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



M C de Wit, M I Srebniak, L C P Govaerts, D Van Opstal, R J H Galjaard, A T J I Go. Ultrasound Obstet Gynecol 2014
Times Cited: 91




List of shared articles



Times cited

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.
Annie Sy Hui, Matthew Hoi Kin Chau, Yiu Man Chan, Ye Cao, Angel Hw Kwan, Xiaofan Zhu, Yvonne K Kwok, Zihan Chen, Terence T Lao, Kwong Wai Choy,[...]. Acta Obstet Gynecol Scand 2021
1

Clinical Application of Easychip 8x15K Platform in 4106 Pregnancies Without Ultrasound Anomalies.
Valeria Orlando, Viola Alesi, Gianluca Di Giacomo, Michela Canestrelli, Chiara Calacci, Anna Maria Nardone, Giusy Calvieri, Maria Teresa Liambo, Ester Sallicandro, Silvia Di Tommaso,[...]. Reprod Sci 2021
0

Chromosomal abnormalities detected by karyotyping and microarray analysis in twins with structural anomalies.
L Li, Z He, X Huang, S Lin, J Wu, L Huang, Y Wan, Q Fang. Ultrasound Obstet Gynecol 2020
0

What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?
Idit Maya, Amihood Singer, Hagith Yonath, Adi Reches, Shlomit Rienstein, Sharon Zeligson, Shay Ben Shachar, Lena Sagi-Dain. Acta Obstet Gynecol Scand 2020
2

The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.
Amber E L van Nisselrooij, Malou A Lugthart, Sally-Ann Clur, Ingeborg H Linskens, Eva Pajkrt, Lukas A Rammeloo, Lieke Rozendaal, Nico A Blom, Jan M M van Lith, Alida C Knegt,[...]. Genet Med 2020
8