemmele, S Fraitag, F Rieux-Laucat, B Neven, N Brousse, Y De Prost, A Fischer, O Goulet, C Bodemer. Br J Dermatol 2009
70
20

Stable hematopoietic cell engraftment after low-intensity nonmyeloablative conditioning in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Lauri M Burroughs, Troy R Torgerson, Rainer Storb, Paul A Carpenter, David J Rawlings, Jean Sanders, Andrew M Scharenberg, Suzanne Skoda-Smith, Janet Englund, Hans D Ochs,[...]. J Allergy Clin Immunol 2010
43
32


Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) associated with pemphigoid nodularis: a case report and review of the literature.
Jamie L McGinness, Mary-Margaret C Bivens, Kenneth E Greer, James W Patterson, Frank T Saulsbury. J Am Acad Dermatol 2006
58
22

Digestive histopathological presentation of IPEX syndrome.
Natacha Patey-Mariaud de Serre, Danielle Canioni, Soléne Ganousse, Frédéric Rieux-Laucat, Olivier Goulet, Frank Ruemmele, Nicole Brousse. Mod Pathol 2009
76
17

Reduced expression of FOXP3 and regulatory T-cell function in severe forms of early-onset autoimmune enteropathy.
Nicolette Moes, Frédéric Rieux-Laucat, Bernadette Begue, Julien Verdier, Bénédicte Neven, Natacha Patey, Troy T Torgerson, Capucine Picard, Marie-Claude Stolzenberg, Corinne Ruemmele,[...]. Gastroenterology 2010
69
18

The spectrum of autoantibodies in IPEX syndrome is broad and includes anti-mitochondrial autoantibodies.
Masanobu Tsuda, Troy R Torgerson, Carlo Selmi, Eleonora Gambineri, Magda Carneiro-Sampaio, Sara Ciullini Mannurita, Patrick S C Leung, Gary L Norman, M Eric Gershwin. J Autoimmun 2010
69
18

Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Keisuke Otsubo, Hirokazu Kanegane, Yoshiro Kamachi, Ichiro Kobayashi, Ikuya Tsuge, Masue Imaizumi, Yoji Sasahara, Akira Hayakawa, Kandai Nozu, Kazumoto Iijima,[...]. Clin Immunol 2011
40
32

Cellular and molecular characterization of the scurfy mouse mutant.
L B Clark, M W Appleby, M E Brunkow, J E Wilkinson, S F Ziegler, F Ramsdell. J Immunol 1999
156
14


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.