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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women
Mylène Badeau, Carmen Lindsay, Jonatan Blais, et al.
Cochrane library (2017) Vol. 2017, Iss. 11
Open Access | Times Cited: 103

Showing 1-25 of 103 citing articles:

Position statement from the International Society for Prenatal Diagnosis on the use of non‐invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies
Lisa Hui, Katie Ellis, Dora Mayen, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 7, pp. 814-828
Open Access | Times Cited: 62
Outcome of publicly funded nationwide first-tier noninvasive prenatal screening
Kris Van Den Bogaert, Lore Lannoo, Nathalie Brison, et al.
Genetics in Medicine (2021) Vol. 23, Iss. 6, pp. 1137-1142
Open Access | Times Cited: 98
Antenatal screening for chromosomal abnormalities
Karl Oliver Kagan, Jiri Sonek, P. Kozlowski
Archives of Gynecology and Obstetrics (2022) Vol. 305, Iss. 4, pp. 825-835
Open Access | Times Cited: 43
Diagnostic accuracy of ultrasound screening for fetal structural abnormalities during the first and second trimester of pregnancy in low-risk and unselected populations
Marieke F.J. Buijtendijk, B. Bet, Mariska Leeflang, et al.
Cochrane library (2024) Vol. 2024, Iss. 5
Closed Access | Times Cited: 15
First trimester ultrasound tests alone or in combination with first trimester serum tests for Down's syndrome screening
S Kate Alldred, Yemisi Takwoingi, Boliang Guo, et al.
Cochrane library (2017) Vol. 2017, Iss. 3
Open Access | Times Cited: 78
A systematic review and meta‐analysis of cell‐free DNA testing for detection of fetal sex chromosome aneuploidy
Matthew A. Shear, Kate Swanson, Ria Garg, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 2, pp. 133-143
Closed Access | Times Cited: 22
Update on the use of exome sequencing in the diagnosis of fetal abnormalities
Lauren Ferretti, Rhiannon Mellis, Lyn S. Chitty
European Journal of Medical Genetics (2019) Vol. 62, Iss. 8, pp. 103663-103663
Open Access | Times Cited: 45
Cell-free DNA in plasma as an essential immune system regulator
Marie Korabečná, Alžběta Zinková, Iva Brynychova, et al.
Scientific Reports (2020) Vol. 10, Iss. 1
Open Access | Times Cited: 43
Next-Generation Sequencing-Based Pre-Implantation Genetic Testing for Aneuploidy (PGT-A): First Report from Saudi Arabia
Yusra Alyafee, Qamre Alam, Abeer Al Tuwaijri, et al.
Genes (2021) Vol. 12, Iss. 4, pp. 461-461
Open Access | Times Cited: 33
Initial Clinical Experience with NIPT for Rare Autosomal Aneuploidies and Large Copy Number Variations
Thomas Harasim, Teresa Neuhann, Anne Behnecke, et al.
Journal of Clinical Medicine (2022) Vol. 11, Iss. 2, pp. 372-372
Open Access | Times Cited: 19
Are People From Black Communities Proportionately Represented in UK and US Studies Examining Views on Screening and Diagnostic Genetic Testing in Pregnancy? A Scoping Review
Michelle Peter, Rashida Baptiste, Celine Lewis, et al.
BJOG An International Journal of Obstetrics & Gynaecology (2025)
Open Access
Psychological and social consequences of non-invasive prenatal testing (NIPT): a scoping review
Valérie Labonté, Dima Alsaid, Britta Lang, et al.
BMC Pregnancy and Childbirth (2019) Vol. 19, Iss. 1
Open Access | Times Cited: 30
Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions: A Health Technology Assessment.

PubMed (2019) Vol. 19, Iss. 4, pp. 1-166
Closed Access | Times Cited: 30
The role of non-invasive prenatal testing and ultrasound in prenatal screening of fetal chromosomal abnormalities in singleton: a retrospective study
Xiying Yuan, Wenjing Yong, Lei Dai, et al.
Annals of Translational Medicine (2023) Vol. 11, Iss. 2, pp. 111-111
Open Access | Times Cited: 10
Non‐invasive prenatal testing (NIPT) in twin pregnancies affected by early single fetal demise: A systematic review of NIPT and vanishing twins
Jacintha C. A. van Eekhout, Mireille N. Bekker, Caroline J. Bax, et al.
Prenatal Diagnosis (2023) Vol. 43, Iss. 7, pp. 829-837
Open Access | Times Cited: 10
Systematic Review of Accuracy Differences in NIPT Methods for Common Aneuploidy Screening
Tamás Marton, Zsófia R. Erdélyi, Minori Takai, et al.
Journal of Clinical Medicine (2025) Vol. 14, Iss. 8, pp. 2813-2813
Open Access
Non-invasive prenatal testing for the detection of trisomy 13, 18, and 21 and sex chromosome aneuploidies in 68,763 cases
Yanchun Zhang, Hongyan Xu, Wen Zhang, et al.
Frontiers in Genetics (2022) Vol. 13
Open Access | Times Cited: 15
47, XXX syndrome with infertility, premature ovarian insufficiency, and streak ovaries
Munazzah Rafique, Solaiman Al-Obaid, Dania Al‐Jaroudi
Clinical Case Reports (2019) Vol. 7, Iss. 6, pp. 1238-1241
Open Access | Times Cited: 24
The Reproductive Journey in the Genomic Era: From Preconception to Childhood
Sandra García-Herrero, Blanca Simon, Javier García‐Planells
Genes (2020) Vol. 11, Iss. 12, pp. 1521-1521
Open Access | Times Cited: 23
Noninvasive Prenatal Testing for Trisomies 21, 18, and 13, Sex Chromosome Aneuploidies, and Microdeletions in Average-Risk Pregnancies: A Cost-Effectiveness Analysis
Xuanqian Xie, Myra Wang, Elaine Goh, et al.
Journal of Obstetrics and Gynaecology Canada (2020) Vol. 42, Iss. 6, pp. 740-749.e12
Closed Access | Times Cited: 21
Trends in the prevalence, prenatal diagnosis, and outcomes of births with chromosomal abnormalities: a hospital-based study in Zhejiang Province, China during 2014–2020
Xinning Chen, Dan Lin, Yinghui Ye, et al.
Orphanet Journal of Rare Diseases (2022) Vol. 17, Iss. 1
Open Access | Times Cited: 14
Non‐Invasive prenatal testing with rolling circle amplification: Real‐world clinical experience in a non‐molecular laboratory
Matthew L. Saidel, Uma Ananth, Donna Rose, et al.
Journal of Clinical Laboratory Analysis (2023) Vol. 37, Iss. 6
Open Access | Times Cited: 8
The Amniotic Fluid Cell-Free Transcriptome Provides Novel Information about Fetal Development and Placental Cellular Dynamics
Hee Jin Park, Hee Young Cho, Dong Hyun
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 5, pp. 2612-2612
Open Access | Times Cited: 17
Non‐invasive prenatal testing for the prenatal screening of sex chromosome aneuploidies: A systematic review and meta‐analysis of diagnostic test accuracy studies
Bounhome Soukkhaphone, Carmen Lindsay, Sylvie Langlois, et al.
Molecular Genetics & Genomic Medicine (2021) Vol. 9, Iss. 5
Open Access | Times Cited: 17
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