| Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis MD Burkhalter, A Sridhar, P Sampaio, R Jacinto, MS Burczyk, C Donow, ... The Journal of clinical investigation 129 (7), 2841-2855, 2019 | 46 | 2019 |
| Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes Study SM Ware, JD Wilkinson, M Tariq, JA Schubert, A Sridhar, SD Colan, L Shi, ... Journal of the American Heart Association 10 (9), e017731, 2021 | 39 | 2021 |
| The genetic architecture of pediatric cardiomyopathy SM Ware, S Bhatnagar, PJ Dexheimer, JD Wilkinson, A Sridhar, X Fan, ... The American Journal of Human Genetics 109 (2), 282-298, 2022 | 31 | 2022 |
| Recurrent copy number variants associated with bronchopulmonary dysplasia A Ahmad, S Bhattacharya, A Sridhar, AM Iqbal, TJ Mariani Pediatric research 79 (6), 940-945, 2016 | 15 | 2016 |
| Cardiac Troponin I–Interacting Kinase Affects Cardiomyocyte S-Phase Activity but Not Cardiomyocyte Proliferation SP Reuter, MH Soonpaa, D Field, E Simpson, M Rubart-von der Lohe, ... Circulation 147 (2), 142-153, 2023 | 11 | 2023 |
| Competence Network for Congenital Heart Defects, I.; Hempel, M.; Walther, P.; et al. Imbalanced mitochondrial function provokes heterotaxy via aberrant ciliogenesis MD Burkhalter, A Sridhar, P Sampaio, R Jacinto, MS Burczyk, C Donow, ... J. Clin. Investig 129, 2841-2855, 2019 | 8 | 2019 |
| Congenital heart defects caused by FOXJ1 MB Padua, BM Helm, JR Wells, AM Smith, HM Bellchambers, A Sridhar, ... Human Molecular Genetics, ddad065, 2023 | 4 | 2023 |
| Analytic Validation of Optical Genome Mapping in Hematological Malignancies AWC Pang, K Kosco, NS Sahajpal, A Sridhar, J Hauenstein, B Clifford, ... Biomedicines 11 (12), 3263, 2023 | 3 | 2023 |
| Clinical Validation of Optical Genome Mapping for the Detection of Structural Variations in Hematological Malignancies AC Pang, K Kosco, N Sahajpal, A Sridhar, J Hauenstein, B Clifford, ... medRxiv, 2022.12. 27.22283973, 2022 | 3 | 2022 |
| Phenotype, but Not Genotype, Determines Survival in Pediatric Dilated Cardiomyopathy: A Study From the NHLBI-Funded Pediatric Cardiomyopathy Registry PF Kantor, SM Ware, L Shi, SA Webber, WK Chung, TM Lee, B Aronow, ... Circulation 138 (Suppl_1), A14210-A14210, 2018 | 1 | 2018 |
| THE FREQUENCY OF MUTATIONS IN KNOWN CARDIOMYOPATHY GENES AMONG CHILDREN WITH HYPERTROPHIC CARDIOMYOPATHY: THE NATIONAL HEART, LUNG AND BLOOD INSTITUTE-FUNDED MULTICENTER … E Pahl, S Ware, L Shi, D Dodd, S Colan, J Wilkinson, A Sridhar, ... Journal of the American College of Cardiology 71 (11S), A663-A663, 2018 | 1 | 2018 |
| Exome Sequencing in a Pediatric Cardiomyopathy Cohort: Findings From the Pediatric Cardiomyopathy Registry SM Ware, JD Wilkinson, M Tariq, JA Schubert, A Sridhar, SD Colan, L Shi, ... Circulation 136 (suppl_1), A16673-A16673, 2017 | 1 | 2017 |
| P480: Validation of optical genome mapping as a laboratory-developed diagnostic test for facioscapulohumeral muscular dystrophy type 1 A Hastie, A Chaubey, K Kosco, A Sridhar Genetics in Medicine Open 1 (1), 2023 | | 2023 |
| Clinical Validation of Optical Genome Mapping for the Detection of Structural Variations in Hematological Malignancies P AwC, K Kosco, N Sahajpal, A Sridhar, J Hauenstein, B Clifford, ... | | 2022 |
| Modeling the ACMG/AMP guidelines as a quantitative approach X Fan, JD Wilkinson, JA Schubert, M Tariq, A Sridhar, SD Colan, ... 69th Annual Meeting of The American Society of Human Genetics, 2019 | | 2019 |
| Identifying causal genes from abnormal clinical microarray results in patients with heterotaxy-spectrum congenital heart defects. A. Sridhar, B.J. Landis, L.R. Elmore, V. Garg, G.C. Geddes, S.R. Lalani, J.H ... 69th Annual Meeting of The American Society of Human Genetics, 2019 | | 2019 |
| SHROOM3 is a novel component of the planar cell polarity pathway whose disruption causes congenital heart disease M.D. Durbin, J. O'Kane, A. Sridhar, S. Ware Midwest Society for Pediatric Research Conference, 2019 | | 2019 |
| Increased burden of variants identified in laterality and cilia related genes in individuals with heterotaxy syndrome A. Sridhar, S.M. Ware Weinstein Cardiovascular Development and Regeneration Meeting, 2019 | | 2019 |
| Understanding the genetic contribution to heterotaxy syndrome A. Sridhar, S.M. Ware 68th Annual Meeting of The American Society of Human Genetics, 2018 | | 2018 |
| Revising Clinical Genetic Panel Test Results for Pediatric Cardiomyopathy After Exome Sequencing T Lee, S Ware, E Miller, P Dexheimer, A Sridhar, S Lipshultz, L Shi, ... Pediatric Academic Societies Meeting, 2018 | | 2018 |
Susana Santos Lopes, Susana Lopes,...Chronic Diseases Research Center, CEDOC, Faculty of Medical Sciences, NOVA Medical School, NMSVerified email at nms.unl.pt
