Markku Ryynänen

Missense Mutations in GJB2 Encoding Connexin-26 Cause the Ectodermal Dysplasia Keratitis-Ichthyosis-Deafness Syndrome

Gabriele Richard, Fatima Rouan, Colin E. Willoughby et al. · The American Journal of Human Genetics · 2002 · 369 citations · Full text

Missense Mutations, Genetic Disorder, Pathogenesis +4

Familial intracranial aneurysms

Antti Ronkainen, Juha Hernesniemi, M Puranen et al. · The Lancet · 1997 · 307 citations

Interventional Neuroradiology, Medicine, Brain Injury +5

The 11q;22q translocation: A European collaborative analysis of 43 cases

M. Fraccaro, J. Lindsten, C. E. Ford et al. · Human Genetics · 1980 · 201 citations

European Collaborative Analysis

Volumes of hippocampus, amygdala and frontal lobe in Alzheimer patients with different apolipoprotein E genotypes

Maarit Lehtovirta, Mikko P. Laakso, Hilkka Soininen et al. · Neuroscience · 1995 · 171 citations

Neuropsychology, Alzheimer's Disease, Dementia +11

Parental decisions regarding termination of pregnancy following prenatal detection of sex chromosome abnormality

M Holmes-Siedle, Markku Ryynänen, R H Lindenbaum · Prenatal Diagnosis · 1987 · 165 citations