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Brody Holohan
Brody Holohan
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Cited by
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Year
Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening
BD Stuart, J Choi, S Zaidi, C Xing, B Holohan, R Chen, M Choi, ...
Nature genetics 47 (5), 512-517, 2015
4702015
Telomeropathies: An emerging spectrum disorder
B Holohan, WE Wright, JW Shay
Journal of Cell Biology 205 (3), 289-299, 2014
2112014
Disruption of Wnt/β-catenin signaling and telomeric shortening are inextricable consequences of tankyrase inhibition in human cells
O Kulak, H Chen, B Holohan, X Wu, H He, D Borek, Z Otwinowski, ...
Molecular and cellular biology 35 (14), 2425-2435, 2015
752015
Impaired telomere maintenance in Alazami syndrome patients with LARP7 deficiency
B Holohan, W Kim, TP Lai, H Hoshiyama, N Zhang, AM Alazami, ...
BMC genomics 17, 79-87, 2016
392016
Decreasing initial telomere length in humans intergenerationally understates age‐associated telomere shortening
B Holohan, T De Meyer, K Batten, M Mangino, SC Hunt, S Bekaert, ...
Aging Cell 14 (4), 669-677, 2015
332015
Perifosine as a potential novel anti-telomerase therapy
B Holohan, MM Hagiopian, TP Lai, E Huang, DR Friedman, WE Wright, ...
Oncotarget 6 (26), 21816, 2015
192015
Impaired telomere maintenance spectrum disorders
B Holohan, WE Wright, JW Shay
J Cell Biol 205, 289-99, 2014
62014
Identifying, Characterizing and Inhibiting the Telomerase Regulatory Network
BC Holohan
2015
A chemicogenetic interrogation of colorectal cancer identifies a shared chemical vulnerability in Wnt signaling and telomere length maintenance.
O Kulak, B Holohan, X Wu, L Lum
Cancer Research 73 (8_Supplement), 2115-2115, 2013
2013
Exome Sequencing Links Loss-of-Function and Missense Mutations in PARN and RTEL1 with Familial Pulmonary Fibrosis and Telomere Shortening
BD Stuart, J Choi, S Zaidi, C Xing, B Holohan, R Chen, M Choi, ...
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