A citation-based method for searching scientific literature

Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
Times Cited: 99



Susan M Wolf, George J Annas, Sherman Elias. Science 2013
Times Cited: 151




List of shared articles



Times cited



A protocol for the identification and validation of novel genetic causes of kidney disease.
Andrew Mallett, Chirag Patel, Barbara Maier, Julie McGaughran, Michael Gabbett, Minoru Takasato, Anne Cameron, Peter Trnka, Stephen I Alexander, Gopala Rangan,[...]. BMC Nephrol 2015
7


Ethical considerations for modern molecular pathology.
Shoko Vos, Paul J van Diest, Margreet Gem Ausems, Marijke R van Dijk, Wendy Wj de Leng, Annelien L Bredenoord. J Pathol 2018
3



Attitudes of non-African American focus group participants toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Michael J Bamshad, Holly K Tabor. Am J Med Genet A 2014
35

Utility of next generation sequencing in clinical primary immunodeficiencies.
Nikita Raje, Sarah Soden, Douglas Swanson, Christina E Ciaccio, Stephen F Kingsmore, Darrell L Dinwiddie. Curr Allergy Asthma Rep 2014
14

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
83


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
36

"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project.
Elizabeth Ormondroyd, Michael P Mackley, Edward Blair, Judith Craft, Julian C Knight, Jenny C Taylor, John Taylor, Hugh Watkins. Genet Med 2018
28

Research participants in NGS studies want to know about incidental findings.
Anne Marie Jelsig, Niels Qvist, Klaus Brusgaard, Lilian Bomme Ousager. Eur J Hum Genet 2015
19