A citation-based method for searching scientific literature

Katie Stoll, Shobana Kubendran, Stephanie A Cohen. Am J Med Genet C Semin Med Genet 2018
Times Cited: 45







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



Times Cited
  Times     Co-cited
Similarity


Evolving Intersection Between Inherited Cancer Genetics and Therapeutic Clinical Trials in Prostate Cancer: A White Paper From the Germline Genetics Working Group of the Prostate Cancer Clinical Trials Consortium.
Maria I Carlo, Veda N Giri, Channing J Paller, Wassim Abida, Joshi J Alumkal, Tomasz M Beer, Himisha Beltran, Daniel J George, Elisabeth I Heath, Celestia S Higano,[...]. JCO Precis Oncol 2018
12
25

Prevalence of Germline Variants in Prostate Cancer and Implications for Current Genetic Testing Guidelines.
Piper Nicolosi, Elisa Ledet, Shan Yang, Scott Michalski, Brandy Freschi, Erin O'Leary, Edward D Esplin, Robert L Nussbaum, Oliver Sartor. JAMA Oncol 2019
65
6

The time-consuming demands of the practice of medical genetics in the era of advanced genomic testing.
Rivka Sukenik-Halevy, Mark David Ludman, Shay Ben-Shachar, Annick Raas-Rothschild. Genet Med 2016
26
11

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
338
6

Clinical models of telehealth in genetics: A regional telegenetics landscape.
Alissa B Terry, Amanda Wylie, Melissa Raspa, Beth Vogel, Kunal Sanghavi, Luba Djurdjinovic, Michele Caggana, Joann Bodurtha. J Genet Couns 2019
14
21

Comparison of Telephone and Televideo Modes for Delivery of Genetic Counseling: a Randomized Trial.
Corrine I Voils, Vickie L Venne, Hollis Weidenbacher, Nina Sperber, Santanu Datta. J Genet Couns 2018
19
15

The importance of genetic counselling in genome-wide sequencing.
Alison M Elliott, Jan M Friedman. Nat Rev Genet 2018
13
23


Should pretest genetic counselling be required for patients pursuing genomic sequencing? Results from a survey of participants in a large genomic implementation study.
Joel E Pacyna, Carmen Radecki Breitkopf, Sarah M Jenkins, Erica J Sutton, Caroline Horrow, Iftikhar J Kullo, Richard R Sharp. J Med Genet 2019
12
25


Recommendations for the integration of genomics into clinical practice.
Sarah Bowdin, Adel Gilbert, Emma Bedoukian, Christopher Carew, Margaret P Adam, John Belmont, Barbara Bernhardt, Leslie Biesecker, Hans T Bjornsson, Miriam Blitzer,[...]. Genet Med 2016
74
6

2013 Review and Update of the Genetic Counseling Practice Based Competencies by a Task Force of the Accreditation Council for Genetic Counseling.
Debra Lochner Doyle, Rawan I Awwad, Jehannine C Austin, Bonnie J Baty, Amanda L Bergner, Stephanie J Brewster, Lori A H Erby, Cathi Rubin Franklin, Anne E Greb, Robin E Grubs,[...]. J Genet Couns 2016
24
12

My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad. Genet Med 2017
17
11

Genetic counseling: Growth of the profession and the professional.
Bonnie J Baty. Am J Med Genet C Semin Med Genet 2018
7
28

Genetic counselors as social and behavioral scientists in the era of precision medicine.
Barbara B Biesecker. Am J Med Genet C Semin Med Genet 2018
8
25

Inherited Mutations in Women With Ovarian Carcinoma.
Barbara M Norquist, Maria I Harrell, Mark F Brady, Tom Walsh, Ming K Lee, Suleyman Gulsuner, Sarah S Bernards, Silvia Casadei, Qian Yi, Robert A Burger,[...]. JAMA Oncol 2016
310
4

Impact of Panel Gene Testing for Hereditary Breast and Ovarian Cancer on Patients.
Heidi S Lumish, Hallie Steinfeld, Carrie Koval, Donna Russo, Elana Levinson, Julia Wynn, James Duong, Wendy K Chung. J Genet Couns 2017
56
4

Report from the National Society of Genetic Counselors service delivery model task force: a proposal to define models, components, and modes of referral.
Stephanie A Cohen, Shanna L Gustafson, Monica L Marvin, Bronson D Riley, Wendy R Uhlmann, S Bonnie Liebers, Julie A Rousseau. J Genet Couns 2012
40
5

