A citation-based method for searching scientific literature


List of co-cited articles
38 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
18

Genetic counselors' views and experiences with the clinical integration of genome sequencing.
Kalotina Machini, Jessica Douglas, Alicia Braxton, Judith Tsipis, Kate Kramer. J Genet Couns 2014
34
18

Return of genomic results to research participants: the floor, the ceiling, and the choices in between.
Gail P Jarvik, Laura M Amendola, Jonathan S Berg, Kyle Brothers, Ellen W Clayton, Wendy Chung, Barbara J Evans, James P Evans, Stephanie M Fullerton, Carlos J Gallego,[...]. Am J Hum Genet 2014
235
18


Implementation and utilization of genetic testing in personalized medicine.
Noura S Abul-Husn, Aniwaa Owusu Obeng, Saskia C Sanderson, Omri Gottesman, Stuart A Scott. Pharmgenomics Pers Med 2014
47
13

Diagnostic clinical genome and exome sequencing.
Leslie G Biesecker, Robert C Green. N Engl J Med 2014
340
13

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
158
13

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
212
13

New approaches to molecular diagnosis.
Bruce R Korf, Heidi L Rehm. JAMA 2013
79
9

Essential elements of personalized medicine.
Wylie Burke, Susan Brown Trinidad, Nancy A Press. Urol Oncol 2014
23
9

Ethical, legal, and social implications of incorporating genomic information into electronic health records.
Ribhi Hazin, Kyle B Brothers, Bradley A Malin, Barbara A Koenig, Saskia C Sanderson, Mark A Rothstein, Marc S Williams, Ellen W Clayton, Iftikhar J Kullo. Genet Med 2013
60
9

Models of consent to return of incidental findings in genomic research.
Paul S Appelbaum, Erik Parens, Cameron R Waldman, Robert Klitzman, Abby Fyer, Josue Martinez, W Nicholson Price, Wendy K Chung. Hastings Cent Rep 2014
49
9

Legislation on direct-to-consumer genetic testing in seven European countries.
Pascal Borry, Rachel E van Hellemondt, Dominique Sprumont, Camilla Fittipaldi Duarte Jales, Emmanuelle Rial-Sebbag, Tade Matthias Spranger, Liam Curren, Jane Kaye, Herman Nys, Heidi Howard. Eur J Hum Genet 2012
70
9

Challenges of translating genetic tests into clinical and public health practice.
Wolf H Rogowski, Scott D Grosse, Muin J Khoury. Nat Rev Genet 2009
77
9


Exome sequencing can improve diagnosis and alter patient management.
Tracy J Dixon-Salazar, Jennifer L Silhavy, Nitin Udpa, Jana Schroth, Stephanie Bielas, Ashleigh E Schaffer, Jesus Olvera, Vineet Bafna, Maha S Zaki, Ghada H Abdel-Salam,[...]. Sci Transl Med 2012
182
9


Ethical issues raised by whole genome sequencing.
Wim Pinxten, Heidi Carmen Howard. Best Pract Res Clin Gastroenterol 2014
31
9

ACMG clinical laboratory standards for next-generation sequencing.
Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet Med 2013
526
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
203
9


To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
105
9


Identifying personal genomes by surname inference.
Melissa Gymrek, Amy L McGuire, David Golan, Eran Halperin, Yaniv Erlich. Science 2013
463
9




ClinGen--the Clinical Genome Resource.
Heidi L Rehm, Jonathan S Berg, Lisa D Brooks, Carlos D Bustamante, James P Evans, Melissa J Landrum, David H Ledbetter, Donna R Maglott, Christa Lese Martin, Robert L Nussbaum,[...]. N Engl J Med 2015
482
9

Gatekeepers or intermediaries? The role of clinicians in commercial genomic testing.
Michelle L McGowan, Jennifer R Fishman, Richard A Settersten, Marcie A Lambrix, Eric T Juengst. PLoS One 2014
22
9

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
9

GINA, genetic discrimination, and genomic medicine.
Robert C Green, Denise Lautenbach, Amy L McGuire. N Engl J Med 2015
95
9

Beyond the patient: the broader impact of genetic discrimination among individuals at risk of Huntington disease.
Yvonne Bombard, JoAnne Palin, Jan M Friedman, Gerry Veenstra, Susan Creighton, Joan L Bottorff, Michael R Hayden. Am J Med Genet B Neuropsychiatr Genet 2012
27
9


Pharmacogenomics: the promise of personalized medicine.
L Mancinelli, M Cronin, W Sadée. AAPS PharmSci 2000
90
9


Kinscapes, timescapes and genescapes: families living with genetic risk.
Paul Atkinson, Katie Featherstone, Maggie Gregory. Sociol Health Illn 2013
24
9

Guidelines for investigating causality of sequence variants in human disease.
D G MacArthur, T A Manolio, D P Dimmock, H L Rehm, J Shendure, G R Abecasis, D R Adams, R B Altman, S E Antonarakis, E A Ashley,[...]. Nature 2014
767
9

Biobanking past, present and future: responsibilities and benefits.
Yvonne G De Souza, John S Greenspan. AIDS 2013
106
9

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
70
4

Readability standards for informed-consent forms as compared with actual readability.
Michael K Paasche-Orlow, Holly A Taylor, Frederick L Brancati. N Engl J Med 2003
380
4

Actionable, pathogenic incidental findings in 1,000 participants' exomes.
Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett,[...]. Am J Hum Genet 2013
268
4

Informed consent for return of incidental findings in genomic research.
Paul S Appelbaum, Cameron R Waldman, Abby Fyer, Robert Klitzman, Erik Parens, Josue Martinez, W Nicholson Price, Wendy K Chung. Genet Med 2014
46
4


Best ethical practices for clinicians and laboratories in the provision of noninvasive prenatal testing.
M A Allyse, L C Sayres, M Havard, J S King, H T Greely, L Hudgins, J Taylor, M E Norton, M K Cho, D Magnus,[...]. Prenat Diagn 2013
39
4

Learning health care systems and justice.
Ruth R Faden, Tom L Beauchamp, Nancy E Kass. Hastings Cent Rep 2011
15
6

It's More Than a Blood Test: Patients' Perspectives on Noninvasive Prenatal Testing.
Ruth M Farrell, Mary Beth Mercer, Patricia K Agatisa, Marissa B Smith, Elliot Philipson. J Clin Med 2014
28
4

Prenatal whole genome sequencing: just because we can, should we?
Greer Donley, Sara Chandros Hull, Benjamin E Berkman. Hastings Cent Rep 2012
36
4


Variation in Mu-Opioid Receptor Gene (OPRM1) as a Moderator of Naltrexone Treatment to Reduce Heavy Drinking in a High Functioning Cohort.
Andrew Ch Chen, Jon Morgenstern, Christine M Davis, Alexis N Kuerbis, Jonathan Covault, Henry R Kranzler. J Alcohol Drug Depend 2013
11
9

Brain-derived neurotrophic factor augments rotational behavior and nigrostriatal dopamine turnover in vivo.
C A Altar, C B Boylan, C Jackson, S Hershenson, J Miller, S J Wiegand, R M Lindsay, C Hyman. Proc Natl Acad Sci U S A 1992
262
4


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.