A citation-based method for searching scientific literature

Chenming Xu, Ting Wang, Chao Liu, Hong Li, Xiaoyan Chen, Huanhuan Zhu, Songchang Chen, Qiuhong Xin, Jing Tao, Liming Huang, Zhengwen Jiang. Clin Chem 2017
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Digital PCR for the molecular detection of fetal chromosomal aneuploidy.
Y M Dennis Lo, Fiona M F Lun, K C Allen Chan, Nancy B Y Tsui, Ka C Chong, Tze K Lau, Tak Y Leung, Benny C Y Zee, Charles R Cantor, Rossa W K Chiu. Proc Natl Acad Sci U S A 2007
288
42

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
28

Non-invasive prenatal diagnosis of paternally inherited disorders from maternal plasma: detection of NF1 and CFTR mutations using droplet digital PCR.
Aurélia Gruber, Mathilde Pacault, Laila Allach El Khattabi, Nicolas Vaucouleur, Lucie Orhant, Thierry Bienvenu, Emmanuelle Girodon, Dominique Vidaud, France Leturcq, Catherine Costa,[...]. Clin Chem Lab Med 2018
16
28

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
28

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
28

Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma.
Fiona M F Lun, Nancy B Y Tsui, K C Allen Chan, Tak Y Leung, Tze K Lau, Pimlak Charoenkwan, Katherine C K Chow, Wyatt Y W Lo, Chanane Wanapirak, Torpong Sanguansermsri,[...]. Proc Natl Acad Sci U S A 2008
228
28

A modified multiplex ligation-dependent probe amplification method for the detection of 22q11.2 copy number variations in patients with congenital heart disease.
Xiaoqing Zhang, Yuejuan Xu, Deyuan Liu, Juan Geng, Sun Chen, Zhengwen Jiang, Qihua Fu, Kun Sun. BMC Genomics 2015
34
28

Screening for fetal aneuploidies at 11 to 13 weeks.
Kypros H Nicolaides. Prenat Diagn 2011
359
14

Screening for trisomies by cell-free DNA testing of maternal blood: consequences of a failed result.
R Revello, L Sarno, A Ispas, R Akolekar, K H Nicolaides. Ultrasound Obstet Gynecol 2016
72
14

Cell-free DNA screening for fetal aneuploidy as a clinical service.
Howard Cuckle, Peter Benn, Eugene Pergament. Clin Biochem 2015
54
14

Selected birth defects data from population-based birth defects surveillance programs in the United States, 2006 to 2010: featuring trisomy conditions.
Cara T Mai, James E Kucik, Jennifer Isenburg, Marcia L Feldkamp, Lisa K Marengo, Erin M Bugenske, Phoebe G Thorpe, Jodi M Jackson, Adolfo Correa, Russel Rickard,[...]. Birth Defects Res A Clin Mol Teratol 2013
63
14

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
14

Epigenetic-genetic chromosome dosage approach for fetal trisomy 21 detection using an autosomal genetic reference marker.
Yu K Tong, Rossa W K Chiu, Ranjit Akolekar, Tak Y Leung, Tze K Lau, Kypros H Nicolaides, Y M Dennis Lo. PLoS One 2010
30
14

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
14

Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samples.
Ron M McCullough, Eyad A Almasri, Xiaojun Guan, Jennifer A Geis, Susan C Hicks, Amin R Mazloom, Cosmin Deciu, Paul Oeth, Allan T Bombard, Bill Paxton,[...]. PLoS One 2014
91
14

Clinical experience and follow-up with large scale single-nucleotide polymorphism-based noninvasive prenatal aneuploidy testing.
Pe'er Dar, Kirsten J Curnow, Susan J Gross, Megan P Hall, Melissa Stosic, Zachary Demko, Bernhard Zimmermann, Matthew Hill, Styrmir Sigurjonsson, Allison Ryan,[...]. Am J Obstet Gynecol 2014
167
14

Detection of aneuploidy with digital polymerase chain reaction.
H Christina Fan, Stephen R Quake. Anal Chem 2007
120
14

Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center.
T K Lau, S W Cheung, P S S Lo, A N Pursley, M K Chan, F Jiang, H Zhang, W Wang, L F J Jong, O K C Yuen,[...]. Ultrasound Obstet Gynecol 2014
100
14

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
14

Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories.
Djie Tjwan Thung, Lean Beulen, Jayne Hehir-Kwa, Brigitte H Faas. Expert Rev Mol Diagn 2015
13
14

Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study.
Laïla Allach El Khattabi, Christelle Rouillac-Le Sciellour, Dominique Le Tessier, Armelle Luscan, Audrey Coustier, Raphael Porcher, Rakia Bhouri, Juliette Nectoux, Valérie Sérazin, Thibaut Quibel,[...]. PLoS One 2016
24
14

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
14

Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery.
Dineika Chandrananda, Natalie P Thorne, Devika Ganesamoorthy, Damien L Bruno, Yuval Benjamini, Terence P Speed, Howard R Slater, Melanie Bahlo. PLoS One 2014
17
14

