A citation-based method for searching scientific literature

Casey Lynnette Overby, Wendy K Chung, George Hripcsak, Rita Kukafka. J Pers Med 2013
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Patient compliance based on genetic medicine: a literature review.
Kai Insa Schneider, Jörg Schmidtke. J Community Genet 2014
24
50

Prenatal versus Postnatal Screening for Familial Retinoblastoma.
Sameh E Soliman, Helen Dimaras, Vikas Khetan, Jane A Gardiner, Helen S L Chan, Elise Héon, Brenda L Gallie. Ophthalmology 2016
32
50

Psychosocial consequences of genetic counseling: a population-based follow-up study.
Ellen M Mikkelsen, Lone Sunde, Christoffer Johansen, Søren P Johnsen. Breast J 2009
14
50

Retinoblastoma.
Helen Dimaras, Timothy W Corson, David Cobrinik, Abby White, Junyang Zhao, Francis L Munier, David H Abramson, Carol L Shields, Guillermo L Chantada, Festus Njuguna,[...]. Nat Rev Dis Primers 2015
205
50

Preimplantation genetic diagnosis for retinoblastoma: the first reported liveborn.
Kangpu Xu, Zev Rosenwaks, Katherine Beaverson, Ina Cholst, Lucinda Veeck, David H Abramson. Am J Ophthalmol 2004
50
50

Are three methods better than one? A comparative assessment of usability evaluation methods in an EHR.
Muhammad F Walji, Elsbeth Kalenderian, Mark Piotrowski, Duong Tran, Krishna K Kookal, Oluwabunmi Tokede, Joel M White, Ram Vaderhobli, Rachel Ramoni, Paul C Stark,[...]. Int J Med Inform 2014
27
25

A report template for molecular genetic tests designed to improve communication between the clinician and laboratory.
Maren T Scheuner, Lee Hilborne, Julie Brown, Ira M Lubin. Genet Test Mol Biomarkers 2012
23
25

Actionable, pathogenic incidental findings in 1,000 participants' exomes.
Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett,[...]. Am J Hum Genet 2013
268
25

ClinVar: public archive of relationships among sequence variation and human phenotype.
Melissa J Landrum, Jennifer M Lee, George R Riley, Wonhee Jang, Wendy S Rubinstein, Deanna M Church, Donna R Maglott. Nucleic Acids Res 2014
25


Exome sequencing can improve diagnosis and alter patient management.
Tracy J Dixon-Salazar, Jennifer L Silhavy, Nitin Udpa, Jana Schroth, Stephanie Bielas, Ashleigh E Schaffer, Jesus Olvera, Vineet Bafna, Maha S Zaki, Ghada H Abdel-Salam,[...]. Sci Transl Med 2012
182
25

The link between providers and patients: how laboratories can ensure quality results with genetic testing.
John M Quillin, Colleen Jackson-Cook, Joann Bodurtha. Clin Leadersh Manag Rev 2003
7
25

Personalized medicine in diabetes mellitus: current opportunities and future prospects.
Jeffrey W Kleinberger, Toni I Pollin. Ann N Y Acad Sci 2015
36
25

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
25

SeqReporter: automating next-generation sequencing result interpretation and reporting workflow in a clinical laboratory.
Somak Roy, Mary Beth Durso, Abigail Wald, Yuri E Nikiforov, Marina N Nikiforova. J Mol Diagn 2014
22
25

Implementation of pharmacogenetics: the University of Maryland Personalized Anti-platelet Pharmacogenetics Program.
Alan R Shuldiner, Kathleen Palmer, Ruth E Pakyz, Tameka D Alestock, Kristin A Maloney, Courtney O'Neill, Shaun Bhatty, Jamie Schub, Casey Lynnette Overby, Richard B Horenstein,[...]. Am J Med Genet C Semin Med Genet 2014
63
25

Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.
Sarah E Calvo, Alison G Compton, Steven G Hershman, Sze Chern Lim, Daniel S Lieber, Elena J Tucker, Adrienne Laskowski, Caterina Garone, Shangtao Liu, David B Jaffe,[...]. Sci Transl Med 2012
307
25

A one-page summary report of genome sequencing for the healthy adult.
Jason L Vassy, Heather M McLaughlin, Calum A MacRae, Christine E Seidman, Denise Lautenbach, Joel B Krier, William J Lane, Isaac S Kohane, Michael F Murray, Amy L McGuire,[...]. Public Health Genomics 2015
28
25

A preliminary investigation of genetic counselors' information needs when receiving a variant of uncertain significance result: a mixed methods study.
Courtney L Scherr, Noralane M Lindor, Teri L Malo, Fergus J Couch, Susan T Vadaparampil. Genet Med 2015
17
25

The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
214
25

A novel clinician interface to improve clinician access to up-to-date genetic results.
Allison R Wilcox, Pamela M Neri, Lynn A Volk, Lisa P Newmark, Eugene H Clark, Lawrence J Babb, Matthew Varugheese, Samuel J Aronson, Heidi L Rehm, David W Bates. J Am Med Inform Assoc 2014
13
25

Usability of a novel clinician interface for genetic results.
Pamela M Neri, Stephanie E Pollard, Lynn A Volk, Lisa P Newmark, Matthew Varugheese, Samantha Baxter, Samuel J Aronson, Heidi L Rehm, David W Bates. J Biomed Inform 2012
24
25

Usability evaluation of pharmacogenomics clinical decision support aids and clinical knowledge resources in a computerized provider order entry system: a mixed methods approach.
Emily Beth Devine, Chia-Ju Lee, Casey L Overby, Neil Abernethy, Jeannine McCune, Joe W Smith, Peter Tarczy-Hornoch. Int J Med Inform 2014
46
25

