Statistics
Publications
11
Citations
294
H-Index
10
Active since
2001
Kai Muru is an author at Tartu University Hospital specializing in developmental biology, molecular genetics, and pathology.
Publications per year
2001–2023
11
11
A novel mutation in the M1S1 gene responsible for gelatinous droplike corneal dystrophy.
Gunnar Tasa, Jaak Kals, Kai Muru et al. · PubMed · 2001 · 68 citations
Mari‐Anne Vals, Tiina Kahre, Pille Mee et al. · Molecular Syndromology · 2015 · 49 citations · Full text
Beckwith-wiedemann Syndrome, Developmental Anomaly, Beckwith-wiedemann Syndromes +15
High incidence of low vitamin B12 levels in Estonian newborns
Karit Reinson, Kadi Künnapas, Annika Kriisa et al. · Molecular Genetics and Metabolism Reports · 2018 · 37 citations · Full text
Natural history of KBG syndrome in a large European cohort
Lorenzo Loberti, Lucia Pia Bruno, Stefania Granata et al. · Human Molecular Genetics · 2022 · 28 citations · Full text
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