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, Wesam Kurdi, Fatima Almusafri, Maha Alnemer, Alya Alkaff, Zeneb Babay, Amal Alhashem, Maha Tulbah, Nada Alsahan, Rubina Khan, Bahauddin Sallout, Elham Al Mardawi, Mohamed Zain Seidahmed, Niema Meriki, Yasser Alsaber, Alya Qari, Ola Khalifa, Wafaa Eyaid, Zuhair Rahbeeni, Ahmed Kurdi, Mais Hashem, Tarfa Alshidi, Eman Al-Obeid, Firdous Abdulwahab, Niema Ibrahim, Nour Ewida, Karen El-Akouri, Mariam Al Mulla, Tawfeg Ben-Omran, Matthias Pergande, Sebahattin Cirak, Saeed Al Tala, Ranad Shaheen, Eissa Faqeih, Fowzan S Alkuraya. Genet Med 2018
Times Cited: 49




List of shared articles



Times cited

Prenatal Exome Sequencing: Background, Current Practice and Future Perspectives-A Systematic Review.
Daniele Guadagnolo, Gioia Mastromoro, Francesca Di Palma, Antonio Pizzuti, Enrica Marchionni. Diagnostics (Basel) 2021
1

Role of whole exome sequencing for unidentified genetic syndromes.
Shagun Aggarwal. Curr Opin Obstet Gynecol 2021
0

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

Molecular autopsy by proxy in preconception counseling.
Malak Ali Alghamdi, Ameinah Alrasheedi, Esra Alghamdi, Nouran Adly, Wajeih Y AlAali, Amal Alhashem, Abdulaziz Alshahrani, Hanan Shamseldin, Fowzan S Alkuraya, Majid Alfadhel. Clin Genet 2021
0

Exome sequencing for perinatal phenotypes: The significance of deep phenotyping.
Shagun Aggarwal, Venugopal Satidevi Vineeth, Aneek Das Bhowmik, Ashwani Tandon, Aditya Kulkarni, Dhanya Lakshmi Narayanan, Amrita Bhattacherjee, Ashwin Dalal. Prenat Diagn 2020
4

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

Importance of complete phenotyping in prenatal whole exome sequencing.
Mahmoud Aarabi, Olivia Sniezek, Huaiyang Jiang, Devereux N Saller, Daniel Bellissimo, Svetlana A Yatsenko, Aleksandar Rajkovic. Hum Genet 2018
30


Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.
Elizabeth A Normand, Alicia Braxton, Salma Nassef, Patricia A Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren E Westerfield, Samantha Stover,[...]. Genome Med 2018
48