A citation-based method for searching scientific literature

Dongyi Yu, Kai Zhang, Meiyan Han, Wei Pan, Ying Chen, Yunfeng Wang, Hongyan Jiao, Ling Duan, Qiying Zhu, Xiaojie Song, Yan Hong, Chen Chen, Juan Wang, Feng Hui, Linzhou Huang, Chongjian Chen, Yang Du. Mol Genet Genomic Med 2019
Times Cited: 21







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



Times Cited
  Times     Co-cited
Similarity


Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma.
Chen Zhao, John Tynan, Mathias Ehrich, Gregory Hannum, Ron McCullough, Juan-Sebastian Saldivar, Paul Oeth, Dirk van den Boom, Cosmin Deciu. Clin Chem 2015
89
38

Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
R Li, J Wan, Y Zhang, F Fu, Y Ou, X Jing, J Li, D Li, C Liao. Ultrasound Obstet Gynecol 2016
39
38

Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.
Kitty K Lo, Evangelia Karampetsou, Christopher Boustred, Fiona McKay, Sarah Mason, Melissa Hill, Vincent Plagnol, Lyn S Chitty. Am J Hum Genet 2016
74
33

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
346
33

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes.
Ronald J Wapner, Joshua E Babiarz, Brynn Levy, Melissa Stosic, Bernhard Zimmermann, Styrmir Sigurjonsson, Nicholas Wayham, Allison Ryan, Milena Banjevic, Phil Lacroute,[...]. Am J Obstet Gynecol 2015
191
33

Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.
Desheng Liang, David S Cram, Hu Tan, Siyuan Linpeng, Yingdi Liu, Huaiyu Sun, Yu Zhang, Feng Tian, Hongmin Zhu, Mengnan Xu,[...]. Genet Med 2019
81
33

Presence of fetal DNA in maternal plasma and serum.
Y M Lo, N Corbetta, P F Chamberlain, V Rai, I L Sargent, C W Redman, J S Wainscoat. Lancet 1997
28

Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA.
Ai-hua Yin, Chun-fang Peng, Xin Zhao, Bennett A Caughey, Jie-xia Yang, Jian Liu, Wei-wei Huang, Chang Liu, Dong-hong Luo, Hai-liang Liu,[...]. Proc Natl Acad Sci U S A 2015
78
28

Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma.
Anupama Srinivasan, Diana W Bianchi, Hui Huang, Amy J Sehnert, Richard P Rava. Am J Hum Genet 2013
173
28

Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA.
Hongtai Liu, Ya Gao, Zhiyang Hu, Linhua Lin, Xuyang Yin, Jun Wang, Dayang Chen, Fang Chen, Hui Jiang, Jinghui Ren,[...]. PLoS One 2016
24
28

Noninvasive prenatal testing for chromosome aneuploidies and subchromosomal microdeletions/microduplications in a cohort of 8141 single pregnancies.
Hua Hu, Li Wang, Jiayan Wu, Peng Zhou, Jingli Fu, Jiuchen Sun, Weiyi Cai, Hailiang Liu, Ying Yang. Hum Genomics 2019
34
28


Chromosomal microarray versus karyotyping for prenatal diagnosis.
Ronald J Wapner, Christa Lese Martin, Brynn Levy, Blake C Ballif, Christine M Eng, Julia M Zachary, Melissa Savage, Lawrence D Platt, Daniel Saltzman, William A Grobman,[...]. N Engl J Med 2012
715
23

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing.
Shengpei Chen, Tze Kin Lau, Chunlei Zhang, Chenming Xu, Zhengfeng Xu, Ping Hu, Jian Xu, Hefeng Huang, Ling Pan, Fuman Jiang,[...]. Prenat Diagn 2013
83
23

Clinical experience with a single-nucleotide polymorphism-based non-invasive prenatal test for five clinically significant microdeletions.
K Martin, S Iyengar, A Kalyan, C Lan, A L Simon, M Stosic, K Kobara, H Ravi, T Truong, A Ryan,[...]. Clin Genet 2018
50
23

