A citation-based method for searching scientific literature

Anna Maria Werling, Edna Grünblatt, Beatrice Oneda, Elise Bobrowski, Ronnie Gundelfinger, Regina Taurines, Marcel Romanos, Anita Rauch, Susanne Walitza. J Neural Transm (Vienna) 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Clinical aspects of prenatally detected congenital heart malformations and the yield of chromosomal microarray analysis.
Rivka Sukenik-Halevy, Shay Sukenik, Arie Koifman, Yoav Alpert, Reli Hershkovitz, Alex Levi, Tal Biron-Shental. Prenat Diagn 2016
11
100

Congenital Heart Disease: Prenatal Diagnosis and Genetic Associations.
Maeve K Hopkins, Lorraine Dugoff, Jeffrey A Kuller. Obstet Gynecol Surv 2019
1
100

Chromosomal Aberrations in Pediatric Patients with Developmental Delay/Intellectual Disability: A Single-Center Clinical Investigation.
Ting Hu, Zhu Zhang, Jiamin Wang, Qinqin Li, Hongmei Zhu, Yi Lai, He Wang, Shanling Liu. Biomed Res Int 2019
5
100

Cardiovascular malformations among preterm infants.
Kirsty Tanner, Nilofer Sabrine, Christopher Wren. Pediatrics 2005
142
100

Attitudes Towards Prenatal Genetic Counseling, Prenatal Genetic Testing, and Termination of Pregnancy among Southeast and East Asian Women in the United States.
Ginger J Tsai, Carrie A Cameron, Jennifer L Czerwinski, Hector Mendez-Figueroa, Susan K Peterson, Sarah Jane Noblin. J Genet Couns 2017
9
100

Chromosome 15q13 microduplication in a fetus with cardiac rhabdomyoma: a case report.
Chen-Zhao Lin, Bi-Ru Qi, Jian-Su Hu, Yu-Dian Huang, Xiu-Qiong Huang. Mol Cytogenet 2019
3
100


A fetus with Kabuki syndrome 2 detected by chromosomal microarray analysis.
Chen-Zhao Lin, Bi-Ru Qi, Jian-Su Hu, Xiu-Qiong Huang. Int J Clin Exp Pathol 2020
4
100

Chromosomal uniparental disomy 16 and fetal intrauterine growth restriction.
Xie Yingjun, Hu Zhiyang, Lin Linhua, Su Fangming, Huang Linhuan, Tan Jinfeng, Pang Qianying, Sun Xiaofang. Eur J Obstet Gynecol Reprod Biol 2017
9
100

Changing Landscape of Congenital Heart Disease.
Berto J Bouma, Barbara J M Mulder. Circ Res 2017
65
100

Detection of copy number variants using chromosomal microarray analysis for the prenatal diagnosis of congenital heart defects with normal karyotype.
Tingting Song, Shanning Wan, Yu Li, Ying Xu, Yinghui Dang, Yunyun Zheng, Chunyan Li, Jiao Zheng, Biliang Chen, Jianfang Zhang. J Clin Lab Anal 2019
7
100

Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies.
Elizabeth Goldmuntz, Prasuna Paluru, Joseph Glessner, Hakon Hakonarson, Jaclyn A Biegel, Peter S White, Xiaowu Gai, Tamim H Shaikh. Congenit Heart Dis 2011
52
100


Congenital heart disease: a global public health concern.
Joseph W Rossano. Lancet Child Adolesc Health 2020
5
100

Cardiovascular anomalies in Turner syndrome: spectrum, prevalence, and cardiac MRI findings in a pediatric and young adult population.
Hee Kyung Kim, William Gottliebson, Kan Hor, Philippe Backeljauw, Iris Gutmark-Little, Shelia R Salisbury, Judy M Racadio, Kathy Helton-Skally, Robert Fleck. AJR Am J Roentgenol 2011
72
100

Chromosome 16p13.11 Microdeletion Syndrome in a Newborn: A Case Study.
Amanda Elizabeth Smith, Amy Jnah, Desi Newberry. Neonatal Netw 2018
3
100

