A citation-based method for searching scientific literature

M Cappelli, M J Esplen, B J Wilson, M Dorval, J L Bottorff, M Ly, J C Carroll, J Allanson, E Humphreys, D Rayson. Clin Genet 2009
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Psychosocial impact of specialized cardiac genetic clinics for hypertrophic cardiomyopathy.
Jodie Ingles, Joanne M Lind, Philayrath Phongsavan, Christopher Semsarian. Genet Med 2008
74
66


Identifying and testing for hereditary susceptibility to common cancers.
Randa Sifri, Sarita Gangadharappa, Louise S Acheson. CA Cancer J Clin 2004
26
33

The psychotherapy of genetics.
Susan H McDaniel. Fam Process 2005
36
33


Methodological issues in the recruitment of cancer pain patients and their caregivers.
Sean Ransom, Lora M Azzarello, Susan C McMillan. Res Nurs Health 2006
29
33

Psychosocial issues in genetic testing for familial adenomatous polyposis: a review of the literature.
K F L Douma, N K Aaronson, H F A Vasen, E M A Bleiker. Psychooncology 2008
33
33

A literature review of the psychological impact of genetic testing on breast cancer patients.
Kathryn J Schlich-Bakker, Herman F J ten Kroode, Margreet G E M Ausems. Patient Educ Couns 2006
63
33



Improving service evaluation in clinical genetics: identifying effects of genetic diseases on individuals and families.
Marion McAllister, Katherine Payne, Stuart Nicholls, Rhona MacLeod, Dian Donnai, Linda M Davies. J Genet Couns 2007
35
33


proFamilies: a psycho-educational multi-family group intervention for cancer patients and their families.
R Chiquelho, S Neves, A Mendes, A P Relvas, L Sousa. Eur J Cancer Care (Engl) 2011
17
33

Interest in and barriers to participation in multiple family groups among head and neck cancer survivors and their primary family caregivers.
Jamie Ostroff, Stephanie Ross, Peter Steinglass, Victor Ronis-Tobin, Bhuvanesh Singh. Fam Process 2004
46
33


Family issues in a psychoeducation group for women with a BRCA mutation.
J Speice, S H McDaniel, P T Rowley, S Loader. Clin Genet 2002
36
33

A multicenter study of supportive-expressive group therapy for women with BRCA1/BRCA2 mutations.
Mary Jane Esplen, Jon Hunter, Molyn Leszcz, Ellen Warner, Steven Narod, Kelly Metcalfe, Gord Glendon, Kate Butler, Alexander Liede, Mary Anne Young,[...]. Cancer 2004
44
33

Experiencing genetic counselling for hereditary cancers: the client's perspective.
A F Mendes, T A Santos, L Sousa. Eur J Cancer Care (Engl) 2011
14
33

Long QT syndrome.
Ilan Goldenberg, Arthur J Moss. J Am Coll Cardiol 2008
295
33

Quality of life and psychological status of patients with implantable cardioverter defibrillators.
Sue Ann Thomas, Erika Friedmann, Chi-Wen Kao, Pia Inguito, Matthew Metcalf, Frances J Kelley, Steven S Gottlieb. Am J Crit Care 2006
73
33

Living with long QT syndrome: a qualitative study of coping with increased risk of sudden cardiac death.
Janice Andersen, Nina Øyen, Cathrine Bjorvatn, Eva Gjengedal. J Genet Couns 2008
28
33

Collaborative care for depression: a cumulative meta-analysis and review of longer-term outcomes.
Simon Gilbody, Peter Bower, Janine Fletcher, David Richards, Alex J Sutton. Arch Intern Med 2006
873
33

The short- and long-term impact of multi-disciplinary clinics in addition to standard nephrology care on patient outcomes.
Bryan M Curtis, Pietro Ravani, F Malberti, Fiona Kennett, Paul A Taylor, Ognjenka Djurdjev, Adeera Levin. Nephrol Dial Transplant 2005
143
33


Models of comprehensive multidisciplinary care for individuals in the United States with genetic disorders.
Scott D Grosse, Michael S Schechter, Roshni Kulkarni, Michele A Lloyd-Puryear, Bonnie Strickland, Edwin Trevathan. Pediatrics 2009
103
33

Standards of care for patients with cystic fibrosis: a European consensus.
Eitan Kerem, Steven Conway, Stuart Elborn, Harry Heijerman. J Cyst Fibros 2005
248
33

Incorporating a Psychological Counselor in a Cancer Risk Assessment Program: Necessity, Acceptability, and Potential Roles.
Alicia K Matthews, Dana L Brandenburg, Shelly Cummings, Olufunmilayo I Olopade. J Genet Couns 2002
7
33

