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Items: 1 to 50 of 140

1.

To Screen or Not to Screen, That Is the Question.

Mital S, Ommen S.

Circulation. 2019 Jul 16;140(3):193-195. doi: 10.1161/CIRCULATIONAHA.119.041021. Epub 2019 Jul 15. No abstract available.

PMID:
31306063
2.

Family screening for hypertrophic cardiomyopathy: Is it time to change practice guidelines?

Lafreniere-Roula M, Bolkier Y, Zahavich L, Mathew J, George K, Wilson J, Stephenson EA, Benson LN, Manlhiot C, Mital S.

Eur Heart J. 2019 Jun 6. pii: ehz396. doi: 10.1093/eurheartj/ehz396. [Epub ahead of print]

PMID:
31170284
3.

Pediatric Outcomes in Transplant: PersOnaliSing Immunosuppression To ImproVe Efficacy (POSITIVE Study): The Collaboration and Design of a National Transplant Precision Medicine Program.

Papaz T, Allen U, Blydt-Hansen T, Birk PE, Min S, Hamiwka L, Phan V, Schechter T, Wall DA, Urschel S, Foster BJ, Mital S.

Transplant Direct. 2018 Nov 27;4(12):e410. doi: 10.1097/TXD.0000000000000842. eCollection 2018 Dec. Erratum in: Transplant Direct. 2019 Feb 14;5(3):1.

4.

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association.

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; American Heart Association Council on Cardiovascular Disease in the Young; Council on Cardiovascular and Stroke Nursing; and Council on Genomic and Precision Medicine.

Circulation. 2018 Nov 20;138(21):e653-e711. doi: 10.1161/CIR.0000000000000606. Erratum in: Circulation. 2018 Nov 20;138(21):e713.

PMID:
30571578
5.

Abnormal fetal cerebral and vascular development in hypoplastic left heart syndrome.

Kinnear C, Haranal M, Shannon P, Jaeggi E, Chitayat D, Mital S.

Prenat Diagn. 2019 Jan;39(1):38-44. doi: 10.1002/pd.5395. Epub 2018 Dec 27.

6.

ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm.

Gould RA, Aziz H, Woods CE, Seman-Senderos MA, Sparks E, Preuss C, Wünnemann F, Bedja D, Moats CR, McClymont SA, Rose R, Sobreira N, Ling H, MacCarrick G, Kumar AA, Luyckx I, Cannaerts E, Verstraeten A, Björk HM, Lehsau AC, Jaskula-Ranga V, Lauridsen H, Shah AA, Bennett CL, Ellinor PT, Lin H, Isselbacher EM, Lino Cardenas CL, Butcher JT, Hughes GC, Lindsay ME; Baylor-Hopkins Center for Mendelian Genomics; MIBAVA Leducq Consortium, Mertens L, Franco-Cereceda A, Verhagen JMA, Wessels M, Mohamed SA, Eriksson P, Mital S, Van Laer L, Loeys BL, Andelfinger G, McCallion AS, Dietz HC.

Nat Genet. 2019 Jan;51(1):42-50. doi: 10.1038/s41588-018-0265-y. Epub 2018 Nov 19.

7.

Novel Association of a De Novo CALM2 Mutation With Long QT Syndrome and Hypertrophic Cardiomyopathy.

Zahavich L, Tarnopolsky M, Yao R, Mital S.

Circ Genom Precis Med. 2018 Oct;11(10):e002255. doi: 10.1161/CIRCGEN.118.002255. No abstract available.

PMID:
30354306
8.

A randomized clinical trial of age and genotype-guided tacrolimus dosing after pediatric solid organ transplantation.

Min S, Papaz T, Lafreniere-Roula M, Nalli N, Grasemann H, Schwartz SM, Kamath BM, Ng V, Parekh RS, Manlhiot C, Mital S.

Pediatr Transplant. 2018 Nov;22(7):e13285. doi: 10.1111/petr.13285. Epub 2018 Sep 3.

PMID:
30178515
9.

Human Pluripotent Stem Cells to Model Congenital Heart Disease.

Mital S.

In: Nakanishi T, Markwald RR, Baldwin HS, Keller BB, Srivastava D, Yamagishi H, editors. Etiology and Morphogenesis of Congenital Heart Disease: From Gene Function and Cellular Interaction to Morphology [Internet]. Tokyo: Springer; 2016. Chapter 45.
2016 Jun 25.