High resolution global chromosomal aberrations from spontaneous miscarriages revealed by low coverage whole genome sequencing.
Hong Qi, Zhao-Ling Xuan, Yang Du, Li-Rong Cai, Han Zhang, Xiao-Hui Wen, Xiang-Dong Kong, Kai Yang, Yang Mi, Xin-Xin Fu,[...]. Eur J Obstet Gynecol Reprod Biol 2018
16
25

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood.
H Christina Fan, Yair J Blumenfeld, Usha Chitkara, Louanne Hudgins, Stephen R Quake. Proc Natl Acad Sci U S A 2008
683
19

Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis.
Sian Taylor-Phillips, Karoline Freeman, Julia Geppert, Adeola Agbebiyi, Olalekan A Uthman, Jason Madan, Angus Clarke, Siobhan Quenby, Aileen Clarke. BMJ Open 2016
174
19

Non-invasive prenatal testing for trisomies 21, 18 and 13: clinical experience from 146,958 pregnancies.
H Zhang, Y Gao, F Jiang, M Fu, Y Yuan, Y Guo, Z Zhu, M Lin, Q Liu, Z Tian,[...]. Ultrasound Obstet Gynecol 2015
206
19

WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme.
Roy Straver, Erik A Sistermans, Henne Holstege, Allerdien Visser, Cees B M Oudejans, Marcel J T Reinders. Nucleic Acids Res 2014
92
19


DNA sequencing versus standard prenatal aneuploidy screening.
Diana W Bianchi, R Lamar Parker, Jeffrey Wentworth, Rajeevi Madankumar, Craig Saffer, Anita F Das, Joseph A Craig, Darya I Chudova, Patricia L Devers, Keith W Jones,[...]. N Engl J Med 2014
405
19


Identification of copy number variants by NGS-based NIPT at low sequencing depth.
Xiaoqing Ye, Shengmou Lin, Xiwei Song, Meihua Tan, Jia Li, Jiayan Wang, Huanchen Yan, Huimin Zhang, Shaoying Li, Dunjin Chen,[...]. Eur J Obstet Gynecol Reprod Biol 2021
6
66

Non-invasive prenatal testing for aneuploidy: current status and future prospects.
P Benn, H Cuckle, E Pergament. Ultrasound Obstet Gynecol 2013
199
14


Analysis of cell-free DNA in maternal blood in screening for aneuploidies: updated meta-analysis.
M M Gil, V Accurti, B Santacruz, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2017
289
14

Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population.
Yijun Song, Congcong Liu, Hong Qi, Yunping Zhang, Xuming Bian, Juntao Liu. Prenat Diagn 2013
131
14

Challenges in non-invasive prenatal screening for sub-chromosomal copy number variations using cell-free DNA.
Henna V Advani, Angela N Barrett, Mark I Evans, Mahesh Choolani. Prenat Diagn 2017
23
14

Noninvasive prenatal molecular karyotyping from maternal plasma.
Stephanie C Y Yu, Peiyong Jiang, Kwong W Choy, Kwan Chee Allen Chan, Hye-Sung Won, Wing C Leung, Elizabeth T Lau, Mary H Y Tang, Tak Y Leung, Yuk Ming Dennis Lo,[...]. PLoS One 2013
63
14

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
348
14

The genetics of microdeletion and microduplication syndromes: an update.
Corey T Watson, Tomas Marques-Bonet, Andrew J Sharp, Heather C Mefford. Annu Rev Genomics Hum Genet 2014
87
14

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.
Peter Benn, Antoni Borrell, Rossa W K Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte Faas, Susan Gross, Tianhua Huang, Joann Johnson, Ron Maymon,[...]. Prenat Diagn 2015
179
14

Clinical validation of a noninvasive prenatal test for genomewide detection of fetal copy number variants.
Roy B Lefkowitz, John A Tynan, Tong Liu, Yijin Wu, Amin R Mazloom, Eyad Almasri, Grant Hogg, Vach Angkachatchai, Chen Zhao, Daniel S Grosu,[...]. Am J Obstet Gynecol 2016
95
14

