A citation-based method for searching scientific literature

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
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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
37

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
37

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
37


Antenatal prognostic factor of fetal echogenic bowel.
Candice Ronin, Pierre Mace, Fabien Stenard, Anderson Loundou, Marianne Capelle, Isabelle Mortier, Marie Christine Pellissier, Sabine Sigaudy, Annie Levy, Claude D'ercole,[...]. Eur J Obstet Gynecol Reprod Biol 2017
13
37

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
31
37

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
7
28

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
33

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
27
25

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
50

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
25


Ultrasonographic fetal soft markers in a low-risk population: prevalence, association with trisomies and invasive tests.
Annika Ahman, Ove Axelsson, Gordan Maras, Christine Rubertsson, Anna Sarkadi, Peter Lindgren. Acta Obstet Gynecol Scand 2014
17
25

Is fetal hyperechoic bowel on second-trimester sonogram an indication for amniocentesis?
B Bromley, P Doubilet, F D Frigoletto, C Krauss, J A Estroff, B R Benacerraf. Obstet Gynecol 1994
100
25

Echogenic bowel on second-trimester ultrasonography: evaluating the risk of adverse pregnancy outcome.
Katherine R Goetzinger, Alison G Cahill, George A Macones, Anthony O Odibo. Obstet Gynecol 2011
37
25

Isolated sonographic markers for detection of fetal Down syndrome in the second trimester of pregnancy.
D A Nyberg, V L Souter, A El-Bastawissi, S Young, F Luthhardt, D A Luthy. J Ultrasound Med 2001
161
25

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
25

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
25

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

Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.
Kitty K Lo, Evangelia Karampetsou, Christopher Boustred, Fiona McKay, Sarah Mason, Melissa Hill, Vincent Plagnol, Lyn S Chitty. Am J Hum Genet 2016
67
12

Chromosomal abnormalities not currently detected by cell-free fetal DNA: a retrospective analysis at a single center.
Hagit Shani, Tamar Goldwaser, Jennifer Keating, Susan Klugman. Am J Obstet Gynecol 2016
23
12



Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
12

Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions.
Rachèl V van Schendel, Carla G van El, Eva Pajkrt, Lidewij Henneman, Martina C Cornel. BMC Health Serv Res 2017
35
12

Noninvasive detection of fetal subchromosomal abnormalities by semiconductor sequencing of maternal plasma DNA.
Ai-hua Yin, Chun-fang Peng, Xin Zhao, Bennett A Caughey, Jie-xia Yang, Jian Liu, Wei-wei Huang, Chang Liu, Dong-hong Luo, Hai-liang Liu,[...]. Proc Natl Acad Sci U S A 2015
65
12

Evolving applications of microarray analysis in prenatal diagnosis.
Melissa S Savage, Mirella J Mourad, Ronald J Wapner. Curr Opin Obstet Gynecol 2011
29
12

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.
Lluís Armengol, Julián Nevado, Clara Serra-Juhé, Alberto Plaja, Carmen Mediano, Fe Amalia García-Santiago, Manel García-Aragonés, Olaya Villa, Elena Mansilla, Cristina Preciado,[...]. Hum Genet 2012
61
12

Chromosome microarrays in human reproduction.
Evica Rajcan-Separovic. Hum Reprod Update 2012
15
12

Why 99% may not be as good as you think it is: limitations of screening for rare diseases.
Monica A Lutgendorf, Katie A Stoll. J Matern Fetal Neonatal Med 2016
7
14

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities.
Francesco Fiorentino, Stefania Napoletano, Fiorina Caiazzo, Mariateresa Sessa, Sara Bono, Letizia Spizzichino, Anthony Gordon, Andrea Nuccitelli, Giuseppe Rizzo, Marina Baldi. Eur J Hum Genet 2013
61
12

Microarray comparative genomic hybridization in prenatal diagnosis: a review.
S C Hillman, D J McMullan, D Williams, E R Maher, M D Kilby. Ultrasound Obstet Gynecol 2012
15
12

Non-invasive prenatal testing: a review of international implementation and challenges.
Megan Allyse, Mollie A Minear, Elisa Berson, Shilpa Sridhar, Margaret Rote, Anthony Hung, Subhashini Chandrasekharan. Int J Womens Health 2015
139
12

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
12

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
40
12


Detection of fetal copy number variants by non-invasive prenatal testing for common aneuploidies.
R Li, J Wan, Y Zhang, F Fu, Y Ou, X Jing, J Li, D Li, C Liao. Ultrasound Obstet Gynecol 2016
34
12


Whole exome sequencing as a diagnostic adjunct to clinical testing in fetuses with structural abnormalities.
F Fu, R Li, Y Li, Z-Q Nie, T Lei, D Wang, X Yang, J Han, M Pan, L Zhen,[...]. Ultrasound Obstet Gynecol 2018
51
12

Extending the PRISMA statement to equity-focused systematic reviews (PRISMA-E 2012): explanation and elaboration.
Vivian Welch, Mark Petticrew, Jennifer Petkovic, David Moher, Elizabeth Waters, Howard White, Peter Tugwell. J Clin Epidemiol 2016
91
12


Adverse Perinatal Conditions Associated With Prenatally Detected Fetal Echogenic Bowel in Nova Scotia.
Rachelle Findley, Victoria M Allen, Jo-Ann K Brock. J Obstet Gynaecol Can 2018
3
33

Foetal magnetic resonance imaging and echogenic bowel.
Xavier Carcopino, Kathia Chaumoitre, Raha Shojai, Reem Akkawi, Michel Panuel, Léon Boubli, Claude D'ercole. Prenat Diagn 2007
10
12

Prognostic implications of fetal echogenic bowel.
R N Slotnick, A Z Abuhamad. Lancet 1996
96
12

Role of second-trimester genetic sonography after Down syndrome screening.
Kjersti M Aagaard-Tillery, Fergal D Malone, David A Nyberg, T Flint Porter, Howard S Cuckle, Karin Fuchs, Lisa Sullivan, Christine H Comstock, George R Saade, Keith Eddleman,[...]. Obstet Gynecol 2009
67
12

Updated guidance for trusted systematic reviews: a new edition of the Cochrane Handbook for Systematic Reviews of Interventions.
Miranda Cumpston, Tianjing Li, Matthew J Page, Jacqueline Chandler, Vivian A Welch, Julian Pt Higgins, James Thomas. Cochrane Database Syst Rev 2019
826
12

Meta-analysis of observational studies in epidemiology: a proposal for reporting. Meta-analysis Of Observational Studies in Epidemiology (MOOSE) group.
D F Stroup, J A Berlin, S C Morton, I Olkin, G D Williamson, D Rennie, D Moher, B J Becker, T A Sipe, S B Thacker. JAMA 2000
12


Hyperechogenic fetal bowel: a prospective analysis of sixty consecutive cases.
I Ghose, G C Mason, D Martinez, K L Harrison, J A Evans, E L Ferriman, M D Stringer. BJOG 2000
31
12

Meta-analysis of second-trimester markers for trisomy 21.
M Agathokleous, P Chaveeva, L C Y Poon, P Kosinski, K H Nicolaides. Ultrasound Obstet Gynecol 2013
119
12


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.