Comparing Outcomes of Genetic Counseling Options in Breast and Ovarian Cancer: An Integrative Review
.
Danielle M Fournier, Angela F Bazzell, Joyce E Dains. Oncol Nurs Forum 2018
13
15

Oncologists' and cancer patients' views on whole-exome sequencing and incidental findings: results from the CanSeq study.
Stacy W Gray, Elyse R Park, Julie Najita, Yolanda Martins, Lara Traeger, Elizabeth Bair, Joshua Gagne, Judy Garber, Pasi A Jänne, Neal Lindeman,[...]. Genet Med 2016
64
4

Errors in delivery of cancer genetics services: implications for practice.
Karina L Brierley, Danielle Campfield, Whitney Ducaine, Lindsay Dohany, Talia Donenberg, Kristen Shannon, Robin C Schwartz, Ellen T Matloff. Conn Med 2010
63
4

A universal genetic testing initiative for patients with high-grade, non-mucinous epithelial ovarian cancer and the implications for cancer treatment.
Erica M Bednar, Holly D Oakley, Charlotte C Sun, Catherine C Burke, Mark F Munsell, Shannon N Westin, Karen H Lu. Gynecol Oncol 2017
24
8

Mainstreamed genetic testing for women with ovarian cancer: first-year experience.
Belinda Rahman, Anne Lanceley, Rebecca S Kristeleit, Jonathan A Ledermann, Michelle Lockley, Mary McCormack, Tim Mould, Lucy Side. J Med Genet 2019
17
11

Are videoconferenced consultations as effective as face-to-face consultations for hereditary breast and ovarian cancer genetic counseling?
Elvira M Zilliacus, Bettina Meiser, Elizabeth A Lobb, Patrick J Kelly, Kristine Barlow-Stewart, Judy A Kirk, Alan D Spigelman, Linda J Warwick, Katherine M Tucker. Genet Med 2011
38
5

Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical center.
Brandie Heald, Thomas Plesec, Xiuli Liu, Rish Pai, Deepa Patil, Jessica Moline, Richard R Sharp, Carol A Burke, Matthew F Kalady, James Church,[...]. J Clin Oncol 2013
106
4

Genetics, genomics, and cancer risk assessment: State of the Art and Future Directions in the Era of Personalized Medicine.
Jeffrey N Weitzel, Kathleen R Blazer, Deborah J MacDonald, Julie O Culver, Kenneth Offit. CA Cancer J Clin 2011
137
4

Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach.
Goli Samimi, Marcus Q Bernardini, Lawrence C Brody, Charlisse F Caga-Anan, Ian G Campbell, Georgia Chenevix-Trench, Fergus J Couch, Michael Dean, Joanne A de Hullu, Susan M Domchek,[...]. J Clin Oncol 2017
29
6

Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers.
T Pal, J-H Lee, A Besharat, Z Thompson, A N A Monteiro, C Phelan, J M Lancaster, K Metcalfe, T A Sellers, S Vadaparampil,[...]. Clin Genet 2014
22
9

Cluster-randomised non-inferiority trial comparing DVD-assisted and traditional genetic counselling in systematic population testing for BRCA1/2 mutations.
Ranjit Manchanda, Matthew Burnell, Kelly Loggenberg, Rakshit Desai, Jane Wardle, Saskia C Sanderson, Sue Gessler, Lucy Side, Nyala Balogun, Ajith Kumar,[...]. J Med Genet 2016
25
8

Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.
Anita Y Kinney, Karin M Butler, Marc D Schwartz, Jeanne S Mandelblatt, Kenneth M Boucher, Lisa M Pappas, Amanda Gammon, Wendy Kohlmann, Sandra L Edwards, Antoinette M Stroup,[...]. J Natl Cancer Inst 2014
70
4

More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling.
Aisha S Sie, Wendy A G van Zelst-Stams, Liesbeth Spruijt, Arjen R Mensenkamp, Marjolijn J L Ligtenberg, Han G Brunner, Judith B Prins, Nicoline Hoogerbrugge. Fam Cancer 2014
30
6

Reaching high-risk underserved individuals for cancer genetic counseling by video-teleconferencing.
Lindsey A Mette, Anna Maria Pulido Saldívar, Natalie E Poullard, Ivette C Torres, Sarah G Seth, Brad H Pollock, Gail E Tomlinson. J Community Support Oncol 2016
16
12

Hereditary breast and ovarian cancer: successful systematic implementation of a group approach to genetic counselling.
Patrick R Benusiglio, Marina Di Maria, Leila Dorling, Anne Jouinot, Antoine Poli, Sophie Villebasse, Marine Le Mentec, Béatrice Claret, Diane Boinon, Olivier Caron. Fam Cancer 2017
9
22

