A citation-based method for searching scientific literature

Y Wang, Y Li, Y Chen, R Zhou, Z Sang, L Meng, J Tan, F Qiao, Q Bao, D Luo, C Peng, Y S Wang, C Luo, P Hu, Z Xu. Ultrasound Obstet Gynecol 2020
Times Cited: 10







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



Times Cited
  Times     Co-cited
Similarity



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
14
30

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
136
30

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
92
30

Added value of chromosomal microarray analysis over karyotyping in early pregnancy loss: systematic review and meta-analysis.
M Pauta, M Grande, L Rodriguez-Revenga, E Kolomietz, A Borrell. Ultrasound Obstet Gynecol 2018
17
30

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
69
20

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
20

Sensitive quantification of mosaicism using high density SNP arrays and the cumulative distribution function.
Thomas C Markello, Hannah Carlson-Donohoe, Murat Sincan, David Adams, David M Bodine, Jason E Farrar, Adrianna Vlachos, Jeffrey M Lipton, Arleen D Auerbach, Elaine A Ostrander,[...]. Mol Genet Metab 2012
13
20


Prenatal Diagnosis of Fetuses With Increased Nuchal Translucency by Genome Sequencing Analysis.
Kwong Wai Choy, Huilin Wang, Mengmeng Shi, Jingsi Chen, Zhenjun Yang, Rui Zhang, Huanchen Yan, Yanfang Wang, Shaoyun Chen, Matthew Hoi Kin Chau,[...]. Front Genet 2019
17
20

Improved assay performance of single nucleotide polymorphism array over conventional karyotyping in analyzing products of conception.
Shao-Bin Lin, Ying-Jun Xie, Zheng Chen, Yi Zhou, Jian-Zhu Wu, Zhi-Qiang Zhang, Shan-Shan Shi, Bao-Jiang Chen, Qun Fang. J Chin Med Assoc 2015
17
20

Cost-effectiveness of cytogenetic evaluation of products of conception in the patient with a second pregnancy loss.
Nastaran Foyouzi, Marcelle I Cedars, Heather G Huddleston. Fertil Steril 2012
33
20

Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage.
Zirui Dong, Junhao Yan, Fengping Xu, Jianying Yuan, Hui Jiang, Huilin Wang, Haixiao Chen, Lei Zhang, Lingfei Ye, Jinjin Xu,[...]. Am J Hum Genet 2019
15
20

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.
Matthew Hoi Kin Chau, Ye Cao, Yvonne Ka Yin Kwok, Samantha Chan, Yiu Man Chan, Huilin Wang, Zhenjun Yang, Hoi Kin Wong, Tak Yeung Leung, Kwong Wai Choy. Am J Obstet Gynecol 2019
12
20

Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
20

Outcomes in pregnancies with a confined placental mosaicism and implications for prenatal screening using cell-free DNA.
Francesca Romana Grati, Jose Ferreira, Peter Benn, Claudia Izzi, Federica Verdi, Elena Vercellotti, Cristina Dalpiaz, Patrizia D'Ajello, Elisa Filippi, Nicola Volpe,[...]. Genet Med 2020
26
20

Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.
T Hassold, M Merrill, K Adkins, S Freeman, S Sherman. Am J Hum Genet 1995
156
20

The nature of aneuploidy with increasing age of the female partner: a review of 15,169 consecutive trophectoderm biopsies evaluated with comprehensive chromosomal screening.
Jason M Franasiak, Eric J Forman, Kathleen H Hong, Marie D Werner, Kathleen M Upham, Nathan R Treff, Richard T Scott. Fertil Steril 2014
362
20


Evidence of Selection against Complex Mitotic-Origin Aneuploidy during Preimplantation Development.
Rajiv C McCoy, Zachary P Demko, Allison Ryan, Milena Banjevic, Matthew Hill, Styrmir Sigurjonsson, Matthew Rabinowitz, Dmitri A Petrov. PLoS Genet 2015
78
20

Array-based comparative genomic hybridization is more informative than conventional karyotyping and fluorescence in situ hybridization in the analysis of first-trimester spontaneous abortion.
Jinsong Gao, Congcong Liu, Fengxia Yao, Na Hao, Jing Zhou, Qian Zhou, Liang Zhang, Xinyan Liu, Xuming Bian, Juntao Liu. Mol Cytogenet 2012
31
20

Diagnostic utility of novel combined arrays for genome-wide simultaneous detection of aneuploidy and uniparental isodisomy in losses of pregnancy.
Stefanie Bug, Beate Solfrank, Felizitas Schmitz, Jana Pricelius, Mona Stecher, Andrew Craig, Marc Botcherby, Claudia Nevinny-Stickel-Hinzpeter. Mol Cytogenet 2014
18
20

Chromosomal copy number analysis on chorionic villus samples from early spontaneous miscarriages by high throughput genetic technology.
Jiandong Shen, Wei Wu, Chao Gao, Humphrey Ochin, Dianyun Qu, Jiazi Xie, Li Gao, Yadong Zhou, Yugui Cui, Jiayin Liu. Mol Cytogenet 2016
23
20

