Author

Kavitha R. Iyer

Observed names: Kavitha Iyer, Kavitha R Iyer, Kavitha Ravee Iyer

Institutions: Victor Chang Cardiac Research Institute, UNSW Sydney

Observed institutions: The University of Western Australia, Victor Chang Cardiac Research Institute, University of Zurich, Harry Perkins Institute of Medical Research, UNSW Sydney, Indian Institute of Science Bangalore

OpenAlex ID: A5111725935

Mapping Protein-Protein Interactions for the Yeast ABC Transporter Ycf1p by Integrated Split-Ubiquitin Membrane Yeast Two-Hybrid Analysis

2007 · Christian M. Paumi, Javier Menendez, et al. · Molecular Cell · 110

Utilizing the Split-Ubiquitin Membrane Yeast Two-Hybrid System to Identify Protein-Protein Interactions of Integral Membrane Proteins

2005 · Kavitha Iyer, Lukas Bürkle, et al. · Science s STKE · 93

Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders

2019 · Justin O. Szot, Carla Campagnolo, et al. · The American Journal of Human Genetics · 52

Functional genomics and gene-environment interaction highlight the complexity of congenital heart disease caused by Notch pathway variants

2019 · Gavin Chapman, Julie L M Moreau, et al. · Human Molecular Genetics · 52

The RNA coregulator SRA, its binding proteins and nuclear receptor signaling activity

2008 · Shane M. Colley, Kavitha R. Iyer, et al. · IUBMB Life · 29

A metabolic signature for NADSYN1-dependent congenital NAD deficiency disorder

2024 · Justin O. Szot, Hartmut Cuny, et al. · Journal of Clinical Investigation · 28

Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

2020 · Ella M M A Martin, Annabelle Enriquez, et al. · Human Molecular Genetics · 26

Limiting the Extent of the RDN1 Heterochromatin Domain by a Silencing Barrier and Sir2 Protein Levels in Saccharomyces cerevisiae

2009 · Moumita Biswas, Nazif Maqani, et al. · Molecular and Cellular Biology · 25

Comprehensive defect detection in mouse embryos and the heart by combining automated phenotyping with novel population averages and atlases

2026 · Ella M.M.A. Martin, Kyle Drover, et al. · Differentiation · 1

A three generation family with VACTERL association is found to have a rare form of diamond-blackfan anaemia

2026 · Iryna Leshchynska, Debjani Das, et al. · European Journal of Human Genetics

Works count: 11

Citation count: 416

H-index: 8

I10-index: 8