A citation-based method for searching scientific literature

Tanya Dwarte, Kristine Barlow-Stewart, Rosie O'Shea, Marcel E Dinger, Bronwyn Terrill. J Genet Couns 2019
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


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
56
100

The importance of genetic counselling in genome-wide sequencing.
Alison M Elliott, Jan M Friedman. Nat Rev Genet 2018
9
66

Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
Amy Nisselle, Ivan Macciocca, Fiona McKenzie, Hannah Vuong, Kate Dunlop, Belinda McClaren, Sylvia Metcalfe, Clara Gaff. J Genet Couns 2019
10
66

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
Zornitza Stark, Tiong Y Tan, Belinda Chong, Gemma R Brett, Patrick Yap, Maie Walsh, Alison Yeung, Heidi Peters, Dylan Mordaunt, Shannon Cowie,[...]. Genet Med 2016
171
66

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.
Sarah E Soden, Carol J Saunders, Laurel K Willig, Emily G Farrow, Laurie D Smith, Josh E Petrikin, Jean-Baptiste LePichon, Neil A Miller, Isabelle Thiffault, Darrell L Dinwiddie,[...]. Sci Transl Med 2014
285
66


Are physicians prepared for whole genome sequencing? a qualitative analysis.
K D Christensen, J L Vassy, L Jamal, L S Lehmann, M J Slashinski, D L Perry, J O Robinson, J Blumenthal-Barby, L Z Feuerman, M F Murray,[...]. Clin Genet 2016
61
33

Nationwide survey for current clinical status of amniocentesis and maternal serum marker test in Japan.
Hidehiko Miyake, Shigehito Yamada, Yosuke Fujii, Hideaki Sawai, Naoko Arimori, Yasuko Yamanouchi, Yuka Ozasa, Makoto Kanai, Haruhiko Sago, Akihiko Sekizawa,[...]. J Hum Genet 2016
2
50

Adverse Events in Genetic Testing: The Fourth Case Series.
Meagan B Farmer, Danielle C Bonadies, Suzanne M Mahon, Maria J Baker, Sumedha M Ghate, Christine Munro, Chinmayee B Nagaraj, Andria G Besser, Kara Bui, Christen M Csuy,[...]. Cancer J 2019
7
33

The past, present and future of service delivery in genetic counseling: Keeping up in the era of precision medicine.
Katie Stoll, Shobana Kubendran, Stephanie A Cohen. Am J Med Genet C Semin Med Genet 2018
38
33

ClinPhen extracts and prioritizes patient phenotypes directly from medical records to expedite genetic disease diagnosis.
Cole A Deisseroth, Johannes Birgmeier, Ethan E Bodle, Jennefer N Kohler, Dena R Matalon, Yelena Nazarenko, Casie A Genetti, Catherine A Brownstein, Klaus Schmitz-Abe, Kelly Schoch,[...]. Genet Med 2019
16
33

The Genetic Counselor in the Pediatric Arrhythmia Clinic: Review and Assessment of Services.
Benjamin M Helm, Samantha L Freeze, Katherine G Spoonamore, Stephanie M Ware, Mark D Ayers, Adam C Kean. J Genet Couns 2018
4
33

Genetic counselor workflow study: The times are they a-changin'?
Courtney A Attard, Erin P Carmany, Angela M Trepanier. J Genet Couns 2019
7
33

Gatekeepers or intermediaries? The role of clinicians in commercial genomic testing.
Michelle L McGowan, Jennifer R Fishman, Richard A Settersten, Marcie A Lambrix, Eric T Juengst. PLoS One 2014
21
33


Physicians' perspectives on receiving unsolicited genomic results.
Douglas B Pet, Ingrid A Holm, Janet L Williams, Melanie F Myers, Laurie L Novak, Kyle B Brothers, Georgia L Wiesner, Ellen W Clayton. Genet Med 2019
21
33

Genetic testing in intellectual disability psychiatry: Opinions and practices of UK child and intellectual disability psychiatrists.
Kate Wolfe, Kerstin Stueber, Andrew McQuillin, Fatima Jichi, Christine Patch, Frances Flinter, André Strydom, Nick Bass. J Appl Res Intellect Disabil 2018
9
33

Access to Genetic Counselors in the Southern United States.
Catalina Villegas, Susanne B Haga. J Pers Med 2019
5
33

The current state of cancer genetic counseling access and availability.
Sara Knapke, Joy Larsen Haidle, Rebecca Nagy, Sara Pirzadeh-Miller. Genet Med 2016
9
33

Analysis of Advantages, Limitations, and Barriers of Genetic Counseling Service Delivery Models.
Stephanie A Cohen, Rachelle C Huziak, Shanna Gustafson, Robin E Grubs. J Genet Couns 2016
22
33

Identification of genetic counseling service delivery models in practice: a report from the NSGC Service Delivery Model Task Force.
Stephanie A Cohen, Monica L Marvin, Bronson D Riley, Hetal S Vig, Julie A Rousseau, Shanna L Gustafson. J Genet Couns 2013
67
33

Follow-up nationwide survey on predictive genetic testing for late-onset hereditary neurological diseases in Japan.
Keiko Tanaka, Yoshiki Sekijima, Kunihiro Yoshida, Mariko Tamai, Tomoki Kosho, Akihiro Sakurai, Keiko Wakui, Shu-ichi Ikeda, Yoshimitsu Fukushima. J Hum Genet 2013
4
33

Oncology health professionals' attitudes toward treatment-focused genetic testing for women newly diagnosed with breast cancer.
Stephanie Burcher, Bettina Meiser, Gillian Mitchell, Christobel Saunders, Belinda Rahman, Kathy Tucker, Kristine Barlow-Stewart, Kaaren Watts, Margaret Gleeson, Judy Kirk. Per Med 2013
5
33