Prenatal diagnosis of congenital heart disease: A review of current knowledge.
Nathalie Jeanne Bravo-Valenzuela, Alberto Borges Peixoto, Edward Araujo Júnior. Indian Heart J 2018
18
100

Global birth prevalence of congenital heart defects 1970-2017: updated systematic review and meta-analysis of 260 studies.
Yingjuan Liu, Sen Chen, Liesl Zühlke, Graeme C Black, Mun-Kit Choy, Ningxiu Li, Bernard D Keavney. Int J Epidemiol 2019
129
100

1q21.1 microduplication in a patient with mental impairment and congenital heart defect.
Guowen Sun, Zhiping Tan, Liangliang Fan, Jian Wang, Yifeng Yang, Weizhi Zhang. Mol Med Rep 2015
6
100


Congenital heart disease and genetic syndromes: new insights into molecular mechanisms.
Giulio Calcagni, Marta Unolt, Maria Cristina Digilio, Anwar Baban, Paolo Versacci, Marco Tartaglia, Antonio Baldini, Bruno Marino. Expert Rev Mol Diagn 2017
17
100

The association between congenital heart disease and Down syndrome in prenatal life.
D Paladini, A Tartaglione, A Agangi, A Teodoro, F Forleo, A Borghese, P Martinelli. Ultrasound Obstet Gynecol 2000
52
100


22q11.2 microduplication syndrome and juvenile glaucoma.
Federico Di Matteo, Paolo Bettin, Giulia Ferrari, Marina Fiori, Carlo Ciampi, Emanuela Manfredini, Alessandro Rabiolo, Francesco Bandello. Ophthalmic Genet 2018
2
100

Genetic basis of congenital cardiovascular malformations.
Seema R Lalani, John W Belmont. Eur J Med Genet 2014
44
100

Pediatric prenatal diagnosis of congenital heart disease.
Stacy A S Killen, Jessica H Mouledoux, Ann Kavanaugh-McHugh. Curr Opin Pediatr 2014
10
100

Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next-generation sequencing.
Xiangyu Zhu, Jie Li, Tong Ru, Yaping Wang, Yan Xu, Ying Yang, Xing Wu, David S Cram, Yali Hu. Prenat Diagn 2016
37
100

Cardiac Surgery in Patients With Trisomy 13 and 18: An Analysis of The Society of Thoracic Surgeons Congenital Heart Surgery Database.
David S Cooper, Kyle W Riggs, Farhan Zafar, Jeffrey P Jacobs, Kevin D Hill, Sara K Pasquali, Sara K Swanson, Sarah K Gelehrter, Amelia Wallace, Marshall L Jacobs,[...]. J Am Heart Assoc 2019
14
100

Congenital heart disease: emerging themes linking genetics and development.
Shiaulou Yuan, Samir Zaidi, Martina Brueckner. Curr Opin Genet Dev 2013
34
100

Next-generation sequencing and the impact on prenatal diagnosis.
Rhiannon Mellis, Natalie Chandler, Lyn S Chitty. Expert Rev Mol Diagn 2018
14
100

Genetics of congenital heart disease.
Jonathan J Edwards, Bruce D Gelb. Curr Opin Cardiol 2016
27
100

Genetic testing practices in infants with congenital heart disease.
Jessica A Connor, Robert B Hinton, Erin M Miller, Kristen L Sund, Jennifer G Ruschman, Stephanie M Ware. Congenit Heart Dis 2014
29
100

Copy number variants detection by microarray and multiplex ligation-dependent probe amplification in congenital heart diseases.
Orsolya Nagy, Katalin Szakszon, Brigitta Orsolya Biró, Gábor Mogyorósy, Dóra Nagy, Bálint Nagy, István Balogh, Anikó Ujfalusi. J Biotechnol 2019
4
100

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.
Amy Breman, Amber N Pursley, Patricia Hixson, Weimin Bi, Patricia Ward, Carlos A Bacino, Chad Shaw, James R Lupski, Arthur Beaudet, Ankita Patel,[...]. Prenat Diagn 2012
74
100

