A citation-based method for searching scientific literature

Judith A Cooksey, Gaetano Forte, Judith Benkendorf, Miriam G Blitzer. Genet Med 2005
Times Cited: 66







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



Times Cited
  Times     Co-cited
Similarity


Familial risk of cancer and knowledge and use of genetic testing.
Heather J Baer, Phyllis Brawarsky, Michael F Murray, Jennifer S Haas. J Gen Intern Med 2010
23
8

Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing.
Christine E Miller, Patti Krautscheid, Erin E Baldwin, Tatiana Tvrdik, Amanda S Openshaw, Kim Hart, Danielle Lagrave. Am J Med Genet A 2014
64
3



The organization and delivery of clinical genetics services.
B A Bernhardt, R E Pyeritz. Pediatr Clin North Am 1992
11
18


Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing.
Peter Benn, Audrey R Chapman, Kristine Erickson, Mark S Defrancesco, Louise Wilkins-Haug, James F X Egan, Jay Schulkin. Prenat Diagn 2014
53
3

Telemedicine for genetic and neurologic evaluation in the neonatal intensive care unit.
T L Wenger, J Gerdes, K Taub, D T Swarr, M A Deardorff, N S Abend. J Perinatol 2014
28
7

Telemedicine: Pediatric Applications.
Bryan L Burke, R W Hall. Pediatrics 2015
125
3

National Estimates of Genetic Testing in Women With a History of Breast or Ovarian Cancer.
Christopher P Childers, Kimberly K Childers, Melinda Maggard-Gibbons, James Macinko. J Clin Oncol 2017
130
3


Promoting appropriate genetic testing: the impact of a combined test review and consultative service.
Carlos J Suarez, Linbo Yu, Natalie Downs, Helio A Costa, David A Stevenson. Genet Med 2017
9
22

Impact of a Patient-Facing Enhanced Genomic Results Report to Improve Understanding, Engagement, and Communication.
Janet L Williams, Alanna Kulchak Rahm, Doris T Zallen, Heather Stuckey, Kara Fultz, Audrey L Fan, Michele Bonhag, Lynn Feldman, Michael M Segal, Marc S Williams. J Genet Couns 2018
15
13

A time study of cancer genetic counselors using a genetic counselor-only patient care model versus a traditional combined genetic counselor plus medical geneticist care model.
Brandie Heald, Shanna Gustafson, Jessica Mester, Patricia Arscott, Katherine Lynch, Jessica Moline, Charis Eng. J Natl Compr Canc Netw 2013
9
22

Surveying the current landscape of clinical genetics residency training.
Caleb P Bupp, Laurie A Demmer, Robert A Saul. Genet Med 2015
6
33

Increasing confidence and changing behaviors in primary care providers engaged in genetic counselling.
Michael S Wilkes, Frank C Day, Tonya L Fancher, Haley McDermott, Erik Lehman, Robert A Bell, Michael J Green. BMC Med Educ 2017
22
9

Implementing Group Prenatal Counseling for Expanded Noninvasive Screening Options.
Betsy L Gammon, Laura Otto, Myra Wick, Kristy Borowski, Megan Allyse. J Genet Couns 2018
9
22

Assessment of clinical workload for general and specialty genetic counsellors at an academic medical center: a tool for evaluating genetic counselling practices.
Brandie Heald, Lisa Rybicki, Diane Clements, Jessica Marquard, Jessica Mester, Ryan Noss, Monica Nardini, Jill Polk, Brittany Psensky, Christina Rigelsky,[...]. NPJ Genom Med 2016
17
11

Primary Care Providers' Initial Evaluation of Children with Global Developmental Delay: A Clinical Vignette Study.
Beth A Tarini, Brian J Zikmund-Fisher, Howard M Saal, Laurie Edmondson, Wendy R Uhlmann. J Pediatr 2015
10
20


Attitudes and practices among internists concerning genetic testing.
Robert Klitzman, Wendy Chung, Karen Marder, Anita Shanmugham, Lisa J Chin, Meredith Stark, Cheng-Shiun Leu, Paul S Appelbaum. J Genet Couns 2013
105
3

Personal genome testing in medical education: student experiences with genotyping in the classroom.
Simone Lucia Vernez, Keyan Salari, Kelly E Ormond, Sandra Soo-Jin Lee. Genome Med 2013
39
5

Views Of Primary Care Providers On Testing Patients For Genetic Risks For Common Chronic Diseases.
Diane Hauser, Aniwaa Owusu Obeng, Kezhen Fei, Michelle A Ramos, Carol R Horowitz. Health Aff (Millwood) 2018
25
8