Factors affecting levels of circulating cell-free fetal DNA in maternal plasma and their implications for noninvasive prenatal testing.
Sarah L Kinnings, Jennifer A Geis, Eyad Almasri, Huiquan Wang, Xiaojun Guan, Ron M McCullough, Allan T Bombard, Juan-Sebastian Saldivar, Paul Oeth, Cosmin Deciu. Prenat Diagn 2015
67
14

Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.
Andrew B Sparks, Craig A Struble, Eric T Wang, Ken Song, Arnold Oliphant. Am J Obstet Gynecol 2012
272
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

Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
Andrew B Sparks, Eric T Wang, Craig A Struble, Wade Barrett, Renee Stokowski, Celeste McBride, Jacob Zahn, Kevin Lee, Naiping Shen, Jigna Doshi,[...]. Prenat Diagn 2012
181
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

Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles.
Gary J W Liao, Fiona M F Lun, Yama W L Zheng, K C Allen Chan, Tak Y Leung, Tze K Lau, Rossa W K Chiu, Y M Dennis Lo. Clin Chem 2011
90
14

Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
Yanlin Wang, Yan Chen, Feng Tian, Jianguang Zhang, Zhuo Song, Yi Wu, Xu Han, Wenjing Hu, Duan Ma, David Cram,[...]. Clin Chem 2014
151
14

Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis.
Paolo Guanciali Franchi, Chiara Palka, Elisena Morizio, Giulia Sabbatinelli, Melissa Alfonsi, Donatella Fantasia, Giammaria Sitar, Peter Benn, Giuseppe Calabrese. PLoS One 2017
7
14


The clinical utility of DNA-based screening for fetal aneuploidy by primary obstetrical care providers in the general pregnancy population.
Glenn E Palomaki, Edward M Kloza, Barbara M O'Brien, Elizabeth E Eklund, Geralyn M Lambert-Messerlian. Genet Med 2017
20
14



A microfluidics approach for the isolation of nucleated red blood cells (NRBCs) from the peripheral blood of pregnant women.
R Huang, T A Barber, M A Schmidt, R G Tompkins, M Toner, D W Bianchi, R Kapur, W L Flejter. Prenat Diagn 2008
84
14

Screening for fetal chromosomal and subchromosomal disorders.
Sarah Harris, Dallas Reed, Neeta L Vora. Semin Fetal Neonatal Med 2018
7
14

Improving the Accuracy of Prenatal Screening with DNA Copy-Number Analysis.
Charles M Strom, Megan D Maxwell, Renius Owen. N Engl J Med 2017
7
14

Targeted sequencing of maternal plasma for haplotype-based non-invasive prenatal testing of spinal muscular atrophy.
M Chen, S Lu, Z F Lai, C Chen, K Luo, Y Yuan, Y S Wang, S Q Li, Y Gao, F Chen,[...]. Ultrasound Obstet Gynecol 2017
9
14

Diagnosis and clinical management of duplications and deletions.
Antonio Capalbo, Laura Rienzi, Filippo Maria Ubaldi. Fertil Steril 2017
13
14

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall,[...]. Eur J Hum Genet 2015
48
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

Patient preferences for prenatal testing of microdeletion and microduplication syndromes.
Elise Calonico, Yair J Blumenfeld, Louanne Hudgins, Joanne Taylor. Prenat Diagn 2016
3
33

Prenatal DNA diagnosis of a single-gene disorder from maternal plasma.
H Saito, A Sekizawa, T Morimoto, M Suzuki, T Yanaihara. Lancet 2000
186
14


Fetoplacental mosaicism: potential implications for false-positive and false-negative noninvasive prenatal screening results.
Francesca R Grati, Francesca Malvestiti, Jose C P B Ferreira, Komal Bajaj, Elisa Gaetani, Cristina Agrati, Beatrice Grimi, Francesca Dulcetti, Anna M Ruggeri, Simona De Toffol,[...]. Genet Med 2014
121
14

Effect of Cell-Free DNA Screening vs Direct Invasive Diagnosis on Miscarriage Rates in Women With Pregnancies at High Risk of Trisomy 21: A Randomized Clinical Trial.
Valérie Malan, Laurence Bussières, Norbert Winer, Jean-Philippe Jais, Amandine Baptiste, Marc Le Lorc'h, Caroline Elie, Neil O'Gorman, Nicolas Fries, Véronique Houfflin-Debarge,[...]. JAMA 2018
37
14

Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples.
Harini Ravi, Gabriel McNeill, Shruti Goel, Steven D Meltzer, Nathan Hunkapiller, Allison Ryan, Brynn Levy, Zachary P Demko. PLoS One 2018
21
14

Noninvasive prenatal testing beyond genomic analysis: what the future holds.
Winnie W I Hui, Rossa W K Chiu. Curr Opin Obstet Gynecol 2016
8
14

Targeted linked-read sequencing for direct haplotype phasing of maternal DMD alleles: a practical and reliable method for noninvasive prenatal diagnosis.
Se Song Jang, Byung Chan Lim, Seong-Keun Yoo, Jong-Yeon Shin, Ki-Joong Kim, Jeong-Sun Seo, Jong-Il Kim, Jong Hee Chae. Sci Rep 2018
16
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.