A citation-based method for searching scientific literature

Annie Sy Hui, Matthew Hoi Kin Chau, Yiu Man Chan, Ye Cao, Angel Hw Kwan, Xiaofan Zhu, Yvonne K Kwok, Zihan Chen, Terence T Lao, Kwong Wai Choy, Tak Yeung Leung. Acta Obstet Gynecol Scand 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

Clinical utility of array comparative genomic hybridisation in prenatal setting.
Luca Lovrecic, Ziga Iztok Remec, Marija Volk, Gorazd Rudolf, Karin Writzl, Borut Peterlin. BMC Med Genet 2016
9
100

European guidelines for constitutional cytogenomic analysis.
Marisa Silva, Nicole de Leeuw, Kathy Mann, Heleen Schuring-Blom, Sian Morgan, Daniela Giardino, Katrina Rack, Ros Hastings. Eur J Hum Genet 2019
31
100

Etiology and perinatal outcome of periviable fetal growth restriction associated with structural or genetic anomaly.
A Dall'Asta, S Girardelli, S Usman, A Lawin-O'Brien, G Paramasivam, T Frusca, C C Lees. Ultrasound Obstet Gynecol 2020
2
100

[Customized and non-customized French intrauterine growth curves. I - Methodology].
A Ego, C Prunet, E Lebreton, B Blondel, M Kaminski, F Goffinet, J Zeitlin. J Gynecol Obstet Biol Reprod (Paris) 2016
52
100

High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power.
Beatrice Oneda, Rosa Baldinger, Regina Reissmann, Irina Reshetnikova, Pavel Krejci, Rahim Masood, Nicole Ochsenbein-Kölble, Deborah Bartholdi, Katharina Steindl, Denise Morotti,[...]. Prenat Diagn 2014
29
100



Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.
Hui Zhu, Shaobin Lin, Linhuan Huang, Zhiming He, Xuan Huang, Yi Zhou, Qun Fang, Yanmin Luo. Prenat Diagn 2016
16
100

Interest of chromosomal microarray analysis in the prenatal diagnosis of fetal intrauterine growth restriction.
Stephanie Brun, Perrine Pennamen, Aurelien Mattuizzi, Frederic Coatleven, Marie Laure Vuillaume, Didier Lacombe, Benoit Arveiler, Jerome Toutain, Caroline Rooryck. Prenat Diagn 2018
4
100


[Chart for estimation of fetal weight 2014 by the French College of Fetal Sonography (CFEF)].
M Massoud, M Duyme, M Fontanges, D Combourieu. J Gynecol Obstet Biol Reprod (Paris) 2016
21
100

Application of chromosomal microarray to investigate genetic causes of isolated fetal growth restriction.
Gang An, Yuan Lin, Liang Pu Xu, Hai Long Huang, Si Ping Liu, Yan Hong Yu, Fang Yang. Mol Cytogenet 2018
3
100

The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker,[...]. Prenat Diagn 2018
15
100

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases.
Francesco Fiorentino, Fiorina Caiazzo, Stefania Napolitano, Letizia Spizzichino, Sara Bono, Mariateresa Sessa, Andrea Nuccitelli, Anil Biricik, Anthony Gordon, Giuseppe Rizzo,[...]. Prenat Diagn 2011
75
100

Chromosomal Microarray Analysis in Fetuses with Growth Restriction and Normal Karyotype: A Systematic Review and Meta-Analysis.
Antoni Borrell, Maribel Grande, Montse Pauta, Laia Rodriguez-Revenga, Francesc Figueras. Fetal Diagn Ther 2018
16
100

Fetal growth retardation: associated malformations and chromosomal abnormalities.
R J Snijders, C Sherrod, C M Gosden, K H Nicolaides. Am J Obstet Gynecol 1993
130
100


Short-term and long-term sequelae in intrauterine growth retardation (IUGR).
Stefania Longo, Lina Bollani, Lidia Decembrino, Amelia Di Comite, Mauro Angelini, M Stronati. J Matern Fetal Neonatal Med 2013
149
100

