A citation-based method for searching scientific literature

Hsu P Chong, Susan Hamilton, Fionnuala Mone, Ka Wang Cheung, Fiona S Togneri, Rachel K Morris, Elizabeth Quinlan-Jones, Denise Williams, Stephanie Allen, Dominic J McMullan, Mark D Kilby. Prenat Diagn 2019
Times Cited: 10







List of co-cited articles
18 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
664
50

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
166
40

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
158
40

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
134
30


Update on the use of exome sequencing in the diagnosis of fetal abnormalities.
Lauren Ferretti, Rhiannon Mellis, Lyn S Chitty. Eur J Med Genet 2019
18
30

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
59
20

Exome sequencing in the assessment of congenital malformations in the fetus and neonate.
Fionnuala Mone, Elizabeth Quinlan-Jones, Andrew K Ewer, Mark D Kilby. Arch Dis Child Fetal Neonatal Ed 2019
9
22

Fetal phenotypes emerge as genetic technologies become robust.
Kathryn J Gray, Louise E Wilkins-Haug, Nancy J Herrig, Neeta L Vora. Prenat Diagn 2019
18
20

Meta-analysis of second-trimester markers for trisomy 21.
M Agathokleous, P Chaveeva, L C Y Poon, P Kosinski, K H Nicolaides. Ultrasound Obstet Gynecol 2013
123
20

Is there still a role for nuchal translucency measurement in the changing paradigm of first trimester screening?
Francesca Bardi, Pien Bosschieter, Joke Verheij, Attie Go, Monique Haak, Mireille Bekker, Esther Sikkel, Audrey Coumans, Eva Pajkrt, Caterina Bilardo. Prenat Diagn 2020
12
20

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
194
20

Exome Sequencing for Prenatal Detection of Genetic Abnormalities in Fetal Ultrasound Anomalies: An Economic Evaluation.
Shahela S Kodabuckus, Elizabeth Quinlan-Jones, Dominic J McMullan, Eamonn R Maher, Matthew E Hurles, Pelham M Barton, Mark D Kilby. Fetal Diagn Ther 2020
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
20

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
97
20

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
42
20


Genomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysis.
M Grande, F A R Jansen, Y J Blumenfeld, A Fisher, A O Odibo, M C Haak, A Borrell. Ultrasound Obstet Gynecol 2015
84
20

Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A Review.
Fionnuala Mone, Elizabeth Quinlan-Jones, Mark D Kilby. Eur J Obstet Gynecol Reprod Biol 2018
11
10

Next-generation sequencing and the impact on prenatal diagnosis.
Rhiannon Mellis, Natalie Chandler, Lyn S Chitty. Expert Rev Mol Diagn 2018
16
10

Dysmorphology demystified.
William Reardon, Dian Donnai. Arch Dis Child Fetal Neonatal Ed 2007
24
10

Implementing Non-Invasive Prenatal Diagnosis (NIPD) in a National Health Service Laboratory; From Dominant to Recessive Disorders.
Suzanne Drury, Sarah Mason, Fiona McKay, Kitty Lo, Christopher Boustred, Lucy Jenkins, Lyn S Chitty. Adv Exp Med Biol 2016
18
10


Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders.
Caroline F Wright, Jeremy F McRae, Stephen Clayton, Giuseppe Gallone, Stuart Aitken, Tomas W FitzGerald, Philip Jones, Elena Prigmore, Diana Rajan, Jenny Lord,[...]. Genet Med 2018
128
10

Implementation of a genomic medicine multi-disciplinary team approach for rare disease in the clinical setting: a prospective exome sequencing case series.
John Taylor, Jude Craft, Edward Blair, Sarah Wordsworth, David Beeson, Saleel Chandratre, Judith Cossins, Tracy Lester, Andrea H Németh, Elizabeth Ormondroyd,[...]. Genome Med 2019
12
10

Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies.
Elizabeth Quinlan-Jones, Jenny Lord, Denise Williams, Sue Hamilton, Tamas Marton, Ruth Y Eberhardt, Gabriele Rinck, Elena Prigmore, Rebecca Keelagher, Dominic J McMullan,[...]. Genet Med 2019
19
10


Genetic Test Availability And Spending: Where Are We Now? Where Are We Going?
Kathryn A Phillips, Patricia A Deverka, Gillian W Hooker, Michael P Douglas. Health Aff (Millwood) 2018
77
10



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
4
25

Consanguineous marriages in the genetic counseling centers of Isfahan and the ethical issues of clinical consultations.
Narges Nouri, Nayereh Nouri, Samane Tirgar, Elham Soleimani, Vida Yazdani, Farzaneh Zahedi, Bagher Larijani. J Med Ethics Hist Med 2017
5
20

Importance of complete phenotyping in prenatal whole exome sequencing.
Mahmoud Aarabi, Olivia Sniezek, Huaiyang Jiang, Devereux N Saller, Daniel Bellissimo, Svetlana A Yatsenko, Aleksandar Rajkovic. Hum Genet 2018
31
10

Race, consanguinity and social features in Birmingham babies: a basis for prospective study.
S Bundey, H Alam, A Kaur, S Mir, R J Lancashire. J Epidemiol Community Health 1990
41
10

Availability of less invasive prenatal, perinatal and paediatric autopsy will improve uptake rates: a mixed-methods study with bereaved parents.
C Lewis, M Riddington, M Hill, O J Arthurs, J C Hutchinson, L S Chitty, C Bevan, J Fisher, J Ward, N J Sebire. BJOG 2019
19
10

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
133
10


First-trimester screening-biomarkers and cell-free DNA.
Ioan Suciu, Slavyana Galeva, Samira Abdel Azim, Lucian Pop, Oana Toader. J Matern Fetal Neonatal Med 2021
3
33

The significance of the second trimester sonographic soft markers in pregnancies after normal first trimester screening.
Marja Kaijomaa, Veli-Matti Ulander, Markku Ryynanen, Vedran Stefanovic. Prenat Diagn 2013
5
20


Uptake of non-invasive prenatal testing in Chinese women: money matters.
J Han, L Zhen, M Pan, X Yang, Y-M Ou, C Liao, D-Z Li. Eur J Obstet Gynecol Reprod Biol 2015
4
25

Second-trimester genetic sonogram for detection of fetal chromosomal abnormalities in a community-based antenatal testing unit.
J N Bottalico, X Chen, M Tartaglia, B Rosario, D Yarabothu, L Nelson. Ultrasound Obstet Gynecol 2009
21
10

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
315
10

The role of ultrasound in women who undergo cell-free DNA screening.
Mary E Norton, Joseph R Biggio, Jeffrey A Kuller, Sean C Blackwell. Am J Obstet Gynecol 2017
51
10

Fetal aneuploidy screening with cell-free DNA in late gestation.
Patricia A Taneja, Tracy L Prosen, Eileen de Feo, Kristina M Kruglyak, Meredith Halks-Miller, Kirsten J Curnow, Sucheta Bhatt. J Matern Fetal Neonatal Med 2017
3
33


Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.
L Beulen, B H W Faas, I Feenstra, J M G van Vugt, M N Bekker. Ultrasound Obstet Gynecol 2017
34
10


Risk of chromosomal abnormalities in patients with idiopathic polyhydramnios.
K Brady, W J Polzin, J N Kopelman, J A Read. Obstet Gynecol 1992
48
10

Third-trimester genetic amniocentesis in mainland China.
Can Liao, Dong-Zhi Li. J Matern Fetal Neonatal Med 2012
5
20


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.