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



Times Cited
  Times     Co-cited
Similarity


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
646
46

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
46

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
38

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
516
30

Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis.
Lijuan Sun, Qingqing Wu, Shi-Wen Jiang, Yani Yan, Xin Wang, Juan Zhang, Yan Liu, Ling Yao, Yuqing Ma, Li Wang. Biomed Res Int 2015
25
30

Chromosome abnormality incidence in fetuses with cerebral ventriculomegaly.
C Gezer, A Ekin, M Ozeren, C E Taner, O Ozer, A Koc, M Bilgin, N S Gezer. J Obstet Gynaecol 2014
17
30

Epidemiology, natural history, progression, and postnatal outcome of severe fetal ventriculomegaly.
Therese Hannon, Peter W G Tennant, Judith Rankin, Stephen C Robson. Obstet Gynecol 2012
41
30

Comprehensive genetic analysis of pregnancy loss by chromosomal microarrays: outcomes, benefits, and challenges.
Trilochan Sahoo, Natasa Dzidic, Michelle N Strecker, Sara Commander, Mary K Travis, Charles Doherty, R Weslie Tyson, Arturo E Mendoza, Mary Stephenson, Craig A Dise,[...]. Genet Med 2017
61
30





Prevalence, natural history, and clinical outcome of mild to moderate ventriculomegaly.
Farah Sethna, Peter W G Tennant, Judith Rankin, Stephen C Robson. Obstet Gynecol 2011
42
23

Prenatal diagnosis by chromosomal microarray analysis.
Brynn Levy, Ronald Wapner. Fertil Steril 2018
89
23

Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities.
Suzanne Drury, Hywel Williams, Natalie Trump, Christopher Boustred, Nicholas Lench, Richard H Scott, Lyn S Chitty. Prenat Diagn 2015
111
15

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
15

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
62
15


Severe apparently isolated fetal ventriculomegaly and neurodevelopmental outcome.
Mathilde Letouzey, Alexandra Chadie, Marie Brasseur-Daudruy, François Proust, Eric Verspyck, Pascal Boileau, Stéphane Marret. Prenat Diagn 2017
10
20

Reference ranges for fetal ventricular width: a non-normal approach.
L J Salomon, J P Bernard, Y Ville. Ultrasound Obstet Gynecol 2007
40
15

The significance of fetal ventriculomegaly: etiology, short- and long-term outcomes.
Pietro Gaglioti, Manuela Oberto, Tullia Todros. Prenat Diagn 2009
83
15

Copy Number Variations with Isolated Fetal Ventriculomegaly.
P Hu, Y Wang, R Sun, L Cao, X Chen, C Liu, C Luo, D Ma, W Wang, X Fu,[...]. Curr Mol Med 2017
11
18

Mild fetal lateral cerebral ventriculomegaly: clinical course and outcome.
B Bromley, F D Frigoletto, B R Benacerraf. Am J Obstet Gynecol 1991
109
15

A prospective study of fetuses with isolated ventriculomegaly investigated by antenatal sonography and in utero MR imaging.
P D Griffiths, M J Reeves, J E Morris, G Mason, S A Russell, M N J Paley, E H Whitby. AJNR Am J Neuroradiol 2010
79
15

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.
Holly N Cukier, Nicole D Dueker, Susan H Slifer, Joycelyn M Lee, Patrice L Whitehead, Eminisha Lalanne, Natalia Leyva, Ioanna Konidari, Ryan C Gentry, William F Hulme,[...]. Mol Autism 2014
136
15

Karyotype versus microarray testing for genetic abnormalities after stillbirth.
Uma M Reddy, Grier P Page, George R Saade, Robert M Silver, Vanessa R Thorsten, Corette B Parker, Halit Pinar, Marian Willinger, Barbara J Stoll, Josefine Heim-Hall,[...]. N Engl J Med 2012
140
15

Autism spectrum disorder is associated with ventricular enlargement in a low birth weight population.
Tammy Z Movsas, Jennifer A Pinto-Martin, Agnes H Whitaker, Judith F Feldman, John M Lorenz, Steven J Korzeniewski, Susan E Levy, Nigel Paneth. J Pediatr 2013
45
15

