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Markku Ryynänen | doi.page

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Markku Ryynänen

Oulu University Hospital(FI)University of Oulu(FI)

Publications by Year

Research Areas

Prenatal Screening and Diagnostics, Pregnancy and preeclampsia studies, Parvovirus B19 Infection Studies, Alzheimer's disease research and treatments, Congenital Anomalies and Fetal Surgery

Most-Cited Works

→ Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome(2002)370 cited
→ Familial intracranial aneurysms(1997)307 cited
→ The 11q;22q translocation: A European collaborative analysis of 43 cases(1980)201 cited
→ Volumes of hippocampus, amygdala and frontal lobe in Alzheimer patients with different apolipoprotein E genotypes(1995)171 cited
→ Parental decisions regarding termination of pregnancy following prenatal detection of sex chromosome abnormality(1987)165 cited
→ A severe loss of choline acetyltransferase in the frontal cortex of Alzheimer patients carrying apolipoprotein ε4 allele(1995)164 cited

→ Clinical and neuropsychological characteristics in familial and sporadic Alzheimer's disease(1996)

155 cited

Human type VII collagen: genetic linkage of the gene (COL7A1) on chromosome 3 to dominant dystrophic epidermolysis bullosa.(1991)

→ Dominant dystrophic epidermolysis bullosa: identification of a Gly-->Ser substitution in the triple-helical domain of type VII collagen.(1994)136 cited

→ Intracranial aneurysms: MR angiographic screening in 400 asymptomatic individuals with increased familial risk.(1995)132 cited