A citation-based method for searching scientific literature

Jacob A Canick, Glenn E Palomaki, Edward M Kloza, Geralyn M Lambert-Messerlian, James E Haddow. Prenat Diagn 2013
Times Cited: 211







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



Times Cited
  Times     Co-cited
Similarity


Sensitive Detection of Minimal Residual Disease in Patients Treated for Early-Stage Breast Cancer.
Heather A Parsons, Justin Rhoades, Sarah C Reed, Gregory Gydush, Priyanka Ram, Pedro Exman, Kan Xiong, Christopher C Lo, Tianyu Li, Mark Fleharty,[...]. Clin Cancer Res 2020
37
2

Liquid biopsy and minimal residual disease - latest advances and implications for cure.
Klaus Pantel, Catherine Alix-Panabières. Nat Rev Clin Oncol 2019
358
1


An ultrasensitive method for quantitating circulating tumor DNA with broad patient coverage.
Aaron M Newman, Scott V Bratman, Jacqueline To, Jacob F Wynne, Neville C W Eclov, Leslie A Modlin, Chih Long Liu, Joel W Neal, Heather A Wakelee, Robert E Merritt,[...]. Nat Med 2014
1

Circulating Tumor DNA Dynamics Predict Benefit from Consolidation Immunotherapy in Locally Advanced Non-Small Cell Lung Cancer.
Everett J Moding, Yufei Liu, Barzin Y Nabet, Jacob J Chabon, Aadel A Chaudhuri, Angela B Hui, Rene F Bonilla, Ryan B Ko, Christopher H Yoo, Linda Gojenola,[...]. Nat Cancer 2020
51
1

Early Detection of Molecular Residual Disease in Localized Lung Cancer by Circulating Tumor DNA Profiling.
Aadel A Chaudhuri, Jacob J Chabon, Alexander F Lovejoy, Aaron M Newman, Henning Stehr, Tej D Azad, Michael S Khodadoust, Mohammad Shahrokh Esfahani, Chih Long Liu, Li Zhou,[...]. Cancer Discov 2017
373
1

Reversible acetylation on Lys501 regulates the activity of RNase II.
Limin Song, Guangyuan Wang, Arun Malhotra, Murray P Deutscher, Wenxing Liang. Nucleic Acids Res 2016
53
1

Somatic mosaicism and neurodevelopmental disease.
Alissa M D'Gama, Christopher A Walsh. Nat Neurosci 2018
104
1

Universal noninvasive detection of solid organ transplant rejection.
Thomas M Snyder, Kiran K Khush, Hannah A Valantine, Stephen R Quake. Proc Natl Acad Sci U S A 2011
223
1

Sequencing small genomic targets with high efficiency and extreme accuracy.
Michael W Schmitt, Edward J Fox, Marc J Prindle, Kate S Reid-Bayliss, Lawrence D True, Jerald P Radich, Lawrence A Loeb. Nat Methods 2015
87
1

Multiplex Cell-Free DNA Reference Materials for Quality Control of Next-Generation Sequencing-Based In Vitro Diagnostic Tests of Colorectal Cancer Tolerance.
Donglai Liu, Xinyuan Zhang, Haiwei Zhou, Xiaojing Lin, Dawei Shi, Shu Shen, Yabin Tian, Bo Du, Henghui Zhang, Haibo Wang,[...]. J Cancer 2018
2
50

Current understanding of the human microbiome.
Jack A Gilbert, Martin J Blaser, J Gregory Caporaso, Janet K Jansson, Susan V Lynch, Rob Knight. Nat Med 2018
657
1

Identification of somatic mutations in single cell DNA-seq using a spatial model of allelic imbalance.
Lovelace J Luquette, Craig L Bohrson, Max A Sherman, Peter J Park. Nat Commun 2019
31
3

Allele-specific PCR in SNP genotyping.
Muriel Gaudet, Anna-Giulia Fara, Isacco Beritognolo, Maurizio Sabatti. Methods Mol Biol 2009
70
1

Trastuzumab Emtansine for Residual Invasive HER2-Positive Breast Cancer.
Gunter von Minckwitz, Chiun-Sheng Huang, Max S Mano, Sibylle Loibl, Eleftherios P Mamounas, Michael Untch, Norman Wolmark, Priya Rastogi, Andreas Schneeweiss, Andres Redondo,[...]. N Engl J Med 2019
767
1



