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
0

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
0

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
1

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

Cytogenomic aberrations in isolated multicystic dysplastic kidney in children.
Tian-Jian Chen, Renfang Song, Adam Janssen, Ihor V Yosypiv. Pediatr Res 2021
0

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
0

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
0

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
8

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

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
0