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CATHRYN WISE, MD
Nephrology Physician
NPI: 1306959127Individual
Specialties, Licenses & Credentials
Nephrology PhysicianPrimary
Internal Medicine — Nephrology
Code: 207RN0300X
MD14059(OR)MD00038221(WA)
Research & Publications (20)
Effects of expansion algorithms on speech reception thresholds.
PMID 18669128·J Am Acad Audiol·2008
8-other
Minimally invasive sacroiliac arthrodesis: outcomes of a new technique.
PMID 19057252·J Spinal Disord Tech·2008
2-rct
Understanding genetic factors in idiopathic scoliosis, a complex disease of childhood.
PMID 19424484·Curr Genomics·2008
8-other
Population-based medical and disease management: an evaluation of cost and quality.
PMID 16466341·Dis Manag·2006
4-observational
Y-chromosome and mitochondrial DNA studies on the population structure of the Christmas Island community.
PMID 15864813·Am J Phys Anthropol·2005
8-other
A standard protocol for single nucleotide primer extension in the human genome using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
PMID 12772276·Rapid Commun Mass Spectrom·2003
8-other
Mutations in CD2BP1 disrupt binding to PTP PEST and are responsible for PAPA syndrome, an autoinflammatory disorder.
PMID 11971877·Hum Mol Genet·2002
8-other
Localization of susceptibility to familial idiopathic scoliosis.
PMID 10984791·Spine (Phila Pa 1976)·2000
8-other
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.
PMID 19169254·Nat Genet·2009
8-other
A genome-wide association study of psoriasis and psoriatic arthritis identifies new disease loci.
PMID 18369459·PLoS Genet·2008
8-other
The infevers autoinflammatory mutation online registry: update with new genes and functions.
PMID 18409191·Hum Mutat·2008
8-other
Personalizing nutrigenomics research through community based participatory research and omics technologies.
PMID 19040372·OMICS·2008
6-review
Autoinflammatory genes and susceptibility to psoriatic juvenile idiopathic arthritis.
PMID 18576390·Arthritis Rheum·2008
8-other
A family-based likelihood ratio test for general pedigree structures that allows for genotyping error and missing data.
PMID 18382089·Hum Hered·2008
8-other
Asymmetric lower-limb malformations in individuals with homeobox PITX1 gene mutation.
PMID 18950742·Am J Hum Genet·2008
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
- 6902 SE LAKE RD, STE 100
MILWAUKIE, OR 97267 - Phone
- (503) 786-1167
Quick Facts
- NPI
- 1306959127
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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