A citation-based method for searching scientific literature

Sharon E Plon, H Paul Cooper, Bethany Parks, Shweta U Dhar, P Adam Kelly, Armin D Weinberg, Stephanie Staggs, Tao Wang, Susan Hilsenbeck. Genet Med 2011
Times Cited: 77







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



Times Cited
  Times     Co-cited
Similarity


Classifying MLH1 and MSH2 variants using bioinformatic prediction, splicing assays, segregation, and tumor characteristics.
Sven Arnold, Daniel D Buchanan, Melissa Barker, Lesley Jaskowski, Michael D Walsh, Genevieve Birney, Michael O Woods, John L Hopper, Mark A Jenkins, Melissa A Brown,[...]. Hum Mutat 2009
52
3

Prediction and assessment of splicing alterations: implications for clinical testing.
Amanda B Spurdle, Fergus J Couch, Frans B L Hogervorst, Paolo Radice, Olga M Sinilnikova. Hum Mutat 2008
89
2

Genetic and histopathologic evaluation of BRCA1 and BRCA2 DNA sequence variants of unknown clinical significance.
Georgia Chenevix-Trench, Sue Healey, Sunil Lakhani, Paul Waring, Margaret Cummings, Ross Brinkworth, Amie M Deffenbaugh, Lynn Anne Burbidge, Dmitry Pruss, Thad Judkins,[...]. Cancer Res 2006
131
2

A timely arrival for genomic medicine.
Alan N Mayer, David P Dimmock, Marjorie J Arca, David P Bick, James W Verbsky, Elizabeth A Worthey, Howard J Jacob, David A Margolis. Genet Med 2011
55
3



Feasibility of screening for Lynch syndrome among patients with colorectal cancer.
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Mark Clendenning, Kaisa Sotamaa, Thomas Prior, Judith A Westman,[...]. J Clin Oncol 2008
523
2

Impact of BRCA1/BRCA2 counseling and testing on newly diagnosed breast cancer patients.
Marc D Schwartz, Caryn Lerman, Barbara Brogan, Beth N Peshkin, Chanita Hughes Halbert, Tiffani DeMarco, William Lawrence, David Main, Clinton Finch, Colette Magnant,[...]. J Clin Oncol 2004
189
2

Clinical genetics issues encountered by family physicians.
Louise S Acheson, Kurt C Stange, Stephen Zyzanski. Genet Med 2005
42
4

Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients.
Heather Hampel, Wendy Frankel, Jenny Panescu, Janet Lockman, Kaisa Sotamaa, Daniel Fix, Ilene Comeras, Jennifer La Jeunesse, Hidewaki Nakagawa, Judith A Westman,[...]. Cancer Res 2006
376
2

Inhibition of poly(ADP-ribose) polymerase in tumors from BRCA mutation carriers.
Peter C Fong, David S Boss, Timothy A Yap, Andrew Tutt, Peijun Wu, Marja Mergui-Roelvink, Peter Mortimer, Helen Swaisland, Alan Lau, Mark J O'Connor,[...]. N Engl J Med 2009
2


Screening for the Lynch syndrome (hereditary nonpolyposis colorectal cancer).
Heather Hampel, Wendy L Frankel, Edward Martin, Mark Arnold, Karamjit Khanduja, Philip Kuebler, Hidewaki Nakagawa, Kaisa Sotamaa, Thomas W Prior, Judith Westman,[...]. N Engl J Med 2005
889
2

An integrative model of shared decision making in medical encounters.
Gregory Makoul, Marla L Clayman. Patient Educ Couns 2006
774
2

Physicians' reactions to uncertainty in the context of shared decision making.
Mary C Politi, France Légaré. Patient Educ Couns 2010
43
4

Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.
Susanne B Haga, Madeline M Carrig, Julianne M O'Daniel, Lori A Orlando, Ley A Killeya-Jones, Geoffrey S Ginsburg, Alex Cho. J Gen Intern Med 2011
52
3

Physicians' propensity to offer genetic testing for Alzheimer's disease: results from a survey.
Gary A Chase, Gail Geller, Suzanne L Havstad, Neil A Holtzman, Susan Spear Bassett. Genet Med 2002
19
10

Use of cancer susceptibility testing among primary care physicians.
R Sifri, R Myers, T Hyslop, B Turner, J Cocroft, T Rothermel, J Grana, N Schlackman. Clin Genet 2003
40
5

Genetic evaluation of cardiomyopathy--a Heart Failure Society of America practice guideline.
Ray E Hershberger, Joann Lindenfeld, Luisa Mestroni, Christine E Seidman, Matthew R G Taylor, Jeffrey A Towbin. J Card Fail 2009
303
2


Increased uptake of BRCA1/2 genetic testing among African American women with a recent diagnosis of breast cancer.
Lisa R Susswein, Cécile Skrzynia, Leslie A Lange, Jessica K Booker, Mark L Graham, James P Evans. J Clin Oncol 2008
42
4

