A citation-based method for searching scientific literature

Karina L Brierley, Erica Blouch, Whitney Cogswell, Jeanne P Homer, Debbie Pencarinha, Christine L Stanislaw, Ellen T Matloff. Cancer J 2012
Times Cited: 62







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



Times Cited
  Times     Co-cited
Similarity




The search for unaffected individuals with Lynch syndrome: do the ends justify the means?
Heather Hampel, Albert de la Chapelle. Cancer Prev Res (Phila) 2011
92
3

Billing for medical genetics and genetic counseling services: a national survey.
Tabitha A Harrison, Debra Lochner Doyle, Caroline McGowan, Leslie Cohen, Elizabeth Repass, Ruthann B Pfau, Trish Brown. J Genet Couns 2010
16
12

A large health system's approach to utilization of the genetic counselor CPT® 96040 code.
Shanna L Gustafson, Gail Pfeiffer, Charis Eng. Genet Med 2011
13
15

A time study of cancer genetic counselors using a genetic counselor-only patient care model versus a traditional combined genetic counselor plus medical geneticist care model.
Brandie Heald, Shanna Gustafson, Jessica Mester, Patricia Arscott, Katherine Lynch, Jessica Moline, Charis Eng. J Natl Compr Canc Netw 2013
7
28

Variants of uncertain significance in breast cancer-related genes: real-world implications for a clinical conundrum. Part one: clinical genetics recommendations.
Susan Miller-Samuel, Deborah J MacDonald, Jeffrey N Weitzel, Ferdy Santiago, Martin A Martino, Tara Namey, Annmarie Augustyn, Rebecca Mueller, Andrea Forman, Angela R Bradbury,[...]. Semin Oncol 2011
12
16

The genetic attributable risk of breast and ovarian cancer.
E B Claus, J M Schildkraut, W D Thompson, N J Risch. Cancer 1996
412
3

Distress among women receiving uninformative BRCA1/2 results: 12-month outcomes.
Suzanne C O'Neill, Christine Rini, Rachel E Goldsmith, Heiddis Valdimarsdottir, Lawrence H Cohen, Marc D Schwartz. Psychooncology 2009
66
3


Multiplex genetic testing for cancer susceptibility: out on the high wire without a net?
Susan M Domchek, Angela Bradbury, Judy E Garber, Kenneth Offit, Mark E Robson. J Clin Oncol 2013
147
3

A review of a multifactorial probability-based model for classification of BRCA1 and BRCA2 variants of uncertain significance (VUS).
Noralane M Lindor, Lucia Guidugli, Xianshu Wang, Maxime P Vallée, Alvaro N A Monteiro, Sean Tavtigian, David E Goldgar, Fergus J Couch. Hum Mutat 2012
128
3

BRCA1/2 sequence variants of uncertain significance: a primer for providers to assist in discussions and in medical management.
Noralane M Lindor, David E Goldgar, Sean V Tavtigian, Sharon E Plon, Fergus J Couch. Oncologist 2013
54
3

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
Diana W Bianchi, Lawrence D Platt, James D Goldberg, Alfred Z Abuhamad, Amy J Sehnert, Richard P Rava. Obstet Gynecol 2012
418
3

DNA sequencing versus standard prenatal aneuploidy screening.
Diana W Bianchi, R Lamar Parker, Jeffrey Wentworth, Rajeevi Madankumar, Craig Saffer, Anita F Das, Joseph A Craig, Darya I Chudova, Patricia L Devers, Keith W Jones,[...]. N Engl J Med 2014
356
3

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
163
3


Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline.
Jacques W M Lenders, Quan-Yang Duh, Graeme Eisenhofer, Anne-Paule Gimenez-Roqueplo, Stefan K G Grebe, Mohammad Hassan Murad, Mitsuhide Naruse, Karel Pacak, William F Young. J Clin Endocrinol Metab 2014
889
3

ASHG Statement* on direct-to-consumer genetic testing in the United States.
Kathy Hudson, Gail Javitt, Wylie Burke, Peter Byers. Obstet Gynecol 2007
80
3

Ethical issues in genetic research: disclosure and informed consent.
P R Reilly, M F Boshar, S H Holtzman. Nat Genet 1997
63
3

Real world experience with cancer genetic counseling via telephone.
Rebecca Sutphen, Barbara Davila, Heather Shappell, Tricia Holtje, Susan Vadaparampil, Sue Friedman, Michele Toscano, Joanne Armstrong. Fam Cancer 2010
25
8

Randomized comparison of phone versus in-person BRCA1/2 predisposition genetic test result disclosure counseling.
Jean Jenkins, Kathleen A Calzone, Eileen Dimond, David J Liewehr, Seth M Steinberg, Oxana Jourkiv, Pam Klein, Peter W Soballe, Sheila A Prindiville, Ilan R Kirsch. Genet Med 2007
47
4


Expanding access to BRCA1/2 genetic counseling with telephone delivery: a cluster randomized trial.
Anita Y Kinney, Karin M Butler, Marc D Schwartz, Jeanne S Mandelblatt, Kenneth M Boucher, Lisa M Pappas, Amanda Gammon, Wendy Kohlmann, Sandra L Edwards, Antoinette M Stroup,[...]. J Natl Cancer Inst 2014
70
3

Increased genetic counseling support improves communication of genetic information in families.
Laura E Forrest, Jo Burke, Sonya Bacic, David J Amor. Genet Med 2008
59
3



Genetic testing by cancer site: pancreas.
Jennifer E Axilbund, Elizabeth A Wiley. Cancer J 2012
9
22

Breast cancer risk elements and nurse practitioners' knowledge, use, and perceived comfort level of breast cancer risk assessment.
Quannetta T Edwards, Ann Maradiegue, Diane Seibert, Sherri Saunders-Goldson, Susanne Humphreys. J Am Acad Nurse Pract 2009
18
11


BRCA testing of breast cancer patients: medical specialists' referral patterns, knowledge and attitudes to genetic testing.
E Van Riel, C C Wárlám-Rodenhuis, S Verhoef, E J T H Rutgers, M G E M Ausems. Eur J Cancer Care (Engl) 2010
38
5

Breast-cancer risk in families with mutations in PALB2.
Antonis C Antoniou, Silvia Casadei, Tuomas Heikkinen, Daniel Barrowdale, Katri Pylkäs, Jonathan Roberts, Andrew Lee, Deepak Subramanian, Kim De Leeneer, Florentia Fostira,[...]. N Engl J Med 2014
444
3


Clinical Application of Multigene Panels: Challenges of Next-Generation Counseling and Cancer Risk Management.
Thomas Paul Slavin, Mariana Niell-Swiller, Ilana Solomon, Bita Nehoray, Christina Rybak, Kathleen R Blazer, Jeffrey N Weitzel. Front Oncol 2015
61
3

Clinical evaluation of a multiple-gene sequencing panel for hereditary cancer risk assessment.
Allison W Kurian, Emily E Hare, Meredith A Mills, Kerry E Kingham, Lisa McPherson, Alice S Whittemore, Valerie McGuire, Uri Ladabaum, Yuya Kobayashi, Stephen E Lincoln,[...]. J Clin Oncol 2014
283
3

Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2.
Efrat Gabai-Kapara, Amnon Lahad, Bella Kaufman, Eitan Friedman, Shlomo Segev, Paul Renbaum, Rachel Beeri, Moran Gal, Julia Grinshpun-Cohen, Karen Djemal,[...]. Proc Natl Acad Sci U S A 2014
178
3

Celebrity disclosures and information seeking: the case of Angelina Jolie.
Robin H Juthe, Amber Zaharchuk, Catharine Wang. Genet Med 2015
35
5

Are physicians prepared for whole genome sequencing? a qualitative analysis.
K D Christensen, J L Vassy, L Jamal, L S Lehmann, M J Slashinski, D L Perry, J O Robinson, J Blumenthal-Barby, L Z Feuerman, M F Murray,[...]. Clin Genet 2016
64
3


Impact of presymptomatic genetic testing on young adults: a systematic review.
Lea Godino, Daniela Turchetti, Leigh Jackson, Catherine Hennessy, Heather Skirton. Eur J Hum Genet 2016
27
7


Rapid progression of prostate cancer in men with a BRCA2 mutation.
S A Narod, S Neuhausen, G Vichodez, S Armel, H T Lynch, P Ghadirian, S Cummings, O Olopade, D Stoppa-Lyonnet, F Couch,[...]. Br J Cancer 2008
87
3

Genetic testing for susceptibility to adult-onset cancer. The process and content of informed consent.
G Geller, J R Botkin, M J Green, N Press, B B Biesecker, B Wilfond, G Grana, M B Daly, K Schneider, M J Kahn. JAMA 1997
91
3

Gene-panel sequencing and the prediction of breast-cancer risk.
Douglas F Easton, Paul D P Pharoah, Antonis C Antoniou, Marc Tischkowitz, Sean V Tavtigian, Katherine L Nathanson, Peter Devilee, Alfons Meindl, Fergus J Couch, Melissa Southey,[...]. N Engl J Med 2015
459
3

ACG clinical guideline: Genetic testing and management of hereditary gastrointestinal cancer syndromes.
Sapna Syngal, Randall E Brand, James M Church, Francis M Giardiello, Heather L Hampel, Randall W Burt. Am J Gastroenterol 2015
581
3

Utilization and Outcomes of BRCA Genetic Testing and Counseling in a National Commercially Insured Population: The ABOUT Study.
Joanne Armstrong, Michele Toscano, Nancy Kotchko, Sue Friedman, Marc D Schwartz, Katherine S Virgo, Kristian Lynch, James E Andrews, Claudia X Aguado Loi, Joseph E Bauer,[...]. JAMA Oncol 2015
72
3

The current state of cancer genetic counseling access and availability.
Sara Knapke, Joy Larsen Haidle, Rebecca Nagy, Sara Pirzadeh-Miller. Genet Med 2016
9
22

Psychological distress with direct-to-consumer genetic testing: a case report of an unexpected BRCA positive test result.
Lindsay Dohany, Shanna Gustafson, Whitney Ducaine, Dana Zakalik. J Genet Couns 2012
17
11

Modes of delivery of genetic testing services and the uptake of cancer risk management strategies in BRCA1 and BRCA2 carriers.
T Pal, J-H Lee, A Besharat, Z Thompson, A N A Monteiro, C Phelan, J M Lancaster, K Metcalfe, T A Sellers, S Vadaparampil,[...]. Clin Genet 2014
22
9

High Satisfaction and Low Distress in Breast Cancer Patients One Year after BRCA-Mutation Testing without Prior Face-to-Face Genetic Counseling.
Aisha S Sie, Liesbeth Spruijt, Wendy A G van Zelst-Stams, Arjen R Mensenkamp, Marjolijn J L Ligtenberg, Han G Brunner, Judith B Prins, Nicoline Hoogerbrugge. J Genet Couns 2016
19
10


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.