A citation-based method for searching scientific literature

David Eric Abel, Amy Alagh. JAAPA 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Procedure-related risk of miscarriage following chorionic villus sampling and amniocentesis.
J Beta, W Zhang, S Geris, V Kostiv, R Akolekar. Ultrasound Obstet Gynecol 2019
21
100


Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort.
Eugene Pergament, Howard Cuckle, Bernhard Zimmermann, Milena Banjevic, Styrmir Sigurjonsson, Allison Ryan, Megan P Hall, Michael Dodd, Phil Lacroute, Melissa Stosic,[...]. Obstet Gynecol 2014
178
100

Causes of aberrant non-invasive prenatal testing for aneuploidy: A systematic review.
Osamu Samura, Aikou Okamoto. Taiwan J Obstet Gynecol 2020
20
100

Fetal fraction-based risk algorithm for non-invasive prenatal testing: screening for trisomies 13 and 18 and triploidy in women with low cell-free fetal DNA.
T McKanna, A Ryan, S Krinshpun, S Kareht, K Marchand, C Grabarits, M Ali, A McElheny, K Gardiner, K LeChien,[...]. Ultrasound Obstet Gynecol 2019
25
100

Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis.
M M Gil, V Accurti, B Santacruz, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2017
289
100



4
100

Most noninvasive prenatal screens failing due to inadequate fetal cell free DNA are negative for trisomy when repeated.
Jaime L Lopes, Guilherme S Lopes, Elizabeth A L Enninga, Hutton M Kearney, Nicole L Hoppman, Ross A Rowsey. Prenat Diagn 2020
7
100

Noninvasive prenatal screening or advanced diagnostic testing: caveat emptor.
Mark I Evans, Ronald J Wapner, Richard L Berkowitz. Am J Obstet Gynecol 2016
55
100

Clinical and cytogenetic results of a large series of amniocentesis cases from Turkey: report of 6124 cases.
Zeynep Ocak, Tülay Özlü, Hasan Fehmi Yazıcıoğlu, Osman Özyurt, Mehmet Aygün. J Obstet Gynaecol Res 2014
15
100

Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy.
Nobuhiro Suzumori, Takeshi Ebara, Takahiro Yamada, Osamu Samura, Junko Yotsumoto, Miyuki Nishiyama, Kiyonori Miura, Hideaki Sawai, Jun Murotsuki, Michihiro Kitagawa,[...]. J Hum Genet 2016
39
100

Earliest gestational age for fetal sexing in cell-free maternal plasma.
R J P Rijnders, R B Van Der Luijt, E D J Peters, J K Goeree, C E Van Der Schoot, J K Ploos Van Amstel, G C M L Christiaens. Prenat Diagn 2003
65
100

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
348
100

Rapid prenatal aneuploidy detection of BACs-on-Beads assay in 4961 cases of amniotic fluid samples.
Hehua Tao, Jinping Shi, Junfeng Wang, Li Zhao, Jieying Ding, Lan Yang. J Matern Fetal Neonatal Med 2021
7
100

ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?
Sara B Hay, Trilochan Sahoo, Mary K Travis, Karine Hovanes, Natasa Dzidic, Charles Doherty, Michelle N Strecker. Prenat Diagn 2018
41
100

Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidies.
Irena Hudecova, Daljit Sahota, Macy M S Heung, Yongjie Jin, Wing S Lee, Tak Y Leung, Yuk Ming Dennis Lo, Rossa W K Chiu. PLoS One 2014
70
100

Circulating cell free DNA testing: are some test failures informative?
G E Palomaki, E M Kloza, G M Lambert-Messerlian, D van den Boom, M Ehrich, C Deciu, A T Bombard, J E Haddow. Prenat Diagn 2015
59
100

Prenatal diagnosis of chromosomal aberrations by chromosomal microarray analysis in fetuses with ultrasound anomalies in the urinary system.
Ting Hu, Zhu Zhang, Jiamin Wang, Qinqin Li, Hongmei Zhu, Yi Lai, He Wang, Shanling Liu. Prenat Diagn 2019
11
100

