| Year |
Citation |
Score |
| 2023 |
Yasuhara J, Manivannan SN, Majumdar U, Gordon DM, Lawrence PJ, Aljuhani M, Myers K, Stiver C, Bigelow AM, Galantowicz M, Yamagishi H, McBride KL, White P, Garg V. Novel pathogenic GATA6 variant associated with congenital heart disease, diabetes mellitus and necrotizing enterocolitis. Pediatric Research. PMID 37700164 DOI: 10.1038/s41390-023-02811-y |
0.336 |
|
| 2023 |
Landis BJ, Helvaty LR, Geddes GC, Lin JI, Yatsenko SA, Lo CW, Border WL, Wechsler SB, Murali CN, Azamian MS, Lalani SR, Hinton RB, Garg V, McBride KL, Hodge JC, et al. A Multicenter Analysis of Abnormal Chromosomal Microarray Findings in Congenital Heart Disease. Journal of the American Heart Association. e029340. PMID 37681527 DOI: 10.1161/JAHA.123.029340 |
0.381 |
|
| 2023 |
Blue EE, White JJ, Dush MK, Gordon WW, Wyatt BH, White P, Marvin CT, Helle E, Ojala T, Priest JR, Jenkins MM, Almli LM, Reefhuis J, Pangilinan F, Brody LC, ... ... Garg V, et al. Rare variants in increase risk for isolated hypoplastic left heart syndrome. Hgg Advances. 4: 100232. PMID 37663545 DOI: 10.1016/j.xhgg.2023.100232 |
0.407 |
|
| 2023 |
Yasuhara J, Schultz K, Bigelow AM, Garg V. Congenital aortic valve stenosis: from pathophysiology to molecular genetics and the need for novel therapeutics. Frontiers in Cardiovascular Medicine. 10: 1142707. PMID 37187784 DOI: 10.3389/fcvm.2023.1142707 |
0.36 |
|
| 2023 |
Ackah RL, Yasuhara J, Garg V. Genetics of aortic valve disease. Current Opinion in Cardiology. PMID 36789772 DOI: 10.1097/HCO.0000000000001028 |
0.307 |
|
| 2022 |
Adhicary S, Ye S, Lin H, Texter K, Garg V, Zhao MT. Establishment of NCHi009-A, an iPSC line from a patient with hypoplastic left heart syndrome (HLHS) carrying a heterozygous NOTCH1 mutation. Stem Cell Research. 66: 103013. PMID 36599283 DOI: 10.1016/j.scr.2022.103013 |
0.407 |
|
| 2022 |
Ye S, Wang C, Xu Z, Lin H, Wan X, Yu Y, Adhicary S, Zhang JZ, Zhou Y, Liu C, Alonzo M, Bi J, Ramirez-Navarro A, Deschenes I, Ma Q, ... Garg V, et al. Impaired Human Cardiac Cell Development due to NOTCH1 Deficiency. Circulation Research. PMID 36583388 DOI: 10.1161/CIRCRESAHA.122.321398 |
0.366 |
|
| 2022 |
Alonzo M, Contreras J, Ye S, Lin H, Hernandez-Rosario L, McBride KL, Texter K, Garg V, Zhao MT. Characterization of an iPSC line NCHi006-A from a patient with hypoplastic left heart syndrome (HLHS). Stem Cell Research. 64: 102892. PMID 35987121 DOI: 10.1016/j.scr.2022.102892 |
0.305 |
|
| 2022 |
Manivannan S, Mansfield C, Zhang X, Kodigepalli KM, Majumdar U, Garg V, Basu M. Single-cell transcriptomic profiling unveils dysregulation of cardiac progenitor cells and cardiomyocytes in a mouse model of maternal hyperglycemia. Communications Biology. 5: 820. PMID 35970860 DOI: 10.1038/s42003-022-03779-x |
0.325 |
|
| 2022 |
Choudhury TZ, Garg V. Molecular genetic mechanisms of congenital heart disease. Current Opinion in Genetics & Development. 75: 101949. PMID 35816939 DOI: 10.1016/j.gde.2022.101949 |
0.398 |
|
| 2022 |
Gordon DM, Cunningham D, Zender G, Lawrence PJ, Penaloza JS, Lin H, Fitzgerald-Butt SM, Myers K, Duong T, Corsmeier DJ, Gaither JB, Kuck HC, Wijeratne S, Moreland B, Kelly BJ, ... Garg V, et al. Exome sequencing in multiplex families with left-sided cardiac defects has high yield for disease gene discovery. Plos Genetics. 18: e1010236. PMID 35737725 DOI: 10.1371/journal.pgen.1010236 |
