A citation-based method for searching scientific literature

Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett, Jerry H Kim, Elisabeth A Rosenthal, Daniel S Kim, Holly K Tabor, Michael J Bamshad, Arno G Motulsky, C Ronald Scott, Colin C Pritchard, Tom Walsh, Wylie Burke, Wendy H Raskind, Peter Byers, Fuki M Hisama, Deborah A Nickerson, Gail P Jarvik. Am J Hum Genet 2013
Times Cited: 268



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: 1513




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

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
0

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
0

Frequency of ClinVar Pathogenic Variants in Chronic Kidney Disease Patients Surveyed for Return of Research Results at a Cleveland Public Hospital.
Dana C Crawford, John Lin, Jessica N Cooke Bailey, Tyler Kinzy, John R Sedor, John F O'Toole, William S Bush. Pac Symp Biocomput 2020
0

Critical assessment of secondary findings in genes linked to primary arrhythmia syndromes.
Isabel Diebold, Ulrike Schön, Florentine Scharf, Anna Benet-Pagès, Andreas Laner, Elke Holinski-Feder, Angela Abicht. Hum Mutat 2020
2

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
5

Actionable Exomic Secondary Findings in 280 Lebanese Participants.
Nadine Jalkh, Cybel Mehawej, Eliane Chouery. Front Genet 2020
1


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
5

Reduced penetrance of pathogenic ACMG variants in a deeply phenotyped cohort study and evaluation of ClinVar classification over time.
Jeroen van Rooij, Pascal Arp, Linda Broer, Joost Verlouw, Frank van Rooij, Robert Kraaij, André Uitterlinden, Annemieke J M H Verkerk. Genet Med 2020
4

Incidental diagnosis of mucopolysaccharidosis type I in an infant with chronic intestinal pseudoobstruction by exome sequencing.
Auriane Cospain, Christèle Dubourg, Swellen Gastineau, Samia Pichard, Virginie Gandemer, Jacinthe Bonneau, Marie de Tayrac, Caroline Moreau, Sylvie Odent, Laurent Pasquier,[...]. Mol Genet Metab Rep 2020
0

Frequency and spectrum of actionable pathogenic secondary findings in Taiwanese exomes.
Chieh-Wen Kuo, Wuh-Liang Hwu, Yin-Hsiu Chien, Ching Hsu, Miao-Zi Hung, I-Lin Lin, Feipei Lai, Ni-Chung Lee. Mol Genet Genomic Med 2020
1

Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.
Caio Robledo D'Angioli Costa Quaio, Caroline Monaco Moreira, Gil Monteiro Novo-Filho, Patricia Rossi Sacramento-Bobotis, Michele Groenner Penna, Sandro Felix Perazzio, Aurelio Pimenta Dutra, Rafael Alves da Silva, Monize Nakamoto Provisor Santos, Vanessa Yurie Nozaki de Arruda,[...]. Am J Med Genet C Semin Med Genet 2020
3



Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
J Delanne, S Nambot, A Chassagne, O Putois, A Pelissier, C Peyron, E Gautier, J Thevenon, E Cretin, A L Bruel,[...]. Eur J Med Genet 2019
17

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
48

Psychiatric genetics researchers' views on offering return of results to individual participants.
Kristin M Kostick, Cody Brannan, Stacey Pereira, Gabriel Lázaro-Muñoz. Am J Med Genet B Neuropsychiatr Genet 2019
12

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

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project.
Ozge Ceyhan-Birsoy, Jaclyn B Murry, Kalotina Machini, Matthew S Lebo, Timothy W Yu, Shawn Fayer, Casie A Genetti, Talia S Schwartz, Pankaj B Agrawal, Richard B Parad,[...]. Am J Hum Genet 2019
55

Beyond medical actionability: Public perceptions of important actions in response to hypothetical genetic testing results.
David J Seiffert, Patricia McCarthy Veach, Bonnie LeRoy, Weihua Guan, Heather Zierhut. J Genet Couns 2019
0

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
14

Secondary actionable findings identified by exome sequencing: expected impact on the organisation of care from the study of 700 consecutive tests.
Christel Thauvin-Robinet, Julien Thevenon, Sophie Nambot, Julian Delanne, Paul Kuentz, Ange-Line Bruel, Aline Chassagne, Elodie Cretin, Aurore Pelissier, Chritine Peyron,[...]. Eur J Hum Genet 2019
6

