A citation-based method for searching scientific literature

Daniele Carrieri, Heidi C Howard, Caroline Benjamin, Angus J Clarke, Sandi Dheensa, Shane Doheny, Naomi Hawkins, Tanya F Halbersma-Konings, Leigh Jackson, Hülya Kayserili, Susan E Kelly, Anneke M Lucassen, Álvaro Mendes, Emmanuelle Rial-Sebbag, Vigdís Stefánsdóttir, Peter D Turnpenny, Carla G van El, Irene M van Langen, Martina C Cornel, Francesca Forzano. Eur J Hum Genet 2019
Times Cited: 39



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, Heidi L Rehm, Julie Richer, Emmanuelle Souzeau, Jason L Vassy, Jennifer K Wagner, Howard P Levy. Am J Hum Genet 2019
Times Cited: 56




List of shared articles



Times cited

Genome Alert!: A standardized procedure for genomic variant reinterpretation and automated gene-phenotype reassessment in clinical routine.
Kevin Yauy, François Lecoquierre, Stéphanie Baert-Desurmont, Detlef Trost, Aicha Boughalem, Armelle Luscan, Jean-Marc Costa, Vanna Geromel, Laure Raymond, Pascale Richard,[...]. Genet Med 2022
0

Preferences for return of germline genome sequencing results for cancer patients and their genetic relatives in a research setting.
Megan C Best, Phyllis Butow, Jacqueline Savard, Chris Jacobs, Nicole Bartley, Grace Davies, Christine E Napier, Mandy L Ballinger, David M Thomas, Barbara Biesecker,[...]. Eur J Hum Genet 2022
1

Reinterpretation, reclassification, and its downstream effects: challenges for clinical laboratory geneticists.
Julia El Mecky, Lennart Johansson, Mirjam Plantinga, Angela Fenwick, Anneke Lucassen, Trijnie Dijkhuizen, Annemieke van der Hout, Kate Lyle, Irene van Langen. BMC Med Genomics 2019
13

Recontacting registry participants with genetic updates through GenomeConnect, the ClinGen patient registry.
Juliann M Savatt, Danielle R Azzariti, David H Ledbetter, Emily Palen, Heidi L Rehm, Erin Rooney Riggs, Christa Lese Martin. Genet Med 2021
3

Ethical challenges of precision cancer medicine.
Eva Caroline Winkler, Bartha Maria Knoppers. Semin Cancer Biol 2020
1

Ethical issues in precision medicine.
Jon J Jonsson, Vigdis Stefansdottir. Ann Clin Biochem 2019
0

Genetic Counseling and Genome Sequencing in Pediatric Rare Disease.
Alison M Elliott. Cold Spring Harb Perspect Med 2020
4

DNA variant classification-reconsidering "allele rarity" and "phenotype" criteria in ACMG/AMP guidelines.
Connor D Davieson, Katie E Joyce, Lakshya Sharma, Claire L Shovlin. Eur J Med Genet 2021
5

Management of amended variant classification laboratory reports by genetic counselors in the United States and Canada: An exploratory study.
Brooke Richardson, Sara M Fitzgerald-Butt, Katherine G Spoonamore, Leah Wetherill, Benjamin M Helm, Amy M Breman. J Genet Couns 2022
0


The role of genetics in cardiovascular disease: arrhythmogenic cardiomyopathy.
Cynthia A James, Petros Syrris, J Peter van Tintelen, Hugh Calkins. Eur Heart J 2020
28

iVar, an Interpretation-Oriented Tool to Manage the Update and Revision of Variant Annotation and Classification.
Sara Castellano, Federica Cestari, Giovanni Faglioni, Elena Tenedini, Marco Marino, Lucia Artuso, Rossella Manfredini, Mario Luppi, Tommaso Trenti, Enrico Tagliafico. Genes (Basel) 2021
1

Patient and public preferences for being recontacted with updated genomic results: a mixed methods study.
Chloe Mighton, Marc Clausen, Agnes Sebastian, Sarah M Muir, Salma Shickh, Nancy N Baxter, Adena Scheer, Emily Glogowski, Kasmintan A Schrader, Kevin E Thorpe,[...]. Hum Genet 2021
0

Letter: Relearning the 3 R's? Reinterpretation, recontact, and return of genetic variants.
Bartha Maria Knoppers, Adrian Thorogood, Ma'n H Zawati. Genet Med 2019
7

Is there a duty to reinterpret genetic data? The ethical dimensions.
Paul S Appelbaum, Erik Parens, Sara M Berger, Wendy K Chung, Wylie Burke. Genet Med 2020
21