A citation-based method for searching scientific literature

Gillian W Hooker, Kelly E Ormond, Kevin Sweet, Barbara B Biesecker. J Genet Couns 2014
Times Cited: 42







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



Times Cited
  Times     Co-cited
Similarity


A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
354
23

From genetic counseling to "genomic counseling".
Kelly E Ormond. Mol Genet Genomic Med 2013
43
23

Genomic counseling: next generation counseling.
Rachel Mills, Susanne B Haga. J Genet Couns 2014
18
50

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
16

A genetic counselor's guide to using next-generation sequencing in clinical practice.
Flavia M Facio, Kristy Lee, Julianne M O'Daniel. J Genet Couns 2014
24
29


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
14

Identification of genetic counseling service delivery models in practice: a report from the NSGC Service Delivery Model Task Force.
Stephanie A Cohen, Monica L Marvin, Bronson D Riley, Hetal S Vig, Julie A Rousseau, Shanna L Gustafson. J Genet Couns 2013
74
11

Assessment of the content and process of genetic counseling: a critical review of empirical studies.
Bettina Meiser, Jennifer Irle, Elizabeth Lobb, Kristine Barlow-Stewart. J Genet Couns 2008
95
11


What does it mean to be genomically literate?: National Human Genome Research Institute Meeting Report.
Belen Hurle, Toby Citrin, Jean F Jenkins, Kimberly A Kaphingst, Neil Lamb, Jo Ellen Roseman, Vence L Bonham. Genet Med 2013
57
11

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
14

Assessing the integration of genomic medicine in genetic counseling training programs.
Jessica Profato, Erynn S Gordon, Shannan Dixon, Andrea Kwan. J Genet Couns 2014
5
100

Conceptualizing genetic counseling as psychotherapy in the era of genomic medicine.
Jehannine Austin, Alicia Semaka, George Hadjipavlou. J Genet Couns 2014
54
11

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
799
11

Communicating genetic risk information for common disorders in the era of genomic medicine.
Denise M Lautenbach, Kurt D Christensen, Jeffrey A Sparks, Robert C Green. Annu Rev Genomics Hum Genet 2013
83
9

Communicating genetic and genomic information: health literacy and numeracy considerations.
D H Lea, K A Kaphingst, D Bowen, I Lipkus, D W Hadley. Public Health Genomics 2011
136
9


Building the genetic counsellor profession in the United Kingdom: two decades of growth and development.
Heather Skirton, Lauren Kerzin-Storrar, Chris Barnes, Georgina Hall, Mark Longmuir, Christine Patch, Gillian Scott, Jan Walford-Moore. J Genet Couns 2013
15
26

Development of a tiered and binned genetic counseling model for informed consent in the era of multiplex testing for cancer susceptibility.
Angela R Bradbury, Linda Patrick-Miller, Jessica Long, Jacquelyn Powers, Jill Stopfer, Andrea Forman, Christina Rybak, Kristin Mattie, Amanda Brandt, Rachelle Chambers,[...]. Genet Med 2015
52
9


Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine.
Keyan Salari, Konrad J Karczewski, Louanne Hudgins, Kelly E Ormond. PLoS One 2013
57
9

Educating health-care professionals about genetics and genomics.
Alan E Guttmacher, Mary E Porteous, Joseph D McInerney. Nat Rev Genet 2007
195
9

Lessons learned from the introduction of personalized genotyping into a medical school curriculum.
David R Walt, Amy Kuhlik, Scott K Epstein, Laurie A Demmer, Meredith Knight, David Chelmow, Michael Rosenblatt, Diana W Bianchi. Genet Med 2011
45
9


Personal genome testing in medical education: student experiences with genotyping in the classroom.
Simone Lucia Vernez, Keyan Salari, Kelly E Ormond, Sandra Soo-Jin Lee. Genome Med 2013
39
10


Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics.
Bruce R Korf, Anna B Berry, Melvin Limson, Ali J Marian, Michael F Murray, P Pearl O'Rourke, Eugene R Passamani, Mary V Relling, John Tooker, Gregory J Tsongalis,[...]. Genet Med 2014
78
9

Looking back and moving forward: an historical perspective from laboratory genetic counselors.
Lindsay H Zetzsche, Katrina E Kotzer, Karen E Wain. J Genet Couns 2014
15
26

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
9

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
190
9


Models of service delivery for cancer genetic risk assessment and counseling.
Angela M Trepanier, Dawn C Allain. J Genet Couns 2014
48
9

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
85
7

Personalized genomic results: analysis of informational needs.
Tara J Schmidlen, Lisa Wawak, Rachel Kasper, J Felipe García-España, Michael F Christman, Erynn S Gordon. J Genet Couns 2014
24
12

How do research participants perceive "uncertainty" in genome sequencing?
Barbara B Biesecker, William Klein, Katie L Lewis, Tyler C Fisher, Martha Frances Wright, Leslie G Biesecker, Paul K Han. Genet Med 2014
50
7


Genetic counseling as a tool for type 2 diabetes prevention: a genetic counseling framework for common polygenetic disorders.
Jessica L Waxler, Kelsey E O'Brien, Linda M Delahanty, James B Meigs, Jose C Florez, Elyse R Park, Barbara R Pober, Richard W Grant. J Genet Couns 2012
23
13

Goals of genetic counseling.
B B Biesecker. Clin Genet 2001
118
7

Genetics patients' perspectives on clinical genomic testing.
Michelle L McGowan, Allison Glinka, Janelle Highland, George Asaad, Richard R Sharp. Per Med 2013
29
10

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
151
7

How can psychological science inform research about genetic counseling for clinical genomic sequencing?
Cynthia M Khan, Christine Rini, Barbara A Bernhardt, J Scott Roberts, Kurt D Christensen, James P Evans, Kyle B Brothers, Myra I Roche, Jonathan S Berg, Gail E Henderson. J Genet Couns 2015
16
18

Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
285
7

Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harms.
Holly K Tabor, Jacquie Stock, Tracy Brazg, Margaret J McMillin, Karin M Dent, Joon-Ho Yu, Jay Shendure, Michael J Bamshad. Am J Med Genet A 2012
82
7

"Not Tied Up Neatly with a Bow": Professionals' Challenging Cases in Informed Consent for Genomic Sequencing.
Ashley N Tomlinson, Debra Skinner, Denise L Perry, Sarah R Scollon, Myra I Roche, Barbara A Bernhardt. J Genet Couns 2016
37
8

Medical and graduate students' attitudes toward personal genomics.
Kelly E Ormond, Louanne Hudgins, Jennifer M Ladd, David M Magnus, Henry T Greely, Mildred K Cho. Genet Med 2011
30
10

The unmet need of education in genomic medicine.
Bradley A Patay, Eric J Topol. Am J Med 2012
24
12

Randomized Trial of Telegenetics vs. In-Person Cancer Genetic Counseling: Cost, Patient Satisfaction and Attendance.
Adam H Buchanan, Santanu K Datta, Celette Sugg Skinner, Gail P Hollowell, Henry F Beresford, Thomas Freeland, Benjamin Rogers, John Boling, P Kelly Marcom, Martha B Adams. J Genet Couns 2015
78
7

Defining the role of laboratory genetic counselor.
Susan Christian, Margaret Lilley, Stacey Hume, Patrick Scott, Martin Somerville. J Genet Couns 2012
18
16



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.