A citation-based method for searching scientific literature

J L Hopper, M A Jenkins, J G Dowty, G S Dite, C Apicella, L Keogh, A K Win, J P Young, D Buchanan, M D Walsh, C Rosty, L Baglietto, G Severi, K A Phillips, E M Wong, A Dobrovic, P Waring, I Winship, S J Ramus, G G Giles, M C Southey. Pathology 2012
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


Morphological predictors of BRCA1 germline mutations in young women with breast cancer.
M C Southey, S J Ramus, J G Dowty, L D Smith, A A Tesoriero, E E M Wong, G S Dite, M A Jenkins, G B Byrnes, I Winship,[...]. Br J Cancer 2011
31
50

Colorectal and other cancer risks for carriers and noncarriers from families with a DNA mismatch repair gene mutation: a prospective cohort study.
Aung Ko Win, Joanne P Young, Noralane M Lindor, Katherine M Tucker, Dennis J Ahnen, Graeme P Young, Daniel D Buchanan, Mark Clendenning, Graham G Giles, Ingrid Winship,[...]. J Clin Oncol 2012
207
33

Use of molecular tumor characteristics to prioritize mismatch repair gene testing in early-onset colorectal cancer.
Melissa C Southey, Mark A Jenkins, Leeanne Mead, Jonathan Whitty, Melanie Trivett, Andrea A Tesoriero, Letitia D Smith, Kim Jennings, Garry Grubb, Simon G Royce,[...]. J Clin Oncol 2005
171
33

Tumour morphology of early-onset breast cancers predicts breast cancer risk for first-degree relatives: the Australian Breast Cancer Family Registry.
Gillian S Dite, Enes Makalic, Daniel F Schmidt, Graham G Giles, John L Hopper, Melissa C Southey. Breast Cancer Res 2012
9
33


Screening for diabetes.
K Backholer, L Chen, J Shaw. Pathology 2012
6
16


The relationships between interest for and participation in health screening and risk of mortality: the Japan Collaborative Cohort Study.
Ai Ikeda, Hiroyasu Iso, Hideaki Toyoshima, Yoshihisa Fujino, Tetsuya Mizoue, Takesumi Yoshimura, Yutaka Inaba, Akiko Tamakoshi. Prev Med 2005
17
16


Screening for lipid disorders.
Damon A Bell, Amanda J Hooper, Robert Bender, Glenn Edwards, Frank M van Bockxmeer, Gerald F Watts, John R Burnett. Pathology 2012
4
25

Prostate cancer screening.
Ken Sikaris. Pathology 2012
7
16



Influence of malpractice history on the practice of screening and surveillance for Barrett's esophagus.
Joel H Rubenstein, Sameer D Saini, Latoya Kuhn, Laurence McMahon, Pratima Sharma, Darrell S Pardi, Philip Schoenfeld. Am J Gastroenterol 2008
27
16


Screening for familial hypercholesterolaemia.
Robert Bender, Damon A Bell, Amanda J Hooper, Glenn Edwards, Frank M van Bockxmeer, Gerald F Watts, John R Burnett. Pathology 2012
24
16

A vision of the future of newborn screening.
Duane Alexander, Peter C van Dyck. Pediatrics 2006
60
16

The ethics of screening for disease.
Martin B Delatycki. Pathology 2012
8
16


Screening for hereditary haemochromatosis.
Itty M Nadakkavukaran, Eng K Gan, John K Olynyk. Pathology 2012
14
16





The effectiveness of family history questionnaires in cancer genetic counseling.
Susan Randall Armel, Jeanna McCuaig, Amy Finch, Rochelle Demsky, Tony Panzarella, Joan Murphy, Barry Rosen. J Genet Couns 2009
18
16

Collection and use of cancer family history in primary care.
Nadeem Qureshi, Brenda Wilson, Pasqualina Santaguida, June Carroll, Judith Allanson, Carolina Ruiz Culebro, Melissa Brouwers, Parminder Raina. Evid Rep Technol Assess (Full Rep) 2007
49
16

Barriers to participating in genetic counseling and BRCA testing during primary treatment for breast cancer.
Kathryn J Schlich-Bakker, Herman F J ten Kroode, Carla C Wárlám-Rodenhuis, Jan van den Bout, Margreet G E M Ausems. Genet Med 2007
54
16

Validity of self reported diagnoses of cancer in a major Spanish prospective cohort study.
C Navarro, M D Chirlaque, M J Tormo, D Pérez-Flores, M Rodríguez-Barranco, A Sánchez-Villegas, A Agudo, G Pera, P Amiano, M Dorronsoro,[...]. J Epidemiol Community Health 2006
33
16

The use of family history questionnaires: an examination of genetic risk estimates and genetic testing eligibility in the non-responder population.
Susan Randall Armel, Kara Hitchman, Kathryn Millar, Laura Zahavich, Rochelle Demsky, Joan Murphy, Barry Rosen. J Genet Couns 2011
4
25

Consistency of self-reported first-degree family history of cancer in a population-based study.
Fernanda Lenara Roth, Suzi Alves Camey, Maira Caleffi, Lavínia Schuler-Faccini, Edenir Inêz Palmero, Carla Bochi, Susana Mayer Moreira, Luciane Kalakun, Roberto Giugliani, Patrícia Ashton-Prolla. Fam Cancer 2009
16
16

Psychological and genetic counseling implications for adolescent daughters of mothers with breast cancer.
M Cappelli, S Verma, Y Korneluk, A Hunter, E Tomiak, J Allanson, C DeGrasse, L Corsini, L Humphreys. Clin Genet 2005
35
16