Cortical overgrowth in fetuses with isolated ventriculomegaly.
Vanessa Kyriakopoulou, Deniz Vatansever, Samia Elkommos, Sarah Dawson, Amy McGuinness, Joanna Allsop, Zoltán Molnár, Joseph Hajnal, Mary Rutherford. Cereb Cortex 2014
37
15

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
301
15

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
23
15

Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs.
Madita Schumann, Andrea Hofmann, Sophia K Krutzke, Alina C Hilger, Florian Marsch, Dietlinde Stienen, Ulrich Gembruch, Michael Ludwig, Waltraut M Merz, Heiko Reutter. J Neurodev Disord 2016
8
25

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.
S C Hillman, D J McMullan, G Hall, F S Togneri, N James, E J Maher, C H Meller, D Williams, R J Wapner, E R Maher,[...]. Ultrasound Obstet Gynecol 2013
154
15

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
146
15

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
52
15

ACOG and SMFM guidelines for prenatal diagnosis: Is karyotyping really sufficient?
Sara B Hay, Trilochan Sahoo, Mary K Travis, Karine Hovanes, Natasa Dzidic, Charles Doherty, Michelle N Strecker. Prenat Diagn 2018
31
15

Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.
I Filges, E Nosova, E Bruder, S Tercanli, K Townsend, W T Gibson, B Röthlisberger, K Heinimann, J G Hall, C Y Gregory-Evans,[...]. Clin Genet 2014
67
7

Epidemiology of congenital diaphragmatic hernia in Europe: a register-based study.
Mark R McGivern, Kate E Best, Judith Rankin, Diana Wellesley, Ruth Greenlees, Marie-Claude Addor, Larraitz Arriola, Hermien de Walle, Ingeborg Barisic, Judit Beres,[...]. Arch Dis Child Fetal Neonatal Ed 2015
114
7

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
798
7

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
814
7


Prenatal whole exome sequencing: the views of clinicians, scientists, genetic counsellors and patient representatives.
Elizabeth Quinlan-Jones, Mark D Kilby, Sheila Greenfield, Michael Parker, Dominic McMullan, Matthew E Hurles, Sarah C Hillman. Prenat Diagn 2016
27
7

Implementing Non-Invasive Prenatal Diagnosis (NIPD) in a National Health Service Laboratory; From Dominant to Recessive Disorders.
Suzanne Drury, Sarah Mason, Fiona McKay, Kitty Lo, Christopher Boustred, Lucy Jenkins, Lyn S Chitty. Adv Exp Med Biol 2016
16
7

Prenatal whole-genome sequencing--is the quest to know a fetus's future ethical?
Ilana R Yurkiewicz, Bruce R Korf, Lisa Soleymani Lehmann. N Engl J Med 2014
19
7

A novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis--further evidence of genotype-phenotype correlation.
Suzanne Drury, Christopher Boustred, Mehmet Tekman, Horia Stanescu, Robert Kleta, Nicholas Lench, Lyn S Chitty, Richard H Scott. Am J Med Genet A 2014
23
7

Offering prenatal diagnostic tests: European guidelines for clinical practice [corrected].
Heather Skirton, Lesley Goldsmith, Leigh Jackson, Celine Lewis, Lyn Chitty. Eur J Hum Genet 2014
26
7

Summarizing and correcting the GC content bias in high-throughput sequencing.
Yuval Benjamini, Terence P Speed. Nucleic Acids Res 2012
412
7


Monitoring the prenatal detection of structural fetal congenital anomalies in England and Wales: register-based study.
Patricia A Boyd, Ann M Tonks, Judith Rankin, Catherine Rounding, Diana Wellesley, Elizabeth S Draper. J Med Screen 2011
35
7

The real cost of sequencing: higher than you think!
Andrea Sboner, Xinmeng Jasmine Mu, Dov Greenbaum, Raymond K Auerbach, Mark B Gerstein. Genome Biol 2011
188
7

Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.
Jennifer J Johnston, Wendy S Rubinstein, Flavia M Facio, David Ng, Larry N Singh, Jamie K Teer, James C Mullikin, Leslie G Biesecker. Am J Hum Genet 2012
159
7


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.