A citation-based method for searching scientific literature

Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
Times Cited: 184



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

Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
S Stern, N Hacohen, V Meiner, S Yagel, S Zenvirt, S Shkedi-Rafid, M Macarov, D V Valsky, S Porat, N Yanai,[...]. Ultrasound Obstet Gynecol 2021
8

The role of chromosomal microarray analysis among fetuses with normal karyotype and single system anomaly or nonspecific sonographic findings.
Annie Sy Hui, Matthew Hoi Kin Chau, Yiu Man Chan, Ye Cao, Angel Hw Kwan, Xiaofan Zhu, Yvonne K Kwok, Zihan Chen, Terence T Lao, Kwong Wai Choy,[...]. Acta Obstet Gynecol Scand 2021
1

Detection of copy number variation associated with ventriculomegaly in fetuses using single nucleotide polymorphism arrays.
Huili Xue, Aili Yu, Na Lin, Xuemei Chen, Min Lin, Yan Wang, Hailong Huang, Liangpu Xu. Sci Rep 2021
1

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

Chromosomal Microarray Analysis for the Prenatal Diagnosis in Fetuses with Nasal Bone Hypoplasia: A Retrospective Cohort Study.
Hailong Huang, Meiying Cai, Wei Ma, Na Lin, Liangpu Xu. Risk Manag Healthc Policy 2021
0

Chromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing.
Xiaoqing Wu, Ying Li, Na Lin, Xiaorui Xie, Linjuan Su, Meiying Cai, Yuan Lin, Linshuo Wang, Meiying Wang, Liangpu Xu,[...]. J Cell Mol Med 2021
1

"It's probably nothing, but…" Couples' experiences of pregnancy following an uncertain prenatal genetic result.
Stina Lou, Kirsten Lomborg, Celine Lewis, Sam Riedijk, Olav Bjørn Petersen, Ida Vogel. Acta Obstet Gynecol Scand 2020
6

Nuchal translucency of 3.0-3.4 mm an indication for NIPT or microarray? Cohort analysis and literature review.
Olav B Petersen, Eric Smith, Diane Van Opstal, Marike Polak, Maarten F C M Knapen, Karin E M Diderich, Caterina M Bilardo, Lidia R Arends, Ida Vogel, Malgorzata I Srebniak. Acta Obstet Gynecol Scand 2020
4

Prenatally detected copy number variants in a national cohort: A postnatal follow-up study.
Joke Muys, Yves Jacquemyn, Bettina Blaumeiser, Laura Bourlard, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Anne De Leener, Marjan De Rademaeker, Julie Désir,[...]. Prenat Diagn 2020
1

Role of late amniocentesis in the era of modern genomic technologies.
H Daum, A Ben David, M Nadjari, S Zenvirt, S Helman, N Yanai, V Meiner, S Yagel, A Frumkin, S Shkedi Rafid. Ultrasound Obstet Gynecol 2019
7


Chromosomal microarray vs. NIPS: analysis of 5541 low-risk pregnancies.
Lena Sagi-Dain, Lital Cohen Vig, Sarit Kahana, Shiri Yacobson, Tamar Tenne, Ifat Agmon-Fishman, Cochava Klein, Reut Matar, Lina Basel-Salmon, Idit Maya. Genet Med 2019
31

Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis.
Matthew Hoi Kin Chau, Ye Cao, Yvonne Ka Yin Kwok, Samantha Chan, Yiu Man Chan, Huilin Wang, Zhenjun Yang, Hoi Kin Wong, Tak Yeung Leung, Kwong Wai Choy. Am J Obstet Gynecol 2019
12


When genotype is not predictive of phenotype: implications for genetic counseling based on 21,594 chromosomal microarray analysis examinations.
Idit Maya, Reuven Sharony, Shiri Yacobson, Sarit Kahana, Josepha Yeshaya, Tamar Tenne, Ifaat Agmon-Fishman, Lital Cohen-Vig, Yael Goldberg, Racheli Berger,[...]. Genet Med 2018
27

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

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

The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
Joke Muys, Bettina Blaumeiser, Yves Jacquemyn, Claude Bandelier, Nathalie Brison, Saskia Bulk, Patrizia Chiarappa, Winnie Courtens, Anne De Leener, Marjan De Rademaeker,[...]. Prenat Diagn 2018
15

Chromosomal Microarray Analysis Results From Pregnancies With Various Ultrasonographic Anomalies.
Lena Sagi-Dain, Idit Maya, Adi Reches, Ayala Frumkin, Julia Grinshpun-Cohen, Reeval Segel, Esther Manor, Morad Khayat, Tamar Tenne, Ehud Banne,[...]. Obstet Gynecol 2018
14

Prenatal diagnosis of susceptibility loci for neurodevelopmental disorders - genetic counseling and pregnancy outcome in 57 cases.
Lutgarde Govaerts, Malgorzata Srebniak, Karin Diderich, Marieke Joosten, Sam Riedijk, Maarten Knapen, Attie Go, Dimitri Papatsonis, Katja de Graaf, Toon Toolenaar,[...]. Prenat Diagn 2017
7