Genetic counseling and testing for Alzheimer disease: joint practice guidelines of the American College of Medical Genetics and the National Society of Genetic Counselors.
Jill S Goldman, Susan E Hahn, Jennifer Williamson Catania, Susan LaRusse-Eckert, Melissa Barber Butson, Malia Rumbaugh, Michelle N Strecker, J Scott Roberts, Wylie Burke, Richard Mayeux,[...]. Genet Med 2011
158
2


Integrated analysis of unclassified variants in mismatch repair genes.
Chiara Pastrello, Elisa Pin, Fabio Marroni, Chiara Bedin, Mara Fornasarig, Maria Grazia Tibiletti, Cristina Oliani, Maurizio Ponz de Leon, Emanuele Damiano Urso, Lara Della Puppa,[...]. Genet Med 2011
30
6

Polymorphisms in genes of nucleotide and base excision repair: risk and prognosis of colorectal cancer.
Victor Moreno, Federica Gemignani, Stefano Landi, Lydie Gioia-Patricola, Amélie Chabrier, Ignacio Blanco, Sara González, Elisabet Guino, Gabriel Capellà, Federico Canzian. Clin Cancer Res 2006
195
2


An analysis of the causes of adverse events from the Quality in Australian Health Care Study.
R M Wilson, B T Harrison, R W Gibberd, J D Hamilton. Med J Aust 1999
192
2


Human genome sequencing in health and disease.
Claudia Gonzaga-Jauregui, James R Lupski, Richard A Gibbs. Annu Rev Med 2012
252
2

Family physicians' awareness and knowledge of the Genetic Information Non-Discrimination Act (GINA).
Amanda L Laedtke, Suzanne M O'Neill, Wendy S Rubinstein, Kristen J Vogel. J Genet Couns 2012
36
5




Genomic medicine: who will practice it? A call to open arms.
A E Guttmacher, J Jenkins, W R Uhlmann. Am J Med Genet 2001
70
2

Understanding adverse events: human factors.
J Reason. Qual Health Care 1995
257
2

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.
Jennifer J Johnston, Wendy S Rubinstein, Flavia M Facio, David Ng, Larry N Singh, Jamie K Teer, James C Mullikin, Leslie G Biesecker. Am J Hum Genet 2012
155
2


The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.
A C Antoniou, A P Cunningham, J Peto, D G Evans, F Lalloo, S A Narod, H A Risch, J E Eyfjord, J L Hopper, M C Southey,[...]. Br J Cancer 2008
295
2

Getting to the point: what women newly diagnosed with breast cancer want to know about treatment-focused genetic testing.
Bettina Meiser, Margaret Gleeson, Kaaren Watts, Michelle Peate, Elvira Zilliacus, Kristine Barlow-Stewart, Christobel Saunders, Gillian Mitchell, Judy Kirk. Oncol Nurs Forum 2012
22
9


Differences and similarities in breast cancer risk assessment models in clinical practice: which model to choose?
Catharina E Jacobi, Geertruida H de Bock, Bob Siegerink, Christi J van Asperen. Breast Cancer Res Treat 2009
53
3

Characteristics of health information gatherers, disseminators, and blockers within families at risk of hereditary cancer: implications for family health communication interventions.
Laura M Koehly, June A Peters, Regina Kenen, Lindsey M Hoskins, Anne L Ersig, Natalia R Kuhn, Jennifer T Loud, Mark H Greene. Am J Public Health 2009
102
2

Communicating genetic risk information within families: a review.
Mel Wiseman, Caroline Dancyger, Susan Michie. Fam Cancer 2010
71
2

Family communication about positive BRCA1 and BRCA2 genetic test results.
Bobbi McGivern, Jessica Everett, Geoffrey G Yager, Robert C Baumiller, Amanda Hafertepen, Howard M Saal. Genet Med 2004
87
2

Communication of BRCA results and family testing in 1,103 high-risk women.
Eleanor L Cheung, Ashley D Olson, Tina M Yu, Pamela Z Han, Mary S Beattie. Cancer Epidemiol Biomarkers Prev 2010
53
3

Selecting a BRCA risk assessment model for use in a familial cancer clinic.
Seema M Panchal, Marguerite Ennis, Sandra Canon, Louise J Bordeleau. BMC Med Genet 2008
31
6

Clinical genetics provider real-time workflow study.
Elizabeth McPherson, Christina Zaleski, Katrina Benishek, Catherine A McCarty, Philip F Giampietro, Kara Reynolds, Kristen Rasmussen. Genet Med 2008
40
5

Use and interpretation of genetic tests in cardiovascular genetics.
Colleen Caleshu, Sharlene Day, Heidi L Rehm, Samantha Baxter. Heart 2010
31
6

Oncology nurses' knowledge, practice, and educational needs regarding cancer genetics.
S K Peterson, P T Rieger, S K Marani, C deMoor, E R Gritz. Am J Med Genet 2001
21
9

Direct to confusion: lessons learned from marketing BRCA testing.
Ellen Matloff, Arthur Caplan. Am J Bioeth 2008
47
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.