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: 106



Michael E Talkowski, Zehra Ordulu, Vamsee Pillalamarri, Carol B Benson, Ian Blumenthal, Susan Connolly, Carrie Hanscom, Naveed Hussain, Shahrin Pereira, Jonathan Picker, Jill A Rosenfeld, Lisa G Shaffer, Louise E Wilkins-Haug, James F Gusella, Cynthia C Morton. N Engl J Med 2012
Times Cited: 119




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

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
2

Prenatal Diagnosis by Whole Exome Sequencing in Fetuses with Ultrasound Abnormalities.
Vanessa Felice, Avinash Abhyankar, Vaidehi Jobanputra. Methods Mol Biol 2019
2

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
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,[...]. Lancet 2019
166

Genetics professionals' attitudes toward prenatal exome sequencing.
Casey E Brew, Brian A Castro, Vivian Pan, Alexa Hart, Bruce Blumberg, Catherine Wicklund. J Genet Couns 2019
7

Evaluation of Diagnostic Yield in Fetal Whole-Exome Sequencing: A Report on 45 Consecutive Families.
Lior Greenbaum, Ben Pode-Shakked, Shlomit Eisenberg-Barzilai, Michal Dicastro-Keidar, Anat Bar-Ziv, Nurit Goldstein, Haike Reznik-Wolf, Hana Poran, Amihai Rigbi, Ortal Barel,[...]. Front Genet 2019
14

Prenatal DNA Sequencing: Clinical, Counseling, and Diagnostic Laboratory Considerations.
Ahmad N Abou Tayoun, Nancy B Spinner, Heidi L Rehm, Robert C Green, Diana W Bianchi. Prenat Diagn 2018
34

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
133

Non invasive prenatal diagnosis of fetal aneuploidy using cell free fetal DNA.
Barbara Renga. Eur J Obstet Gynecol Reprod Biol 2018
11



Intra-familial variability associated with recessive RYR1 mutation diagnosed prenatally by exome sequencing.
Jillian Casey, Karen Flood, Sean Ennis, Emma Doyle, Michael Farrell, Sally Ann Lynch. Prenat Diagn 2016
10

Prenatal and pre-implantation genetic diagnosis.
Joris Robert Vermeesch, Thierry Voet, Koenraad Devriendt. Nat Rev Genet 2016
71

Recent advances in prenatal genetic screening and testing.
Ignatia B Van den Veyver. F1000Res 2016
29


Prenatal exome sequencing for fetuses with structural abnormalities: the next step.
S C Hillman, D Willams, K J Carss, D J McMullan, M E Hurles, M D Kilby. Ultrasound Obstet Gynecol 2015
37

Recent advances of genomic testing in perinatal medicine.
David G Peters, Svetlana A Yatsenko, Urvashi Surti, Aleksandar Rajkovic. Semin Perinatol 2015
17

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

Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.
Lauren E Westerfield, Samantha R Stover, Veena S Mathur, Salma A Nassef, Tiffiney G Carter, Yaping Yang, Christine M Eng, Ignatia B Van den Veyver. Prenat Diagn 2015
31

Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Suzanne Drury, Hywel Williams, Natalie Trump, Christopher Boustred, Nicholas Lench, Richard H Scott, Lyn S Chitty. Prenat Diagn 2015
112