A citation-based method for searching scientific literature

Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall, Michael W Varner, Robert L Goldenberg, Radek Bukowski, Ronald J Wapner, Carolyn D Drews-Botsch, Barbara M O'Brien, Donald J Dudley, Brynn Levy. N Engl J Med 2012
Times Cited: 141







List of shared articles



Times cited

Clinical Practice Guidelines for Prenatal Aneuploidy Screening and Diagnostic Testing from Korean Society of Maternal-Fetal Medicine: (2) Invasive Diagnostic Testing for Fetal Chromosomal Abnormalities.
Ji Yeon Lee, Ji Young Kwon, Sunghun Na, Seung Ah Choe, Hyun Joo Seol, Minhyoung Kim, Min A Kim, Chan Wook Park, Kunwoo Kim, Hyun Mee Ryu,[...]. J Korean Med Sci 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
1

Genetic diagnosis in the fetus.
Monica H Wojcik, Rebecca Reimers, Tabitha Poorvu, Pankaj B Agrawal. J Perinatol 2020
2

A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort.
Lisa Hui, Alice Poulton, Eliza Kluckow, Anthea Lindquist, Briohny Hutchinson, Mark D Pertile, Leonard Bonacquisto, Lucy Gugasyan, Abhijit Kulkarni, James Harraway,[...]. Hum Reprod 2020
2

The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers.
Leslie Durham, Ramesha Papanna, Blair Stevens, Sarah Noblin, David Rodriguez-Buritica, S Shahrukh Hashmi, Nevena Krstic. Prenat Diagn 2019
4

Importance of complete phenotyping in prenatal whole exome sequencing.
Mahmoud Aarabi, Olivia Sniezek, Huaiyang Jiang, Devereux N Saller, Daniel Bellissimo, Svetlana A Yatsenko, Aleksandar Rajkovic. Hum Genet 2018
30

A feasible diagnostic approach for the translocation carrier from the indication of products of conception.
Ye-Qing Qian, Xiao-Ying Fu, Xiao-Qing Wang, Yu-Qin Luo, Min Chen, Kai Yan, Yan-Mei Yang, Bei Liu, Li-Ya Wang, Ying-Zhi Huang,[...]. Mol Cytogenet 2018
1

The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis.
Melissa Stosic, Brynn Levy, Ronald Wapner. Obstet Gynecol Clin North Am 2018
20



Chromosome copy number variants in fetuses with syndromic malformations.
Huilin Wang, Matthew Hoi Kin Chau, Ye Cao, Ka Yin Kwok, Kwong Wai Choy. Birth Defects Res 2017
4