A citation-based method for searching scientific literature

I Maya, S Kahana, J Yeshaya, T Tenne, S Yacobson, I Agmon-Fishman, L Cohen-Vig, A Levi, E Reinstein, L Basel-Vanagaite, R Sharony. Ultrasound Obstet Gynecol 2017
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity



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
47


Aberrant right subclavian artery in fetuses with Down syndrome: a systematic review and meta-analysis.
C Scala, U Leone Roberti Maggiore, M Candiani, P L Venturini, S Ferrero, T Greco, P Cavoretto. Ultrasound Obstet Gynecol 2015
32
41

Second-trimester fetal aberrant right subclavian artery: original study, systematic review and meta-analysis of performance in detection of Down syndrome.
J De León-Luis, F Gámez, C Bravo, J M Tenías, Á Arias, R Pérez, E Maroto, Á Aguarón, L Ortiz-Quintana. Ultrasound Obstet Gynecol 2014
23
41

Aberrant Right Subclavian Artery: Correlation Between Fetal and Neonatal Abnormalities and Abnormal Genetic Screening or Testing.
Angela C Ranzini, Francine Hyman, Emily Jamaer, Tim van Mieghem. J Ultrasound Med 2017
10
70

Aberrant right subclavian artery as a new cardiac sign in second- and third-trimester fetuses with Down syndrome.
Rabih Chaoui, Kai-Sven Heling, Nanette Sarioglu, Michael Schwabe, Anja Dankof, Rainer Bollmann. Am J Obstet Gynecol 2005
83
41

Association of aberrant right subclavian artery with abnormal karyotype and microarray results.
Ran Svirsky, Adi Reches, Dana Brabbing-Goldstein, Anat Bar-Shira, Yuval Yaron. Prenat Diagn 2017
13
53

Prenatal Associated Features in Fetuses Diagnosed with an Aberrant Right Subclavian Artery.
Harmony Pico, Julien Mancini, Antoine Lafouge, Jean-Philippe Bault, Guillaume Gorincour, Edwin Quarello. Fetal Diagn Ther 2016
10
70

Aberrant right subclavian artery: incidence and correlation with other markers of Down syndrome in second-trimester fetuses.
D Paladini, G Sglavo, G Pastore, A Masucci, M R D'Armiento, C Nappi. Ultrasound Obstet Gynecol 2012
28
35

Fetal aberrant right subclavian artery (ARSA) - a potential new soft marker in the genetic scan?
A M Willruth, N Dwinger, J Ritgen, R Stressig, A Geipel, U Gembruch, C Berg. Ultraschall Med 2012
19
35

Aberrant right subclavian artery at 16 to 23 + 6 weeks of gestation: a marker for chromosomal abnormality.
M Borenstein, R Minekawa, V Zidere, K H Nicolaides, L D Allan. Ultrasound Obstet Gynecol 2010
43
35

Aberrant right subclavian artery (ARSA) in unselected population at first and second trimester ultrasonography.
G Rembouskos, U Passamonti, V De Robertis, A Tempesta, G Campobasso, G Volpe, M Gentile, P Volpe. Prenat Diagn 2012
30
35

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
8
75

Aberrant right subclavian artery at 11 + 0 to 13 + 6 weeks of gestation in chromosomally normal and abnormal fetuses.
M Borenstein, P Cavoretto, L Allan, I Huggon, K H Nicolaides. Ultrasound Obstet Gynecol 2008
36
29

Fetal aberrant right subclavian artery in normal and Down syndrome fetuses.
Y Zalel, R Achiron, S Yagel, Z Kivilevitch. Ultrasound Obstet Gynecol 2008
42
29

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
29

Association of chromosome 22q11 deletion with isolated anomalies of aortic arch laterality and branching.
D B McElhinney, B J Clark, P M Weinberg, M L Kenton, D McDonald-McGinn, D A Driscoll, E H Zackai, E Goldmuntz. J Am Coll Cardiol 2001
150
29

Aberrant right subclavian artery in Down syndrome fetuses.
H Fehmi Yazıcıoğlu, Osman Sevket, Hale Akın, Mehmet Aygün, Osman Nuri Özyurt, Ayse Karahasanoğlu. Prenat Diagn 2013
23
29

Incidence of an Aberrant Right Subclavian Artery on Second-Trimester Sonography in an Unselected Population.
Selen Gursoy Erzincan, Burcin Karamustafaoglu Balci, Cengiz Tokgoz, Ibrahim Halil Kalelioglu. J Ultrasound Med 2017
5
100

Detection rate of trisomy 21 in fetuses with isolated and non-isolated aberrant right subclavian artery.
Aytul Corbacioglu Esmer, Ahmet Gul, Aslı Nehir, Atil Yuksel, Ozlem Dural, Ibrahim Kalelioglu, Recep Has, Tanju Demiroren. Fetal Diagn Ther 2013
13
38

