Predicting cancer risk based on family history

por Jacobs, Michelle F
Publicado 2021

Outcomes of Retesting in Patients with Previously Uninformative Cancer Genetics Evaluations

por Dettwyler, Shenin A., Koeppe, Erika S., Jacobs, Michelle F., Stoffel, Elena M.
Publicado 2022

Rare presentations can suggest more than one rare condition: Striking personal and family cancer history in a patient with both CDKN2A and BRCA1 pathogenic variants

por Trupiano, Nicole, Koeppe, Erika, Jacobs, Michelle F., Else, Tobias, Cha, Kelly B.
Publicado 2022

An innovative assessment tool for evaluating narrative feedback quality among Medicine and Biomedical Sciences students

por Jacobs, Michelle M.J., van Son, Pauline M., Scharstuhl, Alwin, van Gurp, Petra J., Tanck, Esther
Publicado 2023

Cannabis-Dependence Risk Relates to Synergism between Neuroticism and Proenkephalin SNPs Associated with Amygdala Gene Expression: Case-Control Study

por Jutras-Aswad, Didier, Jacobs, Michelle M., Yiannoulos, Georgia, Roussos, Panos, Bitsios, Panos, Nomura, Yoko, Liu, Xun, Hurd, Yasmin L.
Publicado 2012

Frontal lobe microglia, neurodegenerative protein accumulation, and cognitive function in people with HIV

por Murray, Jacinta, Meloni, Gregory, Cortes, Etty P., KimSilva, Ariadna, Jacobs, Michelle, Ramkissoon, Alyssa, Crary, John F., Morgello, Susan
Publicado 2022

A Family With a Carotid Body Paraganglioma and Thyroid Neoplasias With a New SDHAF2 Germline Variant

por Wolf, Katherine I, Jacobs, Michelle F, Mehra, Rohit, Begani, Priya, Davenport, Matthew S, Marentette, Lawrence J, Basura, Gregory J, Hughes, David T, Else, Tobias
Publicado 2019

The introduction of genetic counseling in Ethiopia: Results of a training workshop and lessons learned

por Quinonez, Shane C., O’Connor, Bridget C., Jacobs, Michelle F., Mekonnen Tekleab, Atnafu, Marye, Ayalew, Bekele, Delayehu, Yashar, Beverly M., Hanson, Erika, Yeshidinber, Abate, Wedaje, Getahun
Publicado 2021

Tumor Detection Rates in Screening of Individuals with SDHx-related Hereditary Paraganglioma-Pheochromocytoma Syndrome

por Greenberg, Samantha E., Jacobs, Michelle F., Wachtel, Heather, Anson, Amanda, Buchmann, Luke, Cohen, Debbie L., Bonanni, Maria, Bennett, Bonita, Naumer, Anne, Schaefer, Amanda M., Kohlmann, Wendy, Nathanson, Katherine L., Else, Tobias, Fishbein, Lauren
Publicado 2020

BRCA1-Associated RING Domain-1 (BARD1) Loss and GBP1 Expression Enhance Sensitivity to DNA Damage in Ewing Sarcoma

por Maurer, Lisa M., Daley, Jessica D., Mukherjee, Elina, Venier, Rosemarie E., Julian, Claire M., Bailey, Nathanael G., Jacobs, Michelle F., Kumar-Sinha, Chandan, Raphael, Haley, Periyapatna, Nivitha, Weiss, Kurt, Janeway, Katherine A., Mody, Rajen, Lucas, Peter C., McAllister-Lucas, Linda M., Bailey, Kelly M.
Publicado 2022

Assessment of Clinical Benefit of Integrative Genomic Profiling in Advanced Solid Tumors

por Cobain, Erin F., Wu, Yi-Mi, Vats, Pankaj, Chugh, Rashmi, Worden, Francis, Smith, David C., Schuetze, Scott M., Zalupski, Mark M., Sahai, Vaibhav, Alva, Ajjai, Schott, Anne F., Caram, Megan E. V., Hayes, Daniel F., Stoffel, Elena M., Jacobs, Michelle F., Kumar-Sinha, Chandan, Cao, Xuhong, Wang, Rui, Lucas, David, Ning, Yu, Rabban, Erica, Bell, Janice, Camelo-Piragua, Sandra, Udager, Aaron M., Cieslik, Marcin, Lonigro, Robert J., Kunju, Lakshmi P., Robinson, Dan R., Talpaz, Moshe, Chinnaiyan, Arul M.
Publicado 2021