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SARAH JO HEINEN MD
MD
Family Medicine Physician
NPI: 1538697164IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
MD-47344(IA)
Education
INDIANA UNIVERSITY SCHOOL OF MEDICINE
Class of 2017
Research & Publications (20)
An oculomotor decision process revealed by functional magnetic resonance imaging.
PMID 17192434·J Neurosci·2006
4-observational
mSpecs: a software tool for the administration and editing of mass spectral libraries in the field of metabolomics.
PMID 19624850·BMC Bioinformatics·2009
8-other
C3 deposition glomerulopathy due to a functional factor H defect.
PMID 18633337·Kidney Int·2009
5-case
Factor H-related protein 1 (CFHR-1) inhibits complement C5 convertase activity and terminal complex formation.
PMID 19528535·Blood·2009
7-preclinical
Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation.
PMID 18268093·Blood·2008
5-case
Transgenic wheat expressing a barley class II chitinase gene has enhanced resistance against Fusarium graminearum.
PMID 18467324·J Exp Bot·2008
8-other
Performance evaluation of a computer-aided detection algorithm for solid pulmonary nodules in low-dose and standard-dose MDCT chest examinations and its influence on radiologists.
PMID 18941043·Br J Radiol·2008
8-other
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency.
PMID 18006700·Blood·2008
8-other
The effects of microstimulation of the dorsomedial frontal cortex on saccade latency.
PMID 18216220·J Neurophysiol·2008
7-preclinical
Overexpression of defense response genes in transgenic wheat enhances resistance to Fusarium head blight.
PMID 17103001·Plant Cell Rep·2007
8-other
Hemolytic uremic syndrome: a factor H mutation (E1172Stop) causes defective complement control at the surface of endothelial cells.
PMID 17229916·J Am Soc Nephrol·2007
8-other
Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome.
PMID 17367211·PLoS Genet·2007
8-other
Defective complement control of factor H (Y402H) and FHL-1 in age-related macular degeneration.
PMID 17399790·Mol Immunol·2007
7-preclinical
Oculomotor hide and seek: pursuing an accelerating target behind an occluder. Focus on "target acceleration can be extracted and represented within the predictive drive to ocular pursuit".
PMID 17652416·J Neurophysiol·2007
8-other
Complement and diseases: defective alternative pathway control results in kidney and eye diseases.
PMID 16026839·Mol Immunol·2006
6-review
Factor H and atypical hemolytic uremic syndrome: mutations in the C-terminus cause structural changes and defective recognition functions.
PMID 16338962·J Am Soc Nephrol·2006
7-preclinical
A hAT superfamily transposase recruited by the cereal grass genome.
PMID 16468023·Mol Genet Genomics·2006
8-other
De novo gene conversion in the RCA gene cluster (1q32) causes mutations in complement factor H associated with atypical hemolytic uremic syndrome.
PMID 16470555·Hum Mutat·2006
7-preclinical
Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II).
PMID 16612335·Kidney Int·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
Via practice · 2 locations total
- Address
- 104 BUNCOMBE DR
ROCK RAPIDS, IA 51246 - Phone
- (712) 472-3333
Quick Facts
- NPI
- 1538697164
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 9
- Publications
- 20
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