Roelof‐Jan Oostra

An interactive three-dimensional digital atlas and quantitative database of human development

Bernadette S. de Bakker, Kees H. de Jong, Jaco Hagoort et al. · Science · 2016 · 225 citations

Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.

Roelof‐Jan Oostra, P. A. Bolhuis, Frits A. Wijburg et al. · Journal of Medical Genetics · 1994 · 120 citations · Full text

Ocular Disease, Genetics, Visual Outcome +18

Sequence Analysis of the Mitochondrial Genomes from Dutch Pedigrees with Leber Hereditary Optic Neuropathy

Neil Howell, Roelof‐Jan Oostra, P. A. Bolhuis et al. · The American Journal of Human Genetics · 2003 · 107 citations · Full text

Biology, Neurodegenerative Diseases, Mitochondrial Genomes +11

Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells

Jet Bliek, Mariëlle Alders, Saskia M. Maas et al. · European Journal of Human Genetics · 2009 · 98 citations · Full text

Bws Twins, Developmental Biology, Paternal Hypomethylation +12

Mutations in the T (brachyury) gene cause a novel syndrome consisting of sacral agenesis, abnormal ossification of the vertebral bodies and a persistent notochordal canal

Alex V. Postma, Mariëlle Alders, Marc Sylva et al. · Journal of Medical Genetics · 2013 · 69 citations