A citation-based method for searching scientific literature

Shuya Xue, Huanchen Yan, Jingsi Chen, Nan Li, Jiayan Wang, Yu Liu, Huimin Zhang, Shaoying Li, Wei Zhang, Dunjin Chen, Min Chen. Cytogenet Genome Res 2020
Times Cited: 3







List of co-cited articles
9 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
100


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
66

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
130
66

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
66


Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges.
Neeta L Vora, Bradford Powell, Alicia Brandt, Natasha Strande, Emily Hardisty, Kelly Gilmore, Ann Katherine M Foreman, Kirk Wilhelmsen, Chris Bizon, Jason Reilly,[...]. Genet Med 2017
80
66

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
144
66

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
112
66

Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing.
Dominik S Westphal, Gloria S Leszinski, Esther Rieger-Fackeldey, Elisabeth Graf, Gregor Weirich, Thomas Meitinger, Eva Ostermayer, Renate Oberhoffer, Matias Wagner. Clin Genet 2019
9
33

Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A Review.
Fionnuala Mone, Elizabeth Quinlan-Jones, Mark D Kilby. Eur J Obstet Gynecol Reprod Biol 2018
11
33

The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.
Amber E L van Nisselrooij, Malou A Lugthart, Sally-Ann Clur, Ingeborg H Linskens, Eva Pajkrt, Lukas A Rammeloo, Lieke Rozendaal, Nico A Blom, Jan M M van Lith, Alida C Knegt,[...]. Genet Med 2020
10
33

Exome sequencing in the assessment of congenital malformations in the fetus and neonate.
Fionnuala Mone, Elizabeth Quinlan-Jones, Andrew K Ewer, Mark D Kilby. Arch Dis Child Fetal Neonatal Ed 2019
7
33

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
29
33

Next generation sequencing--implications for clinical practice.
Eleanor Raffan, Robert K Semple. Br Med Bull 2011
32
33

Diagnostic power and clinical impact of exome sequencing in a cohort of 500 patients with rare diseases.
Caio Robledo D'Angioli Costa Quaio, Caroline Monaco Moreira, Gil Monteiro Novo-Filho, Patricia Rossi Sacramento-Bobotis, Michele Groenner Penna, Sandro Felix Perazzio, Aurelio Pimenta Dutra, Rafael Alves da Silva, Monize Nakamoto Provisor Santos, Vanessa Yurie Nozaki de Arruda,[...]. Am J Med Genet C Semin Med Genet 2020
3
33

Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
27
33

Preferred reporting items for systematic review and meta-analysis protocols (PRISMA-P) 2015: elaboration and explanation.
Larissa Shamseer, David Moher, Mike Clarke, Davina Ghersi, Alessandro Liberati, Mark Petticrew, Paul Shekelle, Lesley A Stewart. BMJ 2015
33

Novel and recurrent variants identified in fetuses with central nervous system abnormalities by trios-medical exome sequencing.
Hu Tan, Yinong Xie, Fei Chen, Min Chen, Li Yu, Dunjin Chen, Jingsi Chen. Clin Chim Acta 2020
1
100

New genetic testing in prenatal diagnosis.
Natalia Babkina, John M Graham. Semin Fetal Neonatal Med 2014
15
33

Prenatal diagnosis of skeletal dysplasias using whole exome sequencing in China.
Jia Tang, Chenglong Zhou, Haihong Shi, Yuying Mo, Weilan Tan, Tielan Sun, Jinling Zhu, Qing Li, Hui Li, Yuping Li,[...]. Clin Chim Acta 2020
5
33

Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
Qingwei Qi, Yulin Jiang, Xiya Zhou, Hua Meng, Na Hao, Jiazhen Chang, Junjie Bai, Chunli Wang, Mingming Wang, Jiangshan Guo,[...]. Genes (Basel) 2020
2
50

Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting.
Swetha Narayanan, Bruce Blumberg, Marla L Clayman, Vivian Pan, Catherine Wicklund. J Genet Couns 2018
8
33

Genomic medicine for undiagnosed diseases.
Anastasia L Wise, Teri A Manolio, George A Mensah, Josh F Peterson, Dan M Roden, Cecelia Tamburro, Marc S Williams, Eric D Green. Lancet 2019
23
33

Targeted gene sequencing and whole-exome sequencing in autopsied fetuses with prenatally diagnosed kidney anomalies.
M Rasmussen, L Sunde, M L Nielsen, M Ramsing, A Petersen, T D Hjortshøj, T E Olsen, A Tabor, J M Hertz, I Johnsen,[...]. Clin Genet 2018
23
33

Actions and Uncertainty: How Prenatally Diagnosed Variants of Uncertain Significance Become Actionable.
Allison Werner-Lin, Judith L M Mccoyd, Barbara A Bernhardt. Hastings Cent Rep 2019
7
33

Whole-exome sequencing reanalysis at 12 months boosts diagnosis and is cost-effective when applied early in Mendelian disorders.
Lisa J Ewans, Deborah Schofield, Rupendra Shrestha, Ying Zhu, Velimir Gayevskiy, Kevin Ying, Corrina Walsh, Eric Lee, Edwin P Kirk, Alison Colley,[...]. Genet Med 2018
58
33