10.

Trends in non-medical prescription opioids and heroin co-use among adults, 2003-2014.

Mital S, Windle M, Cooper HLF, Crawford ND.

Addict Behav. 2018 Nov;86:17-23. doi: 10.1016/j.addbeh.2018.05.005. Epub 2018 May 16.

PMID:
29778489
11.

Transplant-Free Survival and Interventions at 6 Years in the SVR Trial.

Newburger JW, Sleeper LA, Gaynor JW, Hollenbeck-Pringle D, Frommelt PC, Li JS, Mahle WT, Williams IA, Atz AM, Burns KM, Chen S, Cnota J, Dunbar-Masterson C, Ghanayem NS, Goldberg CS, Jacobs JP, Lewis AB, Mital S, Pizarro C, Eckhauser A, Stark P, Ohye RG; Pediatric Heart Network Investigators.

Circulation. 2018 May 22;137(21):2246-2253. doi: 10.1161/CIRCULATIONAHA.117.029375. Epub 2018 Feb 1.

12.

Prelisting predictions of early postoperative survival in infant heart transplantation using classification and regression tree analysis.

Chen CK, Manlhiot C, Mital S, Schwartz SM, Van Arsdell GS, Caldarone C, McCrindle BW, Dipchand AI.

Pediatr Transplant. 2018 Mar;22(2). doi: 10.1111/petr.13105. Epub 2017 Dec 21.

PMID:
29271030
13.

Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy.

Mathew J, Zahavich L, Lafreniere-Roula M, Wilson J, George K, Benson L, Bowdin S, Mital S.

Clin Genet. 2018 Feb;93(2):310-319. doi: 10.1111/cge.13157. Epub 2017 Dec 26.

PMID:
29053178
14.

Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands.

Jin SC, Homsy J, Zaidi S, Lu Q, Morton S, DePalma SR, Zeng X, Qi H, Chang W, Sierant MC, Hung WC, Haider S, Zhang J, Knight J, Bjornson RD, Castaldi C, Tikhonoa IR, Bilguvar K, Mane SM, Sanders SJ, Mital S, Russell MW, Gaynor JW, Deanfield J, Giardini A, Porter GA Jr, Srivastava D, Lo CW, Shen Y, Watkins WS, Yandell M, Yost HJ, Tristani-Firouzi M, Newburger JW, Roberts AE, Kim R, Zhao H, Kaltman JR, Goldmuntz E, Chung WK, Seidman JG, Gelb BD, Seidman CE, Lifton RP, Brueckner M.

Nat Genet. 2017 Nov;49(11):1593-1601. doi: 10.1038/ng.3970. Epub 2017 Oct 9.

15.

Corrigendum: Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor.

Gillis E, Kumar AA, Luyckx I, Preuss C, Cannaerts E, van de Beek G, Wieschendorf B, Alaerts M, Bolar N, Vandeweyer G, Meester J, Wünnemann F, Gould RA, Zhurayev R, Zerbino D, Mohamed SA, Mital S, Mertens L, Björck HM, Franco-Cereceda A, McCallion AS, Van Laer L, Verhagen JMA, van de Laar IMBH, Wessels MW, Messas E, Goudot G, Nemcikova M, Krebsova A, Kempers M, Salemink S, Duijnhouwer T, Jeunemaitre X, Albuisson J, Eriksson P, Andelfinger G, Dietz HC, Verstraeten A, Loeys BL; Mibava Leducq Consortium.

Front Physiol. 2017 Sep 25;8:730. doi: 10.3389/fphys.2017.00730. eCollection 2017.

16.

Incremental cost-effectiveness of algorithm-driven genetic testing versus no testing for Maturity Onset Diabetes of the Young (MODY) in Singapore.

Nguyen HV, Finkelstein EA, Mital S, Gardner DS.

J Med Genet. 2017 Nov;54(11):747-753. doi: 10.1136/jmedgenet-2017-104670. Epub 2017 Aug 23.

PMID:
28835481
17.

Novel approaches to the prediction, diagnosis and treatment of cardiac late effects in survivors of childhood cancer: a multi-centre observational study.

Skitch A, Mital S, Mertens L, Liu P, Kantor P, Grosse-Wortmann L, Manlhiot C, Greenberg M, Nathan PC.

BMC Cancer. 2017 Aug 3;17(1):519. doi: 10.1186/s12885-017-3505-0.

