A citation-based method for searching scientific literature

B Downe-Wamboldt. Health Care Women Int 1992
Times Cited: 643







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



Times Cited
  Times     Co-cited
Similarity



Three approaches to qualitative content analysis.
Hsiu-Fang Hsieh, Sarah E Shannon. Qual Health Res 2005
22

The qualitative content analysis process.
Satu Elo, Helvi Kyngäs. J Adv Nurs 2008
16


Content analysis: review of methods and their applications in nutrition education.
Nancy L Kondracki, Nancy S Wellman, Daniel R Amundson. J Nutr Educ Behav 2002
293
7

Methodological challenges in qualitative content analysis: A discussion paper.
Ulla H Graneheim, Britt-Marie Lindgren, Berit Lundman. Nurse Educ Today 2017
506
7

Standards for reporting qualitative research: a synthesis of recommendations.
Bridget C O'Brien, Ilene B Harris, Thomas J Beckman, Darcy A Reed, David A Cook. Acad Med 2014
5



Meeting the challenges of implementing rapid genomic testing in acute pediatric care.
Zornitza Stark, Sebastian Lunke, Gemma R Brett, Natalie B Tan, Rachel Stapleton, Smitha Kumble, Alison Yeung, Dean G Phelan, Belinda Chong, Miriam Fanjul-Fernandez,[...]. Genet Med 2018
65
6

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
32
12

Effectiveness of exome and genome sequencing guided by acuity of illness for diagnosis of neurodevelopmental disorders.
Sarah E Soden, Carol J Saunders, Laurel K Willig, Emily G Farrow, Laurie D Smith, Josh E Petrikin, Jean-Baptiste LePichon, Neil A Miller, Isabelle Thiffault, Darrell L Dinwiddie,[...]. Sci Transl Med 2014
309
4

Content analysis and thematic analysis: Implications for conducting a qualitative descriptive study.
Mojtaba Vaismoradi, Hannele Turunen, Terese Bondas. Nurs Health Sci 2013
4


What's in a name? Qualitative description revisited.
Margarete Sandelowski. Res Nurs Health 2010
3



Points to consider for laboratories reporting results from diagnostic genomic sequencing.
D F Vears, K Sénécal, A J Clarke, L Jackson, A M Laberge, L Lovrecic, A Piton, K L I Van Gassen, H G Yntema, B M Knoppers,[...]. Eur J Hum Genet 2018
28
10

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
3

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
792
3

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
3

Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.
Danya F Vears, Emilia Niemiec, Heidi Carmen Howard, Pascal Borry. Eur J Hum Genet 2018
28
10

Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw,[...]. JAMA 2014
558
3


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
20

Purposeful Sampling for Qualitative Data Collection and Analysis in Mixed Method Implementation Research.
Lawrence A Palinkas, Sarah M Horwitz, Carla A Green, Jennifer P Wisdom, Naihua Duan, Kimberly Hoagwood. Adm Policy Ment Health 2015
3

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
799
3

What is an adequate sample size? Operationalising data saturation for theory-based interview studies.
Jill J Francis, Marie Johnston, Clare Robertson, Liz Glidewell, Vikki Entwistle, Martin P Eccles, Jeremy M Grimshaw. Psychol Health 2010
676
3


"In the physio we trust": A qualitative study on patients' preferences for physiotherapy.
Susanne Bernhardsson, Maria E H Larsson, Kajsa Johansson, Birgitta Öberg. Physiother Theory Pract 2017
22
9

Qualitative Descriptive Methods in Health Science Research.
Karen Jiggins Colorafi, Bronwynne Evans. HERD 2016
221
2


Meeting the needs of minority ethnic patients.
Joseph D Cortis. J Adv Nurs 2004
38
5



Culturally congruent care for older people: Finnish care in Sweden.
Kristiina Heikkilä, Anneli Sarvimäki, Sirkka-Liisa Ekman. Scand J Caring Sci 2007
21
9


Health service use in indigenous Sami and non-indigenous youth in North Norway: a population based survey.
Anne Lene Turi, Margrethe Bals, Ingunn B Skre, Siv Kvernmo. BMC Public Health 2009
15
13


Sami speakers are less satisfied with general practitioners' services.
Tove Nystad, Marita Melhus, Eiliv Lund. Int J Circumpolar Health 2008
20
10

Use of health care in the main area of Sami habitation in Norway - catching up with national expenditure rates.
Margrete Gaski, Marita Melhus, Trygve Deraas, Olav H Førde. Rural Remote Health 2011
8
25

Experiences of well-being among Sami and Roma women in a Swedish context.
Lena Alex, Arja Lehti. Health Care Women Int 2013
5
40

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
2

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
42
4


A prospective evaluation of whole-exome sequencing as a first-tier molecular test in infants with suspected monogenic disorders.
Zornitza Stark, Tiong Y Tan, Belinda Chong, Gemma R Brett, Patrick Yap, Maie Walsh, Alison Yeung, Heidi Peters, Dylan Mordaunt, Shannon Cowie,[...]. Genet Med 2016
190
2

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
2


Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit.
Hussein Daoud, Stephanie M Luco, Rui Li, Eric Bareke, Chandree Beaulieu, Olga Jarinova, Nancy Carson, Sarah M Nikkel, Gail E Graham, Julie Richer,[...]. CMAJ 2016
48
4

Experiences with obtaining informed consent for genomic sequencing.
Barbara A Bernhardt, Myra I Roche, Denise L Perry, Sarah R Scollon, Ashley N Tomlinson, Debra Skinner. Am J Med Genet A 2015
63
3


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.