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


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
395
4

Clinical Impact and Cost-Effectiveness of Whole Exome Sequencing as a Diagnostic Tool: A Pediatric Center's Experience.
C Alexander Valencia, Ammar Husami, Jennifer Holle, Judith A Johnson, Yaping Qian, Abhinav Mathur, Chao Wei, Subba Rao Indugula, Fanggeng Zou, Haiying Meng,[...]. Front Pediatr 2015
99
4

The emerging clinical relevance of genomics in cancer medicine.
Michael F Berger, Elaine R Mardis. Nat Rev Clin Oncol 2018
83
4

Use of Whole Genome Sequencing for Diagnosis and Discovery in the Cancer Genetics Clinic.
Samantha B Foley, Jonathan J Rios, Victoria E Mgbemena, Linda S Robinson, Heather L Hampel, Amanda E Toland, Leslie Durham, Theodora S Ross. EBioMedicine 2015
27
7

If we build it ... will they come?--establishing a cancer genetics services clinic for an underserved predominantly Latina cohort.
Charité Ricker, Veronica Lagos, Nancy Feldman, Susan Hiyama, Sue Fuentes, Visanth Kumar, Kelly Gonzalez, Melanie Palomares, Kathleen Blazer, Katrina Lowstuter,[...]. J Genet Couns 2006
39
5

A Comprehensive Program Enabling Effective Delivery of Regional Genetic Counseling.
Jubilee Brown, Aly Athens, David L Tait, Erin K Crane, Robert V Higgins, R Wendel Naumann, Lejla Hadzikadic Gusic, Lisa Amacker-North. Int J Gynecol Cancer 2018
5
40

Genomic education for the next generation of health-care providers.
MaryAnn Campion, Constance Goldgar, Robert J Hopkin, Cynthia A Prows, Shoumita Dasgupta. Genet Med 2019
24
8

Randomized controlled trial of a psychosocial telephone counseling intervention in BRCA1 and BRCA2 mutation carriers.
Kristi D Graves, Lari Wenzel, Marc D Schwartz, George Luta, Paul Wileyto, Steven Narod, Beth N Peshkin, Alfred Marcus, David Cella, Susan Powell Emsbo,[...]. Cancer Epidemiol Biomarkers Prev 2010
32
6

Prevalence and Penetrance of Major Genes and Polygenes for Colorectal Cancer.
Aung Ko Win, Mark A Jenkins, James G Dowty, Antonis C Antoniou, Andrew Lee, Graham G Giles, Daniel D Buchanan, Mark Clendenning, Christophe Rosty, Dennis J Ahnen,[...]. Cancer Epidemiol Biomarkers Prev 2017
113
4

A clinical utility study of exome sequencing versus conventional genetic testing in pediatric neurology.
Lisenka E L M Vissers, Kirsten J M van Nimwegen, Jolanda H Schieving, Erik-Jan Kamsteeg, Tjitske Kleefstra, Helger G Yntema, Rolph Pfundt, Gert Jan van der Wilt, Lotte Krabbenborg, Han G Brunner,[...]. Genet Med 2017
93
4

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
121
4

Clinical exome sequencing: results from 2819 samples reflecting 1000 families.
Daniel Trujillano, Aida M Bertoli-Avella, Krishna Kumar Kandaswamy, Maximilian Er Weiss, Julia Köster, Anett Marais, Omid Paknia, Rolf Schröder, Jose Maria Garcia-Aznar, Martin Werber,[...]. Eur J Hum Genet 2017
159
4

The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking study.
Nick Dragojlovic, Alison M Elliott, Shelin Adam, Clara van Karnebeek, Anna Lehman, Jill C Mwenifumbo, Tanya N Nelson, Christèle du Souich, Jan M Friedman, Larry D Lynd. Genet Med 2018
35
5

How to know when physicians are ready for genomic medicine.
Jason L Vassy, Bruce R Korf, Robert C Green. Sci Transl Med 2015
39
5

Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability.
Glen R Monroe, Gerardus W Frederix, Sanne M C Savelberg, Tamar I de Vries, Karen J Duran, Jasper J van der Smagt, Paulien A Terhal, Peter M van Hasselt, Hester Y Kroes, Nanda M Verhoeven-Duif,[...]. Genet Med 2016
94
4

Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw,[...]. JAMA 2014
533
4

The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders.
Nick Dragojlovic, Clara D M van Karnebeek, Aisha Ghani, Dallas Genereaux, Ellen Kim, Patricia Birch, Alison M Elliott, Jan M Friedman, Larry D Lynd. Genet Med 2020
7
28


Atypical cerebral palsy: genomics analysis enables precision medicine.
Allison M Matthews, Ingrid Blydt-Hansen, Basmah Al-Jabri, John Andersen, Maja Tarailo-Graovac, Magda Price, Katherine Selby, Michelle Demos, Mary Connolly, Britt Drögemoller,[...]. Genet Med 2019
10
20

The Genomic Consultation Service: A clinical service designed to improve patient selection for genome-wide sequencing in British Columbia.
Alison M Elliott, Christèle du Souich, Shelin Adam, Nick Dragojlovic, Clara van Karnebeek, Tanya N Nelson, Anna Lehman, Larry D Lynd, Jan M Friedman. Mol Genet Genomic Med 2018
10
20

