A citation-based method for searching scientific literature

Ting Zeng, Ge Lv, Xuemei Chen, Lu Yang, Lina Zhou, Ying Dou, Xuemei Tang, Jun Yang, Yunfei An, Xiaodong Zhao. J Clin Lab Anal 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


RASGRP1 mutation in autoimmune lymphoproliferative syndrome-like disease.
Huawei Mao, Wanling Yang, Sylvain Latour, Jing Yang, Sarah Winter, Jian Zheng, Ke Ni, Minmin Lv, Chenjing Liu, Hongmei Huang,[...]. J Allergy Clin Immunol 2018
24
100

Long-Term Follow-Up of a Case with Dyskeratosis Congenita Caused by NHP2-V126M/X154R Mutation: Genotype-Phenotype Association.
Melek Erdem, Özlem Tüfekçi, Şebnem Yılmaz, İnci Alacacıoğlu, Hale Ören. Acta Haematol 2019
4
100


Impaired telomere integrity and rRNA biogenesis in PARN-deficient patients and knock-out models.
Maname Benyelles, Harikleia Episkopou, Marie-Françoise O'Donohue, Laëtitia Kermasson, Pierre Frange, Florian Poulain, Fatma Burcu Belen, Meltem Polat, Christine Bole-Feysot, Francina Langa-Vives,[...]. EMBO Mol Med 2019
13
100

Defects in lymphocyte telomere homeostasis contribute to cellular immune phenotype in patients with cartilage-hair hypoplasia.
Geraldine Aubert, Kevin A Strauss, Peter M Lansdorp, Nicholas L Rider. J Allergy Clin Immunol 2017
10
100

Reference values for peripheral blood lymphocyte subsets of healthy children in China.
Yuan Ding, Lina Zhou, Yu Xia, Wei Wang, Ying Wang, Li Li, Zhongxiang Qi, Linqing Zhong, Jinqiao Sun, Wenjing Tang,[...]. J Allergy Clin Immunol 2018
36
100

CD57 identifies T cells with functional senescence before terminal differentiation and relative telomere shortening in patients with activated PI3 kinase delta syndrome.
Paola Cura Daball, Monica Sofia Ventura Ferreira, Sandra Ammann, Christian Klemann, Myriam R Lorenz, Ursula Warthorst, Timothy Ronan Leahy, Niall Conlon, Justin Roche, Pere Soler-Palacín,[...]. Immunol Cell Biol 2018
11
100

Identification and characterization of a human CD5+ pre-naive B cell population.
Jisoo Lee, Stefan Kuchen, Randy Fischer, Sooghee Chang, Peter E Lipsky. J Immunol 2009
97
100

Combined decrease of defined B and T cell subsets in a group of common variable immunodeficiency patients.
Daniele Moratto, Anna Virginia Gulino, Stefania Fontana, Luigi Mori, Silvia Pirovano, Annarosa Soresina, Antonella Meini, Luisa Imberti, Luigi Daniele Notarangelo, Alessandro Plebani,[...]. Clin Immunol 2006
41
100


A POT1 mutation implicates defective telomere end fill-in and telomere truncations in Coats plus.
Hiroyuki Takai, Emma Jenkinson, Shaheen Kabir, Riyana Babul-Hirji, Nasrin Najm-Tehrani, David A Chitayat, Yanick J Crow, Titia de Lange. Genes Dev 2016
45
100

From incomplete penetrance with normal telomere length to severe disease and telomere shortening in a family with monoallelic and biallelic PARN pathogenic variants.
Lois M Dodson, Alessandro Baldan, Mikael Nissbeck, Sethu M R Gunja, Penelope E Bonnen, Geraldine Aubert, Sherri Birchansky, Anders Virtanen, Alison A Bertuch. Hum Mutat 2019
9
100

Telomeres and aging.
Geraldine Aubert, Peter M Lansdorp. Physiol Rev 2008
641
100

Association of immune abnormalities with telomere shortening in autosomal-dominant dyskeratosis congenita.
Matt Knudson, Shashikant Kulkarni, Zuhair K Ballas, Monica Bessler, Frederick Goldman. Blood 2005
55
100

Short telomere syndromes cause a primary T cell immunodeficiency.
Christa L Wagner, Vidya Sagar Hanumanthu, C Conover Talbot, Roshini S Abraham, David Hamm, Dustin L Gable, Christopher G Kanakry, Carolyn D Applegate, Janet Siliciano, J Brooks Jackson,[...]. J Clin Invest 2018
43
100

