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Genes & Development|January 6, 2011
Disruption of telomerase trafficking by TCAB1 mutation causes dyskeratosis congenitaFranklin Zhong, Sharon A Savage, Marina Shkreli, et al.Pediatric Research|May 10, 2017
Bone mineral density in patients with inherited bone marrow failure syndromesRoopa Kanakatti Shankar, Neelam Giri, Maya B Lodish, et al.American Journal of Hematology|May 13, 2015
Immune status of patients with inherited bone marrow failure syndromesNeelam Giri, Blanche P Alter, Keri Penrose, et al.Ebiomedicine|December 20, 2021
Lipoprotein particle alterations due to androgen therapy in individuals with dyskeratosis congenitaMone't B Thompson, Daniel Muldoon, Kelvin C de Andrade, et al.British Journal of Haematology|June 24, 2023
The distribution and accumulation of the shortest telomeres in telomere biology disordersHannah A Raj, Tsung-Po Lai, Marena R Niewisch, et al.Human Molecular Genetics|November 8, 2011
The accumulation and not the specific activity of telomerase ribonucleoprotein determines telomere maintenance deficiency in X-linked dyskeratosis congenitaXi-Lei Zeng, Naresh R Thumati, Helen B Fleisig, et al.Hepatology (Baltimore, Md.)|May 15, 2023
Progression of liver disease and portal hypertension in dyskeratosis congenita and related telomere biology disordersAnusha Vittal, Marena R Niewisch, Sonia Bhala, et al.British Journal of Haematology|May 29, 2010
Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort studyBlanche P Alter, Neelam Giri, Sharon A Savage, et al.Pediatric Blood & Cancer|July 19, 2016
Otologic manifestations of Fanconi anemia and other inherited bone marrow failure syndromesAdedoyin Kalejaiye, Neelam Giri, Carmen C Brewer, et al.Journal of Hematology & Oncology|April 29, 2024
Germline biallelic BRCA2 pathogenic variants and medulloblastoma: an international cohort studySvenja Kastellan, Reinhard Kalb, Bia Sajjad, et al.Pageof 10