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
294
4

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
99
4

Service Delivery Model and Experiences in a Cancer Genetics Clinic for an Underserved Population.
Ashley H Woodson, Jessica L Profato, Minjeong Park, Sarah H Rizvi, Nisreen Elsayegh, Alyssa G Rieber, Banu K Arun. J Health Care Poor Underserved 2015
7
28


Genetic Counseling and the Central Tenets of Practice.
Barbara Biesecker. Cold Spring Harb Perspect Med 2020
3
66

What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
55
4



Artificial intelligence in genetic services delivery: Utopia or apocalypse?
Elizabeth Kearney, Antonina Wojcik, Deepti Babu. J Genet Couns 2020
3
66

Information Mismatch: Cancer Risk Counseling with Diverse Underserved Patients.
Galen Joseph, Rena J Pasick, Dean Schillinger, Judith Luce, Claudia Guerra, Janice Ka Yan Cheng. J Genet Couns 2017
39
5

Effective communication in the era of precision medicine: A pilot intervention with low health literacy patients to improve genetic counseling communication.
Galen Joseph, Robin Lee, Rena J Pasick, Claudia Guerra, Dean Schillinger, Sara Rubin. Eur J Med Genet 2019
14
14

The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations.
Laura M Amendola, Jonathan S Berg, Carol R Horowitz, Frank Angelo, Jeannette T Bensen, Barbara B Biesecker, Leslie G Biesecker, Gregory M Cooper, Kelly East, Kelly Filipski,[...]. Am J Hum Genet 2018
36
5

An approach to pediatric exome and genome sequencing.
Leslie G Biesecker, Barbara B Biesecker. Curr Opin Pediatr 2014
18
11

Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, Stephen Clayton, Jeremy F McRae, Margriet van Kogelenberg, Daniel A King, Kirsty Ambridge, Daniel M Barrett, Tanya Bayzetinova,[...]. Lancet 2015
347
4

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.
Michelle M Clark, Zornitza Stark, Lauge Farnaes, Tiong Y Tan, Susan M White, David Dimmock, Stephen F Kingsmore. NPJ Genom Med 2018
132
4

Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders.
Caroline F Wright, Jeremy F McRae, Stephen Clayton, Giuseppe Gallone, Stuart Aitken, Tomas W FitzGerald, Philip Jones, Elena Prigmore, Diana Rajan, Jenny Lord,[...]. Genet Med 2018
107
4

From genetic counseling to "genomic counseling".
Kelly E Ormond. Mol Genet Genomic Med 2013
42
4

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
28
7


Analysis of state laws on informed consent for clinical genetic testing in the era of genomic sequencing.
Kayte Spector-Bagdady, Anya E R Prince, Joon-Ho Yu, Paul S Appelbaum. Am J Med Genet C Semin Med Genet 2018
4
25

Genetic counseling among minority populations in the era of precision medicine.
Chanita H Halbert, Barbara W Harrison. Am J Med Genet C Semin Med Genet 2018
9
11


Prevalence of childhood and adult obesity in the United States, 2011-2012.
Cynthia L Ogden, Margaret D Carroll, Brian K Kit, Katherine M Flegal. JAMA 2014
2

Engaging populations underrepresented in research through novel approaches to consent.
Stephanie A Kraft, Megan Doerr. Am J Med Genet C Semin Med Genet 2018
14
7

The dawn of consumer-directed testing.
Erica Ramos, Scott M Weissman. Am J Med Genet C Semin Med Genet 2018
25
4

Genetic counseling in industry settings: Opportunities in the era of precision health.
Kirsty McWalter, Megan T Cho, Tara Hart, Rachel Nusbaum, Courtney Sebold, Sara Knapke, Rachel Klein, Bethany Friedman, Rebecca Willaert, Amanda Singleton,[...]. Am J Med Genet C Semin Med Genet 2018
4
25

Evolution of genetic assessment for BRCA-associated gynaecologic malignancies: a Canadian multisociety roadmap.
Jeanna M McCuaig, Tracy L Stockley, Patricia Shaw, Michael Fung-Kee-Fung, Alon D Altman, James Bentley, Marcus Q Bernardini, Beatrice Cormier, Hal Hirte, Katharina Kieser,[...]. J Med Genet 2018
16
6


Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.
Joanne Armstrong, Michele Toscano, Nancy Kotchko, Sue Friedman, Marc D Schwartz, Katherine S Virgo, Kristian Lynch, James E Andrews, Claudia X Aguado Loi, Joseph E Bauer,[...]. JAMA Oncol 2015
72
2

New paradigms for BRCA1/BRCA2 testing in women with ovarian cancer: results of the Genetic Testing in Epithelial Ovarian Cancer (GTEOC) study.
Inga Plaskocinska, Hannah Shipman, James Drummond, Edward Thompson, Vanessa Buchanan, Barbara Newcombe, Charlotte Hodgkin, Elisa Barter, Paul Ridley, Rita Ng,[...]. J Med Genet 2016
31
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.