A citation-based method for searching scientific literature

Layla Shahmirzadi, Elizabeth C Chao, Erika Palmaer, Melissa C Parra, Sha Tang, Kelly D Farwell Gonzalez. Genet Med 2014
Times Cited: 74



Jonathan S Berg, Muin J Khoury, James P Evans. Genet Med 2011
Times Cited: 352




List of shared articles



Times cited

Preferences of Italian patients for return of secondary findings from clinical genome/exome sequencing.
Lea Godino, Liliana Varesco, William Bruno, Carla Bruzzone, Linda Battistuzzi, Marzena Franiuk, Sara Miccoli, Benedetta Bertonazzi, Claudio Graziano, Marco Seri,[...]. J Genet Couns 2021
1

Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study).
Aline Chassagne, Aurore Pélissier, Françoise Houdayer, Elodie Cretin, Elodie Gautier, Dominique Salvi, Sarah Kidri, Aurélie Godard, Christel Thauvin-Robinet, Alice Masurel,[...]. Eur J Hum Genet 2019
5

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
17

Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their child.
Candice Cornelis, Aad Tibben, Wybo Dondorp, Mieke van Haelst, Annelien L Bredenoord, Nine Knoers, Marcus Düwell, Ineke Bolt, Marieke van Summeren. Eur J Hum Genet 2016
13


Management and return of incidental genomic findings in clinical trials.
C Ayuso, J M Millan, R Dal-Re. Pharmacogenomics J 2015
4

Informed Consent in the Genomics Era.
Shannon Rego, Megan E Grove, Mildred K Cho, Kelly E Ormond. Cold Spring Harb Perspect Med 2020
2

Unsolicited findings of next-generation sequencing for tumor analysis within a Dutch consortium: clinical daily practice reconsidered.
Rhodé M Bijlsma, Annelien L Bredenoord, Christa G Gadellaa-Hooijdonk, Martijn Pj Lolkema, Stefan Sleijfer, Emile E Voest, Margreet Gem Ausems, Neeltje Steeghs. Eur J Hum Genet 2016
18

Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.
Ignatia B van den Veyver, Christine M Eng. Cold Spring Harb Perspect Med 2015
26

Participant choices for return of genomic results in the eMERGE Network.
Christin Hoell, Julia Wynn, Luke V Rasmussen, Keith Marsolo, Sharon A Aufox, Wendy K Chung, John J Connolly, Robert R Freimuth, David Kochan, Hakon Hakonarson,[...]. Genet Med 2020
4

Management of Incidental Findings in the Era of Next-generation Sequencing.
Heather L Blackburn, Bradley Schroeder, Clesson Turner, Craig D Shriver, Darrell L Ellsworth, Rachel E Ellsworth. Curr Genomics 2015
26

Preferences for return of incidental findings from genome sequencing among women diagnosed with breast cancer at a young age.
K A Kaphingst, J Ivanovich, B B Biesecker, R Dresser, J Seo, L G Dressler, P J Goodfellow, M S Goodman. Clin Genet 2016
28

Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
47

Acceptability of, and Information Needs Regarding, Next-Generation Sequencing in People Tested for Hereditary Cancer: A Qualitative Study.
Bettina Meiser, Ben Storey, Veronica Quinn, Belinda Rahman, Lesley Andrews. J Genet Couns 2016
10

Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research.
Emmanuelle Souzeau, Kathryn P Burdon, David A Mackey, Alex W Hewitt, Ravi Savarirayan, Margaret Otlowski, Jamie E Craig.  2016
7


A qualitative study among patients with an inherited retinal disease on the meaning of genomic unsolicited findings.
Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Caroline Van Cauwenbergh, Bart P Leroy, Ignaas Devisch, Elfride De Baere. Sci Rep 2021
0

Health outcomes, utility and costs of returning incidental results from genomic sequencing in a Canadian cancer population: protocol for a mixed-methods randomised controlled trial.
Salma Shickh, Marc Clausen, Chloe Mighton, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, Rita Kodida, Emma Reble, Christine Elser, Andrea Eisen, Seema Panchal,[...]. BMJ Open 2019
4

Parents, their children, whole exome sequencing and unsolicited findings: growing towards the child's future autonomy.
Aad Tibben, Wybo Dondorp, Candice Cornelis, Nine Knoers, Eva Brilstra, Marieke van Summeren, Ineke Bolt. Eur J Hum Genet 2021
3


The who, what, and why of research participants' intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study.
Christine Rini, Cynthia M Khan, Elizabeth Moore, Myra I Roche, James P Evans, Jonathan S Berg, Bradford C Powell, Giselle Corbie-Smith, Ann Katherine M Foreman, Ida Griesemer,[...]. Genet Med 2018
13

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

A novel approach to offering additional genomic findings-A protocol to test a two-step approach in the healthcare system.
Melissa Martyn, Anaita Kanga-Parabia, Elly Lynch, Paul A James, Ivan Macciocca, Alison H Trainer, Jane Halliday, Louise Keogh, Janney Wale, Ingrid Winship,[...]. J Genet Couns 2019
3