| 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 | 441 | 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 | 214 | 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 | 163 | 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 | 147 | 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 | 128 | 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 | 112 | 2009 |
| Pectus excavatum and carinatum JM Cobben, RJ Oostra, FS van Dijk European journal of medical genetics 57 (8), 414-417, 2014 | 108 | 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, JB ten Brink, RJ Oostra, FC Riemslag, ... The American Journal of Human Genetics 61 (4), 934-939, 1997 | 81 | 1997 |
| 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 | 72 | 2017 |
| 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 | 71 | 2013 |
| Virtual forensic anthropology: the accuracy of osteometric analysis of 3D bone models derived from clinical computed tomography (CT) scans KL Colman, HH De Boer, JGG Dobbe, NPTJ Liberton, KE Stull, ... Forensic science international 304, 109963, 2019 | 65 | 2019 |
| 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 | 63 | 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 | 62 | 2012 |
| The development of the human notochord K de Bree, BS de Bakker, RJ Oostra PLoS One 13 (10), e0205752, 2018 | 59 | 2018 |
| 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 | 57 | 2016 |
| 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 | 56 | 1996 |
| The applicability of forensic time since death estimation methods for buried bodies in advanced decomposition stages S Pittner, V Bugelli, ME Benbow, B Ehrenfellner, A Zissler, ... PLoS One 15 (12), e0243395, 2020 | 55 | 2020 |
| 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 | 55 | 2017 |
| 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 | 53 | 2014 |
| 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 | 52 | 1994 |