A citation-based method for searching scientific literature

Thessalia Papasavva, Wilfred F J van Ijcken, Christel E M Kockx, Mirjam C G N van den Hout, Petros Kountouris, Loukas Kythreotis, Eleni Kalogirou, Frank G Grosveld, Marina Kleanthous. Eur J Hum Genet 2013
Times Cited: 29







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



Times Cited
  Times     Co-cited
Similarity


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
100
44

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
44

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
539
34

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
119
31

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
206
27

Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma.
Ying Li, Edoardo Di Naro, Angeloantonio Vitucci, Bernhard Zimmermann, Wolfgang Holzgreve, Sinuhe Hahn. JAMA 2005
157
24

Prenatal exclusion of beta thalassaemia major by examination of maternal plasma.
Rossa W K Chiu, Tze K Lau, Tse N Leung, Katherine C K Chow, David H K Chui, Y M Dennis Lo. Lancet 2002
171
24

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
109
24

Non-invasive prenatal diagnostic testing for β-thalassaemia using cell-free fetal DNA and next generation sequencing.
Li Xiong, Angela N Barrett, Rui Hua, Tuan Zea Tan, Sherry Sze Yee Ho, Jerry K Y Chan, Mei Zhong, Mahesh Choolani. Prenat Diagn 2015
34
24

Arrayed primer extension for the noninvasive prenatal diagnosis of beta-thalassemia based on detection of single nucleotide polymorphisms.
Thessalia Papasavva, Ioannis Kalikas, Andreanni Kyrri, Marina Kleanthous. Ann N Y Acad Sci 2008
38
20

Noninvasive prenatal diagnostic assay for the detection of beta-thalassemia.
Thessalia Papasavva, Gabriel Kalakoutis, Ioannis Kalikas, Electra Neokli, Soteroula Papacharalambous, Andreanni Kyrri, Marina Kleanthous. Ann N Y Acad Sci 2006
20
30

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
80
20

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
141
20

Haplotype-based approach for noninvasive prenatal tests of Duchenne muscular dystrophy using cell-free fetal DNA in maternal plasma.
Yan Xu, Xuchao Li, Hui-Juan Ge, Bing Xiao, Yan-Yan Zhang, Xiao-Min Ying, Xiao-Yu Pan, Lei Wang, Wei-Wei Xie, Lin Ni,[...]. Genet Med 2015
40
20

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
273
17

Non-invasive prenatal diagnosis of Duchenne and Becker muscular dystrophies by relative haplotype dosage.
Michael Parks, Samantha Court, Siobhan Cleary, Samuel Clokie, Julie Hewitt, Denise Williams, Trevor Cole, Fiona MacDonald, Mike Griffiths, Stephanie Allen. Prenat Diagn 2016
37
17

Haplotype-based approach for noninvasive prenatal diagnosis of congenital adrenal hyperplasia by maternal plasma DNA sequencing.
Dingyuan Ma, Huijuan Ge, Xuchao Li, Tao Jiang, Fang Chen, Yanyan Zhang, Ping Hu, Shengpei Chen, Jingjing Zhang, Xiuqing Ji,[...]. Gene 2014
28
17

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
83
17

Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemia.
Silvia Galbiati, Barbara Foglieni, Maurizio Travi, Cristina Curcio, Gabriella Restagno, Luca Sbaiz, Maddalena Smid, Federica Pasi, Augusto Ferrari, Maurizio Ferrari,[...]. Haematologica 2008
30
13

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.
Chunming Ding, Rossa W K Chiu, Tze K Lau, Tse N Leung, Li C Chan, Amy Y Y Chan, Pimlak Charoenkwan, Ivy S L Ng, Hai-Yang Law, Edmond S K Ma,[...]. Proc Natl Acad Sci U S A 2004
127
13

Full COLD-PCR protocol for noninvasive prenatal diagnosis of genetic diseases.
Silvia Galbiati, Angela Brisci, Faustina Lalatta, Manuela Seia, G Mike Makrigiorgos, Maurizio Ferrari, Laura Cremonesi. Clin Chem 2011
36
13

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
620
13

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
181
13

Noninvasive prenatal diagnosis of duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus.
Seong-Keun Yoo, Byung Chan Lim, Jiyoung Byeun, Hee Hwang, Ki Joong Kim, Yong Seung Hwang, JoonHo Lee, Joong Shin Park, Yong-Sun Lee, Junghyun Namkung,[...]. Clin Chem 2015
24
16

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
33
13

Droplet digital PCR combined with minisequencing, a new approach to analyze fetal DNA from maternal blood: application to the non-invasive prenatal diagnosis of achondroplasia.
Lucie Orhant, Olivia Anselem, Mélanie Fradin, Pierre Hadrien Becker, Caroline Beugnet, Nathalie Deburgrave, Gilles Tafuri, Franck Letourneur, François Goffinet, Laïla Allach El Khattabi,[...]. Prenat Diagn 2016
24
16

