A citation-based method for searching scientific literature


List of co-cited articles
3 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


The "All of Us" Research Program.
Joshua C Denny, Joni L Rutter, David B Goldstein, Anthony Philippakis, Jordan W Smoller, Gwynne Jenkins, Eric Dishman. N Engl J Med 2019
315
66

The family history--more important than ever.
Alan E Guttmacher, Francis S Collins, Richard H Carmona. N Engl J Med 2004
357
66

Family health history: underused for actionable risk assessment.
Geoffrey S Ginsburg, R Ryanne Wu, Lori A Orlando. Lancet 2019
31
66

An Assessment of Family History Information Captured in an Electronic Health Record.
Fernanda Polubriaginof, Nicholas P Tatonetti, David K Vawdrey. AMIA Annu Symp Proc 2015
23
33

Sending family history questionnaires to patients before a colonoscopy improves genetic counseling for hereditary colorectal cancer.
Koen Kessels, Joey D Eisinger, Tom G Letteboer, G Johan A Offerhaus, Peter D Siersema, Leon M G Moons. J Dig Dis 2017
9
33


Association of Rare Pathogenic DNA Variants for Familial Hypercholesterolemia, Hereditary Breast and Ovarian Cancer Syndrome, and Lynch Syndrome With Disease Risk in Adults According to Family History.
Aniruddh P Patel, Minxian Wang, Akl C Fahed, Heather Mason-Suares, Deanna Brockman, Renee Pelletier, Sami Amr, Kalotina Machini, Megan Hawley, Leora Witkowski,[...]. JAMA Netw Open 2020
28
33

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
33

Automated extraction of family history information from clinical notes.
Robert Bill, Serguei Pakhomov, Elizabeth S Chen, Tamara J Winden, Elizabeth W Carter, Genevieve B Melton. AMIA Annu Symp Proc 2014
21
33

Accuracy of offspring reports of parental cardiovascular disease history: the Framingham Offspring Study.
Joanne M Murabito, Byung-Ho Nam, Ralph B D'Agostino, Donald M Lloyd-Jones, Christopher J O'Donnell, Peter W F Wilson. Ann Intern Med 2004
137
33

Usefulness of cardiovascular family history data for population-based preventive medicine and medical research (the Health Family Tree Study and the NHLBI Family Heart Study).
R R Williams, S C Hunt, G Heiss, M A Province, J T Bensen, M Higgins, R M Chamberlain, J Ware, P N Hopkins. Am J Cardiol 2001
186
33

Million Veteran Program: A mega-biobank to study genetic influences on health and disease.
John Michael Gaziano, John Concato, Mary Brophy, Louis Fiore, Saiju Pyarajan, James Breeling, Stacey Whitbourne, Jennifer Deen, Colleen Shannon, Donald Humphries,[...]. J Clin Epidemiol 2016
359
33

Health family trees: a tool for finding and helping young family members of coronary and cancer prone pedigrees in Texas and Utah.
R R Williams, S C Hunt, G K Barlow, R M Chamberlain, A D Weinberg, H P Cooper, J P Carbonari, A M Gotto. Am J Public Health 1988
72
33

Population-Based Relative Risks for Lung Cancer Based on Complete Family History of Lung Cancer.
Lisa A Cannon-Albright, Shamus R Carr, Wallace Akerley. J Thorac Oncol 2019
9
33

Exploring Gaps of Family History Documentation in EHR for Precision Medicine -A Case Study of Familial Hypercholesterolemia Ascertainment.
Saeed Mehrabi, Yanshan Wang, Donna Ihrke, Hongfang Liu. AMIA Jt Summits Transl Sci Proc 2016
6
33


Development of the Initial Surveys for the All of Us Research Program.
Robert M Cronin, Rebecca N Jerome, Brandy Mapes, Regina Andrade, Rebecca Johnston, Jennifer Ayala, David Schlundt, Kemberlee Bonnet, Sunil Kripalani, Kathryn Goggins,[...]. Epidemiology 2019
11
33

Creating a Common Data Model for Comparative Effectiveness with the Observational Medical Outcomes Partnership.
F FitzHenry, F S Resnic, S L Robbins, J Denton, L Nookala, D Meeker, L Ohno-Machado, M E Matheny. Appl Clin Inform 2015
43
33

UK biobank: an open access resource for identifying the causes of a wide range of complex diseases of middle and old age.
Cathie Sudlow, John Gallacher, Naomi Allen, Valerie Beral, Paul Burton, John Danesh, Paul Downey, Paul Elliott, Jane Green, Martin Landray,[...]. PLoS Med 2015
33



Data model harmonization for the All Of Us Research Program: Transforming i2b2 data into the OMOP common data model.
Jeffrey G Klann, Matthew A H Joss, Kevin Embree, Shawn N Murphy. PLoS One 2019
31
33

Diversity and inclusion for the All of Us research program: A scoping review.
Brandy M Mapes, Christopher S Foster, Sheila V Kusnoor, Marcia I Epelbaum, Mona AuYoung, Gwynne Jenkins, Maria Lopez-Class, Dara Richardson-Heron, Ahmed Elmi, Karl Surkan,[...]. PLoS One 2020
41
33

A SMART on FHIR Prototype for Genomic Test Ordering.
Alejandro Metke-Jimenez, Karen Harrap, David Conlan, Simon Gibson, John Pearson, David Hansen. Stud Health Technol Inform 2019
2
50

