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WILLEM SPEED, MD
MD
Family Medicine Physician
NPI: 1427510148IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
11898958-1205(UT)208512(OR)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE
Class of 2019
Research & Publications (20)
The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.
PMID 18574484·Mol Psychiatry·2010
7-preclinical
Population-specific variation in haplotype composition and heterozygosity at the POLB locus.
PMID 19167932·DNA Repair (Amst)·2009
8-other
Global variation in CYP2C8-CYP2C9 functional haplotypes.
PMID 19381162·Pharmacogenomics J·2009
8-other
Single- and multiple-dose disposition kinetics of sunitinib malate, a multitargeted receptor tyrosine kinase inhibitor: comparative plasma kinetics in non-clinical species.
PMID 19169880·Cancer Chemother Pharmacol·2009
7-preclinical
Global patterns of variation in allele and haplotype frequencies and linkage disequilibrium across the CYP2E1 gene.
PMID 18663376·Pharmacogenomics J·2008
8-other
Ethnic related selection for an ADH Class I variant within East Asia.
PMID 18382665·PLoS One·2008
8-other
Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome.
PMID 18004766·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Multiple superoxide dismutase 1/splicing factor serine alanine 15 variants are associated with the development and progression of diabetic nephropathy: the Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications Genetics study.
PMID 17914031·Diabetes·2008
4-observational
Motoneuron-specific NR3B gene: no association with ALS and evidence for a common null allele.
PMID 17687115·Neurology·2008
8-other
Conservative evolution in duplicated genes of the primate Class I ADH cluster.
PMID 17204375·Gene·2007
7-preclinical
Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations.
PMID 17202997·Eur J Hum Genet·2007
8-other
Developing a SNP panel for forensic identification of individuals.
PMID 16360294·Forensic Sci Int·2006
8-other
Considerable haplotype diversity within the 23kb encompassing the ADH7 gene.
PMID 16385178·Alcohol Clin Exp Res·2005
8-other
Use of autosomal loci for clustering individuals and populations of East Asian origin.
PMID 16028061·Hum Genet·2005
8-other
Formation and antitumor activity of PNU-159682, a major metabolite of nemorubicin in human liver microsomes.
PMID 15746066·Clin Cancer Res·2005
4-observational
Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.
PMID 15303240·Am J Hum Genet·2004
8-other
Bitter receptor gene (TAS2R38), 6-n-propylthiouracil (PROP) bitterness and alcohol intake.
PMID 15547448·Alcohol Clin Exp Res·2004
4-observational
Phase I and pharmacokinetic (PK) study of MAG-CPT (PNU 166148): a polymeric derivative of camptothecin (CPT).
PMID 15187995·Br J Cancer·2004
3-trial
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
- 1140 SW SIMPSON AVE STE 110
BEND, OR 97702 - Phone
- (541) 389-7741
Quick Facts
- NPI
- 1427510148
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 7
- Publications
- 20
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