A citation-based method for searching scientific literature

Maren T Scheuner, Jane Peredo, Kelly Tangney, Diane Schoeff, Taylor Sale, Caroline Lubick-Goldzweig, Alison Hamilton, Lee Hilborne, Martin Lee, Brian Mittman, Elizabeth M Yano, Ira M Lubin. Genet Med 2017
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


The NIH genetic testing registry: a new, centralized database of genetic tests to enable access to comprehensive information and improve transparency.
Wendy S Rubinstein, Donna R Maglott, Jennifer M Lee, Brandi L Kattman, Adriana J Malheiro, Michael Ovetsky, Vichet Hem, Viatcheslav Gorelenkov, Guangfeng Song, Craig Wallin,[...]. Nucleic Acids Res 2013
79
33

Thou shalt versus thou shalt not: a meta-synthesis of GPs' attitudes to clinical practice guidelines.
Benedicte Carlsen, Claire Glenton, Catherine Pope. Br J Gen Pract 2007
160
16

Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.
Ernest Beutler, Vincent J Felitti, James A Koziol, Ngoc J Ho, Terri Gelbart. Lancet 2002
615
16

Improving Molecular Genetic Test Utilization through Order Restriction, Test Review, and Guidance.
Jacquelyn D Riley, Gary W Procop, Kandice Kottke-Marchant, Robert Wyllie, Felicitas L Lacbawan. J Mol Diagn 2015
24
16

Diagnosis and management of hemochromatosis: 2011 practice guideline by the American Association for the Study of Liver Diseases.
Bruce R Bacon, Paul C Adams, Kris V Kowdley, Lawrie W Powell, Anthony S Tavill. Hepatology 2011
312
16

The role of informatics and decision support in utilization management.
Jason M Baron, Anand S Dighe. Clin Chim Acta 2014
28
16

Algorithmic Approach With Clinical Pathology Consultation Improves Access to Specialty Care for Patients With Systemic Lupus Erythematosus.
Lei Chen, Kerry J Welsh, Brian Chang, Laura Kidd, Marylee Kott, Mohammad Zare, Kelley Carroll, Andy Nguyen, Amer Wahed, Ashok Tholpady,[...]. Am J Clin Pathol 2016
3
33


EMQN best practice guidelines for the molecular genetic diagnosis of hereditary hemochromatosis (HH).
Graça Porto, Pierre Brissot, Dorine W Swinkels, Heinz Zoller, Outi Kamarainen, Simon Patton, Isabel Alonso, Michael Morris, Steve Keeney. Eur J Hum Genet 2016
35
16

Implementing guidelines: what works.
Elizabeth Anne Livesey, J Mitchell Noon. Arch Dis Child Educ Pract Ed 2007
20
16

Examining the clinical use of hemochromatosis genetic testing.
Matthew B Lanktree, Bruce B Lanktree, Guillaume Paré, John S Waye, Bekim Sadikovic, Mark A Crowther. Can J Gastroenterol Hepatol 2015
5
20



Stakeholder assessment of the evidence for cancer genomic tests: insights from three case studies.
Patricia A Deverka, Sheri D Schully, Naoko Ishibe, Josh J Carlson, Andrew Freedman, Katrina A B Goddard, Muin J Khoury, Scott D Ramsey. Genet Med 2012
17
16

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.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
799
16

We screen newborns, don't we?: realizing the promise of public health genomics.
James P Evans, Jonathan S Berg, Andrew F Olshan, Terry Magnuson, Barbara K Rimer. Genet Med 2013
44
16

Multilevel research and the challenges of implementing genomic medicine.
Muin J Khoury, Ralph J Coates, Mary L Fennell, Russell E Glasgow, Maren T Scheuner, Sheri D Schully, Marc S Williams, Steven B Clauser. J Natl Cancer Inst Monogr 2012
33
16


