A citation-based method for searching scientific literature

Molly McGuinness, Emily Fassi, Catharine Wang, Claire Hacking, Victoria Ellis. J Genet Couns 2021
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


The impact of a panel of 18 SNPs on breast cancer risk in women attending a UK familial screening clinic: a case-control study.
D Gareth Evans, Adam Brentnall, Helen Byers, Elaine Harkness, Paula Stavrinos, Anthony Howell, William G Newman, Jack Cuzick. J Med Genet 2017
36
66

Association analysis identifies 65 new breast cancer risk loci.
Kyriaki Michailidou, Sara Lindström, Joe Dennis, Jonathan Beesley, Shirley Hui, Siddhartha Kar, Audrey Lemaçon, Penny Soucy, Dylan Glubb, Asha Rostamianfar,[...]. Nature 2017
456
66

Communication and information-giving in high-risk breast cancer consultations: influence on patient outcomes.
E A Lobb, P N Butow, A Barratt, B Meiser, C Gaff, M A Young, E Haan, G Suthers, M Gattas, K Tucker. Br J Cancer 2004
96
66

Uptake of polygenic risk information among women at increased risk of breast cancer.
Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, Maatje Scheepers-Joynt, Simone McInerny, Shelby Taylor, Kristine Barlow-Stewart, Yoland Antill, Lucinda Salmon, Courtney Smyth,[...]. Clin Genet 2020
7
66

Making Sense of SNPs: Women's Understanding and Experiences of Receiving a Personalized Profile of Their Breast Cancer Risks.
Mary-Anne Young, Laura Elenor Forrest, Victoria-Mae Rasmussen, Paul James, Gillian Mitchell, Sarah Dilys Sawyer, Katrina Reeve, Nina Hallowell. J Genet Couns 2018
17
66

The emerging field of polygenic risk scores and perspective for use in clinical care.
Tatiane Yanes, Aideen M McInerney-Leo, Matthew H Law, Shelly Cummings. Hum Mol Genet 2020
6
66


Clinical applications of polygenic breast cancer risk: a critical review and perspectives of an emerging field.
Tatiane Yanes, Mary-Anne Young, Bettina Meiser, Paul A James. Breast Cancer Res 2020
18
66

Psychosocial and behavioral outcomes of genomic testing in cancer: a systematic review.
Tatiane Yanes, Amanda M Willis, Bettina Meiser, Katherine M Tucker, Megan Best. Eur J Hum Genet 2019
26
66

Psychosocial and behavioral impact of breast cancer risk assessed by testing for common risk variants: protocol of a prospective study.
Tatiane Yanes, Bettina Meiser, Mary-Anne Young, Rajneesh Kaur, Gillian Mitchell, Kristine Barlow-Stewart, Tony Roscioli, Jane Halliday, Paul James. BMC Cancer 2017
8
66

Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
393
66

A role for common genomic variants in the assessment of familial breast cancer.
Sarah Sawyer, Gillian Mitchell, Joanne McKinley, Georgia Chenevix-Trench, Jonathan Beesley, Xiao Qing Chen, David Bowtell, Alison H Trainer, Marion Harris, Geoffrey J Lindeman,[...]. J Clin Oncol 2012
57
66

Polygenic risk scores: from research tools to clinical instruments.
Cathryn M Lewis, Evangelos Vassos. Genome Med 2020
75
66

Complementarity between medical geneticists and genetic counsellors: its added value in genetic services in Europe.
Milena Paneque, Clara Serra-Juhé, Rebecka Pestoff, Christophe Cordier, João Silva, Ramona Moldovan, Charlotta Ingvoldstad. Eur J Hum Genet 2017
13
33


Association of Common Genetic Variants With Contralateral Breast Cancer Risk in the WECARE Study.
Mark E Robson, Anne S Reiner, Jennifer D Brooks, Patrick J Concannon, Esther M John, Lene Mellemkjaer, Leslie Bernstein, Kathleen E Malone, Julia A Knight, Charles F Lynch,[...]. J Natl Cancer Inst 2017
19
33

