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American Journal of Human Genetics|February 7, 2008
TINF2, a component of the shelterin telomere protection complex, is mutated in dyskeratosis congenitaSharon A Savage, Neelam Giri, Gabriela M Baerlocher, et al.
ERJ Open Research|November 23, 2019
Prognostic significance of pulmonary function tests in dyskeratosis congenita, a telomere biology disorderNeelam Giri, Sandhiya Ravichandran, Youjin Wang, et al.
Blood Advances|June 2, 2018
Similar telomere attrition rates in androgen-treated and untreated patients with dyskeratosis congenitaPayal P Khincha, Alison A Bertuch, Shahinaz M Gadalla, et al.
Aging Cell|October 11, 2011
The relationship between DNA methylation and telomere length in dyskeratosis congenitaShahinaz M Gadalla, Hormuzd A Katki, Fatma M Shebl, et al.
Haematologica|November 8, 2011
Telomere length is associated with disease severity and declines with age in dyskeratosis congenitaBlanche P Alter, Philip S Rosenberg, Neelam Giri, et al.
American Journal of Hematology|August 30, 2016
Investigation of chromosome X inactivation and clinical phenotypes in female carriers of DKC1 mutationsJialin Xu, Payal P Khincha, Neelam Giri, et al.
Blood|December 1, 2021
Disease progression and clinical outcomes in telomere biology disordersMarena R Niewisch, Neelam Giri, Lisa J McReynolds, et al.
Endocrine Connections|July 20, 2024
Reduced anti-Müllerian hormone levels in males with inherited bone marrow failure syndromesPamela Stratton, Neelam Giri, Sonia Bhala, et al.
BMC Blood Disorders|June 17, 2011
Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature reviewNeelam Giri, Rees Lee, Albert Faro, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Complex phenotype of dyskeratosis congenita and mood dysregulation with novel homozygous RTEL1 and TPH1 variantsRachel A Ungar, Neelam Giri, Maryland Pao, et al.
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