A citation-based method for searching scientific literature

Hongyan Chai, Autumn DiAdamo, Brittany Grommisch, Fang Xu, Qinghua Zhou, Jiadi Wen, Maurice Mahoney, Allen Bale, James McGrath, Michele Spencer-Manzon, Peining Li, Hui Zhang. Front Genet 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Non-invasive prenatal testing to detect chromosome aneuploidies in 57,204 pregnancies.
Ying Xue, Guodong Zhao, Hong Li, Qin Zhang, Jiafeng Lu, Bin Yu, Ting Wang. Mol Cytogenet 2019
13
50

Incidence of X and Y Chromosomal Aneuploidy in a Large Child Bearing Population.
Carole Samango-Sprouse, Eser Kırkızlar, Megan P Hall, Patrick Lawson, Zachary Demko, Susan M Zneimer, Kirsten J Curnow, Susan Gross, Andrea Gropman. PLoS One 2016
13
25

Non-Invasive Prenatal Testing for Sex Chromosome Aneuploidy in Routine Clinical Practice.
Louise Kornman, Ricardo Palma-Dias, Debbie Nisbet, Fergus Scott, Melody Menezes, Fabricio da Silva Costa, Andrew McLennan. Fetal Diagn Ther 2018
23
25

Non-invasive prenatal testing for detection of trisomy 13, 18, 21 and sex chromosome aneuploidies in 8594 cases.
Yunyun Zheng, Shanning Wan, Yinghui Dang, Tingting Song, Biliang Chen, Jianfang Zhang. Ginekol Pol 2019
3
33

Current genetic counseling practice in the United States following positive non-invasive prenatal testing for sex chromosome abnormalities.
Lauren Fleddermann, Syed Shahrukh Hashmi, Blair Stevens, Lauren Murphy, David Rodriguez-Buritica, Lara A Friel, Claire Singletary. J Genet Couns 2019
3
33

The Effect of Freezing on Non-invasive Prenatal Testing.
Xiaolei Xie, Fuguang Li, Weihe Tan, Weiguo Yin, Feiyan Chen, Xiaoyan Guo. Sci Rep 2019
3
33

Clinical experience with sex chromosome aneuploidies detected by noninvasive prenatal testing (NIPT): Accuracy and patient decision-making.
Aarti Ramdaney, Jennifer Hoskovec, Jacqueline Harkenrider, Eleazar Soto, Lauren Murphy. Prenat Diagn 2018
21
25

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
25

Non-invasive prenatal testing in detecting sex chromosome aneuploidy: A large-scale study in Xuzhou area of China.
Feng Suo, Chuangxia Wang, Tianya Liu, Yuan Fang, Qin Wu, Maosheng Gu, Lingshan Gou. Clin Chim Acta 2018
13
25

Expanding the phenotype of Triple X syndrome: A comparison of prenatal versus postnatal diagnosis.
Kristen Wigby, Cheryl D'Epagnier, Susan Howell, Amy Reicks, Rebecca Wilson, Lisa Cordeiro, Nicole Tartaglia. Am J Med Genet A 2016
29
25

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
25

Mosaic Turner syndrome associated with schizophrenia.
Sook Young Jung, Joo Won Park, Dong Hyun Kim, Yong Hoon Jun, Jeong Seop Lee, Ji Eun Lee. Ann Pediatr Endocrinol Metab 2014
5
25

Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood.
Bin Zhang, Bei-Yi Lu, Bin Yu, Fang-Xiu Zheng, Qin Zhou, Ying-Ping Chen, Xiao-Qing Zhang. J Int Med Res 2017
40
25

Laboratory guideline for Turner syndrome.
Daynna J Wolff, Daniel L Van Dyke, Cynthia M Powell. Genet Med 2010
71
25

Gonadal pathology and tumor risk in relation to clinical characteristics in patients with 45,X/46,XY mosaicism.
M Cools, J Pleskacova, H Stoop, P Hoebeke, E Van Laecke, S L S Drop, J Lebl, J W Oosterhuis, L H J Looijenga, K P Wolffenbuttel. J Clin Endocrinol Metab 2011
85
25

High false-positive non-invasive prenatal screening results for sex chromosome abnormalities: Are maternal factors the culprit?
Bin Zhang, Qin Zhou, Yingping Chen, Ye Shi, Fangxiu Zheng, Jianbing Liu, Bin Yu. Prenat Diagn 2020
5
25

Clinical utility of noninvasive prenatal screening for expanded chromosome disease syndromes.
Desheng Liang, David S Cram, Hu Tan, Siyuan Linpeng, Yingdi Liu, Huaiyu Sun, Yu Zhang, Feng Tian, Hongmin Zhu, Mengnan Xu,[...]. Genet Med 2019
52
25

45,X mosaicism in a population-based biobank: implications for Turner syndrome.
Siddharth K Prakash, Melissa L Crenshaw, Philippe F Backeljauw, Michael Silberbach, Cindy Scurlock, Denise D Culin, Kelly C Ranallo, Angela E Lin. Genet Med 2019
4
25

Noninvasive prenatal testing in routine clinical practice--an audit of NIPT and combined first-trimester screening in an unselected Australian population.
Andrew McLennan, Ricardo Palma-Dias, Fabricio da Silva Costa, Simon Meagher, Debbie L Nisbet, Fergus Scott. Aust N Z J Obstet Gynaecol 2016
23
25

Maternal mosaicism of sex chromosome causes discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing.
Leilei Wang, Qian Meng, Xinxin Tang, Ting Yin, Jinglu Zhang, Shuting Yang, Xuyun Wang, Haiqian Wu, Qingxi Shi, Edmund C Jenkins,[...]. Taiwan J Obstet Gynecol 2015
15
25

