A citation-based method for searching scientific literature

Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Désir, Anne Destrée, Koenraad Devriendt, Annelies Dheedene, Armelle Duquenne, Annelies Fieuw, Erik Fransen, Jean-Stéphane Gatot, Mauricette Jamar, Sandra Janssens, Jorien Kerstjens, Kathelijn Keymolen, Damien Lederer, Björn Menten, Bruno Pichon, Sonia Rombout, Yves Sznajer, Ann Van Den Bogaert, Kris Van Den Bogaert, Joris Vermeesch, Katrien Janssens. Prenat Diagn 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Couples experiences of receiving uncertain results following prenatal microarray or exome sequencing: A mixed-methods systematic review.
Eleanor Harding, Jennifer Hammond, Lyn S Chitty, Melissa Hill, Celine Lewis. Prenat Diagn 2020
4
100

Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
630
100

Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management.
Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S Chitty. Genet Med 2018
52
100

Implementation of exome sequencing in fetal diagnostics-Data and experiences from a tertiary center in Denmark.
Naja Becher, Lotte Andreasen, Puk Sandager, Stina Lou, Olav Bjørn Petersen, Rikke Christensen, Ida Vogel. Acta Obstet Gynecol Scand 2020
6
100

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
37
100

Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
26
100




Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.
Amy Breman, Amber N Pursley, Patricia Hixson, Weimin Bi, Patricia Ward, Carlos A Bacino, Chad Shaw, James R Lupski, Arthur Beaudet, Ankita Patel,[...]. Prenat Diagn 2012
74
100

The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker,[...]. Prenat Diagn 2018
14
100

Impacts of variants of uncertain significance on parental perceptions of children after prenatal chromosome microarray testing.
Preeya Desai, Hannah Haber, Jessica Bulafka, Amita Russell, Rebecca Clifton, Julia Zachary, Seonjoo Lee, Tianshu Feng, Ronald Wapner, Catherine Monk,[...]. Prenat Diagn 2018
15
100

Risk of major congenital malformations in relation to maternal overweight and obesity severity: cohort study of 1.2 million singletons.
Martina Persson, Sven Cnattingius, Eduardo Villamor, Jonas Söderling, Björn Pasternak, Olof Stephansson, Martin Neovius. BMJ 2017
80
100


Aiming at multidisciplinary consensus: what should be detected in prenatal diagnosis?
Elisabeth M A Boormans, E Birnie, Alida C Knegt, G Heleen Schuring-Blom, Gouke J Bonsel, Jan M M van Lith. Prenat Diagn 2010
5
100


Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
131
100

Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting.
Swetha Narayanan, Bruce Blumberg, Marla L Clayman, Vivian Pan, Catherine Wicklund. J Genet Couns 2018
7
100

Parents' Perspectives on Variants of Uncertain Significance from Chromosome Microarray Analysis.
Lesli A Kiedrowski, Kailey M Owens, Beverly M Yashar, Jane L Schuette. J Genet Couns 2016
28
100

Preferences for prenatal tests for Down syndrome: an international comparison of the views of pregnant women and health professionals.
Melissa Hill, Jo-Ann Johnson, Sylvie Langlois, Hyun Lee, Stephanie Winsor, Brigid Dineley, Marisa Horniachek, Faustina Lalatta, Luisa Ronzoni, Angela N Barrett,[...]. Eur J Hum Genet 2016
30
100

"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result.
Stina Lou, Kirsten Lomborg, Celine Lewis, Sam Riedijk, Olav Bjørn Petersen, Ida Vogel. Acta Obstet Gynecol Scand 2020
6
100

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.
George McGillivray, Jill A Rosenfeld, R J McKinlay Gardner, Lynn H Gillam. Prenat Diagn 2012
68
100

A taxonomy of medical uncertainties in clinical genome sequencing.
Paul K J Han, Kendall L Umstead, Barbara A Bernhardt, Robert C Green, Steven Joffe, Barbara Koenig, Ian Krantz, Leo B Waterston, Leslie G Biesecker, Barbara B Biesecker. Genet Med 2017
50
100

Impact of prenatal exome sequencing for fetal genetic diagnosis on maternal psychological outcomes and decisional conflict in a prospective cohort.
Asha N Talati, Kelly L Gilmore, Emily E Hardisty, Anne D Lyerly, Christine Rini, Neeta L Vora. Genet Med 2021
1
100



Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
95
100

What results to disclose, when, and who decides? Healthcare professionals' views on prenatal chromosomal microarray analysis.
Shiri Shkedi-Rafid, Angela Fenwick, Sandi Dheensa, Diana Wellesley, Anneke M Lucassen. Prenat Diagn 2016
19
100


The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers.
Leslie Durham, Ramesha Papanna, Blair Stevens, Sarah Noblin, David Rodriguez-Buritica, S Shahrukh Hashmi, Nevena Krstic. Prenat Diagn 2019
3
100

Genetic counselors' perceptions of uncertainty in pretest counseling for genomic sequencing: A qualitative study.
Jessica Park, Kimberly Zayhowski, Ainsley J Newson, Kelly E Ormond. J Genet Couns 2019
5
100

Maternity health care professionals' views and experiences of fetal genomic uncertainty: A review.
Lisa Hui, Emma Szepe, Jane Halliday, Celine Lewis. Prenat Diagn 2020
3
100


A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Lisa Hui, Alice Poulton, Eliza Kluckow, Anthea Lindquist, Briohny Hutchinson, Mark D Pertile, Leonard Bonacquisto, Lucy Gugasyan, Abhijit Kulkarni, James Harraway,[...]. Hum Reprod 2020
2
100

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Christine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, Radha Chari, Bernie N Chodirker, Isabelle DeBie, Jane A Evans, William T Gibson, Elena Kolomietz, Tanya N Nelson,[...]. J Med Genet 2018
25
100

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
152
100

The right to an open future concerning genetic information.
Annelien L Bredenoord, Martine C de Vries, Hans van Delden. Am J Bioeth 2014
15
100

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
122
100


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.