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



Kyle Retterer, Jane Juusola, Megan T Cho, Patrik Vitazka, Francisca Millan, Federica Gibellini, Annette Vertino-Bell, Nizar Smaoui, Julie Neidich, Kristin G Monaghan, Dianalee McKnight, Renkui Bai, Sharon Suchy, Bethany Friedman, Jackie Tahiliani, Daniel Pineda-Alvarez, Gabriele Richard, Tracy Brandt, Eden Haverfield, Wendy K Chung, Sherri Bale. Genet Med 2016
Times Cited: 414




List of shared articles



Times cited

Whole Exome Sequencing Aids the Diagnosis of Fetal Skeletal Dysplasia.
Hui Tang, Qin Zhang, Jingjing Xiang, Linliang Yin, Jing Wang, Ting Wang. Front Genet 2021
0

Genotype-phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders.
Ilaria Mannucci, Nghi D P Dang, Hannes Huber, Jaclyn B Murry, Jeff Abramson, Thorsten Althoff, Siddharth Banka, Gareth Baynam, David Bearden, Ana Beleza-Meireles,[...]. Genome Med 2021
1

Variant interpretation is a component of clinical practice among genetic counselors in multiple specialties.
Karen E Wain, Danielle R Azzariti, Jennifer L Goldstein, Amy Knight Johnson, Patti Krautscheid, Brianna Lepore, Julianne M O'Daniel, Deborah Ritter, Juliann M Savatt, Erin Rooney Riggs,[...]. Genet Med 2020
3

Genetic Examination for Fetuses with Increased Fetal Nuchal Translucency by Genomic Technology.
Shuya Xue, Huanchen Yan, Jingsi Chen, Nan Li, Jiayan Wang, Yu Liu, Huimin Zhang, Shaoying Li, Wei Zhang, Dunjin Chen,[...]. Cytogenet Genome Res 2020
3

Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies.
Korbinian M Riedhammer, Matthias C Braunisch, Roman G√ľnthner, Matias Wagner, Clara Hemmer, Tim M Strom, Christoph Schmaderer, Lutz Renders, Velibor Tasic, Zoran Gucev,[...]. Am J Kidney Dis 2020
8