0.349 |
|
| 2022 |
Hall B, Alonzo M, Texter K, Garg V, Zhao MT. Probing single ventricle heart defects with patient-derived induced pluripotent stem cells and emerging technologies. Birth Defects Research. PMID 35199491 DOI: 10.1002/bdr2.1989 |
0.353 |
|
| 2021 |
Teekakirikul P, Zhu W, Gabriel GC, Young CB, Williams K, Martin LJ, Hill JC, Richards T, Billaud M, Phillippi JA, Wang J, Wu Y, Tan T, Devine W, Lin JH, ... ... Garg V, et al. Common deletion variants causing protocadherin-α deficiency contribute to the complex genetics of BAV and left-sided congenital heart disease. Hgg Advances. 2. PMID 34888534 DOI: 10.1016/j.xhgg.2021.100037 |
0.421 |
|
| 2021 |
Yasuhara J, Garg V. Genetics of congenital heart disease: a narrative review of recent advances and clinical implications. Translational Pediatrics. 10: 2366-2386. PMID 34733677 DOI: 10.21037/tp-21-297 |
0.331 |
|
| 2021 |
Matos-Nieves A, Manivannan S, Majumdar U, McBride KL, White P, Garg V. A Multi-Omics Approach Using a Mouse Model of Cardiac Malformations for Prioritization of Human Congenital Heart Disease Contributing Genes. Frontiers in Cardiovascular Medicine. 8: 683074. PMID 34504875 DOI: 10.3389/fcvm.2021.683074 |
0.41 |
|
| 2021 |
Audain E, Wilsdon A, Breckpot J, Izarzugaza JM, Fitzgerald TW, Kahlert AK, Sifrim A, Wünnemann F, Perez-Riverol Y, Abdul-Khaliq H, Bak M, Bassett AS, Benson WD, Berger F, Daehnert I, ... ... Garg V, et al. Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. Plos Genetics. 17: e1009679. PMID 34324492 DOI: 10.1371/journal.pgen.1009679 |
0.334 |
|
| 2021 |
Lin H, McBride KL, Garg V, Zhao MT. Decoding Genetics of Congenital Heart Disease Using Patient-Derived Induced Pluripotent Stem Cells (iPSCs). Frontiers in Cell and Developmental Biology. 9: 630069. PMID 33585486 DOI: 10.3389/fcell.2021.630069 |
0.332 |
|
| 2020 |
Manivannan SN, Darouich S, Masmoudi A, Gordon D, Zender G, Han Z, Fitzgerald-Butt S, White P, McBride KL, Kharrat M, Garg V. Novel frameshift variant in MYL2 reveals molecular differences between dominant and recessive forms of hypertrophic cardiomyopathy. Plos Genetics. 16: e1008639. PMID 32453731 DOI: 10.1371/Journal.Pgen.1008639 |
0.42 |
|
| 2020 |
Zhao MT, Shao NY, Garg V. Subtype-specific cardiomyocytes for precision medicine: where are we now? Stem Cells (Dayton, Ohio). PMID 32232889 DOI: 10.1002/Stem.3178 |
0.423 |
|
| 2020 |
Zhao M, Ye S, Zhang J, Shao N, Liu C, Zhou Y, Nishiga M, Yang Y, Cui B, Garg V, Wu JC. Abstract 276: NOTCH1 is Essential for Ventricular Cardiomyocyte Differentiation of Human Induced Pluripotent Stem Cells Circulation Research. 127. DOI: 10.1161/res.127.suppl_1.276 |
0.366 |
|
| 2019 |
Majumdar U, Yasuhara J, Garg V. In Vivo and In Vitro Genetic Models of Congenital Heart Disease. Cold Spring Harbor Perspectives in Biology. PMID 31818859 DOI: 10.1101/Cshperspect.A036764 |
0.464 |
|
| 2019 |
Bennett JS, Bernhardt M, McBride KL, Reshmi SC, Zmuda E, Kertesz NJ, Garg V, Fitzgerald-Butt S, Kamp AN. Reclassification of Variants of Uncertain Significance in Children with Inherited Arrhythmia Syndromes is Predicted by Clinical Factors. Pediatric Cardiology. PMID 31535183 DOI: 10.1007/S00246-019-02203-2 |
