LARP7 family proteins have conserved function in telomerase assembly by Collopy, Laura C., Ware, Tracy L., Goncalves, Tomas, í Kongsstovu, Sunnvør, Yang, Qian, Amelina, Hanna, Pinder, Corinne, Alenazi, Ala, Moiseeva, Vera, Pearson, Siân R., Armstrong, Christine A., Tomita, Kazunori

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Fission yeast Ccq1 is a modulator of telomerase activity by Armstrong, Christine A, Moiseeva, Vera, Collopy, Laura C, Pearson, Siân R, Ullah, Tomalika R, Xi, Shidong T, Martin, Jennifer, Subramaniam, Shaan, Marelli, Sara, Amelina, Hanna, Tomita, Kazunori

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Targeted resequencing of 52 bone marrow failure genes in patients with aplastic anemia reveals an increased frequency of novel variants of unknown significance only in SLX4 by Collopy, Laura C, Walne, Amanda J, Vulliamy, Tom J, Dokal, Inderjeet S

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The telomere bouquet facilitates meiotic prophase progression and exit in fission yeast by Moiseeva, Vera, Amelina, Hanna, Collopy, Laura C, Armstrong, Christine A, Pearson, Siân R, Tomita, Kazunori

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Triallelic and epigenetic-like inheritance in human disorders of telomerase by Collopy, Laura C., Walne, Amanda J., Cardoso, Shirleny, de la Fuente, Josu, Mohamed, Mahfuzah, Toriello, Helga, Tamary, Hannah, Ling, AdamJ.Y.V., Lloyd, Timothy, Kassam, Rebecca, Tummala, Hemanth, Vulliamy, Thomas J., Dokal, Inderjeet

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Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita–like phenotypes by Tummala, Hemanth, Collopy, Laura C., Walne, Amanda J., Ellison, Alicia, Cardoso, Shirleny, Aksu, Tekin, Yarali, Nese, Aslan, Deniz, Fikret Akata, Rüştü, Teo, Juliana, Songyang, Zhou, Pontikos, Nikolas, Fitzgibbon, Jude, Tomita, Kazunori, Vulliamy, Tom, Dokal, Inderjeet

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Selective Elimination of Osteosarcoma Cell Lines with Short Telomeres by Ataxia Telangiectasia and Rad3-Related Inhibitors by Goncalves, Tomas, Zoumpoulidou, Georgia, Alvarez-Mendoza, Carlos, Mancusi, Caterina, Collopy, Laura C, Strauss, Sandra J, Mittnacht, Sibylle, Tomita, Kazunori

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Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis by Walne, Amanda J, Collopy, Laura, Cardoso, Shirleny, Ellison, Alicia, Plagnol, Vincent, Albayrak, Canan, Albayrak, Davut, Kilic, Sara Sebnem, Patıroglu, Turkan, Akar, Haluk, Godfrey, Keith, Carter, Tina, Marafie, Makia, Vora, Ajay, Sundin, Mikael, Vulliamy, Thomas, Tummala, Hemanth, Dokal, Inderjeet

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Mutations in CDC45, Encoding an Essential Component of the Pre-initiation Complex, Cause Meier-Gorlin Syndrome and Craniosynostosis by Fenwick, Aimee L., Kliszczak, Maciej, Cooper, Fay, Murray, Jennie, Sanchez-Pulido, Luis, Twigg, Stephen R.F., Goriely, Anne, McGowan, Simon J., Miller, Kerry A., Taylor, Indira B., Logan, Clare, Bozdogan, Sevcan, Danda, Sumita, Dixon, Joanne, Elsayed, Solaf M., Elsobky, Ezzat, Gardham, Alice, Hoffer, Mariette J.V., Koopmans, Marije, McDonald-McGinn, Donna M., Santen, Gijs W.E., Savarirayan, Ravi, de Silva, Deepthi, Vanakker, Olivier, Wall, Steven A., Wilson, Louise C., Yuregir, Ozge Ozalp, Zackai, Elaine H., Ponting, Chris P., Jackson, Andrew P., Wilkie, Andrew O.M., Niedzwiedz, Wojciech, Bicknell, Louise S.

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