TY - JOUR AU - Ginsburg, G. S. AU - Wu, R. R. AU - Orlando, L. A. PY - 2019 DA - 2019// TI - Family health history: underused for actionable risk assessment JO - Lancet. VL - 394 UR - https://doi.org/10.1016/S0140-6736(19)31275-9 DO - 10.1016/S0140-6736(19)31275-9 ID - Ginsburg2019 ER - TY - JOUR AU - Wood, M. E. AU - Stockdale, A. AU - Flynn, B. S. PY - 2008 DA - 2008// TI - Interviews with primary care physicians regarding taking and interpreting the cancer family history JO - Fam Pract VL - 25 UR - https://doi.org/10.1093/fampra/cmn053 DO - 10.1093/fampra/cmn053 ID - Wood2008 ER - TY - JOUR AU - Carey, D. J. AU - Fetterolf, S. N. AU - Davis, F. D. AU - Faucett, W. A. AU - Kirchner, H. L. AU - Mirshahi, U. PY - 2016 DA - 2016// TI - The Geisinger MyCode community health initiative: an electronic health record–linked biobank for precision medicine research JO - Genet Med. VL - 18 UR - https://doi.org/10.1038/gim.2015.187 DO - 10.1038/gim.2015.187 ID - Carey2016 ER - TY - JOUR AU - Hart, M. R. AU - Biesecker, B. B. AU - Blout, C. L. AU - Christensen, K. D. AU - Amendola, L. M. AU - Bergstrom, K. L. PY - 2019 DA - 2019// TI - Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study JO - Genet Med. VL - 21 UR - https://doi.org/10.1038/s41436-018-0308-x DO - 10.1038/s41436-018-0308-x ID - Hart2019 ER - TY - JOUR AU - Reuter, M. S. AU - Walker, S. AU - Thiruvahindrapuram, B. AU - Whitney, J. AU - Cohn, I. AU - Sondheimer, N. PY - 2018 DA - 2018// TI - The Personal Genome Project Canada: findings from whole genome sequences of the inaugural 56 participants JO - CMAJ. VL - 190 UR - https://doi.org/10.1503/cmaj.171151 DO - 10.1503/cmaj.171151 ID - Reuter2018 ER - TY - JOUR AU - Schwartz, M. L. AU - McCormick, C. Z. AU - Lazzeri, A. L. AU - D’Andra, M. L. AU - Hallquist, M. L. AU - Manickam, K. PY - 2018 DA - 2018// TI - A model for genome-first care: returning secondary genomic findings to participants and their healthcare providers in a large research cohort JO - Am J Hum Genet VL - 103 UR - https://doi.org/10.1016/j.ajhg.2018.07.009 DO - 10.1016/j.ajhg.2018.07.009 ID - Schwartz2018 ER - TY - JOUR AU - Turnbull, C. AU - Scott, R. H. AU - Thomas, E. AU - Jones, L. AU - Murugaesu, N. AU - Pretty, F. B. PY - 2018 DA - 2018// TI - The 100 000 Genomes Project: bringing whole genome sequencing to the NHS JO - BMJ. VL - 361 UR - https://doi.org/10.1136/bmj.k1687 DO - 10.1136/bmj.k1687 ID - Turnbull2018 ER - TY - JOUR AU - Grzymski, J. AU - Elhanan, G. AU - Rosado, J. AU - Smith, E. AU - Schlauch, K. AU - Read, R. PY - 2020 DA - 2020// TI - Population genetic screening efficiently identifies carriers of autosomal dominant diseases JO - Nat Med VL - 27 ID - Grzymski2020 ER - TY - JOUR AU - Brothers, K. B. AU - Vassy, J. L. AU - Green, R. C. PY - 2019 DA - 2019// TI - Reconciling opportunistic and population screening in clinical genomics JO - Mayo Clin Proc VL - 94 UR - https://doi.org/10.1016/j.mayocp.2018.08.028 DO - 10.1016/j.mayocp.2018.08.028 ID - Brothers2019 