Neelam Giri, M.D., M.B.B.S., biographical sketch and research interests - NCI

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.

Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature review, BMC Hematology

The Unique Role of Staff Clinicians in DCEG Research - NCI

Dr. Neelam Giri, MD – Rockville, MD

Joel Walker Fund Fanconi Anemia Research Fund

Germline mutation of MDM4, a major p53 regulator, in a familial syndrome of defective telomere maintenance

Neelam GIRI, National Institutes of Health, MD, NIH

Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort

Diverse Applications of Nanomedicine

2012 ASPHO Abstracts Index - The American Society of Pediatric

The Unique Role of Staff Clinicians in DCEG Research - NCI

Genotype-phenotype and outcome associations in patients with Fanconi anemia: the National Cancer Institute cohort

Haematologica, Volume 108, Issue 1 by Haematologica - Issuu

Molecular Hematopoiesis

Secretary Azar and Doctors Fauci and Collins Receive COVID-19 Vaccine

Neelam GIRI, National Institutes of Health, MD, NIH