A citation-based method for searching scientific literature

Shiri Shkedi-Rafid, Angela Fenwick, Sandi Dheensa, Diana Wellesley, Anneke M Lucassen. Prenat Diagn 2016
Times Cited: 20







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



Times Cited
  Times     Co-cited
Similarity


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
643
55

Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
129
50

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
45

Comparing genetic counselor's and patient's perceptions of needs in prenatal chromosomal microarray testing.
Sarah A Walser, Katherine S Kellom, Steven C Palmer, Barbara A Bernhardt. Prenat Diagn 2015
25
40

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges.
Olivier Vanakker, Catheline Vilain, Katrien Janssens, Nathalie Van der Aa, Guillaume Smits, Claude Bandelier, Bettina Blaumeiser, Saskia Bulk, Jean-Hubert Caberg, Anne De Leener,[...]. Eur J Med Genet 2014
61
40


Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.
S L van der Steen, K E M Diderich, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M Joosten, M F C M Knapen, D Van Opstal, M I Srebniak, A Tibben,[...]. Clin Genet 2015
32
35


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
35


"If it helps..." the use of microarray technology in prenatal testing: patient and partners reflections.
Sarah C Hillman, John Skelton, Elizabeth Quinlan-Jones, Amie Wilson, Mark D Kilby. Am J Med Genet A 2013
26
30

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
154
30

The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents' Experiences.
S L van der Steen, S R Riedijk, J Verhagen-Visser, L C P Govaerts, M I Srebniak, D Van Opstal, M Joosten, M F C M Knapen, A Tibben, K E M Diderich,[...]. J Genet Couns 2016
26
30

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
25

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
25

"Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results.
Sarah A Walser, Allison Werner-Lin, Amita Russell, Ronald J Wapner, Barbara A Bernhardt. J Genet Couns 2016
18
27

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
27
25

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
62
25

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
130
25


Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes.
Marina Mikhaelian, Patricia McCarthy Veach, Ian MacFarlane, Bonnie S LeRoy, Matthew Bower. Prenat Diagn 2013
18
22

Couple's Narratives of Communion and Isolation Following Abnormal Prenatal Microarray Testing Results.
Allison Werner-Lin, Frances K Barg, Katherine S Kellom, Kallyn J Stumm, Lisa Pilchman, Ashley N Tomlinson, Barbara A Bernhardt. Qual Health Res 2016
25
20

Balancing Genetics (Science) and Counseling (Art) in Prenatal Chromosomal Microarray Testing.
Allison Werner-Lin, Judith L M McCoyd, Barbara A Bernhardt. J Genet Couns 2016
14
28

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis.
M I Srebniak, M Joosten, M F C M Knapen, L R Arends, M Polak, S van Veen, A T J I Go, D Van Opstal. Ultrasound Obstet Gynecol 2018
40
20

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
15
26

Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study.
Jane L Halliday, Cecile Muller, Taryn Charles, Fiona Norris, Joanne Kennedy, Sharon Lewis, Bettina Meiser, Susan Donath, Zornitza Stark, George McGillivray,[...]. Eur J Hum Genet 2018
11
36


"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
66

Noninvasive whole-genome sequencing of a human fetus.
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
240
15

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow.
Malgorzata Srebniak, Marjan Boter, Grétel Oudesluijs, Marieke Joosten, Lutgarde Govaerts, Diane Van Opstal, Robert-Jan H Galjaard. Eur J Hum Genet 2011
74
15

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
61
15

Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8,700 patients.
Joo Wook Ahn, Susan Bint, Anne Bergbaum, Kathy Mann, Richard P Hall, Caroline Mackie Ogilvie. Mol Cytogenet 2013
36
15

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
70
15


Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
154
15

Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders - genetic counseling and pregnancy outcome in 57 cases.
Lutgarde Govaerts, Malgorzata Srebniak, Karin Diderich, Marieke Joosten, Sam Riedijk, Maarten Knapen, Attie Go, Dimitri Papatsonis, Katja de Graaf, Toon Toolenaar,[...]. Prenat Diagn 2017
7
42

'What do you think?' the collaborative practices of choice and care in a Danish obstetric ultrasound unit.
Stina Lou, Camilla Palmhøj Nielsen, Lone Hvidman, Olav Bjørn Petersen, Mette Bech Risør. Anthropol Med 2016
4
75

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
15

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
136
15

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
15

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
15


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
28
15




When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.
Idit Maya, Reuven Sharony, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, Ifaat Agmon-Fishman, Lital Cohen-Vig, Yael Goldberg, Racheli Berger,[...]. Genet Med 2018
27
15

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
60

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
144
15

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
112
15


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.