Shannon Nees

TitleVolunteer Faculty
InstitutionThomas Jefferson University
DepartmentFaculty Records
Address1015 Walnut St.
Philadelphia PA 19107
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    PMC Citations indicate the number of times the publication was cited by articles in PubMed Central, and the Altmetric score represents citations in news articles and social media. (Note that publications are often cited in additional ways that are not shown here.) Fields are based on how the National Library of Medicine (NLM) classifies the publication's journal and might not represent the specific topic of the publication. Translation tags are based on the publication type and the MeSH terms NLM assigns to the publication. Some publications (especially newer ones and publications not in PubMed) might not yet be assigned Field or Translation tags.) Click a Field or Translation tag to filter the publications.
    1. Sood E, Nees SN, Srivastava S, Ng S, Torres C, Munoz Osorio A, Canter KS, Braley KT, Spradley L, Stein J, Riegel E, Kazak AE. Virtually Delivered Psychosocial Intervention for Prenatally Diagnosed Congenital Heart Disease: Feasibility and Acceptability of HEARTPrep. Pediatr Cardiol. 2023 Jun 24. PMID: 37355506.
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    2. Nees SN, Woo JL, Glickstein JS, Anderson BR. A Spiral and Team Science-Based Research Curriculum Improves Subspecialty Fellowship Research Training and Productivity. J Am Coll Cardiol. 2023 Apr 04; 81(13):1300-1302. PMID: 36990550.
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    3. Griffin EL, Nees SN, Morton SU, Wynn J, Patel N, Jobanputra V, Robinson S, Kochav SM, Tao A, Andrews C, Cross N, Geva J, Lanzilotta K, Ritter A, Taillie E, Thompson A, Meyer C, Akers R, King EC, Cnota JF, Kim RW, Porter GA, Brueckner M, Seidman CE, Shen Y, Gelb BD, Goldmuntz E, Newburger JW, Roberts AE, Chung WK. Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circ Genom Precis Med. 2023 Feb 21; e003791. PMID: 36803080.
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    4. Nees SN, Chung WK. Genetic Basis of Human Congenital Heart Disease. Cold Spring Harb Perspect Biol. 2020 09 01; 12(9). PMID: 31818857.
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    5. Nees SN, Rosenzweig EB, Cohen JL, Valencia Villeda GA, Krishnan US. Targeted Therapy for Pulmonary Hypertension in Premature Infants. Children (Basel). 2020 Aug 15; 7(8). PMID: 32824244.
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    6. Qiao L, Wynn J, Yu L, Hernan R, Zhou X, Duron V, Aspelund G, Farkouh-Karoleski C, Zygumunt A, Krishnan US, Nees S, Khlevner J, Lim FY, Crombleholme T, Cusick R, Azarow K, Danko ME, Chung D, Warner BW, Mychaliska GB, Potoka D, Wagner AJ, Soffer S, Schindel D, McCulley DJ, Shen Y, Chung WK. Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes. Genet Med. 2020 12; 22(12):2020-2028. PMID: 32719394.
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    7. Farooqi KM, Nees SN, Smerling J, Senapathi SH, Lorenzoni R, Pavlicova M, Einstein AJ, Bacha EA, Kalfa D, Chai PJ. Assessment of Anomalous Coronary Arteries by Imagers and Surgeons: Comparison of Imaging Modalities. Ann Thorac Surg. 2021 02; 111(2):672-681. PMID: 32454021.
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    8. Nees SN, Chung WK. The genetics of isolated congenital heart disease. Am J Med Genet C Semin Med Genet. 2020 03; 184(1):97-106. PMID: 31876989.
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    9. Cohen JL, Nees SN, Valencia GA, Rosenzweig EB, Krishnan US. Sildenafil Use in Children with Pulmonary Hypertension. J Pediatr. 2019 02; 205:29-34.e1. PMID: 30396684.
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    10. Okur V, Nees S, Chung WK, Krishnan U. Pulmonary hypertension in patients with 9q34.3 microdeletion-associated Kleefstra syndrome. Am J Med Genet A. 2018 08; 176(8):1773-1777. PMID: 30063093.
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    11. Nees SN, Flyer JN, Chelliah A, Dayton JD, Touchette L, Kalfa D, Chai PJ, Bacha EA, Anderson BR. Patients with anomalous aortic origin of the coronary artery remain at risk after surgical repair. J Thorac Cardiovasc Surg. 2018 06; 155(6):2554-2564.e3. PMID: 29526358.
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    12. Van Batavia JP, Nees SN, Fast AM, Combs AJ, Glassberg KI. Outcomes of vesicoureteral reflux in children with non-neurogenic lower urinary tract dysfunction treated with dextranomer/hyaluronic acid copolymer (Deflux). J Pediatr Urol. 2014 Jun; 10(3):482-7. PMID: 24290224.
