A citation-based method for searching scientific literature

Martin P Nilsson, Erik D Nilsson, Barbro Silfverberg, Åke Borg, Niklas Loman. Genet Med 2019
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


Determinants of genetic counseling uptake and its impact on breast cancer outcome: a population-based study.
Aurélie Ayme, Valeria Viassolo, Elisabetta Rapiti, Gérald Fioretta, Hyma Schubert, Christine Bouchardy, Pierre O Chappuis, Simone Benhamou. Breast Cancer Res Treat 2014
14
100

BRCA1/2 testing in newly diagnosed breast and ovarian cancer patients without prior genetic counselling: the DNA-BONus study.
Hildegunn Høberg-Vetti, Cathrine Bjorvatn, Bent E Fiane, Turid Aas, Kathrine Woie, Helge Espelid, Tone Rusken, Hans Petter Eikesdal, Wenche Listøl, Marianne T Haavind,[...]. Eur J Hum Genet 2016
37
50


Survival analysis of cancer risk reduction strategies for BRCA1/2 mutation carriers.
Allison W Kurian, Bronislava M Sigal, Sylvia K Plevritis. J Clin Oncol 2010
150
50

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
50

More breast cancer patients prefer BRCA-mutation testing without prior face-to-face genetic counseling.
Aisha S Sie, Wendy A G van Zelst-Stams, Liesbeth Spruijt, Arjen R Mensenkamp, Marjolijn J L Ligtenberg, Han G Brunner, Judith B Prins, Nicoline Hoogerbrugge. Fam Cancer 2014
30
50

Randomized noninferiority trial of telephone versus in-person genetic counseling for hereditary breast and ovarian cancer.
Marc D Schwartz, Heiddis B Valdimarsdottir, Beth N Peshkin, Jeanne Mandelblatt, Rachel Nusbaum, An-Tsun Huang, Yaojen Chang, Kristi Graves, Claudine Isaacs, Marie Wood,[...]. J Clin Oncol 2014
148
50

Melanomas and Mechanical Stress Points on the Plantar Surface of the Foot.
Akane Minagawa, Toshikazu Omodaka, Ryuhei Okuyama. N Engl J Med 2016
38
50

Patient Perceptions of Telephone vs. In-Person BRCA1/BRCA2 Genetic Counseling.
Beth N Peshkin, Scott Kelly, Rachel H Nusbaum, Morgan Similuk, Tiffani A DeMarco, Gillian W Hooker, Heiddis B Valdimarsdottir, Andrea D Forman, Jessica Rispoli Joines, Claire Davis,[...]. J Genet Couns 2016
28
50

BRCAsearch: written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer.
Martin P Nilsson, Therese Törngren, Karin Henriksson, Ulf Kristoffersson, Anders Kvist, Barbro Silfverberg, Åke Borg, Niklas Loman. Breast Cancer Res Treat 2018
8
50

Randomized Noninferiority Trial of Telephone Delivery of BRCA1/2 Genetic Counseling Compared With In-Person Counseling: 1-Year Follow-Up.
Anita Y Kinney, Laurie E Steffen, Barbara H Brumbach, Wendy Kohlmann, Ruofei Du, Ji-Hyun Lee, Amanda Gammon, Karin Butler, Saundra S Buys, Antoinette M Stroup,[...]. J Clin Oncol 2016
61
50

Genetic epidemiology of BRCA mutations--family history detects less than 50% of the mutation carriers.
Pål Møller, Anne Irene Hagen, Jaran Apold, Lovise Maehle, Neal Clark, Bent Fiane, Kjell Løvslett, Eivind Hovig, Anita Vabø. Eur J Cancer 2007
82
50

Screening for founder mutations in BRCA1 and BRCA2 in unselected Jewish women.
Kelly A Metcalfe, Aletta Poll, Robert Royer, Marcia Llacuachaqui, Anna Tulman, Ping Sun, Steven A Narod. J Clin Oncol 2010
109
50

The use of telephone in genetic counseling versus in-person counseling: a randomized study on counselees' outcome.
Ulla Platten, Johanna Rantala, Annika Lindblom, Yvonne Brandberg, Gunilla Lindgren, Brita Arver. Fam Cancer 2012
29
50

Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer.
Martin P Nilsson, Christof Winter, Ulf Kristoffersson, Martin Rehn, Christer Larsson, Lao H Saal, Niklas Loman. Fam Cancer 2017
13
50

Risk-Reducing Surgery in Hereditary Breast and Ovarian Cancer.
Lynn C Hartmann, Noralane M Lindor. N Engl J Med 2016
7
50

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
20
50

Patient satisfaction and cancer-related distress among unselected Jewish women undergoing genetic testing for BRCA1 and BRCA2.
K A Metcalfe, A Poll, M Llacuachaqui, S Nanda, A Tulman, N Mian, P Sun, S A Narod. Clin Genet 2010
37
50

Patient outcomes associated with group and individual genetic counseling formats.
Erin Rothwell, Wendy Kohlmann, Kory Jasperson, Amanda Gammon, Bob Wong, Anita Kinney. Fam Cancer 2012
15
50


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
50

The importance of genetic counselling in genome-wide sequencing.
Alison M Elliott, Jan M Friedman. Nat Rev Genet 2018
16
50

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
115
50

Association of Attending Surgeon With Variation in the Receipt of Genetic Testing After Diagnosis of Breast Cancer.
Steven J Katz, Irina Bondarenko, Kevin C Ward, Ann S Hamilton, Monica Morrow, Allison W Kurian, Timothy P Hofer. JAMA Surg 2018
14
50

Utilization of noninvasive prenatal testing: impact on referrals for diagnostic testing.
John Williams, Steve Rad, Sarah Beauchamp, Dalar Ratousi, Vaishnavi Subramaniam, Sayeh Farivar, Margareta D Pisarska. Am J Obstet Gynecol 2015
50
50



Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.
Lauren E Westerfield, Samantha R Stover, Veena S Mathur, Salma A Nassef, Tiffiney G Carter, Yaping Yang, Christine M Eng, Ignatia B Van den Veyver. Prenat Diagn 2015
29
50

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
78
50

Trends in utilization and costs of BRCA testing among women aged 18-64 years in the United States, 2003-2014.
Zhuo Chen, Katherine Kolor, Scott D Grosse, Juan L Rodriguez, Julie A Lynch, Ridgely Fisk Green, W David Dotson, M Scott Bowen, Muin J Khoury. Genet Med 2018
29
50

Comparing Outcomes of Genetic Counseling Options in Breast and Ovarian Cancer: An Integrative Review
.
Danielle M Fournier, Angela F Bazzell, Joyce E Dains. Oncol Nurs Forum 2018
13
50

Utilization of genetic tests: analysis of gene-specific billing in Medicare claims data.
Julie A Lynch, Brygida Berse, W David Dotson, Muin J Khoury, Nicole Coomer, John Kautter. Genet Med 2017
22
50

BRCA Genetic Testing and Receipt of Preventive Interventions Among Women Aged 18-64 Years with Employer-Sponsored Health Insurance in Nonmetropolitan and Metropolitan Areas - United States, 2009-2014.
Katherine Kolor, Zhuo Chen, Scott D Grosse, Juan L Rodriguez, Ridgely Fisk Green, W David Dotson, M Scott Bowen, Julie A Lynch, Muin J Khoury. MMWR Surveill Summ 2017
19
50

Hereditary colorectal cancer diagnostics in southern Sweden: retrospective evaluation and future considerations with emphasis on Lynch syndrome.
Isabelle Henriksson, Karin Henriksson, Hans Ehrencrona, Samuel Gebre-Medhin. J Community Genet 2019
2
50


The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review.
Nick Dragojlovic, Kennedy Borle, Nicola Kopac, Ursula Ellis, Patricia Birch, Shelin Adam, Jan M Friedman, Amy Nisselle, Alison M Elliott, Larry D Lynd. Genet Med 2020
11
50

Introduction of first trimester combined test increases uptake of Down's syndrome screening.
Gillian M Tringham, Tariq S Nawaz, Stephen Holding, Jane Mcfarlane, Stephen W Lindow. Eur J Obstet Gynecol Reprod Biol 2011
3
50

Playing a part in research? University students' attitudes to direct-to-consumer genomics.
Effy Vayena, Christian Ineichen, Elia Stoupka, Ernst Hafen. Public Health Genomics 2014
19
50


Patient acceptance of non-invasive testing for fetal aneuploidy via cell-free fetal DNA.
Sevan A Vahanian, M Baraa Allaf, Corinne Yeh, Martin R Chavez, Wendy L Kinzler, Anthony M Vintzileos. J Matern Fetal Neonatal Med 2014
14
50


Disparities in genetic services utilization in a random sample of young breast cancer survivors.
Christos Nikolaidis, Debra Duquette, Kari E Mendelsohn-Victor, Beth Anderson, Glenn Copeland, Kara J Milliron, Sofia D Merajver, Nancy K Janz, Laurel L Northouse, Sonia A Duffy,[...]. Genet Med 2019
10
50


Budget impact analysis of comprehensive genomic profiling in patients with advanced non-small cell lung cancer.
James Signorovitch, Zhou Zhou, Jason Ryan, Rachel Anhorn, Anita Chawla. J Med Econ 2019
10
50

Impact of a genetic counseling requirement prior to genetic testing.
David D Stenehjem, Trang Au, Amy M Sainski, Hillevi Bauer, Krystal Brown, Johnathan Lancaster, Vanessa Stevens, Diana I Brixner. BMC Health Serv Res 2018
14
50

Current Practice and Utility of Chromosome Microarray Analysis in Infants Undergoing Cardiac Surgery.
Jason R Buckley, Minoo N Kavarana, Shahryar M Chowdhury, Mark A Scheurer. Congenit Heart Dis 2015
8
50


Chorionic villus sampling in the cell-free DNA aneuploidy screening era: careful selection criteria can maximise the clinical utility of screening and invasive testing.
Stefan C Kane, Karen L Reidy, Fiona Norris, Deborah L Nisbet, Louise H Kornman, Ricardo Palma-Dias. Prenat Diagn 2017
6
50

Readiness of clinical genetic healthcare professionals to provide genomic medicine: An Australian census.
Amy Nisselle, Ivan Macciocca, Fiona McKenzie, Hannah Vuong, Kate Dunlop, Belinda McClaren, Sylvia Metcalfe, Clara Gaff. J Genet Couns 2019
15
50

Guidelines for diagnostic next-generation sequencing.
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur J Hum Genet 2016
226
50


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.