A citation-based method for searching scientific literature




Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf, Kent D McKelvey, Kelly E Ormond, C Sue Richards, Christopher N Vlangos, Michael Watson, Christa L Martin, David T Miller. Genet Med 2017
Times Cited: 831




List of shared articles



Times cited

Attitudes among South African university staff and students towards disclosing secondary genetic findings.
Georgina Spies, Jolynne Mokaya, Jacqui Steadman, Nicole Schuitmaker, Martin Kidd, S M J Hemmings, Jonathan A Carr, Helena Kuivaniemi, Soraya Seedat. J Community Genet 2021
0

A survey of aortic disease biorepository participants' preferences for return of research genetic results.
Jamie Love-Nichols, Wendy R Uhlmann, Patricia Arscott, Cristen Willer, Whitney Hornsby, J Scott Roberts. J Genet Couns 2021
2

Please give me a copy of my child's raw genomic data.
Lauren Chad, Michael J Szego. NPJ Genom Med 2021
0

Burden or benefit? Effects of providing education about and the option to request additional genomic findings from diagnostic exome sequencing: A randomized controlled trial.
Christine Rini, Myra I Roche, Feng-Chang Lin, Ann Katherine M Foreman, Cynthia M Khan, Ida Griesemer, Margaret Waltz, Kristy Lee, Julianne M O'Daniel, James P Evans,[...]. Patient Educ Couns 2021
0

Behavioral and psychological impact of genome sequencing: a pilot randomized trial of primary care and cardiology patients.
Kurt D Christensen, Erica F Schonman, Jill O Robinson, J Scott Roberts, Pamela M Diamond, Kaitlyn B Lee, Robert C Green, Amy L McGuire. NPJ Genom Med 2021
0

Enhancing the Impact of Genomics Research in Autism through Integration of Research Results into Routine Care Pathways-A Case Series.
Iskra Peltekova, Daniela Buhas, Lara Stern, Emily Kirby, Afiqah Yusuf, Mayada Elsabbagh. J Pers Med 2021
0

Ethics and Collateral Findings in Pragmatic Clinical Trials.
Stephanie R Morain, Kevin Weinfurt, Juli Bollinger, Gail Geller, Debra Jh Mathews, Jeremy Sugarman. Am J Bioeth 2020
9

Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study.
Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Elfride De Baere, Ignaas Devisch. BMC Med Ethics 2020
7

Why genomics researchers are sometimes morally required to hunt for secondary findings.
Julian J Koplin, Julian Savulescu, Danya F Vears. BMC Med Ethics 2020
4


Return of Individual Research Results: A Guide for Biomedical Researchers Utilizing Human Biospecimens.
Mark E Sobel, Jennifer C Dreyfus, Kelsey Dillehay McKillip, Christi Kolarcik, William A Muller, Melanie J Scott, Gene P Siegal, Kristine Wadosky, Timothy J O'Leary. Am J Pathol 2020
2

Ethical challenges of precision cancer medicine.
Eva Caroline Winkler, Bartha Maria Knoppers. Semin Cancer Biol 2020
0

Integrating Genomics into Psychiatric Practice: Ethical and Legal Challenges for Clinicians.
Eric T Ward, Kristin M Kostick, Gabriel Lázaro-Muñoz. Harv Rev Psychiatry 2019
4

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

Ethical and Policy Considerations for Genomic Testing in Pediatric Research: The Path Toward Disclosing Individual Research Results.
Craig S Wong, Amy J Kogon, Bradley A Warady, Susan L Furth, John D Lantos, Benjamin S Wilfond. Am J Kidney Dis 2019
0

The Responsibility to Recontact Research Participants after Reinterpretation of Genetic and Genomic Research Results.
Yvonne Bombard, Kyle B Brothers, Sara Fitzgerald-Butt, Nanibaa' A Garrison, Leila Jamal, Cynthia A James, Gail P Jarvik, Jennifer B McCormick, Tanya N Nelson, Kelly E Ormond,[...]. Am J Hum Genet 2019
47

Variants in myelin regulatory factor (MYRF) cause autosomal dominant and syndromic nanophthalmos in humans and retinal degeneration in mice.
Sarah J Garnai, Michelle L Brinkmeier, Ben Emery, Tomas S Aleman, Louise C Pyle, Biliana Veleva-Rotse, Robert A Sisk, Frank W Rozsa, Ayse Bilge Ozel, Jun Z Li,[...]. PLoS Genet 2019
24

