Assistant Professor, Pediatrics, Vanderbilt University School of Medicine
Medical Genetics
Dr. Thomas J. Morgan, DO
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Thomas J. Morgan, DO works in the field of Medical Genetics. He studied medicine at Boston University School of Medicine. Boston University School of Medicine has a rank of 30 in research and a 52 in primary care Thomas Morgan is a published doctor. He has 43 papers published. The most current publication "Renal Teratogens." He accepts all Medicare patients.
Publications
- Renal Teratogens.
- Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans.
- Brief report: risk of adverse fetal outcomes associated with immunosuppressive medications for chronic immune-mediated diseases in pregnancy.
- Investigation of genetic risk factors for chronic adult diseases for association with preterm birth.
- Better by the Pound: The Genetics of Birth Weight.
- Genetic Risk Score Does Not Correlate with Body Mass Index of Latina Women in a Clinical Trial.
- Common polymorphisms in human lysyl oxidase genes are not associated with the adolescent idiopathic scoliosis phenotype.
- Variation in recovery: Role of gender on outcomes of young AMI patients (VIRGO) study design.
- L-histidine decarboxylase and Tourette's syndrome.
- Consanguinity mapping of congenital heart disease in a South Indian population.
- National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.
- National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health: August 24-26, 2009.
- Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
- Nonvalidation of reported genetic risk factors for acute coronary syndrome in a large-scale replication study.
- Sequence variants in SLITRK1 are associated with Tourette's syndrome.
- Acute effects of nicotine on serum glucose insulin growth hormone and cortisol in healthy smokers.
- Reporting of model validation procedures in human studies of genetic interactions.
- The education and medical practice of Dr. James McCune Smith (1813-1865), first black American to hold a medical degree.
- Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.
- Maternal smoking and congenital birth defects.
- Investigation of 95 variants identified in a genome-wide study for association with mortality after acute coronary syndrome.
- Vaccines are not associated with metabolic events in children with urea cycle disorders.
- Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies.
- Investigation of 89 candidate gene variants for effects on all-cause mortality following acute coronary syndrome.
- Disruption of contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.
- Additional support for the association of SLITRK1 var321 and Tourette syndrome.
- Overestimation of genetic risks owing to small sample sizes in cardiovascular studies.
- Dietary fish or seafood consumption is not related to cerebrovascular disease risk in twin veterans.
- Individual and combined effects of estrogen/progestin therapy and lovastatin on lipids and flow-mediated vasodilation in postmenopausal women with coronary artery dise...
- Autism in a 15-month-old child.
- A common cardiac sodium channel variant associated with sudden infant death in African Americans, SCN5A S1103Y.
- Hypertension, age, and location predict rupture of small intracranial aneurysms.
- Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth.
- An evolutionary genomic approach to identify genes involved in human birth timing.
- Single nucleotide polymorphisms in the human progesterone receptor gene and spontaneous preterm birth.
- Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
- Population-based estimate of sibling risk for preterm birth, preterm premature rupture of membranes, placental abruption and pre-eclampsia.
- Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
- Surfactant protein-A (SP-A) selectively inhibits prostaglandin F2alpha (PGF2alpha) production in term decidua: implications for the onset of labor.
- Turner syndrome: diagnosis and management.
- Siblings, day-care attendance, and the risk of asthma and wheezing.
- The economic impact of wasted prescription medication in an outpatient population of older adults.
Schools
Oklahoma State University College of Osteopathic Medicine
Doctors Specialties
- Family Medicine
- Medical Genetics
Accepted Insurances
- Aetna
- Assurant Health
- Blue Card PPO
- Great West Healthcare-Cigna PPO
- Commercial Insurance Company
- CoreSource
- Coventry Health Care
- Freedom PPO
- Life and Health Oklahoma
- First Health (Coventry Health Care) PPO
- Health Alliance
- Humana
- Medicaid
- Medicare MCR
- MultiPlan PPO
- PHCS Network PPO
- Tricare
- Choice Plus POS
- Navigate HMO
- Navigate POS
- Options PPO
- United Healthcare
- Universal American
Education
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Yale-New Haven Hospital -
Yale University School of Medicine -
Dartmouth-Hitchcock Medical Center -
Boston University School of Medicine
Hospital
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Vanderbilt Hospital and Clinics
Drug Facts
| NPI NUMBER | 1326054479 | |
| NPPES Provider LastName | MORGAN | |
| NPPES Provider FirstName | THOMAS | |
| NPPES Provider ZIPCode | 741338900 | |
| NPPES Provider State | OK | |
| Specialty Description | Family Practice | |
| Total Claim Count | 1826.0 | |
| Distinct Opioid Count | 3.0 | |
| Opioid Claim Count | 76.0 | |
| Percent Opioid Claims | 4.16 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1326054479 |
| Last Name Of The Provider | MORGAN |
| First Name Of The Provider | THOMAS |
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