A citation-based method for searching scientific literature




Elizabeth A Worthey, Alan N Mayer, Grant D Syverson, Daniel Helbling, Benedetta B Bonacci, Brennan Decker, Jaime M Serpe, Trivikram Dasu, Michael R Tschannen, Regan L Veith, Monica J Basehore, Ulrich Broeckel, Aoy Tomita-Mitchell, Marjorie J Arca, James T Casper, David A Margolis, David P Bick, Martin J Hessner, John M Routes, James W Verbsky, Howard J Jacob, David P Dimmock. Genet Med 2011
Times Cited: 472




List of shared articles



Times cited

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
129

Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.
Josephine Johnston, John D Lantos, Aaron Goldenberg, Flavia Chen, Erik Parens, Barbara A Koenig. Hastings Cent Rep 2018
28

The Human Genome Project, and recent advances in personalized genomics.
Brenda J Wilson, Stuart G Nicholls. Risk Manag Healthc Policy 2015
26

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
29

Views of genetics health professionals on the return of genomic results.
Megan E Grove, Maya N Wolpert, Mildred K Cho, Sandra Soo-Jin Lee, Kelly E Ormond. J Genet Couns 2014
36

Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
Brooke L Levenseller, Danielle J Soucier, Victoria A Miller, Diana Harris, Laura Conway, Barbara A Bernhardt. J Genet Couns 2014
53

The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders.
Vandana Shashi, Allyn McConkie-Rosell, Bruce Rosell, Kelly Schoch, Kasturi Vellore, Marie McDonald, Yong-Hui Jiang, Pingxing Xie, Anna Need, David B Goldstein. Genet Med 2014
151

A genetic counselor's guide to using next-generation sequencing in clinical practice.
Flavia M Facio, Kristy Lee, Julianne M O'Daniel. J Genet Couns 2014
24

Why we should not use the Affordable Care Act to encourage widespread whole genome sequencing.
Pilar N Ossorio, J Paul Kelleher. J Health Polit Policy Law 2014
0

The promise of whole-exome sequencing in medical genetics.
Bahareh Rabbani, Mustafa Tekin, Nejat Mahdieh. J Hum Genet 2014
229

The promise and challenges of next-generation genome sequencing for clinical care.
Katherine A Johansen Taber, Barry D Dickinson, Modena Wilson. JAMA Intern Med 2014
94

An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.
Catherine A Brownstein, Alan H Beggs, Nils Homer, Barry Merriman, Timothy W Yu, Katherine C Flannery, Elizabeth T DeChene, Meghan C Towne, Sarah K Savage, Emily N Price,[...]. Genome Biol 2014
73


Defining and managing incidental findings in genetic and genomic practice.
Shiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, Angela Fenwick, Anneke Lucassen. J Med Genet 2014
37


Self-guided management of exome and whole-genome sequencing results: changing the results return model.
Joon-Ho Yu, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Genet Med 2013
56

Massively parallel sequencing: the new frontier of hematologic genomics.
Jill M Johnsen, Deborah A Nickerson, Alex P Reiner. Blood 2013
14