A citation-based method for searching scientific literature

Morgan Butrick, Scott Kelly, Beth N Peshkin, George Luta, Rachel Nusbaum, Gillian W Hooker, Kristi Graves, Lisa Feeley, Claudine Isaacs, Heiddis B Valdimarsdottir, Lina Jandorf, Tiffani DeMarco, Marie Wood, Wendy McKinnon, Judy Garber, Shelley R McCormick, Marc D Schwartz. Genet Med 2015
Times Cited: 55







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



Times Cited
  Times     Co-cited
Similarity



Utilization of available prenatal screening and diagnosis: effects of the California screen program.
Y J Blumenfeld, J Taylor, H C Lee, L Hudgins, J F Sung, Y Y El-Sayed. J Perinatol 2012
5
20

Uptake of Predictive Genetic Testing and Cardiac Evaluation for Children at Risk for an Inherited Arrhythmia or Cardiomyopathy.
Susan Christian, Joseph Atallah, Robin Clegg, Michael Giuffre, Cathleen Huculak, Tara Dzwiniel, Jillian Parboosingh, Sherryl Taylor, Martin Somerville. J Genet Couns 2018
7
14


Utilization Patterns and Trends in Epidermal Growth Factor Receptor (EGFR) Mutation Testing Among Patients With Newly Diagnosed Metastatic Lung Cancer.
Chan Shen, Kenneth L Kehl, Bo Zhao, George R Simon, Shouhao Zhou, Sharon H Giordano. Clin Lung Cancer 2017
17
5


Uptake of genetic testing by the children of Lynch syndrome variant carriers across three generations.
Toni T Seppälä, Kirsi Pylvänäinen, Jukka-Pekka Mecklin. Eur J Hum Genet 2017
8
12

Using Quality Improvement Methods and Time-Driven Activity-Based Costing to Improve Value-Based Cancer Care Delivery at a Cancer Genetics Clinic.
Ryan Y C Tan, Marie Met-Domestici, Ke Zhou, Alexis B Guzman, Soon Thye Lim, Khee Chee Soo, Thomas W Feeley, Joanne Ngeow. J Oncol Pract 2016
14
7

Provision of Genetic Services for Autism and its Impact on Spanish Families.
Marta Codina-Solà, Luis A Pérez-Jurado, Ivon Cuscó, Clara Serra-Juhé. J Autism Dev Disord 2017
6
16

PRISMA Extension for Scoping Reviews (PRISMA-ScR): Checklist and Explanation.
Andrea C Tricco, Erin Lillie, Wasifa Zarin, Kelly K O'Brien, Heather Colquhoun, Danielle Levac, David Moher, Micah D J Peters, Tanya Horsley, Laura Weeks,[...]. Ann Intern Med 2018
1


An Exploration of Genetic Test Utilization, Genetic Counseling, and Consanguinity within the Inborn Errors of Metabolism Collaborative (IBEMC).
Quinn P Stein, Cate Walsh Vockley, Mathew J Edick, Shaohui Zhai, Sally J Hiner, Rebecca S Loman, Laura Davis-Keppen, Taylor A Zuck, Cynthia A Cameron, Susan A Berry. J Genet Couns 2017
2
50


Diagnostic Impact and Cost-effectiveness of Whole-Exome Sequencing for Ambulant Children With Suspected Monogenic Conditions.
Tiong Yang Tan, Oliver James Dillon, Zornitza Stark, Deborah Schofield, Khurshid Alam, Rupendra Shrestha, Belinda Chong, Dean Phelan, Gemma R Brett, Emma Creed,[...]. JAMA Pediatr 2017
129
1

Women's uptake of non-invasive DNA testing following a high-risk screening test for trisomy 21 within a publicly funded healthcare system: findings from a retrospective review.
Yiu Man Chan, Wing Cheong Leung, Wan Pang Chan, Tak Yeung Leung, Yvonne Kwun Yue Cheng, Daljit Singh Sahota. Prenat Diagn 2015
21
4


