M H Brilliant
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Explore the profile of M H Brilliant including associated specialties, affiliations and a list of published articles.
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51
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1282
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Recent Articles
1.
Bush W, Crosslin D, Owusu-Obeng A, Wallace J, Almoguera B, Basford M, et al.
Clin Pharmacol Ther
. 2016 Feb;
100(2):160-9.
PMID: 26857349
Genetic variation can affect drug response in multiple ways, although it remains unclear how rare genetic variants affect drug response. The electronic Medical Records and Genomics (eMERGE) Network, collaborating with...
2.
Mosley J, Shaffer C, Van Driest S, Weeke P, Wells Q, Karnes J, et al.
Pharmacogenomics J
. 2015 Jul;
16(3):231-7.
PMID: 26169577
The most common side effect of angiotensin-converting enzyme inhibitor (ACEi) drugs is cough. We conducted a genome-wide association study (GWAS) of ACEi-induced cough among 7080 subjects of diverse ancestries in...
3.
Naidoo D, Wu A, Brilliant M, Denny J, Ingram C, Kitchner T, et al.
Pharmacogenomics J
. 2014 Oct;
15(3):272-7.
PMID: 25266681
Several reports have shown that statin treatment benefits patients with asthma; however, inconsistent effects have been observed. The mir-152 family (148a, 148b and 152) has been implicated in asthma. These...
4.
Rasmussen-Torvik L, Stallings S, Gordon A, Almoguera B, Basford M, Bielinski S, et al.
Clin Pharmacol Ther
. 2014 Jun;
96(4):482-9.
PMID: 24960519
We describe here the design and initial implementation of the eMERGE-PGx project. eMERGE-PGx, a partnership of the Electronic Medical Records and Genomics Network and the Pharmacogenomics Research Network, has three...
5.
Hebbring S, Schrodi S, Ye Z, Zhou Z, Page D, Brilliant M
Genes Immun
. 2013 Feb;
14(3):187-91.
PMID: 23392276
HLA-DRB1 codes for a major histocompatibility complex class II cell surface receptor. Genetic variants in and around this gene have been linked to numerous autoimmune diseases. Most notably, an association...
6.
Glurich I, Acharya A, Shukla S, Nycz G, Brilliant M
Oral Dis
. 2012 Mar;
19(1):1-17.
PMID: 22458294
Periodontal disease and diabetes, two diseases that have achieved epidemic status, share a bidirectional relationship driven by micro-inflammatory processes. The present review frames the current understanding of the pathological processes...
7.
Garrison N, Yi Z, Cohen-Barak O, Huizing M, Hartnell L, Gahl W, et al.
J Med Genet
. 2004 Jun;
41(6):e86.
PMID: 15173252
No abstract available.
8.
Newton J, Cohen-Barak O, Hagiwara N, Gardner J, Davisson M, King R, et al.
Am J Hum Genet
. 2001 Sep;
69(5):981-8.
PMID: 11574907
Oculocutaneous albinism (OCA) affects approximately 1/20,000 people worldwide. All forms of OCA exhibit generalized hypopigmentation. Reduced pigmentation during eye development results in misrouting of the optic nerves, nystagmus, alternating strabismus,...
9.
Brilliant M
Pigment Cell Res
. 2001 Apr;
14(2):86-93.
PMID: 11310796
Recessive mutations of the mouse p (pink-eyed dilution) gene lead to hypopigmentation of the eyes, skin, and fur. Mice lacking a functional p protein have pink eyes and light gray...
10.
Cohen-Barak O, Hagiwara N, Arlt M, Horton J, Brilliant M
Gene
. 2001 Mar;
265(1-2):157-64.
PMID: 11255018
The Sox gene family encodes an important group of transcription factors harboring the conserved high-mobility group (HMG) box originally identified in the mouse and human testis determining gene Sry. We...