0.345 |
|
| 2019 |
LaHaye S, Majumdar U, Yasuhara J, Koenig SN, Matos-Nieves A, Kumar R, Garg V. Developmental origins for semilunar valve stenosis identified in mice harboring congenital heart disease-associated mutation. Disease Models & Mechanisms. PMID 31138536 DOI: 10.1242/Dmm.036764 |
0.494 |
|
| 2019 |
Matos-Nieves A, Yasuhara J, Garg V. Another Notch in the Genetic Puzzle of Tetralogy of Fallot. Circulation Research. 124: 462-464. PMID 30763217 DOI: 10.1161/Circresaha.118.314520 |
0.331 |
|
| 2019 |
Mansfield C, Manivannan S, Cameron EM, Garg V, Basu M. Abstract 650: Dose-response Effect of Hyperglycemia in Maternal Diabetes Mediated Congenital Heart Defects Circulation Research. 125. DOI: 10.1161/Res.125.Suppl_1.650 |
0.31 |
|
| 2018 |
Basu M, Garg V. Maternal hyperglycemia and fetal cardiac development: Clinical impact and underlying mechanisms. Birth Defects Research. 110: 1504-1516. PMID 30576094 DOI: 10.1002/Bdr2.1435 |
0.47 |
|
| 2018 |
Pierpont ME, Brueckner M, Chung WK, Garg V, Lacro RV, McGuire AL, Mital S, Priest JR, Pu WT, Roberts A, Ware SM, Gelb BD, Russell MW. Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association. Circulation. 138: e653-e711. PMID 30571578 DOI: 10.1161/Cir.0000000000000606 |
0.467 |
|
| 2018 |
Bosse K, Hans CP, Zhao N, Koenig SN, Huang N, Guggilam A, LaHaye S, Tao G, Lucchesi PA, Lincoln J, Lilly B, Garg V. Corrigendum to "Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease" [J. Mol. Cell. Cardiol. 60 (2013) 27-35]. Journal of Molecular and Cellular Cardiology. PMID 29778253 DOI: 10.1016/J.Yjmcc.2018.04.013 |
0.326 |
|
| 2017 |
Garg V. The Role of Lipoprotein(a) in Calcific Aortic Valve Disease: Insights from a Large-Cohort Genetic Study. Jama Cardiology. PMID 29128867 DOI: 10.1001/Jamacardio.2017.4267 |
0.414 |
|
| 2017 |
Koenig SN, LaHaye S, Feller JD, Rowland P, Hor KN, Trask AJ, Janssen PM, Radtke F, Lilly B, Garg V. Notch1 haploinsufficiency causes ascending aortic aneurysms in mice. Jci Insight. 2. PMID 29093270 DOI: 10.1172/Jci.Insight.91353 |
0.424 |
|
| 2017 |
Basu M, Zhu JY, LaHaye S, Majumdar U, Jiao K, Han Z, Garg V. Epigenetic mechanisms underlying maternal diabetes-associated risk of congenital heart disease. Jci Insight. 2. PMID 29046480 DOI: 10.1172/Jci.Insight.95085 |
0.423 |
|
| 2017 |
Nadorlik H, Bowman JL, Fitzgerald-Butt S, Mah ML, McBride KL, Kovalchin JP, Garg V. Abnormal Longitudinal Growth of the Aorta in Children with Familial Bicuspid Aortic Valve. Pediatric Cardiology. PMID 28948327 DOI: 10.1007/S00246-017-1740-4 |
0.398 |
|
| 2017 |
Hertig V, Nieves AM, Garg V, Villeneuve L, Mamarbachi M, Caland L, Calderone A. Nestin expression is dynamically regulated in cardiomyocytes during embryogenesis. Journal of Cellular Physiology. PMID 28834610 DOI: 10.1002/Jcp.26165 |
0.389 |
|
| 2017 |
Hanchard NA, Umana LA, D'Alessandro L, Azamian M, Poopola M, Morris SA, Fernbach S, Lalani SR, Towbin JA, Zender GA, Fitzgerald-Butt S, Garg V, Bowman J, Zapata G, Hernandez P, et al. Assessment of large copy number variants in patients with apparently isolated congenital left-sided cardiac lesions reveals clinically relevant genomic events. American Journal of Medical Genetics. Part A. PMID 28653806 DOI: 10.1002/Ajmg.A.38309 |
