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: 159



Zirui Dong, Jun Zhang, Ping Hu, Haixiao Chen, Jinjin Xu, Qi Tian, Lu Meng, Yanchou Ye, Jun Wang, Meiyan Zhang, Yun Li, Huilin Wang, Shanshan Yu, Fang Chen, Jiansheng Xie, Hui Jiang, Wei Wang, Kwong Wai Choy, Zhengfeng Xu. Genet Med 2016
Times Cited: 67




List of shared articles



Times cited

Detection of chromosomal abnormalities in spontaneous miscarriage by low‑coverage next‑generation sequencing.
Fen-Xia Li, Mei-Juan Xie, Shou-Fang Qu, Dan He, Long Wu, Zhi-Kun Liang, Ying-Song Wu, Fang Yang, Xue-Xi Yang. Mol Med Rep 2020
1

Copy-number variants in clinical genome sequencing: deployment and interpretation for rare and undiagnosed disease.
Andrew M Gross, Subramanian S Ajay, Vani Rajan, Carolyn Brown, Krista Bluske, Nicole J Burns, Aditi Chawla, Alison J Coffey, Alka Malhotra, Alicia Scocchia,[...]. Genet Med 2019
30

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.
Matthew Hoi Kin Chau, Ye Cao, Yvonne Ka Yin Kwok, Samantha Chan, Yiu Man Chan, Huilin Wang, Zhenjun Yang, Hoi Kin Wong, Tak Yeung Leung, Kwong Wai Choy. Am J Obstet Gynecol 2019
12

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.
Zirui Dong, Junhao Yan, Fengping Xu, Jianying Yuan, Hui Jiang, Huilin Wang, Haixiao Chen, Lei Zhang, Lingfei Ye, Jinjin Xu,[...]. Am J Hum Genet 2019
14

Fecundity in an infertile man with r(15) - a challenge to the current paradigm.
Hamid Kalantari, Hamideh Karimi, Seyed Navid Almadani, Mostafa Fakhri, Pegah Mokhtari, Hamid Gourabi, Anahita Mohseni Meybodi. Reprod Biomed Online 2018
2