A citation-based method for searching scientific literature

Peter E Grant, Maria Pampaka, Katherine Payne, Angus Clarke, Marion McAllister. Eur J Med Genet 2019
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity



The Feelings About genomiC Testing Results (FACToR) Questionnaire: Development and Preliminary Validation.
Meng Li, Caroline S Bennette, Laura M Amendola, M Ragan Hart, Patrick Heagerty, Bryan Comstock, Peter Tarczy-Hornoch, Stephanie M Fullerton, Dean A Regier, Wylie Burke,[...]. J Genet Couns 2019
24
35

A Rapid Systematic Review of Outcomes Studies in Genetic Counseling.
Lisa Madlensky, Angela M Trepanier, Deborah Cragun, Barbara Lerner, Kristen M Shannon, Heather Zierhut. J Genet Couns 2017
51
29

Translation and Adaptation of the Genetic Counselling Outcome Scale (GCOS-24) for Use in Denmark.
Birgitte Rode Diness, Gritt Overbeck, Tina Duelund Hjortshøj, Trine Bjørg Hammer, Susanne Timshel, Else Sørensen, Marion McAllister. J Genet Couns 2017
12
41

Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact.
J Wynn, R Ottman, J Duong, A L Wilson, P Ahimaz, J Martinez, R Rabin, E Rosen, R Webster, C Au,[...]. Clin Genet 2018
26
23

A validated PROM in genetic counselling: the psychometric properties of the Dutch version of the Genetic Counselling Outcome Scale.
Jan S Voorwinden, Mirjam Plantinga, Wim Krijnen, Margreet Ausems, Nine Knoers, Mary Velthuizen, Erwin Birnie, Anneke M Lucassen, Irene M van Langen, Adelita V Ranchor. Eur J Hum Genet 2019
7
57

Evaluating a unique, specialist psychiatric genetic counseling clinic: uptake and impact.
A Inglis, D Koehn, B McGillivray, S E Stewart, J Austin. Clin Genet 2015
69
23



A new definition of Genetic Counseling: National Society of Genetic Counselors' Task Force report.
Robert Resta, Barbara Bowles Biesecker, Robin L Bennett, Sandra Blum, Susan Estabrooks Hahn, Michelle N Strecker, Janet L Williams. J Genet Couns 2006
395
23

Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies.
Jill O Robinson, Julia Wynn, Barbara Biesecker, Leslie G Biesecker, Barbara Bernhardt, Kyle B Brothers, Wendy K Chung, Kurt D Christensen, Robert C Green, Amy L McGuire,[...]. Genet Med 2019
27
23

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.
Michelle M Clark, Zornitza Stark, Lauge Farnaes, Tiong Y Tan, Susan M White, David Dimmock, Stephen F Kingsmore. NPJ Genom Med 2018
206
23

Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders.
Allyn McConkie Rosell, Loren D M Pena, Kelly Schoch, Rebecca Spillmann, Jennifer Sullivan, Stephen R Hooper, Yong-Hui Jiang, Nicolas Mathey-Andrews, David B Goldstein, Vandana Shashi. J Genet Couns 2016
57
17

A brief measure for assessing generalized anxiety disorder: the GAD-7.
Robert L Spitzer, Kurt Kroenke, Janet B W Williams, Bernd Löwe. Arch Intern Med 2006
17


Understanding the Psychosocial Effects of WES Test Results on Parents of Children with Rare Diseases.
Lotte Krabbenborg, L E L M Vissers, J Schieving, T Kleefstra, E J Kamsteeg, J A Veltman, M A Willemsen, S Van der Burg. J Genet Couns 2016
46
17

Using Patient-Reported Outcome Measures for Quality Improvement in Clinical Genetics: an Exploratory Study.
A Costal Tirado, A M McDermott, C Thomas, D Ferrick, J Harris, A Edwards, Marion McAllister. J Genet Couns 2017
17
17

A Systematic Review of Randomized Controlled Trials to Assess Outcomes of Genetic Counseling.
Barbara A Athens, Samantha L Caldwell, Kendall L Umstead, Philip D Connors, Ethan Brenna, Barbara B Biesecker. J Genet Couns 2017
46
17

The impact of cardiovascular genetic counseling on patient empowerment.
Hannah E Ison, Stephanie M Ware, Tae-Hwi Schwantes-An, Samantha Freeze, Lindsey Elmore, Katherine G Spoonamore. J Genet Couns 2019
15
20

Outcome measurement in clinical genetics services: a systematic review of validated measures.
Katherine Payne, Stuart Nicholls, Marion McAllister, Rhona Macleod, Dian Donnai, Linda M Davies. Value Health 2008
71
17

Clinical whole genome sequencing as a first-tier test at a resource-limited dysmorphology clinic in Mexico.
Alicia Scocchia, Kristen M Wigby, Diane Masser-Frye, Miguel Del Campo, Carolina I Galarreta, Erin Thorpe, Julia McEachern, Keisha Robinson, Andrew Gross, Subramanian S Ajay,[...]. NPJ Genom Med 2019
33
17

Translation and Cross-Cultural Adaptation with Preliminary Validation of GCOS-24 for Use in Spain.
Patricia Muñoz-Cabello, Sixto García-Miñaúr, Manuel Eliecer Espinel-Vallejo, Lorenzo Fernández-Franco, Alexandra Stephens, Fernando Santos-Simarro, Pablo Lapunzina-Badía, Marion McAllister. J Genet Couns 2018
7
42

Does genomic sequencing early in the diagnostic trajectory make a difference? A follow-up study of clinical outcomes and cost-effectiveness.
Zornitza Stark, Deborah Schofield, Melissa Martyn, Luke Rynehart, Rupendra Shrestha, Khurshid Alam, Sebastian Lunke, Tiong Y Tan, Clara L Gaff, Susan M White. Genet Med 2019
75
17

