A citation-based method for searching scientific literature

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



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, Susan Klugman, Thomas Scholl, Joe Leigh Simpson, Kimberly McCall, Vimla S Aggarwal, Brian Bunke, Odelia Nahum, Ankita Patel, Allen N Lamb, Elizabeth A Thom, Arthur L Beaudet, David H Ledbetter, Lisa G Shaffer, Laird Jackson. N Engl J Med 2012
Times Cited: 657




List of shared articles



Times cited

Chromosomal microarray analysis in fetuses with central nervous system anomalies: An 8-year long observational study from a tertiary care university hospital.
Maddalena Santirocco, Alberto Plaja, Carlota Rodó, Irene Valenzuela, Silvia Arévalo, Neus Castells, Anna Abuli, Eduardo Tizzano, Nerea Maiz, Elena Carreras. Prenat Diagn 2021
1

The yield of chromosomal microarray analysis among pregnancies terminated due to fetal malformations.
Yael Pasternak, Yair Daykan, Tamar Tenne, Eyal Reinstein, Netanella Miller, Gil Shechter-Maor, Idit Maya, Tal Biron-Shental, Rivka Sukenik Halevy. J Matern Fetal Neonatal Med 2020
1

Chromosome 15q13 microduplication in a fetus with cardiac rhabdomyoma: a case report.
Chen-Zhao Lin, Bi-Ru Qi, Jian-Su Hu, Yu-Dian Huang, Xiu-Qiong Huang. Mol Cytogenet 2019
3


Prenatal Diagnostic Value of Chromosomal Microarray in Fetuses with Nuchal Translucency Greater than 2.5 mm.
Zhu Zhang, Ting Hu, Jiamin Wang, Qinqin Li, He Wang, Shanling Liu. Biomed Res Int 2019
9

Reply.
G Malinger, D Paladini, K K Haratz, A Monteagudo, G Pilu, I E Timor-Tritsch. Ultrasound Obstet Gynecol 2021
0

Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies.
Valeria Orlando, Viola Alesi, Gianluca Di Giacomo, Michela Canestrelli, Chiara Calacci, Anna Maria Nardone, Giusy Calvieri, Maria Teresa Liambo, Ester Sallicandro, Silvia Di Tommaso,[...]. Reprod Sci 2021
0

Prenatal Diagnostic Testing Following High-Risk Result from Serological Screening: Which Shall We Select?
Jing Wang, Xin-Xin Tang, Qin Zhou, Shuting Yang, Ye Shi, Bin Yu, Bin Zhang, Lei-Lei Wang. Int J Womens Health 2021
0


Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.
Desheng Liang, David S Cram, Hu Tan, Siyuan Linpeng, Yingdi Liu, Huaiyu Sun, Yu Zhang, Feng Tian, Hongmin Zhu, Mengnan Xu,[...]. Genet Med 2019
55

Clinical value for the detection of fetal chromosomal deletions/duplications by noninvasive prenatal testing in clinical practice.
Lingshan Gou, Feng Suo, Yi Wang, Na Wang, Qin Wu, Shunan Hu, Peng Wang, Lize Gu, Man Zhang, Chuanxia Wang,[...]. Mol Genet Genomic Med 2021
0

A two-year prospective study assessing the performance of fetal chromosomal microarray analysis and next-generation sequencing in high-risk pregnancies.
Konstantin Ridnõi, Kai Muru, Maria Keernik, Sander Pajusalu, Eva-Liina Ustav, Pille Tammur, Triin Mölter-Väär, Tiina Kahre, Ustina Šamarina, Karin Asser,[...]. Mol Genet Genomic Med 2021
0


Application of chromosome microarray analysis in prenatal diagnosis.
Mingjing Xia, Xinhong Yang, Jing Fu, Zhenjuan Teng, Yan Lv, Lixia Yu. BMC Pregnancy Childbirth 2020
1

Should prenatal chromosomal microarray analysis be offered for isolated fetal growth restriction? A French multicenter study.
Isabelle Monier, Aline Receveur, Véronique Houfflin-Debarge, Valérie Goua, Vanina Castaigne, Jean-Marie Jouannic, Eve Mousty, Anne-Hélène Saliou, Hanane Bouchghoul, Thierry Rousseau,[...]. Am J Obstet Gynecol 2021
0

