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List of co-cited articles
163 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
47

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
656
39

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
387
34

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
608
26

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
676
26

Prenatal Diagnosis Innovation: Genome Sequencing of Maternal Plasma.
Felix C K Wong, Y M Dennis Lo. Annu Rev Med 2016
66
26

Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA.
Fiona M F Lun, Rossa W K Chiu, Kun Sun, Tak Y Leung, Peiyong Jiang, K C Allen Chan, Hao Sun, Y M Dennis Lo. Clin Chem 2013
103
21

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
118
17

Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients.
Peiyong Jiang, Carol W M Chan, K C Allen Chan, Suk Hang Cheng, John Wong, Vincent Wai-Sun Wong, Grace L H Wong, Stephen L Chan, Tony S K Mok, Henry L Y Chan,[...]. Proc Natl Acad Sci U S A 2015
390
17

Nuclear Acids In Human Blood Plasma.
P MANDEL, P METAIS. C R Seances Soc Biol Fil 1948
648
17

Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.
Kitty K Lo, Evangelia Karampetsou, Christopher Boustred, Fiona McKay, Sarah Mason, Melissa Hill, Vincent Plagnol, Lyn S Chitty. Am J Hum Genet 2016
76
17

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
371
17

Liquid biopsies come of age: towards implementation of circulating tumour DNA.
Jonathan C M Wan, Charles Massie, Javier Garcia-Corbacho, Florent Mouliere, James D Brenton, Carlos Caldas, Simon Pacey, Richard Baird, Nitzan Rosenfeld. Nat Rev Cancer 2017
17

Cell-Free DNA: An Upcoming Biomarker in Transplantation.
E M Gielis, K J Ledeganck, B Y De Winter, J Del Favero, J-L Bosmans, F H J Claas, D Abramowicz, M Eikmans. Am J Transplant 2015
101
17

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
49
17

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
61
17


Nonhematopoietically derived DNA is shorter than hematopoietically derived DNA in plasma: a transplantation model.
Yama W L Zheng, K C Allen Chan, Hao Sun, Peiyong Jiang, Xiaoxi Su, Eric Z Chen, Fiona M F Lun, Emily C W Hung, Vincent Lee, John Wong,[...]. Clin Chem 2012
88
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
141
13

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
292
13

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
694
13

Cell-free nucleic acids as biomarkers in cancer patients.
Heidi Schwarzenbach, Dave S B Hoon, Klaus Pantel. Nat Rev Cancer 2011
13

Detection of circulating tumor DNA in early- and late-stage human malignancies.
Chetan Bettegowda, Mark Sausen, Rebecca J Leary, Isaac Kinde, Yuxuan Wang, Nishant Agrawal, Bjarne R Bartlett, Hao Wang, Brandon Luber, Rhoda M Alani,[...]. Sci Transl Med 2014
13

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
402
13

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
181
13

Non-invasive prenatal testing: a review of international implementation and challenges.
Megan Allyse, Mollie A Minear, Elisa Berson, Shilpa Sridhar, Margaret Rote, Anthony Hung, Subhashini Chandrasekharan. Int J Womens Health 2015
171
13

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
92
13

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
320
13

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
13

Detection of the placental epigenetic signature of the maspin gene in maternal plasma.
Stephen S C Chim, Yu K Tong, Rossa W K Chiu, Tze K Lau, Tse N Leung, Lisa Y S Chan, Cees B M Oudejans, Chunming Ding, Y M Dennis Lo. Proc Natl Acad Sci U S A 2005
252
13

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
321
13

Identification of tissue-specific cell death using methylation patterns of circulating DNA.
Roni Lehmann-Werman, Daniel Neiman, Hai Zemmour, Joshua Moss, Judith Magenheim, Adi Vaknin-Dembinsky, Sten Rubertsson, Bengt Nellgård, Kaj Blennow, Henrik Zetterberg,[...]. Proc Natl Acad Sci U S A 2016
349
13


Circulating mutant DNA to assess tumor dynamics.
Frank Diehl, Kerstin Schmidt, Michael A Choti, Katharine Romans, Steven Goodman, Meng Li, Katherine Thornton, Nishant Agrawal, Lori Sokoll, Steve A Szabo,[...]. Nat Med 2008
13

Integrated digital error suppression for improved detection of circulating tumor DNA.
Aaron M Newman, Alexander F Lovejoy, Daniel M Klass, David M Kurtz, Jacob J Chabon, Florian Scherer, Henning Stehr, Chih Long Liu, Scott V Bratman, Carmen Say,[...]. Nat Biotechnol 2016
595
13