Fetal Exome Sequencing on the Horizon.
Karen Wou, Isabelle DeBie, June Carroll, Jo-Ann Brock, R Douglas Wilson. J Obstet Gynaecol Can 2019
5
33

Evaluation of CNV detection tools for NGS panel data in genetic diagnostics.
José Marcos Moreno-Cabrera, Jesús Del Valle, Elisabeth Castellanos, Lidia Feliubadaló, Marta Pineda, Joan Brunet, Eduard Serra, Gabriel Capellà, Conxi Lázaro, Bernat Gel. Eur J Hum Genet 2020
13
33

Recent advances in prenatal genetic screening and testing.
Ignatia B Van den Veyver. F1000Res 2016
26
33

Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice.
Lara De Tomasi, Pierre David, Camille Humbert, Flora Silbermann, Christelle Arrondel, Frédéric Tores, Stéphane Fouquet, Audrey Desgrange, Olivier Niel, Christine Bole-Feysot,[...]. Am J Hum Genet 2017
33
33


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
47
33


Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development.
Carin L Yates, Kristin G Monaghan, Deborah Copenheaver, Kyle Retterer, Julie Scuffins, Cathlin R Kucera, Bethany Friedman, Gabriele Richard, Jane Juusola. Genet Med 2017
59
33

Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE.
Go Hun Seo, Taeho Kim, In Hee Choi, Jung-Young Park, Jungsul Lee, Sehwan Kim, Dhong-Gun Won, Arum Oh, Yena Lee, Jeongmin Choi,[...]. Clin Genet 2020
7
33

Clinical application of medical exome sequencing for prenatal diagnosis of fetal structural anomalies.
Min Chen, Jingsi Chen, Chunli Wang, Fei Chen, Yinong Xie, Yufan Li, Nan Li, Jing Wang, Victor Wei Zhang, Dunjin Chen. Eur J Obstet Gynecol Reprod Biol 2020
4
33

Fetal exome sequencing: yield and limitations in a tertiary referral center.
H Daum, V Meiner, O Elpeleg, T Harel. Ultrasound Obstet Gynecol 2019
20
33

Implementation of exome sequencing in fetal diagnostics-Data and experiences from a tertiary center in Denmark.
Naja Becher, Lotte Andreasen, Puk Sandager, Stina Lou, Olav Bjørn Petersen, Rikke Christensen, Ida Vogel. Acta Obstet Gynecol Scand 2020
6
33


ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
33

Exome Sequencing for Prenatal Diagnosis in Nonimmune Hydrops Fetalis.
Teresa N Sparks, Billie R Lianoglou, Rebecca R Adami, Ilina D Pluym, Kerry Holliman, Jennifer Duffy, Sarah L Downum, Sachi Patel, Amanda Faubel, Nina M Boe,[...]. N Engl J Med 2020
15
33

Clinical diagnosis by whole-genome sequencing of a prenatal sample.
Michael E Talkowski, Zehra Ordulu, Vamsee Pillalamarri, Carol B Benson, Ian Blumenthal, Susan Connolly, Carrie Hanscom, Naveed Hussain, Shahrin Pereira, Jonathan Picker,[...]. N Engl J Med 2012
118
33

Exome Sequencing in Fetuses with Structural Malformations.
Fiona L Mackie, Keren J Carss, Sarah C Hillman, Matthew E Hurles, Mark D Kilby. J Clin Med 2014
12
33

Genetic tests aid in counseling of fetuses with cerebellar vermis defects.
Lushan Li, Fang Fu, Ru Li, Weiqiang Xiao, Qiuxia Yu, Dan Wang, Xiangyi Jing, Yongning Zhang, Xin Yang, Min Pan,[...]. Prenat Diagn 2020
3
33


Introduction of genomics into prenatal diagnostics.
Michael E Talkowski, Heidi L Rehm. Lancet 2019
8
33

Bardet-Biedl syndrome: Antenatal presentation of forty-five fetuses with biallelic pathogenic variants in known Bardet-Biedl syndrome genes.
Laura Mary, Kirsley Chennen, Corinne Stoetzel, Manuela Antin, Anne Leuvrey, Elsa Nourisson, Elisabeth Alanio-Detton, Maria C Antal, Tania Attié-Bitach, Patrice Bouvagnet,[...]. Clin Genet 2019
13
33

The Human Phenotype Ontology in 2021.
Sebastian Köhler, Michael Gargano, Nicolas Matentzoglu, Leigh C Carmody, David Lewis-Smith, Nicole A Vasilevsky, Daniel Danis, Ganna Balagura, Gareth Baynam, Amy M Brower,[...]. Nucleic Acids Res 2021
23
33

Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies.
Elizabeth Quinlan-Jones, Jenny Lord, Denise Williams, Sue Hamilton, Tamas Marton, Ruth Y Eberhardt, Gabriele Rinck, Elena Prigmore, Rebecca Keelagher, Dominic J McMullan,[...]. Genet Med 2019
18
33


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.