Metabolite Signature of Simvastatin Treatment Involves Multiple Metabolic Pathways

por Fernandes Silva, Lilian, Ravi, Rowmika, Vangipurapu, Jagadish, Laakso, Markku
Publicado 2022

Effects of SLCO1B1 Genetic Variant on Metabolite Profile in Participants on Simvastatin Treatment

por Fernandes Silva, Lilian, Ravi, Rowmika, Vangipurapu, Jagadish, Oravilahti, Anniina, Laakso, Markku
Publicado 2022

Metabolite Signature in the Carriers of Pathogenic Genetic Variants for Cardiomyopathy: A Population-Based METSIM Study

por Ravi, Rowmika, Fernandes Silva, Lilian, Vangipurapu, Jagadish, Maria, Maleeha, Raivo, Joose, Helisalmi, Seppo, Laakso, Markku
Publicado 2022

Case Report: Whole exome sequencing reveals a novel frameshift deletion mutation p.G2254fs in COL7A1 associated with autosomal recessive dystrophic epidermolysis bullosa

por Karuthedath Vellarikkal, Shamsudheen, Jayarajan, Rijith, Verma, Ankit, Nair, Sreelata, Ravi, Rowmika, Senthivel, Vigneshwar, Sivasubbu, Sridhar, Scaria, Vinod
Publicado 2016

Case Report: Whole exome sequencing identifies variation c.2308G>A p.E770K in RAG1 associated with B- T- NK+ severe combined immunodeficiency

por Govindaraj, Geeta Madathil, Karuthedath Vellarikkal, Shamsudheen, Jayarajan, Rijith, Ravi, Rowmika, Verma, Ankit, Chakkiyar, Krishnan, Jayakrishnan, Machinari Puthenpurayil, Arakkal, Riyaz, Raj, Revathi, Kunnaruvath, Rajeevan, Sivasubbu, Sridhar, Scaria, Vinod
Publicado 2017

SAGE: a comprehensive resource of genetic variants integrating South Asian whole genomes and exomes

por Hariprakash, Judith Mary, Vellarikkal, Shamsudheen Karuthedath, Verma, Ankit, Ranawat, Anop Singh, Jayarajan, Rijith, Ravi, Rowmika, Kumar, Anoop, Dixit, Vishal, Sivadas, Ambily, Kashyap, Atul Kumar, Senthivel, Vigneshwar, Sehgal, Paras, Mahadevan, Vijayalakshmi, Scaria, Vinod, Sivasubbu, Sridhar
Publicado 2018