A citation-based method for searching scientific literature

Catherine M Scahill, Zsofia Digby, Ian M Sealy, Richard J White, Neha Wali, John E Collins, Derek L Stemple, Elisabeth M Busch-Nentwich. Wellcome Open Res 2017
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Enhancement of premature stop codon readthrough in the CFTR gene by Ataluren (PTC124) derivatives.
Ivana Pibiri, Laura Lentini, Raffaella Melfi, Giulia Gallucci, Andrea Pace, Angelo Spinello, Giampaolo Barone, Aldo Di Leonardo. Eur J Med Chem 2015
32
100

Cancer Biogenesis in Ribosomopathies.
Sergey O Sulima, Kim R Kampen, Kim De Keersmaecker. Cells 2019
24
100

RPS19 mutations in patients with Diamond-Blackfan anemia.
Maria Francesca Campagnoli, Ugo Ramenghi, Marta Armiraglio, Paola Quarello, Emanuela Garelli, Adriana Carando, Federica Avondo, Elisa Pavesi, Sébastien Fribourg, Pierre-Emmanuel Gleizes,[...]. Hum Mutat 2008
75
100

Cancer risks in Fanconi anemia: findings from the German Fanconi Anemia Registry.
Philip S Rosenberg, Blanche P Alter, Wolfram Ebell. Haematologica 2008
125
100

Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene.
N Ishikawa, S Okada, M Miki, K Shirao, H Kihara, M Tsumura, K Nakamura, H Kawaguchi, M Ohtsubo, S Yasunaga,[...]. J Med Genet 2008
40
100

Severe congenital neutropenias.
Julia Skokowa, David C Dale, Ivo P Touw, Cornelia Zeidler, Karl Welte. Nat Rev Dis Primers 2017
100
100

Shwachman-Diamond Syndrome: Molecular Mechanisms and Current Perspectives.
Valentino Bezzerri, Marco Cipolli. Mol Diagn Ther 2019
21
100

Cancer in Fanconi anemia.
Blanche P Alter, Mark H Greene, Isela Velazquez, Philip S Rosenberg. Blood 2003
108
100

Strategies against Nonsense: Oxadiazoles as Translational Readthrough-Inducing Drugs (TRIDs).
Ambra Campofelice, Laura Lentini, Aldo Di Leonardo, Raffaella Melfi, Marco Tutone, Andrea Pace, Ivana Pibiri. Int J Mol Sci 2019
14
100

Readthrough of nonsense mutations in Rett syndrome: evaluation of novel aminoglycosides and generation of a new mouse model.
Cornelia Brendel, Valery Belakhov, Hauke Werner, Eike Wegener, Jutta Gärtner, Igor Nudelman, Timor Baasov, Peter Huppke. J Mol Med (Berl) 2011
70
100

Paternal or Maternal Uniparental Disomy of Chromosome 16 Resulting in Homozygosity of a Mutant Allele Causes Fanconi Anemia.
Frank X Donovan, Danielle C Kimble, Yonghwan Kim, Francis P Lach, Ursula Harper, Aparna Kamat, MaryPat Jones, Erica M Sanborn, Rebecca Tryon, John E Wagner,[...]. Hum Mutat 2016
6
100

[Mutation in the SLC37A4 gene of glycogen storage disease type Ib in 15 families of the mainland of China].
Zheng-qing Qiu, Chao-xia Lu, Wei Wang, Jia-jing Qiu, Min Wei. Zhonghua Er Ke Za Zhi 2011
5
100

Association of clinical severity with FANCB variant type in Fanconi anemia.
Moonjung Jung, Ramanagouda Ramanagoudr-Bhojappa, Sylvie van Twest, Rasim Ozgur Rosti, Vincent Murphy, Winnie Tan, Frank X Donovan, Francis P Lach, Danielle C Kimble, Caroline S Jiang,[...]. Blood 2020
13
100

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.
Roberta Bottega, Elena Nicchia, Enrico Cappelli, Silvia Ravera, Daniela De Rocco, Michela Faleschini, Fabio Corsolini, Filomena Pierri, Michaela Calvillo, Giovanna Russo,[...]. Haematologica 2018
18
100


A lack of premature termination codon read-through efficacy of PTC124 (Ataluren) in a diverse array of reporter assays.
Stuart P McElroy, Toshifumi Nomura, Leah S Torrie, Emma Warbrick, Ulrike Gartner, Gavin Wood, W H Irwin McLean. PLoS Biol 2013
88
100

TCIRG1-associated congenital neutropenia.
Vahagn Makaryan, Elisabeth A Rosenthal, Audrey Anna Bolyard, Merideth L Kelley, Jennifer E Below, Michael J Bamshad, Kathryn M Bofferding, Joshua D Smith, Kati Buckingham, Laurence A Boxer,[...]. Hum Mutat 2014
24
100