Women's experience of telehealth cancer genetic counseling.
Elvira M Zilliacus, Bettina Meiser, Elizabeth A Lobb, Judy Kirk, Linda Warwick, Katherine Tucker. J Genet Couns 2010
31
6

Interventions to improve patient education regarding multifactorial genetic conditions: a systematic review.
Katherine G Meilleur, Marguerite T Littleton-Kearney. Am J Med Genet A 2009
25
8

Keeping it simple: genetics referrals for all invasive serous ovarian cancers.
R Demsky, J McCuaig, M Maganti, K J Murphy, B Rosen, S R Armel. Gynecol Oncol 2013
36
5

Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers,[...]. Genet Med 2013
206
4

The Return of Actionable Variants Empirical (RAVE) Study, a Mayo Clinic Genomic Medicine Implementation Study: Design and Initial Results.
Iftikhar J Kullo, Janet Olson, Xiao Fan, Merin Jose, Maya Safarova, Carmen Radecki Breitkopf, Erin Winkler, David C Kochan, Sara Snipes, Joel E Pacyna,[...]. Mayo Clin Proc 2018
19
10

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
273
4

Factors influencing parental decision making in prenatal diagnosis of sex chromosome aneuploidy.
Gábor Mezei, Csaba Papp, Ernö Tóth-Pál, Artúr Beke, Zoltán Papp. Obstet Gynecol 2004
40
5

The use of noninvasive prenatal testing in obstetric care: educational resources, practice patterns, and barriers reported by a national sample of clinicians.
Ruth M Farrell, Patricia K Agatisa, Mary Beth Mercer, Ariane G Mitchum, Marissa B Coleridge. Prenat Diagn 2016
25
8

Patient-Health Care Provider Conversations About Prenatal Genetic Screening: Recommendation or Personal Choice.
Laura C Colicchia, Cynthia L Holland, Jill A Tarr, Doris M Rubio, Scott D Rothenberger, Judy C Chang. Obstet Gynecol 2016
7
28

Cell-free DNA screening and sex chromosome aneuploidies.
Michael T Mennuti, Suchitra Chandrasekaran, Nahla Khalek, Lorraine Dugoff. Prenat Diagn 2015
32
6

Germline Mutations in ATM and BRCA1/2 Distinguish Risk for Lethal and Indolent Prostate Cancer and are Associated with Early Age at Death.
Rong Na, S Lilly Zheng, Misop Han, Hongjie Yu, Deke Jiang, Sameep Shah, Charles M Ewing, Liti Zhang, Kristian Novakovic, Jacqueline Petkewicz,[...]. Eur Urol 2017
129
4

Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer.
Elena Castro, Chee Goh, David Olmos, Ed Saunders, Daniel Leongamornlert, Malgorzata Tymrakiewicz, Nadiya Mahmud, Tokhir Dadaev, Koveela Govindasami, Michelle Guy,[...]. J Clin Oncol 2013
337
4

Frequent germline deleterious mutations in DNA repair genes in familial prostate cancer cases are associated with advanced disease.
D Leongamornlert, E Saunders, T Dadaev, M Tymrakiewicz, C Goh, S Jugurnauth-Little, I Kozarewa, K Fenwick, I Assiotis, D Barrowdale,[...]. Br J Cancer 2014
73
4

The association between germline BRCA2 variants and sensitivity to platinum-based chemotherapy among men with metastatic prostate cancer.
Mark M Pomerantz, Sandor Spisák, Li Jia, Angel M Cronin, Istvan Csabai, Elisa Ledet, A Oliver Sartor, Irene Rainville, Edward P O'Connor, Zachary T Herbert,[...]. Cancer 2017
103
4

Trends in utilization and costs of BRCA testing among women aged 18-64 years in the United States, 2003-2014.
Zhuo Chen, Katherine Kolor, Scott D Grosse, Juan L Rodriguez, Julie A Lynch, Ridgely Fisk Green, W David Dotson, M Scott Bowen, Muin J Khoury. Genet Med 2018
26
7

Multigene Panel Testing in Oncology Practice: How Should We Respond?
Allison W Kurian, James M Ford. JAMA Oncol 2015
39
5

NCCN Guidelines Insights: Genetic/Familial High-Risk Assessment: Breast and Ovarian, Version 2.2017.
Mary B Daly, Robert Pilarski, Michael Berry, Saundra S Buys, Meagan Farmer, Susan Friedman, Judy E Garber, Noah D Kauff, Seema Khan, Catherine Klein,[...]. J Natl Compr Canc Netw 2017
274
4


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.