A citation-based method for searching scientific literature

Desheng Liang, Ying Peng, Weigang Lv, Linbei Deng, Yanghui Zhang, Haoxian Li, Pu Yang, Jianguang Zhang, Zhuo Song, Genming Xu, David S Cram, Lingqian Wu. J Mol Diagn 2014
Times Cited: 60







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



Times Cited
  Times     Co-cited
Similarity


Traditional karyotyping vs copy number variation sequencing for detection of chromosomal abnormalities associated with spontaneous miscarriage.
S Liu, L Song, D S Cram, L Xiong, K Wang, R Wu, J Liu, K Deng, B Jia, M Zhong,[...]. Ultrasound Obstet Gynecol 2015
36
50


Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
Yanlin Wang, Yan Chen, Feng Tian, Jianguang Zhang, Zhuo Song, Yi Wu, Xu Han, Wenjing Hu, Duan Ma, David Cram,[...]. Clin Chem 2014
137
25

Low-pass whole-genome sequencing in clinical cytogenetics: a validated approach.
Zirui Dong, Jun Zhang, Ping Hu, Haixiao Chen, Jinjin Xu, Qi Tian, Lu Meng, Yanchou Ye, Jun Wang, Meiyan Zhang,[...]. Genet Med 2016
67
25

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
20

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing.
Desheng Liang, Weigang Lv, Hua Wang, Liangpu Xu, Jing Liu, Haoxian Li, Liang Hu, Ying Peng, Lingqian Wu. Prenat Diagn 2013
108
18

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
630
18

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
504
18


Prospective chromosome analysis of 3429 amniocentesis samples in China using copy number variation sequencing.
Jing Wang, Lin Chen, Cong Zhou, Li Wang, Hanbing Xie, Yuanyuan Xiao, Hongmei Zhu, Ting Hu, Zhu Zhang, Qian Zhu,[...]. Am J Obstet Gynecol 2018
25
36

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
13

Technical standards for the interpretation and reporting of constitutional copy-number variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
Erin Rooney Riggs, Erica F Andersen, Athena M Cherry, Sibel Kantarci, Hutton Kearney, Ankita Patel, Gordana Raca, Deborah I Ritter, Sarah T South, Erik C Thorland,[...]. Genet Med 2020
117
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
11

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
376
10

Validation of copy number variation sequencing for detecting chromosome imbalances in human preimplantation embryos.
Li Wang, David S Cram, Jiandong Shen, Xiaohong Wang, Jianguang Zhang, Zhuo Song, Genming Xu, Na Li, Junmei Fan, Shufang Wang,[...]. Biol Reprod 2014
32
18


An integrated map of structural variation in 2,504 human genomes.
Peter H Sudmant, Tobias Rausch, Eugene J Gardner, Robert E Handsaker, Alexej Abyzov, John Huddleston, Yan Zhang, Kai Ye, Goo Jun, Markus Hsi-Yang Fritz,[...]. Nature 2015
903
10

Low-pass genome sequencing versus chromosomal microarray analysis: implementation in prenatal diagnosis.
Huilin Wang, Zirui Dong, Rui Zhang, Matthew Hoi Kin Chau, Zhenjun Yang, Kathy Yin Ching Tsang, Hoi Kin Wong, Baoheng Gui, Zhuo Meng, Kelin Xiao,[...]. Genet Med 2020
19
31

Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population.
Yijun Song, Congcong Liu, Hong Qi, Yunping Zhang, Xuming Bian, Juntao Liu. Prenat Diagn 2013
123
8

Genome-wide detection of single-nucleotide and copy-number variations of a single human cell.
Chenghang Zong, Sijia Lu, Alec R Chapman, X Sunney Xie. Science 2012
568
8


PSCC: sensitive and reliable population-scale copy number variation detection method based on low coverage sequencing.
Xuchao Li, Shengpei Chen, Weiwei Xie, Ida Vogel, Kwong Wai Choy, Fang Chen, Rikke Christensen, Chunlei Zhang, Huijuan Ge, Haojun Jiang,[...]. PLoS One 2014
20
25

Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
Xiangyu Zhu, Jie Li, Tong Ru, Yaping Wang, Yan Xu, Ying Yang, Xing Wu, David S Cram, Yali Hu. Prenat Diagn 2016
37
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
184
6

Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidies.
Irena Hudecova, Daljit Sahota, Macy M S Heung, Yongjie Jin, Wing S Lee, Tak Y Leung, Yuk Ming Dennis Lo, Rossa W K Chiu. PLoS One 2014
63
6

Copy number and SNP arrays in clinical diagnostics.
Christian P Schaaf, Joanna Wiszniewska, Arthur L Beaudet. Annu Rev Genomics Hum Genet 2011
98
6

Genetics of early miscarriage.
Merel M J van den Berg, Merel C van Maarle, Madelon van Wely, Mariëtte Goddijn. Biochim Biophys Acta 2012
110
6

Development and validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of embryos.
Francesco Fiorentino, Anil Biricik, Sara Bono, Letizia Spizzichino, Ettore Cotroneo, Giuliano Cottone, Felix Kokocinski, Claude-Edouard Michel. Fertil Steril 2014
146
6

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
61
6

A robust approach for blind detection of balanced chromosomal rearrangements with whole-genome low-coverage sequencing.
Zirui Dong, Lupin Jiang, Chuanchun Yang, Hua Hu, Xiuhua Wang, Haixiao Chen, Kwong Wai Choy, Huamei Hu, Yanling Dong, Bin Hu,[...]. Hum Mutat 2014
47
8

Computational tools for copy number variation (CNV) detection using next-generation sequencing data: features and perspectives.
Min Zhao, Qingguo Wang, Quan Wang, Peilin Jia, Zhongming Zhao. BMC Bioinformatics 2013
245
6

An integrated map of genetic variation from 1,092 human genomes.
Goncalo R Abecasis, Adam Auton, Lisa D Brooks, Mark A DePristo, Richard M Durbin, Robert E Handsaker, Hyun Min Kang, Gabor T Marth, Gil A McVean. Nature 2012
6


The promise of whole-exome sequencing in medical genetics.
Bahareh Rabbani, Mustafa Tekin, Nejat Mahdieh. J Hum Genet 2014
227
6

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.
Paul Daniel Brady, Barbara Delle Chiaie, Gabrielle Christenhusz, Kris Dierickx, Kris Van Den Bogaert, Bjorn Menten, Sandra Janssens, Paul Defoort, Ellen Roets, Elke Sleurs,[...]. Genet Med 2014
45
8

Structural variation in the human genome.
Lars Feuk, Andrew R Carson, Stephen W Scherer. Nat Rev Genet 2006
6

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
13
30

Copy-Number Variants Detection by Low-Pass Whole-Genome Sequencing.
Zirui Dong, Weiwei Xie, Haixiao Chen, Jinjin Xu, Huilin Wang, Yun Li, Jun Wang, Fang Chen, Kwong Wai Choy, Hui Jiang. Curr Protoc Hum Genet 2017
10
40

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
147
5

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
81
5


Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages.
Anthony J Schaeffer, June Chung, Konstantina Heretis, Andrew Wong, David H Ledbetter, Christa Lese Martin. Am J Hum Genet 2004
145
5

Genomic imbalance in products of conception: single-nucleotide polymorphism chromosomal microarray analysis.
Brynn Levy, Styrmir Sigurjonsson, Barbara Pettersen, Melissa K Maisenbacher, Megan P Hall, Zachary Demko, Ruth B Lathi, Rosina Tao, Vimla Aggarwal, Matthew Rabinowitz. Obstet Gynecol 2014
87
5



Genome analyses of single human oocytes.
Yu Hou, Wei Fan, Liying Yan, Rong Li, Ying Lian, Jin Huang, Jinsen Li, Liya Xu, Fuchou Tang, X Sunney Xie,[...]. Cell 2013
185
5



A PGD pregnancy achieved by embryo copy number variation sequencing with confirmation by non-invasive prenatal diagnosis.
Hui Wang, Li Wang, Minyue Ma, Zhuo Song, Jianguang Zhang, Genming Xu, Junmei Fan, Na Li, David S Cram, Yuanqing Yao. J Genet Genomics 2014
6
50

Massively parallel sequencing for chromosomal abnormality testing in trophectoderm cells of human blastocysts.
XuYang Yin, Ke Tan, Gábor Vajta, Hui Jiang, YueQiu Tan, ChunLei Zhang, Fang Chen, ShengPei Chen, ChunSheng Zhang, XiaoYu Pan,[...]. Biol Reprod 2013
77
5


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.