A citation-based method for searching scientific literature

Jonathan L A Callaway, Lisa G Shaffer, Lyn S Chitty, Jill A Rosenfeld, John A Crolla. Prenat Diagn 2013
Times Cited: 89



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, Susan Klugman, Thomas Scholl, Joe Leigh Simpson, Kimberly McCall, Vimla S Aggarwal, Brian Bunke, Odelia Nahum, Ankita Patel, Allen N Lamb, Elizabeth A Thom, Arthur L Beaudet, David H Ledbetter, Lisa G Shaffer, Laird Jackson. N Engl J Med 2012
Times Cited: 643




List of shared articles



Times cited




Cost-effectiveness analysis of chromosomal microarray as a primary test for prenatal diagnosis in Hong Kong.
Claudia Ching Yan Chung, Kelvin Yuen Kwong Chan, Pui Wah Hui, Patrick Kwok Cheung Au, Wai Keung Tam, Samuel Kai Man Li, Gordon Ka Chun Leung, Jasmine Lee Fong Fung, Marcus Chun Yin Chan, Ho Ming Luk,[...]. BMC Pregnancy Childbirth 2020
2


Fetal Exome Sequencing on the Horizon.
Karen Wou, Isabelle DeBie, June Carroll, Jo-Ann Brock, R Douglas Wilson. J Obstet Gynaecol Can 2019
5

Application of chromosome microarray analysis in prenatal diagnosis.
Mingjing Xia, Xinhong Yang, Jing Fu, Zhenjuan Teng, Yan Lv, Lixia Yu. BMC Pregnancy Childbirth 2020
1


Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong.
Anita S Y Kan, Elizabeth T Lau, W F Tang, Sario S Y Chan, Simon C K Ding, Kelvin Y K Chan, C P Lee, Pui Wah Hui, Brian H Y Chung, K Y Leung,[...]. PLoS One 2014
28

Practice guideline: joint CCMG-SOGC recommendations for the use of chromosomal microarray analysis for prenatal diagnosis and assessment of fetal loss in Canada.
Christine M Armour, Shelley Danielle Dougan, Jo-Ann Brock, Radha Chari, Bernie N Chodirker, Isabelle DeBie, Jane A Evans, William T Gibson, Elena Kolomietz, Tanya N Nelson,[...]. J Med Genet 2018
28


Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing.
Liubing Lan, Lingna She, Bosen Zhang, Yanhong He, Zhiyuan Zheng. J Gene Med 2021
1

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

Cell-free fetal DNA screening for detection of microdeletion syndromes: a cost-effectiveness analysis.
Carmen M Avram, Brian L Shaffer, Teresa N Sparks, Allison J Allen, Aaron B Caughey. J Matern Fetal Neonatal Med 2021
3

Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing.
Jia Zhou, Ziying Yang, Jun Sun, Lipei Liu, Xinyao Zhou, Fengxia Liu, Ya Xing, Shuge Cui, Shiyi Xiong, Xiaoyu Liu,[...]. Genes (Basel) 2021
0

Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray results.
Lena Sagi-Dain, Idit Maya, Tzipora Falik-Zaccai, Michal Feingold-Zadok, Dorit Lev, Hagit Yonath, Ehud Kaliner, Ayala Frumkin, Shay Ben Shachar, Amihood Singer. Eur J Obstet Gynecol Reprod Biol 2018
4

A French Approach to Test Fetuses with Ultrasound Abnormalities Using a Customized Microarray as First-Tier Genetic Test.
Valérie Malan, Jean-Michel Lapierre, Matthieu Egloff, Didier Goidin, Marie-Paule Beaujard, Marie-Laure Maurin, Tania Attié-Bitach, Bettina Bessières, Jean-Pierre Bernard, Philippe Roth,[...]. Cytogenet Genome Res 2015
14

Rapid whole exome sequencing in pregnancies to identify the underlying genetic cause in fetuses with congenital anomalies detected by ultrasound imaging.
Chantal Deden, Kornelia Neveling, Dimitra Zafeiropopoulou, Christian Gilissen, Rolph Pfundt, Tuula Rinne, Nicole de Leeuw, Brigitte Faas, Thatjana Gardeitchik, Suzanne C E H Sallevelt,[...]. Prenat Diagn 2020
7

Copy number variants, aneuploidies, and human disease.
Christa Lese Martin, Brianne E Kirkpatrick, David H Ledbetter. Clin Perinatol 2015
33

Fetal cardiac abnormalities: Genetic etiologies to be considered.
Florencia Petracchi, Silvina Sisterna, Laura Igarzabal, Louise Wilkins-Haug. Prenat Diagn 2019
3

The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland.
Yi Wu, Yanlin Wang, Jiong Tao, Xu Han, Xinrong Zhao, Chunmin Liu, Li Gao, Weiwei Cheng. Eur J Obstet Gynecol Reprod Biol 2017
6

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

Is Prenatal Diagnosis Necessary for Fetal Isolated Nasal Bone Absence or Hypoplasia?
Feng Zhang, Wei Long, Qin Zhou, Jing Wang, Ye Shi, Jianbing Liu, Qiuwei Wang. Int J Gen Med 2021
0


