Concepedia
Statistics
Publications
7
Citations
532
H-Index
Active since
1999
Affiliations
Helsinki University Hospital(Current)
University of Helsinki
University of California, Los Angeles
Institute for Molecular Medicine Finland
The Ohio State University
Mira Kyttälä is an author at Helsinki University Hospital specializing in medical genetics, genetics, and human genetics.
Publications per year
1999–2016
MKS1, encoding a component of the flagellar apparatus basal body proteome, is mutated in Meckel syndrome
Mira Kyttälä, Jonna Tallila, Riitta Salonen et al. · Nature Genetics · 2006 · 252 citations
Life Sciences, Genetics, Molecular Biology +10
Spectrum of<i>MKS1</i>and<i>MKS3</i>mutations in Meckel syndrome: a genotype-phenotype correlation
Rana Khaddour, Ursula M. Smith, Lekbir Baala et al. · Human Mutation · 2007 · 100 citations · Full text
Life Sciences, Genetics, Molecular Genetics +14
WW-Domain-Containing Oxidoreductase Is Associated with Low Plasma HDL-C Levels
Jenny C. Lee, Daphna Weissglas‐Volkov, Mira Kyttälä et al. · The American Journal of Human Genetics · 2008 · 56 citations · Full text
Life Sciences, Biochemistry, Molecular Biology +12
USF1 Contributes to High Serum Lipid Levels in Dutch FCHL Families and U.S. Whites With Coronary Artery Disease
Jenny C. Lee, Daphna Weissglas‐Volkov, Mira Kyttälä et al. · Arteriosclerosis Thrombosis and Vascular Biology · 2007 · 45 citations · Full text
Medicine, Cardiology, Genetics +16
High-Resolution Physical and Genetic Mapping of the Critical Region for Meckel Syndrome and Mulibrey Nanism on Chromosome 17q22–q23
Paulina Paavola, Kristiina Avela, Nina Horelli‐Kuitunen et al. · Genome Research · 1999 · 27 citations · Full text
Life Sciences, Genetics, Molecular Genetics +16
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