A citation-based method for searching scientific literature

Amihood Singer, Idit Maya, Ayala Frumkin, Sharon Zeligson, Sagi Ben Yehoshua Josefsberg, Racheli Berger, Shay Ben Shachar, Lena Sagi-Dain. 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
630
100

Advanced genomic testing may aid in counseling of isolated agenesis of the corpus callosum on prenatal ultrasound.
M C de Wit, F Boekhorst, G M Mancini, L S Smit, I A L Groenenberg, J Dudink, F A T de Vries, A T J I Go, R J H Galjaard. Prenat Diagn 2017
12
100

Chromosomal microarray analysis in fetuses with central nervous system anomalies: An 8-year long observational study from a tertiary care university hospital.
Maddalena Santirocco, Alberto Plaja, Carlota Rodó, Irene Valenzuela, Silvia Arévalo, Neus Castells, Anna Abuli, Eduardo Tizzano, Nerea Maiz, Elena Carreras. Prenat Diagn 2021
1
100

What have we learned from 691 prenatal chromosomal microarrays for ventricular septal defects?
Idit Maya, Amihood Singer, Hagith Yonath, Adi Reches, Shlomit Rienstein, Sharon Zeligson, Shay Ben Shachar, Lena Sagi-Dain. Acta Obstet Gynecol Scand 2020
2
100

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
135
100

Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis.
Lijuan Sun, Qingqing Wu, Shi-Wen Jiang, Yani Yan, Xin Wang, Juan Zhang, Yan Liu, Ling Yao, Yuqing Ma, Li Wang. Biomed Res Int 2015
23
100

Diagnostic imaging of posterior fossa anomalies in the fetus and neonate: part 1, normal anatomy and classification of anomalies.
Teresa Chapman, Sowmya Mahalingam, Gisele E Ishak, Jason N Nixon, Joseph Siebert, Manjiri K Dighe. Clin Imaging 2015
13
100

Epidemiology of Dandy-Walker Malformation in Europe: A EUROCAT Population-Based Registry Study.
Michele Santoro, Alessio Coi, Ingeborg Barišić, Ester Garne, Marie-Claude Addor, Jorieke E H Bergman, Fabrizio Bianchi, Ljubica Boban, Paula Braz, Clara Cavero-Carbonell,[...]. Neuroepidemiology 2019
5
100

Chromosomal aneuploidies and copy number variations in posterior fossa abnormalities diagnosed by prenatal ultrasonography.
Ting Lei, Jie-Ling Feng, Ying-Jun Xie, Hong-Ning Xie, Ju Zheng, Mei-Fang Lin. Prenat Diagn 2017
8
100

Outcomes Associated With Isolated Agenesis of the Corpus Callosum: A Meta-analysis.
Francesco D'Antonio, Giorgio Pagani, Alessandra Familiari, Asma Khalil, Tally-Lerman Sagies, Gustavo Malinger, Zvi Leibovitz, Catherine Garel, Marie Laure Moutard, Gianluigi Pilu,[...]. Pediatrics 2016
51
100

Microarray analysis in pregnancies with isolated unilateral kidney agenesis.
Lena Sagi-Dain, Idit Maya, Amir Peleg, Adi Reches, Ehud Banne, Hagit N Baris, Tamar Tenne, Amihood Singer, Shay Ben-Shachar. Pediatr Res 2018
6
100

Chromosomal microarray should be performed for cases of fetal short long bones detected prenatally.
Keren Tzadikevitch Geffen, Amihood Singer, Idit Maya, Lena Sagi-Dain, Morad Khayat, Shay Ben-Shachar, Hagit Daum, Rachel Michaelson-Cohen, Michal Feingold-Zadok, Rivka Sukenik Halevy. Arch Gynecol Obstet 2021
1
100

Agenesis of the corpus callosum: a clinical approach to diagnosis.
Elizabeth Emma Palmer, David Mowat. Am J Med Genet C Semin Med Genet 2014
35
100

Microarray findings in pregnancies with oligohydramnios - a retrospective cohort study and literature review.
Amihood Singer, Idit Maya, Rivka Sukenik-Halevy, Tamar Tenne, Dorit Lev, Shay Ben Shachar, Lena Sagi-Dain. J Perinat Med 2019
2
100

Prenatal clubfoot increases the risk for clinically significant chromosomal microarray results - Analysis of 269 singleton pregnancies.
Amihood Singer, Idit Maya, Ehud Banne, Hagit Baris Feldman, Chana Vinkler, Shay Ben Shachar, Lena Sagi-Dain. Early Hum Dev 2020
1
100

Diagnostic imaging of posterior fossa anomalies in the fetus.
Ashley James Robinson, M Ashraf Ederies. Semin Fetal Neonatal Med 2016
14
100

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.
Lena Sagi-Dain, Amihood Singer, Ayala Frumkin, Adel Shalata, Arie Koifman, Reeval Segel, Lilach Benyamini, Shlomit Rienstein, Morad Kahyat, Reuven Sharony,[...]. J Perinat Med 2018
2
100

Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Lena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifat Agmon-Fishman, Cochava Klein, Reut Matar, Lina Basel-Salmon, Idit Maya. Genet Med 2019
30
100

Non-visualization of fetal gallbladder in microarray era - a retrospective cohort study and review of the literature.
Lena Sagi-Dain, Amihood Singer, Yarin Hadid, Reuven Sharony, Chana Vinkler, Anat Bar-Shira, Reeval Segel, Shay Ben Shachar, Idit Maya. J Matern Fetal Neonatal Med 2019
2
100

Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal imaging (part 2): neurodevelopmental outcome.
F D'Antonio, A Khalil, C Garel, G Pilu, G Rizzo, T Lerman-Sagie, A Bhide, B Thilaganathan, L Manzoli, A T Papageorghiou. Ultrasound Obstet Gynecol 2016
32
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
43
100

Corpus callosum abnormalities: neuroradiological and clinical correlations.
Aqeela H Al-Hashim, Susan Blaser, Charles Raybaud, Daune MacGregor. Dev Med Child Neurol 2016
17
100


Agenesis of the corpus callosum in California 1983-2003: a population-based study.
Hannah C Glass, Gary M Shaw, Chen Ma, Elliott H Sherr. Am J Med Genet A 2008
116
100

Descriptive epidemiology of cerebellar hypoplasia in the National Birth Defects Prevention Study.
Meredith M Howley, Kim M Keppler-Noreuil, Christopher M Cunniff, Marilyn L Browne. Birth Defects Res 2018
2
100

Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray results.
Lena Sagi-Dain, Idit Maya, Tzipora Falik-Zaccai, Michal Feingold-Zadok, Dorit Lev, Hagit Yonath, Ehud Kaliner, Ayala Frumkin, Shay Ben Shachar, Amihood Singer. Eur J Obstet Gynecol Reprod Biol 2018
4
100

Genetic testing in fetuses with isolated agenesis of the corpus callosum.
Qin She, Fang Fu, Xiaoyan Guo, Weihe Tan, Can Liao. J Matern Fetal Neonatal Med 2021
2
100

Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia.
Zhiyong Zou, Linhuan Huang, Shaobin Lin, Zhiming He, Hui Zhu, Yi Zhang, Qun Fang, Yanmin Luo. Prenat Diagn 2018
10
100

Diagnostic imaging of posterior fossa anomalies in the fetus and neonate: part 2, Posterior fossa disorders.
Teresa Chapman, Sowmya Mahalingam, Gisele E Ishak, Jason N Nixon, Joseph Siebert, Manjiri K Dighe. Clin Imaging 2015
20
100

Congenital basis of posterior fossa anomalies.
Claudia Cotes, Eliana Bonfante, Jillian Lazor, Siddharth Jadhav, Maria Caldas, Leonard Swischuk, Roy Riascos. Neuroradiol J 2015
16
100

Genetic tests aid in counseling of fetuses with cerebellar vermis defects.
Lushan Li, Fang Fu, Ru Li, Weiqiang Xiao, Qiuxia Yu, Dan Wang, Xiangyi Jing, Yongning Zhang, Xin Yang, Min Pan,[...]. Prenat Diagn 2020
3
100

Perinatal and short-term neonatal outcomes of posterior fossa anomalies.
Rim Ghali, Karen Reidy, A Michelle Fink, Ricardo Palma-Dias. Fetal Diagn Ther 2014
5
100

Microarray analysis has no additional value in fetal aberrant right subclavian artery: description of 268 pregnancies and systematic literature review.
L Sagi-Dain, A Singer, S Josefsberg, A Peleg, D Lev, N Nasser Samra, A Bar-Shira, S Zeligson, I Maya, S Ben-Shachar. Ultrasound Obstet Gynecol 2019
5
100

The yield of chromosomal microarray testing for cases of abnormal fetal head circumference.
Yael Pasternak, Amihood Singer, Idit Maya, Lena Sagi-Dain, Shay Ben-Shachar, Morad Khayat, Lior Greenbaum, Michal Feingold-Zadok, Sharon Zeligson, Rivka Sukenik Halevy. J Perinat Med 2020
2
100

Distinguishing 3 classes of corpus callosal abnormalities in consanguineous families.
R M Hanna, S E Marsh, D Swistun, L Al-Gazali, M S Zaki, G M Abdel-Salam, A Al-Tawari, L Bastaki, H Kayserili, A Rajab,[...]. Neurology 2011
22
100

Systematic review and meta-analysis of isolated posterior fossa malformations on prenatal ultrasound imaging (part 1): nomenclature, diagnostic accuracy and associated anomalies.
F D'Antonio, A Khalil, C Garel, G Pilu, G Rizzo, T Lerman-Sagie, A Bhide, B Thilaganathan, L Manzoli, A T Papageorghiou. Ultrasound Obstet Gynecol 2016
31
100



The human motor corpus callosum.
Mathias Wahl, Ulf Ziemann. Rev Neurosci 2008
23
100

Non-visualisation of cavum septi pellucidi: implication in prenatal diagnosis?
K Hosseinzadeh, J Luo, A Borhani, L Hill. Insights Imaging 2013
15
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
13
100

Prenatal exome sequencing in 65 fetuses with abnormality of the corpus callosum: contribution to further diagnostic delineation.
Solveig Heide, Myrtille Spentchian, Stéphanie Valence, Julien Buratti, Corinne Mach, Elodie Lejeune, Valérie Olin, Marta Massimello, Daphné Lehalle, Linda Mouthon,[...]. Genet Med 2020
2
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
152
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
117
100

Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.
Timothy J Edwards, Elliott H Sherr, A James Barkovich, Linda J Richards. Brain 2014
144
100

Microarray analysis in pregnancies with isolated echogenic bowel.
Amihood Singer, Idit Maya, Arie Koifman, Nadra Nasser Samra, Hagit N Baris, Tzipora Falik-Zaccai, Shay Ben Shachar, Lena Sagi-Dain. Early Hum Dev 2018
8
100

Prenatal microarray analysis in right aortic arch-a retrospective cohort study and review of the literature.
Idit Maya, Amihood Singer, Hagit N Baris, Yael Goldberg, Adel Shalata, Morad Khayat, Shay Ben-Shachar, Lena Sagi-Dain. J Perinatol 2018
5
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.