Katarina Lindahl

Genetic epidemiology, prevalence, and genotype–phenotype correlations in the Swedish population with osteogenesis imperfecta

Katarina Lindahl, Eva Åström, Carl‐Johan Rubin et al. · European Journal of Human Genetics · 2015 · 197 citations · Full text

Bone Disease, Bone Health, Genetics +6

COL1 C-propeptide cleavage site mutations cause high bone mass osteogenesis imperfecta

Katarina Lindahl, Aileen M. Barnes, Nadja Fratzl‐Zelman et al. · Human Mutation · 2011 · 137 citations · Full text

Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta – A retrospective cohort study

Kristofer Andersson, Göran Dahllöf, Katarina Lindahl et al. · PLoS ONE · 2017 · 98 citations · Full text

Bone Disease, Developmental Anomaly, Developmental Biology +12

Homozygosity for CREB3L1 premature stop codon in first case of recessive osteogenesis imperfecta associated with OASIS-deficiency to survive infancy

Katarina Lindahl, Eva Åström, Anca Dragomir et al. · Bone · 2018 · 32 citations

Biology, Developmental Anomaly, Recessive Osteogenesis Imperfecta +11

Heterozygosity for a coding SNP in COL1A2 confers a lower BMD and an increased stroke risk

Katarina Lindahl, Carl‐Johan Rubin, Helena Brändström et al. · Biochemical and Biophysical Research Communications · 2009 · 25 citations

Genome-wide Association Study, Lower Bmd, Genetic Disorder +9