Lower detectability of non-invasive prenatal testing compared to prenatal diagnosis in high-risk pregnant women.
Jing Wang, Zhi-Wei Wang, Qin Zhou, Bin Zhang, Ting Yin, Bin Yu, Lei-Lei Wang. Ann Transl Med 2019
3

Case Report: Whole Exome Sequencing Revealed Two Novel Mutations of PIEZO1 Implicated in Nonimmune Hydrops Fetalis.
Yuan Chen, Ying Jiang, Bangwu Chen, Yeqing Qian, Jiao Liu, Mengmeng Yang, Baihui Zhao, Qiong Luo. Front Genet 2021
0

Cell-free fetal DNA screening for detection of microdeletion syndromes: a cost-effectiveness analysis.
Carmen M Avram, Brian L Shaffer, Teresa N Sparks, Allison J Allen, Aaron B Caughey. J Matern Fetal Neonatal Med 2021
3

Role of late amniocentesis in the era of modern genomic technologies.
H Daum, A Ben David, M Nadjari, S Zenvirt, S Helman, N Yanai, V Meiner, S Yagel, A Frumkin, S Shkedi Rafid. Ultrasound Obstet Gynecol 2019
8

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, Ilina D Pluym, Kerry Holliman, Jennifer Duffy, Sarah L Downum, Sachi Patel, Amanda Faubel, Nina M Boe,[...]. N Engl J Med 2020
23

A rapid and simple bead-bashing-based method for genomic DNA extraction from mammalian tissue.
Shan Wei, Brynn Levy, Nataly Hoffman, Claudia Cujar, Reunet Rodney-Sandy, Ronald Wapner, Mary D'Alton, Zev Williams. Biotechniques 2020
2

Study protocol: childhood outcomes of fetal genomic variants: the PrenatAL Microarray (PALM) cohort study.
Lisa Hui, Cecilia Pynaker, Joanne Kennedy, Sharon Lewis, David J Amor, Susan P Walker, Jane Halliday. BMC Pediatr 2021
0

Chances and Challenges of New Genetic Screening Technologies (NIPT) in Prenatal Medicine from a Clinical Perspective: A Narrative Review.
Ivonne Bedei, Aline Wolter, Axel Weber, Fabrizio Signore, Roland Axt-Fliedner. Genes (Basel) 2021
3

Is Prenatal Diagnosis Necessary for Fetal Isolated Nasal Bone Absence or Hypoplasia?
Feng Zhang, Wei Long, Qin Zhou, Jing Wang, Ye Shi, Jianbing Liu, Qiuwei Wang. Int J Gen Med 2021
0

Current landscape of prenatal genetic screening and testing.
Nevena Krstić, Sarah G Običan. Birth Defects Res 2020
3

Are all chromosome microarrays the same? What clinicians need to know.
Brynn Levy, Rachel D Burnside. Prenat Diagn 2019
8

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies.
Jingjing Xiang, Yang Ding, Xiaoyan Song, Jun Mao, Minjuan Liu, Yinghua Liu, Chao Huang, Qin Zhang, Ting Wang. Front Genet 2020
4

Submicroscopic chromosomal imbalances contribute to early abortion.
Haibo Li, Minjuan Liu, Min Xie, Qin Zhang, Jingjing Xiang, Chengying Duan, Yang Ding, Yinghua Liu, Jun Mao, Ting Wang,[...]. Mol Cytogenet 2018
3

A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples.
Xiya Zhou, Xiangbin Chen, Yulin Jiang, Qingwei Qi, Na Hao, Chengkun Liu, Mengnan Xu, David S Cram, Juntao Liu. Life (Basel) 2021
1

The Necessity of Prenatal Diagnosis by CMA for the Women with NIPS-Positive Results.
Jun Xu, Ying Xue, Jing Wang, Qin Zhou, Bin Zhang, Bin Yu, Ting Wang. Int J Genomics 2020
0