Lineage Tracing in Humans Enabled by Mitochondrial Mutations and Single-Cell Genomics.
Leif S Ludwig, Caleb A Lareau, Jacob C Ulirsch, Elena Christian, Christoph Muus, Lauren H Li, Karin Pelka, Will Ge, Yaara Oren, Alison Brack,[...]. Cell 2019
152
1

Comparison of commercially available whole-genome sequencing kits for variant detection in circulating cell-free DNA.
Florence Mauger, Caroline Horgues, Morgane Pierre-Jean, Nouara Oussada, Lilia Mesrob, Jean-François Deleuze. Sci Rep 2020
4
25

Replacing PCR with COLD-PCR enriches variant DNA sequences and redefines the sensitivity of genetic testing.
Jin Li, Lilin Wang, Harvey Mamon, Matthew H Kulke, Ross Berbeco, G Mike Makrigiorgos. Nat Med 2008
277
1


Early recipient chimerism testing in the T- and NK-cell lineages for risk assessment of graft rejection in pediatric patients undergoing allogeneic stem cell transplantation.
S Breuer, S Preuner, G Fritsch, H Daxberger, M Koenig, U Poetschger, A Lawitschka, C Peters, G Mann, T Lion,[...]. Leukemia 2012
42
2

Long-Term Follow-Up of the French Stop Imatinib (STIM1) Study in Patients With Chronic Myeloid Leukemia.
Gabriel Etienne, Joëlle Guilhot, Delphine Rea, Françoise Rigal-Huguet, Franck Nicolini, Aude Charbonnier, Agnès Guerci-Bresler, Laurence Legros, Bruno Varet, Martine Gardembas,[...]. J Clin Oncol 2017
244
1

Assessment of Molecular Relapse Detection in Early-Stage Breast Cancer.
Isaac Garcia-Murillas, Neha Chopra, Iñaki Comino-Méndez, Matthew Beaney, Holly Tovey, Rosalind J Cutts, Claire Swift, Divya Kriplani, Maria Afentakis, Sarah Hrebien,[...]. JAMA Oncol 2019
101
1

Elimination of unaltered DNA in mixed clinical samples via nuclease-assisted minor-allele enrichment.
Chen Song, Yibin Liu, Rachel Fontana, Alexander Makrigiorgos, Harvey Mamon, Matthew H Kulke, G Mike Makrigiorgos. Nucleic Acids Res 2016
43
2

Personalized circulating tumor DNA analysis to detect residual disease after neoadjuvant therapy in breast cancer.
Bradon R McDonald, Tania Contente-Cuomo, Stephen-John Sammut, Ahuva Odenheimer-Bergman, Brenda Ernst, Nieves Perdigones, Suet-Feung Chin, Maria Farooq, Rosa Mejia, Patricia A Cronin,[...]. Sci Transl Med 2019
97
1

Genome-wide cell-free DNA mutational integration enables ultra-sensitive cancer monitoring.
Asaf Zviran, Rafael C Schulman, Minita Shah, Steven T K Hill, Sunil Deochand, Cole C Khamnei, Dillon Maloney, Kristofer Patel, Will Liao, Adam J Widman,[...]. Nat Med 2020
61
1

Adjuvant Capecitabine for Breast Cancer after Preoperative Chemotherapy.
Norikazu Masuda, Soo-Jung Lee, Shoichiro Ohtani, Young-Hyuck Im, Eun-Sook Lee, Isao Yokota, Katsumasa Kuroi, Seock-Ah Im, Byeong-Woo Park, Sung-Bae Kim,[...]. N Engl J Med 2017
607
1


Snakemake--a scalable bioinformatics workflow engine.
Johannes Köster, Sven Rahmann. Bioinformatics 2012
827
1

Measurement and clinical monitoring of human lymphocyte clonality by massively parallel VDJ pyrosequencing.
Scott D Boyd, Eleanor L Marshall, Jason D Merker, Jay M Maniar, Lyndon N Zhang, Bita Sahaf, Carol D Jones, Birgitte B Simen, Bozena Hanczaruk, Khoa D Nguyen,[...]. Sci Transl Med 2009
309
1

Personalized Chimerism Test that Uses Selection of Short Tandem Repeat or Quantitative PCR Depending on Patient's Chimerism Status.
Jennifer Tyler, Lorie Kumer, Carolyn Fisher, Heather Casey, Hiroko Shike. J Mol Diagn 2019
7
14