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
100

Long-Term Outcomes in Single-Ventricle Congenital Heart Disease.
Matthew E Oster, Jessica H Knight, Divya Suthar, Omayma Amin, Lazaros K Kochilas. Circulation 2018
9
100

Chromosome microarray analysis in the investigation of children with congenital heart disease.
Xiao-Li Wu, Ru Li, Fang Fu, Min Pan, Jin Han, Xin Yang, Yong-Ling Zhang, Fa-Tao Li, Can Liao. BMC Pediatr 2017
11
100

Analysis of Imprinted Gene Regulation.
David A Skaar, Randy L Jirtle. Methods Mol Biol 2017
2
100

A New Patient with Potocki-Lupski Syndrome: A Literature Review.
Andrea Domenico Praticò, Raffaele Falsaperla, Renata Rizzo, Martino Ruggieri, Alberto Verrotti, Piero Pavone. J Pediatr Genet 2018
3
100

Molecular screening for 22Q11.2 deletion syndrome in patients with congenital heart disease.
Janaína Huber, Vivian Catarino Peres, Alexandre Luz de Castro, Tiago Jeronimo dos Santos, Lauro da Fontoura Beltrão, Angélica Cerveira de Baumont, Silvia Liliana Cossio, Tiago Pires Dalberto, Mariluce Riegel, Andrés Delgado Cañedo,[...]. Pediatr Cardiol 2014
10
100

1q21.1 Microduplication expression in adults.
Alessia Dolcetti, Candice K Silversides, Christian R Marshall, Anath C Lionel, Dimitri J Stavropoulos, Stephen W Scherer, Anne S Bassett. Genet Med 2013
58
100

What Is New in Genetics of Congenital Heart Defects?
Maria Cristina Digilio, Bruno Marino. Front Pediatr 2016
18
100

[Clinical value of genome-wide high resolution chromosomal microarray analysis in etiological study of fetuses with congenital heart defects].
Xiaoli Wu, Fang Fu, Ru Li, Min Pan, Jin Han, Li Zhen, Xin Yang, Yongling Zhang, Fatao Li, Can Liao. Zhonghua Fu Chan Ke Za Zhi 2014
1
100

Congenital Heart Surgery on In-Hospital Mortality in Trisomy 13 and 18.
Katherine A Kosiv, Jeffrey M Gossett, Shasha Bai, R Thomas Collins. Pediatrics 2017
34
100

Congenital heart defects in recurrent reciprocal 1q21.1 deletion and duplication syndromes: rare association with pulmonary valve stenosis.
M Cristina Digilio, Laura Bernardini, Federica Consoli, Francesca R Lepri, M Grazia Giuffrida, Anwar Baban, Cecilia Surace, Rosangela Ferese, Adriano Angioni, Antonio Novelli,[...]. Eur J Med Genet 2013
24
100

1q21.1 microduplication: large verbal-nonverbal performance discrepancy and ddPCR assays of HYDIN/HYDIN2 copy number.
Jean Xavier, Bo Zhou, Frédéric Bilan, Xianglong Zhang, Brigitte Gilbert-Dussardier, Sylvie Viaux-Savelon, Reenal Pattni, Steve S Ho, David Cohen, Douglas F Levinson,[...]. NPJ Genom Med 2018
4
100

Congenital heart disease and aneuploidy.
R C Wimalasundera, H M Gardiner. Prenat Diagn 2004
38
100

Complex genetics and the etiology of human congenital heart disease.
Bruce D Gelb, Wendy K Chung. Cold Spring Harb Perspect Med 2014
78
100


Advances in the Genetics of Congenital Heart Disease: A Clinician's Guide.
Gillian M Blue, Edwin P Kirk, Eleni Giannoulatou, Gary F Sholler, Sally L Dunwoodie, Richard P Harvey, David S Winlaw. J Am Coll Cardiol 2017
56
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.