Turner Syndrome Genotype and phenotype and their effect on presenting features and timing of Diagnosis.
I Al Alwan, Khadora M, Amir, Nasrat G, Omair A, Brown L, Al Dubayee M, Badri M. Int J Health Sci (Qassim) 2014
23
25

Discordant non-invasive prenatal testing (NIPT) - a systematic review.
Tanja Schlaikjaer Hartwig, Louise Ambye, Steen Sørensen, Finn Stener Jørgensen. Prenat Diagn 2017
85
25

Mosaic Turner syndrome shows reduced penetrance in an adult population study.
Marcus A Tuke, Katherine S Ruth, Andrew R Wood, Robin N Beaumont, Jessica Tyrrell, Samuel E Jones, Hanieh Yaghootkar, Claire L S Turner, Mollie E Donohoe, Antonia M Brooke,[...]. Genet Med 2019
32
25

Clinical Application of Cell-Free DNA Sequencing-Based Noninvasive Prenatal Testing for Trisomies 21, 18, 13 and Sex Chromosome Aneuploidy in a Mixed-Risk Population in Iran.
Masoud Garshasbi, Yicong Wang, Sedigheh Hantoosh Zadeh, Sima Giti, Solmaz Piri, Mohammad Reza Hekmat. Fetal Diagn Ther 2020
6
25

Discordant sex between fetal screening and postnatal phenotype requires evaluation.
Heather M Byers, Whitney Neufeld-Kaiser, Edith Y Chang, Karen Tsuchiya, Erin S Oehler, Margaret P Adam. J Perinatol 2019
10
25

The Clinical Manifestation and Genetic Evaluation in Patients with 45,X/46,XY Mosaicism.
Qinghua Wu, Cong Wang, Huirong Shi, Xiangdong Kong, Shumin Ren, Miao Jiang. Sex Dev 2017
16
25

FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation.
George Koumbaris, Hariklia Hatzisevastou-Loukidou, Angelos Alexandrou, Marios Ioannides, Christodoulos Christodoulou, Tomas Fitzgerald, Diana Rajan, Stephen Clayton, Sophia Kitsiou-Tzeli, Joris R Vermeesch,[...]. Hum Mol Genet 2011
24
25

Cell-free DNA analysis for noninvasive examination of trisomy.
Mary E Norton, Bo Jacobsson, Geeta K Swamy, Louise C Laurent, Angela C Ranzini, Herb Brar, Mark W Tomlinson, Leonardo Pereira, Jean L Spitz, Desiree Hollemon,[...]. N Engl J Med 2015
372
25

Sex chromosome aneuploidy detection by noninvasive prenatal testing: helpful or hazardous?
Rosemary E Reiss, Marie Discenza, Judith Foster, Lori Dobson, Louise Wilkins-Haug. Prenat Diagn 2017
32
25

Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization.
Peining Li, Pawel Pomianowski, Miriam S DiMaio, Joanne R Florio, Michael R Rossi, Bixia Xiang, Fang Xu, Hui Yang, Qian Geng, Jiansheng Xie,[...]. Am J Med Genet A 2011
22
25

Diagnostic cytogenetic testing following positive noninvasive prenatal screening results of sex chromosome abnormalities: Report of five cases and systematic review of evidence.
Xiaolei Xie, Weihe Tan, Fuguang Li, Eric Carrano, Paola Ramirez, Autumn DiAdamo, Brittany Grommisch, Katherine Amato, Hongyan Chai, Jiadi Wen,[...]. Mol Genet Genomic Med 2020
4
25

Clinical features and pregnancy outcomes of women with abnormal cell-free fetal DNA test results.
Qin Zhou, Zhi-Ping Zhu, Bin Zhang, Bin Yu, Zheng-Mao Cai, Pei Yuan. Ann Transl Med 2019
6
25

Non-invasive cell-free fetal DNA testing for aneuploidy: multicenter study of 31 515 singleton pregnancies in southeastern China.
L Xu, H Huang, N Lin, Y Wang, D He, M Zhang, M Chen, L Chen, Y Lin. Ultrasound Obstet Gynecol 2020
12
25

Screening, prenatal diagnosis, and prenatal decision for sex chromosome aneuploidy.
Yong Xu, Liyuan Chen, Yang Liu, Ying Hao, Zhiyong Xu, Liyanyan Deng, Jiansheng Xie. Expert Rev Mol Diagn 2019
7
25

Noninvasive prenatal screening for aneuploidy: positive predictive values based on cytogenetic findings.
Jeanne M Meck, Elizabeth Kramer Dugan, Ludmila Matyakhina, Ayala Aviram, Carolyn Trunca, Daniel Pineda-Alvarez, Swaroop Aradhya, Rachel T Klein, Athena M Cherry. Am J Obstet Gynecol 2015
27
25

Non-invasive prenatal testing for sex chromosome abnormalities: a source of confusion.
Erkan Kalafat, Mehmet Murat Seval, Batuhan Turgay, Acar Koç. BMJ Case Rep 2015
5
25



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
643
25

ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?
Sara B Hay, Trilochan Sahoo, Mary K Travis, Karine Hovanes, Natasa Dzidic, Charles Doherty, Michelle N Strecker. Prenat Diagn 2018
31
25

Association of copy number variants with specific ultrasonographically detected fetal anomalies.
Jennifer C Donnelly, Lawrence D Platt, Andrei Rebarber, Julia Zachary, William A Grobman, Ronald J Wapner. Obstet Gynecol 2014
81
25


The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
62
25

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
25

Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis.
S C Hillman, S Pretlove, A Coomarasamy, D J McMullan, E V Davison, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2011
154
25



Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound.
Lisa G Shaffer, Jill A Rosenfeld, Mindy P Dabell, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Allan J Fisher. Prenat Diagn 2012
138
25

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
513
25



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.