A citation-based method for searching scientific literature

Athena M Cherry, Yassmine M Akkari, Kimberly M Barr, Hutton M Kearney, Nancy C Rose, Sarah T South, James H Tepperberg, Jeanne M Meck. Genet Med 2017
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
234
75

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
294
62

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
185
50

Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood.
Bin Zhang, Bei-Yi Lu, Bin Yu, Fang-Xiu Zheng, Qin Zhou, Ying-Ping Chen, Xiao-Qing Zhang. J Int Med Res 2017
40
50

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
100
37

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
123
37

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
91
37

Non-invasive risk assessment of fetal sex chromosome aneuploidy through directed analysis and incorporation of fetal fraction.
J Hooks, A J Wolfberg, E T Wang, C A Struble, J Zahn, K Juneau, M Mohseni, S Huang, P Bogard, K Song,[...]. Prenat Diagn 2014
34
37

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
348
37


Rare autosomal trisomies, revealed by maternal plasma DNA sequencing, suggest increased risk of feto-placental disease.
Mark D Pertile, Meredith Halks-Miller, Nicola Flowers, Catalin Barbacioru, Sarah L Kinnings, Darcy Vavrek, William K Seltzer, Diana W Bianchi. Sci Transl Med 2017
68
37

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
148
37

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
32
37

Detection of fetal sex chromosome aneuploidy by massively parallel sequencing of maternal plasma DNA: initial experience in a Chinese hospital.
H Yao, F Jiang, H Hu, Y Gao, Z Zhu, H Zhang, Y Wang, Y Guo, L Liu, Y Yuan,[...]. Ultrasound Obstet Gynecol 2014
34
37

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
88
37

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
451
25

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
247
25

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
169
25

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
381
25

Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.
Peter Benn, Antoni Borell, Rossa Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte Faas, Susan Gross, Joann Johnson, Ron Maymon, Mary Norton,[...]. Prenat Diagn 2013
150
25

Positive cell-free fetal DNA testing for trisomy 13 reveals confined placental mosaicism.
April L Hall, Holli M Drendel, Jennifer L Verbrugge, Angela M Reese, Katherine L Schumacher, Christopher B Griffith, David D Weaver, Mary P Abernathy, Christian G Litton, Gail H Vance. Genet Med 2013
54
25

Clinical experience from Thailand: noninvasive prenatal testing as screening tests for trisomies 21, 18 and 13 in 4736 pregnancies.
S Manotaya, H Xu, B Uerpairojkit, F Chen, D Charoenvidhya, H Liu, N Petcharaburanin, Y Liu, S Tang, X Wang,[...]. Prenat Diagn 2016
10
25

Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X.
Hong Yao, Lei Zhang, Hongyun Zhang, Fuman Jiang, Hua Hu, Fang Chen, Hui Jiang, Feng Mu, Lijian Zhao, Zhiqing Liang,[...]. Prenat Diagn 2012
39
25

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
175
25

Genome-wide cfDNA screening: clinical laboratory experience with the first 10,000 cases.
Mathias Ehrich, John Tynan, Amin Mazloom, Eyad Almasri, Ron McCullough, Theresa Boomer, Daniel Grosu, Jason Chibuk. Genet Med 2017
37
25

SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy.
Carole Samango-Sprouse, Milena Banjevic, Allison Ryan, Styrmir Sigurjonsson, Bernhard Zimmermann, Matthew Hill, Megan P Hall, Margaret Westemeyer, Jennifer Saucier, Zachary Demko,[...]. Prenat Diagn 2013
82
25


Non-invasive prenatal diagnosis of fetal aneuploidies using massively parallel sequencing-by-ligation and evidence that cell-free fetal DNA in the maternal plasma originates from cytotrophoblastic cells.
Brigitte H W Faas, Joep de Ligt, Irene Janssen, Alex J Eggink, Lia D E Wijnberger, John M G van Vugt, Lisenka Vissers, Ad Geurts van Kessel. Expert Opin Biol Ther 2012
83
25

Uptake, outcomes, and costs of implementing non-invasive prenatal testing for Down's syndrome into NHS maternity care: prospective cohort study in eight diverse maternity units.
Lyn S Chitty, David Wright, Melissa Hill, Talitha I Verhoef, Rebecca Daley, Celine Lewis, Sarah Mason, Fiona McKay, Lucy Jenkins, Abigail Howarth,[...]. BMJ 2016
85
25

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact.
Dick Oepkes, G C Lieve Page-Christiaens, Caroline J Bax, Mireille N Bekker, Catia M Bilardo, Elles M J Boon, G Heleen Schuring-Blom, Audrey B C Coumans, Brigitte H Faas, Robert-Jan H Galjaard,[...]. Prenat Diagn 2016
83
25

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
159
25

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
572
25

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
361
25

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
67
25


Clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision-making.
Aarti Ramdaney, Jennifer Hoskovec, Jacqueline Harkenrider, Eleazar Soto, Lauren Murphy. Prenat Diagn 2018
21
25

Overall evaluation of the clinical value of prenatal screening for fetal-free DNA in maternal blood.
Bin Yu, Bei-Yi Lu, Bin Zhang, Xiao-Qing Zhang, Ying-Ping Chen, Qin Zhou, Jian Jiang, Hui-Yan Wang. Medicine (Baltimore) 2017
20
25

Non-invasive prenatal testing for fetal aneuploidies in the first trimester of pregnancy.
Y Song, S Huang, X Zhou, Y Jiang, Q Qi, X Bian, J Zhang, Y Yan, D S Cram, J Liu. Ultrasound Obstet Gynecol 2015
36
25

Factors Associated With Informative Redraw After an Initial No Result in Noninvasive Prenatal Testing.
Peter Benn, Elizabeth Valenti, Shailen Shah, Kimberly Martin, Zachary Demko. Obstet Gynecol 2018
18
25


Classification of factors involved in nonreportable results of noninvasive prenatal testing (NIPT) and prediction of success rate of second NIPT.
Nobuhiro Suzumori, Akihiko Sekizawa, Eri Takeda, Osamu Samura, Aiko Sasaki, Rina Akaishi, Seiji Wada, Haruka Hamanoue, Fumiki Hirahara, Hiroko Kuriki,[...]. Prenat Diagn 2019
13
25

Perinatal outcomes following cell-free DNA screening in >32 000 women: Clinical follow-up data from a single tertiary center.
Dong Liang, Ying Lin, Fengchang Qiao, Hang Li, Yan Wang, Jingjing Zhang, An Liu, Xiuqing Ji, Dingyuan Ma, Tao Jiang,[...]. Prenat Diagn 2018
15
25


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
643
25

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
25

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
372
25

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
52
25

Clinical features and pregnancy outcomes of women with abnormal cell-free fetal DNA test results.
Qin Zhou, Zhi-Ping Zhu, Bin Zhang, Bin Yu, Zheng-Mao Cai, Pei Yuan. Ann Transl Med 2019
6
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
25

NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy.
K L Wilson, J L Czerwinski, J M Hoskovec, S J Noblin, C M Sullivan, A Harbison, M W Campion, K Devary, P Devers, C N Singletary. J Genet Couns 2013
70
25


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.