The diagnosis and treatment of dyskeratosis congenita: a review.
M Soledad Fernández García, Julie Teruya-Feldstein. J Blood Med 2014
63
100

Dyskeratosis congenita.
Sharon A Savage, Blanche P Alter. Hematol Oncol Clin North Am 2009
124
100


Circulating CD21low B cells in common variable immunodeficiency resemble tissue homing, innate-like B cells.
Mirzokhid Rakhmanov, Baerbel Keller, Sylvia Gutenberger, Christian Foerster, Manfred Hoenig, Gertjan Driessen, Mirjam van der Burg, Jacques J van Dongen, Elisabeth Wiech, Marcella Visentini,[...]. Proc Natl Acad Sci U S A 2009
215
100

The RNase PARN Controls the Levels of Specific miRNAs that Contribute to p53 Regulation.
Siddharth Shukla, Glen A Bjerke, Denise Muhlrad, Rui Yi, Roy Parker. Mol Cell 2019
25
100

The genetics and clinical manifestations of telomere biology disorders.
Sharon A Savage, Alison A Bertuch. Genet Med 2010
136
100

Extended clinical and genetic spectrum associated with biallelic RTEL1 mutations.
Fabien Touzot, Laetitia Kermasson, Laurent Jullien, Despina Moshous, Christelle Ménard, Aydan Ikincioğullari, Figen Doğu, Sinan Sari, Vannina Giacobbi-Milet, Amos Etzioni,[...]. Blood Adv 2016
11
100

Mutations in STN1 cause Coats plus syndrome and are associated with genomic and telomere defects.
Amos J Simon, Atar Lev, Yong Zhang, Batia Weiss, Anna Rylova, Eran Eyal, Nitzan Kol, Ortal Barel, Keren Cesarkas, Michalle Soudack,[...]. J Exp Med 2016
57
100

Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies.
Cindy S Ma, Natalie Wong, Geetha Rao, Danielle T Avery, James Torpy, Thomas Hambridge, Jacinta Bustamante, Satoshi Okada, Jennifer L Stoddard, Elissa K Deenick,[...]. J Allergy Clin Immunol 2015
121
100

Phenotype and function of human T lymphocyte subsets: consensus and issues.
Victor Appay, Rene A W van Lier, Federica Sallusto, Mario Roederer. Cytometry A 2008
518
100

Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal-Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1.
S W Knight, N S Heiss, T J Vulliamy, C M Aalfs, C McMahon, P Richmond, A Jones, R C Hennekam, A Poustka, P J Mason,[...]. Br J Haematol 1999
152
100

Unraveling the pathogenesis of Hoyeraal-Hreidarsson syndrome, a complex telomere biology disorder.
Galina Glousker, Fabien Touzot, Patrick Revy, Yehuda Tzfati, Sharon A Savage. Br J Haematol 2015
62
100

Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita.
Hemanth Tummala, Amanda Walne, Laura Collopy, Shirleny Cardoso, Josu de la Fuente, Sarah Lawson, James Powell, Nicola Cooper, Alison Foster, Shehla Mohammed,[...]. J Clin Invest 2015
108
100

Clinical and Molecular Heterogeneity of RTEL1 Deficiency.
Carsten Speckmann, Sushree Sangita Sahoo, Marta Rizzi, Shinsuke Hirabayashi, Axel Karow, Nina Kathrin Serwas, Marc Hoemberg, Natalja Damatova, Detlev Schindler, Jean-Baptiste Vannier,[...]. Front Immunol 2017
16
100

Advances in the understanding of dyskeratosis congenita.
Amanda J Walne, Inderjeet Dokal. Br J Haematol 2009
113
100

Telomere measurement by quantitative PCR.
Richard M Cawthon. Nucleic Acids Res 2002
100

Murine regulatory T cells induce death of effector T, B, and NK lymphocytes through a contact-independent mechanism involving telomerase suppression and telomere-associated senescence.
Dmitry D Zhdanov, Yulia A Gladilina, Vadim S Pokrovsky, Dmitry V Grishin, Vladimir A Grachev, Valentina S Orlova, Marina V Pokrovskaya, Svetlana S Alexandrova, Nikolay N Sokolov. Cell Immunol 2018
6
100


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.