A citation-based method for searching scientific literature

Allyn McConkie Rosell, Loren D M Pena, Kelly Schoch, Rebecca Spillmann, Jennifer Sullivan, Stephen R Hooper, Yong-Hui Jiang, Nicolas Mathey-Andrews, David B Goldstein, Vandana Shashi. J Genet Couns 2016
Times Cited: 59



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: 852




List of shared articles



Times cited

Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples.
Allyn McConkie-Rosell, Kelly Schoch, Jennifer Sullivan, Rebecca C Spillmann, Heidi Cope, Queenie K-G Tan, Christina G S Palmer, Stephen R Hooper, Vandana Shashi. J Genet Couns 2022
0

Comparison of medical management and genetic counseling options pre- and post-whole exome sequencing for patients with positive and negative results.
Margret Matias, Katie Wusik, Derek Neilson, Xue Zhang, C Alexander Valencia, Kathleen Collins. J Genet Couns 2019
6

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
40

How do providers discuss the results of pediatric exome sequencing with families?
Sarah A Walser, Allison Werner-Lin, Rebecca Mueller, Victoria A Miller, Sawona Biswas, Barbara A Bernhardt. Per Med 2017
10

Homozygous mutation in PRUNE1 in an Oji-Cree male with a complex neurological phenotype.
Gregory Costain, Andrea Shugar, Pradeep Krishnan, Saadet Mahmutoglu, Suzanne Laughlin, Peter Kannu. Am J Med Genet A 2017
16

Patient perspectives on whole-genome sequencing for undiagnosed diseases.
Debra L Boeldt, Cynthia Cheung, Lauren Ariniello, Burcu F Darst, Sarah Topol, Nicholas J Schork, Athena Philis-Tsimikas, Ali Torkamani, Addie L Fortmann, Cinnamon S Bloss. Per Med 2017
5

Gratitude, protective buffering, and cognitive dissonance: How families respond to pediatric whole exome sequencing in the absence of actionable results.
Allison Werner-Lin, Lori Zaspel, Mae Carlson, Rebecca Mueller, Sarah A Walser, Ria Desai, Barbara A Bernhardt. Am J Med Genet A 2018
15

Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact.
J Wynn, R Ottman, J Duong, A L Wilson, P Ahimaz, J Martinez, R Rabin, E Rosen, R Webster, C Au,[...]. Clin Genet 2018
27

Hope versus reality: Parent expectations of genomic testing.
Katherine E Donohue, Siobhan M Dolan, Dana Watnick, Katie M Gallagher, Jacqueline A Odgis, Sabrina A Suckiel, Nehama Teitelman, Bruce D Gelb, Eimear E Kenny, Melissa P Wasserstein,[...]. Patient Educ Couns 2021
4