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ALBERT ISAACS, MD PHD
MD PHD
Neurological Surgery Physician
NPI: 1427794379Individual
Specialties, Licenses & Credentials
Neurological Surgery PhysicianPrimary
Neurological Surgery
Code: 207T00000X
35.147314(OH)
Research & Publications (20)
The apolipoprotein E gene and its age-specific effects on cognitive function.
PMID 19004527·Neurobiol Aging·2010
8-other
Heparin-induced thrombocytopenia: what clinicians need to know.
PMID 19190810·Thromb Haemost·2009
6-review
Design and synthesis of inhibitors of Hedgehog signaling based on the alkaloid cyclopamine.
PMID 19552464·Org Lett·2009
8-other
Genome-wide linkage analysis of serum creatinine in three isolated European populations.
PMID 19387472·Kidney Int·2009
8-other
Genetic variation in the fibrinogen-alpha and fibrinogen-gamma genes in relation to arterial stiffness: the Rotterdam Study.
PMID 19412134·J Hypertens·2009
8-other
A study of the SORL1 gene in Alzheimer's disease and cognitive function.
PMID 19584446·J Alzheimers Dis·2009
4-observational
Loci influencing lipid levels and coronary heart disease risk in 16 European population cohorts.
PMID 19060911·Nat Genet·2009
8-other
De novo design and in vivo activity of conformationally restrained antimicrobial arylamide foldamers.
PMID 19359494·Proc Natl Acad Sci U S A·2009
7-preclinical
Cortical volumes and atrophy rates in FTD-3 CHMP2B mutation carriers and related non-carriers.
PMID 19150504·Neuroimage·2009
8-other
Presymptomatic generalized brain atrophy in frontotemporal dementia caused by CHMP2B mutation.
PMID 19202337·Dement Geriatr Cogn Disord·2009
5-case
Common variants in the JAZF1 gene associated with height identified by linkage and genome-wide association analysis.
PMID 18952825·Hum Mol Genet·2009
8-other
Evolution of the aging brain transcriptome and synaptic regulation.
PMID 18830410·PLoS One·2008
7-preclinical
Frontotemporal dementia linked to chromosome 3 (FTD-3)--current concepts and the detection of a previously unknown branch of the Danish FTD-3 family.
PMID 18484988·Eur J Neurol·2008
5-case
TDP-43 is a culprit in human neurodegeneration, and not just an innocent bystander.
PMID 18592312·Mamm Genome·2008
6-review
Familial aggregation of preeclampsia and intrauterine growth restriction in a genetically isolated population in The Netherlands.
PMID 18612323·Eur J Hum Genet·2008
8-other
Lack of TAR-DNA binding protein-43 (TDP-43) pathology in human prion diseases.
PMID 18657254·Neuropathol Appl Neurobiol·2008
8-other
Polymorphisms in the vascular endothelial growth factor gene and risk of age-related macular degeneration: the Rotterdam Study.
PMID 18708255·Ophthalmology·2008
8-other
Patterns of hybrid loss of imprinting reveal tissue- and cluster-specific regulation.
PMID 18958286·PLoS One·2008
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 2 locations total
- Address
- 700 CHILDRENS DR
COLUMBUS, OH 43205 - Phone
- (614) 722-2000
Quick Facts
- NPI
- 1427794379
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 2
- Publications
- 20
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