0.445 |
|
| 2017 |
Koenig SN, Lincoln J, Garg V. Genetic basis of aortic valvular disease. Current Opinion in Cardiology. PMID 28157139 DOI: 10.1097/Hco.0000000000000384 |
0.443 |
|
| 2017 |
Majumdar U, Garg V. Notch1 Signaling and Aortic Valve Disease: From Human Genetics to Mouse Models Pediatric Cardiology and Cardiac Surgery. 1: 12-17. DOI: 10.24509/Jpccs.170104 |
0.414 |
|
| 2017 |
L'Italien K, Fitzgerald-Butt S, Simsic J, McBride K, Bowman J, Garg V. UTILITY OF GENETIC TESTING IN INFANTS WITH ISOLATED CONGENITAL HEART DISEASE Journal of the American College of Cardiology. 69: 635. DOI: 10.1016/S0735-1097(17)34024-X |
0.402 |
|
| 2017 |
Cephas A, Basu M, Garg V. Dose-dependent effect of Hyperglycemia during Cardiac Development Journal of Molecular and Cellular Cardiology. 112: 153. DOI: 10.1016/J.Yjmcc.2017.07.069 |
0.312 |
|
| 2016 |
Mital S, Musunuru K, Garg V, Russell MW, Lanfear DE, Gupta RM, Hickey KT, Ackerman MJ, Perez MV, Roden DM, Woo D, Fox CS, Ware S. Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association. Circulation. Cardiovascular Genetics. PMID 27672144 DOI: 10.1161/Hcg.0000000000000031 |
0.355 |
|
| 2016 |
LaHaye S, Corsemeier D, Basu M, Bowman JL, Fitzgerald-Butt S, Zender G, Bosse K, McBride KL, White P, Garg V. Utilization of Whole Exome Sequencing to Identify Causative Mutations in Familial Congenital Heart Disease. Circulation. Cardiovascular Genetics. PMID 27418595 DOI: 10.1161/Circgenetics.115.001324 |
0.465 |
|
| 2016 |
Koenig SN, Bosse K, Majumdar U, Bonachea EM, Radtke F, Garg V. Endothelial Notch1 Is Required for Proper Development of the Semilunar Valves and Cardiac Outflow Tract. Journal of the American Heart Association. 5. PMID 27107132 DOI: 10.1161/Jaha.115.003075 |
0.469 |
|
| 2016 |
Hanchard NA, Swaminathan S, Bucasas K, Furthner D, Fernbach S, Azamian MS, Wang X, Lewin M, Towbin JA, D'Alessandro LC, Morris SA, Dreyer W, Denfield S, Ayres NA, Franklin WJ, ... ... Garg V, et al. A Genome Wide Association Study of Congenital Cardiovascular Left-Sided Lesions Shows Association with a Locus on Chromosome 20. Human Molecular Genetics. PMID 26965164 DOI: 10.1093/Hmg/Ddw071 |
0.363 |
|
| 2015 |
Hinton RB, McBride KL, Bleyl SB, Bowles NE, Border WL, Garg V, Smolarek TA, Lalani SR, Ware SM. Rationale for the Cytogenomics of Cardiovascular Malformations Consortium: A Phenotype Intensive Registry Based Approach. Journal of Cardiovascular Development and Disease. 2: 76-92. PMID 29371513 DOI: 10.3390/Jcdd2020076 |
0.453 |
|
| 2015 |
Horne TE, VandeKopple M, Sauls K, Koenig SN, Anstine LJ, Garg V, Norris RA, Lincoln J. Dynamic Heterogeneity of the Heart Valve Interstitial Cell Population in Mitral Valve Health and Disease. Journal of Cardiovascular Development and Disease. 2: 214-232. PMID 26527432 DOI: 10.3390/Jcdd2030214 |
0.425 |
|
| 2015 |
Backes CH, Huang H, Cua CL, Garg V, Smith CV, Yin H, Galantowicz M, Bauer JA, Hoffman TM. Early versus delayed umbilical cord clamping in infants with congenital heart disease: a pilot, randomized, controlled trial. Journal of Perinatology : Official Journal of the California Perinatal Association. PMID 26226244 DOI: 10.1038/Jp.2015.89 |