Health professionals' evaluation of delivering treatment-focused genetic testing to women newly diagnosed with breast cancer.
Kirsten F L Douma, Bettina Meiser, Judy Kirk, Gillian Mitchell, Christobel Saunders, Belinda Rahman, Mariana S Sousa, Kristine Barlow-Stewart, Margaret Gleeson, Kathy Tucker. Fam Cancer 2015
8
33

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
83
33

A survey of the practice patterns of gynecologic oncologists dealing with hereditary cancer patients in Japan.
Noriko Tanabe, Ayumi Shikama, Hiroko Bando, Toyomi Satoh, Chikako Shimizu. Fam Cancer 2014
4
33

The current use and attitudes towards tumor genome sequencing in breast cancer.
I Gingras, A Sonnenblick, E de Azambuja, M Paesmans, S Delaloge, Philippe Aftimos, M J Piccart, C Sotiriou, M Ignatiadis, H A Azim. Sci Rep 2016
13
33

Rapid genetic counseling and testing in newly diagnosed breast cancer: Patients' and health professionals' attitudes, experiences, and evaluation of effects on treatment decision making.
Marijke R Wevers, Neil K Aaronson, Eveline M A Bleiker, Daniela E E Hahn, Titia Brouwer, Thijs van Dalen, Evert B Theunissen, Bart van Ooijen, Marnix A de Roos, Paul J Borgstein,[...]. J Surg Oncol 2017
7
33

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
6
33

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
5
33

Pulmonary arterial hypertension: Specialists' knowledge, practices, and attitudes of genetic counseling and genetic testing in the USA.
Joseph E Jacher, Lisa J Martin, Wendy K Chung, James E Loyd, William C Nichols. Pulm Circ 2017
8
33

Delivery of genomic medicine for common chronic adult diseases: a systematic review.
Maren T Scheuner, Pauline Sieverding, Paul G Shekelle. JAMA 2008
200
33


Barriers and Facilitators to Adoption of Genomic Services for Colorectal Care within the Veterans Health Administration.
Nina R Sperber, Sara M Andrews, Corrine I Voils, Gregory L Green, Dawn Provenzale, Sara Knight. J Pers Med 2016
8
33

Development of a Streamlined Work Flow for Handling Patients' Genetic Testing Insurance Authorizations.
Wendy R Uhlmann, Katie Schwalm, Victoria M Raymond. J Genet Couns 2017
9
33


Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.
Michelle M Clark, Amber Hildreth, Sergey Batalov, Yan Ding, Shimul Chowdhury, Kelly Watkins, Katarzyna Ellsworth, Brandon Camp, Cyrielle I Kint, Calum Yacoubian,[...]. Sci Transl Med 2019
52
33

Sensorineural Hearing Loss: A Changing Paradigm for Its Evaluation.
Asitha D L Jayawardena, A Eliot Shearer, Richard J H Smith. Otolaryngol Head Neck Surg 2015
9
33

Medical Oncologists' Experiences in Using Genomic Testing for Lung and Colorectal Cancer Care.
Stacy W Gray, Benjamin Kim, Lynette Sholl, Angel Cronin, Aparna R Parikh, Carrie N Klabunde, Katherine L Kahn, David A Haggstrom, Nancy L Keating. J Oncol Pract 2017
9
33

Surveying the current landscape of clinical genetics residency training.
Caleb P Bupp, Laurie A Demmer, Robert A Saul. Genet Med 2015
5
33

Mainstreaming cancer genetics: A model integrating germline BRCA testing into routine ovarian cancer clinics.
Maira Kentwell, Eryn Dow, Yoland Antill, C David Wrede, Orla McNally, Emily Higgs, Anne Hamilton, Sumitra Ananda, Geoffrey J Lindeman, Clare L Scott. Gynecol Oncol 2017
48
33

Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.
Susanne B Haga, Madeline M Carrig, Julianne M O'Daniel, Lori A Orlando, Ley A Killeya-Jones, Geoffrey S Ginsburg, Alex Cho. J Gen Intern Med 2011
49
33

Further Defining the Role of the Laboratory Genetic Counselor.
Lindsey Waltman, Cassandra Runke, Jessica Balcom, Jacquelyn D Riley, Margaret Lilley, Susan Christian, Lindsay Zetzsche, McKinsey L Goodenberger. J Genet Couns 2016
19
33

Genetic consultation embedded in a gynecologic oncology clinic improves compliance with guideline-based care.
Leigha Senter, David M O'Malley, Floor J Backes, Larry J Copeland, Jeffery M Fowler, Ritu Salani, David E Cohn. Gynecol Oncol 2017
15
33

Finding a Balance: Reconciling the Needs of the Institution, Patient, and Genetic Counselor for Optimal Resource Utilization.
Devanshi Patel, Erica L Blouch, Linda H Rodgers-Fouché, Margaret M Emmet, Kristen M Shannon. J Genet Couns 2018
2
50

Implementing a Virtual Health Telemedicine Program in a Community Setting.
Scott M Weissman, Kate Zellmer, Nicole Gill, Deborah Wham. J Genet Couns 2018
12
33

Primary care professionals' perceptions of using a short family history questionnaire.
Shenaz Ahmed, Judith Hayward, Mushtaq Ahmed. Fam Pract 2016
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
12
33

Increasing genetic counseling referral rates through bundled interventions after ovarian cancer diagnosis.
Casey L Swanson, Amanika Kumar, Joy M Maharaj, Jennifer L Kemppainen, Brittany C Thomas, Megan R Weinhold, Kristine M Slaby, Kristin C Mara, Myra J Wick, Jamie N Bakkum-Gamez. Gynecol Oncol 2018
9
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.