A case of prenatal diagnosis of 18p deletion syndrome following noninvasive prenatal testing.
Ganye Zhao, Peng Dai, Shanshan Gao, Xuechao Zhao, Conghui Wang, Lina Liu, Xiangdong Kong. Mol Cytogenet 2019
8
37

Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing.
J Helgeson, J Wardrop, T Boomer, E Almasri, W B Paxton, J S Saldivar, N Dharajiya, T J Monroe, D H Farkas, D S Grosu,[...]. Prenat Diagn 2015
84
14

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
116
14

Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory.
Andrea K Petersen, Sau Wai Cheung, Janice L Smith, Weimin Bi, Patricia A Ward, Sandra Peacock, Alicia Braxton, Ignatia B Van Den Veyver, Amy M Breman. Am J Obstet Gynecol 2017
82
14

Validation of Copy Number Variants Detection from Pregnant Plasma Using Low-Pass Whole-Genome Sequencing in Noninvasive Prenatal Testing-Like Settings.
Michaela Hyblova, Maria Harsanyova, Diana Nikulenkov-Grochova, Jitka Kadlecova, Marcel Kucharik, Jaroslav Budis, Gabriel Minarik. Diagnostics (Basel) 2020
4
75

Application value of NIPT for uncommon fetal chromosomal abnormalities.
Lianli Yin, Yinghua Tang, Qing Lu, Aiping Pan, Mingfang Shi. Mol Cytogenet 2020
4
75

Identification of a de novo fetal variant in osteogenesis imperfecta by targeted sequencing-based noninvasive prenatal testing.
Xiuju Yin, Yang Du, Han Zhang, Zhandong Wang, Juan Wang, Xinxin Fu, Yaoyao Cui, Chongjian Chen, Junbin Liang, Zhaoling Xuan,[...]. J Hum Genet 2018
11
18

Microdeletion and microduplication syndromes.
Anja Weise, Kristin Mrasek, Elisabeth Klein, Milene Mulatinho, Juan C Llerena, David Hardekopf, Sona Pekova, Samarth Bhatt, Nadezda Kosyakova, Thomas Liehr. J Histochem Cytochem 2012
82
9

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach.
Zirui Dong, Jun Zhang, Ping Hu, Haixiao Chen, Jinjin Xu, Qi Tian, Lu Meng, Yanchou Ye, Jun Wang, Meiyan Zhang,[...]. Genet Med 2016
88
9


Global perspectives on clinical adoption of NIPT.
Mollie A Minear, Celine Lewis, Subarna Pradhan, Subhashini Chandrasekharan. Prenat Diagn 2015
89
9

Noninvasive prenatal diagnosis of a fetal microdeletion syndrome.
David Peters, Tianjiao Chu, Svetlana A Yatsenko, Nancy Hendrix, W Allen Hogge, Urvashi Surti, Kimberly Bunce, Mary Dunkel, Patricia Shaw, Aleksandar Rajkovic. N Engl J Med 2011
93
9

Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number Variation.
Han Zhang, Yang-Yu Zhao, Jing Song, Qi-Ying Zhu, Hua Yang, Mei-Ling Zheng, Zhao-Ling Xuan, Yuan Wei, Yang Chen, Peng-Bo Yuan,[...]. Sci Rep 2015
10
20

Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.
M M Gil, M S Quezada, R Revello, R Akolekar, K H Nicolaides. Ultrasound Obstet Gynecol 2015
311
9

New microdeletion and microduplication syndromes: A comprehensive review.
Julián Nevado, Rafaella Mergener, María Palomares-Bralo, Karen Regina Souza, Elena Vallespín, Rocío Mena, Víctor Martínez-Glez, María Ángeles Mori, Fernando Santos, Sixto García-Miñaur,[...]. Genet Mol Biol 2014
57
9



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.