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Age group and sex differences in performance on a computerized neurocognitive battery in children age 8− 21. RC Gur, J Richard, ME Calkins, R Chiavacci, JA Hansen, WB Bilker, ... Neuropsychology 26 (2), 251, 2012 | 602 | 2012 |
Return of genomic results to research participants: the floor, the ceiling, and the choices in between GP Jarvik, LM Amendola, JS Berg, K Brothers, EW Clayton, W Chung, ... The American Journal of Human Genetics 94 (6), 818-826, 2014 | 433 | 2014 |
The Philadelphia Neurodevelopmental Cohort: A publicly available resource for the study of normal and abnormal brain development in youth TD Satterthwaite, JJ Connolly, K Ruparel, ME Calkins, C Jackson, ... Neuroimage 124, 1115-1119, 2016 | 340 | 2016 |
Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases YR Li, J Li, SD Zhao, JP Bradfield, FD Mentch, SM Maggadottir, C Hou, ... Nature medicine 21 (9), 1018-1027, 2015 | 279 | 2015 |
Design and anticipated outcomes of the eMERGE‐PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems LJ Rasmussen‐Torvik, SC Stallings, AS Gordon, B Almoguera, ... Clinical Pharmacology & Therapeutics 96 (4), 482-489, 2014 | 262 | 2014 |
The Philadelphia Neurodevelopmental Cohort: constructing a deep phenotyping collaborative ME Calkins, KR Merikangas, TM Moore, M Burstein, MA Behr, ... Journal of Child Psychology and Psychiatry 56 (12), 1356-1369, 2015 | 257 | 2015 |
Public attitudes toward consent and data sharing in biobank research: a large multi-site experimental survey in the US SC Sanderson, KB Brothers, ND Mercaldo, EW Clayton, ... The American Journal of Human Genetics 100 (3), 414-427, 2017 | 217 | 2017 |
The psychosis spectrum in a young US community sample: findings from the Philadelphia Neurodevelopmental Cohort ME Calkins, TM Moore, KR Merikangas, M Burstein, TD Satterthwaite, ... World Psychiatry 13 (3), 296-305, 2014 | 210 | 2014 |
Association of arrhythmia-related genetic variants with phenotypes documented in electronic medical records SL Van Driest, QS Wells, S Stallings, WS Bush, A Gordon, DA Nickerson, ... Jama 315 (1), 47-57, 2016 | 191 | 2016 |
Genetic variation among 82 pharmacogenes: the PGRNseq data from the eMERGE network WS Bush, DR Crosslin, A Owusu‐Obeng, J Wallace, B Almoguera, ... Clinical Pharmacology & Therapeutics 100 (2), 160-169, 2016 | 190 | 2016 |
GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network B Namjou, T Lingren, Y Huang, S Parameswaran, BL Cobb, IB Stanaway, ... BMC medicine 17, 1-19, 2019 | 134 | 2019 |
Practical challenges in integrating genomic data into the electronic health record AN Kho, LV Rasmussen, JJ Connolly, PL Peissig, J Starren, ... Genetics in Medicine 15 (10), 772-778, 2013 | 113 | 2013 |
Identification of four novel loci in asthma in European American and African American populations B Almoguera, L Vazquez, F Mentch, J Connolly, JA Pacheco, ... American journal of respiratory and critical care medicine 195 (4), 456-463, 2017 | 103 | 2017 |
Harmonizing clinical sequencing and interpretation for the eMERGE III network H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ... The American Journal of Human Genetics 105 (3), 588-605, 2019 | 95 | 2019 |
Genetic sharing and heritability of paediatric age of onset autoimmune diseases YR Li, SD Zhao, J Li, JP Bradfield, M Mohebnasab, L Steel, J Kobie, ... Nature communications 6 (1), 8442, 2015 | 87 | 2015 |
A Genome‐Wide Association Study of Autism Incorporating Autism Diagnostic Interview–Revised, Autism Diagnostic Observation Schedule, and Social Responsiveness Scale JJ Connolly, JT Glessner, H Hakonarson Child development 84 (1), 17-33, 2013 | 87 | 2013 |
Electronic health record based algorithm to identify patients with autism spectrum disorder T Lingren, P Chen, J Bochenek, F Doshi-Velez, P Manning-Courtney, ... PloS one 11 (7), e0159621, 2016 | 83 | 2016 |
The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism D Hadley, Z Wu, C Kao, A Kini, A Mohamed-Hadley, K Thomas, ... Nature communications 5 (1), 4074, 2014 | 73 | 2014 |
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations YR Li, JT Glessner, BP Coe, J Li, M Mohebnasab, X Chang, J Connolly, ... Nature communications 11 (1), 255, 2020 | 70 | 2020 |