18.

Adrenergic receptor genotypes influence postoperative outcomes in infants in the Single-Ventricle Reconstruction Trial.

Ramroop R, Manase G, Lu D, Manase D, Chen S, Kim R, Lee T, Mahle WT, McHugh K, Mitchell M, Tristani-Firouzi M, Wechsler SB, Wilder NS, Zak V, Lafreniere-Roula M, Newburger JW, Gaynor JW, Russell MW, Mital S.

J Thorac Cardiovasc Surg. 2017 Nov;154(5):1703-1710.e3. doi: 10.1016/j.jtcvs.2017.06.041. Epub 2017 Jun 24.

19.

Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor.

Gillis E, Kumar AA, Luyckx I, Preuss C, Cannaerts E, van de Beek G, Wieschendorf B, Alaerts M, Bolar N, Vandeweyer G, Meester J, Wünnemann F, Gould RA, Zhurayev R, Zerbino D, Mohamed SA, Mital S, Mertens L, Björck HM, Franco-Cereceda A, McCallion AS, Van Laer L, Verhagen JMA, van de Laar IMBH, Wessels MW, Messas E, Goudot G, Nemcikova M, Krebsova A, Kempers M, Salemink S, Duijnhouwer T, Jeunemaitre X, Albuisson J, Eriksson P, Andelfinger G, Dietz HC, Verstraeten A, Loeys BL; Mibava Leducq Consortium.

Front Physiol. 2017 Jun 13;8:400. doi: 10.3389/fphys.2017.00400. eCollection 2017. Erratum in: Front Physiol. 2017 Sep 25;8:730.

20.

Results of a phase I/II multi-center investigation of udenafil in adolescents after fontan palliation.

Goldberg DJ, Zak V, Goldstein BH, Chen S, Hamstra MS, Radojewski EA, Maunsell E, Mital S, Menon SC, Schumacher KR, Payne RM, Stylianou M, Kaltman JR, deVries TM, Yeager JL, Paridon SM; Pediatric Heart Network Investigators.

Am Heart J. 2017 Jun;188:42-52. doi: 10.1016/j.ahj.2017.02.030. Epub 2017 Mar 6.

21.

Use of Clinical Exome Sequencing in Isolated Congenital Heart Disease.

Zahavich L, Bowdin S, Mital S.

Circ Cardiovasc Genet. 2017 Jun;10(3). pii: e001581. doi: 10.1161/CIRCGENETICS.116.001581. No abstract available.

PMID:
28473349
22.

Is bronchial thermoplasty cost-effective as treatment for problematic asthma patients? Singapore's perspective on a global model.

Nguyen HV, Bose S, Mital S, Yii ACA, Ang SY, Lam SSW, Anantham D, Finkelstein E, Koh MS.

Respirology. 2017 Aug;22(6):1102-1109. doi: 10.1111/resp.13027. Epub 2017 Mar 31.

23.

Clinical genetic testing in pediatric cardiomyopathy: Is bigger better?

Ouellette AC, Mathew J, Manickaraj AK, Manase G, Zahavich L, Wilson J, George K, Benson L, Bowdin S, Mital S.

Clin Genet. 2018 Jan;93(1):33-40. doi: 10.1111/cge.13024. Epub 2017 Aug 3.

PMID:
28369760
24.

Perspective on precision medicine in paediatric heart failure.

Fridman MD, Mital S.

Clin Sci (Lond). 2017 Mar 1;131(6):439-448. doi: 10.1042/CS20160414. Review.

PMID:
28265035
25.

Management of Pregnancy in Patients With Complex Congenital Heart Disease: A Scientific Statement for Healthcare Professionals From the American Heart Association.

Canobbio MM, Warnes CA, Aboulhosn J, Connolly HM, Khanna A, Koos BJ, Mital S, Rose C, Silversides C, Stout K; American Heart Association Council on Cardiovascular and Stroke Nursing; Council on Clinical Cardiology; Council on Cardiovascular Disease in the Young; Council on Functional Genomics and Translational Biology; and Council on Quality of Care and Outcomes Research.

Circulation. 2017 Feb 21;135(8):e50-e87. doi: 10.1161/CIR.0000000000000458. Epub 2017 Jan 12. Review.

PMID:
28082385
26.

Association between asthma control and asthma cost: Results from a longitudinal study in a primary care setting.

