Ashok Kumar Manickaraj
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Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing
Nature Genetics 48 (9), 1060, 2016
Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
S Al Turki, AK Manickaraj, CL Mercer, SS Gerety, MP Hitz, S Lindsay, ...
The American Journal of Human Genetics 94 (4), 574-585, 2014
Identification of deleterious synonymous variants in human genomes
OJ Buske, AK Manickaraj, S Mital, PN Ray, M Brudno
Bioinformatics 29 (15), 1843-1850, 2013
Genetic determinants of right-ventricular remodeling after tetralogy of Fallot repair
A Jeewa, AK Manickaraj, L Mertens, C Manlhiot, C Kinnear, T Mondal, ...
Pediatric research 72 (4), 407-413, 2012
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect
LCA D’Alessandro, S Al Turki, AK Manickaraj, D Manase, BJM Mulder, ...
Genetics in Medicine 18 (2), 189-198, 2016
Clinical genetic testing in pediatric cardiomyopathy: is bigger better?
AC Ouellette, J Mathew, AK Manickaraj, G Manase, L Zahavich, J Wilson, ...
Clinical genetics 93 (1), 33-40, 2018
Associations for lipoprotein lipase and peroxisome proliferator-activated receptor-γ gene and coronary artery disease in an Indian population
M AshokKumar, NGV Subhashini, S Kanthimathi, R SaiBabu, A Ramesh, ...
Archives of medical research 41 (1), 19-25. e1, 2010
Genetic variants on apolipoprotein gene cluster influence triglycerides with a risk of coronary artery disease among Indians
M AshokKumar, NGV Subhashini, R SaiBabu, A Ramesh, KM Cherian, ...
Molecular biology reports 37 (1), 521-527, 2010
Cardiac Troponin T (TNNT2) mutations are less prevalent in Indian hypertrophic cardiomyopathy patients
D Selvi Rani, P Nallari, PS Dhandapany, S Tamilarasi, A Shah, V Archana, ...
DNA and cell biology 31 (4), 616-624, 2012
An association study of thrombospondin 1 and 2 SNPs with coronary artery disease and myocardial infarction among South Indians
M AshokKumar, C Anbarasan, R SaiBabu, S Kuram, SC Raman, ...
Thrombosis research 128 (4), e49-e53, 2011
Haplotypes on 9p21 modify the risk for coronary artery disease among Indians
M AshokKumar, C Emmanuel, PS Dhandapany, DS Rani, R SaiBabu, ...
DNA and cell biology 30 (2), 105-110, 2011
Factors influencing participation in a population-based biorepository for childhood heart disease
T Papaz, M Safi, AK Manickaraj, C Ogaki, JB Kyryliuk, L Burrill, C Dodge, ...
Pediatrics 130 (5), e1198-e1205, 2012
Personalized medicine in the genomics era: highlights from an international symposium on childhood heart disease
N Farra, AK Manickaraj, J Ellis, S Mital
Future cardiology 8 (2), 157-160, 2012
Genetic variations in hypoxia response genes influence hypertrophic cardiomyopathy phenotype
J Alkon, MK Friedberg, C Manlhiot, AK Manickaraj, C Kinnear, ...
Pediatric research 72 (6), 583-592, 2012
High throughput exome coverage of clinically relevant cardiac genes
D Manase, LCA D’Alessandro, AK Manickaraj, S Al Turki, ME Hurles, ...
BMC medical genomics 7 (1), 1-10, 2014
Personalized medicine in pediatric cardiology: do little changes make a big difference?
AK Manickaraj, S Mital
Current opinion in pediatrics 24 (5), 584-591, 2012
Differential expression of TNF-α signaling molecules and ERK1 in distal and proximal colonic tumors associated with obesity
SS Jain, M AshokKumar, RP Bird
Tumor Biology 32 (5), 1005-1012, 2011
Machine learning identifies clinical and genetic factors associated with anthracycline cardiotoxicity in pediatric cancer survivors
MA Chaix, N Parmar, C Kinnear, M Lafreniere-Roula, O Akinrinade, ...
Cardio Oncology 2 (5), 690-706, 2020
A Machine Learning Approach to Predicting Risk of Anthracycline Cardiotoxicity in Pediatric Cancer Survivors
M Chaix, N Parmar, M Lafreniere-Roula, O Akinrinade, R Yao, A Miron, ...
Circulation 142 (Suppl_3), A14410-A14410, 2020
Genes Associated With Inotrope Requirements in Children Undergoing Tetralogy of Fallot Repair
S Lee, AK Manickaraj, D Lu, R Yao, MA Chan-Seng-Yue, P Laussen, ...
Circulation 134 (suppl_1), A17054-A17054, 2016
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