ER - TY - JOUR AU - Zhang, L. AU - Bao, Y. AU - Riaz, M. AU - Tiller, J. AU - Liew, D. AU - Zhuang, X. PY - 2019 DA - 2019// TI - Population genomic screening of all young adults in a health-care system: a cost-effectiveness analysis JO - Genet Med. VL - 21 UR - https://doi.org/10.1038/s41436-019-0457-6 DO - 10.1038/s41436-019-0457-6 ID - Zhang2019 ER - TY - JOUR AU - Doerr, M. AU - Teng, K. PY - 2012 DA - 2012// TI - Family history: still relevant in the genomics era JO - Cleve Clin J Med VL - 79 UR - https://doi.org/10.3949/ccjm.79a.11065 DO - 10.3949/ccjm.79a.11065 ID - Doerr2012 ER - TY - JOUR AU - Rowley, S. M. AU - Mascarenhas, L. AU - Devereux, L. AU - Li, N. AU - Amarasinghe, K. C. AU - Zethoven, M. PY - 2019 DA - 2019// TI - Population-based genetic testing of asymptomatic women for breast and ovarian cancer susceptibility JO - Genet Med. VL - 21 UR - https://doi.org/10.1038/s41436-018-0277-0 DO - 10.1038/s41436-018-0277-0 ID - Rowley2019 ER - TY - JOUR AU - O'Neill, S. M. AU - Rubinstein, W. S. AU - Wang, C. AU - Yoon, P. W. AU - Acheson, L. S. AU - Rothrock, N. PY - 2009 DA - 2009// TI - Familial risk for common diseases in primary care: the Family Healthware Impact Trial JO - Am J Prev Med VL - 36 UR - https://doi.org/10.1016/j.amepre.2009.03.002 DO - 10.1016/j.amepre.2009.03.002 ID - O'Neill2009 ER - TY - JOUR AU - Carroll, J. C. AU - Campbell-Scherer, D. AU - Permaul, J. A. AU - Myers, J. AU - Manca, D. P. AU - Meaney, C. PY - 2017 DA - 2017// TI - Assessing family history of chronic disease in primary care: prevalence, documentation, and appropriate screening JO - Can Fam Physician VL - 63 ID - Carroll2017 ER - TY - JOUR AU - Yap, J. AU - Lim, W. K. AU - Sahlen, A. AU - Chin, C. W. AU - Chew, K. M. Y. AU - Davila, S. PY - 2019 DA - 2019// TI - Harnessing technology and molecular analysis to understand the development of cardiovascular diseases in Asia: a prospective cohort study (SingHEART) JO - BMC Cardiovasc Disord VL - 19 UR - https://doi.org/10.1186/s12872-019-1248-3 DO - 10.1186/s12872-019-1248-3 ID - Yap2019 ER - TY - JOUR AU - Bylstra, Y. AU - Davila, S. AU - Lim, W. K. AU - Wu, R. AU - Teo, J. X. AU - Kam, S. PY - 2019 DA - 2019// TI - Implementation of genomics in medical practice to deliver precision medicine for an Asian population JO - NPJ Genom Med VL - 4 UR - https://doi.org/10.1038/s41525-019-0085-8 DO - 10.1038/s41525-019-0085-8 ID - Bylstra2019 ER - TY - JOUR AU - Orlando, L. A. AU - Buchanan, A. H. AU - Hahn, S. E. AU - Christianson, C. A. AU - Powell, K. P. AU - Skinner, C. S. PY - 2013 DA - 2013// TI - Development and validation of a primary care-based family health history and decision support program (MeTree) JO - N C Med J VL - 74 ID - Orlando2013 ER - TY - JOUR AU - Wu, R. R. AU - Himmel, T. L. AU - Buchanan, A. H. AU - Powell, K. P. AU - Hauser, E. R. AU - Ginsburg, G. S. PY - 2014 DA - 2014// TI - Quality of family history collection with use of a patient facing family history assessment tool JO - BMC Fam