A citation-based method for searching scientific literature

Megan Latchaw, Kelly Ormond, Maureen Smith, John Richardson, Catherine Wicklund. Genet Med 2010
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


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
20
38


Eligibility criteria in private and public coverage policies for BRCA genetic testing and genetic counseling.
Grace Wang, Mary S Beattie, Ninez A Ponce, Kathryn A Phillips. Genet Med 2011
31
30

Factors influencing health insurers' decisions to cover new genetic technologies.
M M Schoonmaker, B A Bernhardt, N A Holtzman. Int J Technol Assess Health Care 2000
21
23

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
16
23

American Society of Clinical Oncology policy statement update: genetic and genomic testing for cancer susceptibility.
Mark E Robson, Courtney D Storm, Jeffrey Weitzel, Dana S Wollins, Kenneth Offit. J Clin Oncol 2010
298
15




Genetic testing insurance coverage trends: a review of publicly available policies from the largest US payers.
Michael D Graf, Denise F Needham, Nicole Teed, Trisha Brown. Per Med 2013
30
15

The cost of genetic testing for ocular disease: who pays?
Jenina E Capasso. Curr Opin Ophthalmol 2014
16
15



Exploring barriers to payer utilization of genetic counselors.
Nan Doyle, Allison Cirino, Amber Trivedi, Maureen Flynn. J Genet Couns 2015
7
28

Systematic review: family history in risk assessment for common diseases.
Brenda J Wilson, Nadeem Qureshi, Pasqualina Santaguida, Julian Little, June C Carroll, Judith Allanson, Parminder Raina. Ann Intern Med 2009
84
7


Reconsidering the family history in primary care.
Eugene C Rich, Wylie Burke, Caryl J Heaton, Susanne Haga, Linda Pinsky, M Priscilla Short, Louise Acheson. J Gen Intern Med 2004
231
7

Coverage of new genetic technologies: what matters to insurers?
M Schoonmaker, B Bernhardt, N A Holtzman. Am J Hum Genet 1996
5
20


Genetic assessment of breast cancer risk in primary care practice.
Wylie Burke, Julie Culver, Linda Pinsky, Sarah Hall, Susan E Reynolds, Yutaka Yasui, Nancy Press. Am J Med Genet A 2009
53
7


Comparison between US Preventive Services Task Force recommendations and Medicare coverage.
Lenard I Lesser, Alex H Krist, Douglas B Kamerow, Andrew W Bazemore. Ann Fam Med 2011
18
7

Economic considerations for health insurance coverage of emerging genetic tests.
Mita Giacomini, Fiona Miller, Bernie J O'Brien. Community Genet 2003
17
7

The role of financial factors in acceptance of clinical BRCA genetic testing.
Shannon Kieran, Lois J Loescher, Kyung Hee Lim. Genet Test 2007
32
7

Family history of cancer: is it an accurate indicator of cancer risk in the immigrant population?
Heather Orom, Michele L Coté, Hector M González, Willie Underwood, Ann G Schwartz. Cancer 2008
21
7

Cancer risk assessment: examining the family physician's role.
Carl V Tyler, Clint W Snyder. J Am Board Fam Med 2006
46
7

Health plans' coverage determinations for technology-based interventions: the case of electrical bone growth stimulation.
Alison J Huang, Marcel P Gemperli, Linda Bergthold, Sara S Singer, Alan Garber. Am J Manag Care 2004
7
14

Toward evidence-based assessment for coverage and reimbursement of laboratory-based diagnostic and genetic tests.
Scott D Ramsey, David L Veenstra, Louis P Garrison, Rick Carlson, Paul Billings, Josh Carlson, Sean D Sullivan. Am J Manag Care 2006
22
7

National Institutes of Health State-of-the-Science Conference Statement: Family History and Improving Health.
Alfred O Berg, Macaran A Baird, Jeffrey R Botkin, Deborah A Driscoll, Paul A Fishman, Peter D Guarino, Robert A Hiatt, Gail P Jarvik, Sandra Millon-Underwood, Thomas M Morgan,[...]. Ann Intern Med 2009
124
7


Utilization of BRCA1/2 genetic testing in the clinical setting: report from a single institution.
Soo-Chin Lee, Barbara A Bernhardt, Kathy J Helzlsouer. Cancer 2002
46
7

Cancer risk assessment from family history: gaps in primary care practice.
Randa D Sifri, Richard Wender, Nina Paynter. J Fam Pract 2002
37
7

The interface of Medicare coverage decision-making and emerging molecular-based laboratory testing.
Mitchell I Burken, Kathleen S Wilson, Karen Heller, Victoria M Pratt, Michele M Schoonmaker, Eric Seifter. Genet Med 2009
8
12

A coding VKORC1 Asp36Tyr polymorphism predisposes to warfarin resistance.
Ronen Loebstein, Ilana Dvoskin, Hillel Halkin, Manuela Vecsler, Aharon Lubetsky, Gideon Rechavi, Ninette Amariglio, Yoram Cohen, Gie Ken-Dror, Shlomo Almog,[...]. Blood 2007
122
7


Practice parameter: screening and diagnosis of autism: report of the Quality Standards Subcommittee of the American Academy of Neurology and the Child Neurology Society.
P A Filipek, P J Accardo, S Ashwal, G T Baranek, E H Cook, G Dawson, B Gordon, J S Gravel, C P Johnson, R J Kallen,[...]. Neurology 2000
477
7

Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: a systematic review.
L Correia Guedes, J J Ferreira, M M Rosa, M Coelho, V Bonifati, C Sampaio. Parkinsonism Relat Disord 2010
98
7

Clinical genetic testing for patients with autism spectrum disorders.
Yiping Shen, Kira A Dies, Ingrid A Holm, Carolyn Bridgemohan, Magdi M Sobeih, Elizabeth B Caronna, Karen J Miller, Jean A Frazier, Iris Silverstein, Jonathan Picker,[...]. Pediatrics 2010
243
7

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
7





Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study.
Daniel G Healy, Mario Falchi, Sean S O'Sullivan, Vincenzo Bonifati, Alexandra Durr, Susan Bressman, Alexis Brice, Jan Aasly, Cyrus P Zabetian, Stefano Goldwurm,[...]. Lancet Neurol 2008
927
7

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
7

Lost in transition: challenges in the expanding field of adult genetics.
Matthew R G Taylor, Janice G Edwards, Lisa Ku. Am J Med Genet C Semin Med Genet 2006
38
7

The path to personalized medicine.
Margaret A Hamburg, Francis S Collins. N Engl J Med 2010
962
7





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.