Dr. Kristin G. Monaghan PH.D.
Geneticist | Ph.D. Medical Genetics
2799 W Grand Blvd Cfp 4 Detroit MI, 48202About
Dr. Kristin Monaghan practices Genetic Medicine in Detroit, MI. As a geneticist, Dr. Monaghan performs experiments and analyzes data to interpret the inheritance of different traits in patients. A geneticist evaluates, diagnoses, and manages patients? with hereditary conditions or congenital malformations, genetic risk calculations, and mutation analysis. Dr. Monaghan carries out studies, tests, and counsels patients with genetic diseases.
Board Certification
Medical GeneticsAmerican Board of Medical GeneticsABMG
Provider Details
Expert Publications
Data provided by the National Library of Medicine- The risk of cystic fibrosis with prenatally detected echogenic bowel in an ethnically and racially diverse North American population.
- Mutation analysis of the cystic fibrosis and cationic trypsinogen genes in patients with alcohol-related pancreatitis.
- Frequency and clinical significance of the S1235R mutation in the cystic fibrosis transmembrane conductance regulator gene: results from a collaborative study.
- Early gastric cancer in young, asymptomatic carriers of germ-line E-cadherin mutations.
- Prophylactic total gastrectomy for familial gastric cancer.
- Diagnostic testing for Prader-Willi syndrome and Angelman syndrome: a cost comparison.
- Germline E-cadherin mutations in hereditary diffuse gastric cancer: assessment of 42 new families and review of genetic screening criteria.
- Preconception and prenatal cystic fibrosis carrier screening of African Americans reveals unanticipated frequencies for specific mutations.
- Cystic Fibrosis testing among Arab-Americans.
- Prostate cancer risk from occupational exposure to polycyclic aromatic hydrocarbons interacting with the GSTP1 Ile105Val polymorphism.
- Is cystic fibrosis carrier screening cost effective?
- Carrier screening in individuals of Ashkenazi Jewish descent.
- Technical standards and guidelines for reproductive screening in the Ashkenazi Jewish population.
- ACMG Standards and Guidelines for fragile X testing: a revision to the disease-specific supplements to the Standards and Guidelines for Clinical Genetics Laboratories of the American College of Medical Genetics and Genomics.
- Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing Loss.
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Nearby Providers
- Dr. Jacquelyn R. Roberson M.D.Henry Ford Health System Detroit MI 48202
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