A citation-based method for searching scientific literature

Jia Tang, Chenglong Zhou, Haihong Shi, Yuying Mo, Weilan Tan, Tielan Sun, Jinling Zhu, Qing Li, Hui Li, Yuping Li, Songbai Wang, Yan Hong, Ning Li, Qinlong Zeng, Jieliang Tan, Wei Ma, Liangping Luo. Clin Chim Acta 2020
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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
83

Rapid prenatal diagnosis of skeletal dysplasia using medical trio exome sequencing: Benefit for prenatal counseling and pregnancy management.
Jin Han, Yan-Dong Yang, Yi He, Wen-Jie Liu, Li Zhen, Min Pan, Xin Yang, Victor Wei Zhang, Can Liao, Dong-Zhi Li. Prenat Diagn 2020
13
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
134
66

Genetic Analysis in Fetal Skeletal Dysplasias by Trio Whole-Exome Sequencing.
Kai Yang, Ming Shen, Yousheng Yan, Ya Tan, Jing Zhang, Jue Wu, Guangming Yang, Shang Li, Jing Wang, Zhuo Ren,[...]. Biomed Res Int 2019
18
66

Evaluating skeletal dysplasias on prenatal ultrasound: an emphasis on predicting lethality.
Kathryn S Milks, Lyndon M Hill, Keyanoosh Hosseinzadeh. Pediatr Radiol 2017
23
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
133
50

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
50

What Is New in Prenatal Skeletal Dysplasias?
Teresa Victoria, Xiaowei Zhu, Ralph Lachman, Monica Epelman, Edward R Oliver, N Scott Adzick, David M Biko. AJR Am J Roentgenol 2018
10
50

Prenatal sonographic diagnosis of skeletal dysplasias.
T Schramm, K P Gloning, S Minderer, C Daumer-Haas, K Hörtnagel, A Nerlich, B Tutschek. Ultrasound Obstet Gynecol 2009
99
50

Nosology and classification of genetic skeletal disorders: 2019 revision.
Geert R Mortier, Daniel H Cohn, Valerie Cormier-Daire, Christine Hall, Deborah Krakow, Stefan Mundlos, Gen Nishimura, Stephen Robertson, Luca Sangiorgi, Ravi Savarirayan,[...]. Am J Med Genet A 2019
179
50

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
6
33

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
35
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
19
33

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
842
33

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
86
33

Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management.
Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S Chitty. Genet Med 2018
59
33

Achondroplasia.
William A Horton, Judith G Hall, Jacqueline T Hecht. Lancet 2007
280
33

Fetal biometry of skeletal dysplasias: a multicentric study.
L Goncalves, P Jeanty. J Ultrasound Med 1994
37
33

The skeletal dysplasias.
Deborah Krakow, David L Rimoin. Genet Med 2010
109
33

Birth prevalence rates of skeletal dysplasias.
C Stoll, B Dott, M P Roth, Y Alembik. Clin Genet 1989
154
33

Osteogenesis imperfecta - A clinical update.
Symeon Tournis, Anastasia D Dede. Metabolism 2018
42
33

The birth prevalence rates for the skeletal dysplasias.
I M Orioli, E E Castilla, J G Barbosa-Neto. J Med Genet 1986
217
33

Prenatal diagnosis of skeletal dysplasias using a targeted skeletal gene panel.
Xinyao Zhou, Natalie Chandler, Linbei Deng, Jia Zhou, Meizhen Yuan, Luming Sun. Prenat Diagn 2018
22
33

Approach to the diagnosis of skeletal dysplasias: Experience at a center with limited resources.
Manisha Kumar, Seema Thakur, Arunima Haldar, Rama Anand. J Clin Ultrasound 2016
4
50

Two novel mutations of COL1A1 in fetal genetic skeletal dysplasia of Chinese.
Ruibing Li, Jianan Wang, Longxia Wang, Yanping Lu, Chengbin Wang. Mol Genet Genomic Med 2020
6
33

Risk of Adverse Outcomes in Euploid Pregnancies With Isolated Short Fetal Femur and Humerus on Second-Trimester Sonography.
Marja Kaijomaa, Veli-Matti Ulander, Markku Ryynanen, Vedran Stefanovic. J Ultrasound Med 2016
9
33

Midtrimester isolated short femur and perinatal outcomes: A systematic review and meta-analysis.
Valentina D'Ambrosio, Flaminia Vena, Claudia Marchetti, Daniele Di Mascio, Seila Perrone, Chiara Boccherini, Antonio Pizzuti, Pierluigi Benedetti Panici, Antonella Giancotti. Acta Obstet Gynecol Scand 2019
12
33

Chinese fetal biometry: reference equations and comparison with charts from other populations.
Yixiu Zhang, Hua Meng, Yuxin Jiang, Zhonghui Xu, Yunshu Ouyang, Shengli Li, Qian Chen, Qingqing Wu, Rui Li, Tong Ru,[...]. J Matern Fetal Neonatal Med 2019
6
33

Outcome of fetuses with antenatally diagnosed short femur.
A T Papageorghiou, N Fratelli, K Leslie, A Bhide, B Thilaganathan. Ultrasound Obstet Gynecol 2008
43
33

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
13
16

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
16

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
14
16

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
9
16

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
16

Next generation sequencing--implications for clinical practice.
Eleanor Raffan, Robert K Semple. Br Med Bull 2011
33
16

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
5
20

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
16

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
16

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
2
50

New genetic testing in prenatal diagnosis.
Natalia Babkina, John M Graham. Semin Fetal Neonatal Med 2014
15
16

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
3
33

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
16

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
30
16

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
24
16

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
16

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
59
16

Fetal Exome Sequencing on the Horizon.
Karen Wou, Isabelle DeBie, June Carroll, Jo-Ann Brock, R Douglas Wilson. J Obstet Gynaecol Can 2019
5
20

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
21
16


Recent advances in prenatal genetic screening and testing.
Ignatia B Van den Veyver. F1000Res 2016
29
16


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.