Running Genomic Analyses in the Cloud.
Conrad Leonard, Scott Wood, Oliver Holmes, Nic Waddell, Dominique Gorse, David P Hansen, John V Pearson. Stud Health Technol Inform 2019
1
100

Estimating the costs of genomic sequencing in cancer control.
Louisa G Gordon, Nicole M White, Thomas M Elliott, Katia Nones, Anthony G Beckhouse, Astrid J Rodriguez-Acevedo, Penelope M Webb, Xing J Lee, Nicholas Graves, Deborah J Schofield. BMC Health Serv Res 2020
7
33

Learning in the health care enterprise.
William B Rouse, Michael M E Johns, Kara M Pepe. Learn Health Syst 2017
5
33



Australian Genomics: A Federated Model for Integrating Genomics into Healthcare.
Zornitza Stark, Tiffany Boughtwood, Peta Phillips, John Christodoulou, David P Hansen, Jeffrey Braithwaite, Ainsley J Newson, Clara L Gaff, Andrew H Sinclair, Kathryn N North. Am J Hum Genet 2019
38
33

Preparing for genomic medicine: a real world demonstration of health system change.
Clara L Gaff, Ingrid M Winship, Susan M Forrest, David P Hansen, Julian Clark, Paul M Waring, Mike South, Andrew H Sinclair. NPJ Genom Med 2017
52
33

Healthcare System Priorities for Successful Integration of Genomics: An Australian Focus.
Belinda L Burns, Gemma A Bilkey, Emily P Coles, Faye L Bowman, John P Beilby, Nicholas S Pachter, Gareth Baynam, Hugh J S Dawkins, Tarun S Weeramanthri, Kristen J Nowak. Front Public Health 2019
7
33

Budget impact analysis of routinely using whole-genomic sequencing of six multidrug-resistant bacterial pathogens in Queensland, Australia.
Louisa G Gordon, Thomas M Elliott, Brian Forde, Brett Mitchell, Philip L Russo, David L Paterson, Patrick N A Harris. BMJ Open 2021
5
33

The interplay of sun damage and genetic risk in Australian multiple and single primary melanoma cases and controls.
E K McMeniman, D L Duffy, K Jagirdar, K J Lee, E Peach, A M McInerney-Leo, B De'Ambrosis, J E Rayner, B M Smithers, H P Soyer,[...]. Br J Dermatol 2020
11
33

Understanding the Barriers to Genomic Healthcare in Queensland Through an Information Management Lens.
Dana Kai Bradford, John Pearson, Dom Gorse, Alejandro Metke, Hugo Leroux, Kathy Dallest, David Bunker, David Hansen. Stud Health Technol Inform 2019
1
100



Factors influencing cancer genetic somatic mutation test ordering by cancer physician.
Anastassia Demeshko, David J Pennisi, Sushil Narayan, Stacy W Gray, Matthew A Brown, Aideen M McInerney-Leo. J Transl Med 2020
6
33


Adaptive management: from more talk to real action.
Byron K Williams, Eleanor D Brown. Environ Manage 2014
38
33

Building the foundation for genomics in precision medicine.
Samuel J Aronson, Heidi L Rehm. Nature 2015
221
33

Integrating Genomics into Healthcare: A Global Responsibility.
Zornitza Stark, Lena Dolman, Teri A Manolio, Brad Ozenberger, Sue L Hill, Mark J Caulfied, Yves Levy, David Glazer, Julia Wilson, Mark Lawler,[...]. Am J Hum Genet 2019
152
33

Genomic Investigation Reveals Contaminated Detergent as the Source of an Extended-Spectrum-β-Lactamase-Producing Klebsiella michiganensis Outbreak in a Neonatal Unit.
Paul Chapman, Brian M Forde, Leah W Roberts, Haakon Bergh, Debra Vesey, Amy V Jennison, Susan Moss, David L Paterson, Scott A Beatson, Patrick N A Harris. J Clin Microbiol 2020
16
33

What does Australia's investment in genomics mean for public health?
Andrea Belcher, Marie Mangelsdorf, Fiona McDonald, Caitlin Curtis, Nicola Waddell, Karen Hussey. Aust N Z J Public Health 2019
1
100

Evaluation of the efficacy of 3D total-body photography with sequential digital dermoscopy in a high-risk melanoma cohort: protocol for a randomised controlled trial.
Clare Amy Primiero, Aideen M McInerney-Leo, Brigid Betz-Stablein, David C Whiteman, Louisa Gordon, Liam Caffery, Joanne F Aitken, Elizabeth Eakin, Sonya Osborne, Len Gray,[...]. BMJ Open 2019
14
33

Stakeholder engagement: a key component of integrating genomic information into electronic health records.
Andrea Hartzler, Catherine A McCarty, Luke V Rasmussen, Marc S Williams, Murray Brilliant, Erica A Bowton, Ellen Wright Clayton, William A Faucett, Kadija Ferryman, Julie R Field,[...]. Genet Med 2013
44
33

Developing a gene panel for pharmacoresistant epilepsy: a review of epilepsy pharmacogenetics.
Astrid J Rodriguez-Acevedo, Louisa G Gordon, Nicola Waddell, Georgina Hollway, Lata Vadlamudi. Pharmacogenomics 2021
3
33

Precision Medicine: From Science To Value.
Geoffrey S Ginsburg, Kathryn A Phillips. Health Aff (Millwood) 2018
178
33

Protecting trust in medical genetics in the new era of forensics.
Caitlin Curtis, James Hereward, Marie Mangelsdorf, Karen Hussey, John Devereux. Genet Med 2019
5
33



Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.