Indications for genetic testing leading to termination of pregnancy.
Ran Svirsky, Marina Pekar-Zlotin, Uri Rozovski, Ron Maymon. Arch Gynecol Obstet 2019
0

Integrating Microarrays into Routine Prenatal Diagnosis: Determinants of Decision Making.
Marcos Cordoba, Stephanie Andriole, Shara M Evans, David Britt, Melissa Chu Lam, Mark I Evans. Fetal Diagn Ther 2016
3

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing.
Barbara A Bernhardt, Katherine Kellom, Alexandra Barbarese, W Andrew Faucett, Ronald J Wapner. J Genet Couns 2014
37

Clinical Utility of SNP Array Analysis in Prenatal Diagnosis: A Cohort Study of 5000 Pregnancies.
Jingjing Xiang, Yang Ding, Xiaoyan Song, Jun Mao, Minjuan Liu, Yinghua Liu, Chao Huang, Qin Zhang, Ting Wang. Front Genet 2020
3

What's New in Prenatal Genetics? A Review of Current Recommendations and Guidelines.
Annalisa L Post, Amy T Mottola, Jeffrey A Kuller. Obstet Gynecol Surv 2017
1

Copy number variation sequencing for comprehensive diagnosis of chromosome disease syndromes.
Desheng Liang, Ying Peng, Weigang Lv, Linbei Deng, Yanghui Zhang, Haoxian Li, Pu Yang, Jianguang Zhang, Zhuo Song, Genming Xu,[...]. J Mol Diagn 2014
62

Subchromosomal anomalies in small for gestational-age fetuses and newborns.
Ying Ma, Yan Pei, Chenghong Yin, Yuxin Jiang, Jingjing Wang, Xiaofei Li, Lin Li, Karl Oliver Kagan, Qingqing Wu. Arch Gynecol Obstet 2019
2

Dilemmas in genetic counseling for low-penetrance neuro-susceptibility loci detected on prenatal chromosomal microarray analysis.
Dana Brabbing-Goldstein, Adi Reches, Ran Svirsky, Anat Bar-Shira, Yuval Yaron. Am J Obstet Gynecol 2018
13

The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis.
Melissa Stosic, Brynn Levy, Ronald Wapner. Obstet Gynecol Clin North Am 2018
18


Discrepancy of QF-PCR, CMA and karyotyping on a de novo case of mosaic isodicentric Y chromosomes.
Yuan Liu, Li Guo, Hanbiao Chen, Jian Lu, Jingjing Hu, Xianzheng Li, Xing Li, Ting Wang, Fengzhen Li, Aihua Yin. Mol Cytogenet 2019
3

Chromosomal microarray findings in pregnancies with an isolated pelvic kidney.
Lena Sagi-Dain, Amihood Singer, Ayala Frumkin, Adel Shalata, Arie Koifman, Reeval Segel, Lilach Benyamini, Shlomit Rienstein, Morad Kahyat, Reuven Sharony,[...]. J Perinat Med 2018
2

Chromosomal Microarrays in Prenatal Diagnosis: Time for a Change of Policy?
Peter Miny, Friedel Wenzel, Sevgi Tercanli, Isabel Filges. Microarrays (Basel) 2013
8

Benefit versus risk of chromosomal microarray analysis performed in pregnancies with normal and positive prenatal screening results: A retrospective study.
Rami Moshonov, Keren Hod, Bella Azaria, Ifat Abadi-Korek, Rachel Berger, Mordechai Shohat. PLoS One 2021
0

Prenatal diagnosis: the clinical usefulness of array comparative genomic hybridization.
Marta Freitas, Joel Pinto, Carla Ramalho, Sofia Dória. Porto Biomed J 2018
1

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

Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.
Kitty K Lo, Evangelia Karampetsou, Christopher Boustred, Fiona McKay, Sarah Mason, Melissa Hill, Vincent Plagnol, Lyn S Chitty. Am J Hum Genet 2016
67

Clinical utility of array comparative genomic hybridisation in prenatal setting.
Luca Lovrecic, Ziga Iztok Remec, Marija Volk, Gorazd Rudolf, Karin Writzl, Borut Peterlin. BMC Med Genet 2016
9

The use of chromosomal microarray for prenatal diagnosis.
Lorraine Dugoff, Mary E Norton, Jeffrey A Kuller. Am J Obstet Gynecol 2016
62

Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012-2019).
Jenny Patterson, Diana Wellesley, Sian Morgan, Deirdre Cilliers, Stephanie Allen, Carol A Gardiner. Prenat Diagn 2021
0


Cell-free fetal DNA: the new tool in fetal medicine.
T R Everett, L S Chitty. Ultrasound Obstet Gynecol 2015
17

Detection of copy number variants with chromosomal microarray in 10 377 pregnancies at a single laboratory.
Yi-Hui Lin, Yiin-Jeng Jong, Pin-Chia Huang, Chris Tsai. Acta Obstet Gynecol Scand 2020
3

Noninvasive prenatal screening or advanced diagnostic testing: caveat emptor.
Mark I Evans, Ronald J Wapner, Richard L Berkowitz. Am J Obstet Gynecol 2016
47

Prenatal diagnosis of chromosomal imbalances.
Diana G Wellesley, Anneke Lucassen. Arch Dis Child Fetal Neonatal Ed 2014
4

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