Dimitri Avramopoulos
Affiliations: | Johns Hopkins University, Baltimore, MD |
Area:
Genetics, Molecular Biology, Neuroscience BiologyGoogle:
"Dimitri Avramopoulos"Mean distance: 53433
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Publications
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| Posey JE, O'Donnell-Luria AH, Chong JX, et al. (2019) Insights into genetics, human biology and disease gleaned from family based genomic studies. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Payer LM, Steranka JP, Yang WR, et al. (2017) Structural variants caused by Alu insertions are associated with risks for many human diseases. Proceedings of the National Academy of Sciences of the United States of America |
| Guipponi M, Santoni FA, Setola V, et al. (2015) Correction: Exome Sequencing in 53 Sporadic Cases of Schizophrenia Identifies 18 Putative Candidate Genes. Plos One. 10: e0141630 |
| Peters ME, Vaidya V, Drye LT, et al. (2015) Citalopram for the Treatment of Agitation in Alzheimer Dementia: Genetic Influences. Journal of Geriatric Psychiatry and Neurology |
| Chong JX, Buckingham KJ, Jhangiani SN, et al. (2015) The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities. American Journal of Human Genetics. 97: 199-215 |
| Jurgens J, Ling H, Hetrick K, et al. (2015) Assessment of incidental findings in 232 whole-exome sequences from the Baylor-Hopkins Center for Mendelian Genomics. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 782-8 |
| Guipponi M, Santoni FA, Setola V, et al. (2014) Exome sequencing in 53 sporadic cases of schizophrenia identifies 18 putative candidate genes. Plos One. 9: e112745 |
| Brose RD, Avramopoulos D, Smith KD. (2012) SOD2 as a potential modifier of X-linked adrenoleukodystrophy clinical phenotypes. Journal of Neurology. 259: 1440-7 |
| Li Q, Fallin MD, Louis TA, et al. (2010) Detection of SNP-SNP interactions in trios of parents with schizophrenic children. Genetic Epidemiology. 34: 396-406 |
| Balciuniene J, Feng N, Iyadurai K, et al. (2007) Recurrent 10q22-q23 deletions: a genomic disorder on 10q associated with cognitive and behavioral abnormalities. American Journal of Human Genetics. 80: 938-47 |