A citation-based method for searching scientific literature

Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
Times Cited: 504

List of shared articles

Times cited

Genetic testing in fetuses with isolated agenesis of the corpus callosum.
Qin She, Fang Fu, Xiaoyan Guo, Weihe Tan, Can Liao. J Matern Fetal Neonatal Med 2021

Identification of genomic imbalances in oral clefts.
Elaine Lustosa-Mendes, Ana P Dos Santos, Társis P Vieira, Erlane M Ribeiro, Adriana A Rezende, Agnes C Fett-Conte, Denise P Cavalcanti, Têmis M Félix, Isabella L Monlleó, Vera Lúcia Gil-da-Silva-Lopes. J Pediatr (Rio J) 2021

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
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,[...]. Genet Med 2020

High Detection Rate of Copy Number Variations Using Capture Sequencing Data: A Retrospective Study.
Yu Sun, Xiantao Ye, Yanjie Fan, Lili Wang, Xiaomei Luo, Huili Liu, Xueren Gao, Zhuwen Gong, Yu Wang, Wenjuan Qiu,[...]. Clin Chem 2020

Reinterpretation of Chromosomal Microarrays with Detailed Medical History.
Midhat S Farooqi, Shirelle Figueroa, Garrett Gotway, Jason Wang, Hung S Luu, Jason Y Park. J Pediatr 2020

Application of Whole-Exome Sequencing in Detecting Copy Number Variants in Patients with Developmental Delay and/or Multiple Congenital Malformations.
Évelin A Zanardo, Fabíola P Monteiro, Samar N Chehimi, Yanca G Oliveira, Alexandre T Dias, Larissa A Costa, Luiza L Ramos, Gil M Novo-Filho, Marília M Montenegro, Amom M Nascimento,[...]. J Mol Diagn 2020