A citation-based method for searching scientific literature

Amelia K Smit, Ainsley J Newson, Louise Keogh, Megan Best, Kate Dunlop, Kylie Vuong, Judy Kirk, Phyllis Butow, Lyndal Trevena, Anne E Cust. BJGP Open 2019
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Developing and evaluating polygenic risk prediction models for stratified disease prevention.
Nilanjan Chatterjee, Jianxin Shi, Montserrat García-Closas. Nat Rev Genet 2016
290
33

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
422
33


Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
664
16

Exploring general practitioners' experience of informing women about prenatal screening tests for foetal abnormalities: a qualitative focus group study.
Cate Nagle, Sharon Lewis, Bettina Meiser, Jane Gunn, Jane Halliday, Robin Bell. BMC Health Serv Res 2008
13
16

Identification of incestuous parental relationships by SNP-based DNA microarrays.
C P Schaaf, D A Scott, J Wiszniewska, A L Beaudet. Lancet 2011
41
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
842
16

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
37
16

Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
27
16

A routine tool with far-reaching influence: Australian midwives' views on the use of ultrasound during pregnancy.
Kristina Edvardsson, Ingrid Mogren, Ann Lalos, Margareta Persson, Rhonda Small. BMC Pregnancy Childbirth 2015
15
16


Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study.
Jane L Halliday, Cecile Muller, Taryn Charles, Fiona Norris, Joanne Kennedy, Sharon Lewis, Bettina Meiser, Susan Donath, Zornitza Stark, George McGillivray,[...]. Eur J Hum Genet 2018
12
16

The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker,[...]. Prenat Diagn 2018
16
16


Aiming at multidisciplinary consensus: what should be detected in prenatal diagnosis?
Elisabeth M A Boormans, E Birnie, Alida C Knegt, G Heleen Schuring-Blom, Gouke J Bonsel, Jan M M van Lith. Prenat Diagn 2010
5
20

Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.
Sarah A Walser, Katherine S Kellom, Steven C Palmer, Barbara A Bernhardt. Prenat Diagn 2015
26
16

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener,[...]. Eur J Med Genet 2014
61
16




Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
166
16

Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement.
David Moher, Alessandro Liberati, Jennifer Tetzlaff, Douglas G Altman. PLoS Med 2009
16


Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
68
16

Views of American OB/GYNs on the ethics of prenatal whole-genome sequencing.
Michelle J Bayefsky, Amina White, Paul Wakim, Sara Chandros Hull, David Wasserman, Stephanie Chen, Benjamin E Berkman. Prenat Diagn 2016
14
16


Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
134
16


What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.
Shiri Shkedi-Rafid, Angela Fenwick, Sandi Dheensa, Diana Wellesley, Anneke M Lucassen. Prenat Diagn 2016
20
16

Informed Decision-Making in the Context of Prenatal Chromosomal Microarray.
Jessica Baker, Cheryl Shuman, David Chitayat, Syed Wasim, Nan Okun, Johannes Keunen, Renee Hofstedter, Rachel Silver. J Genet Couns 2018
1
100

Increasing possibilities - Increasing dilemmas: A qualitative study of Swedish midwives' experiences of ultrasound use in pregnancy.
Kristina Edvardsson, Ann Lalos, Annika Åhman, Rhonda Small, Sophie Graner Md PhD, Ingrid Mogren. Midwifery 2016
12
16

Chromosomal microarray analysis in prenatal diagnosis: ethical considerations of the Belgian approach.
Joke Muys, Bettina Blaumeiser, Katrien Janssens, Patrick Loobuyck, Yves Jacquemyn. J Med Ethics 2020
7
16

Genomic Literacy of Registered Nurses and Midwives in Australia: A Cross-Sectional Survey.
Helen Wright, Lin Zhao, Melanie Birks, Jane Mills. J Nurs Scholarsh 2019
6
16

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
533
16

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Christine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, Radha Chari, Bernie N Chodirker, Isabelle DeBie, Jane A Evans, William T Gibson, Elena Kolomietz, Tanya N Nelson,[...]. J Med Genet 2018
32
16

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
133
16

Long-term evaluation of benefits, harms, and cost-effectiveness of the National Bowel Cancer Screening Program in Australia: a modelling study.
Jie-Bin Lew, D James B St John, Xiang-Ming Xu, Marjolein J E Greuter, Michael Caruana, Dayna R Cenin, Emily He, Marion Saville, Paul Grogan, Veerle M H Coupé,[...]. Lancet Public Health 2017
50
16

