| Student Name |
|
Year |
|
Plan B Project Title |
|
| Erica Horger |
|
2003 |
|
Factors associated with a heightened perception of risk among African American women with a family history of breast cancer |
|
| Seema Panchal |
|
2003 |
|
Genetic counseling recommendations for Charcot-Marie-Tooth Disease |
|
| Bryanna Cox-Gover |
|
2003 |
|
Identifying barriers to seeking genetics services for children with confirmed hearing loss |
|
| Dima El-Khechen |
|
2004 |
|
Assessing the validity of the CancerGene program, a BRCA1 and BRCA2 gene mutation risk assessment tool, using a chart review |
|
| Jennifer Grffin-Burton |
|
2004 |
|
Undergraduate biology professors' knowledge of and advising practices regarding the field of genetic counseling |
|
| Stephanie Hurst |
|
2004 |
|
Quantifying the female carrier phenotype of Pelizaeus-Merzbacher Disease |
|
| Kate Shane |
|
2004 |
|
Improving cancer risk assessment in primary care |
|
| Elizabeth Herr |
|
2005 |
|
The clinical presentation of women with Charcot-Marie-Tooth Disease Type X (CMTX) |
|
| Tami Friedberg |
|
2005 |
|
Predictors of knowledge of hereditary breast cancer among ethnically diverse breast cancer patients |
|
| Katie Moore-Biro |
|
2005 |
|
Medical students' use of genetics knowledge and skills during the Year 3 clerkships |
|
| Ryan Rodarmer |
|
2005 |
|
Attitudes toward genetic counseling, testing and research |
|
| Karen Metzler |
|
2006 |
|
A self-administered screening tool to select patients at risk for a hereditary breast and ovarian cancer syndrome: A pilot study using a revised family history assessment tool (FHAT) |
|
| Allison Lawrence |
|
2006 |
|
The impact of not proceeding with predictive genetic testing in individuals at risk for Huntington Disease |
|
| Gwenn Sickles |
|
2006 |
|
Women's knowledge and expectations of fetal ultrasound |
|
| Lauren Hickson |
|
2006 |
|
Advice for families: How to communicate BRCA 1/2 results with your relatives |
|
| Rupin Dhamankar |
|
2007 |
|
Outcome of Pregnancies Detected With Non-mosaic Trisomy 16 by Chorionic Villus Sampling |
|
| Stephanie Farner |
|
2007 |
|
Client Expectations of Genetic Counseling: What Are They and Are We Meeting Them? |
|
| Lori Felczak |
|
2007 |
|
The Natural History of Pelizaeus Merzbacher Disease: Patients with Duplications |
|
| Lindsey Weed |
|
2007 |
|
Evaluation of Patient Satisfaction with Genetic Counseling Services |
|
| Jennifer Barrick |
|
2008 |
|
Outcomes of clinical application of published diagnostic criteria for Fetal Alcohol Syndrome Spectrum Disorders |
|
| Lindsey Bennett |
|
2008 |
|
Is Pelizaeus-Merzbacher a Progressive Disorder? |
|
| Jacqueline Gauthier |
|
2008 |
|
Attitudes and Perceptions of Genetic Counseling for Hereditary Breast Cancer Among Arab-American Women? |
|
| Sarah Kramer |
|
2008 |
|
Demographics, Family, and Adherence in Pediatric PKU Patients |
|
| Lindsey Stott |
|
2008 |
|
The Potential Impact of Prenatal Diagnosis of Birth Defects and Elective Termination on Rates of Birth Defects in Michigan |
|
| Emily Swan |
|
2008 |
|
A Quantitative Study of Reproductive Decision-Making in Charcot-Marie Tooth Disease |
|
| Tiara Johnson |
|
2009 |
|
Collecting a Family History of Adult-onset Disorders in a Pediatric Genetic Setting |
|
| Kelly Kennelly |
|
2009 |
|
Assessing the Validity of Family History Collection in a Pediatric Genetics Setting |
|
| Mary Nyhuis |
|
2009 |
|
The Validity of the CancerGene Program to Assess the Probability of BRCA1/2 Mutation: The Impact of Limited Family Structure |
|
| Preethi Premkumar |
|
2009 |
|
Qualitative Evaluation of a New Charcot-Marie-Tooth Disease Neuropathy Scoring System for Children in a Multidisciplinary CMT Clinic |
|
| Abbey Putnam |
|
2009 |
|
Dominant Versus Non-Dominant Hand Strength in CMT1A |
|
| Kate Zellmer |
|
2009 |
|
Comparison of Methods: Family History Questionnaire Versus a 3-Generation Pedigree Interview in an Infertility Setting |
|
| Sohnee Ahmed |
|
2010 |
|
Quality of Life in Caregivers of People with Huntington Disease |
|
| Ghazal Almradi |
|
2010 |
|
Characterizing Family History of Heart Disease in High Risk Women and its Correlation with Risk Reducing Behaviors |
|
| Melissa Dumouchelle |
|
2010 |
|
Reaching the Next Generation of Scientists: What Do High School Textbooks Say about Genomics and Genetic Counseling? |
|
| Veronica Kokavec |
|
2010 |
|
Comparison of Methods: The Utility of a Family History Questionnaire versus a Three-Generation Pedigree Interview in Couples with Infertility |
|
| Stephanie Percich |
|
2010 |
|
Surveillance of BRCA1/2 Genetic Testing Referral and Use |
|
Michael Jay Harrison |
|
2011 |
|
Predictors of consent to donate biological sample data to the NIH Central Repository |
|
Sommer Hayden |
|
2011 |
|
Parental attitudes regarding expanding newborn screening to include Duchenne Muscular Dystrophy: A unique perspective of parents with an affected child |
|
Lauren Isley |
|
2011 |
|
Preimplantation genetic diagnosis: An investigation of knowledge, attitudes, and perceptions of parents of children with muscular dystrophy |
|
Jason Laufman |
|
2011 |
|
Evaluation of state comprehensive cancer control plans for genetics and genomics content |
|
Divya Wilson Mathews |
|
2011 |
|
Non-chromosomal risks associated with low maternal serum estriol levels during pregnancy |
|
Bridget O’Connor |
|
2011 |
|
Education on fetal alcohol syndrome/fetal alcohol spectrum disorders provided at women’s publically funded treatment centers in the state of Michigan |
|
Nikki Hadjuk |
|
2012 |
|
The influence of culture and ethnicity on hereditary breast and ovarian cancer genetic testing and counseling uptake |
|