Alternate Service Delivery Models in Cancer Genetic Counseling: A Mini-Review.
Adam Hudson Buchanan, Alanna Kulchak Rahm, Janet L Williams. Front Oncol 2016
55
3

A pilot study of telegenetics.
J Gray, K Brain, R Iredale, J Alderman, E France, H Hughes. J Telemed Telecare 2000
44
4

Barriers in identification and referral to genetic counseling for familial cancer risk: the perspective of genetic service providers.
Sharon J Rolnick, Alanna K Rahm, Jody M Jackson, Larissa Nekhlyudov, Katrina A B Goddard, Terry Field, Catherine McCarty, Cynthia Nakasato, Douglas Roblin, Christopher P Anderson,[...]. J Genet Couns 2011
24
8

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
22
9

Effectiveness of telemedicine: a systematic review of reviews.
Anne G Ekeland, Alison Bowes, Signe Flottorp. Int J Med Inform 2010
389
3

Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
48
4

Online genetic counseling from the providers' perspective: counselors' evaluations and a time and cost analysis.
Ellen Otten, Erwin Birnie, Adelita V Ranchor, Irene M van Langen. Eur J Hum Genet 2016
20
10

Telegenetics: an Update on Availability and Use of Telemedicine in Clinical Genetics Service.
Irena Vrečar, Dimitar Hristovski, Borut Peterlin. J Med Syst 2017
26
7


Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Laura M Amendola, Michael O Dorschner, Peggy D Robertson, Joseph S Salama, Ragan Hart, Brian H Shirts, Mitzi L Murray, Mari J Tokita, Carlos J Gallego, Daniel Seung Kim,[...]. Genome Res 2015
215
3

Clinical application of whole-exome sequencing across clinical indications.
Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan,[...]. Genet Med 2016
433
3

Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers.
Karoline B Kuchenbaecker, John L Hopper, Daniel R Barnes, Kelly-Anne Phillips, Thea M Mooij, Marie-José Roos-Blom, Sarah Jervis, Flora E van Leeuwen, Roger L Milne, Nadine Andrieu,[...]. JAMA 2017
783
3

Awareness and utilization of BRCA1/2 testing among U.S. primary care physicians.
Cecelia A Bellcross, Katherine Kolor, Katrina A B Goddard, Ralph J Coates, Michele Reyes, Muin J Khoury. Am J Prev Med 2011
111
3


Acceptability of telemedicine and other cancer genetic counseling models of service delivery in geographically remote settings.
Eileen McDonald, Amanda Lamb, Barbara Grillo, Lee Lucas, Susan Miesfeldt. J Genet Couns 2014
29
6

Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.
Anita Y Kinney, Laurie E Steffen, Barbara H Brumbach, Wendy Kohlmann, Ruofei Du, Ji-Hyun Lee, Amanda Gammon, Karin Butler, Saundra S Buys, Antoinette M Stroup,[...]. J Clin Oncol 2016
61
3

A profile of the genetic counsellor and genetic nurse profession in European countries.
Cristophe Cordier, Debby Lambert, Marie-Antoinette Voelckel, Ulrika Hosterey-Ugander, Heather Skirton. J Community Genet 2012
28
7

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
3

Nursing genetics and genomics: The International Society of Nurses in Genetics (ISONG) survey.
Kathleen T Hickey, Jacquelyn Y Taylor, Taura L Barr, Nicole R Hauser, Haomiao Jia, Teresa C Riga, Maria Katapodi. Nurse Educ Today 2018
8
25

Meeting the challenges of implementing rapid genomic testing in acute pediatric care.
Zornitza Stark, Sebastian Lunke, Gemma R Brett, Natalie B Tan, Rachel Stapleton, Smitha Kumble, Alison Yeung, Dean G Phelan, Belinda Chong, Miriam Fanjul-Fernandez,[...]. Genet Med 2018
65
3

Racial disparities in BRCA testing and cancer risk management across a population-based sample of young breast cancer survivors.
Deborah Cragun, Anne Weidner, Courtney Lewis, Devon Bonner, Jongphil Kim, Susan T Vadaparampil, Tuya Pal. Cancer 2017
82
3

Prioritizing diversity in human genomics research.
Lucia A Hindorff, Vence L Bonham, Lawrence C Brody, Margaret E C Ginoza, Carolyn M Hutter, Teri A Manolio, Eric D Green. Nat Rev Genet 2018
121
3

Precision medicine meets public health: population screening for BRCA1 and BRCA2.
Ephrat Levy-Lahad, Amnon Lahad, Mary-Claire King. J Natl Cancer Inst 2014
36
5

Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
518
3

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
3



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.