The prevalence of a family history of cancer in general practice.
N Johnson, T Lancaster, A Fuller, S V Hodgson. Fam Pract 1995
37
16

The accuracy of diagnoses as reported in families with cancer: a retrospective study.
F S Douglas, L C O'Dair, M Robinson, D G Evans, S A Lynch. J Med Genet 1999
90
16

Limited family structure and BRCA gene mutation status in single cases of breast cancer.
Jeffrey N Weitzel, Veronica I Lagos, Carey A Cullinane, Patricia J Gambol, Julie O Culver, Kathleen R Blazer, Melanie R Palomares, Katrina J Lowstuter, Deborah J MacDonald. JAMA 2007
130
16

Clinically relevant changes in family history of cancer over time.
Argyrios Ziogas, Nora K Horick, Anita Y Kinney, Jan T Lowery, Susan M Domchek, Claudine Isaacs, Constance A Griffin, Patricia G Moorman, Karen L Edwards, Deirdre A Hill,[...]. JAMA 2011
34
16

Cancer family history reporting: impact of method and psychosocial factors.
Kimberly M Kelly, Randi Shedlosky-Shoemaker, Kyle Porter, Amber Remy, Philip DeSimone, Michael A Andrykowski. J Genet Couns 2007
19
16

The current state of cancer family history collection tools in primary care: a systematic review.
Nadeem Qureshi, June C Carroll, Brenda Wilson, Pasqualina Santaguida, Judith Allanson, Melissa Brouwers, Parminder Raina. Genet Med 2009
68
16

Accuracy of reporting of family history of colorectal cancer.
R J Mitchell, D Brewster, H Campbell, M E M Porteous, A H Wyllie, C C Bird, M G Dunlop. Gut 2004
148
16

Establishing a family risk assessment clinic for breast cancer.
Jurgen Mulsow, James Lee, Cathriona Dempsey, Jane Rothwell, James G Geraghty. Breast J 2009
6
16

Factors influencing patients' decisions to decline cancer genetic counseling services.
K P Geer, M E Ropka, W F Cohn, S M Jones, S Miesfeldt. J Genet Couns 2001
62
16

Log odds of carrying an Ancestral Mutation in BRCA1 or BRCA2 for a Defined personal and family history in an Ashkenazi Jewish woman (LAMBDA).
Carmel Apicella, Lesley Andrews, Shirley V Hodgson, Sheila A Fisher, Cathryn M Lewis, Ellen Solomon, Katherine Tucker, Michael Friedlander, Agnes Bankier, Melissa C Southey,[...]. Breast Cancer Res 2003
32
16

PALB2/FANCN: recombining cancer and Fanconi anemia.
Marc Tischkowitz, Bing Xia. Cancer Res 2010
122
16

Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women.
William D Foulkes, Parviz Ghadirian, Mohammed Reza Akbari, Nancy Hamel, Sylvie Giroux, Nelly Sabbaghian, Andrew Darnel, Robert Royer, Aletta Poll, Eve Fafard,[...]. Breast Cancer Res 2007
105
16

A PALB2 germline mutation associated with hereditary breast cancer in Italy.
Laura Papi, Anna Laura Putignano, Caterina Congregati, Irene Piaceri, Ines Zanna, Francesco Sera, Doralba Morrone, Maurizio Genuardi, Domenico Palli. Fam Cancer 2010
37
16

Population-based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066-6T>G (IVS10-6T>G) from the Breast Cancer Family Registry.
J L Bernstein, S Teraoka, M C Southey, M A Jenkins, I L Andrulis, J A Knight, E M John, R Lapinski, A L Wolitzer, A S Whittemore,[...]. Hum Mutat 2006
66
16

Analysis of cancer risk and BRCA1 and BRCA2 mutation prevalence in the kConFab familial breast cancer resource.
Graham J Mann, Heather Thorne, Rosemary L Balleine, Phyllis N Butow, Christine L Clarke, Edward Edkins, Gerda M Evans, Sián Fereday, Eric Haan, Michael Gattas,[...]. Breast Cancer Res 2006
124
16

The Breast Cancer Family Registry: an infrastructure for cooperative multinational, interdisciplinary and translational studies of the genetic epidemiology of breast cancer.
Esther M John, John L Hopper, Jeanne C Beck, Julia A Knight, Susan L Neuhausen, Ruby T Senie, Argyrios Ziogas, Irene L Andrulis, Hoda Anton-Culver, Norman Boyd,[...]. Breast Cancer Res 2004
234
16

Interobserver agreement and reproducibility in classification of invasive breast carcinoma: an NCI breast cancer family registry study.
Teri A Longacre, Marguerite Ennis, Louise A Quenneville, Anita L Bane, Ira J Bleiweiss, Beverley A Carter, Edison Catelano, Michael R Hendrickson, Hanina Hibshoosh, Lester J Layfield,[...]. Mod Pathol 2006
77
16

Relationship of patients' age to histopathological features of breast tumours in BRCA1 and BRCA2 and mutation-negative breast cancer families.
Hannaleena Eerola, Päivi Heikkilä, Anitta Tamminen, Kristiina Aittomäki, Carl Blomqvist, Heli Nevanlinna. Breast Cancer Res 2005
44
16

Histological features of medullary carcinoma and prognosis in triple-negative basal-like carcinomas of the breast.
Felicia Marginean, Emad A Rakha, Bernard C Ho, Ian O Ellis, Andrew H S Lee. Mod Pathol 2010
26
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.