A citation-based method for searching scientific literature

Susan T Vadaparampil, Deborah Cragun. Transl Behav Med 2018
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors.
Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, Barbara Biesecker, Rebecca Dresser, Ashley Elrick, Cindy Matsen, Melody Goodman. Transl Behav Med 2018
13
50

Will Precision Medicine Improve Population Health?
Muin J Khoury, Sandro Galea. JAMA 2016
105
25


Heart disease risk information, encouragement, and physical activity among Mexican-origin couples: Self- or spouse-driven change?
Kaley F Skapinsky, Susan Persky, Megan Lewis, Andrea Goergen, Sato Ashida, Hendrik D de Heer, Donald Hadley, Anna V Wilkinson, Laura M Koehly. Transl Behav Med 2018
5
25

Patient communication of cancer genetic test results in a diverse population.
Charité N Ricker, Rachel B Koff, Chenxu Qu, Julie Culver, Duveen Sturgeon, Kerry E Kingham, Katrina Lowstuter, Nicolette M Chun, Courtney Rowe-Teeter, Alexandra Lebensohn,[...]. Transl Behav Med 2018
13
25

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
25

Genetic test reporting of CDKN2A provides informational and motivational benefits for managing melanoma risk.
Lisa G Aspinwall, Tammy K Stump, Jennifer M Taber, Danielle M Drummond, Wendy Kohlmann, Marjan Champine, Sancy A Leachman. Transl Behav Med 2018
9
25

Introduction to the special series on health disparities in genomic medicine.
Kristi D Graves, Kenneth P Tercyak. Health Psychol 2015
2
50

The impact of raw DNA availability and corresponding online interpretation services: A mixed-methods study.
Caitlin G Allen, Jazmine Gabriel, Maureen Flynn, Tricia N Cunningham, Catharine Wang. Transl Behav Med 2018
14
25

Factors influencing the impact of pharmacogenomic prescribing on adherence to nicotine replacement therapy: A qualitative study of participants from a randomized controlled trial.
Alison J Wright, Stephen Sutton, David Armstrong, Paul Aveyard, Ann Louise Kinmonth, Theresa M Marteau. Transl Behav Med 2018
3
33

Potentially Preventable Deaths Among the Five Leading Causes of Death - United States, 2010 and 2014.
Macarena C García, Brigham Bastian, Lauren M Rossen, Robert Anderson, Arialdi Miniño, Paula W Yoon, Mark Faul, Greta Massetti, Cheryll C Thomas, Yuling Hong,[...]. MMWR Morb Mortal Wkly Rep 2016
25
25

Communication of cancer-related genetic and genomic information: A landscape analysis of reviews.
Emily B Peterson, Wen-Ying Sylvia Chou, Anna Gaysynsky, Melinda Krakow, Ashley Elrick, Muin J Khoury, Kimberly A Kaphingst. Transl Behav Med 2018
17
25

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
25

Parental attitudes and expectations towards receiving genomic test results in healthy children.
Alanna Kulchak Rahm, Lindsay Bailey, Kara Fultz, Audrey Fan, Janet L Williams, Adam Buchanan, F Daniel Davis, Michael F Murray, Marc S Williams. Transl Behav Med 2018
8
25

Social and behavioral science priorities for genomic translation.
Laura M Koehly, Susan Persky, Erica Spotts, Gillian Acca. Transl Behav Med 2018
2
50


Toward the implementation of genomic applications for smoking cessation and smoking-related diseases.
Alex T Ramsey, Li-Shiun Chen, Sarah M Hartz, Nancy L Saccone, Sherri L Fisher, Enola K Proctor, Laura J Bierut. Transl Behav Med 2018
8
25

Effect of co-payment on behavioral response to consumer genomic testing.
Wendy Liu, Jessica J Outlaw, Nathan Wineinger, Debra Boeldt, Cinnamon S Bloss. Transl Behav Med 2018
2
50

A comparison of views regarding the use of de-identified data.
Deborah Goodman, Catherine O Johnson, Deborah Bowen, Megan Smith, Lari Wenzel, Karen L Edwards. Transl Behav Med 2018
2
50

The research participant perspective related to the conduct of genomic cohort studies: A systematic review of the quantitative literature.
Deborah Goodman, Deborah Bowen, Lari Wenzel, Paris Tehrani, Francis Fernando, Araksi Khacheryan, Farihah Chowdhury, Catherine O Johnson, Karen Edwards. Transl Behav Med 2018
12
25

Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics.
Liza-Marie Johnson, Jessica M Valdez, Emily A Quinn, April D Sykes, Rose B McGee, Regina Nuccio, Stacy J Hines-Dowell, Justin N Baker, Chimene Kesserwan, Kim E Nichols,[...]. Cancer 2017
28
25


Statistical challenges in the evaluation of treatments for small patient populations.
Edward L Korn, Lisa M McShane, Boris Freidlin. Sci Transl Med 2013
33
25

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience.
C Alexander Valencia, Ammar Husami, Jennifer Holle, Judith A Johnson, Yaping Qian, Abhinav Mathur, Chao Wei, Subba Rao Indugula, Fanggeng Zou, Haiying Meng,[...]. Front Pediatr 2015
105
25

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
45
25

HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum.
Rhian L Clissold, Alexander J Hamilton, Andrew T Hattersley, Sian Ellard, Coralie Bingham. Nat Rev Nephrol 2015
115
25

Bringing genetics into primary care: findings from a national evaluation of pilots in England.
Graham Martin, Graeme Currie, Rachael Finn. J Health Serv Res Policy 2009
12
25

Prevalence of kidney damage in Australian adults: The AusDiab kidney study.
Steven J Chadban, Esther M Briganti, Peter G Kerr, David W Dunstan, Timothy A Welborn, Paul Z Zimmet, Robert C Atkins. J Am Soc Nephrol 2003
475
25

