A citation-based method for searching scientific literature

Bartha Maria Knoppers, Adrian Thorogood, Ma'n H Zawati. Genet Med 2019
Times Cited: 7







List of co-cited articles
20 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG).
Karen L David, Robert G Best, Leslie Manace Brenman, Lynn Bush, Joshua L Deignan, David Flannery, Jodi D Hoffman, Ingrid Holm, David T Miller, James O'Leary,[...]. Genet Med 2019
54
71

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.
Daniele Carrieri, Heidi C Howard, Caroline Benjamin, Angus J Clarke, Sandi Dheensa, Shane Doheny, Naomi Hawkins, Tanya F Halbersma-Konings, Leigh Jackson, Hülya Kayserili,[...]. Eur J Hum Genet 2019
39
71

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
56
71

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
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,[...]. Genet Med 2017
936
57


Reinterpretation of sequence variants: one diagnostic laboratory's experience, and the need for standard guidelines.
Caitlin Chisholm, Hussein Daoud, Mahdi Ghani, Gabrielle Mettler, Jean McGowan-Jordan, Liz Sinclair-Bourque, Amanda Smith, Olga Jarinova. Genet Med 2018
18
42

Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature.
Ellen Otten, Mirjam Plantinga, Erwin Birnie, Marian A Verkerk, Anneke M Lucassen, Adelita V Ranchor, Irene M Van Langen. Genet Med 2015
55
42

A duty to recontact in genetics: context matters.
Noor A A Giesbertz, Wim H van Harten, Annelien L Bredenoord. Nat Rev Genet 2019
10
42

Physicians' duty to recontact and update genetic advice.
Yvonne A Stevens, Grant D Senner, Gary E Marchant. Per Med 2017
12
42

Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.
Danya F Vears, Emilia Niemiec, Heidi Carmen Howard, Pascal Borry. Eur J Hum Genet 2018
36
28


A Model for Genome-First Care: Returning Secondary Genomic Findings to Participants and Their Healthcare Providers in a Large Research Cohort.
Marci L B Schwartz, Cara Zayac McCormick, Amanda L Lazzeri, D'Andra M Lindbuchler, Miranda L G Hallquist, Kandamurugu Manickam, Adam H Buchanan, Alanna Kulchak Rahm, Monica A Giovanni, Lauren Frisbie,[...]. Am J Hum Genet 2018
77
28

Variant classification changes over time in BRCA1 and BRCA2.
Chloe Mighton, George S Charames, Marina Wang, Kathleen-Rose Zakoor, Andrew Wong, Salma Shickh, Nicholas Watkins, Matthew S Lebo, Yvonne Bombard, Jordan Lerner-Ellis. Genet Med 2019
16
28

Recontacting in clinical practice: the views and expectations of patients in the United Kingdom.
Daniele Carrieri, Sandi Dheensa, Shane Doheny, Angus J Clarke, Peter D Turnpenny, Anneke M Lucassen, Susan E Kelly. Eur J Hum Genet 2017
17
28

A 'joint venture' model of recontacting in clinical genomics: challenges for responsible implementation.
Sandi Dheensa, Daniele Carrieri, Susan Kelly, Angus Clarke, Shane Doheny, Peter Turnpenny, Anneke Lucassen. Eur J Med Genet 2017
23
28

Return of individual genomic research results: are laws and policies keeping step?
Adrian Thorogood, Gratien Dalpé, Bartha Maria Knoppers. Eur J Hum Genet 2019
45
28


Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).
Joshua L Deignan, Wendy K Chung, Hutton M Kearney, Kristin G Monaghan, Catherine W Rehder, Elizabeth C Chao. Genet Med 2019
53
28

From Genetics to Genomics: Facing the Liability Implications in Clinical Care.
Gary Marchant, Mark Barnes, James P Evans, Bonnie LeRoy, Susan M Wolf. J Law Med Ethics 2020
16
28

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
28



CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record.
Brian H Shirts, Joseph S Salama, Samuel J Aronson, Wendy K Chung, Stacy W Gray, Lucia A Hindorff, Gail P Jarvik, Sharon E Plon, Elena M Stoffel, Peter Z Tarczy-Hornoch,[...]. J Am Med Inform Assoc 2015
55
14

