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

Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland, Daniel Pineda-Alvarez, Swaroop Aradhya, Christa Lese Martin. Genet Med 2020
Times Cited: 117

List of shared articles

Times cited

Risk of Clinically Significant Chromosomal Microarray Analysis Findings in Fetuses With Nuchal Translucency From 3.0 mm Through 3.4 mm.
Lena Sagi-Dain, Amihood Singer, Shay Ben Shachar, Sagi Josefsberg Ben Yehoshua, Michal Feingold-Zadok, Lior Greenbaum, Idit Maya. Obstet Gynecol 2021

Identification of copy number variants by NGS-based NIPT at low sequencing depth.
Xiaoqing Ye, Shengmou Lin, Xiwei Song, Meihua Tan, Jia Li, Jiayan Wang, Huanchen Yan, Huimin Zhang, Shaoying Li, Dunjin Chen,[...]. Eur J Obstet Gynecol Reprod Biol 2021

Rare and low frequency genomic variants impacting neuronal functions modify the Dup7q11.23 phenotype.
Farah Qaiser, Yue Yin, Carolyn B Mervis, Colleen A Morris, Bonita P Klein-Tasman, Elaine Tam, Lucy R Osborne, Ryan K C Yuen. Orphanet J Rare Dis 2021

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

Cytogenomic aberrations in isolated multicystic dysplastic kidney in children.
Tian-Jian Chen, Renfang Song, Adam Janssen, Ihor V Yosypiv. Pediatr Res 2021

Detection of cytogenomic abnormalities by OncoScan microarray assay for products of conception from formalin-fixed paraffin-embedded and fresh fetal tissues.
Jiadi Wen, Brittany Grommisch, Autumn DiAdamo, Hongyan Chai, Sok Meng Evelyn Ng, Pei Hui, Allen Bale, Winifred Mak, Guilin Wang, Peining Li. Mol Cytogenet 2021

Array-comparative Genomic Hybridization Results in Clinically Affected Cases with Apparently Balanced Chromosomal Rearrangements.
N B Satkin, B Karaman, S Ergin, H Kayserili, I H Kalelioglu, R Has, A Yuksel, S Basaran. Balkan J Med Genet 2021

Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort.
Xinran Dong, Bo Liu, Lin Yang, Huijun Wang, Bingbing Wu, Renchao Liu, Hongbo Chen, Xiang Chen, Sha Yu, Bin Chen,[...]. J Med Genet 2020

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

Limited diagnostic impact of duplications <1 Mb of uncertain clinical significance: a 10-year retrospective analysis of reporting practices at the Mayo Clinic.
Cherisse A Marcou, Beth Pitel, Clinton E Hagen, Nicole J Boczek, Ross A Rowsey, Linda B Baughn, Nicole L Hoppman, Erik C Thorland, Hutton M Kearney. Genet Med 2020