Egeland, T.
Norwegian University of Life Sciences
3 papers on CoChatORCID 0000-0002-3465-8885
Most cited papers
- Verified
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome
Gilfillan, G. D., Selmer, K. K., Roxrud, I., Smith, R., Kyllerman, M., Eiklid, K., Kroken, M., Mattingsdal, M., Egeland, T., Stenmark, H., et al. (2008) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 232
- Verified
Cross-sex pattern of bone mineral density in early onset gender identity disorder
Haraldsen, I. R., Haug, E., Falch, J., Egeland, T., & Opjordsmoen, S. (2007) · Hormones and Behavior
LGBTQ Health, Identity, and PolicySexual Differentiation and Disorders
Cited by 113
- Verified
Bifidobacterial Succession and Correlation Networks in a Large Unselected Cohort of Mothers and Their Children
Avershina, E., Storrø, O., Øien, T., Johnsen, R., Wilson, R., Egeland, T., & Rudi, K. (2013) · Applied and Environmental Microbiology
Gut microbiota and healthInfant Nutrition and Health
Cited by 101
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