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Times Cited: 37
Times Cited: 37
Times Cited
Times Co-cited
Similarity
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Desheng Liang, David S Cram, Hu Tan, Siyuan Linpeng, Yingdi Liu, Huaiyu Sun, Yu Zhang, Feng Tian, Hongmin Zhu, Mengnan Xu,[...]. Genet Med 2019
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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
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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
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Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
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Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.
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Jacob A Canick, Glenn E Palomaki, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow. Prenat Diagn 2013
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Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma.
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Fetal fraction and noninvasive prenatal testing: What clinicians need to know.
Lisa Hui, Diana W Bianchi. Prenat Diagn 2020
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Clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision-making.
Aarti Ramdaney, Jennifer Hoskovec, Jacqueline Harkenrider, Eleazar Soto, Lauren Murphy. Prenat Diagn 2018
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Clinical Experience of Non-Invasive Prenatal Chromosomal Aneuploidy Testing in 190,277 Patient Samples.
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Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.
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Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
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Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma.
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Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus.
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Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnancies.
Ying Xue, Guodong Zhao, Hong Li, Qin Zhang, Jiafeng Lu, Bin Yu, Ting Wang. Mol Cytogenet 2019
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Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing.
Can Liao, Ai-hua Yin, Chun-fang Peng, Fang Fu, Jie-xia Yang, Ru Li, Yang-yi Chen, Dong-hong Luo, Yong-ling Zhang, Yan-mei Ou,[...]. Proc Natl Acad Sci U S A 2014
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Non-invasive cell-free fetal DNA testing for aneuploidy: multicenter study of 31 515 singleton pregnancies in southeastern China.
L Xu, H Huang, N Lin, Y Wang, D He, M Zhang, M Chen, L Chen, Y Lin. Ultrasound Obstet Gynecol 2020
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Screening, prenatal diagnosis, and prenatal decision for sex chromosome aneuploidy.
Yong Xu, Liyuan Chen, Yang Liu, Ying Hao, Zhiyong Xu, Liyanyan Deng, Jiansheng Xie. Expert Rev Mol Diagn 2019
Yong Xu, Liyuan Chen, Yang Liu, Ying Hao, Zhiyong Xu, Liyanyan Deng, Jiansheng Xie. Expert Rev Mol Diagn 2019
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ACMG statement on noninvasive prenatal screening for fetal aneuploidy.
Anthony R Gregg, S J Gross, R G Best, K G Monaghan, K Bajaj, B G Skotko, B H Thompson, M S Watson. Genet Med 2013
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TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.
Karuna R M van der Meij, Erik A Sistermans, Merryn V E Macville, Servi J C Stevens, Caroline J Bax, Mireille N Bekker, Caterina M Bilardo, Elles M J Boon, Marjan Boter, Karin E M Diderich,[...]. Am J Hum Genet 2019
Karuna R M van der Meij, Erik A Sistermans, Merryn V E Macville, Servi J C Stevens, Caroline J Bax, Mireille N Bekker, Caterina M Bilardo, Elles M J Boon, Marjan Boter, Karin E M Diderich,[...]. Am J Hum Genet 2019
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Rare autosomal trisomies: Important and not so rare.
Fergus Scott, Michael Bonifacio, Rhiannon Sandow, Katie Ellis, Maria-Elisabeth Smet, Andrew McLennan. Prenat Diagn 2018
Fergus Scott, Michael Bonifacio, Rhiannon Sandow, Katie Ellis, Maria-Elisabeth Smet, Andrew McLennan. Prenat Diagn 2018
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Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
Andrea K Petersen, Sau Wai Cheung, Janice L Smith, Weimin Bi, Patricia A Ward, Sandra Peacock, Alicia Braxton, Ignatia B Van Den Veyver, Amy M Breman. Am J Obstet Gynecol 2017
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DNA sequencing versus standard prenatal aneuploidy screening.
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Screening for Fetal Chromosomal Abnormalities: ACOG Practice Bulletin, Number 226.
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Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.
Kitty K Lo, Evangelia Karampetsou, Christopher Boustred, Fiona McKay, Sarah Mason, Melissa Hill, Vincent Plagnol, Lyn S Chitty. Am J Hum Genet 2016
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Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population.