Uptake of Preimplantation Genetic Diagnosis in Female BRCA1 and BRCA2 Mutation Carriers.
Pnina Mor, Sarah Brennenstuhl, Kelly A Metcalfe. J Genet Couns 2018
8
12

Implementation of a pharmacogenomics service in a community pharmacy.
Stefanie P Ferreri, Angelo J Greco, Natasha M Michaels, Shanna K O'Connor, Rebecca W Chater, Anthony J Viera, Hawazin Faruki, Howard L McLeod, Mary W Roederer. J Am Pharm Assoc (2003) 2014
46
2

Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
Charlotte J Dommering, Lidewij Henneman, Annemarie H van der Hout, Marianne A Jonker, Carli M J Tops, Ans M W van den Ouweland, Rob B van der Luijt, Arjen R Mensenkamp, Frans B L Hogervorst, Egbert J W Redeker,[...]. Fam Cancer 2017
8
12

Uptake of noninvasive prenatal testing at a large academic referral center.
Sebastian Larion, Steven L Warsof, Letty Romary, Margaret Mlynarczyk, David Peleg, Alfred Z Abuhamad. Am J Obstet Gynecol 2014
61
1

Clinical utility of noninvasive fetal trisomy (NIFTY) test--early experience.
Tze Kin Lau, Mei Ki Chan, Pui Shan Salome Lo, Hon Yee Connie Chan, Wai Sze Kim Chan, Tik Yee Koo, Hoi Yan Joyce Ng, Ritsuko K Pooh. J Matern Fetal Neonatal Med 2012
44
2

Budget Impact of Next-Generation Sequencing for Molecular Assessment of Advanced Non-Small Cell Lung Cancer.
Tiffany M Yu, Carl Morrison, Edward J Gold, Alison Tradonsky, Renée J G Arnold. Value Health 2018
13
7

Uptake of KRAS mutation testing in patients with metastatic colorectal cancer in Europe, Latin America and Asia.
Fortunato Ciardiello, Sabine Tejpar, Nicola Normanno, Domenica Mercadante, Tracey Teague, Bruno Wohlschlegel, Eric Van Cutsem. Target Oncol 2011
40
2

Cell-free DNA testing after combined test: factors affecting the uptake.
Nerea Maiz, Irune Alzola, Emerson J Murua, Javier Rodríguez Santos. J Matern Fetal Neonatal Med 2016
5
20

Cancer whole-genome sequencing: present and future.
H Nakagawa, C P Wardell, M Furuta, H Taniguchi, A Fujimoto. Oncogene 2015
55
1

Impact of nationwide health insurance coverage for non-invasive prenatal testing.
Valentina Vinante, Bettina Keller, Evelyn A Huhn, Dorothy Huang, Olav Lapaire, Gwendolin Manegold-Brauer. Int J Gynaecol Obstet 2018
5
20

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
338
1

Parents' perceptions of genetics services for congenital heart disease: the role of demographic, clinical, and psychological factors in determining service attendance.
Nadine A Kasparian, Blake Fidock, Gary F Sholler, Christoph Camphausen, David N Murphy, Stephen G Cooper, Ritik Kaul, Owen Jones, David S Winlaw, Edwin P E Kirk. Genet Med 2014
10
10


Impact of subsidies on cancer genetic testing uptake in Singapore.
Shao-Tzu Li, Jeanette Yuen, Ke Zhou, Nur Diana Binte Ishak, Yanni Chen, Marie Met-Domestici, Sock Hoai Chan, Yee Pin Tan, John Carson Allen, Soon Thye Lim,[...]. J Med Genet 2017
15
6


Population-Based Study of Attitudes toward BRCA Genetic Testing among Orthodox Jewish Women.
Eve Y Tang, Meghna S Trivedi, Rita Kukafka, Wendy K Chung, Raven David, Leah Respler, Sarah Leifer, Isaac Schechter, Katherine D Crew. Breast J 2017
6
16

