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



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

Clinical utility of expanded non-invasive prenatal screening and chromosomal microarray analysis in high-risk pregnancy.
X Zhu, M Chen, H Wang, Y Guo, M H K Chau, H Yan, Y Cao, Y K Y Kwok, J Chen, A S Y Hui,[...]. Ultrasound Obstet Gynecol 2021
4

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021
6

Variants of uncertain significance in prenatal microarrays: a retrospective cohort study.
A H Mardy, A P Wiita, B V Wayman, K Drexler, T N Sparks, M E Norton. BJOG 2021
0

A study of normal copy number variations in Israeli population.
Idit Maya, Pola Smirin-Yosef, Sarit Kahana, Sne Morag, Shiri Yacobson, Ifaat Agmon-Fishman, Reut Matar, Elisheva Bitton, Mordechai Shohat, Lina Basel-Salmon,[...]. Hum Genet 2021
1

Precise variant interpretation, phenotype ascertainment, and genotype-phenotype correlation of children in the EARLY PRO-TECT Alport trial.
Jan Boeckhaus, Julia Hoefele, Korbinian M Riedhammer, Burkhard Tönshoff, Rasmus Ehren, Lars Pape, Kay Latta, Henry Fehrenbach, Baerbel Lange-Sperandio, Matthias Kettwig,[...]. Clin Genet 2021
0

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

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

ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data.
Andre E Minoche, Ben Lundie, Greg B Peters, Thomas Ohnesorg, Mark Pinese, David M Thomas, Andreas Zankl, Tony Roscioli, Nicole Schonrock, Sarah Kummerfeld,[...]. Genome Med 2021
1


The genetic landscape of intellectual disability and epilepsy in adults and the elderly: a systematic genetic work-up of 150 individuals.
Pia Zacher, Thomas Mayer, Frank Brandhoff, Tobias Bartolomaeus, Diana Le Duc, Martin Finzel, Anja Heinze, Susanne Horn, Chiara Klöckner, Gudrun Körber,[...]. Genet Med 2021
0

Exome sequencing as the first-tier test for pediatric respiratory diseases: A single-center study.
Chanjuan Hao, Ruolan Guo, Jun Liu, Xuyun Hu, Jun Guo, Yao Yao, Zhipeng Zhao, Zhan Qi, Jun Yin, Lanqin Chen,[...]. Hum Mutat 2021
0


Renal and Skeletal Anomalies in a Cohort of Individuals With Clinically Presumed Hereditary Nephropathy Analyzed by Molecular Genetic Testing.
Michaela Stippel, Korbinian M Riedhammer, Bärbel Lange-Sperandio, Michaela Geßner, Matthias C Braunisch, Roman Günthner, Martin Bald, Miriam Schmidts, Peter Strotmann, Velibor Tasic,[...]. Front Genet 2021
0

Abnormal Microarray, Clinical Outcomes, and Surgical Risk Scores in Young Children with Cardiac Disease.
Kelsey McAfee, Will T Rosenow, Sara Cherny, Catherine A Collins, Lauren C Balmert, Gregory Webster. Pediatr Cardiol 2021
0

Copy number variations and multiallelic variants in Korean patients with Leber congenital amaurosis.
Dongheon Surl, Saeam Shin, Seung-Tae Lee, Jong Rak Choi, Junwon Lee, Suk Ho Byeon, Sueng-Han Han, Hyun Taek Lim, Jinu Han. Mol Vis 2020
2

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

High-frequency low-penetrance copy-number variant classification: should we revise the existing guidelines?
Idit Maya, Lina Basel-Salmon, Ami Singer, Lena Sagi-Dain. Genet Med 2020
3

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
1