A citation-based method for searching scientific literature

Hemanth Tummala, Amanda Walne, Laura Collopy, Shirleny Cardoso, Josu de la Fuente, Sarah Lawson, James Powell, Nicola Cooper, Alison Foster, Shehla Mohammed, Vincent Plagnol, Thomas Vulliamy, Inderjeet Dokal. J Clin Invest 2015
Times Cited: 102



Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
Times Cited: 547




List of shared articles



Times cited

Molecular mechanisms of telomere biology disorders.
Sherilyn Grill, Jayakrishnan Nandakumar. J Biol Chem 2021
3

NHP2 deficiency impairs rRNA biogenesis and causes pulmonary fibrosis and Høyeraal-Hreidarsson syndrome.
Maname Benyelles, Marie-Françoise O'Donohue, Laëtitia Kermasson, Elodie Lainey, Raphael Borie, Chantal Lagresle-Peyrou, Hilario Nunes, Clarisse Cazelles, Cécile Fourrage, Emmanuelle Ollivier,[...]. Hum Mol Genet 2020
9

Loss of Human TGS1 Hypermethylase Promotes Increased Telomerase RNA and Telomere Elongation.
Lu Chen, Caitlin M Roake, Alessandra Galati, Francesca Bavasso, Emanuela Micheli, Isabella Saggio, Stefan Schoeftner, Stefano Cacchione, Maurizio Gatti, Steven E Artandi,[...]. Cell Rep 2020
7

Small-Molecule PAPD5 Inhibitors Restore Telomerase Activity in Patient Stem Cells.
Neha Nagpal, Jianing Wang, Jing Zeng, Emily Lo, Diane H Moon, Kevin Luk, Roman O Braun, Lauri M Burroughs, Sioban B Keel, Christopher Reilly,[...]. Cell Stem Cell 2020
15

Chemical inhibition of PAPD5/7 rescues telomerase function and hematopoiesis in dyskeratosis congenita.
Siddharth Shukla, Ho-Chang Jeong, Christopher M Sturgeon, Roy Parker, Luis Francisco Zirnberger Batista. Blood Adv 2020
6


Molecular mechanisms of telomere biology disorders.
Sherilyn Grill, Jayakrishnan Nandakumar. J Biol Chem 2020
4

Posttranscriptional modulation of TERC by PAPD5 inhibition rescues hematopoietic development in dyskeratosis congenita.
Wilson Chun Fok, Siddharth Shukla, Alexandre Teixeira Vessoni, Kirsten Ann Brenner, Roy Parker, Christopher M Sturgeon, Luis Francisco Zirnberger Batista. Blood 2019
17


Novel variants in Nordic patients referred for genetic testing of telomere-related disorders.
Anna Norberg, Anna Rosén, Klas Raaschou-Jensen, Lars Kjeldsen, Jukka S Moilanen, Ylva Paulsson-Karlsson, Panagiotis Baliakas, Olli Lohi, Aymen Ahmed, Astrid O Kittang,[...]. Eur J Hum Genet 2018
8

Telomerase Mechanism of Telomere Synthesis.
R Alex Wu, Heather E Upton, Jacob M Vogan, Kathleen Collins. Annu Rev Biochem 2017
91

Genetics in Idiopathic Pulmonary Fibrosis Pathogenesis, Prognosis, and Treatment.
Amarpreet Kaur, Susan K Mathai, David A Schwartz. Front Med (Lausanne) 2017
49

The wide-ranging clinical implications of the short telomere syndromes.
P M Barbaro, D S Ziegler, R R Reddel. Intern Med J 2016
16

Telomerase gene therapy rescues telomere length, bone marrow aplasia, and survival in mice with aplastic anemia.
Christian Bär, Juan Manuel Povedano, Rosa Serrano, Carlos Benitez-Buelga, Miriam Popkes, Ivan Formentini, Maria Bobadilla, Fatima Bosch, Maria A Blasco. Blood 2016
33

Inhibition of telomerase RNA decay rescues telomerase deficiency caused by dyskerin or PARN defects.
Siddharth Shukla, Jens C Schmidt, Katherine C Goldfarb, Thomas R Cech, Roy Parker. Nat Struct Mol Biol 2016
61

p53 downregulates the Fanconi anaemia DNA repair pathway.
Sara Jaber, Eléonore Toufektchan, Vincent Lejour, Boris Bardot, Franck Toledo. Nat Commun 2016
21

Hypo- and Hyper-Assembly Diseases of RNA-Protein Complexes.
Siddharth Shukla, Roy Parker. Trends Mol Med 2016
40

The short and long telomere syndromes: paired paradigms for molecular medicine.
Susan E Stanley, Mary Armanios. Curr Opin Genet Dev 2015
67