A citation-based method for searching scientific literature

T Rigter, C J A van Aart, M W Elting, Q Waisfisz, M C Cornel, L Henneman. Clin Genet 2014
Times Cited: 30



Tessel Rigter, Lidewij Henneman, Ulf Kristoffersson, Alison Hall, Helger G Yntema, Pascal Borry, Holger Tönnies, Quinten Waisfisz, Mariet W Elting, Wybo J Dondorp, Martina C Cornel. Hum Mutat 2013
Times Cited: 39




List of shared articles



Times cited

Incidental or secondary findings: an integrative and patient-inclusive approach to the current debate.
Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
12


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 2021
0

Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual Understanding.
Leandra K Tolusso, Kathleen Collins, Xue Zhang, Jennifer R Holle, C Alexander Valencia, Melanie F Myers. J Genet Couns 2017
10

College of American Pathologists' laboratory standards for next-generation sequencing clinical tests.
Nazneen Aziz, Qin Zhao, Lynn Bry, Denise K Driscoll, Birgit Funke, Jane S Gibson, Wayne W Grody, Madhuri R Hegde, Gerald A Hoeltge, Debra G B Leonard,[...]. Arch Pathol Lab Med 2015
196

Patients' views on incidental findings from clinical exome sequencing.
Kristin E Clift, Colin M E Halverson, Alexander S Fiksdal, Ashok Kumbamu, Richard R Sharp, Jennifer B McCormick. Appl Transl Genom 2015
57