Nguyen HV, Nadkarni NV, Sankari U, Mital S, Lye WK, Tan NC.

Respirology. 2017 Apr;22(3):454-459. doi: 10.1111/resp.12930. Epub 2016 Nov 10.

27.

Enhancing Literacy in Cardiovascular Genetics: A Scientific Statement From the American Heart Association.

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; American Heart Association Council on Functional Genomics and Translational Biology; Council on Cardiovascular Disease in the Young; Council on Cardiovascular and Stroke Nursing; Stroke Council; Council on Lifestyle and Cardiometabolic Health; and Council on Quality of Care and Outcomes Research.

Circ Cardiovasc Genet. 2016 Oct;9(5):448-467. Epub 2016 Sep 26.

PMID:
27672144
28.

Cost-effectiveness of a National Telemedicine Diabetic Retinopathy Screening Program in Singapore.

Nguyen HV, Tan GS, Tapp RJ, Mital S, Ting DS, Wong HT, Tan CS, Laude A, Tai ES, Tan NC, Finkelstein EA, Wong TY, Lamoureux EL.

Ophthalmology. 2016 Dec;123(12):2571-2580. doi: 10.1016/j.ophtha.2016.08.021. Epub 2016 Oct 7.

PMID:
27726962
29.

Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.

Sifrim A, Hitz MP, Wilsdon A, Breckpot J, Turki SH, Thienpont B, McRae J, Fitzgerald TW, Singh T, Swaminathan GJ, Prigmore E, Rajan D, Abdul-Khaliq H, Banka S, Bauer UM, Bentham J, Berger F, Bhattacharya S, Bu'Lock F, Canham N, Colgiu IG, Cosgrove C, Cox H, Daehnert I, Daly A, Danesh J, Fryer A, Gewillig M, Hobson E, Hoff K, Homfray T; INTERVAL Study, Kahlert AK, Ketley A, Kramer HH, Lachlan K, Lampe AK, Louw JJ, Manickara AK, Manase D, McCarthy KP, Metcalfe K, Moore C, Newbury-Ecob R, Omer SO, Ouwehand WH, Park SM, Parker MJ, Pickardt T, Pollard MO, Robert L, Roberts DJ, Sambrook J, Setchfield K, Stiller B, Thornborough C, Toka O, Watkins H, Williams D, Wright M, Mital S, Daubeney PE, Keavney B, Goodship J; UK10K Consortium, Abu-Sulaiman RM, Klaassen S, Wright CF, Firth HV, Barrett JC, Devriendt K, FitzPatrick DR, Brook JD; Deciphering Developmental Disorders Study, Hurles ME.

Nat Genet. 2016 Sep;48(9):1060-5. doi: 10.1038/ng.3627. Epub 2016 Aug 1.

30.

Avoiding false discovery in biomarker research.

Patel P, Kuzmanov U, Mital S.

BMC Biochem. 2016 Jul 30;17(1):17. doi: 10.1186/s12858-016-0073-x.

31.

Progressive Cerebellar Atrophy and a Novel Homozygous Pathogenic DNAJC19 Variant as a Cause of Dilated Cardiomyopathy Ataxia Syndrome.

Al Teneiji A, Siriwardena K, George K, Mital S, Mercimek-Mahmutoglu S.

Pediatr Neurol. 2016 Sep;62:58-61. doi: 10.1016/j.pediatrneurol.2016.03.020. Epub 2016 Jun 4. Review.

PMID:
27426421
32.

De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.

Priest JR, Osoegawa K, Mohammed N, Nanda V, Kundu R, Schultz K, Lammer EJ, Girirajan S, Scheetz T, Waggott D, Haddad F, Reddy S, Bernstein D, Burns T, Steimle JD, Yang XH, Moskowitz IP, Hurles M, Lifton RP, Nickerson D, Bamshad M, Eichler EE, Mital S, Sheffield V, Quertermous T, Gelb BD, Portman M, Ashley EA.

PLoS Genet. 2016 Apr 8;12(4):e1005963. doi: 10.1371/journal.pgen.1005963. eCollection 2016 Apr.

33.

Opportunities for the Cardiovascular Community in the Precision Medicine Initiative.

Shah SH, Arnett D, Houser SR, Ginsburg GS, MacRae C, Mital S, Loscalzo J, Hall JL.

