Professor of Medicine, Washington University St Louis
Medical Genetics
Dr. Alison J. Whelan, MD
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Dr. Alison J. Whelan is an expert in the field of Medical Genetics. She attended Washington University School of Medicine in St. Louis. She received awards:"America's Top Doctors", "America's Top Doctors for Cancer" and "St. Louis Magazine: Top Doctors". Alison Whelan is a published doctor. She has 53 publications published. The most current publication "Correlation of platelet Fc gammaRIIA polymorphism in refractory idiopathic (immune) thrombocytopenic purpura." She accepts Medicare.
Publications
- Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2015.
- Primary care specialty choices of United States medical graduates, 1997-2006.
- DICER1 mutations in familial pleuropulmonary blastoma.
- Mutations in the GGCX and ABCC6 genes in a family with pseudoxanthoma elasticum-like phenotypes.
- Attrition during graduate medical education: medical school perspective.
- Characteristics and career intentions of the emerging MD/PhD workforce.
- Reaping what we sow: the emerging academic medicine workforce.
- Clustering of Lynch syndrome malignancies with no evidence for a role of DNA mismatch repair.
- The changing paradigm of contemporary U.S. allopathic medical school graduates' career paths: analysis of the 1997-2004 national AAMC Graduation Questionnaire database.
- Which U.S. medical graduates plan to become specialty-board certified? Analysis of the 1997-2004 national association of American Medical Colleges Graduation Questionn...
- Educational responses to declining student interest in internal medicine careers.
- What predicts USMLE Step 3 performance?
- Genetic red flags: clues to thinking genetically in primary care practice.
- What predicts surgical internship performance?
- Penetrance and expressivity of MSH6 germline mutations in seven kindreds not ascertained by family history.
- Clinical genetic testing and early surgical intervention in patients with multiple endocrine neoplasia type 1 (MEN 1).
- Recent trends in match process outcomes for U.S. senior medical students.
- A new first-year course designed and taught by a senior medical student.
- MSI in endometrial carcinoma: absence of MLH1 promoter methylation is associated with increased familial risk for cancers.
- Correlation of platelet Fc gammaRIIA polymorphism in refractory idiopathic (immune) thrombocytopenic purpura.
- Evaluation of clinical guidelines for the management of Staphylococcus aureus bacteraemia.
- Serum levels of soluble CD163 correlate with the inflammatory process in coeliac disease.
- Reforming the core clerkship in internal medicine: the SGIM/CDIM Project. Society of General Internal Medicine/Clerkship Directors in Internal Medicine.
- Biomedical education in the 21st century.
- Expression and characterization of human mutant (glutamic acid304) medium-chain acyl-coenzyme A dehydrogenase in mammalian cells.
- Molecular characterization of medium-chain acyl-CoA dehydrogenase deficiency causing sudden death.
- Molecular characterization of inherited medium-chain acyl-CoA dehydrogenase deficiency.
- Klippel-Trenaunay-Weber syndrome associated with a 5:11 balanced translocation.
- Mapping human telomere regions with YAC and P1 clones: chromosome-specific markers for 27 telomeres including 149 STSs and 24 polymorphisms for 14 proterminal regions.
- Human telomerase RNA mutations and bone marrow failure.
- Washington University School of Medicine.
- Human glucagon-like peptide-1 receptor gene in NIDDM. Identification and use of simple sequence repeat polymorphisms in genetic analysis.
- Washington University in St. Louis School of Medicine.
- A novel missense mutation in the MEN1 gene in a patient with multiple endocrine neoplasia type 1.
- Plexiform neurofibromatosis of the liver: case report and review of the literature.
- Perceptions of genetic risk assessment and education among first-degree relatives of colorectal cancer patients and implications for physicians.
- Molecular basis of inherited medium-chain acyl-CoA dehydrogenase deficiency causing sudden child death.
- Safety and pharmacokinetics of agalsidase alfa in patients with Fabry disease and end-stage renal disease.
- Low frequency of CDKN2 mutation in endometrial carcinomas.
- Prophylactic oophorectomy and ovarian cancer surveillance. Patient perceptions and satisfaction.
- An 11-year-old boy with mosaic ring chromosome 6 and dilated aortic root.
- Educational assessment guidelines: a Clerkship Directors in Internal Medicine commentary.
- Bringing the human genome and the revolution in bioinformatics to the medical school classroom: a case report from Washington University School of Medicine.
- Brief report: a familial syndrome of pancreatic cancer and melanoma with a mutation in the CDKN2 tumor-suppressor gene.
- Evaluation of the family history collection process and the accuracy of cancer reporting among a series of women with endometrial cancer.
- Comparing medical students' performances and their achievements as residents: similar findings.
- The future of medical student education in internal medicine.
- A practical approach to familial and hereditary colorectal cancer.
- How competitive is my surgical specialty?
- Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability.
- Atypical clustering of gynecologic malignancies: A family study including molecular analysis of candidate genes.
- Epitope-positive truncating MLH1 mutation and loss of PMS2: implications for IHC-directed genetic testing for Lynch syndrome.
Schools
Washington Center School of Medicine
Barneshosp Wash University
Barnes Jewish Hospital
St Louis Chldns Hospital Wash University
Doctors Specialties
- Clinical Genetics
- Internal Medicine
- Medical Genetics
Accepted Insurances
Awards
- America's Top Doctors
- America's Top Doctors for Cancer
- St. Louis Magazine: Top Doctors
Education
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Washington University - Barnes-Jewish Hospital -
Washington University School of Medicine in St. Louis
Hospital
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Barnes-Jewish Hospital -
St. Louis Children's Hospital
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1487670709 |
| Last Name Of The Provider | WHELAN |
| First Name Of The Provider | ALISON |
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