Recent Publications
Everett SS, Bomback M, Roth P, Goldshtrom N, Polin RA, Lyford A, Hays T. Nine is the New Ten of Apgar Scores: An Observational Retrospective Cohort Study. J Pediatr. 2024 Jun 15;273:114150. doi: 10.1016/j.jpeds.2024.114150.
Zhao E, Bomback M, Khan A, Krishna Murthy S, Solowiejczyk D, Vora NL, Gilmore KL, Giordano JL, Wapner RJ, Sanna-Cherchi S, Lyford A, Jelin AC, Gharavi AG, Hays T. The expanded spectrum of human disease associated with GREB1L likely includes complex congenital heart disease. Prenat Diagn. 2024 Jan 29. doi: 10.1002/pd.6527.
Richter F, Rutherford KD, Cooke AJ, Meshkati M, Eddy-Abrams V, Greene D, Kosowsky J, Park Y, Aggarwal S, Burke RJ, Chang W, Connors J, Giannone PJ, Hays T, Khattar D, Polak M, Senaldi L, Smith-Raska M, Sridhar S, Steiner L, Swanson JR, Tauber KA, Barbosa M, Guttmann KF, Turro E. A Deep Intronic PKHD1 Variant Identified by SpliceAI in a Deceased Neonate With Autosomal Recessive Polycystic Kidney Disease. Am J Kidney Dis. 2024 Jan 9:S0272-6386(24)00010-6. doi: 10.1053/j.ajkd.2023.12.011.
Brar BK, Blakemore K, Hertenstein C, Miller JL, Miller KA, Shamseldin H, Maddirevula S, Hays T, Lianoglou B, Dukhovny S, Baker LA, Sparks TN, Wapner R, Alkuraya FS, Norton ME, Jelin AC; Fetal Sequencing Consortium. The utility of gene sequencing in identifying an underlying genetic disorder in prenatally suspected lower urinary tract obstruction. Prenat Diagn. 2023 Aug 18. doi: 10.1002/pd.6425
Selin S. Everett, Miles Bomback, Rakesh Sahni, Ronald J. Wapner, Veeral N. Tolia, Reese H. Clark, Alex Lyford, Thomas Hays. Prevalence and Clinical Significance of Commonly Diagnosed Genetic Disorders in Preterm Infants. medRxiv 2023.07.14.23292662; doi: https://doi.org/10.1101/2023.07.14.23292662 [Preprint].
Miles Bomback, Selin Everett, Alex Lyford, Rakesh Sahni, Faith Kim, Caitlin Baptiste, Joshua Motelow, Veeral Tolia, Reese Clark, Thomas Hays. The Contribution of Commonly Diagnosed Genetic Disorders to Small for Gestational Age Birth and Subsequent Morbidity and Mortality in Preterm Infants. medRxiv 2023.07.14.23292682; doi: https://doi.org/10.1101/2023.07.14.23292682 [Preprint].
Hays T, Hernan R, Disco M, Griffin E, Goldshtrom N, Vargas D, Krishnamurthy G, Bomback M, Rehman AU, Wilson AT, Guha S, Phadke S, Okur V, Robinson D, Felice V, Abhyankar A, Jobanputra V, Chung WK. Implementation of Rapid Genome Sequencing for Critically Ill Infants with Complex Congenital Heart Disease. Circulation: Genomic and Precision Medicine. 2023;0:e004050. https://doi.org/10.1161/CIRCGEN.122.004050.
Moran GW, Steinman JB, Tilotson CV, Carpenter CP, Hays T, Ham JN, Li B. Virilization of a 46,XX Fetus Following Aromatase Inhibitor Treatment of Breast Cancer. Pediatrics. 2023 Jun1;151(6). PMID: 37128841.
Ahram, et al. Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis. JASN. 2023 Jun 1; 34(6):1105-1119. PMID: 36995132.
Hays T, The genetic basis of congenital kidney anomalies. In Neonatology Questions and Controversies, 4th Ed. Edited by Richard Polin. 2023.
Hays T, Thompson MV, Bateman DA, Sahni R, Tolia VN, Clark RH, Gharavi AG. The Prevalence and Clinical Significance of Congenital Anomalies of the Kidney and Urinary Tract in Preterm Infants. JAMA Network Open. 2022 Sep 1;5(9):e2231626. doi: 10.1001/jamanetworkopen.2022.31626. PMID: 36103177; PMCID: PMC9475384.
Hays T, Wapner RJ. Genetic testing for unexplained perinatal disorders. Current Opinion in Pediatrics. 2021 Apr 1;33(2):195-202. doi: 10.1097/MOP.0000000000000999. PMID: 33605625; PMCID: PMC8221376.
Hays T, Groopman EE, Gharavi AG. Genetic testing for kidney disease of unknown etiology. Kidney International. 2020 Sep;98(3):590-600. doi: 10.1016/j.kint.2020.03.031. Epub 2020 Apr 24. PMID: 32739203; PMCID: PMC7784921.
A complete list of publications can be found on PubMed or Google Scholar.
Other Media
Delphi Neonatal Innovations Lecture 2022
Alianza Médica Para La Salud 2022