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DANIEL FREDMAN, M.D.
M.D.
Psychiatry Physician
NPI: 1700984127Individual
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
7555A(WY)11948(AZ)10612(MT)
Research & Publications (16)
Web-based tools and approaches to study long-range gene regulation in Metazoa.
PMID 19605518·Brief Funct Genomic Proteomic·2009
6-review
The phenotype and genotype experiment object model (PaGE-OM): a robust data structure for information related to DNA variation.
PMID 19479963·Hum Mutat·2009
8-other
Genetic structures of copy number variants revealed by genotyping single sperm.
PMID 19384415·PLoS One·2009
8-other
The transcriptional network that controls growth arrest and differentiation in a human myeloid leukemia cell line.
PMID 19377474·Nat Genet·2009
8-other
Systematic human/zebrafish comparative identification of cis-regulatory activity around vertebrate developmental transcription factor genes.
PMID 19073165·Dev Biol·2009
7-preclinical
Ancora: a web resource for exploring highly conserved noncoding elements and their association with developmental regulatory genes.
PMID 18279518·Genome Biol·2008
7-preclinical
Retroviral enhancer detection insertions in zebrafish combined with comparative genomics reveal genomic regulatory blocks - a fundamental feature of vertebrate genomes.
PMID 18047696·Genome Biol·2007
6-review
Genomic regulatory blocks encompass multiple neighboring genes and maintain conserved synteny in vertebrates.
PMID 17387144·Genome Res·2007
4-observational
Evolutionary turnover of mammalian transcription start sites.
PMID 16687732·Genome Res·2006
4-observational
Nonsynonymous SNPs: validation characteristics, derived allele frequency patterns, and suggestive evidence for natural selection.
PMID 16429399·Hum Mutat·2006
8-other
Complex SNP-related sequence variation in segmental genome duplications.
PMID 15247918·Nat Genet·2004
8-other
DFold: PCR design that minimizes secondary structure and optimizes downstream genotyping applications.
PMID 15221783·Hum Mutat·2004
8-other
HGVbase: a curated resource describing human DNA variation and phenotype relationships.
PMID 14681471·Nucleic Acids Res·2004
8-other
HGVbase: a human sequence variation database emphasizing data quality and a broad spectrum of data sources.
PMID 11752345·Nucleic Acids Res·2002
8-other
SNP association studies in Alzheimer's disease highlight problems for complex disease analysis.
PMID 11418222·Trends Genet·2001
6-review
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2800 E AJO WAY
TUCSON, AZ 85713 - Phone
- (520) 307-0682
Quick Facts
- NPI
- 1700984127
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 16
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