The Global State of the Genetic Counseling Profession.
MaryAnn Abacan, Lamia Alsubaie, Kristine Barlow-Stewart, Beppy Caanen, Christophe Cordier, Eliza Courtney, Emeline Davoine, Janice Edwards, Niby J Elackatt, Kate Gardiner,[...]. Eur J Hum Genet 2019
66
33

Women's responses and understanding of polygenic breast cancer risk information.
T Yanes, R Kaur, B Meiser, M Scheepers-Joynt, S McInerny, K Barlow-Stewart, Y Antill, L Salmon, C Smyth, P A James,[...]. Fam Cancer 2020
3
33

Validation of a genetic risk score for Arkansas women of color.
Athena Starlard-Davenport, Richard Allman, Gillian S Dite, John L Hopper, Erika Spaeth Tuff, Stewart Macleod, Susan Kadlubar, Michael Preston, Ronda Henry-Tillman. PLoS One 2018
7
33


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
33

Patient participation in the medical specialist encounter: does physicians' patient-centred communication matter?
Linda C Zandbelt, Ellen M A Smets, Frans J Oort, Mieke H Godfried, Hanneke C J M de Haes. Patient Educ Couns 2007
55
33

Evaluation of three polygenic risk score models for the prediction of breast cancer risk in Singapore Chinese.
Claire Hian Tzer Chan, Prabhakaran Munusamy, Sau Yeen Loke, Geok Ling Koh, Audrey Zhi Yi Yang, Hai Yang Law, Chui Sheun Yoon, Chow Yin Wong, Wei Sean Yong, Nan Soon Wong,[...]. Oncotarget 2018
10
33

Genetic counseling as a tool for type 2 diabetes prevention: a genetic counseling framework for common polygenetic disorders.
Jessica L Waxler, Kelsey E O'Brien, Linda M Delahanty, James B Meigs, Jose C Florez, Elyse R Park, Barbara R Pober, Richard W Grant. J Genet Couns 2012
23
33

Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk.
Iris Kramer, Maartje J Hooning, Nasim Mavaddat, Michael Hauptmann, Renske Keeman, Ewout W Steyerberg, Daniele Giardiello, Antonis C Antoniou, Paul D P Pharoah, Sander Canisius,[...]. Am J Hum Genet 2020
7
33

High-risk women's risk perception after receiving personalized polygenic breast cancer risk information.
Laura Elenor Forrest, Sarah Dilys Sawyer, Nina Hallowell, Paul Andrew James, Mary-Anne Young. J Community Genet 2019
11
33

Opening the "black box" of informed consent appointments for genome sequencing: a multisite observational study.
Saskia C Sanderson, Celine Lewis, Christine Patch, Melissa Hill, Maria Bitner-Glindzicz, Lyn S Chitty. Genet Med 2019
6
33

Illustrating Cancer Risk: Patient Risk Communication Preferences and Interest regarding a Novel BRCA1/2 Genetic Risk Modifier Test.
Jada G Hamilton, Margaux Genoff Garzon, Ibrahim H Shah, Kechna Cadet, Elyse Shuk, Joy S Westerman, Jennifer L Hay, Kenneth Offit, Mark E Robson. Public Health Genomics 2020
3
33

Exploration of experiences with and understanding of polygenic risk scores for bipolar disorder.
Sophie Putt, Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, Janice M Fullerton, Kristine Barlow-Stewart, Peter R Schofield, Claudio Toma, Holly Peay, Philip B Mitchell. J Affect Disord 2020
4
33

Addition of a 161-SNP polygenic risk score to family history-based risk prediction: impact on clinical management in non-BRCA1/2 breast cancer families.
Inge M M Lakeman, Florentine S Hilbers, Mar Rodríguez-Girondo, Andrew Lee, Maaike P G Vreeswijk, Antoinette Hollestelle, Caroline Seynaeve, Hanne Meijers-Heijboer, Jan C Oosterwijk, Nicoline Hoogerbrugge,[...]. J Med Genet 2019
14
33

Communication in cancer genetic counselling: does it reflect counselees' previsit needs and preferences?
A H Pieterse, A M van Dulmen, M G E M Ausems, F A Beemer, J M Bensing. Br J Cancer 2005
51
33