Introduction to the 4th National Conference on Genomics and Public Health.
Colleen M McBride, Scott M Bowen, Sheri D Shully, Muin J Khoury. Public Health Genomics 2012
1
100


Integrating Advanced Molecular Technologies into Public Health.
Marta Gwinn, Duncan R MacCannell, Rima F Khabbaz. J Clin Microbiol 2017
22
16

Making genomic medicine evidence-based and patient-centered: a structured review and landscape analysis of comparative effectiveness research.
Kathryn A Phillips, Patricia A Deverka, Harold C Sox, Muin J Khoury, Lewis G Sandy, Geoffrey S Ginsburg, Sean R Tunis, Lori A Orlando, Michael P Douglas. Genet Med 2017
37
16

Long-term follow-up to ensure quality care of individuals diagnosed with newborn screening conditions: early experience in New England.
Inderneel Sahai, Roger B Eaton, Jaime E Hale, Eleanor A Mulcahy, Anne Marie Comeau. Genet Med 2010
8
16

Child-Parent Familial Hypercholesterolemia Screening in Primary Care.
David S Wald, Jonathan P Bestwick, Joan K Morris, Ken Whyte, Lucy Jenkins, Nicholas J Wald. N Engl J Med 2016
148
16

Current priorities for public health practice in addressing the role of human genomics in improving population health.
Muin J Khoury, Michael S Bowen, Wylie Burke, Ralph J Coates, Nicole F Dowling, James P Evans, Michele Reyes, Jeannette St Pierre. Am J Prev Med 2011
51
16

Utilization of genetic tests: analysis of gene-specific billing in Medicare claims data.
Julie A Lynch, Brygida Berse, W David Dotson, Muin J Khoury, Nicole Coomer, John Kautter. Genet Med 2017
22
16

Which BRCA genetic testing programs are ready for implementation in health care? A systematic review of economic evaluations.
Elvira D'Andrea, Carolina Marzuillo, Corrado De Vito, Marco Di Marco, Erica Pitini, Maria Rosaria Vacchio, Paolo Villari. Genet Med 2016
41
16

Advances in Public Health Surveillance and Information Dissemination at the Centers for Disease Control and Prevention.
Chesley L Richards, Michael F Iademarco, Delton Atkinson, Robert W Pinner, Paula Yoon, William R Mac Kenzie, Brian Lee, Judith R Qualters, Thomas R Frieden. Public Health Rep 2017
26
16

A curated gene list for reporting results of newborn genomic sequencing.
Ozge Ceyhan-Birsoy, Kalotina Machini, Matthew S Lebo, Tim W Yu, Pankaj B Agrawal, Richard B Parad, Ingrid A Holm, Amy McGuire, Robert C Green, Alan H Beggs,[...]. Genet Med 2017
36
16

Clinical utility of family history for cancer screening and referral in primary care: a report from the Family Healthware Impact Trial.
Wendy S Rubinstein, Louise S Acheson, Suzanne M O'Neill, Mack T Ruffin, Catharine Wang, Jennifer L Beaumont, Nan Rothrock. Genet Med 2011
62
16

The current state of implementation science in genomic medicine: opportunities for improvement.
Megan C Roberts, Amy E Kennedy, David A Chambers, Muin J Khoury. Genet Med 2017
63
16

Newborn Sequencing in Genomic Medicine and Public Health.
Jonathan S Berg, Pankaj B Agrawal, Donald B Bailey, Alan H Beggs, Steven E Brenner, Amy M Brower, Julie A Cakici, Ozge Ceyhan-Birsoy, Kee Chan, Flavia Chen,[...]. Pediatrics 2017
89
16

The human microbiome.
Hubert E Blum. Adv Med Sci 2017
63
16

The Evaluation of Genomic Applications in Practice and Prevention (EGAPP) Initiative: methods of the EGAPP Working Group.
Steven M Teutsch, Linda A Bradley, Glenn E Palomaki, James E Haddow, Margaret Piper, Ned Calonge, W David Dotson, Michael P Douglas, Alfred O Berg. Genet Med 2009
463
16

