A citation-based method for searching scientific literature

Aaron J Goldenberg, Daniel S Dodson, Matthew M Davis, Beth A Tarini. Genet Med 2014
Times Cited: 55







List of co-cited articles
286 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
36


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
371
23

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
46

Ethical issues with newborn screening in the genomics era.
Beth A Tarini, Aaron J Goldenberg. Annu Rev Genomics Hum Genet 2012
68
20

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
256
18

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
45

Whole-genome sequencing in newborn screening programs.
Bartha M Knoppers, Karine Sénécal, Pascal Borry, Denise Avard. Sci Transl Med 2014
44
20

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
69

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
20
40

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
424
14

Genomics in newborn screening.
Yuval E Landau, Uta Lichter-Konecki, Harvey L Levy. J Pediatr 2014
39
20

Parental Views on Expanded Newborn Screening Using Whole-Genome Sequencing.
Galen Joseph, Flavia Chen, Julie Harris-Wai, Jennifer M Puck, Charlotte Young, Barbara A Koenig. Pediatrics 2016
21
38

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
48
16

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
16


Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
12


Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
344
12

Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children.
J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin Genet 2014
86
12


Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am J Hum Genet 2015
220
12

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
53
13

Newborn screening: the genomic challenge.
Harvey L Levy. Mol Genet Genomic Med 2014
16
37

Interest in newborn genetic testing: a survey of prospective parents and the general public.
Holly Etchegary, Elizabeth Dicks, Jane Green, Kathleen Hodgkinson, Daryl Pullman, Patrick Parfrey. Genet Test Mol Biomarkers 2012
11
54

Potential Psychosocial Risks of Sequencing Newborns.
Leslie Ann Frankel, Stacey Pereira, Amy L McGuire. Pediatrics 2016
32
18

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing.
Jonathan S Berg, Ann Katherine M Foreman, Julianne M O'Daniel, Jessica K Booker, Lacey Boshe, Timothy Carey, Kristy R Crooks, Brian C Jensen, Eric T Juengst, Kristy Lee,[...]. Genet Med 2016
53
11

Genomic newborn screening: public health policy considerations and recommendations.
Jan M Friedman, Martina C Cornel, Aaron J Goldenberg, Karla J Lister, Karine Sénécal, Danya F Vears. BMC Med Genomics 2017
39
15

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
831
10

The BabySeq project: implementing genomic sequencing in newborns.
Ingrid A Holm, Pankaj B Agrawal, Ozge Ceyhan-Birsoy, Kurt D Christensen, Shawn Fayer, Leslie A Frankel, Casie A Genetti, Joel B Krier, Rebecca C LaMay, Harvey L Levy,[...]. BMC Pediatr 2018
45
13

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
9

Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
207
9

Making a definitive diagnosis: successful clinical application of whole exome sequencing in a child with intractable inflammatory bowel disease.
Elizabeth A Worthey, Alan N Mayer, Grant D Syverson, Daniel Helbling, Benedetta B Bonacci, Brennan Decker, Jaime M Serpe, Trivikram Dasu, Michael R Tschannen, Regan L Veith,[...]. Genet Med 2011
474
9



Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
809
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
182
9

Parent and public interest in whole-genome sequencing.
Daniel S Dodson, Aaron J Goldenberg, Matthew M Davis, Dianne C Singer, Beth A Tarini. Public Health Genomics 2015
16
31

A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
Zornitza Stark, Tiong Y Tan, Belinda Chong, Gemma R Brett, Patrick Yap, Maie Walsh, Alison Yeung, Heidi Peters, Dylan Mordaunt, Shannon Cowie,[...]. Genet Med 2016
200
9

Supporting Parental Decisions About Genomic Sequencing for Newborn Screening: The NC NEXUS Decision Aid.
Megan A Lewis, Ryan S Paquin, Myra I Roche, Robert D Furberg, Christine Rini, Jonathan S Berg, Cynthia M Powell, Donald B Bailey. Pediatrics 2016
28
17

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
62

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
9

Parents perspectives on whole genome sequencing for their children: qualified enthusiasm?
J A Anderson, M S Meyn, C Shuman, R Zlotnik Shaul, L E Mantella, M J Szego, S Bowdin, N Monfared, R Z Hayeems. J Med Ethics 2017
31
16

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
93
9

Reconsidering reproductive benefit through newborn screening: a systematic review of guidelines on preconception, prenatal and newborn screening.
Yvonne Bombard, Fiona A Miller, Robin Z Hayeems, Denise Avard, Bartha M Knoppers. Eur J Hum Genet 2010
35
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
11

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
26


Reflections on the cost of "low-cost" whole genome sequencing: framing the health policy debate.
Timothy Caulfield, Jim Evans, Amy McGuire, Christopher McCabe, Tania Bubela, Robert Cook-Deegan, Jennifer Fishman, Stuart Hogarth, Fiona A Miller, Vardit Ravitsky,[...]. PLoS Biol 2013
52
7

The 'thousand-dollar genome': an ethical exploration.
Wybo J Dondorp, Guido M W R de Wert. Eur J Hum Genet 2013
36
11


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.