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.
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
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.
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.
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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Next-generation genotype imputation service and methods.
Sayantan Das;Lukas Forer;Sebastian Schönherr;Carlo Sidore;Carlo Sidore.
Nature Genetics (2016)
A reference panel of 64,976 haplotypes for genotype imputation
Shane McCarthy;Sayantan Das;Warren Kretzschmar;Olivier Delaneau.
Nature Genetics (2016)
Retinal Repair by Transplantation of Photoreceptor Precursors
R. E. MacLaren;R. A. Pearson;A. MacNeil;R. H. Douglas.
A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants
Lars G. Fritsche;Wilmar Igl;Jessica N.Cooke Bailey;Felix Grassmann.
Nature Genetics (2016)
Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region.
Carl C. T. Ton;Harri Hirvonen;Hiroshi Miwa;Michael M. Weil.
Nrl is required for rod photoreceptor development
Alan J. Mears;Mineo Kondo;Mineo Kondo;Prabodha K. Swain;Yuichiro Takada.
Nature Genetics (2001)
Seven new loci associated with age-related macular degeneration
Lars G. Fritsche;Lars G. Fritsche;Wei Chen;Wei Chen;Matthew Schu;Brian L. Yaspan.
Nature Genetics (2013)
The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4
John A. Sayer;John A. Sayer;Edgar A. Otto;John F. O'Toole;Gudrun Nurnberg.
Nature Genetics (2006)
Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration
Wei Chen;Dwight Stambolian;Albert O. Edwards;Kari E. Branham.
Proceedings of the National Academy of Sciences of the United States of America (2010)
Transcriptional regulation of photoreceptor development and homeostasis in the mammalian retina.
Anand Swaroop;Douglas Kim;Douglas Kim;Douglas Forrest.
Nature Reviews Neuroscience (2010)
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