A citation-based method for searching scientific literature

Kuntharee Traisrisilp, Fuanglada Tongprasert, Kasemsri Srisupundit, Suchaya Luewan, Theera Tongsong. Obstet Gynecol Sci 2020
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome.
Erica Schindewolf, Nahla Khalek, Mark P Johnson, Juliana Gebb, Beverly Coleman, Terrence Blaine Crowley, Elaine H Zackai, Donna M McDonald-McGinn, Julie S Moldenhauer. Am J Med Genet A 2018
15
66


Right-sided aortic arch in the age of microarray.
Edward F O'Mahony, Darren P Hutchinson, George McGillivray, Debbie L Nisbet, Ricardo Palma-Dias. Prenat Diagn 2017
12
66

Chromosomal Microarray Analysis for the Fetuses with Aortic Arch Abnormalities and Normal Karyotype.
Xiaoqing Wu, Ying Li, Linjuan Su, Xiaorui Xie, Meiying Cai, Na Lin, Hailong Huang, Yuan Lin, Liangpu Xu. Mol Diagn Ther 2020
3
66

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
59
66

Risk of 22q11.2 deletion in fetuses with right aortic arch and without intracardiac anomalies.
A Perolo, V De Robertis, I Cataneo, N Volpe, G Campobasso, T Frusca, T Ghi, D Prandstraller, G Pilu, P Volpe. Ultrasound Obstet Gynecol 2016
14
66

Prenatal diagnosis and outcome of right aortic arch without significant intracardiac anomaly.
Yaron Razon, Michael Berant, Rami Fogelman, Gabriel Amir, Einat Birk. J Am Soc Echocardiogr 2014
44
66

The presentation and management of vascular rings: an otolaryngology perspective.
Rahul K Shah, Bassem N Mora, Emile Bacha, Laureen M Sena, Carlo Buonomo, Pedro Del Nido, Reza Rahbar. Int J Pediatr Otorhinolaryngol 2007
38
66

Prenatal diagnosis of right aortic arch: associated findings, pregnancy outcome, and clinical significance of vascular rings.
A Galindo, O Nieto, M T Nieto, M O Rodríguez-Martín, I Herraiz, D Escribano, M A Granados. Prenat Diagn 2009
57
66

Prenatal echocardiographic assessment of right aortic arch.
C M Campanale, L Pasquini, T P Santangelo, F S Iorio, P Bagolan, S P Sanders, A Toscano. Ultrasound Obstet Gynecol 2019
14
66

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
154
66

The significance of a prenatal diagnosis of right aortic arch.
Anna Wójtowicz, Maria Respondek-Liberska, Maciej Słodki, Paulina Kordjalik, Joanna Płużańska, Anna Knafel, Hubert Huras. Prenat Diagn 2017
10
66

Incidence of chromosomal anomalies in fetuses with isolated right aortic arch: A meta-analysis.
Qingyi Luo, Jian Chen, Yu Zhang, Jianhua Li, Xuan Su, Qinghui Wang, Yunchuan Ding. Prenat Diagn 2020
2
100

Right aortic arch in the fetus.
V Zidere, E G Tsapakis, I C Huggon, L D Allan. Ultrasound Obstet Gynecol 2006
63
66

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
283
66

Anatomic classification of the right aortic arch.
Sudesh Prabhu, Siddhant Mehra, Srikanth Kasturi, Rishi Tiwari, Abhijit Joshi, Colin John, Tom R Karl. Cardiol Young 2020
3
66

Postnatal Outcome and Associated Anomalies of Prenatally Diagnosed Right Aortic Arch with Concomitant Right Ductal Arch: A Systematic Review and Meta-Analysis.
Paolo Ivo Cavoretto, Alexandros Sotiriadis, Serena Girardelli, Silvia Spinillo, Massimo Candiani, Silvia Amodeo, Antonio Farina, Vlasta Fesslova. Diagnostics (Basel) 2020
3
66

Right aortic arch diagnosed antenatally: associations and outcome in 98 fetuses.
Joana O Miranda, Nicky Callaghan, Owen Miller, John Simpson, Gurleen Sharland. Heart 2014
39
66

Anomalies of the fetal aortic arch: a novel sonographic approach to in-utero diagnosis.
R Achiron, Z Rotstein, J Heggesh, M Bronshtein, S Zimand, S Lipitz, S Yagel. Ultrasound Obstet Gynecol 2002
88
66

Characteristics of prenatally detected right aortic arch cases in a single institution.
Melih Velipasaoglu, Metin Sentürk, Reyhan Ayaz, Barbaros Atesli, H Mete Tanir. J Obstet Gynaecol 2018
5
66

Perinatal outcomes and anomalies associated with fetal right aortic arch.
Ahmet Gül, Kemal Güngördük, Gökhan Yıldırım. J Turk Ger Gynecol Assoc 2012
8
66

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
8
66



Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome.
P J Scambler, A H Carey, R K Wyse, S Roach, J P Dumanski, M Nordenskjold, R Williamson. Genomics 1991
188
33

Screening for 22q11.2 deletion syndrome by two non-invasive prenatal testing methodologies: A case with discordant results.
Liang-Ming Lo, Chii-Shinn Shiau, Kuang-Chao Chen, S W S Shaw, Peter Benn. Taiwan J Obstet Gynecol 2019
1
100

