A citation-based method for searching scientific literature

Sarah T South, Charles Lee, Allen N Lamb, Anne W Higgins, Hutton M Kearney. Genet Med 2013
Times Cited: 158



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: 630




List of shared articles



Times cited

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

Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan, Sarah E Graham, Maddalena Marasà, Hyunwoo Kim, Tze Y Lim, Patricia L Weng, Elena Sánchez-Rodríguez,[...]. J Am Soc Nephrol 2021
0

The role of chromosomal microarray and exome sequencing in prenatal diagnosis.
Matthew Hoi Kin Chau, Kwong Wai Choy. Curr Opin Obstet Gynecol 2021
0


Practice patterns of prenatal and perinatal testing in Canadian cytogenetics laboratories.
Tamara Ashfield, Elizabeth McCready, Mary Shago, Hong Wang, Elizabeth Sinclair-Bourque, Eva Cappa, Amanda Piche Marolt, Kathy Chun. Prenat Diagn 2021
0

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

Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing.
Xiaoqing Wu, Ying Li, Na Lin, Xiaorui Xie, Linjuan Su, Meiying Cai, Yuan Lin, Linshuo Wang, Meiying Wang, Liangpu Xu,[...]. J Cell Mol Med 2021
0

Expanding the Scope of Non-invasive Prenatal Testing to Detect Fetal Chromosomal Copy Number Variations.
Songchang Chen, Lanlan Zhang, Jiong Gao, Shuyuan Li, Chunxin Chang, Yiyao Chen, Hongjun Fei, Junyu Zhang, Yanlin Wang, Hefeng Huang,[...]. Front Mol Biosci 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
1

Nonimmune hydrops fetalis: Genetic analysis and clinical outcome.
Qiong Deng, Fang Fu, Qiuxia Yu, Ru Li, Fucheng Li, Dan Wang, Tingying Lei, Xin Yang, Can Liao. Prenat Diagn 2020
1

Detection of chromosomal abnormalities in spontaneous miscarriage by low‑coverage next‑generation sequencing.
Fen-Xia Li, Mei-Juan Xie, Shou-Fang Qu, Dan He, Long Wu, Zhi-Kun Liang, Ying-Song Wu, Fang Yang, Xue-Xi Yang. Mol Med Rep 2020
1

Analysis of tissue from pregnancy loss and aborted fetus with ultrasound anomaly using subtelomeric MLPA and chromosomal array analysis.
Jiwu Lou, Manna Sun, Ying Zhao, Youqing Fu, Haiming Yuan, Yunshi Dai, Fuxiao Liang, Yi He, Yanhui Liu. J Matern Fetal Neonatal Med 2020
1

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


Chromosomal microarray analysis in fetuses with an isolated congenital heart defect: A retrospective, nationwide, multicenter study in France.
Marguerite Hureaux, Sarah Guterman, Bérénice Hervé, Marianne Till, Sylvie Jaillard, Sylvie Redon, Myléne Valduga, Charles Coutton, Chantal Missirian, Fabienne Prieur,[...]. Prenat Diagn 2019
4

Cytogenetic microarray in structurally normal and abnormal foetuses: a five year experience elucidating increasing acceptance and clinical utility.
Meenakshi Lallar, Priyanka Srivastava, Archana Rai, Deepti Saxena, Kausik Mandal, Shubha R Phadke. J Genet 2019
0

Genetic and expression changes in TNF-α as a risk factor for rheumatoid arthritis pathogenesis in northeast India.
Somdatta Das, Chitralekha Baruah, Anjan Kumar Saikia, Diptika Tiwari, Sujoy Bose. J Genet 2019
0

The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy.
Gorazd Rudolf, Luca Lovrečić, Nataša Tul, Nataša Teran, Borut Peterlin. Mol Genet Genomic Med 2019
3

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.
Matthew Hoi Kin Chau, Ye Cao, Yvonne Ka Yin Kwok, Samantha Chan, Yiu Man Chan, Huilin Wang, Zhenjun Yang, Hoi Kin Wong, Tak Yeung Leung, Kwong Wai Choy. Am J Obstet Gynecol 2019
12

Subchromosomal anomalies in small for gestational-age fetuses and newborns.
Ying Ma, Yan Pei, Chenghong Yin, Yuxin Jiang, Jingjing Wang, Xiaofei Li, Lin Li, Karl Oliver Kagan, Qingqing Wu. Arch Gynecol Obstet 2019
2

A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings.
Hongyan Chai, Autumn DiAdamo, Brittany Grommisch, Fang Xu, Qinghua Zhou, Jiadi Wen, Maurice Mahoney, Allen Bale, James McGrath, Michele Spencer-Manzon,[...]. Front Genet 2019
3

Genetic basis of human congenital anomalies of the kidney and urinary tract.
Simone Sanna-Cherchi, Rik Westland, Gian Marco Ghiggeri, Ali G Gharavi. J Clin Invest 2018
30

Genomic medicine for kidney disease.
Emily E Groopman, Hila Milo Rasouly, Ali G Gharavi. Nat Rev Nephrol 2018
43

The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis.
Melissa Stosic, Brynn Levy, Ronald Wapner. Obstet Gynecol Clin North Am 2018
18