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REBECCA WEINSHILBOUM, DO
DO
Pediatrics Physician
NPI: 1801889589Individual
Specialties, Licenses & Credentials
Pediatrics PhysicianPrimary
Pediatrics
Code: 208000000X
97-00155(NC)
Research & Publications (20)
Cytosolic 5'-nucleotidase III (NT5C3): gene sequence variation and functional genomics.
PMID 19623099·Pharmacogenet Genomics·2009
7-preclinical
Thiopurine methyltransferase activity is related to the risk of relapse of childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study.
PMID 18987654·Leukemia·2009
4-observational
Very important pharmacogene summary: sulfotransferase 1A1.
PMID 19451861·Pharmacogenet Genomics·2009
6-review
Methotrexate/6-mercaptopurine maintenance therapy influences the risk of a second malignant neoplasm after childhood acute lymphoblastic leukemia: results from the NOPHO ALL-92 study.
PMID 19224761·Blood·2009
8-other
Catechol O-methyltransferase pharmacogenomics: human liver genotype-phenotype correlation and proximal promoter studies.
PMID 19641441·Pharmacogenet Genomics·2009
8-other
Human S-adenosylhomocysteine hydrolase: common gene sequence variation and functional genomic characterization.
PMID 19619139·J Neurochem·2009
8-other
SLC6A4 variation and citalopram response.
PMID 18618621·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Thiopurine S-methyltransferase pharmacogenetics: autophagy as a mechanism for variant allozyme degradation.
PMID 18820593·Pharmacogenet Genomics·2008
8-other
Interindividual variability in acetaminophen sulfation by human fetal liver: implications for pharmacogenetic investigations of drug-induced birth defects.
PMID 18232020·Birth Defects Res A Clin Mol Teratol·2008
8-other
Cytochrome P450 2D6 and homeobox 13/interleukin-17B receptor: combining inherited and tumor gene markers for prediction of tamoxifen resistance.
PMID 18794098·Clin Cancer Res·2008
8-other
Sulfotransferase gene copy number variation: pharmacogenetics and function.
PMID 19287157·Cytogenet Genome Res·2008
6-review
Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization.
PMID 18457970·Mol Genet Metab·2008
7-preclinical
Human phenylethanolamine N-methyltransferase genetic polymorphisms and exercise-induced epinephrine release.
PMID 18349382·Physiol Genomics·2008
7-preclinical
Gemcitabine pharmacogenomics: deoxycytidine kinase and cytidylate kinase gene resequencing and functional genomics.
PMID 18556440·Drug Metab Dispos·2008
8-other
Structural basis of substrate recognition in thiopurine s-methyltransferase.
PMID 18484748·Biochemistry·2008
7-preclinical
Pharmacogenomics: candidate gene identification, functional validation and mechanisms.
PMID 18852207·Hum Mol Genet·2008
6-review
Breast cancer risk reduction and membrane-bound catechol O-methyltransferase genetic polymorphisms.
PMID 18632656·Cancer Res·2008
8-other
Glutathione s-transferase p1: gene sequence variation and functional genomic studies.
PMID 18559526·Cancer Res·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
- Address
- 3746 VEST MILL RD
WINSTON SALEM, NC 27103 - Phone
- (336) 774-0710
Quick Facts
- NPI
- 1801889589
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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