The utilization and choices of aneuploidy screening in a midwestern population.
Jeffrey M Dicke, Lindsey Van Duyne, Rachael Bradshaw. J Genet Couns 2014
3
33

Genome sequencing identifies major causes of severe intellectual disability.
Christian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, Maartje van de Vorst, Bregje W M van Bon, Marjolein H Willemsen, Michael Kwint, Irene M Janssen, Alexander Hoischen, Annette Schenck,[...]. Nature 2014
612
1

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
50
2

Uptake of noninvasive prenatal testing (NIPT) in women following positive aneuploidy screening.
Shilpa Chetty, Matthew J Garabedian, Mary E Norton. Prenat Diagn 2013
117
1

Growth of molecular diagnostics and genetic testing in the USA, 2008-2011: analysis and implications.
Jeanne De Sa, Brantley Carlson, Nadine Caputo, Deneen Vojta, Lewis Sandy, Simon Stevens. Per Med 2013
8
12

Compliance for genetic screening in the Arab population in Israel.
Rivka Sukenik-Halevy, Ulfat Abu Leil-Zoabi, Lilach Peled-Perez, Joel Zlotogora, Stavit Allon-Shalev. Isr Med Assoc J 2012
10
10

Expanded carrier screening: a current survey of physician utilization and attitudes.
Allison Briggs, Parvaneh K Nouri, Michael Galloway, Kathleen O'Leary, Nigel Pereira, Steven R Lindheim. J Assist Reprod Genet 2018
11
9

Utilization of Genetic Counseling after Direct-to-Consumer Genetic Testing: Findings from the Impact of Personal Genomics (PGen) Study.
Diane R Koeller, Wendy R Uhlmann, Deanna Alexis Carere, Robert C Green, J Scott Roberts. J Genet Couns 2017
19
5

NIPT in a clinical setting: an analysis of uptake in the first months of clinical availability.
Joanne B Taylor, Valerie Y Chock, Louanne Hudgins. J Genet Couns 2014
35
2

Cost Implications of Reactive Versus Prospective Testing for Dihydropyrimidine Dehydrogenase Deficiency in Patients With Colorectal Cancer: A Single-Institution Experience.
Con Murphy, Stephen Byrne, Gul Ahmed, Andrew Kenny, James Gallagher, Harry Harvey, Eoin O'Farrell, Brian Bird. Dose Response 2018
9
11

Trends in the use of prenatal testing services for fetal aneuploidy in Ontario: a descriptive study.
Tianhua Huang, Shelley Dougan, Mark Walker, Christine M Armour, Nan Okun.  2018
5
20

Chromosomal microarray use among women undergoing invasive prenatal diagnosis.
Mariam Naqvi, Ilona T Goldfarb, Kaitlin J Hanmer, Allison Bryant. Prenat Diagn 2016
8
12


Prospective comparison of the cost-effectiveness of clinical whole-exome sequencing with that of usual care overwhelmingly supports early use and reimbursement.
Zornitza Stark, Deborah Schofield, Khurshid Alam, William Wilson, Nessie Mupfeki, Ivan Macciocca, Rupendra Shrestha, Susan M White, Clara Gaff. Genet Med 2017
103
1

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
62
1

NSCLC molecular testing in Central and Eastern European countries.
Ales Ryska, Peter Berzinec, Luka Brcic, Tanja Cufer, Rafal Dziadziuszko, Maya Gottfried, Ilona Kovalszky, Włodzimierz Olszewski, Buge Oz, Lukas Plank,[...]. BMC Cancer 2018
11
9

Genetic test utilization and diagnostic yield in adult patients with neurological disorders.
Tanya M Bardakjian, Ingo Helbig, Colin Quinn, Lauren B Elman, Leo F McCluskey, Steven S Scherer, Pedro Gonzalez-Alegre. Neurogenetics 2018
7
14

Use of combinatorial pharmacogenomic guidance in treating psychiatric disorders.
Joachim Benitez, Christina L Cool, Dennis J Scotti. Per Med 2018
7
14


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.