An association study of PCQAP polymorphisms and schizophrenia.
Harinder K Sandhu, Nancy Hollenbeck, Thomas H Wassink, Robert A Philibert. Psychiatr Genet 2004
8
33




Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review.
Chih-Ping Chen, Jian-Pei Huang, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Jun-Wei Su, Yu-Ting Chen, Wen-Lin Chen, Wayseen Wang. Gene 2013
13
33

Chromosome 22q11.2 microdeletion syndrome.
Marion G Molesky. Neonatal Netw 2011
3
33


Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion.
Yen-Ni Chen, Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Pei-Chen Wu, Tung-Yao Chang, Peih-Shan Wu, Chien-Wen Yang, Wayseen Wang. Taiwan J Obstet Gynecol 2016
2
50

Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects.
Yu-Ling Kuo, Chih-Ping Chen, Liang-Kai Wang, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Shu-Yuan Chang. Taiwan J Obstet Gynecol 2014
6
33

Evidence for involvement of GNB1L in autism.
Ying-Zhang Chen, Mark Matsushita, Santhosh Girirajan, Mark Lisowski, Elizabeth Sun, Youngmee Sul, Raphael Bernier, Annette Estes, Geraldine Dawson, Nancy Minshew,[...]. Am J Med Genet B Neuropsychiatr Genet 2012
15
33

Prenatal diagnosis of mosaic 22q11.2 microdeletion.
Chih-Ping Chen, Schu-Rern Chern, Chen-Chi Lee, Shuan-Pei Lin, Tung-Yao Chang, Wayseen Wang. Prenat Diagn 2004
9
33

Association study between GNB1L and three major mental disorders in Chinese Han populations.
You Li, Qian Zhao, Ti Wang, Jie Liu, Junyan Li, Tao Li, Zhen Zeng, Guoyin Feng, Lin He, Yongyong Shi. Psychiatry Res 2011
12
33

Recurrent 22q11.2 deletion in a sibship suggestive of parental germline mosaicism in velocardiofacial syndrome.
P Sandrin-Garcia, C Macedo, L R Martelli, E S Ramos, M L Guion-Almeida, A Richieri-Costa, G A S Passos. Clin Genet 2002
30
33

A rare mosaic 22q11.2 microdeletion identified in a Chinese family with recurrent fetal conotruncal defects.
Weicheng Chen, Xiaodi Li, Liqun Sun, Wei Sheng, Guoying Huang. Mol Genet Genomic Med 2019
2
50

The velo-cardio-facial syndrome: a clinical and genetic analysis.
R J Shprintzen, R B Goldberg, D Young, L Wolford. Pediatrics 1981
233
33

Renal and urological tract malformations caused by a 22q11 deletion.
K Devriendt, A Swillen, J P Fryns, W Proesmans, M Gewillig. J Med Genet 1996
34
33

Genitourinary malformations in chromosome 22q11.2 deletion.
Hsi-Yang Wu, Susan L Rusnack, Richard D Bellah, Natalie Plachter, Donna M McDonald-McGinn, Elaine H Zackai, Douglas A Canning. J Urol 2002
33
33

Genomic disorders on chromosome 22.
Shihui Yu, William D Graf, Robert J Shprintzen. Curr Opin Pediatr 2012
15
33

Prenatal diagnosis of rearrangements in the fetal 22q11.2 region.
Suping Li, Yuxia Jin, Jing Yang, Li Yang, Ping Tang, Chiyan Zhou, Liping Wu, Jinhua Dong, Jie Chen, Huaxiang Shen. Mol Cytogenet 2020
4
33

Association study between CAG trinucleotide repeats in the PCQAP gene (PC2 glutamine/Q-rich-associated protein) and schizophrenia.
Alessandro De Luca, Emanuela Conti, Nicoletta Grifone, Francesca Amati, Gianfranco Spalletta, Carlo Caltagirone, Giuseppina Bonaviri, Augusto Pasini, Massimo Gennarelli, Bignotti Stefano,[...]. Am J Med Genet B Neuropsychiatr Genet 2003
14
33

22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect: prenatal diagnosis by array comparative genomic hybridization.
Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Fuu-Jen Tsai, Jonathan Kwei Hwang, Wayseen Wang. Taiwan J Obstet Gynecol 2009
13
33

The 22q11 deletion syndromes.
P J Scambler. Hum Mol Genet 2000
343
33

The UFD1L rs5992403 polymorphism is associated with age at onset of schizophrenia.
Vanessa Kiyomi Ota, Sintia Iole Belangero, Ary Gadelha, Fernanda Teixeira Bellucco, Denise Maria Christofolini, Tatiane Iris Mancini, Andrea Kelly Ribeiro-dos-Santos, Sidney Emanuel Santos, Jair de Jesus Mari, Rodrigo Affonseca Bressan,[...]. J Psychiatr Res 2010
8
33

Practice guidelines for performance of the routine mid-trimester fetal ultrasound scan.
L J Salomon, Z Alfirevic, V Berghella, C Bilardo, E Hernandez-Andrade, S L Johnsen, K Kalache, K-Y Leung, G Malinger, H Munoz,[...]. Ultrasound Obstet Gynecol 2011
462
33


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.