Steiner, Robert D.
Oregon Health & Science University · Doernbecher Children's Hospital · Marshfield Clinic Research Foundation · Marshfield Clinic Research Institute
4 papers on CoChatORCID 0000-0003-4177-4590
Most cited papers
- Verified
Mutations in the Human Sterol Δ7-Reductase Gene at 11q12-13 Cause Smith-Lemli-Opitz Syndrome
Wassif, C. A., Maslen, C., Kachilele-Linjewile, S., Lin, D., Linck, L. M., Connor, W. E., Steiner, R. D., & Porter, F. D. (1998) · The American Journal of Human Genetics
Cholesterol and Lipid MetabolismMetabolism and Genetic Disorders
Cited by 418
- Verified
The near universal presence of autism spectrum disorders in children with Smith–Lemli–Opitz syndrome
Sikora, D. M., Pettit‐Kekel, K., Penfield, J., Merkens, L. S., & Steiner, R. D. (2006) · American Journal of Medical Genetics Part A
Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders
Cited by 196
- Verified
Apolipoprotein E–low density lipoprotein receptor interaction affects spatial memory retention and brain ApoE levels in an isoform-dependent manner
Johnson, L. A., Olsen, R. H. J., Merkens, L. S., DeBarber, A., Steiner, R. D., Sullivan, P. M., Maeda, N., & Raber, J. (2014) · Neurobiology of Disease
Alzheimer's disease research and treatmentsCholesterol and Lipid Metabolism
Cited by 107
- Verified
Shared familial transmission of autism spectrum and attention‐deficit/hyperactivity disorders
Musser, E. D., Hawkey, E., Kachan‐Liu, S. S., Lees, P., Roullet, J., Goddard, K., Steiner, R. D., & Nigg, J. T. (2014) · Journal of Child Psychology and Psychiatry
Autism Spectrum Disorder ResearchAttention Deficit Hyperactivity Disorder
Cited by 97
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