A citation-based method for searching scientific literature

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



Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
Times Cited: 199




List of shared articles



Times cited



A closer look at the recommended criteria for disclosing genetic results: perspectives of medical genetic specialists, genomic researchers, and institutional review board chairs.
Debra S Brandt, Laura Shinkunas, Stephen L Hillis, Sandra E Daack-Hirsch, Martha Driessnack, Nancy R Downing, Megan F Liu, Lisa L Shah, Janet K Williams, Christian M Simon. J Genet Couns 2013
21

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
55

Disclosing incidental findings in genetics contexts: a review of the empirical ethical research.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Med Genet 2013
27

Incidental findings from clinical genome-wide sequencing: a review.
Z Lohn, S Adam, P H Birch, J M Friedman. J Genet Couns 2014
30

Case Report: Direct Access Genetic Testing and A False-Positive Result For Long QT Syndrome.
Sarah Predham, Sara Hamilton, Alison M Elliott, William T Gibson. J Genet Couns 2016
1

Attitudes of French populations towards the disclosure of unsolicited findings in medical genetics.
Marion Rosier, Myriam Guedj, Patrick Calvas, Sophie Julia, Christelle Garnier, Anne Cambon-Thomsen, Maria Teresa Muñoz Sastre. J Health Psychol 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

The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing.
G M Christenhusz, K Devriendt, H Peeters, H Van Esch, K Dierickx. Clin Genet 2014
17


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

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.
M Reiff, K Ross, S Mulchandani, K J Propert, R E Pyeritz, N B Spinner, B A Bernhardt. Clin Genet 2013
43

Genetic medicine and incidental findings: it is more complicated than deciding whether to disclose or not.
Gillian Crawford, Nicola Foulds, Angela Fenwick, Nina Hallowell, Anneke Lucassen. Genet Med 2013
21