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

Malgorzata I Srebniak, Karin Em Diderich, Marieke Joosten, Lutgarde Cp Govaerts, Jeroen Knijnenburg, Femke At de Vries, Marjan Boter, Debora Lont, Maarten Fcm Knapen, Merel C de Wit, Attie Tji Go, Robert-Jan H Galjaard, Diane Van Opstal. Eur J Hum Genet 2016
Times Cited: 37

List of shared articles

Times cited

Benefit versus risk of chromosomal microarray analysis performed in pregnancies with normal and positive prenatal screening results: A retrospective study.
Rami Moshonov, Keren Hod, Bella Azaria, Ifat Abadi-Korek, Rachel Berger, Mordechai Shohat. PLoS One 2021

The frequency of CNVs in a cohort population of consecutive fetuses with congenital anomalies after the termination of pregnancy.
Gorazd Rudolf, Luca Lovrečić, Nataša Tul, Nataša Teran, Borut Peterlin. Mol Genet Genomic Med 2019

A Retrospective Analysis of 10-Year Data Assessed the Diagnostic Accuracy and Efficacy of Cytogenomic Abnormalities in Current Prenatal and Pediatric Settings.
Hongyan Chai, Autumn DiAdamo, Brittany Grommisch, Fang Xu, Qinghua Zhou, Jiadi Wen, Maurice Mahoney, Allen Bale, James McGrath, Michele Spencer-Manzon,[...]. Front Genet 2019

Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH.
A Vetro, D Goidin, I Lesende, I Limongelli, G N Ranzani, F Novara, M C Bonaglia, B Rinaldi, F Franchi, E Manolakos,[...]. Clin Genet 2018

The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis.
Melissa Stosic, Brynn Levy, Ronald Wapner. Obstet Gynecol Clin North Am 2018