A citation-based method for searching scientific literature

Holly K Tabor, Benjamin E Berkman, Sara Chandros Hull, Michael J Bamshad. Am J Med Genet A 2011
Times Cited: 93



Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers, Nancy A Press, Lainie Friedman Ross, Mark A Rothstein, Howard Saal, Wendy R Uhlmann, Benjamin Wilfond, Susan M Wolf, Ron Zimmern. Genet Med 2013
Times Cited: 213




List of shared articles



Times cited

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
17


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
26

Ethical issues raised by whole genome sequencing.
Wim Pinxten, Heidi Carmen Howard. Best Pract Res Clin Gastroenterol 2014
32

Institutional review board perspectives on obligations to disclose genetic incidental findings to research participants.
Catherine Gliwa, Ilana R Yurkiewicz, Lisa Soleymani Lehmann, Sara Chandros Hull, Nathan Jones, Benjamin E Berkman. Genet Med 2016
15

Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular Pathology.
Madhuri Hegde, Sherri Bale, Pinar Bayrak-Toydemir, Jane Gibson, Linda Jo Bone Jeng, Loren Joseph, Jordan Laser, Ira M Lubin, Christine E Miller, Lainie F Ross,[...]. J Mol Diagn 2015
35

Grappling with genomic incidental findings in the clinical realm.
Sara Chandros Hull, Benjamin E Berkman. Chest 2014
3

Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.
Joon-Ho Yu, Tanya M Harrell, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Hum Genet 2014
86

Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results.
Holly K Tabor, Paul L Auer, Seema M Jamal, Jessica X Chong, Joon-Ho Yu, Adam S Gordon, Timothy A Graubert, Christopher J O'Donnell, Stephen S Rich, Deborah A Nickerson,[...]. Am J Hum Genet 2014
64

Whole exome or genome sequencing: nurses need to prepare families for the possibilities.
Cynthia A Prows, Grace Tran, Beverly Blosser. J Adv Nurs 2014
7

Next-generation sequencing applied to rare diseases genomics.
Krissi Danielsson, Liew Jun Mun, Amanda Lordemann, Jimmy Mao, Cheng-Ho Jimmy Lin. Expert Rev Mol Diagn 2014
15



A framework for analyzing the ethics of disclosing genetic research findings.
Lisa Eckstein, Jeremy R Garrett, Benjamin E Berkman. J Law Med Ethics 2014
23