A citation-based method for searching scientific literature

Barbara A Bernhardt, Danielle Soucier, Karen Hanson, Melissa S Savage, Laird Jackson, Ronald J Wapner. Genet Med 2013
Times Cited: 129

List of shared articles

Times cited

Variants of uncertain significance in prenatal microarrays: a retrospective cohort study.
A H Mardy, A P Wiita, B V Wayman, K Drexler, T N Sparks, M E Norton. BJOG 2021

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

Information Women Choose to Receive About Prenatal Chromosomal Microarray Analysis.
Hagit Hochner, Hagit Daum, Liza Douiev, Naama Zvi, Ayala Frumkin, Michal Macarov, Adva Kimchi-Shaal, Nuphar Hacohen, Avital Eilat, Duha Faham,[...]. Obstet Gynecol 2020

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 D├ęsir,[...]. Prenat Diagn 2020

The utilization of prenatal microarray: A survey of current genetic counseling practices and barriers.
Leslie Durham, Ramesha Papanna, Blair Stevens, Sarah Noblin, David Rodriguez-Buritica, S Shahrukh Hashmi, Nevena Krstic. Prenat Diagn 2019

Ethical considerations in prenatal testing: Genomic testing and medical uncertainty.
Anastasia Richardson, Kelly E Ormond. Semin Fetal Neonatal Med 2018

Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study.
Jane L Halliday, Cecile Muller, Taryn Charles, Fiona Norris, Joanne Kennedy, Sharon Lewis, Bettina Meiser, Susan Donath, Zornitza Stark, George McGillivray,[...]. Eur J Hum Genet 2018

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

Whole Exome Sequencing: Applications in Prenatal Genetics.
Angie C Jelin, Neeta Vora. Obstet Gynecol Clin North Am 2018

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

Exploring the Issues Surrounding Clinical Exome Sequencing in the Prenatal Setting.
Swetha Narayanan, Bruce Blumberg, Marla L Clayman, Vivian Pan, Catherine Wicklund. J Genet Couns 2018

Impacts of variants of uncertain significance on parental perceptions of children after prenatal chromosome microarray testing.
Preeya Desai, Hannah Haber, Jessica Bulafka, Amita Russell, Rebecca Clifton, Julia Zachary, Seonjoo Lee, Tianshu Feng, Ronald Wapner, Catherine Monk,[...]. Prenat Diagn 2018

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

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