Clinical exome sequencing vs. usual care for hereditary colorectal cancer diagnosis: A pilot comparative effectiveness study.
Xin Niu, Laura M Amendola, Ragan Hart, Caroline S Bennette, Patrick Heagerty, Martha Horike-Pyne, Susan B Trinidad, Elisabeth A Rosenthal, Bryan Comstock, Chris Nefcy,[...]. Contemp Clin Trials 2019
4


Improved ethical guidance for the return of results from psychiatric genomics research.
G Lázaro-Muñoz, M S Farrell, J J Crowley, D M Filmyer, R A Shaughnessy, R C Josiassen, P F Sullivan. Mol Psychiatry 2018
20

Ethical issues in neurogenetics.
Wendy R Uhlmann, J Scott Roberts. Handb Clin Neurol 2018
5

Precision medicine screening using whole-genome sequencing and advanced imaging to identify disease risk in adults.
Bradley A Perkins, C Thomas Caskey, Pamila Brar, Eric Dec, David S Karow, Andrew M Kahn, Ying-Chen Claire Hou, Naisha Shah, Debbie Boeldt, Erin Coughlin,[...]. Proc Natl Acad Sci U S A 2018
42

The Right to Know: A Revised Standard for Reporting Incidental Findings.
G Owen Schaefer, Julian Savulescu. Hastings Cent Rep 2018
10

The Genomics ADvISER: development and usability testing of a decision aid for the selection of incidental sequencing results.
Yvonne Bombard, Marc Clausen, Chloe Mighton, Lindsay Carlsson, Selina Casalino, Emily Glogowski, Kasmintan Schrader, Michael Evans, Adena Scheer, Nancy Baxter,[...]. Eur J Hum Genet 2018
23


Genomic sequencing identifies secondary findings in a cohort of parent study participants.
Michelle L Thompson, Candice R Finnila, Kevin M Bowling, Kyle B Brothers, Matthew B Neu, Michelle D Amaral, Susan M Hiatt, Kelly M East, David E Gray, James M J Lawlor,[...]. Genet Med 2018
13


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

Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations.
Pascal Pujol, Pierre Vande Perre, Laurence Faivre, Damien Sanlaville, Carole Corsini, Bernard Baertschi, Michèle Anahory, Dominique Vaur, Sylviane Olschwang, Nadem Soufir,[...]. Eur J Hum Genet 2018
14

What People Want to Know About Their Genes: A Critical Review of the Literature on Large-Scale Genome Sequencing Studies.
Courtney L Scherr, Sharon Aufox, Amy A Ross, Sanjana Ramesh, Catherine A Wicklund, Maureen Smith. Healthcare (Basel) 2018
11

Return of individual results in epilepsy genomic research: A view from the field.
Ruth Ottman, Catharine Freyer, Heather C Mefford, Annapurna Poduri, Daniel H Lowenstein. Epilepsia 2018
5

Approaches to carrier testing and results disclosure in translational genomics research: The clinical sequencing exploratory research consortium experience.
Kathryn M Porter, Tia L Kauffman, Barbara A Koenig, Katie L Lewis, Heidi L Rehm, Carolyn Sue Richards, Natasha T Strande, Holly K Tabor, Susan M Wolf, Yaping Yang,[...]. Mol Genet Genomic Med 2018
7

Ethical and counseling challenges in prenatal exome sequencing.
Sarah Harris, Kelly Gilmore, Emily Hardisty, Anne Drapkin Lyerly, Neeta L Vora. Prenat Diagn 2018
12

Ethical Issues in Contemporary Clinical Genetics.
Genna Braverman, Zachary E Shapiro, Jonathan A Bernstein. Mayo Clin Proc Innov Qual Outcomes 2018
4

Which Results to Return: Subjective Judgments in Selecting Medically Actionable Genes.
Gabriel Lázaro-Muñoz, John M Conley, Arlene M Davis, Anya E R Prince, R Jean Cadigan. Genet Test Mol Biomarkers 2017
14

Ethical considerations surrounding germline next-generation sequencing of children with cancer.
Liza-Marie Johnson, Kayla V Hamilton, Jessica M Valdez, Esther Knapp, Justin N Baker, Kim E Nichols. Expert Rev Mol Diagn 2017
11