Korenberg, Julie R.
University of Utah
11 papers on CoChatORCID 0000-0001-5264-9109
Most cited papers
- Verified
The genetic architecture of down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies
Korbel, J. O., Tirosh-Wagner, T., Urban, A. E., Chen, X.-N., Kasowski, M., Dai, L., Grubert, F., Erdman, C., Gao, M. C., Lange, K., et al. (2009) · Proceedings of the National Academy of Sciences
Down syndrome and intellectual disability researchGenomic variations and chromosomal abnormalities
Cited by 399
- Verified
“Everybody in the world is my friend” hypersociability in young children with Williams syndrome
Doyle, T. F., Bellugi, U., Korenberg, J. R., & Graham, J. (2004) · American Journal of Medical Genetics Part A
Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders
Cited by 296
- Verified
VI. Genome structure and cognitive map of Williams syndrome
Korenberg, J. R., Chen, X.-N., Hirota, H., Lai, Z., Bellugi, U., Burian, D., Roe, B., & Matsuoka, R. (2000) · Journal of Cognitive Neuroscience
Williams Syndrome ResearchGenomic variations and chromosomal abnormalities
Cited by 285
- Verified
A human neurodevelopmental model for Williams syndrome
Chailangkarn, T., Trujillo, C. A., Freitas, B. C., Hrvoj-Mihic, B., Herai, R. H., Yu, D. X., Brown, T. T., Marchetto, M. C., Bardy, C., McHenry, L., et al. (2016) · Nature
Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders
Cited by 195
- Verified
Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior
Järvinen-Pasley, A., Bellugi, U., Reilly, J., MILLS, D. L., Galaburda, A., Reiss, A. L., & Korenberg, J. R. (2008) · Development and Psychopathology
Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders
Cited by 177
- Verified
The social phenotype of Williams syndrome
Järvinen, A., Korenberg, J. R., & Bellugi, U. (2013) · Current Opinion in Neurobiology
Williams Syndrome ResearchNeuroendocrine regulation and behavior
Cited by 161
- Verified
Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on Chromosome 7q11.23
Hirota, H., Matsuoka, R., Chen, X.-N., Salandanan, L. S., Lincoln, A., Rose, F. E., Sunahara, M., Osawa, M., Bellugi, U., & Korenberg, J. R. (2003) · Genetics in Medicine
Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders
Cited by 123
- Verified
Oxytocin and vasopressin are dysregulated in Williams Syndrome, a genetic disorder affecting social behavior
Dai, L., Carter, C. S., Ying, J., Bellugi, U., Pournajafi-Nazarloo, H., & Korenberg, J. R. (2012) · PLoS ONE
Williams Syndrome ResearchNeuroendocrine regulation and behavior
Cited by 119
- Verified
Affiliative behavior in Williams syndrome: social perception and real-life social behavior
Järvinen-Pasley, A., Adolphs, R., Yam, A., Hill, K. J., Grichanik, M., Reilly, J., Mills, D., Reiss, A. L., Korenberg, J. R., & Bellugi, U. (2010) · Neuropsychologia
Williams Syndrome ResearchFace Recognition and Perception
Cited by 63
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Intelligence in Williams Syndrome is related to STX1A, which encodes a component of the presynaptic SNARE complex
Gao, M. C., Bellugi, U., Dai, L., Mills, D. L., Sobel, E. M., Lange, K., & Korenberg, J. R. (2010) · PLoS ONE
Williams Syndrome ResearchGenetics and Neurodevelopmental Disorders
Cited by 42
- Verified
A preliminary study of orbitofrontal activation and hypersociability in Williams Syndrome
Mimura, M., Hoeft, F., Kato, M., Kobayashi, N., Sheau, K., Piggot, J., Mills, D., Galaburda, A., Korenberg, J. R., Bellugi, U., et al. (2010) · Journal of Neurodevelopmental Disorders
Williams Syndrome ResearchFace Recognition and Perception
Cited by 38
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