Public health action in genomics is now needed beyond newborn screening.
M S Bowen, K Kolor, W D Dotson, R M Ned, M J Khoury. Public Health Genomics 2012
37
16

Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children.
Alex R Kemper, Nancy S Green, Ned Calonge, Wendy K K Lam, Anne M Comeau, Aaron J Goldenberg, Jelili Ojodu, Lisa A Prosser, Susan Tanksley, Joseph A Bocchini. Genet Med 2014
57
16

Evidence synthesis and guideline development in genomic medicine: current status and future prospects.
Sheri D Schully, Tram Kim Lam, W David Dotson, Christine Q Chang, Naomi Aronson, Marian L Birkeland, Stephanie Jo Brewster, Stefania Boccia, Adam H Buchanan, Ned Calonge,[...]. Genet Med 2015
13
16

A standardized, evidence-based protocol to assess clinical actionability of genetic disorders associated with genomic variation.
Jessica Ezzell Hunter, Stephanie A Irving, Leslie G Biesecker, Adam Buchanan, Brian Jensen, Kristy Lee, Christa Lese Martin, Laura Milko, Kristin Muessig, Annie D Niehaus,[...]. Genet Med 2016
53
16




Genetic identification of familial hypercholesterolemia within a single U.S. health care system.
Noura S Abul-Husn, Kandamurugu Manickam, Laney K Jones, Eric A Wright, Dustin N Hartzel, Claudia Gonzaga-Jauregui, Colm O'Dushlaine, Joseph B Leader, H Lester Kirchner, D'Andra M Lindbuchler,[...]. Science 2016
186
16

CDC Grand Rounds: Family History and Genomics as Tools for Cancer Prevention and Control.
Juan L Rodriguez, Cheryll C Thomas, Greta M Massetti, Debra Duquette, Lindsay Avner, John Iskander, Muin J Khoury, Lisa C Richardson. MMWR Morb Mortal Wkly Rep 2016
6
16

The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.
Muin J Khoury, Colleen M McBride, Sheri D Schully, John P A Ioannidis, W Gregory Feero, A Cecile J W Janssens, Marta Gwinn, Denise G Simons-Morton, Jay M Bernhardt, Michele Cargill,[...]. Genet Med 2009
150
16

Precision Public Health for the Era of Precision Medicine.
Muin J Khoury, Michael F Iademarco, William T Riley. Am J Prev Med 2016
205
16

Strategies, actions, and outcomes of pilot state programs in public health genomics, 2003-2008.
Jeanette St Pierre, Janice Bach, Debra Duquette, Kristen Oehlke, Robert Nystrom, Kerry Silvey, Amy Zlot, Rebecca Giles, Jenny Johnson, H Mack Anders,[...]. Prev Chronic Dis 2014
9
16

Will Precision Medicine Improve Population Health?
Muin J Khoury, Sandro Galea. JAMA 2016
105
16

Public awareness and use of direct-to-consumer personal genomic tests from four state population-based surveys, and implications for clinical and public health practice.
Katherine Kolor, Debra Duquette, Amy Zlot, Joan Foland, Beth Anderson, Rebecca Giles, Jennifer Wrathall, Muin J Khoury. Genet Med 2012
32
16

The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service.
Gareth Baynam, Nicholas Pachter, Fiona McKenzie, Sharon Townshend, Jennie Slee, Cathy Kiraly-Borri, Anand Vasudevan, Anne Hawkins, Stephanie Broley, Lyn Schofield,[...]. Orphanet J Rare Dis 2016
32
16

Experiences from a pilot program bringing BRCA1/2 genetic screening to theUS Ashkenazi Jewish population.
Chana Wiesman, Esther Rose, Allison Grant, Adam Zimilover, Susan Klugman, Nicole Schreiber-Agus. Genet Med 2017
10
16


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.