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
73
25

Enhancing genomic laboratory reports: A qualitative analysis of provider review.
Janet L Williams, Alanna Kulchak Rahm, Heather Stuckey, Jamie Green, Lynn Feldman, Doris T Zallen, Michele Bonhag, Michael M Segal, Audrey L Fan, Marc S Williams. Am J Med Genet A 2016
23
25

Integrating genetic information resources with an EHR.
Guilherme Del Fiol, Marc S Williams, Naveen Maram, Roberto A Rocha, Grant M Wood, Joyce A Mitchell. AMIA Annu Symp Proc 2006
12
25

Usability study of clinical exome analysis software: top lessons learned and recommendations.
Casper Shyr, Andre Kushniruk, Wyeth W Wasserman. J Biomed Inform 2014
9
25

Electronic medical records and personalized medicine.
Mark A Hoffman, Marc S Williams. Hum Genet 2011
37
25

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.
Jason L Vassy, Denise M Lautenbach, Heather M McLaughlin, Sek Won Kong, Kurt D Christensen, Joel Krier, Isaac S Kohane, Lindsay Z Feuerman, Jennifer Blumenthal-Barby, J Scott Roberts,[...]. Trials 2014
100
25

Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
Allison W Kurian, Emily E Hare, Meredith A Mills, Kerry E Kingham, Lisa McPherson, Alice S Whittemore, Valerie McGuire, Uri Ladabaum, Yuya Kobayashi, Stephen E Lincoln,[...]. J Clin Oncol 2014
312
25

Implementations of the HL7 Context-Aware Knowledge Retrieval ("Infobutton") Standard: challenges, strengths, limitations, and uptake.
Guilherme Del Fiol, Vojtech Huser, Howard R Strasberg, Saverio M Maviglia, Clayton Curtis, James J Cimino. J Biomed Inform 2012
44
25


Creating a scalable clinical pharmacogenomics service with automated interpretation and medical record result integration - experience from a pediatric tertiary care facility.
Shannon F Manzi, Vincent A Fusaro, Laura Chadwick, Catherine Brownstein, Catherine Clinton, Kenneth D Mandl, Wendy A Wolf, Jared B Hawkins. J Am Med Inform Assoc 2017
24
25

Taxonomizing, sizing, and overcoming the incidentalome.
Isaac S Kohane, Michael Hsing, Sek Won Kong. Genet Med 2012
90
25

Genetic Counseling for Diabetes Mellitus.
Stephanie A Stein, Kristin L Maloney, Toni I Pollin. Curr Genet Med Rep 2014
7
25

Return of results in the genomic medicine projects of the eMERGE network.
Iftikhar J Kullo, Ra'ad Haddad, Cynthia A Prows, Ingrid Holm, Saskia C Sanderson, Nanibaa' A Garrison, Richard R Sharp, Maureen E Smith, Helena Kuivaniemi, Erwin P Bottinger,[...]. Front Genet 2014
31
25

ClinVar: public archive of interpretations of clinically relevant variants.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Jeffrey Hoover,[...]. Nucleic Acids Res 2016
25

Cascade effects of medical technology.
Richard A Deyo. Annu Rev Public Health 2002
119
25

A systematic approach to the reporting of medically relevant findings from whole genome sequencing.
Heather M McLaughlin, Ozge Ceyhan-Birsoy, Kurt D Christensen, Isaac S Kohane, Joel Krier, William J Lane, Denise Lautenbach, Matthew S Lebo, Kalotina Machini, Calum A MacRae,[...]. BMC Med Genet 2014
61
25


SEIPS 2.0: a human factors framework for studying and improving the work of healthcare professionals and patients.
Richard J Holden, Pascale Carayon, Ayse P Gurses, Peter Hoonakker, Ann Schoofs Hundt, A Ant Ozok, A Joy Rivera-Rodriguez. Ergonomics 2013
350
25

Using Workflow Modeling to Identify Areas to Improve Genetic Test Processes in the University of Maryland Translational Pharmacogenomics Project.
Elizabeth M Cutting, Casey L Overby, Meghan Banchero, Toni Pollin, Mark Kelemen, Alan R Shuldiner, Amber L Beitelshees. AMIA Annu Symp Proc 2015
3
33

Making pharmacogenomic-based prescribing alerts more effective: A scenario-based pilot study with physicians.
Casey Lynnette Overby, Emily Beth Devine, Neil Abernethy, Jeannine S McCune, Peter Tarczy-Hornoch. J Biomed Inform 2015
20
25

Achieving optimal cancer outcomes in East Africa through multidisciplinary partnership: a case study of the Kenyan National Retinoblastoma Strategy group.
Jessica A Hill, Kahaki Kimani, Abby White, Faith Barasa, Morgan Livingstone, Brenda L Gallie, Helen Dimaras. Global Health 2016
12
25

Cancer genetics education in a low- to middle-income country: evaluation of an interactive workshop for clinicians in Kenya.
Jessica A Hill, Su Yeon Lee, Lucy Njambi, Timothy W Corson, Helen Dimaras. PLoS One 2015
11
25


[Retinoblastoma in Kenya: survival and prognostic factors].
E N Gichigo, M M Kariuki-Wanyoike, K Kimani, M M Nentwich. Ophthalmologe 2015
12
25

The incidence and distribution of retinoblastoma in Kenya.
Joseph M Nyamori, Kahaki Kimani, Margaret W Njuguna, Helen Dimaras. Br J Ophthalmol 2012
22
25

Genetic testing for inherited breast cancer risk in African Americans.
Chanita Hughes Halbert, Lisa Jay Kessler, Edith Mitchell. Cancer Invest 2005
44
25

Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
53
25


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.