KEVIN GLINTON

TitleAssistant Professor
InstitutionBaylor College of Medicine
DepartmentDepartment of Molecular & Human Genetics
AddressOne Baylor Plaza
Houston, TX 77030
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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. Slater B, Glinton K, Dai H, Lay E, Karaviti L, Mizerik E, Murali CN, Lalani SR, Bacino CA, Rossetti LZ. Sudden infant death with dysgenesis of the testes syndrome in a non-Amish infant: A case report. Am J Med Genet A. 2020 11; 182(11):2751-2754. PMID: 32885560.
      Citations:    
    2. Alaimo JT, Glinton KE, Liu N, Xiao J, Yang Y, Reid Sutton V, Elsea SH. Integrated analysis of metabolomic profiling and exome data supplements sequence variant interpretation, classification, and diagnosis. Genet Med. 2020 Sep; 22(9):1560-1566. PMID: 32439973.
      Citations:    Fields:    
    3. Nguyen JM, Kaushal S, Glinton KE, Marom R. A Somnolent Neonate With Hypothermia and Posturing. Clin Pediatr (Phila). 2020 Jul; 59(8):841-843. PMID: 32400174.
      Citations:    Fields:    
    4. Birjiniuk A, Glinton KE, Villafranco N, Boyer S, Laufman J, Mizerik E, Scott D, Elsea SH, Galambos C, Varghese NP, Scaglia F. Multiple mitochondrial dysfunctions syndrome 1: An unusual cause of developmental pulmonary hypertension. . 2020 04; 182(4):755-761. PMID: 31970900.
      Citations:    
    5. Glinton KE, Elsea SH. