A citation-based method for searching scientific literature

Chan Tian, Tao Deng, Xiuhuang Zhu, Chen Gong, Yangyu Zhao, Yuan Wei, Rong Li, Xiufeng Xu, Miaonan He, Zhiwei Zhang, Jing Cheng, Mol BenWillem, Jie Qiao. Sci China Life Sci 2020
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


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
42

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
42

Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
422
42

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
42

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
42

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies.
Fuman Jiang, Jinghui Ren, Fang Chen, Yuqiu Zhou, Jiansheng Xie, Shan Dan, Yue Su, Jianhong Xie, Baomin Yin, Wen Su,[...]. BMC Med Genomics 2012
109
28

The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies.
Jacob A Canick, Glenn E Palomaki, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow. Prenat Diagn 2013
216
28

Discordant noninvasive prenatal testing and cytogenetic results: a study of 109 consecutive cases.
Jia-Chi Wang, Trilochan Sahoo, Steven Schonberg, Kimberly A Kopita, Leslie Ross, Kyla Patek, Charles M Strom. Genet Med 2015
60
28

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.
Y M Lo, M S Tein, T K Lau, C J Haines, T N Leung, P M Poon, J S Wainscoat, P J Johnson, A M Chang, N M Hjelm. Am J Hum Genet 1998
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

An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing.
Ting Wang, Quanze He, Haibo Li, Jie Ding, Ping Wen, Qin Zhang, Jingjing Xiang, Qiong Li, Liming Xuan, Lingyin Kong,[...]. PLoS One 2016
16
28

Noninvasive prenatal testing in the general obstetric population: clinical performance and counseling considerations in over 85 000 cases.
Patricia A Taneja, Holly L Snyder, Eileen de Feo, Kristina M Kruglyak, Meredith Halks-Miller, Kirsten J Curnow, Sucheta Bhatt. Prenat Diagn 2016
35
28


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
28

Non-invasive cell-free fetal DNA testing for aneuploidy: multicenter study of 31 515 singleton pregnancies in southeastern China.
L Xu, H Huang, N Lin, Y Wang, D He, M Zhang, M Chen, L Chen, Y Lin. Ultrasound Obstet Gynecol 2020
20
28

Screening for trisomies by cfDNA testing of maternal blood in twin pregnancy: update of The Fetal Medicine Foundation results and meta-analysis.
M M Gil, S Galeva, J Jani, L Konstantinidou, R Akolekar, M N Plana, K H Nicolaides. Ultrasound Obstet Gynecol 2019
52
28

Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors.
Shan Dan, Wei Wang, Jinghui Ren, Yali Li, Hua Hu, Zhengfeng Xu, Tze Kin Lau, Jianhong Xie, Weihua Zhao, Hefeng Huang,[...]. Prenat Diagn 2012
163
28

Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA.
Richard P Porreco, Thomas J Garite, Kimberly Maurel, Barbara Marusiak, Mathias Ehrich, Dirk van den Boom, Cosmin Deciu, Allan Bombard. Am J Obstet Gynecol 2014
112
28

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
28

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
28

International Committee for Monitoring Assisted Reproductive Technologies world report: assisted reproductive technology 2012†.
Jacques de Mouzon, Georgina M Chambers, Fernando Zegers-Hochschild, Ragaa Mansour, Osamu Ishihara, Manish Banker, Silke Dyer, Markus Kupka, G David Adamson. Hum Reprod 2020
57
28


ACMG statement on noninvasive prenatal screening for fetal aneuploidy.
Anthony R Gregg, S J Gross, R G Best, K G Monaghan, K Bajaj, B G Skotko, B H Thompson, M S Watson. Genet Med 2013
181
14

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

Fast gapped-read alignment with Bowtie 2.
Ben Langmead, Steven L Salzberg. Nat Methods 2012
14

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
14

Diagnostic tests 2: Predictive values.
D G Altman, J M Bland. BMJ 1994
14

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
14


Interrater reliability: the kappa statistic.
Mary L McHugh. Biochem Med (Zagreb) 2012
14

Expanding the phenotype associated with 17q12 duplication: case report and review of the literature.
Tatjana Bierhals, Satish Babu Maddukuri, Kerstin Kutsche, Katta Mohan Girisha. Am J Med Genet A 2013
23
14

Current Status of Testing for Microdeletion Syndromes and Rare Autosomal Trisomies Using Cell-Free DNA Technology.
Yuval Yaron, Jacques Jani, Maximilian Schmid, Dick Oepkes. Obstet Gynecol 2015
35
14

