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: 513



Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey, Rhiannon Mellis, Sarah Robart, Ian R Berry, Kate E Chandler, Deirdre Cilliers, Lara Cresswell, Sandra L Edwards, Carol Gardiner, Alex Henderson, Simon T Holden, Tessa Homfray, Tracy Lester, Rebecca A Lewis, Ruth Newbury-Ecob, Katrina Prescott, Oliver W Quarrell, Simon C Ramsden, Eileen Roberts, Dagmar Tapon, Madeleine J Tooley, Pradeep C Vasudevan, Astrid P Weber, Diana G Wellesley, Paul Westwood, Helen White, Michael Parker, Denise Williams, Lucy Jenkins, Richard H Scott, Mark D Kilby, Lyn S Chitty, Matthew E Hurles, Eamonn R Maher. Lancet 2019
Times Cited: 144




List of shared articles



Times cited

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
1

Combined exome sequencing and deep phenotyping in highly selected fetuses with skeletal dysplasia during the first and second trimesters improves diagnostic yield.
Xinyue Zhang, Yuan Ren, Rui Song, Longxia Wang, Hong Xu, Xiaoxiao Xie, Honghui Zhou, Pei Sun, Manli Zhang, Qingdong Zhao,[...]. Prenat Diagn 2021
0

Contribution of single-gene defects to congenital cardiac left-sided lesions in the prenatal setting.
H Sun, T Yi, X Hao, H Yan, J Wang, Q Li, X Gu, X Zhou, S Wang, X Wang,[...]. Ultrasound Obstet Gynecol 2020
12

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

Maternity health care professionals' views and experiences of fetal genomic uncertainty: A review.
Lisa Hui, Emma Szepe, Jane Halliday, Celine Lewis. Prenat Diagn 2020
3

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

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
10