Neelam Giri, M.D., M.B.B.S., biographical sketch and research interests - NCI
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Dr. Neelam Giri conducts clinical and laboratory research focused on the various diseases that are being studied as part of the DCEG Inherited Bone Marrow Failure Syndromes Program, including Fanconi's anemia, dyskeratosis congenita, Diamond-Blackfan anemia and Shwachman-Diamond syndrome.
Blanche Alter Retires after 21 Years at NCI - NCI
PDF) Pathogenic germline IKZF1 variant alters hematopoietic gene expression profiles
Germline mutation of MDM4, a major p53 regulator, in a familial syndrome of defective telomere maintenance
Joel Walker Fund Fanconi Anemia Research Fund
Neelam GIRI, National Institutes of Health, MD, NIH
The incidence and spectrum of congenital hand differences in patients with Fanconi anaemia: analysis of 48 patients - Grainne Bourke, Daniel Wilks, Sally Kinsey, Richard G. Feltbower, Neelam Giri, Blanche P. Alter, 2022
Disease progression and clinical outcomes in telomere biology disorders - ScienceDirect
Professor Sunil Lakhani - Centre for Clinical Research - University of Queensland
Dr. Neelam Giri, MD – Rockville, MD
Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature review, BMC Hematology
Pregnancy outcomes in mothers of offspring with inherited bone marrow failure syndromes - Giri - 2018 - Pediatric Blood & Cancer - Wiley Online Library
Neelam GIRI, National Institutes of Health, MD, NIH
Diverse Applications of Nanomedicine
Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort
Frontiers Variable Clinical Features in a Large Family With Diamond Blackfan Anemia Caused by a Pathogenic Missense Mutation in RPS19
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