A citation-based method for searching scientific literature

Elizabeth A Normand, Joseph T Alaimo, Ignatia B Van den Veyver. Fertil Steril 2018
Times Cited: 9







List of co-cited articles
13 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
33

The Genetics of Infertility: Current Status of the Field.
Michelle Zorrilla, Alexander N Yatsenko. Curr Genet Med Rep 2013
47
33

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
592
22

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
117
22

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
740
22

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
76
22

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
104
22

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
720
22

Comprehensive carrier genetic test using next-generation deoxyribonucleic acid sequencing in infertile couples wishing to conceive through assisted reproductive technology.
Julio Martin, Asan, Yuting Yi, Trinidad Alberola, Beatriz Rodríguez-Iglesias, Jorge Jiménez-Almazán, Qin Li, Huiqian Du, Pilar Alama, Amparo Ruiz,[...]. Fertil Steril 2015
35
22


Recent developments in genetics and medically assisted reproduction: from research to clinical applications.
J C Harper, K Aittomäki, P Borry, M C Cornel, G de Wert, W Dondorp, J Geraedts, L Gianaroli, K Ketterson, I Liebaers,[...]. Eur J Hum Genet 2018
35
22

National, regional, and global trends in infertility prevalence since 1990: a systematic analysis of 277 health surveys.
Maya N Mascarenhas, Seth R Flaxman, Ties Boerma, Sheryl Vanderpoel, Gretchen A Stevens. PLoS Med 2012
613
22

ACMG clinical laboratory standards for next-generation sequencing.
Heidi L Rehm, Sherri J Bale, Pinar Bayrak-Toydemir, Jonathan S Berg, Kerry K Brown, Joshua L Deignan, Michael J Friez, Birgit H Funke, Madhuri R Hegde, Elaine Lyon. Genet Med 2013
504
22

Ultrasound findings provide clues to investigate founder mutations expressed as runs of homozygosity in chromosomal microarray studies.
Hagit Daum, Israela Lerer, Ayala Frumkin, Daniel Rosenak, Nili Yanai, Shay Porat, Simcha Yagel, Vardiella Meiner. Prenat Diagn 2018
5
20

Detection of clinically relevant copy number variants with whole-exome sequencing.
Joep de Ligt, Philip M Boone, Rolph Pfundt, Lisenka E L M Vissers, Todd Richmond, Joel Geoghegan, Kathleen O'Moore, Nicole de Leeuw, Christine Shaw, Han G Brunner,[...]. Hum Mutat 2013
75
11

Exome sequence read depth methods for identifying copy number changes.
Latha Kadalayil, Sajjad Rafiq, Matthew J J Rose-Zerilli, Reuben J Pengelly, Helen Parker, David Oscier, Jonathan C Strefford, William J Tapper, Jane Gibson, Sarah Ennis,[...]. Brief Bioinform 2015
43
11

Chromosomal microarray analysis and prenatal diagnosis.
Jamie O Lo, Brian L Shaffer, Cori D Feist, Aaron B Caughey. Obstet Gynecol Surv 2014
11
11


Increased nuchal translucency thickness and normal karyotype: time for parental reassurance.
C M Bilardo, M A Müller, E Pajkrt, S A Clur, M M van Zalen, E K Bijlsma. Ultrasound Obstet Gynecol 2007
88
11


Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies.
Christina L Alamillo, Zöe Powis, Kelly Farwell, Layla Shahmirzadi, Elaine C Weltmer, John Turocy, Thomas Lowe, Christine Kobelka, Emily Chen, Donald Basel,[...]. Prenat Diagn 2015
52
11

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
25
11

Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families.
R Harripaul, N Vasli, A Mikhailov, M A Rafiq, K Mittal, C Windpassinger, T I Sheikh, A Noor, H Mahmood, S Downey,[...]. Mol Psychiatry 2018
63
11

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
52
11

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
101
11

Increased nuchal translucency in euploid fetuses--what should we be telling the parents?
C M Bilardo, E Timmerman, E Pajkrt, M van Maarle. Prenat Diagn 2010
61
11

Termination of pregnancy due to fetal abnormalities performed after 32 weeks' gestation: survey of 57 fetuses from a single medical center.
Noa Feldman, Yaakov Melcer, Edward Hod, Orna Levinsohn-Tavor, Ran Svirsky, Ron Maymon. J Matern Fetal Neonatal Med 2018
5
20

The sequence of sequencers: The history of sequencing DNA.
James M Heather, Benjamin Chain. Genomics 2016
222
11

Genomic landscape of oxidative DNA damage and repair reveals regioselective protection from mutagenesis.
Anna R Poetsch, Simon J Boulton, Nicholas M Luscombe. Genome Biol 2018
19
11

The Role of Next-Generation Sequencing in Pharmacogenetics and Pharmacogenomics.
Ute I Schwarz, Markus Gulilat, Richard B Kim. Cold Spring Harb Perspect Med 2019
14
11

BMDExpress 2: enhanced transcriptomic dose-response analysis workflow.
Jason R Phillips, Daniel L Svoboda, Arpit Tandon, Shyam Patel, Alex Sedykh, Deepak Mav, Byron Kuo, Carole L Yauk, Longlong Yang, Russell S Thomas,[...]. Bioinformatics 2019
34
11