Pract VL - 15 UR - https://doi.org/10.1186/1471-2296-15-31 DO - 10.1186/1471-2296-15-31 ID - Wu2014 ER - TY - JOUR AU - Orlando, L. A. AU - Wu, R. R. AU - Beadles, C. AU - Himmel, T. AU - Buchanan, A. H. AU - Powell, K. P. PY - 2014 DA - 2014// TI - Implementing family health history risk stratification in primary care: impact of guideline criteria on populations and resource demand JO - Am J Med Genet C Semin Med Genet VL - 166C UR - https://doi.org/10.1002/ajmg.c.31388 DO - 10.1002/ajmg.c.31388 ID - Orlando2014 ER - TY - JOUR AU - Wu, R. R. AU - Myers, R. A. AU - McCarty, C. A. AU - Dimmock, D. AU - Farrell, M. AU - Cross, D. PY - 2015 DA - 2015// TI - Protocol for the “implementation, adoption, and utility of family history in diverse care settings” study JO - Implement Sci VL - 10 UR - https://doi.org/10.1186/s13012-015-0352-8 DO - 10.1186/s13012-015-0352-8 ID - Wu2015 ER - TY - JOUR AU - Facio, F. M. AU - Feero, W. G. AU - Linn, A. AU - Oden, N. AU - Manickam, K. AU - Biesecker, L. G. PY - 2010 DA - 2010// TI - Validation of My Family Health Portrait for six common heritable conditions JO - Genet Med VL - 12 UR - https://doi.org/10.1097/GIM.0b013e3181e15bd5 DO - 10.1097/GIM.0b013e3181e15bd5 ID - Facio2010 ER - TY - JOUR AU - Bensen, J. T. AU - Liese, A. D. AU - Rushing, J. T. AU - Province, M. AU - Folsom, A. R. AU - Rich, S. S. PY - 1999 DA - 1999// TI - Accuracy of proband reported family history: the NHLBI Family Heart Study (FHS) JO - Genet Epidemiol VL - 17 UR - https://doi.org/3.0.CO;2-Q DO - 3.0.CO;2-Q ID - Bensen1999 ER - TY - STD TI - Network NCC. Genetic/Familial High-Risk Assessment: Breast and Ovarian (Version 3.2019). Available from: https://www.nccn.org/professionals/physician_gls/pdf/genetics_screening.pdf. Accessed 1 Mar 2019. UR - https://www.nccn.org/professionals/physician_gls/pdf/genetics_screening.pdf ID - ref23 ER - TY - STD TI - Network NCC. Genetic/Familial High-Risk Assessment: Colorectal Version1.2018-July 12, 2018. Available from: https://www.nccn.org/professionals/physician_gls/pdf/genetics_colon.pdf. Accessed 1 Mar 2019. UR - https://www.nccn.org/professionals/physician_gls/pdf/genetics_colon.pdf ID - ref24 ER - TY - JOUR AU - Kluijt, I. AU - Sijmons, R. H. AU - Hoogerbrugge, N. AU - Plukker, J. T. AU - Jong, D. AU - Krieken, J. H. PY - 2012 DA - 2012// TI - Familial gastric cancer: guidelines for diagnosis, treatment and periodic surveillance JO - Familial Cancer VL - 11 UR - https://doi.org/10.1007/s10689-012-9521-y DO - 10.1007/s10689-012-9521-y ID - Kluijt2012 ER - TY - JOUR AU - Post, R. S. AU - Vogelaar, I. P. AU - Carneiro, F. AU - Guilford, P. AU - Huntsman, D. AU - Hoogerbrugge, N. PY - 2015 DA - 2015// TI - Hereditary diffuse gastric cancer: updated clinical guidelines with an emphasis on germline CDH1 mutation carriers JO - J Med Genet VL - 52 UR - https://doi.org/10.1136/jmedgenet-2015-103094 DO - 10.1136/jmedgenet-2015-103094 ID - Post2015 ER - TY - JOUR AU - Zhang, J. AU - Walsh, M. F. AU - Wu, G. AU - Edmonson, M. N. AU - Gruber, T. A. AU - Easton, J. PY - 2015 DA - 2015// TI - Germline mutations in predisposition genes in pediatric cancer JO - N Engl J Med VL - 373 UR - https://doi.org/10.1056/NEJMoa1508054 DO - 10.1056/NEJMoa1508054 ID - Zhang2015 ER - TY - JOUR AU - Rahman, N. PY - 2014 DA - 2014// TI - Realizing the promise of cancer predisposition genes JO - Nature. VL - 505 UR - https://doi.org/10.1038/nature12981 DO - 10.1038/nature12981 ID - Rahman2014 ER - TY - JOUR AU - Huang, K. L. AU - Mashl, R. J. AU - Wu, Y. AU - Ritter, D. I. AU - Wang, J. AU - Oh, C. PY - 2018 DA - 2018// TI - Pathogenic germline variants in 10,389 adult cancers JO - Cell. VL - 173 UR - https://doi.org/10.1016/j.cell.2018.03.039 DO - 10.1016/j.cell.2018.03.039 ID - Huang2018 ER - TY - JOUR AU - Hamosh, A. AU - Scott, A. F. AU - Amberger, J. S. AU - Bocchini, C. A. AU - McKusick, V. A. PY - 2005 DA - 2005// TI - Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders JO - Nucleic Acids Res VL - 33 ID - Hamosh2005 ER - TY - JOUR AU - Rehm, H. L. AU - Berg, J. S. AU - Brooks, L. D. AU - Bustamante, C. D. AU - Evans, J. P. AU - Landrum, M. J. PY - 2015 DA - 2015// TI - ClinGen—the clinical genome resource JO - N Engl J Med. VL - 372 UR - https://doi.org/10.1056/NEJMsr1406261 DO - 10.1056/NEJMsr1406261 ID - Rehm2015 ER - TY - JOUR AU - Kalia, S. S. AU - Adelman, K. AU - Bale, S. J. AU - Chung, W. K. AU - Eng, C. AU - Evans, J. P. PY - 2017 DA - 2017// TI - Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics JO - Genet Med. VL - 19 UR - https://doi.org/10.1038/gim.2016.190 DO - 10.1038/gim.2016.190 ID - Kalia2017 ER - TY - JOUR AU - Landrum, M. J. AU - Lee, J. M. AU - Benson, M. AU - Brown, G. AU - Chao, C. AU - Chitipiralla, S. PY - 2016 DA - 2016// TI - ClinVar: public archive of interpretations of clinically relevant variants JO - Nucleic Acids Res VL - 44 UR - https://doi.org/10.1093/nar/gkv1222 DO - 10.1093/nar/gkv1222 ID - Landrum2016 ER - TY - JOUR AU - Tian, Y. AU - Pesaran, T. AU - Chamberlin, A. AU - Fenwick, R. B. AU - Li, S. AU - Gau, C. L. PY - 2019 DA - 2019// TI - REVEL and BayesDel outperform other in silico meta-predictors for clinical variant classification JO - Sci Rep VL - 9 UR - https://doi.org/10.1038/s41598-019-49224-8 DO - 10.1038/s41598-019-49224-8 ID - Tian2019 ER - TY - JOUR AU - Stenson, P. D. AU - Mort, M. AU - Ball, E. V. AU - Evans, K. AU - Hayden, M. AU - Heywood, S. PY - 2017 DA - 2017// TI - The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies JO - Hum Genet VL - 136 UR - https://doi.org/10.1007/s00439-017-1779-6 DO - 10.1007/s00439-017-1779-6 ID - Stenson2017 ER - TY - JOUR AU - Allot, A. AU - Peng, Y. AU - Wei, C. H. AU - Lee, K. AU - Phan, L. AU - Lu, Z. PY - 2018 DA - 2018// TI - LitVar: a semantic search engine for linking genomic variant data in PubMed and PMC JO - Nucleic Acids Res VL - 46 UR - https://doi.org/10.1093/nar/gky355 DO - 10.1093/nar/gky355 ID - Allot2018 ER - TY - JOUR AU - Richards, S. AU - Aziz, N. AU - Bale, S. AU - Bick, D. AU - Das, S. AU - Gastier-Foster, J. PY - 2015 DA - 2015// TI - Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology JO - Genet Med. VL - 17 UR - https://doi.org/10.1038/gim.2015.30 DO - 10.1038/gim.2015.30 ID - Richards2015 ER - TY - BOOK AU - Altman, D. G. PY - 1990 DA - 1990// TI - Practical statistics for medical research PB - CRC Press CY - London UR - https://doi.org/10.1201/9780429258589 DO - 10.1201/9780429258589 ID - Altman1990 ER - TY - JOUR AU - Li, Q. AU - Wang, K. PY - 2017 DA - 2017// TI - InterVar: clinical interpretation of genetic variants by the 2015 ACMG-AMP guidelines JO - Am J Hum Genet VL - 100 UR - https://doi.org/10.1016/j.ajhg.2017.01.004 DO - 10.1016/j.ajhg.2017.01.004 ID - Li2017 ER - TY - JOUR AU - Wu, R. R. AU - Sultana, R. AU - Bylstra, Y. AU - Jamuar, S. AU - Davila, S. AU - Lim, W. K. PY - 2020 DA - 2020// TI - Evaluation of family health history collection methods impact on data and risk assessment outcomes JO - Prev Med Rep VL - 18 UR - https://doi.org/10.1016/j.pmedr.2020.101072 DO - 10.1016/j.pmedr.2020.101072 ID - Wu2020 ER - TY - JOUR AU - Thompson, M. L. AU - Finnila, C. R. AU - Bowling, K. M. AU - Brothers, K. B. AU - Neu, M. B. AU - Amaral, M. D. PY - 2018 DA - 2018// TI - Genomic sequencing identifies secondary findings in a cohort of parent study participants JO - Genet Med. VL - 20 UR - https://doi.org/10.1038/gim.2018.53 DO - 10.1038/gim.2018.53 ID - Thompson2018 ER - TY - JOUR AU - Haer-Wigman, L. AU - Schoot, V. AU - Feenstra, I. AU - Vulto-van Silfhout, A. T. AU - Gilissen, C. AU - Brunner, H. G. PY - 2019 DA - 2019// TI - 1 in 38 individuals at risk of a dominant medically actionable disease JO - Eur J Hum Genet VL - 27 UR - https://doi.org/10.1038/s41431-018-0284-2 DO - 10.1038/s41431-018-0284-2 ID - Haer-Wigman2019 ER - TY - JOUR AU - Jamuar, S. S. AU - Kuan, J. L. AU - Brett, M. AU - Tiang, Z. AU - Tan, W. L. AU - Lim, J. Y. PY - 2016 DA - 2016// TI - Incidentalome from genomic sequencing: a barrier to personalized medicine? JO - EBioMed VL - 5 UR - https://doi.org/10.1016/j.ebiom.2016.01.030 DO - 10.1016/j.ebiom.2016.01.030 ID - Jamuar2016 ER - TY - JOUR AU - Antoniou, A. C. AU - Casadei, S. AU - Heikkinen, T. AU - Barrowdale, D. AU - Pylkäs, K. AU - Roberts, J. PY - 2014 DA - 2014// TI - Breast-cancer risk in families with mutations in PALB2 JO - N Engl J Med VL - 371 UR - https://doi.org/10.1056/NEJMoa1400382 DO - 10.1056/NEJMoa1400382 ID - Antoniou2014 ER - TY - JOUR AU - Taeubner, J. AU - Wieczorek, D. AU - Yasin, L. AU - Brozou, T. AU - Borkhardt, A. AU - Kuhlen, M. PY - 2018 DA - 2018// TI - Penetrance and expressivity in inherited cancer predisposing syndromes JO - Trends Cancer VL - 4 UR - https://doi.org/10.1016/j.trecan.2018.09.002 DO - 10.1016/j.trecan.2018.09.002 ID - Taeubner2018 ER - TY - JOUR AU - Schroeder, S. A. PY - 2007 DA - 2007// TI - We can do better — improving the health of the American people JO - N Engl J Med VL - 357 UR - https://doi.org/10.1056/NEJMsa073350 