Rapid whole-genome sequencing decreases infant morbidity and cost of hospitalization.
Lauge Farnaes, Amber Hildreth, Nathaly M Sweeney, Michelle M Clark, Shimul Chowdhury, Shareef Nahas, Julie A Cakici, Wendy Benson, Robert H Kaplan, Richard Kronick,[...]. NPJ Genom Med 2018
168
17

Perceived utility of biological testing for autism spectrum disorder is associated with child and family functioning.
Afiqah Yusuf, Iskra Peltekova, Tal Savion-Lemieux, Jennifer Frei, Ruth Bruno, Ridha Joober, Jennifer Howe, Stephen W Scherer, Mayada Elsabbagh. Res Dev Disabil 2020
5
60

Personal utility in genomic testing: a systematic literature review.
Jennefer N Kohler, Erin Turbitt, Barbara B Biesecker. Eur J Hum Genet 2017
64
17


Beyond diagnostic accuracy: the clinical utility of diagnostic tests.
Patrick M M Bossuyt, Johannes B Reitsma, Kristian Linnet, Karel G M Moons. Clin Chem 2012
184
17

Defining personal utility in genomics: A Delphi study.
J N Kohler, E Turbitt, K L Lewis, B S Wilfond, L Jamal, H L Peay, L G Biesecker, B B Biesecker. Clin Genet 2017
42
17

Evaluating empowerment in genetic counseling using patient-reported outcomes.
Jeanette Yuen, Suat Y Lee, Eliza Courtney, John Lim, Hazel Soh, Shao T Li, Yanni Chen, Marion McAllister, Eva K Fenwick, Joanne Ngeow. Clin Genet 2020
10
30

Research electronic data capture (REDCap)--a metadata-driven methodology and workflow process for providing translational research informatics support.
Paul A Harris, Robert Taylor, Robert Thielke, Jonathon Payne, Nathaniel Gonzalez, Jose G Conde. J Biomed Inform 2009
17

Development and Validation of a Genomic Knowledge Scale to Advance Informed Decision Making Research in Genomic Sequencing.
Michelle M Langer, Myra I Roche, Noel T Brewer, Jonathan S Berg, Cynthia M Khan, Cristina Leos, Elizabeth Moore, Michelle Brown, Christine Rini. MDM Policy Pract 2017
20
11

Design and psychometric evaluation of the Psychological Adaptation to Genetic Information Scale.
Catherine Y Read, Donna J Perry, Mary E Duffy. J Nurs Scholarsh 2005
41
11

Pediatric Whole Exome Sequencing: an Assessment of Parents' Perceived and Actual Understanding.
Leandra K Tolusso, Kathleen Collins, Xue Zhang, Jennifer R Holle, C Alexander Valencia, Melanie F Myers. J Genet Couns 2017
11
18

A brief assessment of concerns associated with genetic testing for cancer: the Multidimensional Impact of Cancer Risk Assessment (MICRA) questionnaire.
David Cella, Chanita Hughes, Amy Peterman, Chih-Hung Chang, Beth N Peshkin, Marc D Schwartz, Lari Wenzel, Amy Lemke, Alfred C Marcus, Caryn Lerman. Health Psychol 2002
173
11

The PHQ-9: validity of a brief depression severity measure.
K Kroenke, R L Spitzer, J B Williams. J Gen Intern Med 2001
11

New developmental syndromes: Understanding the family experience.
Cara N Inglese, Alison M Elliott, Anna Lehman. J Genet Couns 2019
13
15


Parents' experiences of receiving their child's genetic diagnosis: a qualitative study to inform clinical genetics practice.
Setareh Ashtiani, Nancy Makela, Prescilla Carrion, Jehannine Austin. Am J Med Genet A 2014
28
11

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock,[...]. Genet Med 2019
158
11

Evaluating the utility of personal genomic information.
Morris W Foster, John J Mulvihill, Richard R Sharp. Genet Med 2009
128
11

Pathways from autism spectrum disorder diagnosis to genetic testing.
Krysta S Barton, Holly K Tabor, Helene Starks, Nanibaa' A Garrison, Mercy Laurino, Wylie Burke. Genet Med 2018
18
11

Parents' Experience with Pediatric Microarray: Transferrable Lessons in the Era of Genomic Counseling.
R Z Hayeems, R Babul-Hirji, N Hoang, R Weksberg, C Shuman. J Genet Couns 2016
25
11

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
11

Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder.
Ryan K C Yuen, Daniele Merico, Matt Bookman, Jennifer L Howe, Bhooma Thiruvahindrapuram, Rohan V Patel, Joe Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang,[...]. Nat Neurosci 2017
376
11

Quality criteria were proposed for measurement properties of health status questionnaires.
Caroline B Terwee, Sandra D M Bot, Michael R de Boer, Daniëlle A W M van der Windt, Dirk L Knol, Joost Dekker, Lex M Bouter, Henrica C W de Vet. J Clin Epidemiol 2007
11

Coming full circle: a reciprocal-engagement model of genetic counseling practice.
Patricia McCarthy Veach, Dianne M Bartels, Bonnie S Leroy. J Genet Couns 2007
145
11

The need to develop an evidence base for genetic counselling in Europe.
Marion McAllister, Ramona Moldovan, Milena Paneque, Heather Skirton. Eur J Hum Genet 2016
10
20

Assessment of the content and process of genetic counseling: a critical review of empirical studies.
Bettina Meiser, Jennifer Irle, Elizabeth Lobb, Kristine Barlow-Stewart. J Genet Couns 2008
100
11

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
83
11


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.