0.3 |
|
| 2015 |
Fitzgerald-Butt SM, Bodine A, Fry KM, Ash J, Zaidi AN, Garg V, Gerhardt CA, McBride KL. Measuring genetic knowledge: a brief survey instrument for adolescents and adults. Clinical Genetics. PMID 26032340 DOI: 10.1111/Cge.12618 |
0.313 |
|
| 2015 |
Koenig SN, Bosse KM, Nadorlik HA, Lilly B, Garg V. Evidence of Aortopathy in Mice with Haploinsufficiency of Notch1 in Nos3-Null Background. Journal of Cardiovascular Development and Disease. 2: 17-30. PMID 25914885 DOI: 10.3390/Jcdd2010017 |
0.374 |
|
| 2014 |
Cheng J, Koenig SN, Kuivaniemi HS, Garg V, Hans CP. Pharmacological inhibitor of notch signaling stabilizes the progression of small abdominal aortic aneurysm in a mouse model. Journal of the American Heart Association. 3: e001064. PMID 25349182 DOI: 10.1161/Jaha.114.001064 |
0.306 |
|
| 2014 |
Bonachea EM, Zender G, White P, Corsmeier D, Newsom D, Fitzgerald-Butt S, Garg V, McBride KL. Use of a targeted, combinatorial next-generation sequencing approach for the study of bicuspid aortic valve. Bmc Medical Genomics. 7: 56. PMID 25260786 DOI: 10.1186/1755-8794-7-56 |
0.426 |
|
| 2014 |
Lincoln J, Garg V. Etiology of valvular heart disease-genetic and developmental origins. Circulation Journal : Official Journal of the Japanese Circulation Society. 78: 1801-7. PMID 24998280 DOI: 10.1253/Circj.Cj-14-0510 |
0.502 |
|
| 2014 |
Misra C, Chang SW, Basu M, Huang N, Garg V. Disruption of myocardial Gata4 and Tbx5 results in defects in cardiomyocyte proliferation and atrioventricular septation. Human Molecular Genetics. 23: 5025-35. PMID 24858909 DOI: 10.1093/Hmg/Ddu215 |
0.456 |
|
| 2014 |
Hu H, Roach JC, Coon H, Guthery SL, Voelkerding KV, Margraf RL, Durtschi JD, Tavtigian SV, Shankaracharya, Wu W, Scheet P, Wang S, Xing J, Glusman G, Hubley R, ... ... Garg V, et al. A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data. Nature Biotechnology. 32: 663-9. PMID 24837662 DOI: 10.1038/Nbt.2895 |
0.55 |
|
| 2014 |
Bonachea EM, Chang SW, Zender G, LaHaye S, Fitzgerald-Butt S, McBride KL, Garg V. Rare GATA5 sequence variants identified in individuals with bicuspid aortic valve. Pediatric Research. 76: 211-6. PMID 24796370 DOI: 10.1038/Pr.2014.67 |
0.421 |
|
| 2014 |
LaHaye S, Lincoln J, Garg V. Genetics of valvular heart disease. Current Cardiology Reports. 16: 487. PMID 24743897 DOI: 10.1007/S11886-014-0487-2 |
0.491 |
|
| 2014 |
Garg V, Basu M. Cohort study: Beyond genetics: Focusing on maternal environment for congenital heart disease prevention Evidence-Based Medicine. 19: e8. PMID 24282172 DOI: 10.1136/Eb-2013-101556 |
0.417 |
|
| 2013 |
Chang SW, Mislankar M, Misra C, Huang N, Dajusta DG, Harrison SM, McBride KL, Baker LA, Garg V. Genetic abnormalities in FOXP1 are associated with congenital heart defects. Human Mutation. 34: 1226-30. PMID 23766104 DOI: 10.1002/Humu.22366 |
0.49 |
|
| 2013 |
Bosse K, Hans CP, Zhao N, Koenig SN, Huang N, Guggilam A, LaHaye S, Tao G, Lucchesi PA, Lincoln J, Lilly B, Garg V. Endothelial nitric oxide signaling regulates Notch1 in aortic valve disease. Journal of Molecular and Cellular Cardiology. 60: 27-35. PMID 23583836 DOI: 10.1016/J.Yjmcc.2013.04.001 |
