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KATHY WIMMER, MD
MD
Family Medicine Physician
NPI: 1700855814IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
30204(MN)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UNIVERSITY OF MINNESOTA MEDICAL SCHOOL
Class of 1985
Research & Publications (20)
Shape coexistence near neutron number N=20: first identification of the E0 decay from the deformed first excited Jpi=0+ state in 30Mg.
PMID 19659139·Phys Rev Lett·2009
8-other
Synthesis and crystal structures of bis(diphenylphosphanyl)methanides of lithium and calcium as well as of their borane adducts.
PMID 19352522·Dalton Trans·2009
8-other
Synthesis and antigenic properties of C-7-modified Kdo mono- and disaccharide ligands and Kdo disaccharide interresidue lactones.
PMID 19665108·Carbohydr Res·2009
7-preclinical
AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes.
PMID 19306356·Genes Chromosomes Cancer·2009
8-other
Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome.
PMID 19293170·J Med Genet·2009
5-case
The operating regime of local computations in primary visual cortex.
PMID 19221143·Cereb Cortex·2009
8-other
Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?
PMID 18709565·Hum Genet·2008
6-review
Adaptation and selective information transmission in the cricket auditory neuron AN2.
PMID 18818723·PLoS Comput Biol·2008
7-preclinical
RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference.
PMID 18030674·Hum Mutat·2008
8-other
Childhood T-cell non-Hodgkin's lymphoma, colorectal carcinoma and brain tumor in association with café-au-lait spots caused by a novel homozygous PMS2 mutation.
PMID 18007577·Leukemia·2008
5-case
Dynamics of orientation tuning in cat v1 neurons depend on location within layers and orientation maps.
PMID 18982125·Front Neurosci·2007
8-other
Type 2 NF1 deletions are highly unusual by virtue of the absence of nonallelic homologous recombination hotspots and an apparent preference for female mitotic recombination.
PMID 17999360·Am J Hum Genet·2007
8-other
Intraorbital plexiform neurofibroma in an NF-1-negative patient.
PMID 17536094·Dentomaxillofac Radiol·2007
5-case
Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5' splice-site disruption.
PMID 17311297·Hum Mutat·2007
8-other
Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion.
PMID 17115058·Nat Genet·2006
4-observational
Spectrum of single- and multiexon NF1 copy number changes in a cohort of 1,100 unselected NF1 patients.
PMID 16283621·Genes Chromosomes Cancer·2006
8-other
GAB2 is a novel target of 11q amplification in AML/MDS.
PMID 16736498·Genes Chromosomes Cancer·2006
8-other
Pitfalls of automated comparative sequence analysis as a single platform for routine clinical testing for NF1.
PMID 15863657·J Med Genet·2005
8-other
Silver-Russell syndrome-like features in a patient carrying a novel NF1 mutation.
PMID 16306205·Pediatr Res·2005
5-case
[Neurofibromatosis: the most frequent hereditary tumor predisposition syndrome].
PMID 16035388·Wien Med Wochenschr·2005
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
- 680 PILLSBURY ST N
PILLAGER, MN 56473 - Phone
- (218) 746-4527
Quick Facts
- NPI
- 1700855814
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 41
- Publications
- 20
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