A citation-based method for searching scientific literature

Jiping Shi, Runling Zhang, Jinming Li, Rui Zhang. Crit Rev Clin Lab Sci 2019
Times Cited: 5







List of co-cited articles
23 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
40

Universal Haplotype-Based Noninvasive Prenatal Testing for Single Gene Diseases.
Winnie W I Hui, Peiyong Jiang, Yu K Tong, Wing-Shan Lee, Yvonne K Y Cheng, Maria I New, Rezan A Kadir, K C Allen Chan, Tak Y Leung, Y M Dennis Lo,[...]. Clin Chem 2017
58
40

Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA.
Jinglan Zhang, Jianli Li, Jennifer B Saucier, Yanming Feng, Yanjun Jiang, Jefferson Sinson, Anne K McCombs, Eric S Schmitt, Sandra Peacock, Stella Chen,[...]. Nat Med 2019
95
40

Accurate whole-genome sequencing and haplotyping from 10 to 20 human cells.
Brock A Peters, Bahram G Kermani, Andrew B Sparks, Oleg Alferov, Peter Hong, Andrei Alexeev, Yuan Jiang, Fredrik Dahl, Y Tom Tang, Juergen Haas,[...]. Nature 2012
160
40

Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: next-generation sequencing allows for a safer, more accurate, and comprehensive approach.
Lyn S Chitty, Sarah Mason, Angela N Barrett, Fiona McKay, Nicholas Lench, Rebecca Daley, Lucy A Jenkins. Prenat Diagn 2015
94
40

Haplotype-resolved genome sequencing: experimental methods and applications.
Matthew W Snyder, Andrew Adey, Jacob O Kitzman, Jay Shendure. Nat Rev Genet 2015
99
40

Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing.
Sasan Amini, Dmitry Pushkarev, Lena Christiansen, Emrah Kostem, Tom Royce, Casey Turk, Natasha Pignatelli, Andrew Adey, Jacob O Kitzman, Kandaswamy Vijayan,[...]. Nat Genet 2014
102
40

Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus.
Y M Dennis Lo, K C Allen Chan, Hao Sun, Eric Z Chen, Peiyong Jiang, Fiona M F Lun, Yama W Zheng, Tak Y Leung, Tze K Lau, Charles R Cantor,[...]. Sci Transl Med 2010
629
40

Haplotype-resolved genome sequencing of a Gujarati Indian individual.
Jacob O Kitzman, Alexandra P Mackenzie, Andrew Adey, Joseph B Hiatt, Rupali P Patwardhan, Peter H Sudmant, Sarah B Ng, Can Alkan, Ruolan Qiu, Evan E Eichler,[...]. Nat Biotechnol 2011
171
40


The Biology of Cell-free DNA Fragmentation and the Roles of DNASE1, DNASE1L3, and DFFB.
Diana S C Han, Meng Ni, Rebecca W Y Chan, Vicken W H Chan, Kathy O Lui, Rossa W K Chiu, Y M Dennis Lo. Am J Hum Genet 2020
54
40

Integrated digital error suppression for improved detection of circulating tumor DNA.
Aaron M Newman, Alexander F Lovejoy, Daniel M Klass, David M Kurtz, Jacob J Chabon, Florian Scherer, Henning Stehr, Chih Long Liu, Scott V Bratman, Carmen Say,[...]. Nat Biotechnol 2016
561
40

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
40

Synthetic Circulating Cell-free DNA as Quality Control Materials for Somatic Mutation Detection in Liquid Biopsy for Cancer.
Rui Zhang, Rongxue Peng, Ziyang Li, Peng Gao, Shiyu Jia, Xin Yang, Jiansheng Ding, Yanxi Han, Jiehong Xie, Jinming Li. Clin Chem 2017
27
40

Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends.
K C Allen Chan, Peiyong Jiang, Kun Sun, Yvonne K Y Cheng, Yu K Tong, Suk Hang Cheng, Ada I C Wong, Irena Hudecova, Tak Y Leung, Rossa W K Chiu,[...]. Proc Natl Acad Sci U S A 2016
91
40

External Quality Assessment for Detection of Fetal Trisomy 21, 18, and 13 by Massively Parallel Sequencing in Clinical Laboratories.
Rui Zhang, Hongyun Zhang, Yulong Li, Yanxi Han, Jiehong Xie, Jinming Li. J Mol Diagn 2016
10
40


Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing.
Stephanie C Y Yu, K C Allen Chan, Yama W L Zheng, Peiyong Jiang, Gary J W Liao, Hao Sun, Ranjit Akolekar, Tak Y Leung, Attie T J I Go, John M G van Vugt,[...]. Proc Natl Acad Sci U S A 2014
177
40

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
40

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
40

Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma.
Felix C K Wong, Y M Dennis Lo. Annu Rev Med 2016
62
40

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
40

High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screening.
Noah C Welker, Albert K Lee, Rachel A S Kjolby, Helen Y Wan, Mark R Theilmann, Diana Jeon, James D Goldberg, Kevin R Haas, Dale Muzzey, Clement S Chu. Genet Med 2021
10
40

Noninvasive prenatal diagnosis of 21-Hydroxylase deficiency using target capture sequencing of maternal plasma DNA.
Dingyuan Ma, Yuan Yuan, Chunyu Luo, Yaoshen Wang, Tao Jiang, Fengyu Guo, Jingjing Zhang, Chao Chen, Yun Sun, Jian Cheng,[...]. Sci Rep 2017
6
20

Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA.
Nancy B Y Tsui, Rezan A Kadir, K C Allen Chan, Claudia Chi, Gillian Mellars, Edward G Tuddenham, Tak Y Leung, Tze K Lau, Rossa W K Chiu, Y M Dennis Lo. Blood 2011
156
20

Targeted sequencing by proximity ligation for comprehensive variant detection and local haplotyping.
Paula J P de Vree, Elzo de Wit, Mehmet Yilmaz, Monique van de Heijning, Petra Klous, Marjon J A M Verstegen, Yi Wan, Hans Teunissen, Peter H L Krijger, Geert Geeven,[...]. Nat Biotechnol 2014
136
20

Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness.
Meng Meng, Xuchao Li, Huijuan Ge, Fang Chen, Mingyu Han, Yanyan Zhang, Dongyang Kang, Weiwei Xie, Zhiying Gao, Xiaoyu Pan,[...]. Genet Med 2014
34
20

Noninvasive detection of F8 int22h-related inversions and sequence variants in maternal plasma of hemophilia carriers.
Irena Hudecova, Peiyong Jiang, Joanna Davies, Y M Dennis Lo, Rezan A Kadir, Rossa W K Chiu. Blood 2017
25
20

Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18.
Mary E Norton, Herb Brar, Jonathan Weiss, Ardeshir Karimi, Louise C Laurent, Aaron B Caughey, M Hellen Rodriguez, John Williams, Michael E Mitchell, Charles D Adair,[...]. Am J Obstet Gynecol 2012
367
20


Whole-genome haplotyping approaches and genomic medicine.
Gustavo Glusman, Hannah C Cox, Jared C Roach. Genome Med 2014
38
20


Novel approach to genetic analysis and results in 3000 hemophilia patients enrolled in the My Life, Our Future initiative.
Jill M Johnsen, Shelley N Fletcher, Haley Huston, Sarah Roberge, Beth K Martin, Martin Kircher, Neil C Josephson, Jay Shendure, Sarah Ruuska, Marion A Koerper,[...]. Blood Adv 2017
50
20

Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma.
Yan Xu, Xuchao Li, Hui-Juan Ge, Bing Xiao, Yan-Yan Zhang, Xiao-Min Ying, Xiao-Yu Pan, Lei Wang, Wei-Wei Xie, Lin Ni,[...]. Genet Med 2015
47
20

Direct quantification of cell-free, circulating DNA from unpurified plasma.
Sarah Breitbach, Suzan Tug, Susanne Helmig, Daniela Zahn, Thomas Kubiak, Matthias Michal, Tommaso Gori, Tobias Ehlert, Thomas Beiter, Perikles Simon. PLoS One 2014
91
20

The status of carrier and prenatal diagnosis of haemophilia in China.
J Dai, Y Lu, Q Ding, H Wang, X Xi, X Wang. Haemophilia 2012
9
20

DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.
Glenn E Palomaki, Cosmin Deciu, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow, Louis M Neveux, Mathias Ehrich, Dirk van den Boom, Allan T Bombard, Wayne W Grody,[...]. Genet Med 2012
366
20

