Roelof-Jan Oostra
Roelof-Jan Oostra
hoogleraar Anatomie en Embryologie
Verified email at
Cited by
Cited by
Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.
DA Mackey, RJ Oostra, T Rosenberg, E Nikoskelainen, J Bronte-Stewart, ...
American journal of human genetics 59 (2), 481, 1996
An interactive three-dimensional digital atlas and quantitative database of human development
BS de Bakker, KH de Jong, J Hagoort, K de Bree, CT Besselink, ...
Science 354 (6315), aag0053, 2016
The anatomy in relation to injury of the lateral collateral ligaments of the ankle: a current concepts review
MPJ Van Den Bekerom, RJ Oostra, PG Alvarez, CN Van Dijk
Clinical anatomy 21 (7), 619-626, 2008
Leber's hereditary optic neuropathy: correlations between mitochondrial genotype and visual outcome.
RJ Oostra, PA Bolhuis, FA Wijburg, G Zorn-Ende, ...
Journal of medical genetics 31 (4), 280-286, 1994
Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy
N Howell, RJ Oostra, PA Bolhuis, L Spruijt, LA Clarke, DA Mackey, ...
The American Journal of Human Genetics 72 (6), 1460-1469, 2003
Lessons from BWS twins: complex maternal and paternal hypomethylation and a common source of haematopoietic stem cells
J Bliek, M Alders, SM Maas, RJ Oostra, DM Mackay, K Van Der Lip, ...
European Journal of Human Genetics 17 (12), 1625-1634, 2009
Pectus excavatum and carinatum
JM Cobben, RJ Oostra, FS van Dijk
European journal of medical genetics 57 (8), 414-417, 2014
A gene for X-linked optic atrophy is closely linked to the Xp11. 4-Xp11. 2 region of the X chromosome
JJM Assink, NT Tijmes, B Jacoline, RJ Oostra, FC Riemslag, ...
The American Journal of Human Genetics 61 (4), 934-939, 1997
Development of the hearts of lizards and snakes and perspectives to cardiac evolution
B Jensen, G van den Berg, R van den Doel, RJ Oostra, T Wang, ...
PLoS One 8 (6), e63651, 2013
An aquatic decomposition scoring method to potentially predict the postmortem submersion interval of bodies recovered from the North Sea
MA van Daalen, DS de Kat, BFL Oude Grotebevelsborg, R De Leeuwe, ...
Journal of forensic sciences 62 (2), 369-373, 2017
No evidence for ‘skewed’inactivation of the X-chromosome as cause of Leber's hereditary optic neuropathy in female carriers
RJ Oostra, S Kemp, PA Bolhuis, EM Sleeker-Wagemakers
Human genetics 97, 500-505, 1996
Leber's hereditary optic neuropathy: no significant evidence for primary or secondary pathogenicity of the 15257 mutation
RJ Oostra, PA Bolhuis, I Zorn-Ende, MM de Kok-Nazaruk, ...
Human genetics 94, 265-270, 1994
Development of a mRNA profiling multiplex for the inference of organ tissues
A Lindenbergh, M van den Berge, RJ Oostra, C Cleypool, A Bruggink, ...
International journal of legal medicine 127, 891-900, 2013
Towards a 3-dimensional atlas of the developing human embryo: the Amsterdam experience
BS de Bakker, KH de Jong, J Hagoort, RJ Oostra, AFM Moorman
Reproductive Toxicology 34 (2), 225-236, 2012
The mitochondrial DNA mutation ND6* 14,484 C associated with Leber hereditary optic neuropathy, leads to deficiency of complex I of the respiratory chain
RJ Oostra, MJM Vangalen, PA Bolhuis, EM Bleekerwagemakers, ...
Biochemical and biophysical research communications 215 (3), 1001-1005, 1995
The hypertrabeculated (noncompacted) left ventricle is different from the ventricle of embryos and ectothermic vertebrates
B Jensen, P Agger, BA de Boer, RJ Oostra, M Pedersen, AC van der Wal, ...
Biochimica et Biophysica Acta (BBA)-Molecular Cell Research 1863 (7), 1696-1706, 2016
The geometrical precision of virtual bone models derived from clinical computed tomography data for forensic anthropology
KL Colman, JGG Dobbe, KE Stull, JM Ruijter, RJ Oostra, RR Van Rijn, ...
International journal of legal medicine 131, 1155-1163, 2017
In patients with pseudoxanthoma elasticum a thicker and more elastic carotid artery is associated with elastin fragmentation and proteoglycans accumulation
L Kornet, AAB Bergen, APG Hoeks, JP Cleutjens, RJ Oostra, MJ Daemen, ...
Ultrasound in medicine & biology 30 (8), 1041-1048, 2004
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
AV Postma, M Alders, M Sylva, CM Bilardo, E Pajkrt, RR van Rijn, ...
Journal of Medical Genetics 51 (2), 90-97, 2014
Congenital anomalies in the teratological collection of Museum Vrolik in Amsterdam, The Netherlands. II: Skeletal dysplasias
RJ Oostra, B Baljet, PF Dijkstra, RCM Hennekam
American journal of medical genetics 77 (2), 116-134, 1998
The system can't perform the operation now. Try again later.
Articles 1–20