Meeting report of the 2017 KidGen Renal Genetics Symposium.
Kushani Jayasinghe, Cathy Quinlan, Zornitza Stark, Chirag Patel, Matthew G Sampson, Moin Saleem, Andrew J Mallett. Hum Genomics 2018
1
100

Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis.
Christine Gast, Reuben J Pengelly, Matthew Lyon, David J Bunyan, Eleanor G Seaby, Nikki Graham, Gopalakrishnan Venkat-Raman, Sarah Ennis. Nephrol Dial Transplant 2016
100
25

Consensus opinion on diagnosis and management of thrombotic microangiopathy in Australia and New Zealand.
Lucy C Fox, Solomon J Cohney, Joshua Y Kausman, Jake Shortt, Peter D Hughes, Erica M Wood, Nicole M Isbel, Theo de Malmanche, Anne Durkan, Pravin Hissaria,[...]. Nephrology (Carlton) 2018
9
25

Disease modeling in genetic kidney diseases: zebrafish.
Heiko Schenk, Janina Müller-Deile, Mark Kinast, Mario Schiffer. Cell Tissue Res 2017
15
25

Differential risk of remission and ESRD in childhood FSGS.
Debbie S Gipson, Hyunsook Chin, Trevor P Presler, Caroline Jennette, Maria E Ferris, Susan Massengill, Keisha Gibson, David B Thomas. Pediatr Nephrol 2006
83
25

Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome.
Jamie M Ellingford, Panagiotis I Sergouniotis, Rachel Lennon, Sanjeev Bhaskar, Simon G Williams, Kate A Hillman, James O'Sullivan, Georgina Hall, Simon C Ramsden, I Christopher Lloyd,[...]. Lancet 2015
17
25

Nephropathic cystinosis: an international consensus document.
Francesco Emma, Galina Nesterova, Craig Langman, Antoine Labbé, Stephanie Cherqui, Paul Goodyer, Mirian C Janssen, Marcella Greco, Rezan Topaloglu, Ewa Elenberg,[...]. Nephrol Dial Transplant 2014
89
25

Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.
Kyle B Brothers, Kelly M East, Whitley V Kelley, M Frances Wright, Matthew J Westbrook, Carla A Rich, Kevin M Bowling, Edward J Lose, E Martina Bebin, Shirley Simmons,[...]. Genet Med 2017
25
25

Early angiotensin-converting enzyme inhibition in Alport syndrome delays renal failure and improves life expectancy.
Oliver Gross, Christoph Licht, Hans J Anders, Bernd Hoppe, Bodo Beck, Burkhard Tönshoff, Britta Höcker, Simone Wygoda, Jochen H H Ehrich, Lars Pape,[...]. Kidney Int 2012
154
25

A protocol for the identification and validation of novel genetic causes of kidney disease.
Andrew Mallett, Chirag Patel, Barbara Maier, Julie McGaughran, Michael Gabbett, Minoru Takasato, Anne Cameron, Peter Trnka, Stephen I Alexander, Gopala Rangan,[...]. BMC Nephrol 2015
7
25

Common Elements in Rare Kidney Diseases: Conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference.
Ségolène Aymé, Detlef Bockenhauer, Simon Day, Olivier Devuyst, Lisa M Guay-Woodford, Julie R Ingelfinger, Jon B Klein, Nine V A M Knoers, Ronald D Perrone, Julia Roberts,[...]. Kidney Int 2017
16
25

Coming of age: ten years of next-generation sequencing technologies.
Sara Goodwin, John D McPherson, W Richard McCombie. Nat Rev Genet 2016
25

Variant detection sensitivity and biases in whole genome and exome sequencing.
Alison M Meynert, Morad Ansari, David R FitzPatrick, Martin S Taylor. BMC Bioinformatics 2014
124
25

Complement genes strongly predict recurrence and graft outcome in adult renal transplant recipients with atypical hemolytic and uremic syndrome.
M Le Quintrec, J Zuber, B Moulin, N Kamar, M Jablonski, A Lionet, V Chatelet, C Mousson, G Mourad, F Bridoux,[...]. Am J Transplant 2013
153
25

Exploring the genetic basis of early-onset chronic kidney disease.
Asaf Vivante, Friedhelm Hildebrandt. Nat Rev Nephrol 2016
134
25

Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
46
25

Technology: The $1,000 genome.
Erika Check Hayden. Nature 2014
206
25

Innovative research methods for studying treatments for rare diseases: methodological review.
Joshua J Gagne, Lauren Thompson, Kelly O'Keefe, Aaron S Kesselheim. BMJ 2014
89
25

Can we further enrich autosomal dominant polycystic kidney disease clinical trials for rapidly progressive patients? Application of the PROPKD score in the TEMPO trial.
Emilie Cornec-Le Gall, Jaime D Blais, Maria V Irazabal, Olivier Devuyst, Ron T Gansevoort, Ron D Perrone, Arlene B Chapman, Frank S Czerwiec, John Ouyang, Christina M Heyer,[...]. Nephrol Dial Transplant 2018
14
25

Prevalence of genetic renal disease in children.
Jeffery Fletcher, Stephen McDonald, Stephen I Alexander. Pediatr Nephrol 2013
20
25

Generation of kidney organoids from human pluripotent stem cells.
Minoru Takasato, Pei X Er, Han S Chiu, Melissa H Little. Nat Protoc 2016
113
25

A systematic review of factors that act as barriers to patient referral to genetic services.
Türem Delikurt, Graham R Williamson, Violetta Anastasiadou, Heather Skirton. Eur J Hum Genet 2015
73
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.