A citation-based method for searching scientific literature

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, Holly K Tabor, Michael J Bamshad, Evan E Eichler, Jay Shendure. Sci Transl Med 2012
Times Cited: 240







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



Times Cited
  Times     Co-cited
Similarity


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
578
49

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

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
213
40

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
563
30

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
649
30

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
384
24

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
579
21

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
455
19

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
657
18

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
171
18

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
385
16

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
90
17

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
475
15

Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci.
Bernhard Zimmermann, Matthew Hill, George Gemelos, Zachary Demko, Milena Banjevic, Johan Baner, Allison Ryan, Styrmir Sigurjonsson, Nikhil Chopra, Michael Dodd,[...]. Prenat Diagn 2012
193
15

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
14

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
377
14

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
105
14

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
702
13

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
13

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
129
13

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
73
17

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
219
12

Noninvasive prenatal diagnosis of a fetal microdeletion syndrome.
David Peters, Tianjiao Chu, Svetlana A Yatsenko, Nancy Hendrix, W Allen Hogge, Urvashi Surti, Kimberly Bunce, Mary Dunkel, Patricia Shaw, Aleksandar Rajkovic. N Engl J Med 2011
91
13

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
176
12

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
175
12

Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Suzanne Drury, Hywel Williams, Natalie Trump, Christopher Boustred, Nicholas Lench, Richard H Scott, Lyn S Chitty. Prenat Diagn 2015
111
12

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
353
11

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
364
11

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
295
11

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
132
11

Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population.
Kypros H Nicolaides, Argyro Syngelaki, Ghalia Ashoor, Cahit Birdir, Gisele Touzet. Am J Obstet Gynecol 2012
237
10


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
222
10

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting.
Mathias Ehrich, Cosmin Deciu, Tricia Zwiefelhofer, John A Tynan, Lesley Cagasan, Roger Tim, Vivian Lu, Ron McCullough, Erin McCarthy, Anders O H Nygren,[...]. Am J Obstet Gynecol 2011
339
10

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
324
10

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
203
10

Cell-free DNA Comprises an In Vivo Nucleosome Footprint that Informs Its Tissues-Of-Origin.
Matthew W Snyder, Martin Kircher, Andrew J Hill, Riza M Daza, Jay Shendure. Cell 2016
509
10

Update on procedure-related risks for prenatal diagnosis techniques.
Ann Tabor, Zarko Alfirevic. Fetal Diagn Ther 2010
226
9

Advances in prenatal screening: the ethical dimension.
Antina de Jong, Wybo J Dondorp, Suzanna G M Frints, Christine E M de Die-Smulders, Guido M W R de Wert. Nat Rev Genet 2011
80
11

The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made.
Nicholas Lench, Angela Barrett, Sarah Fielding, Fiona McKay, Melissa Hill, Lucy Jenkins, Helen White, Lyn S Chitty. Prenat Diagn 2013
89
10

Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma.
Taylor J Jensen, Zeljko Dzakula, Cosmin Deciu, Dirk van den Boom, Mathias Ehrich. Clin Chem 2012
83
10

Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma.
Fiona M F Lun, Rossa W K Chiu, K C Allen Chan, Tak Yeung Leung, Tze Kin Lau, Y M Dennis Lo. Clin Chem 2008
290
9

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
Rachèl V van Schendel, Johanna H Kleinveld, Wybo J Dondorp, Eva Pajkrt, Danielle R M Timmermans, Kim C A Holtkamp, Margreet Karsten, Anne L Vlietstra, Augusta M A Lachmeijer, Lidewij Henneman. Eur J Hum Genet 2014
72
12

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
155
9

Women's experiences receiving abnormal prenatal chromosomal microarray testing results.
Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
132
9


ACMG position statement on prenatal/preconception expanded carrier screening.
Wayne W Grody, Barry H Thompson, Anthony R Gregg, Lora H Bean, Kristin G Monaghan, Adele Schneider, Roger V Lebo. Genet Med 2013
173
9


Prenatal whole-exome sequencing: parental attitudes.
Eve J Kalynchuk, Andrew Althouse, Lisa S Parker, Devereux N Saller, Aleksandar Rajkovic. Prenat Diagn 2015
33
27



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.