A citation-based method for searching scientific literature

Svetlana Vakkilainen, Mervi Taskinen, Outi Mäkitie. Scand J Immunol 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Ataxia telangiectasia: a review.
Cynthia Rothblum-Oviatt, Jennifer Wright, Maureen A Lefton-Greif, Sharon A McGrath-Morrow, Thomas O Crawford, Howard M Lederman. Orphanet J Rare Dis 2016
185
66

A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency.
David A Parry, Tim D Holmes, Nikita Gamper, Walid El-Sayed, Nishani T Hettiarachchi, Mushtaq Ahmed, Graham P Cook, Clare V Logan, Colin A Johnson, Shelagh Joss,[...]. J Allergy Clin Immunol 2016
22
33

Hyper IgE syndromes: clinical and molecular characteristics.
Taha Al-Shaikhly, Hans D Ochs. Immunol Cell Biol 2019
27
33

T Cell Impairment Is Predictive for a Severe Clinical Course in NEMO Deficiency.
Stephanie Heller, Uwe Kölsch, Thomas Magg, Renate Krüger, Andrea Scheuern, Holm Schneider, Anna Eichinger, Volker Wahn, Nadine Unterwalder, Myriam Lorenz,[...]. J Clin Immunol 2020
3
33

Insights into the renal pathogenesis in Schimke immuno-osseous dysplasia: A renal histological characterization and expression analysis.
Sanjay Sarin, Ashkan Javidan, Felix Boivin, Iakovina Alexopoulou, Dusan Lukic, Bruno Svajger, Stephanie Chu, Alireza Baradaran-Heravi, Cornelius F Boerkoel, Norman D Rosenblum,[...]. J Histochem Cytochem 2015
8
33

Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee.
Stuart G Tangye, Waleed Al-Herz, Aziz Bousfiha, Talal Chatila, Charlotte Cunningham-Rundles, Amos Etzioni, Jose Luis Franco, Steven M Holland, Christoph Klein, Tomohiro Morio,[...]. J Clin Immunol 2020
267
33



Variable immune deficiency related to deletion size in chromosome 22q11.2 deletion syndrome.
Blaine Crowley, Melanie Ruffner, Donna M McDonald McGinn, Kathleen E Sullivan. Am J Med Genet A 2018
21
33

Chromosome instability syndromes.
A Malcolm R Taylor, Cynthia Rothblum-Oviatt, Nathan A Ellis, Ian D Hickson, Stefan Meyer, Thomas O Crawford, Agata Smogorzewska, Barbara Pietrucha, Corry Weemaes, Grant S Stewart. Nat Rev Dis Primers 2019
34
33

Human hyper-IgE syndrome: singular or plural?
Qian Zhang, Bertrand Boisson, Vivien Béziat, Anne Puel, Jean-Laurent Casanova. Mamm Genome 2018
31
33

Update on DNA-Double Strand Break Repair Defects in Combined Primary Immunodeficiency.
Mary A Slatter, Andrew R Gennery. Curr Allergy Asthma Rep 2020
1
100

Clinical Utility Gene Card for: PGM3 defective congenital disorder of glycosylation.
Jaak Jaeken, Dirk J Lefeber, Gert Matthijs. Eur J Hum Genet 2019
2
50

CHARGE syndrome: a review.
Peter Hsu, Alan Ma, Meredith Wilson, George Williams, John Curotta, Craig F Munns, Sam Mehr. J Paediatr Child Health 2014
71
33

A novel NEMO gene mutation causing osteopetrosis, lymphoedema, hypohidrotic ectodermal dysplasia and immunodeficiency (OL-HED-ID).
Catherine M L Roberts, Janet E Angus, Ian H Leach, Elizabeth M McDermott, David A Walker, Jane C Ravenscroft. Eur J Pediatr 2010
24
33

Wiskott-Aldrich syndrome: a comprehensive review.
Michel J Massaad, Narayanaswamy Ramesh, Raif S Geha. Ann N Y Acad Sci 2013
148
33


Recent advances in understanding and managing adenosine deaminase and purine nucleoside phosphorylase deficiencies.
Eyal Grunebaum, Amos Cohen, Chaim M Roifman. Curr Opin Allergy Clin Immunol 2013
47
33

Pediatric neurological syndromes and inborn errors of purine metabolism.
Marcella Camici, Vanna Micheli, Piero Luigi Ipata, Maria Grazia Tozzi. Neurochem Int 2010
51
33

The immune deficiency of chromosome 22q11.2 deletion syndrome.
Megan Morsheimer, Terri F Brown Whitehorn, Jennifer Heimall, Kathleen E Sullivan. Am J Med Genet A 2017
33
33

Ataxia-telangiectasia: A review of clinical features and molecular pathology.
Parisa Amirifar, Mohammad Reza Ranjouri, Reza Yazdani, Hassan Abolhassani, Asghar Aghamohammadi. Pediatr Allergy Immunol 2019
48
33

How I manage patients with Wiskott Aldrich syndrome.
Elizabeth Rivers, Austen Worth, Adrian J Thrasher, Siobhan O Burns. Br J Haematol 2019
13
33

ORAI1 deficiency and lack of store-operated Ca2+ entry cause immunodeficiency, myopathy, and ectodermal dysplasia.
Christie-Ann McCarl, Capucine Picard, Sara Khalil, Takumi Kawasaki, Jens Röther, Alexander Papolos, Jeffery Kutok, Claire Hivroz, Francoise Ledeist, Katrin Plogmann,[...]. J Allergy Clin Immunol 2009
215
33

