A citation-based method for searching scientific literature

Brynn Levy, Ronald Wapner. Fertil Steril 2018
Times Cited: 96







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



Times Cited
  Times     Co-cited
Similarity


Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.
Ioannis Papoulidis, Alexandros Sotiriadis, Elisavet Siomou, Elena Papageorgiou, Makarios Eleftheriades, Vasilios Papadopoulos, Eirini Oikonomidou, Sandro Orru, Emmanouil Manolakos, Apostolos Athanasiadis. Prenat Diagn 2015
23
13

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.
A Novelli, F R Grati, L Ballarati, L Bernardini, D Bizzoco, L Camurri, R Casalone, L Cardarelli, P Cavalli, R Ciccone,[...]. Ultrasound Obstet Gynecol 2012
44
6



Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory Considerations.
Ahmad N Abou Tayoun, Nancy B Spinner, Heidi L Rehm, Robert C Green, Diana W Bianchi. Prenat Diagn 2018
34
8


Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies.
Diana W Bianchi, Darya Chudova, Amy J Sehnert, Sucheta Bhatt, Kathryn Murray, Tracy L Prosen, Judy E Garber, Louise Wilkins-Haug, Neeta L Vora, Stephen Warsof,[...]. JAMA 2015
203
3

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
132
3




An isolated intracardiac echogenic focus as a marker for aneuploidy.
Kathleen E Bradley, Thomas S Santulli, Kimberly D Gregory, William Herbert, Dru E Carlson, Lawrence D Platt. Am J Obstet Gynecol 2005
22
13




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
10

Is high fetal nuchal translucency associated with submicroscopic chromosomal abnormalities on array CGH?
J Huang, L C Poon, R Akolekar, K W Choy, T Y Leung, K H Nicolaides. Ultrasound Obstet Gynecol 2014
32
9

Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound.
Keren J Carss, Sarah C Hillman, Vijaya Parthiban, Dominic J McMullan, Eamonn R Maher, Mark D Kilby, Matthew E Hurles. Hum Mol Genet 2014
105
3

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
3

Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities.
F Fu, R Li, Y Li, Z-Q Nie, T Lei, D Wang, X Yang, J Han, M Pan, L Zhen,[...]. Ultrasound Obstet Gynecol 2018
53
5

Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, David Hardekopf, Sona Pekova, Samarth Bhatt, Nadezda Kosyakova, Thomas Liehr. J Histochem Cytochem 2012
78
3

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
12
25

Chromosomal microarray analysis in prenatal diagnosis: ethical considerations of the Belgian approach.
Joke Muys, Bettina Blaumeiser, Katrien Janssens, Patrick Loobuyck, Yves Jacquemyn. J Med Ethics 2020
7
42

Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
Xiangyu Zhu, Jie Li, Tong Ru, Yaping Wang, Yan Xu, Ying Yang, Xing Wu, David S Cram, Yali Hu. Prenat Diagn 2016
39
7

First and second trimester screening for fetal structural anomalies.
Lindsay Edwards, Lisa Hui. Semin Fetal Neonatal Med 2018
32
9

Molecular cytogenetic characterization of a mosaic small supernumerary marker chromosome derived from chromosome Y in an azoospermic male: A case report.
Hongguo Zhang, Xiangyin Liu, Dongfeng Geng, Fagui Yue, Yuting Jiang, Ruizhi Liu, Ruixue Wang. Medicine (Baltimore) 2019
6
50


Cut-off value of nuchal translucency as indication for chromosomal microarray analysis.
I Maya, S Yacobson, S Kahana, J Yeshaya, T Tenne, I Agmon-Fishman, L Cohen-Vig, M Shohat, L Basel-Vanagaite, R Sharony. Ultrasound Obstet Gynecol 2017
21
14

Risk of selected structural abnormalities in infants after increased nuchal translucency measurement.
Rebecca J Baer, Mary E Norton, Gary M Shaw, Monica C Flessel, Sara Goldman, Robert J Currier, Laura L Jelliffe-Pawlowski. Am J Obstet Gynecol 2014
54
5

Clinical utility of array comparative genomic hybridisation in prenatal setting.
Luca Lovrecic, Ziga Iztok Remec, Marija Volk, Gorazd Rudolf, Karin Writzl, Borut Peterlin. BMC Med Genet 2016
9
33


Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG).
Athena M Cherry, Yassmine M Akkari, Kimberly M Barr, Hutton M Kearney, Nancy C Rose, Sarah T South, James H Tepperberg, Jeanne M Meck. Genet Med 2017
9
33

Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies.
Hua Hu, Li Wang, Jiayan Wu, Peng Zhou, Jingli Fu, Jiuchen Sun, Weiyi Cai, Hailiang Liu, Ying Yang. Hum Genomics 2019
26
11


Mosaicism and uniparental disomy in prenatal diagnosis.
Thomas Eggermann, Lukas Soellner, Karin Buiting, Dieter Kotzot. Trends Mol Med 2015
58
5

European guidelines for constitutional cytogenomic analysis.
Marisa Silva, Nicole de Leeuw, Kathy Mann, Heleen Schuring-Blom, Sian Morgan, Daniela Giardino, Katrina Rack, Ros Hastings. Eur J Hum Genet 2019
33
9

Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
Yanlin Wang, Yan Chen, Feng Tian, Jianguang Zhang, Zhuo Song, Yi Wu, Xu Han, Wenjing Hu, Duan Ma, David Cram,[...]. Clin Chem 2014
144
3


Exome sequencing improves genetic diagnosis of fetal increased nuchal translucency.
Xin Yang, Lv-Yin Huang, Min Pan, Li-Li Xu, Li Zhen, Jin Han, Dong-Zhi Li. Prenat Diagn 2020
8
37

Genetic Examination for Fetuses with Increased Fetal Nuchal Translucency by Genomic Technology.
Shuya Xue, Huanchen Yan, Jingsi Chen, Nan Li, Jiayan Wang, Yu Liu, Huimin Zhang, Shaoying Li, Wei Zhang, Dunjin Chen,[...]. Cytogenet Genome Res 2020
4
75

Systematic analysis of copy-number variations associated with early pregnancy loss.
Y Wang, Y Li, Y Chen, R Zhou, Z Sang, L Meng, J Tan, F Qiao, Q Bao, D Luo,[...]. Ultrasound Obstet Gynecol 2020
14
21


Chromosomal Microarray Analysis in Fetuses with Growth Restriction and Normal Karyotype: A Systematic Review and Meta-Analysis.
Antoni Borrell, Maribel Grande, Montse Pauta, Laia Rodriguez-Revenga, Francesc Figueras. Fetal Diagn Ther 2018
17
17


Prenatal diagnosis by array-CGH.
L Rickman, H Fiegler, N P Carter, M Bobrow. Eur J Med Genet 2005
42
4

Chromosome abnormalities identified in 347 spontaneous abortions collected in Japan.
Masaji Nagaishi, Tatsuo Yamamoto, Kazuso Iinuma, Katsunori Shimomura, Sue Ann Berend, Judith Knops. J Obstet Gynaecol Res 2004
72
2

Circulating levels of inhibin A, activin A and follistatin in missed and recurrent miscarriages.
S Muttukrishna, E Jauniaux, N Greenwold, H McGarrigle, S Jivraj, S Carter, S Elgaddal, N Groome, L Regan. Hum Reprod 2002
46
4

Genetics of early miscarriage.
Merel M J van den Berg, Merel C van Maarle, Madelon van Wely, MariĆ«tte Goddijn. Biochim Biophys Acta 2012
117
2




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.