A citation-based method for searching scientific literature

Aaron J Goldenberg, Richard R Sharp. JAMA 2012
Times Cited: 66







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



Times Cited
  Times     Co-cited
Similarity


Ethical issues with newborn screening in the genomics era.
Beth A Tarini, Aaron J Goldenberg. Annu Rev Genomics Hum Genet 2012
69
36

Mandatory versus voluntary consent for newborn screening?
Lainie Friedman Ross. Kennedy Inst Ethics J 2010
46
34

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
24

Rapid whole-genome sequencing for genetic disease diagnosis in neonatal intensive care units.
Carol Jean Saunders, Neil Andrew Miller, Sarah Elizabeth Soden, Darrell Lee Dinwiddie, Aaron Noll, Noor Abu Alnadi, Nevene Andraws, Melanie LeAnn Patterson, Lisa Ann Krivohlavek, Joel Fellis,[...]. Sci Transl Med 2012
375
22

Parents' interest in whole-genome sequencing of newborns.
Aaron J Goldenberg, Daniel S Dodson, Matthew M Davis, Beth A Tarini. Genet Med 2014
54
27


State newborn screening in the tandem mass spectrometry era: more tests, more false-positive results.
Beth A Tarini, Dimitri A Christakis, H Gilbert Welch. Pediatrics 2006
89
15

From public health emergency to public health service: the implications of evolving criteria for newborn screening panels.
Scott D Grosse, Coleen A Boyle, Aileen Kenneson, Muin J Khoury, Benjamin S Wilfond. Pediatrics 2006
86
15

Genomics in newborn screening.
Yuval E Landau, Uta Lichter-Konecki, Harvey L Levy. J Pediatr 2014
39
25



Expanded newborn screening for biochemical disorders: the effect of a false-positive result.
Elizabeth A Gurian, Daniel D Kinnamon, Judith J Henry, Susan E Waisbren. Pediatrics 2006
139
12


Ethical, legal, and social concerns about expanded newborn screening: fragile X syndrome as a prototype for emerging issues.
Donald B Bailey, Debra Skinner, Arlene M Davis, Ian Whitmarsh, Cynthia Powell. Pediatrics 2008
72
12

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
431
12

Applying Genomic Analysis to Newborn Screening.
B D Solomon, D E Pineda-Alvarez, K A Bear, J C Mullikin, J P Evans. Mol Syndromol 2012
15
53

Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
259
12


Decision-making process for conditions nominated to the recommended uniform screening panel: statement of the US Department of Health and Human Services Secretary's Advisory Committee on Heritable Disorders in Newborns and Children.
Alex R Kemper, Nancy S Green, Ned Calonge, Wendy K K Lam, Anne M Comeau, Aaron J Goldenberg, Jelili Ojodu, Lisa A Prosser, Susan Tanksley, Joseph A Bocchini. Genet Med 2014
57
14

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
100
10

Effect of expanded newborn screening for biochemical genetic disorders on child outcomes and parental stress.
Susan E Waisbren, Simone Albers, Steve Amato, Mary Ampola, Thomas G Brewster, Laurie Demmer, Roger B Eaton, Robert Greenstein, Mark Korson, Cecilia Larson,[...]. JAMA 2003
223
10

Recommendations for effective newborn screening communication: results of focus groups with parents, providers, and experts.
Terry C Davis, Sharon G Humiston, Connie L Arnold, Joseph A Bocchini, Pat F Bass, Estela M Kennen, Anna Bocchini, Penny Kyler, Michele Lloyd-Puryear. Pediatrics 2006
87
10

Information and informed consent for neonatal screening: opinions and preferences of parents.
Symone Detmar, Esther Hosli, Nynke Dijkstra, Niels Nijsingh, Marlies Rijnders, Marcel Verweij. Birth 2007
36
19

State laws regarding the retention and use of residual newborn screening blood samples.
Michelle H Lewis, Aaron Goldenberg, Rebecca Anderson, Erin Rothwell, Jeffrey Botkin. Pediatrics 2011
59
11



Public attitudes about genetic testing in the newborn period.
Holly Etchegary, Elizabeth Dicks, Kathleen Hodgkinson, Daryl Pullman, Jane Green, Patrick Parfey. J Obstet Gynecol Neonatal Nurs 2012
21
33

Whole-genome sequencing in newborn screening programs.
Bartha M Knoppers, Karine Sénécal, Pascal Borry, Denise Avard. Sci Transl Med 2014
45
15

Expanding newborn screening: process, policy, and priorities.
Virginia A Moyer, Ned Calonge, Steven M Teutsch, Jeffrey R Botkin. Hastings Cent Rep 2008
56
10


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
10

Parents' experiences of expanded newborn screening evaluations.
Jane M DeLuca, Margaret H Kearney, Sally A Norton, Georgianne L Arnold. Pediatrics 2011
39
15

Challenges in the clinical application of whole-genome sequencing.
Kelly E Ormond, Matthew T Wheeler, Louanne Hudgins, Teri E Klein, Atul J Butte, Russ B Altman, Euan A Ashley, Henry T Greely. Lancet 2010
153
9

Patients-in-waiting: Living between sickness and health in the genomics era.
Stefan Timmermans, Mara Buchbinder. J Health Soc Behav 2010
143
9

Public attitudes regarding the use of residual newborn screening specimens for research.
Jeffrey R Botkin, Erin Rothwell, Rebecca Anderson, Louisa Stark, Aaron Goldenberg, Michelle Lewis, Matthew Burbank, Bob Wong. Pediatrics 2012
53
11

Citizens' values regarding research with stored samples from newborn screening in Canada.
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, June C Carroll, Denise Avard, Brenda J Wilson, Julian Little, Jessica P Bytautas, Judith Allanson, Renata Axler,[...]. Pediatrics 2012
34
17



Exome sequencing identifies the cause of a mendelian disorder.
Sarah B Ng, Kati J Buckingham, Choli Lee, Abigail W Bigham, Holly K Tabor, Karin M Dent, Chad D Huff, Paul T Shannon, Ethylin Wang Jabs, Deborah A Nickerson,[...]. Nat Genet 2010
9

Carrier testing for severe childhood recessive diseases by next-generation sequencing.
Callum J Bell, Darrell L Dinwiddie, Neil A Miller, Shannon L Hateley, Elena E Ganusova, Joann Mudge, Ray J Langley, Lu Zhang, Clarence C Lee, Faye D Schilkey,[...]. Sci Transl Med 2011
431
9

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
14

Public views on participating in newborn screening using genome sequencing.
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, Carolyn Barg, Celine Cressman, June C Carroll, Brenda J Wilson, Julian Little, Denise Avard, Michael Painter-Main,[...]. Eur J Hum Genet 2014
20
30

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
346
9

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Sarah E Soden, Julie A Cakici, Suzanne M Herd, Greyson Twist,[...]. Lancet Respir Med 2015
187
9

The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
214
7


A vision of the future of newborn screening.
Duane Alexander, Peter C van Dyck. Pediatrics 2006
60
8

Noninvasive whole-genome sequencing of a human fetus.
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
241
7


From genetics to genomics: ethics, policy, and parental decision-making.
Benjamin Wilfond, Lainie Friedman Ross. J Pediatr Psychol 2009
55
9


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.