A citation-based method for searching scientific literature

Jinglan Zhang, Jianli Li, Jennifer B Saucier, Yanming Feng, Yanjun Jiang, Jefferson Sinson, Anne K McCombs, Eric S Schmitt, Sandra Peacock, Stella Chen, Hongzheng Dai, Xiaoyan Ge, Guoli Wang, Chad A Shaw, Hui Mei, Amy Breman, Fan Xia, Yaping Yang, Anne Purgason, Alan Pourpak, Zhao Chen, Xia Wang, Yue Wang, Shashikant Kulkarni, Kwong Wai Choy, Ronald J Wapner, Ignatia B Van den Veyver, Arthur Beaudet, Sheetal Parmar, Lee-Jun Wong, Christine M Eng. Nat Med 2019
Times Cited: 90







List of co-cited articles
541 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
34

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
618
24

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
18

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
678
15

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
14

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
218
14

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
13

Sequencing of Circulating Cell-free DNA during Pregnancy.
Diana W Bianchi, Rossa W K Chiu. N Engl J Med 2018
128
13

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
225
13

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
413
12

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
85
12

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
187
12

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
703
11

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
282
11

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015
345
11


Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping.
Carlo Vermeulen, Geert Geeven, Elzo de Wit, Marjon J A M Verstegen, Rumo P M Jansen, Melissa van Kranenburg, Ewart de Bruijn, Sara L Pulit, Evelien Kruisselbrink, Zahra Shahsavari,[...]. Am J Hum Genet 2017
40
25


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
56
17

Non-invasive prenatal measurement of the fetal genome.
H Christina Fan, Wei Gu, Jianbin Wang, Yair J Blumenfeld, Yasser Y El-Sayed, Stephen R Quake. Nature 2012
224
11

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
188
10

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
580
10

Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma.
Maria I New, Yu K Tong, Tony Yuen, Peiyong Jiang, Christian Pina, K C Allen Chan, Ahmed Khattab, Gary J W Liao, Mabel Yau, Se-Min Kim,[...]. J Clin Endocrinol Metab 2014
135
10

Size distributions of maternal and fetal DNA in maternal plasma.
K C Allen Chan, Jun Zhang, Angela B Y Hui, Nathalie Wong, Tze K Lau, Tse N Leung, Kwok-Wai Lo, Dolly W S Huang, Y M Dennis Lo. Clin Chem 2004
393
10

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
401
10

Noninvasive Prenatal Diagnosis of Single-Gene Diseases: The Next Frontier.
Elizabeth Scotchman, Natalie J Chandler, Rhiannon Mellis, Lyn S Chitty. Clin Chem 2020
19
47

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
170
8

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
223
8

Bayesian-based noninvasive prenatal diagnosis of single-gene disorders.
Tom Rabinowitz, Avital Polsky, David Golan, Artem Danilevsky, Guy Shapira, Chen Raff, Lina Basel-Salmon, Reut Tomashov Matar, Noam Shomron. Genome Res 2019
15
53

Discordant non-invasive prenatal testing (NIPT) - a systematic review.
Tanja Schlaikjaer Hartwig, Louise Ambye, Steen Sørensen, Finn Stener Jørgensen. Prenat Diagn 2017
100
8

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
160
8

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
76
10

Noninvasive prenatal diagnosis of monogenic diseases by targeted massively parallel sequencing of maternal plasma: application to β-thalassemia.
Kwan-Wood G Lam, Peiyong Jiang, Gary J W Liao, K C Allen Chan, Tak Y Leung, Rossa W K Chiu, Y M Dennis Lo. Clin Chem 2012
111
8

Size-tagged preferred ends in maternal plasma DNA shed light on the production mechanism and show utility in noninvasive prenatal testing.
Kun Sun, Peiyong Jiang, Ada I C Wong, Yvonne K Y Cheng, Suk Hang Cheng, Haiqiang Zhang, K C Allen Chan, Tak Y Leung, Rossa W K Chiu, Y M Dennis Lo. Proc Natl Acad Sci U S A 2018
69
11

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
347
8

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
230
8

Amniocentesis and chorionic villus sampling for prenatal diagnosis.
Zarko Alfirevic, Kate Navaratnam, Faris Mujezinovic. Cochrane Database Syst Rev 2017
61
13

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
7

Pilot study of a novel multi-functional noninvasive prenatal test on fetus aneuploidy, copy number variation, and single-gene disorder screening.
Yuqin Luo, Bei Jia, Kai Yan, Siping Liu, Xiaojie Song, Mingfa Chen, Fan Jin, Yang Du, Juan Wang, Yan Hong,[...]. Mol Genet Genomic Med 2019
15
46

Noninvasive whole-genome sequencing of a human fetus.
Jacob O Kitzman, Matthew W Snyder, Mario Ventura, Alexandra P Lewis, Ruolan Qiu, Lavone E Simmons, Hilary S Gammill, Craig E Rubens, Donna A Santillan, Jeffrey C Murray,[...]. Sci Transl Med 2012
245
7

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
286
7

A novel high-throughput molecular counting method with single base-pair resolution enables accurate single-gene NIPT.
David S Tsao, Sukrit Silas, Brian P Landry, Nelda P Itzep, Amy B Nguyen, Samuel Greenberg, Celeste K Kanne, Vivien A Sheehan, Rani Sharma, Rahul Shukla,[...]. Sci Rep 2019
10
70

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
213
7

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
7


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
229
7

Noninvasive prenatal diagnosis by genome-wide haplotyping of cell-free plasma DNA.
Huiwen Che, Darine Villela, Eftychia Dimitriadou, Cindy Melotte, Nathalie Brison, Maria Neofytou, Kris Van Den Bogaert, Olga Tsuiko, Koen Devriendt, Eric Legius,[...]. Genet Med 2020
12
58


Digital PCR analysis of maternal plasma for noninvasive detection of sickle cell anemia.
Angela N Barrett, Thomas C R McDonnell, K C Allen Chan, Lyn S Chitty. Clin Chem 2012
122
6

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
217
6


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.