Author details

Skip to Main Content

Full Name

Harsha K Rajasimha

Affiliation

ORCID

Career Start Year

2008

Papers

15

H Index

11

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37180411	Building cross-border collaborations to increase diversity and accelerate rare disease drug development - meeting report from the inaugural IndoUSrare Annual Conference 2021.		2022
32226924	Recent Advances in Systems and Network Medicine: Meeting Report from the First International Conference in Systems and Network Medicine.	Syst Med (New Rochelle)	2020
25520388	Differential gene expression and alternative splicing between diploid and tetraploid watermelon.	Journal of Experimental Botany	2015
24899048	Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.	Hum Mol Genet	2014
25579084	Organization for rare diseases India (ORDI) - addressing the challenges and opportunities for the Indian rare diseases' community.	Genet Res (Camb)	2014
24456465	Toward more transparent and reproducible omics studies through a common metadata checklist and data publications.	OMICS	2014
23495178	Developing rods transplanted into the degenerating retina of Crx-knockout mice exhibit neural activity similar to native photoreceptors.	Stem Cells	2013
27447251	Toward More Transparent and Reproducible Omics Studies Through a Common Metadata Checklist and Data Publications.	Big Data	2013
23272214	Non-random mtDNA segregation patterns indicate a metastable heteroplasmic segregation unit in m.3243A>G cybrid cells.	PLoS One	2012
22688718	Exome sequencing: capture and sequencing of all human coding regions for disease gene discovery.	Methods Mol Biol	2012
22688717	Retinal transcriptome profiling by directional next-generation sequencing using 100 ng of total RNA.	Methods Mol Biol	2012
22605924	Transcriptome analysis using next generation sequencing reveals molecular signatures of diabetic retinopathy and efficacy of candidate drugs.	Mol Vis	2012
22162623	Next-generation sequencing facilitates quantitative analysis of wild-type and Nrl(-/-) retinal transcriptomes.	Mol Vis	2011
18223651	A reduction of mitochondrial DNA molecules during embryogenesis explains the rapid segregation of genotypes.	Nat Genet	2008
18252214	Selection against pathogenic mtDNA mutations in a stem cell population leads to the loss of the 3243A-->G mutation in blood.	Am J Hum Genet	2008

1 - 15 of 15

National Eye Institute, National Institutes of Health

Co-authored papers 6

David C Samuels

Vanderbilt University

Co-authored papers 3

Preveen Ramamoorthy

Co-authored papers 3

Co-authored papers 3

Patrick F Chinnery

School of Clinical Medicine, University of Cambridge

Co-authored papers 3

William S Hancock

Northeastern University

Co-authored papers 2

Rinki Ratnapriya

National Eye Institute, National Institutes of Health

Co-authored papers 2

Elizabeth Montague

Co-authored papers 2

Lennart Martens

Co-authored papers 2

Gordon A Anderson

Co-authored papers 2

Montana State University

Co-authored papers 2

J. Craig Venter Institute

Co-authored papers 2

Co-authored papers 2

Co-authored papers 2

Center for the Study of Biological Complexity, Virginia Commonwealth University

Co-authored papers 2

Co-authored papers 2

Sanjeeva Srivastava

Indian Institute of Technology Bombay

Co-authored papers 2

Co-authored papers 2

Larissa Stanberry

Co-authored papers 2

Kenneth Verheggen

Co-authored papers 2

Harvard Medical School

Co-authored papers 2

Co-authored papers 2

Co-authored papers 2

Robert L Grossman

University of Chicago

Co-authored papers 2

Michigan State University

Co-authored papers 2

Co-authored papers 2

Stanford University

Co-authored papers 2

Courtney MacNealy-Koch

Co-authored papers 2

Rui Chen

Stanford University

Co-authored papers 2

Joseph W Kemnitz

Co-authored papers 2

1 - 30