Non-invasive prenatal diagnosis of beta-thalassemia and sickle-cell disease using pyrophosphorolysis-activated polymerization and melting curve analysis.
Marion Phylipsen, Supawadee Yamsri, Emmely E Treffers, Diahann T S L Jansen, Warsha A Kanhai, Elles M J Boon, Piero C Giordano, Supan Fucharoen, Egbert Bakker, Cornelis L Harteveld. Prenat Diagn 2012
25
12

Direct selection of human genomic loci by microarray hybridization.
Thomas J Albert, Michael N Molla, Donna M Muzny, Lynne Nazareth, David Wheeler, Xingzhi Song, Todd A Richmond, Chris M Middle, Matthew J Rodesch, Charles J Packard,[...]. Nat Methods 2007
426
10

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
201
10

Updates of the HbVar database of human hemoglobin variants and thalassemia mutations.
Belinda Giardine, Joseph Borg, Emmanouil Viennas, Cristiana Pavlidis, Kamran Moradkhani, Philippe Joly, Marina Bartsakoulia, Cathy Riemer, Webb Miller, Giannis Tzimas,[...]. Nucleic Acids Res 2014
233
10

A minimal set of SNPs for the noninvasive prenatal diagnosis of β-thalassaemia.
Thessalia E Papasavva, Carsten W Lederer, Jan Traeger-Synodinos, Ariadne Mavrou, Emmanuel Kanavakis, Christiana Ioannou, Christiana Makariou, Marina Kleanthous. Ann Hum Genet 2013
11
27

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
356
10

Size fractionation of cell-free DNA in maternal plasma improves the detection of a paternally inherited beta-thalassemia point mutation by MALDI-TOF mass spectrometry.
Ying Li, Edoardo Di Naro, Angeloantonio Vitucci, Simon Grill, Xiao Yan Zhong, Wolfgang Holzgreve, Sinuhe Hahn. Fetal Diagn Ther 2009
25
12

Update on procedure-related risks for prenatal diagnosis techniques.
Ann Tabor, Zarko Alfirevic. Fetal Diagn Ther 2010
206
10

Beta-thalassemia.
Antonio Cao, Renzo Galanello. Genet Med 2010
336
10

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
180
10

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
199
10

Diagnostic accuracy of routine antenatal determination of fetal RHD status across gestation: population based cohort study.
Lyn S Chitty, Kirstin Finning, Angela Wade, Peter Soothill, Bill Martin, Kerry Oxenford, Geoff Daniels, Edwin Massey. BMJ 2014
58
10

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
90
10

Initial clinical laboratory experience in noninvasive prenatal testing for fetal aneuploidy from maternal plasma DNA samples.
Tracy Futch, John Spinosa, Sucheta Bhatt, Eileen de Feo, Richard P Rava, Amy J Sehnert. Prenat Diagn 2013
112
10

Beta-thalassemia.
Renzo Galanello, Raffaella Origa. Orphanet J Rare Dis 2010
470
10

Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemia.
Silvia Galbiati, Angela Brisci, Francesco Damin, Barbara Gentilin, Cristina Curcio, Gabriella Restagno, Laura Cremonesi, Maurizio Ferrari. Expert Opin Biol Ther 2012
8
37

Noninvasive prenatal diagnosis in a fetus at risk for methylmalonic acidemia.
Wei Gu, Winston Koh, Yair J Blumenfeld, Yasser Y El-Sayed, Louanne Hudgins, Susan R Hintz, Stephen R Quake. Genet Med 2014
16
18

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
10


Noninvasive prenatal testing for autosomal recessive conditions by maternal plasma sequencing in a case of congenital deafness.
Meng Meng, Xuchao Li, Huijuan Ge, Fang Chen, Mingyu Han, Yanyan Zhang, Dongyang Kang, Weiwei Xie, Zhiying Gao, Xiaoyu Pan,[...]. Genet Med 2014
34
10

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
50
10

Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage.
Michael Parks, Samantha Court, Benjamin Bowns, Siobhan Cleary, Samuel Clokie, Julie Hewitt, Denise Williams, Trevor Cole, Fiona MacDonald, Mike Griffiths,[...]. Eur J Hum Genet 2017
32
10

COLD-PCR and microarray: two independent highly sensitive approaches allowing the identification of fetal paternally inherited mutations in maternal plasma.
Silvia Galbiati, Alessandra Monguzzi, Francesco Damin, Nadia Soriani, Marianna Passiu, Carlo Castellani, Federica Natacci, Cristina Curcio, Manuela Seia, Faustina Lalatta,[...]. J Med Genet 2016
15
20

The prevalence and spectrum of alpha and beta thalassaemia in Guangdong Province: implications for the future health burden and population screening.
X M Xu, Y Q Zhou, G X Luo, C Liao, M Zhou, P Y Chen, J P Lu, S Q Jia, G F Xiao, X Shen,[...]. J Clin Pathol 2004
215
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.