A citation-based method for searching scientific literature

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



Ruqayyah Abdul-Karim, Benjamin E Berkman, David Wendler, Annette Rid, Javed Khan, Tom Badgett, Sara Chandros Hull. Pediatrics 2013
Times Cited: 52




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


The psychosocial and service delivery impact of genomic testing for inherited retinal dystrophies.
Eleanor McVeigh, Harriet Jones, Graeme Black, Georgina Hall. J Community Genet 2019
0

A qualitative study of healthcare providers' perspectives on the implications of genome-wide testing in pediatric clinical practice.
Marian Reiff, Rebecca Mueller, Surabhi Mulchandani, Nancy B Spinner, Reed E Pyeritz, Barbara A Bernhardt. J Genet Couns 2014
16

Next-generation sequencing for research and diagnostics in kidney disease.
Kirsten Y Renkema, Marijn F Stokman, Rachel H Giles, Nine V A M Knoers. Nat Rev Nephrol 2014
57

Incidental variants are critical for genomics.
Leslie G Biesecker. Am J Hum Genet 2013
30

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