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Inderjeet Dokal | doi.page

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Inderjeet Dokal

Queen Mary University of London(GB)Barts Health NHS Trust(GB)

Publications by Year

Research Areas

Telomeres, Telomerase, and Senescence, DNA Repair Mechanisms, Acute Myeloid Leukemia Research, Blood disorders and treatments, Hematopoietic Stem Cell Transplantation

Most-Cited Works

→ X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions(1998)955 cited
→ The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita(2001)951 cited
→ Guidelines for the diagnosis and management of adult aplastic anaemia(2015)737 cited
→ The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity(2019)600 cited
→ Dyskeratosis congenita in all its forms(2000)569 cited
→ Guidelines for the diagnosis and management of aplastic anaemia(2009)553 cited

→ Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC(2004)

460 cited

→ A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M(2005)448 cited

→ Mutations in dyskeratosis congenita: their impact on telomere length and the diversity of clinical presentation(2005)336 cited

→ Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita(2008)327 cited