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







List of shared articles



Times cited

Genotype-first in a cohort of 95 fetuses with multiple congenital abnormalities: when exome sequencing reveals unexpected fetal phenotype-genotype correlations.
Mathilde Lefebvre, Ange-Line Bruel, Emilie Tisserant, Nicolas Bourgon, Yannis Duffourd, Sophie Collardeau-Frachon, Tania Attie-Bitach, Paul Kuentz, Mirna Assoum, Elise Schaefer,[...]. J Med Genet 2021
0

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
2

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
6

Considerations for whole exome sequencing unique to prenatal care.
Ahmad Abou Tayoun, Heather Mason-Suares. Hum Genet 2020
6

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

Application of exome sequencing for prenatal diagnosis: a rapid scoping review.
Misty Pratt, Chantelle Garritty, Micere Thuku, Leila Esmaeilisaraji, Candyce Hamel, Taila Hartley, Kathryn Millar, Becky Skidmore, Shelley Dougan, Christine M Armour. Genet Med 2020
7

Exome sequencing of fetal anomaly syndromes: novel phenotype-genotype discoveries.
Nicole Meier, Elisabeth Bruder, Olav Lapaire, Irene Hoesli, Anjeung Kang, J├╝rgen Hench, Sylvia Hoeller, Julie De Geyter, Peter Miny, Karl Heinimann,[...]. Eur J Hum Genet 2019
21

Update on the use of exome sequencing in the diagnosis of fetal abnormalities.
Lauren Ferretti, Rhiannon Mellis, Lyn S Chitty. Eur J Med Genet 2019
18

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

A Dysmorphology Based Systematic Approach Toward Perinatal Genetic Diagnosis in a Fetal Autopsy Series.
Shagun Aggarwal, Ashwani Tandon, Aneek Das Bhowmik, Jamal Mohamed Nurul Jain Safarulla, Ashwin Dalal. Fetal Pediatr Pathol 2018
0


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



Next-Generation Sequencing Using a Cardiac Gene Panel in Prenatally Diagnosed Cardiac Anomalies.
Ryan E Lamont, Yanwei Xi, Claire Popko, Joanna Lazier, Francois P Bernier, Julie L Lauzon, A Micheil Innes, Jillian S Parboosingh, Mary Ann Thomas. J Obstet Gynaecol Can 2018
2



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

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