Calculating the fetal fraction for noninvasive prenatal testing based on genome-wide nucleosome profiles.
Roy Straver, Cees B M Oudejans, Erik A Sistermans, Marcel J T Reinders. Prenat Diagn 2016
56
20

Detection of the placental epigenetic signature of the maspin gene in maternal plasma.
Stephen S C Chim, Yu K Tong, Rossa W K Chiu, Tze K Lau, Tse N Leung, Lisa Y S Chan, Cees B M Oudejans, Chunming Ding, Y M Dennis Lo. Proc Natl Acad Sci U S A 2005
250
20

Dnase1l3 deletion causes aberrations in length and end-motif frequencies in plasma DNA.
Lee Serpas, Rebecca W Y Chan, Peiyong Jiang, Meng Ni, Kun Sun, Ali Rashidfarrokhi, Chetna Soni, Vanja Sisirak, Wing-Shan Lee, Suk Hang Cheng,[...]. Proc Natl Acad Sci U S A 2019
71
20

Cell-free DNA levels as a prognostic marker in acute myocardial infarction.
Dionisios Antonatos, Sotirios Patsilinakos, Stavros Spanodimos, Panagiotis Korkonikitas, D Tsigas. Ann N Y Acad Sci 2006
73
20

Mutational Landscape of cfDNA Identifies Distinct Molecular Features Associated With Therapeutic Response to First-Line Platinum-Based Doublet Chemotherapy in Patients with Advanced NSCLC.
Tao Jiang, Xuefei Li, Jianfei Wang, Chunxia Su, Wenbo Han, Chao Zhao, Fengying Wu, Guanghui Gao, Wei Li, Xiaoxia Chen,[...]. Theranostics 2017
21
20

Circulating Cell-Free DNA and RNA Analysis as Liquid Biopsy: Optimal Centrifugation Protocol.
Laure Sorber, Karen Zwaenepoel, Julie Jacobs, Koen De Winne, Sofie Goethals, Pablo Reclusa, Kaat Van Casteren, Elien Augustus, Filip Lardon, Geert Roeyen,[...]. Cancers (Basel) 2019
41
20

Guidelines for the Preanalytical Conditions for Analyzing Circulating Cell-Free DNA.
Romain Meddeb, Ekaterina Pisareva, Alain R Thierry. Clin Chem 2019
77
20

Orientation-aware plasma cell-free DNA fragmentation analysis in open chromatin regions informs tissue of origin.
Kun Sun, Peiyong Jiang, Suk Hang Cheng, Timothy H T Cheng, John Wong, Vincent W S Wong, Simon S M Ng, Brigette B Y Ma, Tak Y Leung, Stephen L Chan,[...]. Genome Res 2019
86
20

Quick assessment of cell-free DNA in seminal fluid and fragment size for early non-invasive prostate cancer diagnosis.
Giovanni Ponti, Monia Maccaferri, Marco Manfredini, Salvatore Micali, Federica Torricelli, Riccardo Milandri, Chiara Del Prete, Alessia Ciarrocchi, Cristel Ruini, Luisa Benassi,[...]. Clin Chim Acta 2019
16
20

Persistent aberrations in circulating DNA integrity after radiotherapy are associated with poor prognosis in nasopharyngeal carcinoma patients.
K C Allen Chan, Sing-Fai Leung, Sze-Wan Yeung, Anthony T C Chan, Y M Dennis Lo. Clin Cancer Res 2008
50
20

DNA integrity assay: a plasma-based screening tool for the detection of prostate cancer.
Robert Hanley, Kimberly M Rieger-Christ, David Canes, Norah R Emara, Anthony P Shuber, Kevin A Boynton, John A Libertino, Ian C Summerhayes. Clin Cancer Res 2006
41
20

Nonhematopoietically derived DNA is shorter than hematopoietically derived DNA in plasma: a transplantation model.
Yama W L Zheng, K C Allen Chan, Hao Sun, Peiyong Jiang, Xiaoxi Su, Eric Z Chen, Fiona M F Lun, Emily C W Hung, Vincent Lee, John Wong,[...]. Clin Chem 2012
84
20

Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments.
Kun Sun, Peiyong Jiang, K C Allen Chan, John Wong, Yvonne K Y Cheng, Raymond H S Liang, Wai-kong Chan, Edmond S K Ma, Stephen L Chan, Suk Hang Cheng,[...]. Proc Natl Acad Sci U S A 2015
361
20


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.