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Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 8, 2017
Observed frequency and challenges of variant reclassification in a hereditary cancer clinicSarah Macklin, Nisha Durand, Paldeep Atwal, et al.Journal of Women'S Health (2002)|November 8, 2017
Women's Health Endocrine UpdateEkta Kapoor, Stephanie Faubion, Stephanie Hines, et al.Clinical Case Reports|February 9, 2017
<i>BARD1</i> nonsense variant c.1921C>T in a patient with recurrent breast cancerJennifer Gass, Madeline Tatro, Patrick Blackburn, et al.Pharmacy Practice|October 25, 2013
Job satisfaction among chain community pharmacists: results from a pilot studyAna L Hincapie, Stephanie Yandow, Stephanie Hines, et al.Familial Cancer|June 24, 2017
The role of screening MRI in the era of next generation sequencing and moderate-risk genetic mutationsSarah Macklin, Jennifer Gass, Ghada Mitri, et al.Familial Cancer|April 5, 2017
A case of contralateral breast cancer and skin cancer associated with NBN heterozygous pathogenic variant c.698_701delAACAJennifer Gass, Jessica Jackson, Sarah Macklin, et al.American Journal of Disaster Medicine|February 13, 2015
Willingness to respond for radiologic incidents: a hands-on approachJohn Richard Ludtke, Roopsi Narayan, Ameer Matariyeh, et al.Journal of Community Genetics|August 22, 2019
Patients' views on variants of uncertain significance across indicationsKristin Clift, Sarah Macklin, Colin Halverson, et al.Medicina (Kaunas, Lithuania)|May 18, 2019
Genomic Observations of a Rare/Pathogenic <i>SMAD3</i> Variant in Loeys⁻Dietz Syndrome 3 Confirmed by Protein Informatics and Structural InvestigationsJohn E Richter, Ayesha Samreen, Charitha Vadlamudi, et al.Supportive Cancer Therapy|July 18, 2008
Phase II Evaluation of Desipramine for the Treatment of Hot FlashesDebra L Barton, Charles L Loprinzi, Pamela Atherton, et al.Pageof 2