A citation-based method for searching scientific literature

H Sun, T Yi, X Hao, H Yan, J Wang, Q Li, X Gu, X Zhou, S Wang, X Wang, P Wan, L Han, J Chen, H Zhu, H Zhang, Y He. Ultrasound Obstet Gynecol 2020
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
66

Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study.
Jenny Lord, Dominic J McMullan, Ruth Y Eberhardt, Gabriele Rinck, Susan J Hamilton, Elizabeth Quinlan-Jones, Elena Prigmore, Rebecca Keelagher, Sunayna K Best, Georgina K Carey,[...]. Lancet 2019
144
41

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.
Slavé Petrovski, Vimla Aggarwal, Jessica L Giordano, Melissa Stosic, Karen Wou, Louise Bier, Erica Spiegel, Kelly Brennan, Nicholas Stong, Vaidehi Jobanputra,[...]. Lancet 2019
112
41

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
41

Lessons from exome sequencing in prenatally diagnosed heart defects: A basis for prenatal testing.
Dominik S Westphal, Gloria S Leszinski, Esther Rieger-Fackeldey, Elisabeth Graf, Gregor Weirich, Thomas Meitinger, Eva Ostermayer, Renate Oberhoffer, Matias Wagner. Clin Genet 2019
9
44

Promises, pitfalls and practicalities of prenatal whole exome sequencing.
Sunayna Best, Karen Wou, Neeta Vora, Ignatia B Van der Veyver, Ronald Wapner, Lyn S Chitty. Prenat Diagn 2018
130
33

Clinical application of targeted next-generation sequencing in fetuses with congenital heart defect.
P Hu, F Qiao, Y Wang, L Meng, X Ji, C Luo, T Xu, R Zhou, J Zhang, B Yu,[...]. Ultrasound Obstet Gynecol 2018
16
33

Whole-exome sequencing on deceased fetuses with ultrasound anomalies: expanding our knowledge of genetic disease during fetal development.
Carin L Yates, Kristin G Monaghan, Deborah Copenheaver, Kyle Retterer, Julie Scuffins, Cathlin R Kucera, Bethany Friedman, Gabriele Richard, Jane Juusola. Genet Med 2017
59
33

Exome sequencing in the assessment of congenital malformations in the fetus and neonate.
Fionnuala Mone, Elizabeth Quinlan-Jones, Andrew K Ewer, Mark D Kilby. Arch Dis Child Fetal Neonatal Ed 2019
7
42

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.
Jason Homsy, Samir Zaidi, Yufeng Shen, James S Ware, Kaitlin E Samocha, Konrad J Karczewski, Steven R DePalma, David McKean, Hiroko Wakimoto, Josh Gorham,[...]. Science 2015
331
25

Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder.
Elizabeth A Normand, Alicia Braxton, Salma Nassef, Patricia A Ward, Francesco Vetrini, Weimin He, Vipulkumar Patel, Chunjing Qu, Lauren E Westerfield, Samantha Stover,[...]. Genome Med 2018
45
25

Molecular autopsy by trio exome sequencing (ES) and postmortem examination in fetuses and neonates with prenatally identified structural anomalies.
Elizabeth Quinlan-Jones, Jenny Lord, Denise Williams, Sue Hamilton, Tamas Marton, Ruth Y Eberhardt, Gabriele Rinck, Elena Prigmore, Rebecca Keelagher, Dominic J McMullan,[...]. Genet Med 2019
18
25

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.
Sheng Chih Jin, Jason Homsy, Samir Zaidi, Qiongshi Lu, Sarah Morton, Steven R DePalma, Xue Zeng, Hongjian Qi, Weni Chang, Michael C Sierant,[...]. Nat Genet 2017
260
25

From diagnostic yield to clinical impact: a pilot study on the implementation of prenatal exome sequencing in routine care.
Maayke A de Koning, Monique C Haak, Phebe N Adama van Scheltema, Cacha M P C D Peeters-Scholte, Tamara T Koopmann, Esther A R Nibbeling, Emmelien Aten, Nicolette S den Hollander, Claudia A L Ruivenkamp, Mariëtte J V Hoffer,[...]. Genet Med 2019
15
25

Prenatal exome sequencing in anomalous fetuses: new opportunities and challenges.
Neeta L Vora, Bradford Powell, Alicia Brandt, Natasha Strande, Emily Hardisty, Kelly Gilmore, Ann Katherine M Foreman, Kirk Wilhelmsen, Chris Bizon, Jason Reilly,[...]. Genet Med 2017
80
25

Intellectual disability and non-compaction cardiomyopathy with a de novo NONO mutation identified by exome sequencing.
Eyal Reinstein, Shay Tzur, Rony Cohen, Concetta Bormans, Doron M Behar. Eur J Hum Genet 2016
8
37

Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO.
Daryl A Scott, Andres Hernandez-Garcia, Mahshid S Azamian, Valerie K Jordan, Bum Jun Kim, Molly Starkovich, Jinglan Zhang, Lee-Jun Wong, Sandra A Darilek, Amy M Breman,[...]. J Med Genet 2017
9
33

