A citation-based method for searching scientific literature

Eyal Reinstein. Genet Res (Camb) 2015
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
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,[...]. Genet Med 2013
50

Ethical issues with newborn screening in the genomics era.
Beth A Tarini, Aaron J Goldenberg. Annu Rev Genomics Hum Genet 2012
63
50

Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.
Anne Andermann, Ingeborg Blancquaert, Sylvie Beauchamp, Véronique Déry. Bull World Health Organ 2008
414
33


Parental rights, child welfare, and public health: the case of PKU screening.
R R Faden, N A Holtzman, A J Chwalow. Am J Public Health 1982
37
33

Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes.
Heidi Carmen Howard, Bartha Maria Knoppers, Martina C Cornel, Ellen Wright Clayton, Karine Sénécal, Pascal Borry. Eur J Hum Genet 2015
47
33

Whole Genome Sequencing and Newborn Screening.
Jeffrey R Botkin, Erin Rothwell. Curr Genet Med Rep 2016
23
33

Development of DNA confirmatory and high-risk diagnostic testing for newborns using targeted next-generation DNA sequencing.
Arindam Bhattacharjee, Tanya Sokolsky, Stacia K Wyman, Martin G Reese, Erik Puffenberger, Kevin Strauss, Holmes Morton, Richard B Parad, Edwin W Naylor. Genet Med 2015
38
33

Utility of whole-genome sequencing for detection of newborn screening disorders in a population cohort of 1,696 neonates.
Dale L Bodian, Elisabeth Klein, Ramaswamy K Iyer, Wendy S W Wong, Prachi Kothiyal, Daniel Stauffer, Kathi C Huddleston, Amber D Gaither, Irina Remsburg, Alina Khromykh,[...]. Genet Med 2016
50
33

Newborn screening: the genomic challenge.
Harvey L Levy. Mol Genet Genomic Med 2014
16
33

Psychosocial Factors Influencing Parental Interest in Genomic Sequencing of Newborns.
Susan E Waisbren, Caroline M Weipert, Rebecca C Walsh, Carter R Petty, Robert C Green. Pediatrics 2016
13
33

Point-counterpoint. Ethics and genomic incidental findings.
Amy L McGuire, Steven Joffe, Barbara A Koenig, Barbara B Biesecker, Laurence B McCullough, Jennifer S Blumenthal-Barby, Timothy Caulfield, Sharon F Terry, Robert C Green. Science 2013
128
33




Parents are interested in newborn genomic testing during the early postpartum period.
Susan E Waisbren, Danielle K Bäck, Christina Liu, Sarah S Kalia, Steven A Ringer, Ingrid A Holm, Robert C Green. Genet Med 2015
28
33

Detection of structural variation using target captured next-generation sequencing data for genetic diagnostic testing.
Wenbo Mu, Bing Li, Sitao Wu, Jefferey Chen, Divya Sain, Dong Xu, Mary Helen Black, Rachid Karam, Katrina Gillespie, Kelly D Farwell Hagman,[...]. Genet Med 2019
11
33

Next generation sequencing as a follow-up test in an expanded newborn screening programme.
Andraz Smon, Barbka Repic Lampret, Urh Groselj, Mojca Zerjav Tansek, Jernej Kovac, Dasa Perko, Sara Bertok, Tadej Battelino, Katarina Trebusak Podkrajsek. Clin Biochem 2018
17
33

Clinical Validation of Copy Number Variant Detection from Targeted Next-Generation Sequencing Panels.
Jennifer Kerkhof, Laila C Schenkel, Jack Reilly, Sheri McRobbie, Erfan Aref-Eshghi, Alan Stuart, C Anthony Rupar, Paul Adams, Robert A Hegele, Hanxin Lin,[...]. J Mol Diagn 2017
66
33

Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.
Mads Vilhelm Hollegaard, Jonas Grauholm, Ronni Nielsen, Jakob Grove, Susanne Mandrup, David Michael Hougaard. Mol Genet Metab 2013
41
33

Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
Aziz Belkadi, Alexandre Bolze, Yuval Itan, Aurélie Cobat, Quentin B Vincent, Alexander Antipenko, Lei Shang, Bertrand Boisson, Jean-Laurent Casanova, Laurent Abel. Proc Natl Acad Sci U S A 2015
243
33

Newborn Sequencing in Genomic Medicine and Public Health.
Jonathan S Berg, Pankaj B Agrawal, Donald B Bailey, Alan H Beggs, Steven E Brenner, Amy M Brower, Julie A Cakici, Ozge Ceyhan-Birsoy, Kee Chan, Flavia Chen,[...]. Pediatrics 2017
89
33

Noninvasive prenatal testing.
Jamie O Lo, Feist Cori D, Mary E Norton, Aaron B Caughey. Obstet Gynecol Surv 2014
19
16