Direct detection of early-stage cancers using circulating tumor DNA.
Jillian Phallen, Mark Sausen, Vilmos Adleff, Alessandro Leal, Carolyn Hruban, James White, Valsamo Anagnostou, Jacob Fiksel, Stephen Cristiano, Eniko Papp,[...]. Sci Transl Med 2017
578
13

Free DNA in the serum of cancer patients and the effect of therapy.
S A Leon, B Shapiro, D M Sklaroff, M J Yaros. Cancer Res 1977
13

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
17
17

Non-invasive prenatal diagnosis of thalassemias using maternal plasma cell free DNA.
Irena Hudecova, Rossa W K Chiu. Best Pract Res Clin Obstet Gynaecol 2017
27
13

cfDNA screening and diagnosis of monogenic disorders - where are we heading?
Eunice Ka Long Chiu, Winnie Wai In Hui, Rossa Wai Kwun Chiu. Prenat Diagn 2018
32
13

Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57.
Deborah J G Mackay, Jonathan L A Callaway, Sophie M Marks, Helen E White, Carlo L Acerini, Susanne E Boonen, Pinar Dayanikli, Helen V Firth, Judith A Goodship, Andreas P Haemers,[...]. Nat Genet 2008
352
8

Mosaic maternal uniparental disomy of chromosome 11 in a patient with Silver-Russell syndrome.
H Bullman, M Lever, D O Robinson, D J G Mackay, S E Holder, E L Wakeling. J Med Genet 2008
52
8

Epimutations of the IG-DMR and the MEG3-DMR at the 14q32.2 imprinted region in two patients with Silver-Russell Syndrome-compatible phenotype.
Masayo Kagami, Seiji Mizuno, Keiko Matsubara, Kazuhiko Nakabayashi, Shinichiro Sano, Tomoko Fuke, Maki Fukami, Tsutomu Ogata. Eur J Hum Genet 2015
52
8

Additional molecular findings in 11p15-associated imprinting disorders: an urgent need for multi-locus testing.
Thomas Eggermann, Ann-Kathrin Heilsberg, Susanne Bens, Reiner Siebert, Jasmin Beygo, Karin Buiting, Matthias Begemann, Lukas Soellner. J Mol Med (Berl) 2014
37
8

Mutations in NALP7 cause recurrent hydatidiform moles and reproductive wastage in humans.
Sharlene Murdoch, Ugljesa Djuric, Batool Mazhar, Muheiddine Seoud, Rabia Khan, Rork Kuick, Rashmi Bagga, Renate Kircheisen, Asangla Ao, Bhawna Ratti,[...]. Nat Genet 2006
318
8

Clinical features of three girls with mosaic genome-wide paternal uniparental isodisomy.
Jennifer M Kalish, Laura K Conlin, Tricia R Bhatti, Holly A Dubbs, Mary Catherine Harris, Kosuke Izumi, Sogol Mostoufi-Moab, Surabhi Mulchandani, Sulagna Saitta, Lisa J States,[...]. Am J Med Genet A 2013
48
8

Novel deletions affecting the MEG3-DMR provide further evidence for a hierarchical regulation of imprinting in 14q32.
Jasmin Beygo, Miriam Elbracht, Karel de Groot, Matthias Begemann, Deniz Kanber, Konrad Platzer, Gabriele Gillessen-Kaesbach, Anne Vierzig, Andrew Green, Raoul Heller,[...]. Eur J Hum Genet 2015
39
8

Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).
Esther Meyer, Derek Lim, Shanaz Pasha, Louise J Tee, Fatimah Rahman, John R W Yates, C Geoffrey Woods, Wolf Reik, Eamonn R Maher. PLoS Genet 2009
163
8

CDKN1C mutation affecting the PCNA-binding domain as a cause of familial Russell Silver syndrome.
F Brioude, I Oliver-Petit, A Blaise, F Praz, S Rossignol, M Le Jule, N Thibaud, A-M Faussat, M Tauber, Y Le Bouc,[...]. J Med Genet 2013
90
8

Methylation analysis in tongue tissue of BWS patients identifies the (EPI)genetic cause in 3 patients with normal methylation levels in blood.
Mariëlle Alders, Saskia M Maas, Daniël J M Kadouch, Karin van der Lip, Jet Bliek, Chantal M A M van der Horst, Marcel M A M Mannens. Eur J Med Genet 2014
20
10


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.