Partial functional correction of xeroderma pigmentosum group A cells by suppressor tRNA.
R G Panchal, S Wang, J McDermott, C J Link. Hum Gene Ther 1999
19
100


Readthrough of ACTN3 577X nonsense mutation produces full-length α-actinin-3 protein.
Nagakatsu Harada, Adzumi Hatakeyama, Maiko Okuyama, Yumiko Miyatake, Tadahiko Nakagawa, Masashi Kuroda, Saeko Masumoto, Rie Tsutsumi, Yutaka Nakaya, Hiroshi Sakaue. Biochem Biophys Res Commun 2018
6
100

Suppression of premature termination codons as a therapeutic approach.
Kim M Keeling, Dan Wang, Sara E Conard, David M Bedwell. Crit Rev Biochem Mol Biol 2012
66
100

Novel small molecules potentiate premature termination codon readthrough by aminoglycosides.
Alireza Baradaran-Heravi, Aruna D Balgi, Carla Zimmerman, Kunho Choi, Fahimeh S Shidmoossavee, Jason S Tan, Célia Bergeaud, Alexandra Krause, Stéphane Flibotte, Yoko Shimizu,[...]. Nucleic Acids Res 2016
40
100

The Genetic Landscape of Diamond-Blackfan Anemia.
Jacob C Ulirsch, Jeffrey M Verboon, Shideh Kazerounian, Michael H Guo, Daniel Yuan, Leif S Ludwig, Robert E Handsaker, Nour J Abdulhay, Claudia Fiorini, Giulio Genovese,[...]. Am J Hum Genet 2019
9
100

Novel recurrent chromosome anomalies in Shwachman-Diamond syndrome.
Roberto Valli, Elena De Paoli, Lucia Nacci, Annalisa Frattini, Francesco Pasquali, Emanuela Maserati. Pediatr Blood Cancer 2017
10
100

Ataluren stimulates ribosomal selection of near-cognate tRNAs to promote nonsense suppression.
Bijoyita Roy, Westley J Friesen, Yuki Tomizawa, John D Leszyk, Jin Zhuo, Briana Johnson, Jumana Dakka, Christopher R Trotta, Xiaojiao Xue, Venkateshwar Mutyam,[...]. Proc Natl Acad Sci U S A 2016
89
100

Suppression of CFTR premature termination codons and rescue of CFTR protein and function by the synthetic aminoglycoside NB54.
Steven M Rowe, Peter Sloane, Li Ping Tang, Kyle Backer, Marina Mazur, Jessica Buckley-Lanier, Igor Nudelman, Valery Belakhov, Zsuzsa Bebok, Erik Schwiebert,[...]. J Mol Med (Berl) 2011
52
100

Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression.
T N Willig, N Draptchinskaia, I Dianzani, S Ball, C Niemeyer, U Ramenghi, K Orfali, P Gustavsson, E Garelli, A Brusco,[...]. Blood 1999
152
100


Biallelic mutations in DNAJC21 cause Shwachman-Diamond syndrome.
Santhosh Dhanraj, Anna Matveev, Hongbing Li, Supanun Lauhasurayotin, Lawrence Jardine, Michaela Cada, Bozana Zlateska, Chetankumar S Tailor, Joseph Zhou, Roberto Mendoza-Londono,[...]. Blood 2017
62
100


Clinical phenotype and genetic analysis of RPS19, RPL5, and RPL11 genes in Greek patients with Diamond Blackfan Anemia.
Polyxeni Delaporta, Christalena Sofocleous, Eftichia Stiakaki, Sophia Polychronopoulou, Marina Economou, Lydia Kossiva, Stavroula Kostaridou, Antonis Kattamis. Pediatr Blood Cancer 2014
11
100

Stable long-term risk of leukaemia in patients with severe congenital neutropenia maintained on G-CSF therapy.
Philip S Rosenberg, Cornelia Zeidler, Audrey A Bolyard, Blanche P Alter, Mary A Bonilla, Laurence A Boxer, Yigal Dror, Sally Kinsey, Daniel C Link, Peter E Newburger,[...]. Br J Haematol 2010
128
100

Aminoglycoside interactions and impacts on the eukaryotic ribosome.
Irina Prokhorova, Roger B Altman, Muminjon Djumagulov, Jaya P Shrestha, Alexandre Urzhumtsev, Angelica Ferguson, Cheng-Wei Tom Chang, Marat Yusupov, Scott C Blanchard, Gulnara Yusupova. Proc Natl Acad Sci U S A 2017
66
100

ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
955
100


Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.
Daniela De Rocco, Roberta Bottega, Enrico Cappelli, Simona Cavani, Maria Criscuolo, Elena Nicchia, Fabio Corsolini, Chiara Greco, Adriana Borriello, Johanna Svahn,[...]. Haematologica 2014
28
100

Pharmaceutical therapies to recode nonsense mutations in inherited diseases.
Hui-Ling Rose Lee, Joseph P Dougherty. Pharmacol Ther 2012
88
100

Inhibition of nonsense-mediated mRNA decay rescues the phenotype in Ullrich's disease.
Fusako Usuki, Akio Yamashita, Itsuro Higuchi, Tetsuo Ohnishi, Tadafumi Shiraishi, Mitsuhiro Osame, Shigeo Ohno. Ann Neurol 2004
66
100

A novel large deletion and single nucleotide insertion in the Wiskott-Aldrich syndrome protein gene.
Vera Gulácsy, Beáta Soltész, Carmen Petrescu, Mihaela Bataneant, Edit Gyimesi, Margit Serban, László Maródi, Beáta Tóth. Eur J Haematol 2015
1
100

Shwachman-Diamond syndrome with exocrine pancreatic dysfunction and bone marrow failure maps to the centromeric region of chromosome 7.
S Goobie, M Popovic, J Morrison, L Ellis, H Ginzberg, G R Boocock, N Ehtesham, C Bétard, C G Brewer, N M Roslin,[...]. Am J Hum Genet 2001
85
100

Ten novel Diamond-Blackfan anemia mutations and three polymorphisms within the rps19 gene.
Alexis Proust, Lydie Da Costa, Patricia Rince, Anaely Landois, Hannah Tamary, Rina Zaizov, Gil Tchernia, Jean Delaunay. Hematol J 2003
24
100

X-linked VACTERL with hydrocephalus syndrome: further delineation of the phenotype caused by FANCB mutations.
Joanna McCauley, Navta Masand, Ruth McGowan, Sulekha Rajagopalan, Alasdair Hunter, Jacques L Michaud, Kate Gibson, Jeremy Robertson, Fiona Vaz, Stephen Abbs,[...]. Am J Med Genet A 2011
30
100

The role of nonsense-mediated decay in neuronal ceroid lipofuscinosis.
Jake N Miller, Chun-Hung Chan, David A Pearce. Hum Mol Genet 2013
35
100

Repairing faulty genes by aminoglycosides: development of new derivatives of geneticin (G418) with enhanced suppression of diseases-causing nonsense mutations.
Igor Nudelman, Dana Glikin, Boris Smolkin, Mariana Hainrichson, Valery Belakhov, Timor Baasov. Bioorg Med Chem 2010
85
100

A homozygous FANCM frameshift pathogenic variant causes male infertility.
Hao Yin, Hui Ma, Sajjad Hussain, Huan Zhang, Xuefeng Xie, Long Jiang, Xiaohua Jiang, Furhan Iqbal, Ihtisham Bukhari, Hanwei Jiang,[...]. Genet Med 2019
40
100

Severe congenital neutropenia resulting from G6PC3 deficiency with increased neutrophil CXCR4 expression and myelokathexis.
David H McDermott, Suk See De Ravin, Hyun Sik Jun, Qian Liu, Debra A Long Priel, Pierre Noel, Clifford M Takemoto, Teresa Ojode, Scott M Paul, Kimberly P Dunsmore,[...]. Blood 2010
56
100

Abnormalities of the large ribosomal subunit protein, Rpl35a, in Diamond-Blackfan anemia.
Jason E Farrar, Michelle Nater, Emi Caywood, Michael A McDevitt, Jeanne Kowalski, Clifford M Takemoto, C Conover Talbot, Paul Meltzer, Diane Esposito, Alan H Beggs,[...]. Blood 2008
171
100

DKC1 is a transcriptional target of GATA1 and drives upregulation of telomerase activity in normal human erythroblasts.
Laura A Richards, Ashu Kumari, Kathy Knezevic, Julie Ai Thoms, Georg von Jonquieres, Christine E Napier, Zara Ali, Rosemary O'Brien, Jonathon Marks-Bluth, Michelle F Maritz,[...]. Haematologica 2020
7
100

Ataluren/ivacaftor combination therapy: Two N-of-1 trials in cystic fibrosis patients with nonsense mutations.
Jacelyn E Peabody Lever, Venkateshwar Mutyam, Heather Y Hathorne, Ning Peng, Jyoti Sharma, Lloyd J Edwards, Steven M Rowe. Pediatr Pulmonol 2020
5
100

Implementing Keytruda/Pembrolizumab Testing in Clinical Practice.
Dmitry Ratner, Jochen K Lennerz. Oncologist 2018
3
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.