Richard C Sallari
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Explore the profile of Richard C Sallari including associated specialties, affiliations and a list of published articles.
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7
Citations
3667
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Recent Articles
1.
Morton A, Dogan-Artun N, Faber Z, MacLeod G, Bartels C, Piazza M, et al.
Cell
. 2019 Nov;
179(6):1330-1341.e13.
PMID: 31761532
Non-coding regions amplified beyond oncogene borders have largely been ignored. Using a computational approach, we find signatures of significant co-amplification of non-coding DNA beyond the boundaries of amplified oncogenes across...
2.
Currall B, Chen M, Sallari R, Cotter M, Wong K, Robertson N, et al.
Hum Mol Genet
. 2019 Jun;
28(10):1753-1754.
PMID: 31222336
No abstract available.
3.
Currall B, Chen M, Sallari R, Cotter M, Wong K, Robertson N, et al.
Hum Mol Genet
. 2018 Sep;
27(24):4194-4203.
PMID: 30169630
Great strides in gene discovery have been made using a multitude of methods to associate phenotypes with genetic variants, but there still remains a substantial gap between observed symptoms and...
4.
Ahmed M, Sallari R, Guo H, Moore J, He H, Lupien M
BioData Min
. 2017 Feb;
10:9.
PMID: 28239419
Background: Genetic predispositions to diseases populate the noncoding regions of the human genome. Delineating their functional basis can inform on the mechanisms contributing to disease development. However, this remains a...
5.
Bailey S, Desai K, Kron K, Mazrooei P, Sinnott-Armstrong N, Treloar A, et al.
Nat Genet
. 2016 Aug;
48(10):1260-6.
PMID: 27571262
Sustained expression of the estrogen receptor-α (ESR1) drives two-thirds of breast cancer and defines the ESR1-positive subtype. ESR1 engages enhancers upon estrogen stimulation to establish an oncogenic expression program. Somatic...
6.
Dunning A, Michailidou K, Kuchenbaecker K, Thompson D, French J, Beesley J, et al.
Nat Genet
. 2016 Mar;
48(4):374-86.
PMID: 26928228
We analyzed 3,872 common genetic variants across the ESR1 locus (encoding estrogen receptor α) in 118,816 subjects from three international consortia. We found evidence for at least five independent causal...
7.
Kundaje A, Meuleman W, Ernst J, Bilenky M, Yen A, Heravi-Moussavi A, et al.
Nature
. 2015 Feb;
518(7539):317-30.
PMID: 25693563
The reference human genome sequence set the stage for studies of genetic variation and its association with human disease, but epigenomic studies lack a similar reference. To address this need,...