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Yijun Song, Congcong Liu, Hong Qi, Yunping Zhang, Xuming Bian, Juntao Liu. Prenat Diagn 2013
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Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Jinglan Zhang, Jianli Li, Jennifer B Saucier, Yanming Feng, Yanjun Jiang, Jefferson Sinson, Anne K McCombs, Eric S Schmitt, Sandra Peacock, Stella Chen,[...]. Nat Med 2019
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Sequencing shorter cfDNA fragments improves the fetal DNA fraction in noninvasive prenatal testing.
Longwei Qiao, Bin Yu, Yuting Liang, Chunhua Zhang, Xiaojuan Wu, Ying Xue, Cong Shen, Quanze He, Jiafeng Lu, Jingjing Xiang,[...]. Am J Obstet Gynecol 2019
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Sex chromosome aneuploidy detection by noninvasive prenatal testing: helpful or hazardous?
Rosemary E Reiss, Marie Discenza, Judith Foster, Lori Dobson, Louise Wilkins-Haug. Prenat Diagn 2017
Rosemary E Reiss, Marie Discenza, Judith Foster, Lori Dobson, Louise Wilkins-Haug. Prenat Diagn 2017
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Global perspectives on clinical adoption of NIPT.
Mollie A Minear, Celine Lewis, Subarna Pradhan, Subhashini Chandrasekharan. Prenat Diagn 2015
Mollie A Minear, Celine Lewis, Subarna Pradhan, Subhashini Chandrasekharan. Prenat Diagn 2015
10
Current Status of Testing for Microdeletion Syndromes and Rare Autosomal Trisomies Using Cell-Free DNA Technology.
Yuval Yaron, Jacques Jani, Maximilian Schmid, Dick Oepkes. Obstet Gynecol 2015
Yuval Yaron, Jacques Jani, Maximilian Schmid, Dick Oepkes. Obstet Gynecol 2015
11
Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications.
Maria C Neofytou, Kyriakos Tsangaras, Elena Kypri, Charalambos Loizides, Marios Ioannides, Achilleas Achilleos, Petros Mina, Anna Keravnou, Carolina Sismani, George Koumbaris,[...]. PLoS One 2017
Maria C Neofytou, Kyriakos Tsangaras, Elena Kypri, Charalambos Loizides, Marios Ioannides, Achilleas Achilleos, Petros Mina, Anna Keravnou, Carolina Sismani, George Koumbaris,[...]. PLoS One 2017
14
Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.
Pe'er Dar, Kirsten J Curnow, Susan J Gross, Megan P Hall, Melissa Stosic, Zachary Demko, Bernhard Zimmermann, Matthew Hill, Styrmir Sigurjonsson, Allison Ryan,[...]. Am J Obstet Gynecol 2014
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The clinical utility of genome-wide non invasive prenatal screening.
Francesco Fiorentino, Sara Bono, Francesca Pizzuti, Sara Duca, Arianna Polverari, Monica Faieta, Marina Baldi, Laura Diano, Francesca Spinella. Prenat Diagn 2017
Francesco Fiorentino, Sara Bono, Francesca Pizzuti, Sara Duca, Arianna Polverari, Monica Faieta, Marina Baldi, Laura Diano, Francesca Spinella. Prenat Diagn 2017
10
Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease.
Mark D Pertile, Meredith Halks-Miller, Nicola Flowers, Catalin Barbacioru, Sarah L Kinnings, Darcy Vavrek, William K Seltzer, Diana W Bianchi. Sci Transl Med 2017
Mark D Pertile, Meredith Halks-Miller, Nicola Flowers, Catalin Barbacioru, Sarah L Kinnings, Darcy Vavrek, William K Seltzer, Diana W Bianchi. Sci Transl Med 2017
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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
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
10
Current controversies in prenatal diagnosis 1: should NIPT routinely include microdeletions/microduplications?
Nancy C Rose, Peter Benn, Aubrey Milunsky. Prenat Diagn 2016
Nancy C Rose, Peter Benn, Aubrey Milunsky. Prenat Diagn 2016
16
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.