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MICHAEL BRILLIANT, MD

MD

Psychiatry Physician

NPI: 1588779151IndividualAccepts Medicare

Specialties, Licenses & Credentials

Psychiatry PhysicianPrimary

Psychiatry & Neurology — Psychiatry

Code: 2084P0800X

036-102551(IL)

CMS Specialties

PrimaryPSYCHIATRY

Education

OTHER

Class of 1981

Research & Publications (17)

A splice site mutation is the cause of the high prevalence of oculocutaneous albinism type 2 in the Kuna population.
PMID 19397757·Pigment Cell Melanoma Res·2009
8-other
Critical parameters for genome editing using zinc finger nucleases.
PMID 18537722·Mini Rev Med Chem·2008
6-review
Stem cell transplantation demonstrates that Sox6 represses epsilon y globin expression in definitive erythropoiesis of adult mice.
PMID 17309816·Exp Hematol·2007
7-preclinical
Sox6 directly silences epsilon globin expression in definitive erythropoiesis.
PMID 16462943·PLoS Genet·2006
7-preclinical
Meningococccal meningitis and complement component 6 deficiency associated with oculocutaneous albinism.
PMID 15565285·Eur J Pediatr·2005
5-case
P gene mutations in patients with oculocutaneous albinism and findings suggestive of Hermansky-Pudlak syndrome.
PMID 15173252·J Med Genet·2004
5-case
Sox6 regulation of cardiac myocyte development.
PMID 14530442·Nucleic Acids Res·2003
7-preclinical
Nonneuronal expression of the GABA(A) beta3 subunit gene is required for normal palate development in mice.
PMID 12606284·Dev Biol·2003
7-preclinical
A 122.5-kilobase deletion of the P gene underlies the high prevalence of oculocutaneous albinism type 2 in the Navajo population.
PMID 12469324·Am J Hum Genet·2003
8-other
Mutations in the human orthologue of the mouse underwhite gene (uw) underlie a new form of oculocutaneous albinism, OCA4.
PMID 11574907·Am J Hum Genet·2001
7-preclinical
Melanosomal pH, pink locus protein and their roles in melanogenesis.
PMID 11511323·J Invest Dermatol·2001
7-preclinical
Defense use and defense understanding in children.
PMID 11339801·J Pers·2001
8-other
The mouse p (pink-eyed dilution) and human P genes, oculocutaneous albinism type 2 (OCA2), and melanosomal pH.
PMID 11310796·Pigment Cell Res·2001
6-review
Cloning, characterization and chromosome mapping of the human SOX6 gene.
PMID 11255018·Gene·2001
8-other
Aberrant pH of melanosomes in pink-eyed dilution (p) mutant melanocytes.
PMID 10998131·J Invest Dermatol·2000
7-preclinical
The underwhite (uw) locus acts autonomously and reduces the production of melanin.
PMID 10998130·J Invest Dermatol·2000
7-preclinical
Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death.
PMID 10760285·Proc Natl Acad Sci U S A·2000
7-preclinical

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
1786 MOON LAKE BLVD, SUITE 104
HOFFMAN ESTATES, IL 60194

Location

Practice Location

1786 MOON LAKE BLVD, HOFFMAN ESTATES, IL
(847) 755-8090

Quick Facts

NPI
1588779151
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
45
Publications
17

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