Discrepancy of QF-PCR, CMA and karyotyping on a de novo case of mosaic isodicentric Y chromosomes.
Yuan Liu, Li Guo, Hanbiao Chen, Jian Lu, Jingjing Hu, Xianzheng Li, Xing Li, Ting Wang, Fengzhen Li, Aihua Yin. Mol Cytogenet 2019
3

The role of chromosomal microarray and exome sequencing in prenatal diagnosis.
Matthew Hoi Kin Chau, Kwong Wai Choy. Curr Opin Obstet Gynecol 2021
1


Benefit versus risk of chromosomal microarray analysis performed in pregnancies with normal and positive prenatal screening results: A retrospective study.
Rami Moshonov, Keren Hod, Bella Azaria, Ifat Abadi-Korek, Rachel Berger, Mordechai Shohat. PLoS One 2021
0

Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic Bowel.
Xiangqun Fan, Hailong Huang, Xiyao Lin, Huili Xue, Meiying Cai, Na Lin, Liangpu Xu. Risk Manag Healthc Policy 2021
0


Chromosome microarray analysis should be offered to all invasive prenatal diagnostic testing following a normal rapid aneuploidy test result.
Laia Rodriguez-Revenga, Irene Madrigal, Antoni Borrell, Josep M Martinez, Joan Sabria, Lourdes Martin, Wladimiro Jimenez, Aurea Mira, Celia Badenas, Montserrat Milà. Clin Genet 2020
2

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

Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012-2019).
Jenny Patterson, Diana Wellesley, Sian Morgan, Deirdre Cilliers, Stephanie Allen, Carol A Gardiner. Prenat Diagn 2021
0

Cytogenetic and molecular diagnostic testing associated with prenatal and postnatal birth defects.
Stela Z Berisha, Shashi Shetty, Thomas W Prior, Anna L Mitchell. Birth Defects Res 2020
2

Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases.
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,[...]. Prenat Diagn 2019
8

How genomics is changing the practice of prenatal testing.
Isabel Filges, Peter Miny, Wolfgang Holzgreve, Sevgi Tercanli. J Perinat Med 2021
1

Exome Sequencing and Its Emerging Role in Prenatal Genetic Diagnosis.
Maeve K Hopkins, Lorraine Dugoff, Jeffrey A Kuller. Obstet Gynecol Surv 2020
0

Detection of copy number variants with chromosomal microarray in 10 377 pregnancies at a single laboratory.
Yi-Hui Lin, Yiin-Jeng Jong, Pin-Chia Huang, Chris Tsai. Acta Obstet Gynecol Scand 2020
3

The Significance of Fetal Brain Ventricular Asymmetry Without Dilation.
Raanan Meyer, Omer Bar-Yosef, Eran Barzilay, Igal Radinsky, Chen Key Segal, Tomer Ziv-Baran, Hagit Shani, Gabriel Levin, Eldad Katorza. J Ultrasound Med 2021
0

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study.
Hailong Huang, Meiying Cai, Wei Ma, Na Lin, Liangpu Xu. Risk Manag Healthc Policy 2021
0

"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result.
Stina Lou, Kirsten Lomborg, Celine Lewis, Sam Riedijk, Olav Bjørn Petersen, Ida Vogel. Acta Obstet Gynecol Scand 2020
6

First data from the new, unified database of the Hungarian case-control surveillance of congenital abnormalities.
Nándor Ács, Ákos Mátrai, András Kaposi. J Matern Fetal Neonatal Med 2021
0

Prenatal Diagnosis by Chromosome Microarray Analysis, An Indian Experience.
Meena Bajaj Lall, Shruti Agarwal, Preeti Paliwal, Pushpa Saviour, Anju Joshi, Arti Joshi, Surbhi Mahajan, Sunita Bijarnia-Mahay, Ratna Dua Puri, I C Verma. J Obstet Gynaecol India 2021
0

C-banding and AgNOR-staining were still effective complementary methods to indentify chromosomal heteromorphisms and some structural abnormalities in prenatal diagnosis.
Jian Jiang Zhu, Hong Qi, Li Rong Cai, Xiao Hui Wen, Wen Zeng, Guo Dong Tang, Yao Luo, Ran Meng, Xue Qun Mao, Shao Qin Zhang. Mol Cytogenet 2019
0