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Špela Miroševič, Zalika Klemenc-Ketiš & Borut Peterlin. (2022) Family history tools for primary care: A systematic review. European Journal of General Practice 28:1, pages 75-86.
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Yuval Barak-Corren, David Tsurel, Daphna Keidar, Ilan Gofer, Dafna Shahaf, Maya Leventer-Roberts, Noam Barda & Ben Y Reis. (2023) The value of parental medical records for the prediction of diabetes and cardiovascular disease: a novel method for generating and incorporating family histories. Journal of the American Medical Informatics Association 30:12, pages 1915-1924.
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Laura Hays. (2023) The Three-Generation Pedigree. Advances in Family Practice Nursing 5:1, pages 77-91.
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Molly Dineen, Kate Sidaway-Lee, Denis Pereira Gray & Philip H Evans. (2022) Family history recording in UK general practice: the lIFeLONG study. Family Practice 39:4, pages 610-615.
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Michelle Hämmerle, Lukas Forer, Sebastian Schönherr, Annette Peters, Harald GrallertFlorian Kronenberg, Christian Gieger & Claudia Lamina. (2022) A Family and a Genome-Wide Polygenic Risk Score Are Independently Associated With Stroke in a Population-Based Study. Stroke 53:7, pages 2331-2339.
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Kathleen F. Mittendorf, Chinedu Ukaegbu, Marian J. Gilmore, Nangel M. Lindberg, Tia L. Kauffman, Donna J. Eubanks, Elizabeth Shuster, Jake Allen, Carmit McMullen, Heather Spencer Feigelson, Katherine P. Anderson, Michael C. Leo, Jessica Ezzell Hunter, Sonia Okuyama Sasaki, Jamilyn M. Zepp, Sapna Syngal, Benjamin S. Wilfond & Katrina A. B. Goddard. (2021) Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population. Familial Cancer 21:2, pages 167-180.
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Yu-Lyu Yeh, Ming Li, Oi-Man Kwok, Ping Ma & Lei-Shih Chen. (2021) Chinese Americans’ Family History of Colorectal Cancer Communication With Primary Care Physicians. Health Education & Behavior 49:1, pages 169-178.
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Kristin Clift, Sarah Macklin-Mantia, Margaret Barnhorst, Lindsey Millares, Zacharay King, Anjali Agarwal & Richard John Presutti. (2022) Comparison of a Focused Family Cancer History Questionnaire to Family History Documentation in the Electronic Medical Record. Journal of Primary Care & Community Health 13, pages 215013192110697.
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James M. Gudgeon, Jeremy C. Wallentine, Emily M. Bonham, Hannah D. McLaughlin & Mark K. Dodson. (2022) Determination of test performance of two contemporary screening tests for Lynch syndrome in endometrial cancer: A clinical trial. Gynecologic Oncology 164:1, pages 34-38.
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Ann F. Chou, Ashten R. Duncan, Gene Hallford, David M. Kelley & Lori Williamson Dean. (2021) Barriers and strategies to integrate medical genetics and primary care in underserved populations: a scoping review. Journal of Community Genetics 12:3, pages 291-309.
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Luis Lino & Henrique Martins. (2021) Medical History Taking Using Electronic Medical Records: A Systematic Review. International Journal of Digital Health 1:1.
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Philip H Evans, Imran Rafi, Judith Hayward, Molly Dineen & Fiona M. Walter. (2020) Primary care genomic research: One eye on the future. InnovAiT: Education and inspiration for general practice 14:2, pages 131-136.
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Peter Taber, Parveen Ghani, Joshua D Schiffman, Wendy Kohlmann, Rachel Hess, Valli Chidambaram, Kensaku Kawamoto, Rosalie G Waller, Damian Borbolla, Guilherme Del Fiol & Charlene Weir. (2020) Physicians’ strategies for using family history data: having the data is not the same as using the data. JAMIA Open 3:3, pages 378-385.
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Norita Hussein, Tun Firzara Abdul Malik, Hani Salim, Azah Samad, Nadeem Qureshi & Chirk Jenn Ng. (2020) Is family history still underutilised? Exploring the views and experiences of primary care doctors in Malaysia. Journal of Community Genetics 11:4, pages 413-420.
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Susanne B Haga & Lori A Orlando. (2020) The enduring importance of family health history in the era of genomic medicine and risk assessment. Personalized Medicine 17:3, pages 229-239.
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Polona Selič, Zalika Klemenc-Ketiš, Erika Zelko, Andrej Kravos, Janez Rifel, Irena Makivić, Antonija Poplas Susič, Špela Tevžič, Metka Cerovič, Borut Peterlin & Nena Kopčavar Guček. (2020) Development of an Algorithm for Determining of Genetic Risk at the Primary Healthcare Level – A New Tool for Primary Prevention: A Study Protocol. Slovenian Journal of Public Health 59:1, pages 27-32.
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Sarah N. Thomas, Shelly R. Hovick, Naomi Tan, Amy C. Sturm & Kevin Sweet. (2018) How Online Family History Tool Design and Message Content Impact User Perceptions: An Examination of Family Health<b><i>Link</i></b>. Public Health Genomics 21:1-2, pages 53-66.
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Kate McReynolds & Sara Lewis. (2017) Genetic counseling for hereditary cancer. The Nurse Practitioner 42:7, pages 22-28.
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Roya Kelishadi & Parinaz Poursafa. (2014) A Review on the Genetic, Environmental, and Lifestyle Aspects of the Early-Life Origins of Cardiovascular Disease. Current Problems in Pediatric and Adolescent Health Care 44:3, pages 54-72.
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