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DOUGLAS GEIGER, D.M.D.
D.M.D.
Dentist
NPI: 1538250774Individual
Specialties, Licenses & Credentials
DentistPrimary
Dentist
Code: 122300000X
7094(NC)
Research & Publications (20)
Speeding up HMM algorithms for genetic linkage analysis via chain reductions of the state space.
PMID 19477987·Bioinformatics·2009
8-other
Parent and professional agreement on cognitive level of children with autism.
PMID 12199135·J Autism Dev Disord·2002
8-other
64-Section multi-detector row CT in the preoperative diagnosis of peritoneal carcinomatosis: correlation with histopathological findings.
PMID 19455272·Abdom Imaging·2010
8-other
Heteromeric AtKC1{middle dot}AKT1 channels in Arabidopsis roots facilitate growth under K+-limiting conditions.
PMID 19509299·J Biol Chem·2009
8-other
Diffuse osteopenia and myelopathy in a puppy fed a diet composed of an organic premix and raw ground beef.
PMID 19366336·J Am Vet Med Assoc·2009
5-case
Spinal muscular atrophy with pontocerebellar hypoplasia is caused by a mutation in the VRK1 gene.
PMID 19646678·Am J Hum Genet·2009
8-other
Optimisation of a high-resolution whole-body MR angiography protocol with parallel imaging and biphasic administration of a single bolus of Gd-BOPTA: preliminary experience in the systemic evaluation of atherosclerotic burden in patients referred for endovascular procedures.
PMID 19430733·Radiol Med·2009
4-observational
Gadofosveset-enhanced MR angiography of carotid arteries: does steady-state imaging improve accuracy of first-pass imaging? Comparison with selective digital subtraction angiography.
PMID 19401574·Radiology·2009
4-observational
Inferring ancestries efficiently in admixed populations with linkage disequilibrium.
PMID 19645595·J Comput Biol·2009
8-other
Encephalomyelopathy and polyneuropathy associated with neuronal vacuolation in two Boxer littermates.
PMID 19605909·Vet Pathol·2009
5-case
Panel construction for mapping in admixed populations via expected mutual information.
PMID 18353806·Genome Res·2008
8-other
Alopecia, neurological defects, and endocrinopathy syndrome caused by decreased expression of RBM28, a nucleolar protein associated with ribosome biogenesis.
PMID 18439547·Am J Hum Genet·2008
8-other
64-MDCT imaging of the coronary arteries and systemic arterial vascular tree in a single examination: optimisation of the scan protocol and contrast-agent administration.
PMID 18594763·Radiol Med·2008
4-observational
Diagnosing mycobacterial lymphadenitis in children using fine needle aspiration biopsy: cytomorphology, ZN staining and autofluorescence -- making more of less.
PMID 18335554·Diagn Cytopathol·2008
4-observational
Electron holography with a Cs-corrected transmission electron microscope.
PMID 18096096·Microsc Microanal·2008
8-other
Variational upper and lower bounds for probabilistic graphical models.
PMID 18652528·J Comput Biol·2008
7-preclinical
[Successful individualized and targeted therapy of an NSCLC patient with Gefitinib based on a predictive assessment of the EGF-receptor mutation status].
PMID 17455141·Pneumologie·2007
8-other
Familial steroid-sensitive nephrotic syndrome in Southern Israel: clinical and genetic observations.
PMID 17219184·Pediatr Nephrol·2007
8-other
Results of the prospective, randomized, multicenter Food and Drug Administration investigational device exemption study of the ProDisc-L total disc replacement versus circumferential fusion for the treatment of 1-level degenerative disc disease.
PMID 17495770·Spine (Phila Pa 1976)·2007
4-observational
A deleterious mutation in SAMD9 causes normophosphatemic familial tumoral calcinosis.
PMID 16960814·Am J Hum Genet·2006
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 321 S POLK ST STE 2A
PINEVILLE, NC 28134 - Phone
- (704) 889-7395
Quick Facts
- NPI
- 1538250774
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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