Expanding the genetic and clinical spectrum of the NONO-associated X-linked intellectual disability syndrome.
Colleen M Carlston, Steven B Bleyl, Ashley Andrews, Lindsay Meyers, Sara Brown, Pinar Bayrak-Toydemir, James F Bale, Lorenzo D Botto. Am J Med Genet A 2019
6
50


Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohorts.
Emmi Helle, Aldo Córdova-Palomera, Tiina Ojala, Priyanka Saha, Praneetha Potiny, Stefan Gustafsson, Erik Ingelsson, Michael Bamshad, Deborah Nickerson, Jessica X Chong,[...]. Genet Epidemiol 2019
12
16

Identification of de novo mutations and rare variants in hypoplastic left heart syndrome.
M Iascone, R Ciccone, L Galletti, D Marchetti, F Seddio, A R Lincesso, L Pezzoli, A Vetro, D Barachetti, L Boni,[...]. Clin Genet 2012
70
16

Fetal exome sequencing: yield and limitations in a tertiary referral center.
H Daum, V Meiner, O Elpeleg, T Harel. Ultrasound Obstet Gynecol 2019
20
16

Reproductive genetic counseling challenges associated with diagnostic exome sequencing in a large academic private reproductive genetic counseling practice.
Lauren E Westerfield, Samantha R Stover, Veena S Mathur, Salma A Nassef, Tiffiney G Carter, Yaping Yang, Christine M Eng, Ignatia B Van den Veyver. Prenat Diagn 2015
29
16

De novo mutations in histone-modifying genes in congenital heart disease.
Samir Zaidi, Murim Choi, Hiroko Wakimoto, Lijiang Ma, Jianming Jiang, John D Overton, Angela Romano-Adesman, Robert D Bjornson, Roger E Breitbart, Kerry K Brown,[...]. Nature 2013
517
16

Genetics and Genomics of Congenital Heart Disease.
Samir Zaidi, Martina Brueckner. Circ Res 2017
140
16


Exome sequencing improves genetic diagnosis of structural fetal abnormalities revealed by ultrasound.
Keren J Carss, Sarah C Hillman, Vijaya Parthiban, Dominic J McMullan, Eamonn R Maher, Mark D Kilby, Matthew E Hurles. Hum Mol Genet 2014
103
16

Genomic study of severe fetal anomalies and discovery of GREB1L mutations in renal agenesis.
Sarah Boissel, Catherine Fallet-Bianco, David Chitayat, Valérie Kremer, Christina Nassif, Françoise Rypens, Marie-Ange Delrue, Dorothée Dal Soglio, Luc L Oligny, Natalie Patey,[...]. Genet Med 2018
30
16

Prenatal and perinatal history in Kabuki Syndrome.
Chen E Rosenberg, Tara Daly, Christina Hung, Irene Hsueh, Andrew W Lindsley, Olaf Bodamer. Am J Med Genet A 2020
3
66

Diagnosis of lethal or prenatal-onset autosomal recessive disorders by parental exome sequencing.
Karen L Stals, Matthew Wakeling, Júlia Baptista, Richard Caswell, Andrew Parrish, Julia Rankin, Carolyn Tysoe, Garan Jones, Adam C Gunning, Hana Lango Allen,[...]. Prenat Diagn 2018
32
16

Importance of complete phenotyping in prenatal whole exome sequencing.
Mahmoud Aarabi, Olivia Sniezek, Huaiyang Jiang, Devereux N Saller, Daniel Bellissimo, Svetlana A Yatsenko, Aleksandar Rajkovic. Hum Genet 2018
26
16

Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES).
Gordon K C Leung, Christopher C Y Mak, Jasmine L F Fung, Wilfred H S Wong, Mandy H Y Tsang, Mullin H C Yu, Steven L C Pei, K S Yeung, Gary T K Mok, C P Lee,[...]. BMC Med Genomics 2018
15
16

Mutations in NONO lead to syndromic intellectual disability and inhibitory synaptic defects.
Dennis Mircsof, Maéva Langouët, Marlène Rio, Sébastien Moutton, Karine Siquier-Pernet, Christine Bole-Feysot, Nicolas Cagnard, Patrick Nitschke, Ludmila Gaspar, Matej Žnidarič,[...]. Nat Neurosci 2015
40
16

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
799
16

Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis.
Denise van der Linde, Elisabeth E M Konings, Maarten A Slager, Maarten Witsenburg, Willem A Helbing, Johanna J M Takkenberg, Jolien W Roos-Hesselink. J Am Coll Cardiol 2011
16

The prevalence of genetic diagnoses in fetuses with severe congenital heart defects.
Amber E L van Nisselrooij, Malou A Lugthart, Sally-Ann Clur, Ingeborg H Linskens, Eva Pajkrt, Lukas A Rammeloo, Lieke Rozendaal, Nico A Blom, Jan M M van Lith, Alida C Knegt,[...]. Genet Med 2020
10
20

