Concepedia

Natasha Kraeva

NK

Statistics

Publications

5

Citations

245

H-Index

5

Active since

2007

Affiliations

University of Toronto(Current)

Toronto General Hospital

Howard Hughes Medical Institute

Harvard University

Natasha Kraeva is an author at University of Toronto specializing in molecular genetics, ion channel disorders, and ryanodine receptor mutations.

ORCID

Publications per year

2007–2014

5

Publications

5

An <i>Ryr1</i> <sup> <i>I4895T</i> </sup> mutation abolishes Ca <sup>2+</sup> release channel function and delays development in homozygous offspring of a mutant mouse line

Elena Zvaritch, Frederic Depreux, Natasha Kraeva et al. · Proceedings of the National Academy of Sciences · 2007 · 81 citations

, , +17

Ca <sup>2+</sup> dysregulation in <i> Ryr1 <sup>I4895T/wt</sup> </i> mice causes congenital myopathy with progressive formation of minicores, cores, and nemaline rods

Elena Zvaritch, Natasha Kraeva, Éric Bombardier et al. · Proceedings of the National Academy of Sciences · 2009 · 74 citations · Full text

, , +17

Ryanodine receptor type 1 gene mutations found in the Canadian malignant hyperthermia population

Natasha Kraeva, Sheila Riazi, Julian Loke et al. · Canadian Journal of Anesthesia/Journal canadien d anesthésie · 2011 · 55 citations · Full text

, , +6

Exome analysis identifies <scp>B</scp>rody myopathy in a family diagnosed with malignant hyperthermia susceptibility

Nyamkhishig Sambuughin, Elena Zvaritch, Natasha Kraeva et al. · Molecular Genetics & Genomic Medicine · 2014 · 23 citations · Full text

, , +17

Genetic variation and cognitive dysfunction one year after cardiac surgery

Alastair G. Stewart, Rita Katznelson, Natasha Kraeva et al. · Anaesthesia · 2013 · 12 citations · Full text

, , +17

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