World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
74
Citations
20151
World Ranking
5585
National Ranking
433

Research.com Recognitions

  • Fellow of The Academy of Medical Sciences, United Kingdom
  • Fellow of The Academy of Medical Sciences, United Kingdom
  • Fellow of The Academy of Medical Sciences, United Kingdom

Overview

Inderjeet Dokal is affiliated with Queen Mary University of London in the United Kingdom and contributes primarily to the fields of Medicine and Biochemistry, Genetics and Molecular Biology. Their work focuses extensively on molecular biology, genetics, physiology, hematology, and immunology.

The scientist's research addresses key topics including:

  • Telomeres, Telomerase, and Senescence
  • Acute Myeloid Leukemia Research
  • Blood disorders and treatments
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Immunodeficiency and Autoimmune Disorders
  • Hematopoietic Stem Cell Transplantation
  • Muscle Physiology and Disorders

Recent significant papers authored by Inderjeet Dokal and collaborators include:

  • "The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants" (2020), published in Nature Communications
  • "Guidelines for the diagnosis and management of adult aplastic anaemia: A British Society for Haematology Guideline" (2024), published in British Journal of Haematology
  • "Inherited bone marrow failure in the pediatric patient" (2022), published in Blood
  • "The biology and management of dyskeratosis congenita and related disorders of telomeres" (2022), published in Expert Review of Hematology
  • "The Clinical Picture of the ERCC6L2 Disease - from Bone Marrow Failure to Acute Leukemia" (2023), published in Blood

Inderjeet Dokal has coauthored extensively with researchers such as Tom Vulliamy, Amanda J. Walne, Hemanth Tummala, Jenna Alnajar, and Nikolas Pontikos. Collaboration within this group has facilitated research across hematology and genetics.

Their work frequently appears in major publications including Blood, Faculty Opinions - Post-Publication Peer Review of the Biomedical Literature, British Journal of Haematology, The American Journal of Human Genetics, and Nature Communications.

Additionally, Inderjeet Dokal has been recognized as a Fellow of The Academy of Medical Sciences, United Kingdom.

Best Publications

  • X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

    Nina S. Heiss;Stuart W. Knight;Tom J. Vulliamy;Sabine M. Klauck

  • The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita

    Tom Vulliamy;Anna Marrone;Frederick Goldman;Andrew Dearlove

  • Guidelines for the diagnosis and management of adult aplastic anaemia.

    Sally B Killick;Nick Bown;Jamie Cavenagh;Inderjeet Dokal

  • Dyskeratosis congenita in all its forms.

    Inderjeet Dokal

  • Guidelines for the diagnosis and management of aplastic anaemia

    Judith C. W. Marsh;Sarah E. Ball;Jamie Cavenagh;Phil Darbyshire

  • The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity

    Markus G. Seidel;Gerhard Kindle;Benjamin Gathmann;Isabella Quinti

  • A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.

    Amom Ruhikanta Meetei;Annette L Medhurst;Chen Ling;Yutong Xue

  • Disease anticipation is associated with progressive telomere shortening in families with dyskeratosis congenita due to mutations in TERC

    Tom Vulliamy;Anna Marrone;Richard Szydlo;Amanda Walne

  • Mutations in dyskeratosis congenita: their impact on telomere length and the diversity of clinical presentation.

    Tom J. Vulliamy;Tom J. Vulliamy;Tom J. Vulliamy;Anna Marrone;Anna Marrone;Anna Marrone;Stuart W. Knight;Stuart W. Knight;Stuart W. Knight;Amanda Walne;Amanda Walne;Amanda Walne

  • Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita

    Tom Vulliamy;Richard Beswick;Michael Kirwan;Anna Marrone

  • Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10.

    Amanda J. Walne;Tom Vulliamy;Anna Marrone;Richard Beswick

  • Association between aplastic anaemia and mutations in telomerase RNA

    Tom Vulliamy;Anna Marrone;Inderjeet Dokal;Philip J Mason

  • TINF2 mutations result in very short telomeres: analysis of a large cohort of patients with dyskeratosis congenita and related bone marrow failure syndromes

    Amanda J Walne;Thomas J Vulliamy;Richard Beswick;Michael Kirwan

  • Association of complementation group and mutation type with clinical outcome in Fanconi anemia

    Laurence Faivre;Philippe Guardiola;Cathryn Lewis;Inderjeet Dokal

  • Dyskeratosis congenita: a genetic disorder of many faces.

    M Kirwan;I Dokal

  • X-Linked Dyskeratosis Congenita Is Predominantly Caused by Missense Mutations in the DKC1 Gene

    S.W. Knight;N.S. Heiss;T.J. Vulliamy;S. Greschner

  • Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.

    J.R. Lo Ten Foe;M.L. <b Kwee;M.A. Rooimans;A.B. Oostra

  • Constitutional mutations in RTEL1 cause severe dyskeratosis congenita.

    Amanda J. Walne;Tom Vulliamy;Michael Kirwan;Vincent Plagnol

  • Very short telomeres in the peripheral blood of patients with X-linked and autosomal dyskeratosis congenita.

    Tom J Vulliamy;Stuart W Knight;Philip J Mason;Inderjeet Dokal

  • Outcome of 69 allogeneic stem cell transplantations for Fanconi anemia using HLA-matched unrelated donors : a study on behalf of the European Group for Blood and Marrow Transplantation

    Ph. Guardiola;R. Pasquini;I. Dokal;J. J. Ortega

Frequent Co-Authors

Tom Vulliamy
Tom Vulliamy Queen Mary University of London
Philip J. Mason
Philip J. Mason Children's Hospital of Philadelphia
Irene Roberts
Irene Roberts University of Oxford
Judith C. W. Marsh
Judith C. W. Marsh King's College London
Jude Fitzgibbon
Jude Fitzgibbon Queen Mary University of London
Neil V. Morgan
Neil V. Morgan University of Birmingham
Christopher G. Mathew
Christopher G. Mathew King's College London
Vincent Plagnol
Vincent Plagnol University College London
Eliane Gluckman
Eliane Gluckman Université Paris Cité
Monica Bessler
Monica Bessler Children's Hospital of Philadelphia

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