0.393 |
|
| 2013 |
Misra C, Garg V. Compacting the heart with Notch Nature Medicine. 19: 133-134. PMID 23389606 DOI: 10.1038/Nm.3071 |
0.472 |
|
| 2012 |
Misra C, Sachan N, McNally CR, Koenig SN, Nichols HA, Guggilam A, Lucchesi PA, Pu WT, Srivastava D, Garg V. Congenital heart disease-causing Gata4 mutation displays functional deficits in vivo. Plos Genetics. 8: e1002690. PMID 22589735 DOI: 10.1371/Journal.Pgen.1002690 |
0.606 |
|
| 2012 |
Payne AR, Chang SW, Koenig SN, Zinn AR, Garg V. Submicroscopic chromosomal copy number variations identified in children with hypoplastic left heart syndrome. Pediatric Cardiology. 33: 757-63. PMID 22349727 DOI: 10.1007/S00246-012-0208-9 |
0.415 |
|
| 2012 |
Bhoj EJ, Ramos P, Baker LA, Garg V, Cost N, Nordenskjöld A, Elder FF, Bleyl SB, Bowles NE, Arrington CB, Delhomme B, Vanhoutteghem A, Djian P, Zinn AR. Erratum: Human balanced translocation and mouse gene inactivation implicate Basonuclin 2 in distal urethral development (European Journal of Human Genetics (2011) DOI: 10.1038/ejhg.2010.245) European Journal of Human Genetics. 20. DOI: 10.1038/Ejhg.2011.137 |
0.338 |
|
| 2011 |
Acharya A, Hans CP, Koenig SN, Nichols HA, Galindo CL, Garner HR, Merrill WH, Hinton RB, Garg V. Inhibitory role of Notch1 in calcific aortic valve disease. Plos One. 6: e27743. PMID 22110751 DOI: 10.1371/Journal.Pone.0027743 |
0.411 |
|
| 2011 |
Roach JC, Glusman G, Hubley R, Montsaroff SZ, Holloway AK, Mauldin DE, Srivastava D, Garg V, Pollard KS, Galas DJ, Hood L, Smit AF. Chromosomal haplotypes by genetic phasing of human families. American Journal of Human Genetics. 89: 382-97. PMID 21855840 DOI: 10.1016/J.Ajhg.2011.07.023 |
0.51 |
|
| 2011 |
McBride KL, Garg V. Heredity of bicuspid aortic valve: is family screening indicated? Heart (British Cardiac Society). 97: 1193-5. PMID 21459929 DOI: 10.1136/Hrt.2011.222489 |
0.43 |
|
| 2010 |
Richards AA, Garg V. Genetics of congenital heart disease. Current Cardiology Reviews. 6: 91-7. PMID 21532774 DOI: 10.2174/157340310791162703 |
0.493 |
|
| 2010 |
McBride KL, Garg V. Impact of Mendelian inheritance in cardiovascular disease. Annals of the New York Academy of Sciences. 1214: 122-37. PMID 20958326 DOI: 10.1111/J.1749-6632.2010.05791.X |
0.458 |
|
| 2010 |
Maitra M, Koenig SN, Srivastava D, Garg V. Identification of GATA6 sequence variants in patients with congenital heart defects. Pediatric Research. 68: 281-5. PMID 20581743 DOI: 10.1203/PDR.0b013e3181ed17e4 |
0.638 |
|
| 2010 |
Richards AA, Garg V. Genetics of congenital heart disease Current Cardiology Reviews. 6: 91-97. DOI: 10.2174/157340310791162703 |
0.399 |
|
| 2009 |
Pan H, Richards AA, Zhu X, Joglar JA, Yin HL, Garg V. A novel mutation in LAMIN A/C is associated with isolated early-onset atrial fibrillation and progressive atrioventricular block followed by cardiomyopathy and sudden cardiac death. Heart Rhythm. 6: 707-10. PMID 19328042 DOI: 10.1016/J.Hrthm.2009.01.037 |
0.486 |
|
| 2009 |
Maitra M, Schluterman MK, Nichols HA, Richardson JA, Lo CW, Srivastava D, Garg V. Interaction of Gata4 and Gata6 with Tbx5 is critical for normal cardiac development. Developmental Biology. 326: 368-77. PMID 19084512 DOI: 10.1016/J.Ydbio.2008.11.004 |
