A citation-based method for searching scientific literature

Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
Times Cited: 254







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



Times Cited
  Times     Co-cited
Similarity




Direct-to-Consumer Testing 2.0: Emerging Models of Direct-to-Consumer Genetic Testing.
Megan A Allyse, David H Robinson, Matthew J Ferber, Richard R Sharp. Mayo Clin Proc 2018
53
5

The NSIGHT1-randomized controlled trial: rapid whole-genome sequencing for accelerated etiologic diagnosis in critically ill infants.
Josh E Petrikin, Julie A Cakici, Michelle M Clark, Laurel K Willig, Nathaly M Sweeney, Emily G Farrow, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Lee Zellmer,[...]. NPJ Genom Med 2018
72
4

Cystic Fibrosis Transmembrane Conductance Regulator-Related Metabolic Syndrome and Cystic Fibrosis Screen Positive, Inconclusive Diagnosis.
Clement L Ren, Drucy S Borowitz, Tanja Gonska, Michelle S Howenstine, Hara Levy, John Massie, Carlos Milla, Anne Munck, Kevin W Southern. J Pediatr 2017
48
6

The usefulness of whole-exome sequencing in routine clinical practice.
Alejandro Iglesias, Kwame Anyane-Yeboa, Julia Wynn, Ashley Wilson, Megan Truitt Cho, Edwin Guzman, Rebecca Sisson, Claire Egan, Wendy K Chung. Genet Med 2014
127
3

Newborn screening technology: proceed with caution.
Jeffrey R Botkin, Ellen Wright Clayton, Norman C Fost, Wylie Burke, Thomas H Murray, Mary Ann Baily, Benjamin Wilfond, Alfred Berg, Lainie Friedman Ross. Pediatrics 2006
98
3

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
6

Newborn Screening for Cystic Fibrosis in California.
Martin Kharrazi, Juan Yang, Tracey Bishop, Shellye Lessing, Suzanne Young, Steven Graham, Michelle Pearl, Helen Chow, Thomson Ho, Robert Currier,[...]. Pediatrics 2015
65
4


False-positive results released by direct-to-consumer genetic tests highlight the importance of clinical confirmation testing for appropriate patient care.
Stephany Tandy-Connor, Jenna Guiltinan, Kate Krempely, Holly LaDuca, Patrick Reineke, Stephanie Gutierrez, Phillip Gray, Brigette Tippin Davis. Genet Med 2018
109
3

Variation among Consent Forms for Clinical Whole Exome Sequencing.
Sara A Fowler, Carol J Saunders, Mark A Hoffman. J Genet Couns 2018
10
30

Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
55
5

Disclosure of incidental findings from next-generation sequencing in pediatric genomic research.
Ruqayyah Abdul-Karim, Benjamin E Berkman, David Wendler, Annette Rid, Javed Khan, Tom Badgett, Sara Chandros Hull. Pediatrics 2013
53
5

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
3

A systematic approach to assessing the clinical significance of genetic variants.
H Duzkale, J Shen, H McLaughlin, A Alfares, M A Kelly, T J Pugh, B H Funke, H L Rehm, M S Lebo. Clin Genet 2013
106
3

Reconciling Opportunistic and Population Screening in Clinical Genomics.
Kyle B Brothers, Jason L Vassy, Robert C Green. Mayo Clin Proc 2019
14
21


Eliciting preferences on secondary findings: the Preferences Instrument for Genomic Secondary Results.
Kyle B Brothers, Kelly M East, Whitley V Kelley, M Frances Wright, Matthew J Westbrook, Carla A Rich, Kevin M Bowling, Edward J Lose, E Martina Bebin, Shirley Simmons,[...]. Genet Med 2017
25
12


ClinVar: improving access to variant interpretations and supporting evidence.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth R Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Wonhee Jang,[...]. Nucleic Acids Res 2018
815
3

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
961
3

Genomic Contextualism: Shifting the Rhetoric of Genetic Exceptionalism.
Nanibaa' A Garrison, Kyle B Brothers, Aaron J Goldenberg, John A Lynch. Am J Bioeth 2019
27
11

The Exome Clinic and the role of medical genetics expertise in the interpretation of exome sequencing results.
Dustin Baldridge, Jennifer Heeley, Marisa Vineyard, Linda Manwaring, Tomi L Toler, Emily Fassi, Elise Fiala, Sarah Brown, Charles W Goss, Marcia Willing,[...]. Genet Med 2017
47
6


Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation.
Michelle M Clark, Amber Hildreth, Sergey Batalov, Yan Ding, Shimul Chowdhury, Kelly Watkins, Katarzyna Ellsworth, Brandon Camp, Cyrielle I Kint, Calum Yacoubian,[...]. Sci Transl Med 2019
67
4

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
6

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
16
18



Pediatric research and the return of individual research results.
Denise Avard, Karine Sénécal, Parvaz Madadi, Daniel Sinnett. J Law Med Ethics 2011
28
7

Clinical Pharmacogenetics Implementation Consortium guidelines for cytochrome P450 2D6 genotype and codeine therapy: 2014 update.
K R Crews, A Gaedigk, H M Dunnenberger, J S Leeder, T E Klein, K E Caudle, C E Haidar, D D Shen, J T Callaghan, S Sadhasivam,[...]. Clin Pharmacol Ther 2014
368
2

Incidental findings in pediatric research.
Benjamin S Wilfond, Katherine J Carpenter. J Law Med Ethics 2008
31
6


Parents' attitudes toward pediatric genetic testing for common disease risk.
Kenneth P Tercyak, Sharon Hensley Alford, Karen M Emmons, Isaac M Lipkus, Benjamin S Wilfond, Colleen M McBride. Pediatrics 2011
49
4

An international survey of predictive genetic testing in children for adult onset conditions.
Rony E Duncan, Julian Savulescu, Lynn Gillam, Robert Williamson, Martin B Delatycki. Genet Med 2005
55
3

Growing up in the genomic era: implications of whole-genome sequencing for children, families, and pediatric practice.
Christopher H Wade, Beth A Tarini, Benjamin S Wilfond. Annu Rev Genomics Hum Genet 2013
42
4



Predictive genetic testing for adult-onset disorders in minors: a critical analysis of the arguments for and against the 2013 ACMG guidelines.
J A Anderson, R Z Hayeems, C Shuman, M J Szego, N Monfared, S Bowdin, R Zlotnik Shaul, M S Meyn. Clin Genet 2015
27
7

Genetic Testing for Minors: Comparison between Italian and British Guidelines.
Pamela Tozzo, Luciana Caenazzo, Daniele Rodriguez. Genet Res Int 2012
5
40

Constructing "best interests": genetic testing of children in families with hypertrophic cardiomyopathy.
Els Geelen, Ine Van Hoyweghen, Pieter A Doevendans, Carlo L M Marcelis, Klasien Horstman. Am J Med Genet A 2011
17
11

The right to an open future concerning genetic information.
Annelien L Bredenoord, Martine C de Vries, Hans van Delden. Am J Bioeth 2014
15
13

'You don't make genetic test decisions from one day to the next'--using time to preserve moral space.
Jackie Leach Scully, Rouven Porz, Christoph Rehmann-Sutter. Bioethics 2007
27
7

Consensus statement for standard of care in spinal muscular atrophy.
Ching H Wang, Richard S Finkel, Enrico S Bertini, Mary Schroth, Anita Simonds, Brenda Wong, Annie Aloysius, Leslie Morrison, Marion Main, Thomas O Crawford,[...]. J Child Neurol 2007
445
2

Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children.
Ned Calonge, Nancy S Green, Piero Rinaldo, Michele Lloyd-Puryear, Denise Dougherty, Coleen Boyle, Michael Watson, Tracy Trotter, Sharon F Terry, R Rodney Howell. Genet Med 2010
59
3

Childhood spinal muscular atrophy: controversies and challenges.
Eugenio Mercuri, Enrico Bertini, Susan T Iannaccone. Lancet Neurol 2012
167
2

Seize the day: Newborn screening for SMA.
Kathryn J Swoboda. Am J Med Genet A 2010
14
14

Newborn blood spot screening test using multiplexed real-time PCR to simultaneously screen for spinal muscular atrophy and severe combined immunodeficiency.
Jennifer L Taylor, Francis K Lee, Golriz Khadem Yazdanpanah, John F Staropoli, Mei Liu, John P Carulli, Chao Sun, Steven F Dobrowolski, W Harry Hannon, Robert F Vogt. Clin Chem 2015
46
4

Evidence-based path to newborn screening for Duchenne muscular dystrophy.
Jerry R Mendell, Chris Shilling, Nancy D Leslie, Kevin M Flanigan, Roula al-Dahhak, Julie Gastier-Foster, Kelley Kneile, Diane M Dunn, Brett Duval, Alexander Aoyagi,[...]. Ann Neurol 2012
424
2


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.