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EDWARD EICHLER, MD
MD
Hematology & Oncology Physician
NPI: 1801869235Individual
Specialties, Licenses & Credentials
Hematology & Oncology PhysicianPrimary
Internal Medicine — Hematology & Oncology
Code: 207RH0003X
F9393(TX)
Research & Publications (20)
Programmed loss of millions of base pairs from a vertebrate genome.
PMID 19561299·Proc Natl Acad Sci U S A·2009
7-preclinical
Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance.
PMID 19592580·Hum Mol Genet·2009
8-other
A method for rapid, targeted CNV genotyping identifies rare variants associated with neurocognitive disease.
PMID 19506092·Genome Res·2009
8-other
Tissue-specific variation in DNA methylation levels along human chromosome 1.
PMID 19505295·Epigenetics Chromatin·2009
8-other
Duplication hotspots, rare genomic disorders, and common disease.
PMID 19477115·Curr Opin Genet Dev·2009
6-review
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding.
PMID 19546169·Genome Res·2009
8-other
Combinatorial algorithms for structural variation detection in high-throughput sequenced genomes.
PMID 19447966·Genome Res·2009
8-other
New insights into centromere organization and evolution from the white-cheeked gibbon and marmoset.
PMID 19429672·Mol Biol Evol·2009
7-preclinical
Linkage disequilibrium between two high-frequency deletion polymorphisms: implications for association studies involving the glutathione-S transferase (GST) genes.
PMID 19424424·PLoS Genet·2009
7-preclinical
The genome sequence of taurine cattle: a window to ruminant biology and evolution.
PMID 19390049·Science·2009
7-preclinical
Characterization of six human disease-associated inversion polymorphisms.
PMID 19383631·Hum Mol Genet·2009
7-preclinical
Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
PMID 19372089·J Med Genet·2009
8-other
Lineage-specific biology revealed by a finished genome assembly of the mouse.
PMID 19468303·PLoS Biol·2009
7-preclinical
A burst of segmental duplications in the genome of the African great ape ancestor.
PMID 19212409·Nature·2009
7-preclinical
Deletion of the late cornified envelope LCE3B and LCE3C genes as a susceptibility factor for psoriasis.
PMID 19169253·Nat Genet·2009
8-other
Population analysis of large copy number variants and hotspots of human genetic disease.
PMID 19166990·Am J Hum Genet·2009
8-other
Copy number variation of CCL3-like genes affects rate of progression to simian-AIDS in Rhesus Macaques (Macaca mulatta).
PMID 19165326·PLoS Genet·2009
7-preclinical
Sequencing primate genomes: what have we learned?
PMID 19630567·Annu Rev Genomics Hum Genet·2009
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
- 2604 ST. MICHAEL DR, SUITE 210
TEXARKANA, TX 75503 - Phone
- (903) 614-5510
Quick Facts
- NPI
- 1801869235
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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