0.647 |
|
| 2008 |
Ransom JF, King IN, Garg V, Srivastava D. A rare human sequence variant reveals myocardin autoinhibition. The Journal of Biological Chemistry. 283: 35845-52. PMID 18852265 DOI: 10.1074/Jbc.M805909200 |
0.578 |
|
| 2008 |
Richards AA, Santos LJ, Nichols HA, Crider BP, Elder FF, Hauser NS, Zinn AR, Garg V. Cryptic chromosomal abnormalities identified in children with congenital heart disease. Pediatric Research. 64: 358-63. PMID 18535492 DOI: 10.1203/Pdr.0B013E31818095D0 |
0.386 |
|
| 2007 |
Tomita-Mitchell A, Maslen CL, Morris CD, Garg V, Goldmuntz E. GATA4 sequence variants in patients with congenital heart disease. Journal of Medical Genetics. 44: 779-83. PMID 18055909 DOI: 10.1136/Jmg.2007.052183 |
0.475 |
|
| 2007 |
Rajagopal SK, Ma Q, Obler D, Shen J, Manichaikul A, Tomita-Mitchell A, Boardman K, Briggs C, Garg V, Srivastava D, Goldmuntz E, Broman KW, Benson DW, Smoot LB, Pu WT. Spectrum of heart disease associated with murine and human GATA4 mutation. Journal of Molecular and Cellular Cardiology. 43: 677-85. PMID 17643447 DOI: 10.1016/J.Yjmcc.2007.06.004 |
0.619 |
|
| 2007 |
Schluterman MK, Krysiak AE, Kathiriya IS, Abate N, Chandalia M, Srivastava D, Garg V. Screening and biochemical analysis of GATA4 sequence variations identified in patients with congenital heart disease. American Journal of Medical Genetics. Part A. 143: 817-23. PMID 17352393 DOI: 10.1002/Ajmg.A.31652 |
0.609 |
|
| 2006 |
Garg V. Molecular genetics of aortic valve disease Current Opinion in Cardiology. 21: 180-184. PMID 16601454 DOI: 10.1097/01.Hco.0000221578.18254.70 |
0.466 |
|
| 2006 |
Garg V. Insights into the genetic basis of congenital heart disease Cellular and Molecular Life Sciences. 63: 1141-1148. PMID 16568242 DOI: 10.1007/S00018-005-5532-2 |
0.494 |
|
| 2005 |
Garg V, Muth AN, Ransom JF, Schluterman MK, Barnes R, King IN, Grossfeld PD, Srivastava D. Mutations in NOTCH1 cause aortic valve disease. Nature. 437: 270-4. PMID 16025100 DOI: 10.1038/Nature03940 |
0.589 |
|
| 2003 |
Garg V, Kathiriya IS, Barnes R, Schluterman MK, King IN, Butler CA, Rothrock CR, Eapen RS, Hirayama-Yamada K, Joo K, Matsuoka R, Cohen JC, Srivastava D. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5. Nature. 424: 443-7. PMID 12845333 DOI: 10.1038/Nature01827 |
0.634 |
|
| 2001 |
Kunte A, Ivey K, Yamagishi C, Garg V, Yamagishi H, Srivastava D. A common cis-acting sequence in the DiGeorge critical region regulates bi-directional transcription of UFD1L and CDC45L Mechanisms of Development. 108: 81-92. PMID 11578863 DOI: 10.1016/S0925-4773(01)00489-0 |
0.537 |
|
| 2001 |
Garg V, Yamagishi C, Hu T, Kathiriya IS, Yamagishi H, Srivastava D. Tbx1, a DiGeorge syndrome candidate gene, is regulated by sonic hedgehog during pharyngeal arch development. Developmental Biology. 235: 62-73. PMID 11412027 DOI: 10.1006/Dbio.2001.0283 |
0.543 |
|
| 1999 |
Yamagishi H, Garg V, Matsuoka R, Thomas T, Srivastava D. A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects. Science (New York, N.Y.). 283: 1158-61. PMID 10024240 DOI: 10.1126/Science.283.5405.1158 |
0.579 |
|
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