A citation-based method for searching scientific literature

Antonio Capalbo, Laura Rienzi, Filippo Maria Ubaldi. Fertil Steril 2017
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Human embryos commonly form abnormal nuclei during development: a mechanism of DNA damage, embryonic aneuploidy, and developmental arrest.
Daniel H Kort, Gloryn Chia, Nathan R Treff, Akemi J Tanaka, Tongji Xing, Lauren Bauer Vensand, Stephanie Micucci, Robert Prosser, Roger A Lobo, Mark V Sauer,[...]. Hum Reprod 2016
40
25

Mouse model of chromosome mosaicism reveals lineage-specific depletion of aneuploid cells and normal developmental potential.
Helen Bolton, Sarah J L Graham, Niels Van der Aa, Parveen Kumar, Koen Theunis, Elia Fernandez Gallardo, Thierry Voet, Magdalena Zernicka-Goetz. Nat Commun 2016
168
25

Assessing the true incidence of mosaicism in preimplantation embryos.
Maria Vera-Rodriguez, Carmen Rubio. Fertil Steril 2017
50
25

Detailed investigation into the cytogenetic constitution and pregnancy outcome of replacing mosaic blastocysts detected with the use of high-resolution next-generation sequencing.
Santiago Munné, Joshua Blazek, Michael Large, Pedro A Martinez-Ortiz, Haley Nisson, Emmeline Liu, Nicoletta Tarozzi, Andrea Borini, Amie Becker, John Zhang,[...]. Fertil Steril 2017
121
25

Analysis of implantation and ongoing pregnancy rates following the transfer of mosaic diploid-aneuploid blastocysts.
Elpida Fragouli, Samer Alfarawati, Katharina Spath, Dhruti Babariya, Nicoletta Tarozzi, Andrea Borini, Dagan Wells. Hum Genet 2017
105
25

A single trophectoderm biopsy at blastocyst stage is mathematically unable to determine embryo ploidy accurately enough for clinical use.
Norbert Gleicher, Jacob Metzger, Gist Croft, Vitaly A Kushnir, David F Albertini, David H Barad. Reprod Biol Endocrinol 2017
54
25


Detecting mosaicism in trophectoderm biopsies: current challenges and future possibilities.
Antonio Capalbo, Filippo Maria Ubaldi, Laura Rienzi, Richard Scott, Nathan Treff. Hum Reprod 2017
66
25

Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA.
Ai-hua Yin, Chun-fang Peng, Xin Zhao, Bennett A Caughey, Jie-xia Yang, Jian Liu, Wei-wei Huang, Chang Liu, Dong-hong Luo, Hai-liang Liu,[...]. Proc Natl Acad Sci U S A 2015
65
25

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

Molecular origin of mitotic aneuploidies in preimplantation embryos.
Eleni Mantikou, Kai Mee Wong, Sjoerd Repping, Sebastiaan Mastenbroek. Biochim Biophys Acta 2012
69
16

Micronucleus formation causes perpetual unilateral chromosome inheritance in mouse embryos.
Cayetana Vázquez-Diez, Kazuo Yamagata, Shardul Trivedi, Jenna Haverfield, Greg FitzHarris. Proc Natl Acad Sci U S A 2016
42
16

The origin, mechanisms, incidence and clinical consequences of chromosomal mosaicism in humans.
Tyl H Taylor, Susan A Gitlin, Jennifer L Patrick, Jack L Crain, J Michael Wilson, Darren K Griffin. Hum Reprod Update 2014
170
16

Chromosome instability is common in human cleavage-stage embryos.
Evelyne Vanneste, Thierry Voet, Cédric Le Caignec, Michèle Ampe, Peter Konings, Cindy Melotte, Sophie Debrock, Mustapha Amyere, Miikka Vikkula, Frans Schuit,[...]. Nat Med 2009
495
16


Why do euploid embryos miscarry? A case-control study comparing the rate of aneuploidy within presumed euploid embryos that resulted in miscarriage or live birth using next-generation sequencing.
Susan M Maxwell, Pere Colls, Brooke Hodes-Wertz, David H McCulloh, Caroline McCaffrey, Dagan Wells, Santiago Munné, James A Grifo. Fertil Steril 2016
96
16

Healthy Babies after Intrauterine Transfer of Mosaic Aneuploid Blastocysts.
Ermanno Greco, Maria Giulia Minasi, Francesco Fiorentino. N Engl J Med 2015
247
16

Human female meiosis revised: new insights into the mechanisms of chromosome segregation and aneuploidies from advanced genomics and time-lapse imaging.
Antonio Capalbo, Eva R Hoffmann, Danilo Cimadomo, Filippo Maria Ubaldi, Laura Rienzi. Hum Reprod Update 2017
72
16

In vitro fertilization with single euploid blastocyst transfer: a randomized controlled trial.
Eric J Forman, Kathleen H Hong, Kathleen M Ferry, Xin Tao, Deanne Taylor, Brynn Levy, Nathan R Treff, Richard T Scott. Fertil Steril 2013
299
16

Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
R Li, J Wan, Y Zhang, F Fu, Y Ou, X Jing, J Li, D Li, C Liao. Ultrasound Obstet Gynecol 2016
34
16

Performance Evaluation of NIPT in Detection of Chromosomal Copy Number Variants Using Low-Coverage Whole-Genome Sequencing of Plasma DNA.
Hongtai Liu, Ya Gao, Zhiyang Hu, Linhua Lin, Xuyang Yin, Jun Wang, Dayang Chen, Fang Chen, Hui Jiang, Jinghui Ren,[...]. PLoS One 2016
20
16