Multiplexed enrichment of rare DNA variants via sequence-selective and temperature-robust amplification.
Lucia R Wu, Sherry X Chen, Yalei Wu, Abhijit A Patel, David Yu Zhang. Nat Biomed Eng 2017
43
2

ctDNA monitoring using patient-specific sequencing and integration of variant reads.
Jonathan C M Wan, Katrin Heider, Davina Gale, Suzanne Murphy, Eyal Fisher, Florent Mouliere, Andrea Ruiz-Valdepenas, Angela Santonja, James Morris, Dineika Chandrananda,[...]. Sci Transl Med 2020
55
1

Somatic mutations predict poor outcome in patients with myelodysplastic syndrome after hematopoietic stem-cell transplantation.
Rafael Bejar, Kristen E Stevenson, Bennett Caughey, R Coleman Lindsley, Brenton G Mar, Petar Stojanov, Gad Getz, David P Steensma, Jerome Ritz, Robert Soiffer,[...]. J Clin Oncol 2014
273
1

Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum.
Hiroshi Honda, Norio Miharu, Yoko Ohashi, Osamu Samura, Masayuki Kinutani, Tetsuaki Hara, Koso Ohama. Hum Genet 2002
125
1


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
34
2

Noninvasive prenatal testing using cell-free fetal DNA in maternal plasma.
Nilesh Dharajiya, Tricia Zwiefelhofer, Xiaojun Guan, Vach Angkachatchai, Juan-Sebastian Saldivar. Curr Protoc Hum Genet 2015
2
50

The correlation between clinical characteristics of preeclampsia and the concentration of fetal DNA in maternal circulation.
Karina Engel, Tomasz Płonka, Marek Bilar, Agnieszka Orzinska, Ewa Brojer, Elzbieta Ronin-Walknowska. Eur J Obstet Gynecol Reprod Biol 2008
4
25

A novel approach toward the challenge of accurately quantifying fetal DNA in maternal plasma.
Tianjiao Chu, Kimberly Bunce, W Allen Hogge, David G Peters. Prenat Diagn 2010
11
9

Concordance of various chromosomal errors among different parts of the embryo and the value of re-biopsy in embryos with segmental aneuploidies.
Rostislav Navratil, Jakub Horak, Miroslav Hornak, David Kubicek, Maria Balcova, Gabriela Tauwinklova, Pavel Travnik, Katerina Vesela. Mol Hum Reprod 2020
18
5

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
127
1

Chromosomal mosaicism in human blastocysts: the ultimate challenge of preimplantation genetic testing?
M Popovic, A Dheedene, C Christodoulou, J Taelman, L Dhaenens, F Van Nieuwerburgh, D Deforce, E Van den Abbeel, P De Sutter, B Menten,[...]. Hum Reprod 2018
62
1


Characterization of Prevalence and Health Consequences of Uniparental Disomy in Four Million Individuals from the General Population.
Priyanka Nakka, Samuel Pattillo Smith, Anne H O'Donnell-Luria, Kimberly F McManus, Joanna L Mountain, Sohini Ramachandran, J Fah Sathirapongsasuti. Am J Hum Genet 2019
33
3

Characterization of chromosomal abnormalities in pregnancy losses reveals critical genes and loci for human early development.
Yiyun Chen, Justin Bartanus, Desheng Liang, Hongmin Zhu, Amy M Breman, Janice L Smith, Hua Wang, Zhilin Ren, Ankita Patel, Pawel Stankiewicz,[...]. Hum Mutat 2017
15
6

Using outcome data from one thousand mosaic embryo transfers to formulate an embryo ranking system for clinical use.
Manuel Viotti, Andrea R Victor, Frank L Barnes, Christo G Zouves, Andria G Besser, James A Grifo, En-Hui Cheng, Maw-Sheng Lee, Jose A Horcajadas, Laura Corti,[...]. Fertil Steril 2021
27
3

Optimized NGS Approach for Detection of Aneuploidies and Mosaicism in PGT-A and Imbalances in PGT-SR.
Carmen M García-Pascual, Luis Navarro-Sánchez, Roser Navarro, Lucía Martínez, Jorge Jiménez, Lorena Rodrigo, Carlos Simón, Carmen Rubio. Genes (Basel) 2020
15
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.