A citation-based method for searching scientific literature




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

Comprehension and personal value of negative non-diagnostic genetic panel testing.
Christin Hoell, Sharon Aufox, Nora Nashawaty, Melanie F Myers, Maureen E Smith. J Genet Couns 2021
0

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
2

Amino Acid-Level Signal-to-Noise Analysis Aids in Pathogenicity Prediction of Incidentally Identified TTN-Encoded Titin Truncating Variants.
Patrick S Connell, Amy M Berkman, BriAnna M Souder, Elisa J Pirozzi, Julia J Lovin, Jill A Rosenfeld, Pengfei Liu, Hari Tunuguntla, Hugh D Allen, Susan W Denfield,[...]. Circ Genom Precis Med 2021
3


Prenatal Exome Sequencing: Background, Current Practice and Future Perspectives-A Systematic Review.
Daniele Guadagnolo, Gioia Mastromoro, Francesca Di Palma, Antonio Pizzuti, Enrica Marchionni. Diagnostics (Basel) 2021
1

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


Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Adam S Gordon, Laura M Amendola, Kathy Adelman, Sherri J Bale, Wendy K Chung, Michael H Gollob, Steven M Harrison, Gail E Herman,[...]. Genet Med 2021
11

Ethical Challenges in Pediatric Oncology Care and Clinical Trials.
Daniel J Benedetti, Jonathan M Marron. Recent Results Cancer Res 2021
0

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes.
Julia K Goodrich, Moriel Singer-Berk, Rachel Son, Abigail Sveden, Jordan Wood, Eleina England, Joanne B Cole, Ben Weisburd, Nick Watts, Lizz Caulkins,[...]. Nat Commun 2021
1

Genomic medicine and the "loss of chance" medical malpractice doctrine.
Jennifer K Wagner, Michelle N Meyer. HGG Adv 2021
0

Interpretation of Incidental Genetic Findings Localizing to Genes Associated With Cardiac Channelopathies and Cardiomyopathies.
Jordan E Ezekian, Catherine Rehder, Priya S Kishnani, Andrew P Landstrom. Circ Genom Precis Med 2021
0



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

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
2

Adolescents' and Parents' Genomic Testing Decisions: Associations With Age, Race, and Sex.
Melanie F Myers, Lisa J Martin, Cynthia A Prows. J Adolesc Health 2020
4


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


Integrating Rules for Genomic Research, Clinical Care, Public Health Screening and DTC Testing: Creating Translational Law for Translational Genomics.
Susan M Wolf, Pilar N Ossorio, Susan A Berry, Henry T Greely, Amy L McGuire, Michelle A Penny, Sharon F Terry. J Law Med Ethics 2020
7

Pediatric reporting of genomic results study (PROGRESS): a mixed-methods, longitudinal, observational cohort study protocol to explore disclosure of actionable adult- and pediatric-onset genomic variants to minors and their parents.
Juliann M Savatt, Jennifer K Wagner, Steven Joffe, Alanna Kulchak Rahm, Marc S Williams, Angela R Bradbury, F Daniel Davis, Julie Hergenrather, Yirui Hu, Melissa A Kelly,[...]. BMC Pediatr 2020
3

Management of Secondary Genomic Findings.
Alexander E Katz, Robert L Nussbaum, Benjamin D Solomon, Heidi L Rehm, Marc S Williams, Leslie G Biesecker. Am J Hum Genet 2020
6

Attitudes toward and current status of disclosure of secondary findings from next-generation sequencing: a nation-wide survey of clinical genetics professionals in Japan.
Mio Tsuchiya, Takahiro Yamada, Rina Akaishi, Haruka Hamanoue, Akira Hirasawa, Maki Hyodo, Issei Imoto, Tomoki Kosho, Kenji Kurosawa, Hiromi Murakami,[...]. J Hum Genet 2020
1

Health-care practitioners' preferences for the return of secondary findings from next-generation sequencing: a discrete choice experiment.
Shan Jiang, Aslam H Anis, Ian Cromwell, Tima Mohammadi, Kasmintan A Schrader, Janet Lucas, Christine M Armour, Marc Clausen, Yvonne Bombard, Dean A Regier. Genet Med 2020
0