Prenatal diagnosis of BACs-on-Beads assay in 1520 cases from Fujian Province, China.
Yan Wang, Min Zhang, Lingji Chen, Hailong Huang, Liangpu Xu. Mol Genet Genomic Med 2020
5
100

Screening for trisomies by cell-free DNA testing of maternal blood: consequences of a failed result.
R Revello, L Sarno, A Ispas, R Akolekar, K H Nicolaides. Ultrasound Obstet Gynecol 2016
72
100

A New Stepwise Molecular Work-Up After Chorionic Villi Sampling in Women With an Early Pregnancy Loss.
Montse Pauta, Cèlia Badenas, Laia Rodriguez-Revenga, Anna Soler, Maribel Grande, Joan Sabrià, Carmen Illanes, Virginia Borobio, Antoni Borrell. Front Genet 2021
1
100

Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing.
Jing Wang, Lin Chen, Cong Zhou, Li Wang, Hanbing Xie, Yuanyuan Xiao, Daishu Yin, Yang Zeng, Feng Tang, Yunyuan Yang,[...]. Sci Rep 2018
10
100

Application of the BACs-on-Beads assay for the prenatal diagnosis of chromosomal abnormalities in Quanzhou, China.
Jianlong Zhuang, Chunnuan Chen, Yuying Jiang, Qi Luo, Shuhong Zeng, Chunling Lv, Yuanbai Wang, Wanyu Fu. BMC Pregnancy Childbirth 2021
3
100

Update on procedure-related risks for prenatal diagnosis techniques.
Ann Tabor, Zarko Alfirevic. Fetal Diagn Ther 2010
234
100

Molecular and cytogenetic analysis in stillbirth: results from 481 consecutive cases.
Ellika Sahlin, Peter Gustavsson, Agne Liedén, Nikos Papadogiannakis, Linus Bjäreborn, Karin Pettersson, Magnus Nordenskjöld, Erik Iwarsson. Fetal Diagn Ther 2014
14
100


[Application of Chromosomal Microarray Analysis for Chromosomal Abnormalities of Spontaneously Aborted Fetuses].
Ting Hu, Hong-Mei Zhu, Zhu Zhang, Jia-Min Wang, Hai-Xia Zhang, Ze Du, Ling-Pingi Li, He Wang, Shan-Ling Liu. Sichuan Da Xue Xue Bao Yi Xue Ban 2017
1
100

Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
422
100


Added value of chromosomal microarray analysis over karyotyping in early pregnancy loss: systematic review and meta-analysis.
M Pauta, M Grande, L Rodriguez-Revenga, E Kolomietz, A Borrell. Ultrasound Obstet Gynecol 2018
25
100

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.
Peter Benn, Antoni Borrell, Rossa W K Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte Faas, Susan Gross, Tianhua Huang, Joann Johnson, Ron Maymon,[...]. Prenat Diagn 2015
179
100

Experimental factors are associated with fetal fraction in size selection noninvasive prenatal testing.
Longwei Qiao, Jun Mao, Minjuan Liu, Yinghua Liu, Xiaoyan Song, Hui Tang, Qing Zhang, Hong Li, Yaojuan Lu, Yuting Liang,[...]. Am J Transl Res 2019
6
100

Added value of chromosomal microarray analysis over conventional karyotyping in stillbirth work-up: systematic review and meta-analysis.
R J Martinez-Portilla, M Pauta, A Hawkins-Villarreal, M Rial-Crestelo, F Paz Y Miño, I Madrigal, F Figueras, A Borrell. Ultrasound Obstet Gynecol 2019
9
100

Clinical experience across the fetal-fraction spectrum of a non-invasive prenatal screening approach with low test-failure rate.
S Hancock, R Ben-Shachar, C Adusei, C B Oyolu, E A Evans, H P Kang, C Haverty, D Muzzey. Ultrasound Obstet Gynecol 2020
10
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.