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
14

Laying Anchor: Inserting Precision Health into a Public Health Genetics Policy Course.
Stephen M Modell, Toby Citrin, Sharon L R Kardia. Healthcare (Basel) 2018
18
14

Editorial: Precision Public Health.
Tarun Stephen Weeramanthri, Hugh J S Dawkins, Gareth Baynam, Matthew Bellgard, Ori Gudes, James Bernard Semmens. Front Public Health 2018
28
14



Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Laura M Amendola, Michael O Dorschner, Peggy D Robertson, Joseph S Salama, Ragan Hart, Brian H Shirts, Mitzi L Murray, Mari J Tokita, Carlos J Gallego, Daniel Seung Kim,[...]. Genome Res 2015
238
14


From public health genomics to precision public health: a 20-year journey.
Muin J Khoury, M Scott Bowen, Mindy Clyne, W David Dotson, Marta L Gwinn, Ridgely Fisk Green, Katherine Kolor, Juan L Rodriguez, Anja Wulf, Wei Yu. Genet Med 2018
64
14

Children are not just small adults: the urgent need for high-quality trial evidence in children.
Terry P Klassen, Lisa Hartling, Jonathan C Craig, Martin Offringa. PLoS Med 2008
116
14

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
75
14

Germline Mutations in Predisposition Genes in Pediatric Cancer.
Jinghui Zhang, Michael F Walsh, Gang Wu, Michael N Edmonson, Tanja A Gruber, John Easton, Dale Hedges, Xiaotu Ma, Xin Zhou, Donald A Yergeau,[...]. N Engl J Med 2015
588
14




Rethinking the "open future" argument against predictive genetic testing of children.
Jeremy R Garrett, John D Lantos, Leslie G Biesecker, Janet E Childerhose, Wendy K Chung, Ingrid A Holm, Barbara A Koenig, Jean E McEwen, Benjamin S Wilfond, Kyle Brothers. Genet Med 2019
19
14


[Value of bacteriologic studies of the ejaculate in examining men in infertile marriages].
Iu T Voronin, V M Mazurova, Ia A P'ianzina. Akush Ginekol (Mosk) 1983
2
50

ClinVar at five years: Delivering on the promise.
Melissa J Landrum, Brandi L Kattman. Hum Mutat 2018
87
14

Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disorders.
Lisa J Ewans, Deborah Schofield, Rupendra Shrestha, Ying Zhu, Velimir Gayevskiy, Kevin Ying, Corrina Walsh, Eric Lee, Edwin P Kirk, Alison Colley,[...]. Genet Med 2018
71
14

Parents' and children's attitudes toward the enrollment of minors in genetic susceptibility research: implications for informed consent.
Barbara A Bernhardt, Ellen S Tambor, Gertrude Fraser, Lawrence S Wissow, Gail Geller. Am J Med Genet A 2003
52
14

Cytarabine anaphylaxis.
J Slater. Am J Dis Child 1988
1
100


[The cell membrane combustible battery, electrodialyser, and electromechanic energy converter].
C Eyraud, J Lenoir, G Duperray, C Bardot, C Fourcade, A Thomasset. C R Acad Hebd Seances Acad Sci D 1969
5
20


eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes.
Giulia Babbi, Pier Luigi Martelli, Giuseppe Profiti, Samuele Bovo, Castrense Savojardo, Rita Casadio. BMC Genomics 2017
29
14

Cost-effectiveness of HLA-DQB1/HLA-B pharmacogenetic-guided treatment and blood monitoring in US patients taking clozapine.
François R Girardin, Antoine Poncet, Arnaud Perrier, Nathalie Vernaz, Mark Pletscher, Caroline F Samer, Jeffrey A Lieberman, Jean Villard. Pharmacogenomics J 2019
17
14

Pharmacogenomics: personalizing pediatric heart transplantation.
Sara L Van Driest, Steven A Webber. Circulation 2015
7
14


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.