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    13. Sanna-Cherchi S, Sampogna RV, Papeta N, Burgess KE, Nees SN, Perry BJ, Choi M, Bodria M, Liu Y, Weng PL, Lozanovski VJ, Verbitsky M, Lugani F, Sterken R, Paragas N, Caridi G, Carrea A, Dagnino M, Materna-Kiryluk A, Santamaria G, Murtas C, Ristoska-Bojkovska N, Izzi C, Kacak N, Bianco B, Giberti S, Gigante M, Piaggio G, Gesualdo L, Vukic DK, Vukojevic K, Saraga-Babic M, Saraga M, Gucev Z, Allegri L, Latos-Bielenska A, Casu D, State M, Scolari F, Ravazzolo R, Kiryluk K, Al-Awqati Q, D'Agati VD, Drummond IA, Tasic V, Lifton RP, Ghiggeri GM, Gharavi AG. Mutations in DSTYK and dominant urinary tract malformations. N Engl J Med. 2013 Aug 15; 369(7):621-9. PMID: 23862974.
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    14. Ndao DH, Ladas EJ, Bao Y, Cheng B, Nees SN, Levine JM, Kelly KM. Use of complementary and alternative medicine among children, adolescent, and young adult cancer survivors: a survey study. J Pediatr Hematol Oncol. 2013 May; 35(4):281-8. PMID: 23612379.
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    15. Fast AM, Nees SN, Van Batavia JP, Combs AJ, Glassberg KI. Outcomes of targeted treatment for vesicoureteral reflux in children with nonneurogenic lower urinary tract dysfunction. J Urol. 2013 Sep; 190(3):1028-32. PMID: 23473909.
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    16. Van Batavia JP, Fast AM, Nees SN, Mercado MA, Gaselberti A, Glassberg KI. Incidence, significance and natural history of persistent retrograde venous flow after varicocelectomy in children and adolescents: correlation with catch-up growth. J Urol. 2013 Aug; 190(2):689-95. PMID: 23473906.
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    17. Shen L, Peng HC, Nees SN, Zhao SP, Xu DY. Proprotein convertase subtilisin/kexin type 9 potentially influences cholesterol uptake in macrophages and reverse cholesterol transport. FEBS Lett. 2013 May 02; 587(9):1271-4. PMID: 23499248.
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    18. MacLachlan LS, Nees SN, Fast AM, Glassberg KI. Intratesticular varicoceles: are they significant? J Pediatr Urol. 2013 Dec; 9(6 Pt A):851-5. PMID: 23218754.
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    19. Sanna-Cherchi S, Kiryluk K, Burgess KE, Bodria M, Sampson MG, Hadley D, Nees SN, Verbitsky M, Perry BJ, Sterken R, Lozanovski VJ, Materna-Kiryluk A, Barlassina C, Kini A, Corbani V, Carrea A, Somenzi D, Murtas C, Ristoska-Bojkovska N, Izzi C, Bianco B, Zaniew M, Flogelova H, Weng PL, Kacak N, Giberti S, Gigante M, Arapovic A, Drnasin K, Caridi G, Curioni S, Allegri F, Ammenti A, Ferretti S, Goj V, Bernardo L, Jobanputra V, Chung WK, Lifton RP, Sanders S, State M, Clark LN, Saraga M, Padmanabhan S, Dominiczak AF, Foroud T, Gesualdo L, Gucev Z, Allegri L, Latos-Bielenska A, Cusi D, Scolari F, Tasic V, Hakonarson H, Ghiggeri GM, Gharavi AG. Copy-number disorders are a common cause of congenital kidney malformations. Am J Hum Genet. 2012 Dec 07; 91(6):987-97. PMID: 23159250.
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    20. Nees SN, Glassberg KI. Observations on hydroceles following adolescent varicocelectomy. J Urol. 2011 Dec; 186(6):2402-7. PMID: 22019156.
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    21. Korets R, Woldu SL, Nees SN, Spencer BA, Glassberg KI. Testicular symmetry and adolescent varicocele--does it need followup? J Urol. 2011 Oct; 186(4 Suppl):1614-8. PMID: 21862060.
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    22. Sanna-Cherchi S, Burgess KE, Nees SN, Caridi G, Weng PL, Dagnino M, Bodria M, Carrea A, Allegretta MA, Kim HR, Perry BJ, Gigante M, Clark LN, Kisselev S, Cusi D, Gesualdo L, Allegri L, Scolari F, D'Agati V, Shapiro LS, Pecoraro C, Palomero T, Ghiggeri GM, Gharavi AG. Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome. Kidney Int. 2011 Aug; 80(4):389-96. PMID: 21697813.
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