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
115
16

The expansion of newborn screening: is reproductive benefit an appropriate pursuit?
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, Denise Avard, Bartha M Knoppers, Martina C Cornel, Pascal Borry. Nat Rev Genet 2009
15
16

Next generation sequencing and the future of genetic diagnosis.
Katja Lohmann, Christine Klein. Neurotherapeutics 2014
76
16


Pre-natal origins of childhood leukemia.
Mel Greaves. Rev Clin Exp Hematol 2003
60
16

Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians.
Hui Shen, Jian Li, Jigang Zhang, Chao Xu, Yan Jiang, Zikai Wu, Fuping Zhao, Li Liao, Jun Chen, Yong Lin,[...]. PLoS One 2013
37
16

Use of cell-free fetal DNA in maternal plasma for noninvasive prenatal screening.
Amy J Wagner, Michael E Mitchell, Aoy Tomita-Mitchell. Clin Perinatol 2014
11
16


Predictors of genetic testing decisions: a systematic review and critique of the literature.
Kate Sweeny, Arezou Ghane, Angela M Legg, Ho Phi Huynh, Sara E Andrews. J Genet Couns 2014
32
16

Status of newborn screening programs in the United States.
Bradford L Therrell, Alissa Johnson, Donna Williams. Pediatrics 2006
61
16

Newborn screening for cystic fibrosis: evaluation of benefits and risks and recommendations for state newborn screening programs.
Scott D Grosse, Coleen A Boyle, Jeffrey R Botkin, Anne Marie Comeau, Martin Kharrazi, Margaret Rosenfeld, Benjamin S Wilfond. MMWR Recomm Rep 2004
147
16

Genetics professionals' opinions of whole-genome sequencing in the newborn period.
Elizabeth Ulm, W Gregory Feero, Richard Dineen, Joel Charrow, Catherine Wicklund. J Genet Couns 2015
8
16


Cell-free DNA screening for fetal aneuploidy as a clinical service.
Howard Cuckle, Peter Benn, Eugene Pergament. Clin Biochem 2015
51
16

Parents' interest in whole-genome sequencing of newborns.
Aaron J Goldenberg, Daniel S Dodson, Matthew M Davis, Beth A Tarini. Genet Med 2014
55
16

Evaluating the utility of personal genomic information.
Morris W Foster, John J Mulvihill, Richard R Sharp. Genet Med 2009
123
16

FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project.
Chandree L Beaulieu, Jacek Majewski, Jeremy Schwartzentruber, Mark E Samuels, Bridget A Fernandez, Francois P Bernier, Michael Brudno, Bartha Knoppers, Janet Marcadier, David Dyment,[...]. Am J Hum Genet 2014
147
16

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.
Kelly D Farwell, Layla Shahmirzadi, Dima El-Khechen, Zöe Powis, Elizabeth C Chao, Brigette Tippin Davis, Ruth M Baxter, Wenqi Zeng, Cameron Mroske, Melissa C Parra,[...]. Genet Med 2015
285
16

A framework to start the debate on neonatal screening policies in the EU: an Expert Opinion Document.
Martina C Cornel, Tessel Rigter, Stephanie S Weinreich, Peter Burgard, Georg F Hoffmann, Martin Lindner, J Gerard Loeber, Kathrin Rupp, Domenica Taruscio, Luciano Vittozzi. Eur J Hum Genet 2014
36
16

Genomics in newborn screening.
Yuval E Landau, Uta Lichter-Konecki, Harvey L Levy. J Pediatr 2014
36
16

Review of Current International Decision-Making Processes for Newborn Screening: Lessons for Australia.
Selina Carolyne Metternick-Jones, Karla Jane Lister, Hugh J S Dawkins, Craig Anthony White, Tarun Stephen Weeramanthri.  2015
4
25

Government-funded universal newborn hearing screening and genetic analyses of deafness predisposing genes in Taiwan.
Chun-Wei Chu, Yann-Jang Chen, Yi-Hui Lee, Sian-Jang Jaung, Fei-Peng Lee, Hung-Meng Huang. Int J Pediatr Otorhinolaryngol 2015
9
16


How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples.
Sumit Middha, Noralane M Lindor, Shannon K McDonnell, Janet E Olson, Kiley J Johnson, Eric D Wieben, Gianrico Farrugia, James R Cerhan, Stephen N Thibodeau. Front Genet 2015
6
16

International perspectives on newborn screening.
R J Pollitt. J Inherit Metab Dis 2006
42
16


Improving test properties for neonatal cystic fibrosis screening in the Netherlands before the nationwide start by May 1st 2011.
Martina C Cornel, Johan J P Gille, J Gerard Loeber, Annette M M Vernooij-van Langen, Jeannette Dankert-Roelse, Piet A Bolhuis. J Inherit Metab Dis 2012
6
16


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.