A citation-based method for searching scientific literature

Johnson Nameirakpam, Rashmi Rikhi, Sanjay Singh Rawat, Jyoti Sharma, Deepti Suri. Genes Dis 2019
Times Cited: 3







List of co-cited articles
32 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
66


CRISPR-based gene editing enables FOXP3 gene repair in IPEX patient cells.
M Goodwin, E Lee, U Lakshmanan, S Shipp, L Froessl, F Barzaghi, L Passerini, M Narula, A Sheikali, C M Lee,[...]. Sci Adv 2020
24
66

Point mutants of forkhead box P3 that cause immune dysregulation, polyendocrinopathy, enteropathy, X-linked have diverse abilities to reprogram T cells into regulatory T cells.
Alicia N McMurchy, Jana Gillies, Sarah E Allan, Laura Passerini, Eleonora Gambineri, Maria Grazia Roncarolo, Rosa Bacchetta, Megan K Levings. J Allergy Clin Immunol 2010
36
66

Severe gastritis in an insulin-dependent child with an IPEX syndrome.
M Scaillon, S Van Biervliet, P Bontems, H Dorchy, L Hanssens, A Ferster, V Segers, S Cadranel. J Pediatr Gastroenterol Nutr 2009
18
66

Late-onset of immunodysregulation, polyendocrinopathy, enteropathy, x-linked syndrome (IPEX) with intractable diarrhea.
Daniele Zama, Ilaria Cocchi, Riccardo Masetti, Fernando Specchia, Patrizia Alvisi, Eleonora Gambineri, Mario Lima, Andrea Pession. Ital J Pediatr 2014
17
66

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
66

From IPEX syndrome to FOXP3 mutation: a lesson on immune dysregulation.
Rosa Bacchetta, Federica Barzaghi, Maria-Grazia Roncarolo. Ann N Y Acad Sci 2018
140
66

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
66

Novel mutations of FOXP3 in two Japanese patients with immune dysregulation, polyendocrinopathy, enteropathy, X linked syndrome (IPEX).
I Kobayashi, R Shiari, M Yamada, N Kawamura, M Okano, A Yara, A Iguchi, N Ishikawa, T Ariga, Y Sakiyama,[...]. J Med Genet 2001
84
66


Clinical, Immunological, and Genetic Features in Patients with Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) and IPEX-like Syndrome.
Mahnaz Jamee, Majid Zaki-Dizaji, Bernice Lo, Hassan Abolhassani, Fatemeh Aghamahdi, Mehdi Mosavian, Zohreh Nademi, Hamed Mohammadi, Farhad Jadidi-Niaragh, Manuel Rojas,[...]. J Allergy Clin Immunol Pract 2020
12
66


Renal involvement in the immunodysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) disorder.
Yuri Sheikine, Craig B Woda, Pui Y Lee, Talal A Chatila, Sevgi Keles, Louis-Marie Charbonnier, Birgitta Schmidt, Seymour Rosen, Nancy M Rodig. Pediatr Nephrol 2015
18
66

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
66

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
66

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
66

Suppression by human FOXP3+ regulatory T cells requires FOXP3-TIP60 interactions.
Khalid Bin Dhuban, Eva d'Hennezel, Yasuhiro Nagai, Yan Xiao, Steven Shao, Roman Istomine, Fernando Alvarez, Moshe Ben-Shoshan, Hans Ochs, Bruce Mazer,[...]. Sci Immunol 2017
29
66

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
66

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
66

Use of sirolimus in IPEX and IPEX-like children.
Pierre L Yong, Pierre Russo, Kathleen E Sullivan. J Clin Immunol 2008
69
66

Long-term follow-up of IPEX syndrome patients after different therapeutic strategies: An international multicenter retrospective study.
Federica Barzaghi, Laura Cristina Amaya Hernandez, Benedicte Neven, Silvia Ricci, Zeynep Yesim Kucuk, Jack J Bleesing, Zohreh Nademi, Mary Anne Slatter, Erlinda Rose Ulloa, Anna Shcherbina,[...]. J Allergy Clin Immunol 2018
105
66

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
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
66

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
66

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
66

Clinical heterogeneity of immunodysregulation, polyendocrinopathy, enteropathy, X-linked: pulmonary involvement as a non-classical disease manifestation.
Safa Baris, Ilka Schulze, Ahmet Ozen, Elif Karakoç Aydıner, Emel Altuncu, Gulsun Tezcan Karasu, Nilufer Ozturk, Myriam Lorenz, Klaus Schwarz, Thomas Vraetz,[...]. J Clin Immunol 2014
23
66

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
66

Clinical, Immunological, and Molecular Heterogeneity of 173 Patients With the Phenotype of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked (IPEX) Syndrome.
Eleonora Gambineri, Sara Ciullini Mannurita, David Hagin, Marina Vignoli, Stephanie Anover-Sombke, Stacey DeBoer, Gesmar R S Segundo, Eric J Allenspach, Claudio Favre, Hans D Ochs,[...]. Front Immunol 2018
58
66