Implementation of genomics in medical practice to deliver precision medicine for an Asian population.
Yasmin Bylstra, Sonia Davila, Weng Khong Lim, Ryanne Wu, Jing Xian Teo, Sylvia Kam, Tamra Lysaght, Steve Rozen, Bin Tean Teh, Khung Keong Yeo,[...]. NPJ Genom Med 2019
9

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
7

Genomic testing in pediatric epilepsy.
Drew M Thodeson, Jason Y Park. Cold Spring Harb Mol Case Stud 2019
4

Open-Sourced CIViC Annotation Pipeline to Identify and Annotate Clinically Relevant Variants Using Single-Molecule Molecular Inversion Probes.
Erica K Barnell, Adam Waalkes, Matt C Mosior, Kelsi Penewit, Kelsy C Cotto, Arpad M Danos, Lana M Sheta, Katie M Campbell, Kilannin Krysiak, Damian Rieke,[...]. JCO Clin Cancer Inform 2019
2

Return of genetic and genomic research findings: experience of a pediatric biorepository.
Tanya Papaz, Eriskay Liston, Laura Zahavich, Dimitri J Stavropoulos, Rebekah K Jobling, Raymond H Kim, Miriam Reuter, Anastasia Miron, Erwin Oechslin, Tapas Mondal,[...]. BMC Med Genomics 2019
5

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

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

Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals.
Yumi Yamaguchi-Kabata, Jun Yasuda, Osamu Tanabe, Yoichi Suzuki, Hiroshi Kawame, Nobuo Fuse, Masao Nagasaki, Yosuke Kawai, Kaname Kojima, Fumiki Katsuoka,[...]. J Hum Genet 2018
19

Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact.
J Wynn, R Ottman, J Duong, A L Wilson, P Ahimaz, J Martinez, R Rabin, E Rosen, R Webster, C Au,[...]. Clin Genet 2018
23

A literature review at genome scale: improving clinical variant assessment.
Christopher A Cassa, Daniel M Jordan, Ivan Adzhubei, Shamil Sunyaev. Genet Med 2018
1

[Changes in clinical practice related to the arrival of next-generation sequencing in the genetic diagnosis of developmental diseases].
L Demougeot, F Houdayer, A Pélissier, F Mohrez, J Thevenon, Y Duffourd, S Nambot, E Gautier, C Binquet, M Rossi,[...]. Arch Pediatr 2018
1

Incidental and clinically actionable genetic variants in 1005 whole exomes and genomes from Qatar.
Abhinav Jain, Shrey Gandhi, Remya Koshy, Vinod Scaria. Mol Genet Genomics 2018
6

Tensions in ethics and policy created by National Precision Medicine Programs.
Jusaku Minari, Kyle B Brothers, Michael Morrison. Hum Genomics 2018
15

Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.
Sumit Punj, Yassmine Akkari, Jennifer Huang, Fei Yang, Allison Creason, Christine Pak, Amiee Potter, Michael O Dorschner, Deborah A Nickerson, Peggy D Robertson,[...]. Am J Hum Genet 2018
14

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
11

Adolescent and Parental Attitudes About Return of Genomic Research Results: Focus Group Findings Regarding Decisional Preferences.
Michelle L McGowan, Cynthia A Prows, Melissa DeJonckheere, William B Brinkman, Lisa Vaughn, Melanie F Myers. J Empir Res Hum Res Ethics 2018
14

Opportunities and Challenges for Genetic Studies of End-Stage Renal Disease in Canada.
Vinusha Kalatharan, Mathieu Lemaire, Matthew B Lanktree. Can J Kidney Health Dis 2018
3

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


Secondary findings in 421 whole exome-sequenced Chinese children.
Wen Chen, Wenke Li, Yi Ma, Yujing Zhang, Bianmei Han, Xuewen Liu, Kun Zhao, Meixian Zhang, Jie Mi, Yuanyuan Fu,[...]. Hum Genomics 2018
2

Cost Analyses of Genomic Sequencing: Lessons Learned from the MedSeq Project.
Kurt D Christensen, Kathryn A Phillips, Robert C Green, Dmitry Dukhovny. Value Health 2018
6

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