A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
354
33


Development and Validation of a Clinical Polygenic Risk Score to Predict Breast Cancer Risk.
Elisha Hughes, Placede Tshiaba, Shannon Gallagher, Susanne Wagner, Thaddeus Judkins, Benjamin Roa, Eric Rosenthal, Susan Domchek, Judy Garber, Johnathan Lancaster,[...]. JCO Precis Oncol 2020
6
33

Development and pilot testing of a leaflet informing women with breast cancer about genomic testing for polygenic risk.
Rajneesh Kaur, Bettina Meiser, Tatiane Yanes, Mary-Anne Young, Kristine Barlow-Stewart, Tony Roscioli, Sian Smith, Paul A James. Fam Cancer 2019
4
33

Differences in individual approaches: communication in the familial breast cancer consultation and the effect on patient outcomes.
Elizabeth A Lobb, Phyllis Butow, Alexandra Barratt, Bettina Meiser, Katherine Tucker. J Genet Couns 2005
24
33

Analyzing communication in genetic consultations--a systematic review.
Jean Paul, Sylvia Metcalfe, Lesley Stirling, Brenda Wilson, Jan Hodgson. Patient Educ Couns 2015
26
33

European polygenic risk score for prediction of breast cancer shows similar performance in Asian women.
Weang-Kee Ho, Min-Min Tan, Nasim Mavaddat, Mei-Chee Tai, Shivaani Mariapun, Jingmei Li, Peh-Joo Ho, Joe Dennis, Jonathan P Tyrer, Manjeet K Bolla,[...]. Nat Commun 2020
19
33

Genetic testing and insurance in Australia.
Margaret Otlowski, Kristine Barlow-Stewart, Paul Lacaze, Jane Tiller. Aust J Gen Pract 2019
4
33

BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors.
Andrew Lee, Nasim Mavaddat, Amber N Wilcox, Alex P Cunningham, Tim Carver, Simon Hartley, Chantal Babb de Villiers, Angel Izquierdo, Jacques Simard, Marjanka K Schmidt,[...]. Genet Med 2019
118
33

Association analyses identify 31 new risk loci for colorectal cancer susceptibility.
Philip J Law, Maria Timofeeva, Ceres Fernandez-Rozadilla, Peter Broderick, James Studd, Juan Fernandez-Tajes, Susan Farrington, Victoria Svinti, Claire Palles, Giulia Orlando,[...]. Nat Commun 2019
53
33

GP attitudes to and expectations for providing personal genomic risk information to the public: a qualitative study.
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
5
33

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer.
Kyriaki Michailidou, Jonathan Beesley, Sara Lindstrom, Sander Canisius, Joe Dennis, Michael J Lush, Mel J Maranian, Manjeet K Bolla, Qin Wang, Mitul Shah,[...]. Nat Genet 2015
331
33

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility.
Maria Teresa Landi, D Timothy Bishop, Stuart MacGregor, Mitchell J Machiela, Alexander J Stratigos, Paola Ghiorzo, Myriam Brossard, Donato Calista, Jiyeon Choi, Maria Concetta Fargnoli,[...]. Nat Genet 2020
24
33

Outcomes for implementation research: conceptual distinctions, measurement challenges, and research agenda.
Enola Proctor, Hiie Silmere, Ramesh Raghavan, Peter Hovmand, Greg Aarons, Alicia Bunger, Richard Griffey, Melissa Hensley. Adm Policy Ment Health 2011
33

Validation of a scale for assessing attitudes towards outcomes of genetic cancer testing among primary care providers and breast specialists.
Anne-Deborah Bouhnik, Khadim N'Diaye, D Gareth Evans, Hilary Harris, Aad Tibben, Christi van Asperen, Joerg Schmidtke, Irmgard Nippert, Julien Mancini, Claire Julian-Reynier. PLoS One 2017
4
33

Preparing Medical Specialists to Practice Genomic Medicine: Education an Essential Part of a Broader Strategy.
Erin Crellin, Belinda McClaren, Amy Nisselle, Stephanie Best, Clara Gaff, Sylvia Metcalfe. Front Genet 2019
18
33

The personal and clinical utility of polygenic risk scores.
Ali Torkamani, Nathan E Wineinger, Eric J Topol. Nat Rev Genet 2018
369
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.