What is he best known for?
The fields of study he is best known for:
His primary scientific interests are in Genetics, Cell biology, Macular degeneration, Molecular biology and Gene.
Allele, Genome-wide association study, Retinitis pigmentosa, Genotype and Retinal degeneration are the core of his Genetics study.
His Genome-wide association study research is multidisciplinary, incorporating perspectives in Genetic variation and Genetic association.
His studies examine the connections between Cell biology and genetics, as well as such issues in Retina, with regards to Retinal, Cellular differentiation and Progenitor cell.
His Macular degeneration research is multidisciplinary, incorporating elements of Factor H, Disease, Genetic predisposition, Case-control study and Age related.
His Molecular biology study combines topics from a wide range of disciplines, such as Homeobox, Gene expression, Transcription factor, Microarray and Leucine zipper.
His most cited work include:
- A global reference for human genetic variation. (7825 citations)
- A reference panel of 64,976 haplotypes for genotype imputation (1312 citations)
- Next-generation genotype imputation service and methods. (1165 citations)
What are the main themes of his work throughout his whole career to date?
Anand Swaroop mainly investigates Genetics, Cell biology, Retinal, Retina and Gene.
Anand Swaroop regularly links together related areas like Macular degeneration in his Genetics studies.
His Macular degeneration research also works with subjects such as
- Internal medicine which is related to area like Oncology,
- Genome-wide association study that connect with fields like Genetic association.
His studies deal with areas such as Regulation of gene expression, Rod Photoreceptors, Gene expression and Anatomy as well as Cell biology.
His Retinal research incorporates themes from Induced pluripotent stem cell and Organoid.
Anand Swaroop has researched Gene in several fields, including Molecular biology and Computational biology.
He most often published in these fields:
- Genetics (36.02%)
- Cell biology (33.64%)
- Retinal (17.15%)
What were the highlights of his more recent work (between 2016-2021)?
- Cell biology (33.64%)
- Retinal (17.15%)
- Retina (17.41%)
In recent papers he was focusing on the following fields of study:
Cell biology, Retinal, Retina, Transcriptome and Macular degeneration are his primary areas of study.
His research investigates the link between Cell biology and topics such as Retinal degeneration that cross with problems in Retinitis pigmentosa.
His Retina study combines topics in areas such as Cell type and Disease.
The Macular degeneration study combines topics in areas such as Eye disease, Internal medicine, Age related and Genome-wide association study.
Single-nucleotide polymorphism and Genetics are the main areas of his Genome-wide association study studies.
His primary area of study in Genetics is in the field of Phenotype.
Between 2016 and 2021, his most popular works were:
- Nrl knockdown by AAV-delivered CRISPR/Cas9 prevents retinal degeneration in mice (144 citations)
- Molecular Anatomy of the Developing Human Retina (106 citations)
- Retinal transcriptome and eQTL analyses identify genes associated with age-related macular degeneration (90 citations)
In his most recent research, the most cited papers focused on:
His primary areas of investigation include Retina, Retinal, Cell biology, Macular degeneration and Internal medicine.
His studies in Retina integrate themes in fields like Transcriptome, Disease and Cell type.
His biological study spans a wide range of topics, including Epithelium, Adherent Culture, Induced pluripotent stem cell, Mitochondrion and In vivo.
In general Cell biology, his work in Organoid is often linked to Presynaptic active zone, Active zone, Pikachurin and Ribbon synapse linking many areas of study.
His work carried out in the field of Macular degeneration brings together such families of science as Eye disease, Oncology and Atrophy.
Single-nucleotide polymorphism is a primary field of his research addressed under Genetics.
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