Fetal aortic wall thickness: a marker of hypertension in IUGR children?
Vincenzo Zanardo, Silvia Visentin, Daniele Trevisanuto, Martina Bertin, Francesco Cavallin, Erich Cosmi. Hypertens Res 2013
31
100

Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeks.
M C de Wit, M I Srebniak, M Joosten, L C P Govaerts, R F Kornelisse, D N M Papatsonis, K de Graaff, M F C M Knapen, H T Bruggenwirth, F A T de Vries,[...]. Ultrasound Obstet Gynecol 2017
10
100

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021
8
100

Birth weight in relation to morbidity and mortality among newborn infants.
D D McIntire, S L Bloom, B M Casey, K J Leveno. N Engl J Med 1999
798
100

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases.
Ignatia B Van den Veyver, Ankita Patel, Chad A Shaw, Amber N Pursley, Sung-Hae L Kang, Marcia J Simovich, Patricia A Ward, Sandra Darilek, Anthony Johnson, Sarah E Neill,[...]. Prenat Diagn 2009
139
100

Genomic Microarray in Fetuses with Early Growth Restriction: A Multicenter Study.
Antoni Borrell, Maribel Grande, Eva Meler, Joan Sabrià, Edurne Mazarico, Anna Muñoz, Laia Rodriguez-Revenga, Cèlia Badenas, Francesc Figueras. Fetal Diagn Ther 2017
11
100

Fetal growth restriction and intra-uterine growth restriction: guidelines for clinical practice from the French College of Gynaecologists and Obstetricians.
C Vayssière, L Sentilhes, A Ego, C Bernard, D Cambourieu, C Flamant, G Gascoin, A Gaudineau, G Grangé, V Houfflin-Debarge,[...]. Eur J Obstet Gynecol Reprod Biol 2015
98
100

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


Major risk factors for stillbirth in high-income countries: a systematic review and meta-analysis.
Vicki Flenady, Laura Koopmans, Philippa Middleton, J Frederik Frøen, Gordon C Smith, Kristen Gibbons, Michael Coory, Adrienne Gordon, David Ellwood, Harold David McIntyre,[...]. Lancet 2011
633
100


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
100

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011.
A Novelli, F R Grati, L Ballarati, L Bernardini, D Bizzoco, L Camurri, R Casalone, L Cardarelli, P Cavalli, R Ciccone,[...]. Ultrasound Obstet Gynecol 2012
44
100

Array CGH analysis in high-risk pregnancies: comparing DNA from cultured cells and cell-free fetal DNA.
Nicolas Gruchy, Matthieu Decamp, Nicolas Richard, Corinne Jeanne-Pasquier, Guillaume Benoist, Hervé Mittre, Nathalie Leporrier. Prenat Diagn 2012
23
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

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Christine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, Radha Chari, Bernie N Chodirker, Isabelle DeBie, Jane A Evans, William T Gibson, Elena Kolomietz, Tanya N Nelson,[...]. J Med Genet 2018
28
100

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype.
Linda Kleeman, Diana W Bianchi, Lisa G Shaffer, Emily Rorem, Janet Cowan, Sabrina D Craigo, Hocine Tighiouart, Louise E Wilkins-Haug. Prenat Diagn 2009
78
100

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.
Lisa G Shaffer, Mindy P Dabell, Allan J Fisher, Justine Coppinger, Anne M Bandholz, Jay W Ellison, J Britt Ravnan, Beth S Torchia, Blake C Ballif, Jill A Rosenfeld. Prenat Diagn 2012
136
100

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
154
100

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
100

Infant neurodevelopment following fetal growth restriction: relationship with antepartum surveillance parameters.
A A Baschat, R M Viscardi, B Hussey-Gardner, N Hashmi, C Harman. Ultrasound Obstet Gynecol 2009
68
100

Karyotype versus genomic hybridization for the prenatal diagnosis of chromosomal abnormalities: a metaanalysis.
Wilmar Saldarriaga, Herney Andrés García-Perdomo, Johanna Arango-Pineda, Javier Fonseca. Am J Obstet Gynecol 2015
18
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.