Cell-Free DNA as a Diagnostic Blood-Based Biomarker for Colorectal Cancer: A Systematic Review.
Joel Petit, Georgia Carroll, Tiffany Gould, Peter Pockney, Matthew Dun, Rodney J Scott. J Surg Res 2019
17
11

Testicular transcriptome alterations in zebrafish (Danio rerio) exposure to 17β-estradiol.
Yao Zheng, Julin Yuan, Shunlong Meng, Jiazhang Chen, Zhimin Gu. Chemosphere 2019
7
14

Identification of RNA biomarkers for chemical safety screening in mouse embryonic stem cells using RNA deep sequencing analysis.
Hidenori Tani, Jun-Ichi Takeshita, Hiroshi Aoki, Kaoru Nakamura, Ryosuke Abe, Akinobu Toyoda, Yasunori Endo, Sadaaki Miyamoto, Masashi Gamo, Hiroaki Sato,[...]. PLoS One 2017
5
20

Utilizing toxicogenomic data to understand chemical mechanism of action in risk assessment.
Vickie S Wilson, Nagalakshmi Keshava, Susan Hester, Deborah Segal, Weihsueh Chiu, Chad M Thompson, Susan Y Euling. Toxicol Appl Pharmacol 2013
32
11

Three-Dimensional (3D) HepaRG Spheroid Model With Physiologically Relevant Xenobiotic Metabolism Competence and Hepatocyte Functionality for Liver Toxicity Screening.
Sreenivasa C Ramaiahgari, Suramya Waidyanatha, Darlene Dixon, Michael J DeVito, Richard S Paules, Stephen S Ferguson. Toxicol Sci 2017
16
11

Technical guide for applications of gene expression profiling in human health risk assessment of environmental chemicals.
Julie A Bourdon-Lacombe, Ivy D Moffat, Michelle Deveau, Mainul Husain, Scott Auerbach, Daniel Krewski, Russell S Thomas, Pierre R Bushel, Andrew Williams, Carole L Yauk. Regul Toxicol Pharmacol 2015
37
11

Ultra-deep sequencing detects ovarian cancer cells in peritoneal fluid and reveals somatic TP53 mutations in noncancerous tissues.
Jeffrey D Krimmel, Michael W Schmitt, Maria I Harrell, Kathy J Agnew, Scott R Kennedy, Mary J Emond, Lawrence A Loeb, Elizabeth M Swisher, Rosa Ana Risques. Proc Natl Acad Sci U S A 2016
84
11


Comparison of RNA-seq and microarray-based models for clinical endpoint prediction.
Wenqian Zhang, Ying Yu, Falk Hertwig, Jean Thierry-Mieg, Wenwei Zhang, Danielle Thierry-Mieg, Jian Wang, Cesare Furlanello, Viswanath Devanarayan, Jie Cheng,[...]. Genome Biol 2015
148
11


Drug-induced liver injury: recent advances in diagnosis and risk assessment.
Gerd A Kullak-Ublick, Raul J Andrade, Michael Merz, Peter End, Andreas Benesic, Alexander L Gerbes, Guruprasad P Aithal. Gut 2017
160
11

Tissue- and strain-specific effects of a genotoxic carcinogen 1,3-butadiene on chromatin and transcription.
Jennifer W Israel, Grace A Chappell, Jeremy M Simon, Sebastian Pott, Alexias Safi, Lauren Lewis, Paul Cotney, Hala S Boulos, Wanda Bodnar, Jason D Lieb,[...]. Mamm Genome 2018
9
11

Identification of tubular injury microRNA biomarkers in urine: comparison of next-generation sequencing and qPCR-based profiling platforms.
Rounak Nassirpour, Sachin Mathur, Mark M Gosink, Yizheng Li, Ahmed M Shoieb, Joanna Wood, Shawn P O'Neil, Bruce L Homer, Laurence O Whiteley. BMC Genomics 2014
61
11


Coming of age: ten years of next-generation sequencing technologies.
Sara Goodwin, John D McPherson, W Richard McCombie. Nat Rev Genet 2016
11

What People Want to Know About Their Genes: A Critical Review of the Literature on Large-Scale Genome Sequencing Studies.
Courtney L Scherr, Sharon Aufox, Amy A Ross, Sanjana Ramesh, Catherine A Wicklund, Maureen Smith. Healthcare (Basel) 2018
8
12

TBBPA exposure during a sensitive developmental window produces neurobehavioral changes in larval zebrafish.
Jiangfei Chen, Robert L Tanguay, Yanyan Xiao, Derik E Haggard, Xiaoqing Ge, Yinhang Jia, Yi Zheng, Qiaoxiang Dong, Changjiang Huang, Kuangfei Lin. Environ Pollut 2016
38
11

The Rat microRNA body atlas; Evaluation of the microRNA content of rat organs through deep sequencing and characterization of pancreas enriched miRNAs as biomarkers of pancreatic toxicity in the rat and dog.
Aaron Smith, John Calley, Sachin Mathur, Hui-Rong Qian, Han Wu, Mark Farmen, Florian Caiment, Pierre R Bushel, Jianying Li, Craig Fisher,[...]. BMC Genomics 2016
30
11

Nanopore-based fourth-generation DNA sequencing technology.
Yanxiao Feng, Yuechuan Zhang, Cuifeng Ying, Deqiang Wang, Chunlei Du. Genomics Proteomics Bioinformatics 2015
135
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.