Immunodeficiency in CHARGE syndrome.
Sam Mehr, Peter Hsu, Dianne Campbell. Am J Med Genet C Semin Med Genet 2017
7
33

Ataxia-telangiectasia, an evolving phenotype.
Helen H Chun, Richard A Gatti. DNA Repair (Amst) 2004
279
33

Screening for Wiskott-Aldrich syndrome by flow cytometry.
Samuel C C Chiang, Sue M Vergamini, Ammar Husami, Lisa Neumeier, Kathryn Quinn, Teresa Ellerhorst, Linda Sheppard, Carrie Gifford, David Buchbinder, Avni Joshi,[...]. J Allergy Clin Immunol 2018
6
33


Wiskott-Aldrich syndrome: diagnosis, current management, and emerging treatments.
David Buchbinder, Diane J Nugent, Alexandra H Fillipovich. Appl Clin Genet 2014
45
33

ZNF341 controls STAT3 expression and thereby immunocompetence.
Stefanie Frey-Jakobs, Julia M Hartberger, Manfred Fliegauf, Claudia Bossen, Magdalena L Wehmeyer, Johanna C Neubauer, Alla Bulashevska, Michele Proietti, Philipp Fröbel, Christina Nöltner,[...]. Sci Immunol 2018
56
33

Purine nucleoside phosphorylase deficiency: a mutation update.
P L C Walker, Adele Corrigan, Monica Arenas, Emilia Escuredo, Lynette Fairbanks, Anthony Marinaki. Nucleosides Nucleotides Nucleic Acids 2011
21
33

Health supervision for people with Bloom syndrome.
Christopher Cunniff, Amir Reza Djavid, Steven Carrubba, Bernard Cohen, Nathan A Ellis, Carolyn Fein Levy, Stacy Jeong, Howard M Lederman, Maria Vogiatzi, Michael F Walsh,[...]. Am J Med Genet A 2018
13
33

The First Purine Nucleoside Phosphorylase Deficiency Patient Resembling IgA Deficiency and a Review of the Literature.
Saba Fekrvand, Reza Yazdani, Hassan Abolhassani, Javad Ghaffari, Asghar Aghamohammadi. Immunol Invest 2019
5
33

Purine nucleoside phosphorylase deficiency presenting as severe combined immune deficiency.
Raz Somech, Atar Lev, Galia Grisaru-Soen, Shelly I Shiran, Amos J Simon, Eyal Grunebaum. Immunol Res 2013
24
33

An Update on Syndromes with a Hyper-IgE Phenotype.
Jenna R E Bergerson, Alexandra F Freeman. Immunol Allergy Clin North Am 2019
22
33

CHARGE Syndrome.
Alexandra Hudson, Carrie-Lee Trider, Kim Blake. Pediatr Rev 2017
5
33




PNPASE regulates RNA import into mitochondria.
Geng Wang, Hsiao-Wen Chen, Yavuz Oktay, Jin Zhang, Eric L Allen, Geoffrey M Smith, Kelly C Fan, Jason S Hong, Samuel W French, J Michael McCaffery,[...]. Cell 2010
215
33

TRIM Proteins and Their Roles in Antiviral Host Defenses.
Michiel van Gent, Konstantin M J Sparrer, Michaela U Gack. Annu Rev Virol 2018
77
33


Mutations in RNA Polymerase III genes and defective DNA sensing in adults with varicella-zoster virus CNS infection.
Madalina E Carter-Timofte, Anders F Hansen, Mette Christiansen, Søren R Paludan, Trine H Mogensen. Genes Immun 2019
26
33

Pattern Recognition Receptors in Multiple Sclerosis and Its Animal Models.
M Elizabeth Deerhake, Debolina D Biswas, William E Barclay, Mari L Shinohara. Front Immunol 2019
10
33

Cryo-EM Structure of the Human Ribonuclease P Holoenzyme.
Jian Wu, Shuangshuang Niu, Ming Tan, Chenhui Huang, Mingyue Li, Yang Song, Qianmin Wang, Juan Chen, Shaohua Shi, Pengfei Lan,[...]. Cell 2018
17
33

Accurate processing of a eukaryotic precursor ribosomal RNA by ribonuclease MRP in vitro.
Z Lygerou, C Allmang, D Tollervey, B Séraphin. Science 1996
203
33

Heterodimerization of the human RNase P/MRP subunits Rpp20 and Rpp25 is a prerequisite for interaction with the P3 arm of RNase MRP RNA.
Katherine L D Hands-Taylor, Luigi Martino, Renée Tata, Jeffrey J Babon, Tam T Bui, Alex F Drake, Rebecca L Beavil, Ger J M Pruijn, Paul R Brown, Maria R Conte. Nucleic Acids Res 2010
28
33


Antibodies in human serum that precipitate ribonuclease P.
H A Gold, J Craft, J A Hardin, M Bartkiewicz, S Altman. Proc Natl Acad Sci U S A 1988
65
33

Roles of RNase P and Its Subunits.
Nayef Jarrous. Trends Genet 2017
25
33

Intracellular sensing of viral genomes and viral evasion.
Hyun-Cheol Lee, Kiramage Chathuranga, Jong-Soo Lee. Exp Mol Med 2019
91
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.