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
16

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
16

Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.
Andrew B Sparks, Eric T Wang, Craig A Struble, Wade Barrett, Renee Stokowski, Celeste McBride, Jacob Zahn, Kevin Lee, Naiping Shen, Jigna Doshi,[...]. Prenat Diagn 2012
175
16

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
80
16

Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing.
Can Liao, Ai-hua Yin, Chun-fang Peng, Fang Fu, Jie-xia Yang, Ru Li, Yang-yi Chen, Dong-hong Luo, Yong-ling Zhang, Yan-mei Ou,[...]. Proc Natl Acad Sci U S A 2014
82
16


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
16

Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal Sex.
George Koumbaris, Elena Kypri, Kyriakos Tsangaras, Achilleas Achilleos, Petros Mina, Maria Neofytou, Voula Velissariou, Georgia Christopoulou, Ioannis Kallikas, Alicia González-Liñán,[...]. Clin Chem 2016
27
16

Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications.
Maria C Neofytou, Kyriakos Tsangaras, Elena Kypri, Charalambos Loizides, Marios Ioannides, Achilleas Achilleos, Petros Mina, Anna Keravnou, Carolina Sismani, George Koumbaris,[...]. PLoS One 2017
22
16


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
16

Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.
Peter Benn, Antoni Borrell, Rossa W K Chiu, Howard Cuckle, Lorraine Dugoff, Brigitte Faas, Susan Gross, Tianhua Huang, Joann Johnson, Ron Maymon,[...]. Prenat Diagn 2015
164
16

Mosaicism between trophectoderm and inner cell mass.
Antonio Capalbo, Laura Rienzi. Fertil Steril 2017
42
16

Evolutionarily conserved replication timing profiles predict long-range chromatin interactions and distinguish closely related cell types.
Tyrone Ryba, Ichiro Hiratani, Junjie Lu, Mari Itoh, Michael Kulik, Jinfeng Zhang, Thomas C Schulz, Allan J Robins, Stephen Dalton, David M Gilbert. Genome Res 2010
351
16

Inconclusive chromosomal assessment after blastocyst biopsy: prevalence, causative factors and outcomes after re-biopsy and re-vitrification. A multicenter experience.
Danilo Cimadomo, Laura Rienzi, Valeria Romanelli, Erminia Alviggi, Paolo Emanuele Levi-Setti, Elena Albani, Ludovica Dusi, Letizia Papini, Claudia Livi, Francesca Benini,[...]. Hum Reprod 2018
20
16

Genome-wide copy number profiling of single cells in S-phase reveals DNA-replication domains.
Niels Van der Aa, Jiqiu Cheng, Ligia Mateiu, Masoud Zamani Esteki, Parveen Kumar, Eftychia Dimitriadou, Evelyne Vanneste, Yves Moreau, Joris Robert Vermeesch, Thierry Voet. Nucleic Acids Res 2013
49
16

Clinical outcomes after the transfer of blastocysts characterized as mosaic by high resolution Next Generation Sequencing- further insights.
Santiago Munné, Francesca Spinella, Jamie Grifo, John Zhang, Monica Parriego Beltran, Elpida Fragouli, Francesco Fiorentino. Eur J Med Genet 2020
26
16

Distribution patterns of segmental aneuploidies in human blastocysts identified by next-generation sequencing.
María Vera-Rodríguez, Claude-Edouard Michel, Amparo Mercader, Alex J Bladon, Lorena Rodrigo, Felix Kokocinski, Emilia Mateu, Nasser Al-Asmar, David Blesa, Carlos Simón,[...]. Fertil Steril 2016
60
16

The incidence and origin of segmental aneuploidy in human oocytes and preimplantation embryos.
D Babariya, E Fragouli, S Alfarawati, K Spath, D Wells. Hum Reprod 2017
48
16

New microdeletion and microduplication syndromes: A comprehensive review.
Julián Nevado, Rafaella Mergener, María Palomares-Bralo, Karen Regina Souza, Elena Vallespín, Rocío Mena, Víctor Martínez-Glez, María Ángeles Mori, Fernando Santos, Sixto García-Miñaur,[...]. Genet Mol Biol 2014
54
16

Concordance between different trophectoderm biopsy sites and the inner cell mass of chromosomal composition measured with a next-generation sequencing platform.
Tzu-Hsuan Chuang, Jhih-Yuan Hsieh, Meng-Ju Lee, Hsing-Hua Lai, Chia-Lin Hsieh, Huai-Lin Wang, Yu-Jen Chang, Shee-Uan Chen. Mol Hum Reprod 2018
21
16

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
381
16

Development of prenatal screening--A historical overview.
Howard Cuckle, Ron Maymon. Semin Perinatol 2016
25
16


Recent trends in prenatal genetic screening and testing.
Ondrej Pös, Jaroslav Budiš, Tomáš Szemes. F1000Res 2019
14
16

Prenatal Diagnosis: Screening and Diagnostic Tools.
Laura M Carlson, Neeta L Vora. Obstet Gynecol Clin North Am 2017
37
16

Incidence of chromosomal mosaicism in morphologically normal nonhuman primate preimplantation embryos.
Cathérine Dupont, James Segars, Alan DeCherney, Barry D Bavister, D Randall Armant, Carol A Brenner. Fertil Steril 2010
18
8


Grandmothering, menopause, and the evolution of human life histories.
K Hawkes, J F O'Connell, N G Jones, H Alvarez, E L Charnov. Proc Natl Acad Sci U S A 1998
478
8


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.