A citation-based method for searching scientific literature

Jonathan S Berg, Muin J Khoury, James P Evans. Genet. Med. 2011
Times Cited: 328

Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay, Narayanan Veeraraghavan, Alicia Hawes, Theodore Chiang, Magalie Leduc, Joke Beuten, Jing Zhang, Weimin He, Jennifer Scull, Alecia Willis, Megan Landsverk, William J Craigen, Mir Reza Bekheirnia, Asbjorg Stray-Pedersen, Pengfei Liu, Shu Wen, Wendy Alcaraz, Hong Cui, Magdalena Walkiewicz, Jeffrey Reid, Matthew Bainbridge, Ankita Patel, Eric Boerwinkle, Arthur L Beaudet, James R Lupski, Sharon E Plon, Richard A Gibbs, Christine M Eng. JAMA 2014
Times Cited: 661

List of shared articles

Times cited

Beyond medically actionable results: an analytical pipeline for decreasing the burden of returning all clinically significant secondary findings.
Emma Reble, Mariana Gutierrez Salazar, Kathleen-Rose Zakoor, Sam Khalouei, Marc Clausen, Rita Kodida, Salma Shickh, Chloe Mighton, Iris Cohn, Kasmintan A Schrader,[...]. Hum. Genet. 2020

Diagnostic yield and clinical utility of whole exome sequencing using an automated variant prioritization system, EVIDENCE.
Go Hun Seo, Taeho Kim, In Hee Choi, Jung-Young Park, Jungsul Lee, Sehwan Kim, Dhong-Gun Won, Arum Oh, Yena Lee, Jeongmin Choi,[...]. Clin. Genet. 2020

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019

Genetics professionals' attitudes toward prenatal exome sequencing.
Casey E Brew, Brian A Castro, Vivian Pan, Alexa Hart, Bruce Blumberg, Catherine Wicklund. J Genet Couns 2019

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

Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing.
Ahmed Alfares, Taghrid Aloraini, Lamia Al Subaie, Abdulelah Alissa, Ahmed Al Qudsi, Ahmed Alahmad, Fuad Al Mutairi, Abdulrahman Alswaid, Ali Alothaim, Wafaa Eyaid,[...]. Genet. Med. 2018

New technologies to uncover the molecular basis of disorders of sex development.
Hayk Barseghyan, Emmanuèle C Délot, Eric Vilain. Mol. Cell. Endocrinol. 2018

My46: a Web-based tool for self-guided management of genomic test results in research and clinical settings.
Holly K Tabor, Seema M Jamal, Joon-Ho Yu, Julia M Crouch, Aditi G Shankar, Karin M Dent, Nick Anderson, Damon A Miller, Brett T Futral, Michael J Bamshad. Genet. Med. 2017

Clinical and Counseling Experiences of Early Adopters of Whole Exome Sequencing.
Shubhangi Arora, Eden Haverfield, Gabriele Richard, Susanne B Haga, Rachel Mills. J Genet Couns 2016