A citation-based method for searching scientific literature

Keren J Carss, Sarah C Hillman, Vijaya Parthiban, Dominic J McMullan, Eamonn R Maher, Mark D Kilby, Matthew E Hurles. Hum Mol Genet 2014
Times Cited: 105



Hanan E Shamseldin, Abdulrahman Swaid, Fowzan S Alkuraya. Genet Med 2013
Times Cited: 26




List of shared articles



Times cited

Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities.
Kimia Najafi, Zohreh Mehrjoo, Fariba Ardalani, Siavash Ghaderi-Sohi, Ariana Kariminejad, Roxana Kariminejad, Hossein Najmabadi. Sci Rep 2021
1

Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations.
Wei Guo, Yuchen Lai, Zhiqiang Yan, Yuqian Wang, Yanli Nie, Shuo Guan, Ying Kuo, Wenxin Zhang, Xiaohui Zhu, Mei Peng,[...]. Hum Mutat 2020
5

Potential genetic causes of miscarriage in euploid pregnancies: a systematic review.
Emily Colley, Susan Hamilton, Paul Smith, Neil V Morgan, Arri Coomarasamy, Stephanie Allen. Hum Reprod Update 2019
27

Genetic testing and PGD for unexplained recurrent fetal malformations with MAGEL2 gene mutation.
Wei Guo, Yanli Nie, Zhiqiang Yan, Xiaohui Zhu, Yuqian Wang, Shuo Guan, Ying Kuo, Wenxin Zhang, Xu Zhi, Yuan Wei,[...]. Sci China Life Sci 2019
3

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
132

Molecular autopsy in maternal-fetal medicine.
Hanan E Shamseldin, Wesam Kurdi, Fatima Almusafri, Maha Alnemer, Alya Alkaff, Zeneb Babay, Amal Alhashem, Maha Tulbah, Nada Alsahan, Rubina Khan,[...]. Genet Med 2018
49



Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies.
Christina L Alamillo, Zöe Powis, Kelly Farwell, Layla Shahmirzadi, Elaine C Weltmer, John Turocy, Thomas Lowe, Christine Kobelka, Emily Chen, Donald Basel,[...]. Prenat Diagn 2015
56

Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.
Ignatia B van den Veyver, Christine M Eng. Cold Spring Harb Perspect Med 2015
26