Analogies in Genomics Policymaking: Debates and Drawbacks.
John A Lynch, Aaron J Goldenberg, Nanibaa' A Garrison, Kyle B Brothers. Am J Hum Genet 2020
0


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
10

The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.
Hila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, David A Fasel, Adele Mitrotti, Rik Westland, Louise Bier, Chunhua Weng, Zhong Ren, Brett Copeland,[...]. Ann Intern Med 2019
21

Reconciling Opportunistic and Population Screening in Clinical Genomics.
Kyle B Brothers, Jason L Vassy, Robert C Green. Mayo Clin Proc 2019
14

Genomic Contextualism: Shifting the Rhetoric of Genetic Exceptionalism.
Nanibaa' A Garrison, Kyle B Brothers, Aaron J Goldenberg, John A Lynch. Am J Bioeth 2019
29

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

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

Clinical application of next-generation sequencing to the practice of neurology.
Jessica Rexach, Hane Lee, Julian A Martinez-Agosto, Andrea H Németh, Brent L Fogel. Lancet Neurol 2019
29

Translating genomics to the clinical diagnosis of disorders/differences of sex development.
Abhinav Parivesh, Hayk Barseghyan, Emmanuèle Délot, Eric Vilain. Curr Top Dev Biol 2019
9

Germline-focussed analysis of tumour-only sequencing: recommendations from the ESMO Precision Medicine Working Group.
D Mandelker, M Donoghue, S Talukdar, C Bandlamudi, P Srinivasan, M Vivek, S Jezdic, H Hanson, K Snape, A Kulkarni,[...]. Ann Oncol 2019
34

Points-to-consider on the return of results in epigenetic research.
Stephanie O M Dyke, Katie M Saulnier, Charles Dupras, Amy P Webster, Karen Maschke, Mark Rothstein, Reiner Siebert, Jörn Walter, Stephan Beck, Tomi Pastinen,[...]. Genome Med 2019
7

Improving recommendations for genomic medicine: building an evolutionary process from clinical practice advisory documents to guidelines.
Wylie Burke, Ellen Wright Clayton, Susan M Wolf, Susan A Berry, Barbara J Evans, James P Evans, Ralph Hall, Diane Korngiebel, Anne-Marie Laberge, Bonnie S LeRoy,[...]. Genet Med 2019
7


Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathy.
Edward G Jones, Neda Mazaheri, Reza Maroofian, Mina Zamani, Tahereh Seifi, Alireza Sedaghat, Gholamreza Shariati, Yalda Jamshidi, Hugh D Allen, Xander H T Wehrens,[...]. Sci Rep 2019
8

Dissecting in silico Mutation Prediction of Variants in African Genomes: Challenges and Perspectives.
Christian Domilongo Bope, Emile R Chimusa, Victoria Nembaware, Gaston K Mazandu, Jantina de Vries, Ambroise Wonkam. Front Genet 2019
8

Genomes in Context.
Wylie Burke. Am J Bioeth 2019
0



The congenital disorder of glycosylation in PGM1 (PGM1-CDG) can cause severe cardiomyopathy and unexpected sudden cardiac death in childhood.
Eva Fernlund, Oskar Andersson, Rada Ellegård, Hanna Klang Årstrand, Henrik Green, Hans Olsson, Cecilia Gunnarsson. Forensic Sci Int Genet 2019
5

Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.
Lainie Friedman Ross, Ellen Wright Clayton. Pediatrics 2019
10

Privacy and ethical challenges in next-generation sequencing.
Nicole Martinez-Martin, David Magnus. Expert Rev Precis Med Drug Dev 2019
3

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
10

Variation among Consent Forms for Clinical Whole Exome Sequencing.
Sara A Fowler, Carol J Saunders, Mark A Hoffman. J Genet Couns 2018
11

Towards precision nephrology: the opportunities and challenges of genomic medicine.
Jordan G Nestor, Emily E Groopman, Ali G Gharavi. J Nephrol 2018
6