Circulation. 2016 Jan 12;133(2):226-31. doi: 10.1161/CIRCULATIONAHA.115.019475.

PMID:
27028435
34.

Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans.

Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LCA, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'Lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, FitzPatrick DR; UK10K Consortium, Wilson DI, Mital S, Hurles ME.

Am J Hum Genet. 2016 Mar 3;98(3):592. doi: 10.1016/j.ajhg.2016.02.016. Epub 2016 Mar 3. No abstract available.

35.

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies.

Homsy J, Zaidi S, Shen Y, Ware JS, Samocha KE, Karczewski KJ, DePalma SR, McKean D, Wakimoto H, Gorham J, Jin SC, Deanfield J, Giardini A, Porter GA Jr, Kim R, Bilguvar K, López-Giráldez F, Tikhonova I, Mane S, Romano-Adesman A, Qi H, Vardarajan B, Ma L, Daly M, Roberts AE, Russell MW, Mital S, Newburger JW, Gaynor JW, Breitbart RE, Iossifov I, Ronemus M, Sanders SJ, Kaltman JR, Seidman JG, Brueckner M, Gelb BD, Goldmuntz E, Lifton RP, Seidman CE, Chung WK.

Science. 2015 Dec 4;350(6265):1262-6. doi: 10.1126/science.aac9396.

36.

Human induced pluripotent stem cell derived neurons as a model for Williams-Beuren syndrome.

Khattak S, Brimble E, Zhang W, Zaslavsky K, Strong E, Ross PJ, Hendry J, Mital S, Salter MW, Osborne LR, Ellis J.

Mol Brain. 2015 Nov 24;8(1):77. doi: 10.1186/s13041-015-0168-0.

37.

Heroin shortage in Coastal Kenya: A rapid assessment and qualitative analysis of heroin users' experiences.

Mital S, Miles G, McLellan-Lemal E, Muthui M, Needle R.

Int J Drug Policy. 2016 Apr;30:91-8. doi: 10.1016/j.drugpo.2015.08.010. Epub 2015 Aug 22.

38.

Renin-angiotensin-aldosterone system genotype and serum BNP in a contemporary cohort of adults late after Fontan palliation.

Burchill LJ, Redington AN, Silversides CK, Ross HJ, Jimenez-Juan L, Mital S, Oechslin EN, Dragulescu A, Slorach C, Mertens L, Wald RM.

Int J Cardiol. 2015 Oct 15;197:209-15. doi: 10.1016/j.ijcard.2015.06.018. Epub 2015 Jun 18.

PMID:
26142965
39.

Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.

D'Alessandro LC, Al Turki S, Manickaraj AK, Manase D, Mulder BJ, Bergin L, Rosenberg HC, Mondal T, Gordon E, Lougheed J, Smythe J, Devriendt K, Bhattacharya S, Watkins H, Bentham J, Bowdin S, Hurles ME, Mital S.

Genet Med. 2016 Feb;18(2):189-98. doi: 10.1038/gim.2015.60. Epub 2015 May 21.

40.

Congenital heart disease in the older adult: a scientific statement from the American Heart Association.

Bhatt AB, Foster E, Kuehl K, Alpert J, Brabeck S, Crumb S, Davidson WR Jr, Earing MG, Ghoshhajra BB, Karamlou T, Mital S, Ting J, Tseng ZH; American Heart Association Council on Clinical Cardiology.

Circulation. 2015 May 26;131(21):1884-931. doi: 10.1161/CIR.0000000000000204. Epub 2015 Apr 20. No abstract available. Erratum in: Circulation. 2015 May 26;131(21):e510.

PMID:
25896865
41.

High throughput exome coverage of clinically relevant cardiac genes.

Manase D, D'Alessandro LC, Manickaraj AK, Al Turki S, Hurles ME, Mital S.

BMC Med Genomics. 2014 Dec 11;7:67. doi: 10.1186/s12920-014-0067-8.

42.

Identification of deleterious synonymous variants in human genomes.

Buske OJ, Manickaraj A, Mital S, Ray PN, Brudno M.

Bioinformatics. 2015 Mar 1;31(5):799. doi: 10.1093/bioinformatics/btu765. Epub 2014 Dec 8. No abstract available.

PMID:
25488928
43.

Prevalence of rape and client-initiated gender-based violence among female sex workers: Kampala, Uganda, 2012.

