A citation-based method for searching scientific literature

Yanlin Wang, Yan Chen, Feng Tian, Jianguang Zhang, Zhuo Song, Yi Wu, Xu Han, Wenjing Hu, Duan Ma, David Cram, Weiwei Cheng. Clin Chem 2014
Times Cited: 149







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



Times Cited
  Times     Co-cited
Similarity


Noninvasive Prenatal Testing and Incidental Detection of Occult Maternal Malignancies.
Diana W Bianchi, Darya Chudova, Amy J Sehnert, Sucheta Bhatt, Kathryn Murray, Tracy L Prosen, Judy E Garber, Louise Wilkins-Haug, Neeta L Vora, Stephen Warsof,[...]. JAMA 2015
217
35

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
308
32

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

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
408
26

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
332
26

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
398
25

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
187
25

Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism-based noninvasive prenatal test.
Kirsten J Curnow, Louise Wilkins-Haug, Allison Ryan, Eser Kırkızlar, Melissa Stosic, Megan P Hall, Styrmir Sigurjonsson, Zachary Demko, Matthew Rabinowitz, Susan J Gross. Am J Obstet Gynecol 2015
91
25

Fetal sex chromosome testing by maternal plasma DNA sequencing: clinical laboratory experience and biology.
Diana W Bianchi, Saba Parsa, Sucheta Bhatt, Meredith Halks-Miller, Kathryn Kurtzman, Amy J Sehnert, Amy Swanson. Obstet Gynecol 2015
92
25

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
209
23

Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease.
C Michael Osborne, Emily Hardisty, Patricia Devers, Kathleen Kaiser-Rogers, Melissa A Hayden, William Goodnight, Neeta L Vora. Prenat Diagn 2013
127
22

DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study.
Glenn E Palomaki, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow, Louis M Neveux, Mathias Ehrich, Dirk van den Boom, Allan T Bombard, Cosmin Deciu, Wayne W Grody,[...]. Genet Med 2011
590
22

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
161
22

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
200
22

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
690
21

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
84
25

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
83
25

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing.
Diana W Bianchi, Lawrence D Platt, James D Goldberg, Alfred Z Abuhamad, Amy J Sehnert, Richard P Rava. Obstet Gynecol 2012
459
20

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
119
20

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
670
19


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
174
18

X chromosome loss and ageing.
L M Russell, P Strike, C E Browne, P A Jacobs. Cytogenet Genome Res 2007
104
17

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
575
17

Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service.
Tze Kin Lau, Fu Man Jiang, Robert J Stevenson, Tsz Kin Lo, Lin Wai Chan, Mei Ki Chan, Pui Shan Salome Lo, Wei Wang, Hong-Yun Zhang, Fang Chen,[...]. Prenat Diagn 2013
94
17

Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast.
M Alberry, D Maddocks, M Jones, M Abdel Hadi, S Abdel-Fattah, N Avent, P W Soothill. Prenat Diagn 2007
229
15

The type of feto-placental aneuploidy detected by cfDNA testing may influence the choice of confirmatory diagnostic procedure.
Francesca Romana Grati, Komal Bajaj, Francesca Malvestiti, Cristina Agrati, Beatrice Grimi, Barbara Malvestiti, Eva Pompilii, Federico Maggi, Susan Gross, Giuseppe Simoni,[...]. Prenat Diagn 2015
40
37

Gestational age and maternal weight effects on fetal cell-free DNA in maternal plasma.
Eric Wang, Annette Batey, Craig Struble, Thomas Musci, Ken Song, Arnold Oliphant. Prenat Diagn 2013
224
15

Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: relation to maternal and fetal characteristics.
G Ashoor, A Syngelaki, L C Y Poon, J C Rezende, K H Nicolaides. Ultrasound Obstet Gynecol 2013
214
15

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
168
15

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
357
14

Sex chromosome aneuploidy detection by noninvasive prenatal testing: helpful or hazardous?
Rosemary E Reiss, Marie Discenza, Judith Foster, Lori Dobson, Louise Wilkins-Haug. Prenat Diagn 2017
34
41

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
98
13

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
58
22

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
85
15

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
129
13

Maternal X chromosome copy number variations are associated with discordant fetal sex chromosome aneuploidies detected by noninvasive prenatal testing.
Shaowei Wang, Shuai Huang, Linlin Ma, Lin Liang, Junrong Zhang, Jianguang Zhang, David S Cram. Clin Chim Acta 2015
19
68

Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort.
Eugene Pergament, Howard Cuckle, Bernhard Zimmermann, Milena Banjevic, Styrmir Sigurjonsson, Allison Ryan, Megan P Hall, Michael Dodd, Phil Lacroute, Melissa Stosic,[...]. Obstet Gynecol 2014
173
13

Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma.
Amin R Mazloom, Željko Džakula, Paul Oeth, Huiquan Wang, Taylor Jensen, John Tynan, Ron McCullough, Juan-Sebastian Saldivar, Mathias Ehrich, Dirk van den Boom,[...]. Prenat Diagn 2013
126
13

Overview of the impact of noninvasive prenatal testing on diagnostic procedures.
Steven L Warsof, Sebastian Larion, Alfred Z Abuhamad. Prenat Diagn 2015
80
16

Discordant non-invasive prenatal testing (NIPT) - a systematic review.
Tanja Schlaikjaer Hartwig, Louise Ambye, Steen Sørensen, Finn Stener Jørgensen. Prenat Diagn 2017
94
13

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
106
12

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.
Rossa W K Chiu, Ranjit Akolekar, Yama W L Zheng, Tak Y Leung, Hao Sun, K C Allen Chan, Fiona M F Lun, Attie T J I Go, Elizabeth T Lau, William W K To,[...]. BMJ 2011
484
12

Rapid clearance of fetal DNA from maternal plasma.
Y M Lo, J Zhang, T N Leung, T K Lau, A M Chang, N M Hjelm. Am J Hum Genet 1999
724
12

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.
Desheng Liang, Ying Peng, Weigang Lv, Linbei Deng, Yanghui Zhang, Haoxian Li, Pu Yang, Jianguang Zhang, Zhuo Song, Genming Xu,[...]. J Mol Diagn 2014
72
16


Circulating fetal cell-free DNA fractions differ in autosomal aneuploidies and monosomy X.
Richard P Rava, Anupama Srinivasan, Amy J Sehnert, Diana W Bianchi. Clin Chem 2014
102
12

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
78
15

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
11

Chromosome abnormalities detected by current prenatal screening and noninvasive prenatal testing.
Mary E Norton, Laura L Jelliffe-Pawlowski, Robert J Currier. Obstet Gynecol 2014
67
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.