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MILAN MUKERJI, MD
MD
Psychiatry Physician
NPI: 1497746044Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
ME 18292(FL)
Research & Publications (20)
Utilizing linkage disequilibrium information from Indian Genome Variation Database for mapping mutations: SCA12 case study.
PMID 19417544·J Genet·2009
8-other
SCA-LSVD: a repeat-oriented locus-specific variation database for genotype to phenotype correlations in spinocerebellar ataxias.
PMID 19370769·Hum Mutat·2009
8-other
Whole genome expression and biochemical correlates of extreme constitutional types defined in Ayurveda.
PMID 18782426·J Transl Med·2008
8-other
From diversity to delivery: the case of the Indian Genome Variation initiative.
PMID 18802420·Nat Rev Genet·2008
6-review
Non-random genomic divergence in repetitive sequences of human and chimpanzee in genes of different functional categories.
PMID 17375324·Mol Genet Genomics·2007
4-observational
SCA 1, SCA 2 & SCA 3/MJD mutations in ataxia syndromes in southern India.
PMID 18160752·Indian J Med Res·2007
8-other
Utility of microwave processed cell blocks as a complement to cervico-vaginal smears.
PMID 17497657·Diagn Cytopathol·2007
8-other
Genome-wide prediction of G4 DNA as regulatory motifs: role in Escherichia coli global regulation.
PMID 16651665·Genome Res·2006
4-observational
MLC1 gene is associated with schizophrenia and bipolar disorder in Southern India.
PMID 15992519·Biol Psychiatry·2005
4-observational
Post-zygotic de novo trinucleotide repeat expansion at spinocerebellar ataxia type 7 locus: evidence from an Indian family.
PMID 15750685·J Hum Genet·2005
4-observational
Founder haplotype for Machado-Joseph disease in the Indian population: novel insights from history and polymorphism studies.
PMID 15824265·Arch Neurol·2005
8-other
Insights into the mutational history and prevalence of SCA1 in the Indian population through anchored polymorphisms.
PMID 16133185·Hum Genet·2005
7-preclinical
Evidence of a common founder for SCA12 in the Indian population.
PMID 16138911·Ann Hum Genet·2005
8-other
Alu repeat analysis in the complete human genome: trends and variations with respect to genomic composition.
PMID 14751968·Bioinformatics·2004
8-other
SMARCA2 and THAP11: potential candidates for polyglutamine disorders as evidenced from polymorphism and protein-folding simulation studies.
PMID 15368101·J Hum Genet·2004
4-observational
Complex phenotypes in an Indian family with homozygous SCA2 mutations.
PMID 14705123·Ann Neurol·2004
5-case
Evolution and distribution of RNA polymerase II regulatory sites from RNA polymerase III dependant mobile Alu elements.
PMID 15461819·BMC Evol Biol·2004
8-other
Nonrandom distribution of alu elements in genes of various functional categories: insight from analysis of human chromosomes 21 and 22.
PMID 12832639·Mol Biol Evol·2003
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1350 HICKORY ST
MELBOURNE, FL 32901 - Phone
- (321) 434-1771
Quick Facts
- NPI
- 1497746044
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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