A citation-based method for searching scientific literature

Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Sarah E Soden, Julie A Cakici, Suzanne M Herd, Greyson Twist, Aaron Noll, Mitchell Creed, Patria M Alba, Shannon L Carpenter, Mark A Clements, Ryan T Fischer, J Allyson Hays, Howard Kilbride, Ryan J McDonough, Jamie L Rosterman, Sarah L Tsai, Lee Zellmer, Emily G Farrow, Stephen F Kingsmore. Lancet Respir Med 2015
Times Cited: 178



Ozge Ceyhan-Birsoy, Jaclyn B Murry, Kalotina Machini, Matthew S Lebo, Timothy W Yu, Shawn Fayer, Casie A Genetti, Talia S Schwartz, Pankaj B Agrawal, Richard B Parad, Ingrid A Holm, Amy L McGuire, Robert C Green, Heidi L Rehm, Alan H Beggs. Am J Hum Genet 2019
Times Cited: 60




List of shared articles



Times cited

Genetic testing for unexplained perinatal disorders.
Thomas Hays, Ronald J Wapner. Curr Opin Pediatr 2021
1

Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).
Kandamurugu Manickam, Monica R McClain, Laurie A Demmer, Sawona Biswas, Hutton M Kearney, Jennifer Malinowski, Lauren J Massingham, Danny Miller, Timothy W Yu, Fuki M Hisama. Genet Med 2021
1

Prospective, phenotype-driven selection of critically ill neonates for rapid exome sequencing is associated with high diagnostic yield.
Cynthia S Gubbels, Grace E VanNoy, Jill A Madden, Deborah Copenheaver, Sandra Yang, Monica H Wojcik, Nina B Gold, Casie A Genetti, Joan Stoler, Richard B Parad,[...]. Genet Med 2020
26

Clinical utility of ultra-rapid whole-genome sequencing in an infant with atypical presentation of WT1-associated nephrotic syndrome type 4.
Erica Sanford, Terence Wong, Katarzyna A Ellsworth, Elizabeth Ingulli, Stephen F Kingsmore. Cold Spring Harb Mol Case Stud 2020
1

Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing.
Stephen F Kingsmore, Audrey Henderson, Mallory J Owen, Michelle M Clark, Christian Hansen, David Dimmock, Christina D Chambers, Laura L Jeliffe-Pawlowski, Charlotte Hobbs. NPJ Genom Med 2020
0

An RCT of Rapid Genomic Sequencing among Seriously Ill Infants Results in High Clinical Utility, Changes in Management, and Low Perceived Harm.
David P Dimmock, Michelle M Clark, Mary Gaughran, Julie A Cakici, Sara A Caylor, Christina Clarke, Michele Feddock, Shimul Chowdhury, Lisa Salz, Cynthia Cheung,[...]. Am J Hum Genet 2020
11

A Prospective Study of Parental Perceptions of Rapid Whole-Genome and -Exome Sequencing among Seriously Ill Infants.
Julie A Cakici, David P Dimmock, Sara A Caylor, Mary Gaughran, Christina Clarke, Cynthia Triplett, Michelle M Clark, Stephen F Kingsmore, Cinnamon S Bloss. Am J Hum Genet 2020
9

Measurement of genetic diseases as a cause of mortality in infants receiving whole genome sequencing.
Stephen F Kingsmore, Audrey Henderson, Mallory J Owen, Michelle M Clark, Christian Hansen, David Dimmock, Christina D Chambers, Laura L Jeliffe-Pawlowski, Charlotte Hobbs. NPJ Genom Med 2020
3

A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill Infants.
Stephen F Kingsmore, Julie A Cakici, Michelle M Clark, Mary Gaughran, Michele Feddock, Sergey Batalov, Matthew N Bainbridge, Jeanne Carroll, Sara A Caylor, Christina Clarke,[...]. Am J Hum Genet 2019
68

Clinical utility of genomic sequencing.
Matthew B Neu, Kevin M Bowling, Gregory M Cooper. Curr Opin Pediatr 2019
6

FDA oversight of NSIGHT genomic research: the need for an integrated systems approach to regulation.
Laura V Milko, Flavia Chen, Kee Chan, Amy M Brower, Pankaj B Agrawal, Alan H Beggs, Jonathan S Berg, Steven E Brenner, Ingrid A Holm, Barbara A Koenig,[...]. NPJ Genom Med 2019
0