Recurrent miscarriage.
Raj Rai, Lesley Regan. Lancet 2006
718
20

Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.
Trilochan Sahoo, Natasa Dzidic, Michelle N Strecker, Sara Commander, Mary K Travis, Charles Doherty, R Weslie Tyson, Arturo E Mendoza, Mary Stephenson, Craig A Dise,[...]. Genet Med 2017
60
20

Potential genetic causes of miscarriage in euploid pregnancies: a systematic review.
Emily Colley, Susan Hamilton, Paul Smith, Neil V Morgan, Arri Coomarasamy, Stephanie Allen. Hum Reprod Update 2019
20
20

Diagnostic utility of microarray testing in pregnancy loss.
J A Rosenfeld, M E Tucker, L F Escobar, N J Neill, B S Torchia, L D McDaniel, R A Schultz, K Chong, D Chitayat. Ultrasound Obstet Gynecol 2015
27
20


Genetic aspects of miscarriage.
M Goddijn, N J Leschot. Baillieres Best Pract Res Clin Obstet Gynaecol 2000
133
20

Clinical application of SNP array analysis in first-trimester pregnancy loss: a prospective study.
Y Wang, Q Cheng, L Meng, C Luo, H Hu, J Zhang, J Cheng, T Xu, T Jiang, D Liang,[...]. Clin Genet 2017
36
20

The effect of maternal age on chromosomal anomaly rate and spectrum in recurrent miscarriage.
Maribel Grande, Antoni Borrell, Raul Garcia-Posada, Virginia Borobio, Miriam Muñoz, Montserrat Creus, Anna Soler, Aurora Sanchez, Juan Balasch. Hum Reprod 2012
50
20

Maternal age and fetal loss: population based register linkage study.
A M Nybo Andersen, J Wohlfahrt, P Christens, J Olsen, M Melbye. BMJ 2000
788
20


New insights into mechanisms behind miscarriage.
Elisabeth Clare Larsen, Ole Bjarne Christiansen, Astrid Marie Kolte, Nick Macklon. BMC Med 2013
199
20

Circular binary segmentation for the analysis of array-based DNA copy number data.
Adam B Olshen, E S Venkatraman, Robert Lucito, Michael Wigler. Biostatistics 2004
20

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.
Amy Breman, Amber N Pursley, Patricia Hixson, Weimin Bi, Patricia Ward, Carlos A Bacino, Chad Shaw, James R Lupski, Arthur Beaudet, Ankita Patel,[...]. Prenat Diagn 2012
74
20

ESHRE guideline: recurrent pregnancy loss.
Ruth Bender Atik, Ole Bjarne Christiansen, Janine Elson, Astrid Marie Kolte, Sheena Lewis, Saskia Middeldorp, Willianne Nelen, Braulio Peramo, Siobhan Quenby, Nathalie Vermeulen,[...]. Hum Reprod Open 2018
141
20

Karyotype versus microarray testing for genetic abnormalities after stillbirth.
Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall,[...]. N Engl J Med 2012
140
20

Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.
Elizabeth A Normand, Alicia Braxton, Salma Nassef, Patricia A Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren E Westerfield, Samantha Stover,[...]. Genome Med 2018
45
20

Causal Genetic Variants in Stillbirth.
Kate E Stanley, Jessica Giordano, Vanessa Thorsten, Christie Buchovecky, Amanda Thomas, Mythily Ganapathi, Jun Liao, Avinash V Dharmadhikari, Anya Revah-Politi, Michelle Ernst,[...]. N Engl J Med 2020
11
20


Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
130
20

De novo PMP2 mutations in families with type 1 Charcot-Marie-Tooth disease.
William W Motley, Paulius Palaima, Sabrina W Yum, Michael A Gonzalez, Feifei Tao, Julia V Wanschitz, Alleene V Strickland, Wolfgang N Löscher, Els De Vriendt, Stefan Koppi,[...]. Brain 2016
24
10

Mutational, functional, and expression studies of the TCF4 gene in Pitt-Hopkins syndrome.
Loïc de Pontual, Yves Mathieu, Christelle Golzio, Marlène Rio, Valérie Malan, Nathalie Boddaert, Christine Soufflet, Capucine Picard, Anne Durandy, Angus Dobbie,[...]. Hum Mutat 2009
102
10

Mechanisms for Complex Chromosomal Insertions.
Shen Gu, Przemyslaw Szafranski, Zeynep Coban Akdemir, Bo Yuan, Mitchell L Cooper, Maria A Magriñá, Carlos A Bacino, Seema R Lalani, Amy M Breman, Janice L Smith,[...]. PLoS Genet 2016
26
10

Comprehensively benchmarking applications for detecting copy number variation.
Le Zhang, Wanyu Bai, Na Yuan, Zhenglin Du. PLoS Comput Biol 2019
16
10

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.
Desheng Liang, Ying Peng, Weigang Lv, Linbei Deng, Yanghui Zhang, Haoxian Li, Pu Yang, Jianguang Zhang, Zhuo Song, Genming Xu,[...]. J Mol Diagn 2014
62
10

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
10

Development of coupling controlled polymerizations by adapter-ligation in mate-pair sequencing for detection of various genomic variants in one single assay.
Zirui Dong, Xia Zhao, Qiaoling Li, Zhenjun Yang, Yang Xi, Andrei Alexeev, Hanjie Shen, Ou Wang, Jie Ruan, Han Ren,[...]. DNA Res 2019
5
20

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
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.