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
66

Clinical Heterogeneity of Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome: A French Multicenter Retrospective Study.
R Duclaux-Loras, F Charbit-Henrion, B Neven, J Nowak, S Collardeau-Frachon, C Malcus, P F Ray, D Moshous, J Beltrand, O Goulet,[...]. Clin Transl Gastroenterol 2018
14
66


Current status and prospects of primary immunodeficiency diseases in Asia.
Rakesh Kumar Pilania, Himanshi Chaudhary, Ankur Kumar Jindal, Amit Rawat, Surjit Singh. Genes Dis 2019
10
33

Recent advances in chronic granulomatous disease.
Gummadi Anjani, Pandiarajan Vignesh, Vibhu Joshi, Jitendra Kumar Shandilya, Dharmagat Bhattarai, Jyoti Sharma, Amit Rawat. Genes Dis 2019
9
33

Selective immunoglobulin A deficiency (SIgAD) primarily leads to recurrent infections and autoimmune diseases: A retrospective study of Chinese patients in the past 40 years.
Wei Wang, Tianhao Yao, Tianyi Zhang, Meiying Quan, Changyan Wang, Chen Wang, Lejia Zhang, Xiaoyan Tang, Shan Jian, Hongmei Song. Genes Dis 2019
2
50

Clinical phenotype of a Chinese patient with RIPK1 deficiency due to novel mutation.
Li Lin, Ying Wang, Luyao Liu, Wenjing Ying, Wenjie Wang, Bijun Sun, Jinqiao Sun, Xiaochuan Wang. Genes Dis 2019
5
33

Leukocyte adhesion defect: Where do we stand circa 2019?
Jhumki Das, Avinash Sharma, Ankur Jindal, Vaishali Aggarwal, Amit Rawat. Genes Dis 2019
9
33

Transcriptomic changes associated with PCK1 overexpression in hepatocellular carcinoma cells detected by RNA-seq.
Jin Xiang, Yuhong Zhang, Lin Tuo, Rui Liu, Dongmei Gou, Li Liang, Chang Chen, Jie Xia, Ni Tang, Kai Wang. Genes Dis 2019
2
50

Three-dimensional printed tissue engineered bone for canine mandibular defects.
Li Zhang, Junling Tang, Libo Sun, Ting Zheng, Xianzhi Pu, Yue Chen, Kai Yang. Genes Dis 2019
1
100

Novel biallelic TRNT1 mutations lead to atypical SIFD and multiple immune defects.
Lu Yang, Xiuhong Xue, Ting Zeng, Xuemei Chen, Qin Zhao, Xuemei Tang, Jun Yang, Yunfei An, Xiaodong Zhao. Genes Dis 2020
5
33

An update on the genetics and pathogenesis of hereditary angioedema.
Aaqib Zaffar Banday, Anit Kaur, Ankur Kumar Jindal, Amit Rawat, Surjit Singh. Genes Dis 2019
11
33

An updated review on activated PI3 kinase delta syndrome (APDS).
Ankita Singh, Vibhu Joshi, Ankur Kumar Jindal, Babu Mathew, Amit Rawat. Genes Dis 2019
9
33

Platelets in Kawasaki disease: Is this only a numbers game or something beyond?
Kanika Arora, Sandesh Guleria, Ankur Kumar Jindal, Amit Rawat, Surjit Singh. Genes Dis 2019
8
33

Recent advances in elucidating the genetics of common variable immunodeficiency.
Vaishali Aggarwal, Aaqib Zaffar Banday, Ankur Kumar Jindal, Jhumki Das, Amit Rawat. Genes Dis 2019
16
33

Genetics of severe combined immunodeficiency.
Rajni Kumrah, Pandiarajan Vignesh, Pratap Patra, Ankita Singh, Gummadi Anjani, Poonam Saini, Madhubala Sharma, Anit Kaur, Amit Rawat. Genes Dis 2019
9
33

An updated review on phenocopies of primary immunodeficiency diseases.
Ankita Singh, Ankur K Jindal, Vibhu Joshi, Gummadi Anjani, Amit Rawat. Genes Dis 2019
8
33

Gene therapy and genome editing for primary immunodeficiency diseases.
Zhi-Yong Zhang, Adrian J Thrasher, Fang Zhang. Genes Dis 2019
11
33

IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity.
Hans D Ochs, Eleonora Gambineri, Troy R Torgerson. Immunol Res 2007
112
33

Intrauterine IPEX.
Magda Carneiro-Sampaio, Carlos Alberto Moreira-Filho, Silvia Yumi Bando, Jocelyne Demengeot, Antonio Coutinho. Front Pediatr 2020
2
50

Familial IPEX syndrome: different glomerulopathy in two siblings.
Eujin Park, Hye Jin Chang, Jae Il Shin, Beom Jin Lim, Hyeon Joo Jeong, Kyoung Bun Lee, Kyoung Chul Moon, Hee Gyung Kang, Il-Soo Ha, Hae Il Cheong. Pediatr Int 2015
13
33


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.