Genome-wide association study of colorectal cancer identifies six new susceptibility loci.
Fredrick R Schumacher, Stephanie L Schmit, Shuo Jiao, Christopher K Edlund, Hansong Wang, Ben Zhang, Li Hsu, Shu-Chen Huang, Christopher P Fischer, John F Harju,[...]. Nat Commun 2015
95
16

The use of a risk assessment and decision support tool (CRISP) compared with usual care in general practice to increase risk-stratified colorectal cancer screening: study protocol for a randomised controlled trial.
Jennifer G Walker, Finlay Macrae, Ingrid Winship, Jasmeen Oberoi, Sibel Saya, Shakira Milton, Adrian Bickerstaffe, James G Dowty, Richard De Abreu Lourenço, Malcolm Clark,[...]. Trials 2018
6
16

Increasing incidence of colorectal cancer in young adults in Europe over the last 25 years.
Fanny Er Vuik, Stella Av Nieuwenburg, Marc Bardou, Iris Lansdorp-Vogelaar, Mário Dinis-Ribeiro, Maria J Bento, Vesna Zadnik, María Pellisé, Laura Esteban, Michal F Kaminski,[...]. Gut 2019
167
16

Risk Prediction Models for Colorectal Cancer Incorporating Common Genetic Variants: A Systematic Review.
Luke McGeoch, Catherine L Saunders, Simon J Griffin, Jon D Emery, Fiona M Walter, Deborah J Thompson, Antonis C Antoniou, Juliet A Usher-Smith. Cancer Epidemiol Biomarkers Prev 2019
15
16

Breast cancer risk prediction using a clinical risk model and polygenic risk score.
Yiwey Shieh, Donglei Hu, Lin Ma, Scott Huntsman, Charlotte C Gard, Jessica W T Leung, Jeffrey A Tice, Celine M Vachon, Steven R Cummings, Karla Kerlikowske,[...]. Breast Cancer Res Treat 2016
67
16

Quantifying the utility of single nucleotide polymorphisms to guide colorectal cancer screening.
Mark A Jenkins, Enes Makalic, James G Dowty, Daniel F Schmidt, Gillian S Dite, Robert J MacInnis, Driss Ait Ouakrim, Mark Clendenning, Louisa B Flander, Oliver K Stanesby,[...]. Future Oncol 2016
26
16

Use of Single-Nucleotide Polymorphisms and Mammographic Density Plus Classic Risk Factors for Breast Cancer Risk Prediction.
Elke M van Veen, Adam R Brentnall, Helen Byers, Elaine F Harkness, Susan M Astley, Sarah Sampson, Anthony Howell, William G Newman, Jack Cuzick, D Gareth R Evans. JAMA Oncol 2018
58
16

The CRISP colorectal cancer risk prediction tool: an exploratory study using simulated consultations in Australian primary care.
Jennifer G Walker, Adrian Bickerstaffe, Nadira Hewabandu, Sanjay Maddumarachchi, James G Dowty, Mark Jenkins, Marie Pirotta, Fiona M Walter, Jon D Emery. BMC Med Inform Decis Mak 2017
14
16

Cohort Profile: The Colon Cancer Family Registry Cohort (CCFRC).
Mark A Jenkins, Aung Ko Win, Allyson S Templeton, Maggie S Angelakos, Daniel D Buchanan, Michelle Cotterchio, Jane C Figueiredo, Stephen N Thibodeau, John A Baron, John D Potter,[...]. Int J Epidemiol 2018
23
16

External validation of risk prediction models for incident colorectal cancer using UK Biobank.
J A Usher-Smith, A Harshfield, C L Saunders, S J Sharp, J Emery, F M Walter, K Muir, S J Griffin. Br J Cancer 2018
24
16


An updated Asia Pacific Consensus Recommendations on colorectal cancer screening.
J J Y Sung, S C Ng, F K L Chan, H M Chiu, H S Kim, T Matsuda, S S M Ng, J Y W Lau, S Zheng, S Adler,[...]. Gut 2015
245
16

Meta-analysis of genome-wide association data identifies four new susceptibility loci for colorectal cancer.
Richard S Houlston, Emily Webb, Peter Broderick, Alan M Pittman, Maria Chiara Di Bernardo, Steven Lubbe, Ian Chandler, Jayaram Vijayakrishnan, Kate Sullivan, Steven Penegar,[...]. Nat Genet 2008
434
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.