A citation-based method for searching scientific literature




Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey, Vrunda Sheth, Jimmy E Woodward, Heather E Peckham, Gary P Schroth, Ryan W Kim, Stephen F Kingsmore. Sci Transl Med 2011
Times Cited: 428




List of shared articles



Times cited


Tay-Sachs disease: current perspectives from Australia.
Raelia M Lew, Leslie Burnett, AnnĂ© L Proos, Martin B Delatycki. Appl Clin Genet 2015
14

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

Adult genetic risk screening.
C Thomas Caskey, Manuel L Gonzalez-Garay, Stacey Pereira, Amy L McGuire. Annu Rev Med 2014
10

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


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

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

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