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Thomas Hays, MD, PhD
Thomas Hays, MD, PhD
Assistant Professor of Pediatrics, Columbia University
在 cumc.columbia.edu 的电子邮件经过验证
标题
引用次数
年份
A deep intronic PKHD1 variant identified by SpliceAI in a deceased neonate with autosomal recessive polycystic kidney disease
F Richter, KD Rutherford, AJ Cooke, M Meshkati, V Eddy-Abrams, ...
American Journal of Kidney Diseases 83 (6), 829-833, 2024
12024
APOL1 variants in HIV-associated nephropathy: just one piece of the puzzle
T Hays, CM Wyatt
Kidney international 82 (3), 259-260, 2012
152012
Archeological Testing at Fort St. Leon (16PL35), Plaquemines Parish, Louisiana
K Gilmore, VE Noble, TR Hays, RT Saucier, BC Yates, ...
Institute of Applied Sciences, North Texas State University, 1983
11983
Brc1-mediated rescue of Smc5/6 deficiency: requirement for multiple nucleases and a novel Rad18 function
KM Lee, S Nizza, T Hayes, KL Bass, A Irmisch, JM Murray, MJ O'Connell
Genetics 175 (4), 1585-1595, 2007
452007
Components of the Spindle Assembly Checkpoint Regulate the Anaphase-Promoting Complex During Meiosis in Caenorhabditis elegans
KK Stein, ES Davis, T Hays, A Golden
Genetics 175 (1), 107-123, 2007
522007
Congenital anomalies of the kidney and urinary tract (CAKUT) in critically ill infants: a multicenter cohort study
EH Leow, JH Lee, CP Hornik, YH Ng, T Hays, RH Clark, VN Tolia, ...
Pediatric Nephrology 38 (1), 161-172, 2023
52023
Exploratory laparoscopy for rotational abnormality of the intestine in a child with leukocyte adhesion deficiency type II
T Hays, E Feuille, E Schussler, C Cunningham-Rundles, P Midulla
Journal of Pediatric Surgery Case Reports 1 (8), 244-246, 2013
2013
Genetic Causes of Congenital Anomalies of the Kidney and Urinary Tract
T Hays
Neonatology Questions and Controversies: Renal, Fluid & Electrolyte …, 2023
2023
Genetic testing for kidney disease of unknown etiology
T Hays, EE Groopman, AG Gharavi
Kidney international 98 (3), 590-600, 2020
582020
Genetic testing for unexplained perinatal disorders
T Hays, RJ Wapner
Current opinion in pediatrics 33 (2), 195-202, 2021
172021
Genomic identification of potential risk factors during acetaminophen-induced liver disease in susceptible and resistant strains of mice
KD Welch, TP Reilly, M Bourdi, T Hays, CA Pise-Masison, MF Radonovich, ...
Chemical research in toxicology 19 (2), 223-233, 2006
612006
Glomerular MYH9 expression is reduced by HIV-1
T Hays, VD D’Agati, JA Garellek, T Warren, ME Trubin, DP Hyink, JC He, ...
Aids 26 (7), 797-803, 2012
212012
Implementation of rapid genome sequencing for critically ill infants with complex congenital heart disease
T Hays, R Hernan, M Disco, EL Griffin, N Goldshtrom, D Vargas, ...
Circulation: Genomic and Precision Medicine 16 (5), 415-420, 2023
82023
Implementation of Rapid Genome Sequencing for Infants with Congenital Heart Disease
T Hays, R Hernan, M Disco, E Griffin, N Goldshtrom, D Vargas, ...
medRxiv, 2022.12. 16.22283479, 2022
2022
Learning the Language of Medical Device Innovation: A Longitudinal Interdisciplinary Elective for Medical Students
LM Maloney, M Hakimi, T Hays, J Adachi, A Chau, BS Esper, V Koulouris, ...
Academic Medicine 97 (9), 1341-1345, 2022
32022
Nine is the New Ten of Apgar Scores: An Observational Retrospective Cohort Study
SS Everett, M Bomback, P Roth, N Goldshtrom, RA Polin, A Lyford, T Hays
The Journal of Pediatrics, 114150, 2024
2024
PhDs: Israel also trains plenty
T Hays
Nature 473 (7347), 284-284, 2011
2011
Prevalence and Clinical Significance of Commonly Diagnosed Genetic Disorders in Preterm Infants
SS Everett, M Bomback, R Sahni, RJ Wapner, VN Tolia, RH Clark, ...
medRxiv, 2023.07. 14.23292662, 2023
2023
Prevalence and Clinical Significance of Commonly Diagnosed Genetic Disorders in Preterm Infants
T Hays, SS Everett, M Bomback, R Sahni, RJ Wapner, VN Tolia, RH Clark, ...
2023
Proteomics analysis of the non-muscle myosin heavy chain IIa-enriched actin-myosin complex reveals multiple functions within the podocyte
T Hays, A Ma’ayan, NR Clark, CM Tan, A Teixeira, A Teixeira, JW Choi, ...
PLoS One 9 (6), e100660, 2014
182014
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