Impact of MYH6 variants in hypoplastic left heart syndrome.
Aoy Tomita-Mitchell, Karl D Stamm, Donna K Mahnke, Min-Su Kim, Pip M Hidestrand, Huan Ling Liang, Mary A Goetsch, Mats Hidestrand, Pippa Simpson, Andrew N Pelech,[...]. Physiol Genomics 2016
34
16

Deficiency of NONO is associated with impaired cardiac function and fibrosis in mice.
Xingli Xu, Hong Jiang, Yue Lu, Meng Zhang, Cheng Cheng, Fei Xue, Meng Zhang, Cheng Zhang, Mei Ni, Yun Zhang. J Mol Cell Cardiol 2019
4
50

Genetics, Clinical Features, and Long-Term Outcome of Noncompaction Cardiomyopathy.
Jaap I van Waning, Kadir Caliskan, Yvonne M Hoedemaekers, Karin Y van Spaendonck-Zwarts, Annette F Baas, S Matthijs Boekholdt, Joost P van Melle, Arco J Teske, Folkert W Asselbergs, Ad P C M Backx,[...]. J Am Coll Cardiol 2018
108
16

Clinical and genetic insights into non-compaction: a meta-analysis and systematic review on 7598 individuals.
Elham Kayvanpour, Farbod Sedaghat-Hamedani, Weng-Tein Gi, Oguz Firat Tugrul, Ali Amr, Jan Haas, Feng Zhu, Philipp Ehlermann, Lorenz Uhlmann, Hugo A Katus,[...]. Clin Res Cardiol 2019
20
16

Genetic diagnosis by whole exome capture and massively parallel DNA sequencing.
Murim Choi, Ute I Scholl, Weizhen Ji, Tiewen Liu, Irina R Tikhonova, Paul Zumbo, Ahmet Nayir, Ayşin Bakkaloğlu, Seza Ozen, Sami Sanjad,[...]. Proc Natl Acad Sci U S A 2009
833
16

Hypoplastic left heart syndrome: current considerations and expectations.
Jeffrey A Feinstein, D Woodrow Benson, Anne M Dubin, Meryl S Cohen, Dawn M Maxey, William T Mahle, Elfriede Pahl, Juan Villafañe, Ami B Bhatt, Lynn F Peng,[...]. J Am Coll Cardiol 2012
270
16

Systematic Review of Genotype-Phenotype Correlations in Noncompaction Cardiomyopathy.
Jaap I van Waning, Joost Moesker, Daphne Heijsman, Eric Boersma, Danielle Majoor-Krakauer. J Am Heart Assoc 2019
17
16

Targeted panel sequencing in adult patients with left ventricular non-compaction reveals a large genetic heterogeneity.
Pascale Richard, Flavie Ader, Maguelonne Roux, Erwan Donal, Jean-Christophe Eicher, Nadia Aoutil, Olivier Huttin, Christine Selton-Suty, Damien Coisne, Guillaume Jondeau,[...]. Clin Genet 2019
20
16

Characteristics of Cardiac Phenotype in Prenatal Familial Cases With NONO Mutations.
Hairui Sun, Xiaoxue Zhou, Xiaoyan Hao, Ye Zhang, Hongjia Zhang, Yihua He. Circ Genom Precis Med 2020
2
100

Cardiac Phenotypes, Genetics, and Risks in Familial Noncompaction Cardiomyopathy.
Jaap I van Waning, Kadir Caliskan, Michelle Michels, Arend F L Schinkel, Alexander Hirsch, Michiel Dalinghaus, Yvonne M Hoedemaekers, Marja W Wessels, Arne S IJpma, Robert M W Hofstra,[...]. J Am Coll Cardiol 2019
25
16

Clinical utility of exome sequencing in the prenatal diagnosis of congenital anomalies: A Review.
Fionnuala Mone, Elizabeth Quinlan-Jones, Mark D Kilby. Eur J Obstet Gynecol Reprod Biol 2018
11
18

COngenital heart disease and the Diagnostic yield with Exome sequencing (CODE) study: prospective cohort study and systematic review.
F Mone, R Y Eberhardt, R K Morris, M E Hurles, D J McMullan, E R Maher, J Lord, L S Chitty, J L Giordano, R J Wapner,[...]. Ultrasound Obstet Gynecol 2021
5
40

Prenatal exome sequencing in fetuses with congenital heart defects.
Ru Li, Fang Fu, Qiuxia Yu, Dan Wang, Xiangyi Jing, Yongling Zhang, Fucheng Li, Fatao Li, Jin Han, Min Pan,[...]. Clin Genet 2020
2
100

Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management.
Natalie Chandler, Sunayna Best, Jane Hayward, Francesca Faravelli, Sahar Mansour, Emma Kivuva, Dagmar Tapon, Alison Male, Catherine DeVile, Lyn S Chitty. Genet Med 2018
57
16


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.