DO - 10.1056/NEJMsa073350 ID - Schroeder2007 ER - TY - JOUR AU - Scheuner, M. T. AU - Wang, S. J. AU - Raffel, L. J. AU - Larabell, S. K. AU - Rotter, J. I. PY - 1997 DA - 1997// TI - Family history: a comprehensive genetic risk assessment method for the chronic conditions of adulthood JO - Am J Med Genet VL - 71 UR - https://doi.org/3.0.CO;2-N DO - 3.0.CO;2-N ID - Scheuner1997 ER - TY - JOUR AU - Yoon, P. W. AU - Scheuner, M. T. AU - Peterson-Oehlke, K. L. AU - Gwinn, M. AU - Faucett, A. AU - Khoury, M. J. PY - 2002 DA - 2002// TI - Can family history be used as a tool for public health and preventive medicine? JO - Genet Med. VL - 4 UR - https://doi.org/10.1097/00125817-200207000-00009 DO - 10.1097/00125817-200207000-00009 ID - Yoon2002 ER - TY - JOUR AU - Lowery, J. T. AU - Ahnen, D. J. AU - Schroy, P. C. AU - Hampel, H. AU - Baxter, N. AU - Boland, C. R. PY - 2016 DA - 2016// TI - Understanding the contribution of family history to colorectal cancer risk and its clinical implications: a state-of-the-science review JO - Cancer. VL - 122 UR - https://doi.org/10.1002/cncr.30080 DO - 10.1002/cncr.30080 ID - Lowery2016 ER - TY - JOUR AU - Smith, R. A. AU - Andrews, K. S. AU - Brooks, D. AU - Fedewa, S. A. AU - Manassaram-Baptiste, D. AU - Saslow, D. PY - 2019 DA - 2019// TI - Cancer screening in the United States, 2019: a review of current American Cancer Society guidelines and current issues in cancer screening JO - CA Cancer J Clin VL - 69 UR - https://doi.org/10.3322/caac.21557 DO - 10.3322/caac.21557 ID - Smith2019 ER - TY - JOUR AU - Liu, W. AU - Dong, X. AU - Mai, M. AU - Seelan, R. S. AU - Taniguchi, K. AU - Krishnadath, K. K. PY - 2000 DA - 2000// TI - Mutations in AXIN2 cause colorectal cancer with defective mismatch repair by activating β-catenin/TCF signalling JO - Nat Genet VL - 26 UR - https://doi.org/10.1038/79859 DO - 10.1038/79859 ID - Liu2000 ER - TY - JOUR AU - Ndugga-Kabuye, M. K. AU - Issaka, R. B. PY - 2019 DA - 2019// TI - Inequities in multi-gene hereditary cancer testing: lower diagnostic yield and higher VUS rate in individuals who identify as Hispanic, African or Asian and Pacific Islander as compared to European JO - Fam Can VL - 18 UR - https://doi.org/10.1007/s10689-019-00144-6 DO - 10.1007/s10689-019-00144-6 ID - Ndugga-Kabuye2019 ER - TY - JOUR AU - Wideroff, L. AU - Garceau, A. O. AU - Greene, M. H. AU - Dunn, M. AU - McNeel, T. AU - Mai, P. PY - 2010 DA - 2010// TI - Coherence and completeness of population-based family cancer reports JO - Cancer Epidemiol Biomark Prev VL - 19 UR - https://doi.org/10.1158/1055-9965.EPI-09-1138 DO - 10.1158/1055-9965.EPI-09-1138 ID - Wideroff2010 ER - TY - JOUR AU - Murff, H. J. AU - Spigel, D. R. AU - Syngal, S. PY - 2004 DA - 2004// TI - Does this patient have a family history of cancer? An evidence-based analysis of the accuracy of family cancer history JO - JAMA. VL - 292 UR - https://doi.org/10.1001/jama.292.12.1480 DO - 10.1001/jama.292.12.1480 ID - Murff2004 ER -