Schwitters A, Swaminathan M, Serwadda D, Muyonga M, Shiraishi RW, Benech I, Mital S, Bosa R, Lubwama G, Hladik W.

AIDS Behav. 2015 Feb;19 Suppl 1:S68-76. doi: 10.1007/s10461-014-0957-y.

44.

Adrenergic receptor genotype influences heart failure severity and β-blocker response in children with dilated cardiomyopathy.

Reddy S, Fung A, Manlhiot C, Tierney ES, Chung WK, Blume E, Kaufman BD, Goldmuntz E, Colan S, Mital S.

Pediatr Res. 2015 Feb;77(2):363-9. doi: 10.1038/pr.2014.183. Epub 2014 Nov 19.

45.

Uncoupling of microbial community structure and function in decomposing litter across beech forest ecosystems in Central Europe.

Purahong W, Schloter M, Pecyna MJ, Kapturska D, Däumlich V, Mital S, Buscot F, Hofrichter M, Gutknecht JL, Krüger D.

Sci Rep. 2014 Nov 12;4:7014. doi: 10.1038/srep07014.

46.

Validation of association of the apolipoprotein E ε2 allele with neurodevelopmental dysfunction after cardiac surgery in neonates and infants.

Gaynor JW, Kim DS, Arrington CB, Atz AM, Bellinger DC, Burt AA, Ghanayem NS, Jacobs JP, Lee TM, Lewis AB, Mahle WT, Marino BS, Miller SG, Newburger JW, Pizarro C, Ravishankar C, Santani AB, Wilder NS, Jarvik GP, Mital S, Russell MW.

J Thorac Cardiovasc Surg. 2014 Dec;148(6):2560-6. doi: 10.1016/j.jtcvs.2014.07.052. Epub 2014 Aug 1.

47.

New mechanistic and therapeutic targets for pediatric heart failure: report from a National Heart, Lung, and Blood Institute working group.

Burns KM, Byrne BJ, Gelb BD, Kühn B, Leinwand LA, Mital S, Pearson GD, Rodefeld M, Rossano JW, Stauffer BL, Taylor MD, Towbin JA, Redington AN.

Circulation. 2014 Jul 1;130(1):79-86. doi: 10.1161/CIRCULATIONAHA.113.007980. No abstract available.

48.

Transplantation-free survival and interventions at 3 years in the single ventricle reconstruction trial.

Newburger JW, Sleeper LA, Frommelt PC, Pearson GD, Mahle WT, Chen S, Dunbar-Masterson C, Mital S, Williams IA, Ghanayem NS, Goldberg CS, Jacobs JP, Krawczeski CD, Lewis AB, Pasquali SK, Pizarro C, Gruber PJ, Atz AM, Khaikin S, Gaynor JW, Ohye RG; Pediatric Heart Network Investigators.

Circulation. 2014 May 20;129(20):2013-20. doi: 10.1161/CIRCULATIONAHA.113.006191. Epub 2014 Apr 4.

49.

Rare variants in NR2F2 cause congenital heart defects in humans.

Al Turki S, Manickaraj AK, Mercer CL, Gerety SS, Hitz MP, Lindsay S, D'Alessandro LC, Swaminathan GJ, Bentham J, Arndt AK, Louw J, Low J, Breckpot J, Gewillig M, Thienpont B, Abdul-Khaliq H, Harnack C, Hoff K, Kramer HH, Schubert S, Siebert R, Toka O, Cosgrove C, Watkins H, Lucassen AM, O'Kelly IM, Salmon AP, Bu'lock FA, Granados-Riveron J, Setchfield K, Thornborough C, Brook JD, Mulder B, Klaassen S, Bhattacharya S, Devriendt K, Fitzpatrick DF; UK10K Consortium, Wilson DI, Mital S, Hurles ME.

Am J Hum Genet. 2014 Apr 3;94(4):574-85. doi: 10.1016/j.ajhg.2014.03.007. Erratum in: Am J Hum Genet. 2014 Jul 3;95(1):126. Am J Hum Genet. 2016 Mar 3;98(3):592. Low, Jacoba [corrected to Louw, Jacoba].

50.

Heart failure in congenital heart disease: a confluence of acquired and congenital.

Fahed AC, Roberts AE, Mital S, Lakdawala NK.

Heart Fail Clin. 2014 Jan;10(1):219-27. doi: 10.1016/j.hfc.2013.09.017. Review.

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