Mira Kyttälä

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

Signal Transduction, Developmental Biology, Mendelian Disorder +7

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

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

Oxysterol, Biochemistry, Reactive Oxygen Specie +4

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

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

Trancript Map, Developmental Biology, Mendelian Disorder +15