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
23

Associated anomalies and outcome of fetal aberrant right subclavian artery.
Ahmet Gul, Aytul Corbacioglu, Isil Turan Bakirci, Yavuz Ceylan. Arch Gynecol Obstet 2012
15
26


Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities.
Debra D'Angelo, Sébastien Lebon, Qixuan Chen, Sandra Martin-Brevet, LeeAnne Green Snyder, Loyse Hippolyte, Ellen Hanson, Anne M Maillard, W Andrew Faucett, Aurélien Macé,[...]. JAMA Psychiatry 2016
104
23

Rare and common variants at 16p11.2 are associated with schizophrenia.
Hong Chang, Lingyi Li, Ming Li, Xiao Xiao. Schizophr Res 2017
19
23

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.
A M Maillard, A Ruef, F Pizzagalli, E Migliavacca, L Hippolyte, S Adaszewski, J Dukart, C Ferrari, P Conus, K Männik,[...]. Mol Psychiatry 2015
93
23

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
23


Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies.
Francesca Romana Grati, Denise Molina Gomes, Jose Carlos Pinto B Ferreira, Celine Dupont, Viola Alesi, Laetitia Gouas, Nina Horelli-Kuitunen, Kwong Wai Choy, Sandra García-Herrero, Alberto Gonzalez de la Vega,[...]. Prenat Diagn 2015
154
17

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
58
17

Prenatal diagnosis of aberrant right subclavian artery in an unselected population.
Mi Jin Song, Byoung Hee Han, Young-Hwa Kim, So Young Yoon, Yoo Mi Lee, Hye Su Jeon, Bo Kyung Park. Ultrasonography 2017
9
33

Association of copy number variants with specific ultrasonographically detected fetal anomalies.
Jennifer C Donnelly, Lawrence D Platt, Andrei Rebarber, Julia Zachary, William A Grobman, Ronald J Wapner. Obstet Gynecol 2014
81
11

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
138
11

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
11

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
D M McDonald-McGinn, R Kirschner, E Goldmuntz, K Sullivan, P Eicher, M Gerdes, E Moss, C Solot, P Wang, I Jacobs,[...]. Genet Couns 1999
311
11

Refining analyses of copy number variation identifies specific genes associated with developmental delay.
Bradley P Coe, Kali Witherspoon, Jill A Rosenfeld, Bregje W M van Bon, Anneke T Vulto-van Silfhout, Paolo Bosco, Kathryn L Friend, Carl Baker, Serafino Buono, Lisenka E L M Vissers,[...]. Nat Genet 2014
323
11

Congenital Variants and Anomalies of the Aortic Arch.
Kate Hanneman, Beverley Newman, Frandics Chan. Radiographics 2017
75
11


An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
286
11


Renal malformations in patients with Turner syndrome: imaging in 141 patients.
B Lippe, M E Geffner, R B Dietrich, M I Boechat, H Kangarloo. Pediatrics 1988
68
11


Prenatal chromosomal microarray analysis in fetuses with congenital heart disease: a prospective cohort study.
Yan Wang, Li Cao, Dong Liang, Lulu Meng, Yun Wu, Fengchang Qiao, Xiuqing Ji, Chunyu Luo, Jingjing Zhang, Tianhui Xu,[...]. Am J Obstet Gynecol 2018
22
11

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
11

Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics.
Anthony R Gregg, Brian G Skotko, Judith L Benkendorf, Kristin G Monaghan, Komal Bajaj, Robert G Best, Susan Klugman, Michael S Watson. Genet Med 2016
294
11

ISUOG Practice Guidelines (updated): sonographic screening examination of the fetal heart.
International Society of Ultrasound in Obstetrics and Gynecology, J S Carvalho, L D Allan, R Chaoui, J A Copel, G R DeVore, K Hecher, W Lee, H Munoz, D Paladini,[...]. Ultrasound Obstet Gynecol 2013
257
11

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.
Heather C Mefford, Andrew J Sharp, Carl Baker, Andy Itsara, Zhaoshi Jiang, Karen Buysse, Shuwen Huang, Viv K Maloney, John A Crolla, Diana Baralle,[...]. N Engl J Med 2008
514
11

Recurrent deletions and duplications of chromosome 2q11.2 and 2q13 are associated with variable outcomes.
Kacie N Riley, Lisa M Catalano, John A Bernat, Stacie D Adams, Donna M Martin, Seema R Lalani, Ankita Patel, Rachel D Burnside, Jeffrey W Innis, M Katharine Rudd. Am J Med Genet A 2015
23
11

Right aortic arch detected in fetal life.
C Berg, F Bender, M Soukup, A Geipel, R Axt-Fliedner, J Breuer, U Herberg, U Gembruch. Ultrasound Obstet Gynecol 2006
57
11


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.