A citation-based method for searching scientific literature

Lena Sagi-Dain, Amihood Singer, Shay Ben Shachar, Sagi Josefsberg Ben Yehoshua, Michal Feingold-Zadok, Lior Greenbaum, Idit Maya. Obstet Gynecol 2021
Times Cited: 1

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

Times Cited
  Times     Co-cited

Array comparative genomic hybridization and fetal congenital heart defects: a systematic review and meta-analysis.
F A R Jansen, Y J Blumenfeld, A Fisher, J M Cobben, A O Odibo, A Borrell, M C Haak. Ultrasound Obstet Gynecol 2015

When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.
Idit Maya, Reuven Sharony, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, Ifaat Agmon-Fishman, Lital Cohen-Vig, Yael Goldberg, Racheli Berger,[...]. Genet Med 2018

Comparative genomic hybridisation shows a partial de novo deletion 16p11.2 in a neonate with multiple congenital malformations.
C Hernando, A Plaja, M A Rigola, M M Pérez, T Vendrell, J Egocue, C Fuster. J Med Genet 2002

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

Women's Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results.
Rachèl V van Schendel, G C M Lieve Page-Christiaens, Lean Beulen, Caterina M Bilardo, Marjon A de Boer, Audrey B C Coumans, Brigitte H W Faas, Irene M van Langen, Klaske D Lichtenbelt, Merel C van Maarle,[...]. J Genet Couns 2017

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

Procedure-related risk of miscarriage following amniocentesis and chorionic villus sampling: a systematic review and meta-analysis.
R Akolekar, J Beta, G Picciarelli, C Ogilvie, F D'Antonio. Ultrasound Obstet Gynecol 2015

Association of combined first-trimester screen and noninvasive prenatal testing on diagnostic procedures.
Sebastian Larion, Steven L Warsof, Letty Romary, Margaret Mlynarczyk, David Peleg, Alfred Z Abuhamad. Obstet Gynecol 2014

Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review.
Olav B Petersen, Eric Smith, Diane Van Opstal, Marike Polak, Maarten F C M Knapen, Karin E M Diderich, Caterina M Bilardo, Lidia R Arends, Ida Vogel, Malgorzata I Srebniak. Acta Obstet Gynecol Scand 2020

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall,[...]. Eur J Hum Genet 2015

The contribution of chromosomal abnormalities to congenital heart defects: a population-based study.
Robert J Hartman, Sonja A Rasmussen, Lorenzo D Botto, Tiffany Riehle-Colarusso, Christa L Martin, Janet D Cragan, Mikyong Shin, Adolfo Correa. Pediatr Cardiol 2011

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

Noninherited risk factors and congenital cardiovascular defects: current knowledge: a scientific statement from the American Heart Association Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics.
Kathy J Jenkins, Adolfo Correa, Jeffrey A Feinstein, Lorenzo Botto, Amy E Britt, Stephen R Daniels, Marsha Elixson, Carole A Warnes, Catherine L Webb. Circulation 2007

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta-analysis.
M I Srebniak, M Joosten, M F C M Knapen, L R Arends, M Polak, S van Veen, A T J I Go, D Van Opstal. Ultrasound Obstet Gynecol 2018

A familial 593-kb microdeletion of 16p11.2 associated with mental retardation and hemivertebrae.
Keiko Shimojima, Takehiko Inoue, Yuji Fujii, Kousaku Ohno, Toshiyuki Yamamoto. Eur J Med Genet 2009

Value of increased nuchal translucency in the era of noninvasive prenatal testing with cell-free DNA.
Iris Holzer, Peter W Husslein, Dieter Bettelheim, Julia Scheidl, Herbert Kiss, Alex Farr. Int J Gynaecol Obstet 2019

Detection of fetal chromosomal anomalies: does nuchal translucency measurement have added value in the era of non-invasive prenatal testing?
K D Lichtenbelt, B D M Diemel, M P H Koster, G T R Manten, J Siljee, G H Schuring-Blom, G C M L Page-Christiaens. Prenat Diagn 2015

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

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

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.