What is he best known for?
The fields of study he is best known for:
His scientific interests lie mostly in Dyskeratosis congenita, Hoyeraal-Hreidarsson syndrome, Dyskerin, Telomerase and Genetics.
His work on Dyskeratosis congenita is being expanded to include thematically relevant topics such as Bone marrow.
His study in Hoyeraal-Hreidarsson syndrome is interdisciplinary in nature, drawing from both Mutation and TINF2.
His Dyskerin study combines topics in areas such as X chromosome and Pathology.
His Telomerase research includes elements of Telomere and Cancer research.
Inderjeet Dokal works mostly in the field of Genetics, limiting it down to topics relating to Molecular biology and, in certain cases, Mitotic crossover.
His most cited work include:
- The RNA component of telomerase is mutated in autosomal dominant dyskeratosis congenita (803 citations)
- X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions (725 citations)
- Dyskeratosis congenita in all its forms. (432 citations)
What are the main themes of his work throughout his whole career to date?
Dyskeratosis congenita, Genetics, Bone marrow failure, Telomerase and Immunology are his primary areas of study.
His work in Dyskeratosis congenita tackles topics such as Pathology which are related to areas like Dermatology.
His research investigates the connection with Genetics and areas like Molecular biology which intersect with concerns in Exon.
His study looks at the relationship between Bone marrow failure and fields such as Leukemia, as well as how they intersect with chemical problems.
His studies in Telomerase integrate themes in fields like Genetic heterogeneity and Cancer research.
His work deals with themes such as Internal medicine, Fanconi anemia and Haematopoiesis, which intersect with Immunology.
He most often published in these fields:
- Dyskeratosis congenita (52.41%)
- Genetics (36.90%)
- Bone marrow failure (32.62%)
What were the highlights of his more recent work (between 2014-2021)?
- Genetics (36.90%)
- Bone marrow failure (32.62%)
- Dyskeratosis congenita (52.41%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Genetics, Bone marrow failure, Dyskeratosis congenita, Germline and Gene.
Mutation and Human genetics are among the areas of Genetics where he concentrates his study.
His studies deal with areas such as Hoyeraal-Hreidarsson syndrome and Allele as well as Mutation.
His Bone marrow failure research is multidisciplinary, relying on both Cancer research, In vitro, Fanconi anemia, Progenitor cell and Signal transduction.
As part of his inquiry into Telomere and Telomerase, Inderjeet Dokal is doing Dyskeratosis congenita research.
His Gene study combines topics from a wide range of disciplines, such as Molecular biology and Acute leukemia.
Between 2014 and 2021, his most popular works were:
- Guidelines for the diagnosis and management of adult aplastic anaemia. (255 citations)
- The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity (123 citations)
- Poly(A)-specific ribonuclease deficiency impacts telomere biology and causes dyskeratosis congenita (107 citations)
In his most recent research, the most cited papers focused on:
Inderjeet Dokal mostly deals with Genetics, Dyskeratosis congenita, Mutation, Germline and Gene.
Within one scientific family, Inderjeet Dokal focuses on topics pertaining to RNA under Dyskeratosis congenita, and may sometimes address concerns connected to Human genetics and Cancer research.
In the subject of general Mutation, his work in Exome sequencing is often linked to HSPA8, thereby combining diverse domains of study.
The various areas that he examines in his Germline study include Germline mutation and Myeloid leukemia.
His research integrates issues of Myeloid, Hematopoietic stem cell, Bone marrow failure and RRNA 2'-O-methylation in his study of Germline mutation.
His Telomere, Telomerase, Exome and Hoyeraal-Hreidarsson syndrome study are his primary interests in Gene.
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