Novel one-stop multidisciplinary follow-up clinic significantly improves cancer risk management in BRCA1/2 carriers.
G Pichert, C Jacobs, I Jacobs, U Menon, R Manchanda, M Johnson, H Hamed, C Firth, M Evison, A Tutt,[...]. Fam Cancer 2010
12
33

Clinical practice. Long-QT syndrome.
Dan M Roden. N Engl J Med 2008
268
33


Recurrence rates for sudden infant death syndrome (SIDS): the importance of risk stratification.
M J Campbell, D Hall, T Stephenson, C Bacon, J Madan. Arch Dis Child 2008
5
33

Improving access to breast health services with an interdisciplinary model of care.
Mario R Castellanos, Joseph Conte, Dina Abi Fadel, Carolyn Raia, Frank Forte, Kathleen Ahern, Marianne Smith, Danny Elsayeh, Shalom Buchbinder. Breast J 2008
15
33


The science of team science: overview of the field and introduction to the supplement.
Daniel Stokols, Kara L Hall, Brandie K Taylor, Richard P Moser. Am J Prev Med 2008
252
33

Role of congenital long-QT syndrome in unexplained sudden infant death: proposal for an electrocardiographic screening in relatives.
Alban-Elouen Baruteau, Julien Baruteau, Ryad Joomye, Raphael Martins, Frédéric Treguer, Remi Baruteau, Jean-Claude Daubert, Philippe Mabo, Michel Roussey. Eur J Pediatr 2009
7
33

Preferences of cardiologists and clinical geneticists for the future organization of genetic care in hypertrophic cardiomyopathy: a survey.
I M van Langen, E Birnie, E Schuurman, H L Tan, N Hofman, G J Bonsel, A A M Wilde. Clin Genet 2005
16
33

Experience over fifteen years with a protocol for predictive testing for Huntington disease.
Suzanne Dufrasne, Madeleine Roy, Maria Galvez, David S Rosenblatt. Mol Genet Metab 2011
54
33

Effectiveness of a multidisciplinary clinic in managing children with chronic kidney disease.
Shina Menon, Rudolph P Valentini, Gaurav Kapur, Sandra Layfield, Tej K Mattoo. Clin J Am Soc Nephrol 2009
34
33


Prevalence of long-QT syndrome gene variants in sudden infant death syndrome.
Marianne Arnestad, Lia Crotti, Torleiv O Rognum, Roberto Insolia, Matteo Pedrazzini, Chiara Ferrandi, Ashild Vege, Dao W Wang, Troy E Rhodes, Alfred L George,[...]. Circulation 2007
336
33


Good care for people with cystic fibrosis.
J M Littlewood. Paediatr Respir Rev 2000
8
33

Genetic counseling and cardiac care in predictively tested hypertrophic cardiomyopathy mutation carriers: the patients' perspective.
Imke Christiaans, Irene M van Langen, Erwin Birnie, Gouke J Bonsel, Arthur A M Wilde, Ellen M A Smets. Am J Med Genet A 2009
42
33

Clinical considerations for allied professionals: ethical issues in cardiogenetics.
Michelle A Mullen, Christina R Honeywell, Robert M Gow. Heart Rhythm 2007
1
100


Impact of MYH6 variants in hypoplastic left heart syndrome.
Aoy Tomita-Mitchell, Karl D Stamm, Donna K Mahnke, Min-Su Kim, Pip M Hidestrand, Huan Ling Liang, Mary A Goetsch, Mats Hidestrand, Pippa Simpson, Andrew N Pelech,[...]. Physiol Genomics 2016
45
33

A Screening Approach to Identify Clinically Actionable Variants Causing Congenital Heart Disease in Exome Data.
Justin O Szot, Hartmut Cuny, Gillian M Blue, David T Humphreys, Eddie Ip, Katrina Harrison, Gary F Sholler, Eleni Giannoulatou, Paul Leo, Emma L Duncan,[...]. Circ Genom Precis Med 2018
45
33

Interdisciplinary psychosocial care for families with inherited cardiovascular diseases.
Colleen Caleshu, Nadine A Kasparian, Katharine S Edwards, Laura Yeates, Christopher Semsarian, Marco Perez, Euan Ashley, Christian J Turner, Joshua W Knowles, Jodie Ingles. Trends Cardiovasc Med 2016
38
33

Three year experience of a clinical cardiovascular genetics program for infants with congenital heart disease.
Gabrielle C Geddes, Erin Syverson, Michael G Earing. Congenit Heart Dis 2019
5
33

Genetic counseling in congenital heart disease.
Karlene B Coleman. Crit Care Nurs Q 2002
5
33


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.