A citation-based method for searching scientific literature

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, Benjamin S Wilfond, Joseph D McInerney. Am J Hum Genet 2015
Times Cited: 231







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



Times Cited
  Times     Co-cited
Similarity


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
263
30

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
27

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
902
26


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
16

The psychological impact of genetic information on children: a systematic review.
Claire E Wakefield, Lucy V Hanlon, Katherine M Tucker, Andrea F Patenaude, Christina Signorelli, Jordana K McLoone, Richard J Cohn. Genet Med 2016
58
24


Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.
Pascal Borry, Gerry Evers-Kiebooms, Martina C Cornel, Angus Clarke, Kris Dierickx. Eur J Hum Genet 2009
118
9

A curated gene list for reporting results of newborn genomic sequencing.
Ozge Ceyhan-Birsoy, Kalotina Machini, Matthew S Lebo, Tim W Yu, Pankaj B Agrawal, Richard B Parad, Ingrid A Holm, Amy McGuire, Robert C Green, Alan H Beggs,[...]. Genet Med 2017
38
23

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
126
8



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
53
15

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
102
8

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
214
7

Experience with genetic counseling: the adolescent perspective.
Amanda Pichini, Cheryl Shuman, Karen Sappleton, Miriam Kaufman, David Chitayat, Riyana Babul-Hirji. J Genet Couns 2016
12
58

Adolescents' preferences regarding disclosure of incidental findings in genomic sequencing that are not medically actionable in childhood.
Sophia B Hufnagel, Lisa J Martin, Amy Cassedy, Robert J Hopkin, Armand H Matheny Antommaria. Am J Med Genet A 2016
18
38


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
201
7

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
18
38

Adolescent and Parental Attitudes About Return of Genomic Research Results: Focus Group Findings Regarding Decisional Preferences.
Michelle L McGowan, Cynthia A Prows, Melissa DeJonckheere, William B Brinkman, Lisa Vaughn, Melanie F Myers. J Empir Res Hum Res Ethics 2018
18
38

"It was the missing piece": adolescent experiences of predictive genetic testing for adult-onset conditions.
Cara Mand, Lynn Gillam, Rony E Duncan, Martin B Delatycki. Genet Med 2013
30
20

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study.
Anita Villani, Ari Shore, Jonathan D Wasserman, Derek Stephens, Raymond H Kim, Harriet Druker, Bailey Gallinger, Anne Naumer, Wendy Kohlmann, Ana Novokmet,[...]. Lancet Oncol 2016
250
6


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
573
6

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
94
6


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
45
13

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
353
6


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
72
8

"You're one of us now": young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP).
Rony E Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G Rogers, Martin B Delatycki. Am J Med Genet C Semin Med Genet 2008
65
7

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
159
5

Return of genetic testing results in the era of whole-genome sequencing.
Bartha Maria Knoppers, Ma'n H Zawati, Karine Sénécal. Nat Rev Genet 2015
92
5

Return of whole-genome sequencing results in paediatric research: a statement of the P3G international paediatrics platform.
Bartha Maria Knoppers, Denise Avard, Karine Sénécal, Ma'n H Zawati. Eur J Hum Genet 2014
46
10

Parents' and children's communication about genetic risk: a qualitative study, learning from families' experiences.
Alison Metcalfe, Gill Plumridge, Jane Coad, Andrew Shanks, Paramjit Gill. Eur J Hum Genet 2011
69
7

Professionally Responsible Disclosure of Genomic Sequencing Results in Pediatric Practice.
Laurence B McCullough, Kyle B Brothers, Wendy K Chung, Steven Joffe, Barbara A Koenig, Benjamin Wilfond, Joon-Ho Yu. Pediatrics 2015
15
33

Should Genetic Testing be Offered for Children? The Perspectives of Adolescents and Emerging Adults in Families with Li-Fraumeni Syndrome.
Melissa A Alderfer, Robert B Lindell, Claire I Viadro, Kristin Zelley, Jessica Valdez, Belinda Mandrell, Carol A Ford, Kim E Nichols. J Genet Couns 2017
22
22

Potential Psychosocial Risks of Sequencing Newborns.
Leslie Ann Frankel, Stacey Pereira, Amy L McGuire. Pediatrics 2016
33
15

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
88
5

Stakeholders' opinions on the implementation of pediatric whole exome sequencing: implications for informed consent.
Brooke L Levenseller, Danielle J Soucier, Victoria A Miller, Diana Harris, Laura Conway, Barbara A Bernhardt. J Genet Couns 2014
55
9

Sequencing Newborns: A Call for Nuanced Use of Genomic Technologies.
Josephine Johnston, John D Lantos, Aaron Goldenberg, Flavia Chen, Erik Parens, Barbara A Koenig. Hastings Cent Rep 2018
35
14


Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome.
Christian P Kratz, Maria Isabel Achatz, Laurence Brugières, Thierry Frebourg, Judy E Garber, Mary-Louise C Greer, Jordan R Hansford, Katherine A Janeway, Wendy K Kohlmann, Rose McGee,[...]. Clin Cancer Res 2017
214
4


Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers,[...]. Genet Med 2013
218
4

Clinical application of whole-exome sequencing across clinical indications.
Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan,[...]. Genet Med 2016
498
4

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
49
8

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
85
4

Genetic testing in Li-Fraumeni syndrome: uptake and psychosocial consequences.
Chantal R M Lammens, Neil K Aaronson, Anja Wagner, Rolf H Sijmons, Margreet G E M Ausems, Annette H J T Vriends, Mariëlle W G Ruijs, Theo A M van Os, Liesbeth Spruijt, Encarna B Gómez García,[...]. J Clin Oncol 2010
73
5


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.