A citation-based method for searching scientific literature

Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers, Nancy A Press, Lainie Friedman Ross, Mark A Rothstein, Howard Saal, Wendy R Uhlmann, Benjamin Wilfond, Susan M Wolf, Ron Zimmern. Genet Med 2013
Times Cited: 213

Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond, Heidi L Rehm, Michael S Watson, Marc S Williams, Leslie G Biesecker. Genet Med 2013
Times Cited: 1537

List of shared articles

Times cited

Disclosure of secondary findings in exome sequencing of 2480 Japanese cancer patients.
Yasue Horiuchi, Hiroyuki Matsubayashi, Yoshimi Kiyozumi, Seiichiro Nishimura, Satomi Higashigawa, Nobuhiro Kado, Takeshi Nagashima, Maki Mizuguchi, Sumiko Ohnami, Makoto Arai,[...]. Hum Genet 2021

A decision aid for additional findings in genomic sequencing: Development and pilot testing.
Amanda S Freed, Inga Gruß, Carmit K McMullen, Michael C Leo, Tia L Kauffman, Kathryn M Porter, Kristin R Muessig, Donna Eubanks, Katrina A B Goddard, Benjamin S Wilfond,[...]. Patient Educ Couns 2021

Evaluating the resource implications of different service delivery models for offering additional genomic findings.
Martin Vu, Koen Degeling, Melissa Martyn, Elly Lynch, Belinda Chong, Clara Gaff, Maarten J IJzerman. Genet Med 2021

Actionable secondary findings in 1116 Hong Kong Chinese based on exome sequencing data.
Mullin Ho Chung Yu, Christopher Chun Yu Mak, Jasmine Lee Fong Fung, Mianne Lee, Mandy Ho Yin Tsang, Jeffrey Fong Ting Chau, Patrick Ho-Yu Chung, Wanling Yang, Godfrey Chi Fung Chan, So Lun Lee,[...]. J Hum Genet 2021

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics.
Guido de Wert, Wybo Dondorp, Angus Clarke, Elisabeth M C Dequeker, Christophe Cordier, Zandra Deans, Carla G van El, Florence Fellmann, Ros Hastings, Sabine Hentze,[...]. Eur J Hum Genet 2021

Massively Parallel Sequencing for Rare Genetic Disorders: Potential and Pitfalls.
Aideen M McInerney-Leo, Emma L Duncan. Front Endocrinol (Lausanne) 2021

Utility and Diversity: Challenges for Genomic Medicine.
Wylie Burke. Annu Rev Genomics Hum Genet 2021

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

Ethical Challenges in Pediatric Oncology Care and Clinical Trials.
Daniel J Benedetti, Jonathan M Marron. Recent Results Cancer Res 2021

Exploring the motivations of research participants who chose not to learn medically actionable secondary genetic findings about themselves.
Will Schupmann, Skye A Miner, Haley K Sullivan, Jamie R Glover, Janet E Hall, Shepherd H Schurman, Benjamin E Berkman. Genet Med 2021

Decisional conflict among adolescents and parents making decisions about genomic sequencing results.
Preethi Raghuram Pillai, Cynthia A Prows, Lisa J Martin, Melanie F Myers. Clin Genet 2020

Primary care provider perspectives on using genomic sequencing in the care of healthy children.
Esha Joshi, Chloe Mighton, Marc Clausen, Selina Casalino, Theresa H M Kim, Christine Kowal, Catherine Birken, Jonathon L Maguire, Yvonne Bombard. Eur J Hum Genet 2020

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

Understanding and information needs of cancer patients regarding treatment-focused genomic testing: A systematic review.
Kamil Wolyniec, Jessica Sharp, Smaro Lazarakis, Linda Mileshkin, Penelope Schofield. Psychooncology 2020

Design and Reporting Considerations for Genetic Screening Tests.
Jill Hagenkord, Birgit Funke, Emily Qian, Madhuri Hegde, Kevin B Jacobs, Matthew Ferber, Matthew Lebo, Adam Buchanan, David Bick. J Mol Diagn 2020

Experiences and lessons learned by genetic counselors in returning secondary genetic findings to patients.
Carly Rost, Karin M Dent, Jeffrey Botkin, Erin Rothwell. J Genet Couns 2020

Clinical utility of genomic sequencing: a measurement toolkit.
Robin Z Hayeems, David Dimmock, David Bick, John W Belmont, Robert C Green, Brendan Lanpher, Vaidehi Jobanputra, Roberto Mendoza, Shashi Kulkarni, Megan E Grove,[...]. NPJ Genom Med 2020

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019

Giving adolescents a voice: the types of genetic information adolescents choose to learn and why.
Josie Pervola, Melanie F Myers, Michelle L McGowan, Cynthia A Prows. Genet Med 2019

Returning a Genomic Result for an Adult-Onset Condition to the Parents of a Newborn: Insights From the BabySeq Project.
Ingrid A Holm, Amy McGuire, Stacey Pereira, Heidi Rehm, Robert C Green, Alan H Beggs. Pediatrics 2019

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

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

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

Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.
Lainie Friedman Ross, Ellen Wright Clayton. Pediatrics 2019

Great expectations: patient perspectives and anticipated utility of non-diagnostic genomic-sequencing results.
Robyn Hylind, Maureen Smith, Laura Rasmussen-Torvik, Sharon Aufox. J Community Genet 2018

Legal issues in governing genetic biobanks: the Italian framework as a case study for the implications for citizen's health through public-private initiatives.
Cinzia Piciocchi, Rossana Ducato, Lucia Martinelli, Silvia Perra, Marta Tomasi, Carla Zuddas, Deborah Mascalzoni. J Community Genet 2018

Towards precision nephrology: the opportunities and challenges of genomic medicine.
Jordan G Nestor, Emily E Groopman, Ali G Gharavi. J Nephrol 2018

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

Is It Our Duty To Hunt for Pathogenic Mutations?
Roel H P Wouters, Rhodé M Bijlsma, Geert W J Frederix, Margreet G E M Ausems, Johannes J M van Delden, Emile E Voest, Annelien L Bredenoord. Trends Mol Med 2018

Preferences for learning different types of genome sequencing results among young breast cancer patients: Role of psychological and clinical factors.
Kimberly A Kaphingst, Jennifer Ivanovich, Sarah Lyons, Barbara Biesecker, Rebecca Dresser, Ashley Elrick, Cindy Matsen, Melody Goodman. Transl Behav Med 2018

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018

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

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

Ethical conundrums in pediatric genomics.
Seth J Rotz, Eric Kodish. Hematology Am Soc Hematol Educ Program 2018

Developing a Process for Returning Medically Actionable Genomic Variants to Latino Patients in a Federally Qualified Health Center.
Gabriel Q Shaibi, Iftikhar J Kullo, Davinder P Singh, Richard R Sharp, Eleanna De Filippis, Idali Cuellar, Valentina Hernandez, Sharon Levey, Carmen Radecki Breitkopf, Janet E Olson,[...]. Public Health Genomics 2018

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017

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

Discussing molecular testing in oncology care: Comparing patient and physician information preferences.
Ana P M Pinheiro, Rachel H Pocock, Jeffrey M Switchenko, Margie D Dixon, Walid L Shaib, Suresh S Ramalingam, Rebecca D Pentz. Cancer 2017

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

Public's Views toward Return of Secondary Results in Genomic Sequencing: It's (Almost) All about the Choice.
Kerry A Ryan, Raymond G De Vries, Wendy R Uhlmann, J Scott Roberts, Michele C Gornick. J Genet Couns 2017