Noninvasive prenatal testing/noninvasive prenatal diagnosis: the position of the National Society of Genetic Counselors.
Patricia L Devers, Amy Cronister, Kelly E Ormond, Flavia Facio, Campbell K Brasington, Pamela Flodman. J Genet Couns 2013
136
14


Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications.
Maria C Neofytou, Kyriakos Tsangaras, Elena Kypri, Charalambos Loizides, Marios Ioannides, Achilleas Achilleos, Petros Mina, Anna Keravnou, Carolina Sismani, George Koumbaris,[...]. PLoS One 2017
28
14

Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing.
Tze Kin Lau, Fang Chen, Xiaoyu Pan, Ritsuko K Pooh, Fuman Jiang, Yihan Li, Hui Jiang, Xuchao Li, Shengpei Chen, Xiuqing Zhang. J Matern Fetal Neonatal Med 2012
87
14

Enrichment of the fetal fraction in non-invasive prenatal screening reduces maternal background interference.
Bo Liang, Hong Li, Quanze He, Haibo Li, Lingyin Kong, Liming Xuan, Yingying Xia, Jingjing Shen, Yan Mao, Yixue Li,[...]. Sci Rep 2018
15
14

Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing.
Eric Z Chen, Rossa W K Chiu, Hao Sun, Ranjit Akolekar, K C Allen Chan, Tak Y Leung, Peiyong Jiang, Yama W L Zheng, Fiona M F Lun, Lisa Y S Chan,[...]. PLoS One 2011
204
14

Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases.
George Koumbaris, Achilleas Achilleos, Michalis Nicolaou, Charalambos Loizides, Kyriakos Tsangaras, Elena Kypri, Petros Mina, Carolina Sismani, Voula Velissariou, Georgia Christopoulou,[...]. Mol Cytogenet 2019
11
14

Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12.
Sandesh Chakravarthy Sreenath Nagamani, Ayelet Erez, Joseph Shen, Chumei Li, Elizabeth Roeder, Sarah Cox, Lefkothea Karaviti, Margret Pearson, Sung-Hae L Kang, Trilochan Sahoo,[...]. Eur J Hum Genet 2010
88
14

Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma.
Rossa W K Chiu, K C Allen Chan, Yuan Gao, Virginia Y M Lau, Wenli Zheng, Tak Y Leung, Chris H F Foo, Bin Xie, Nancy B Y Tsui, Fiona M F Lun,[...]. Proc Natl Acad Sci U S A 2008
589
14

Informative priors on fetal fraction increase power of the noninvasive prenatal screen.
Hanli Xu, Shaowei Wang, Lin-Lin Ma, Shuai Huang, Lin Liang, Qian Liu, Yang-Yang Liu, Ke-Di Liu, Ze-Min Tan, Hao Ban,[...]. Genet Med 2018
8
14

Birth defects surveillance in China.
Li Dai, Jun Zhu, Juan Liang, Yan-Ping Wang, He Wang, Meng Mao. World J Pediatr 2011
71
14

Environmental and developmental origins of ovarian reserve.
M C Richardson, M Guo, B C J M Fauser, N S Macklon. Hum Reprod Update 2014
64
14

Fetal Aneuploidy Detection by Cell-Free DNA Sequencing for Multiple Pregnancies and Quality Issues with Vanishing Twins.
Sebastian Grömminger, Erbil Yagmur, Sanli Erkan, Sándor Nagy, Ulrike Schöck, Joachim Bonnet, Patricia Smerdka, Mathias Ehrich, Rolf-Dieter Wegner, Wera Hofmann,[...]. J Clin Med 2014
60
14

Copy-number variation and false positive prenatal aneuploidy screening results.
Matthew W Snyder, LaVone E Simmons, Jacob O Kitzman, Bradley P Coe, Jessica M Henson, Riza M Daza, Evan E Eichler, Jay Shendure, Hilary S Gammill. N Engl J Med 2015
89
14

Clinical Experience of Non-Invasive Prenatal Chromosomal Aneuploidy Testing in 190,277 Patient Samples.
H Hu, H Liu, C Peng, T Deng, X Fu, C Chung, E Zhang, C Lu, K Zhang, Z Liang,[...]. Curr Mol Med 2016
24
14

Clinical performance of non-invasive prenatal served as a first-tier screening test for trisomy 21, 18, 13 and sex chromosome aneuploidy in a pilot city in China.
Yanhui Liu, Hailiang Liu, Yi He, Wanfang Xu, Qiulin Ma, Yuzhen He, Wei Lei, Guoquan Chen, Zheng He, Jiayi Huang,[...]. Hum Genomics 2020
12
14


Accurate description of DNA-based noninvasive prenatal screening.
Sau W Cheung, Ankita Patel, Tak Y Leung. N Engl J Med 2015
26
14


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.