A citation-based method for searching scientific literature

Qiong Deng, Lihua Huang, Juan Liu, Fu Fang, Zequn Liu, Yongling Zhang, Fatao Li, Can Liao. J Matern Fetal Neonatal Med 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


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
100

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
100

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
62
100

Prenatal diagnosis of sex chromosomal inversion, translocation and deletion.
Lin Zhang, Meihong Ren, Guining Song, Yang Zhang, Xuexia Liu, Xiaohong Zhang, Jianliu Wang. Mol Med Rep 2018
4
100

A French Approach to Test Fetuses with Ultrasound Abnormalities Using a Customized Microarray as First-Tier Genetic Test.
Valérie Malan, Jean-Michel Lapierre, Matthieu Egloff, Didier Goidin, Marie-Paule Beaujard, Marie-Laure Maurin, Tania Attié-Bitach, Bettina Bessières, Jean-Pierre Bernard, Philippe Roth,[...]. Cytogenet Genome Res 2015
14
100

Combination of QF-PCR and aCGH is an efficient diagnostic strategy for the detection of chromosome aberrations in recurrent miscarriage.
Luca Lovrečić, Nina Pereza, Helena Jaklič, Saša Ostojić, Borut Peterlin. Mol Genet Genomic Med 2019
2
100


Prenatal and pre-implantation genetic diagnosis.
Joris Robert Vermeesch, Thierry Voet, Koenraad Devriendt. Nat Rev Genet 2016
66
100

Traditional banding of chromosomes for cytogenetic analysis.
Jane Bayani, Jeremy A Squire. Curr Protoc Cell Biol 2004
12
100

Chromosomal microarray testing.
W Andrew Faucett, Melissa Savage. JAAPA 2012
1
100

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
100

Comparison of cytogenetics and molecular karyotyping for chromosome testing of miscarriage specimens.
Meera Sridhar Shah, Cengiz Cinnioglu, Melissa Maisenbacher, Ioanna Comstock, Jonathan Kort, Ruth Bunker Lathi. Fertil Steril 2017
24
100

The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis.
Melissa Stosic, Brynn Levy, Ronald Wapner. Obstet Gynecol Clin North Am 2018
18
100

Array-Based Comparative Genomic Hybridization (aCGH).
Chengsheng Zhang, Eliza Cerveira, Mallory Romanovitch, Qihui Zhu. Methods Mol Biol 2017
3
100

Chromosome microarrays in human reproduction.
Evica Rajcan-Separovic. Hum Reprod Update 2012
15
100

Microarray-based comparative genomic hybridisation reveals additional recurrent aberrations in adult patients evaluated for myelodysplastic syndrome with normal karyotype.
Ines Ouahchi, Luduo Zhang, Ramon Benitez Brito, Rudolf Benz, Rouven Müller, Nicolas Bonadies, Joëlle Tchinda. Br J Haematol 2019
2
100

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
100

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
100

Microarrays in prenatal diagnosis.
Beatrice Oneda, Anita Rauch. Best Pract Res Clin Obstet Gynaecol 2017
20
100

Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.
Ioannis Papoulidis, Alexandros Sotiriadis, Elisavet Siomou, Elena Papageorgiou, Makarios Eleftheriades, Vasilios Papadopoulos, Eirini Oikonomidou, Sandro Orru, Emmanouil Manolakos, Apostolos Athanasiadis. Prenat Diagn 2015
23
100

Genomic answers for recurrent spontaneous abortion in Saudi Arabia: An array comparative genomic hybridization approach.
Sajjad Karim, Hasan Salleh Jamal, Abdullraheem Rouzi, Mohammed Salleh M Ardawi, Hans-Juergen Schulten, Zeenat Mirza, Nuha A Alansari, Maha M Al-Quaiti, Heba Abusamra, Muhammad Imran Naseer,[...]. Reprod Biol 2017
6
100

Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome Sequence.
Christa Lese Martin, Dorothy Warburton. Annu Rev Genomics Hum Genet 2015
23
100

Traditional Prenatal Diagnosis: Past to Present.
Brynn Levy, Melissa Stosic. Methods Mol Biol 2019
7
100

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
100

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.
Lena Sagi-Dain, Idit Maya, Adi Reches, Ayala Frumkin, Julia Grinshpun-Cohen, Reeval Segel, Esther Manor, Morad Khayat, Tamar Tenne, Ehud Banne,[...]. Obstet Gynecol 2018
14
100

Noninvasive prenatal diagnosis.
Wei-Lun Cheng, Ching-Hua Hsiao, Hua-Wei Tseng, Tai-Ping Lee. Taiwan J Obstet Gynecol 2015
9
100

The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland.
Yi Wu, Yanlin Wang, Jiong Tao, Xu Han, Xinrong Zhao, Chunmin Liu, Li Gao, Weiwei Cheng. Eur J Obstet Gynecol Reprod Biol 2017
6
100


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.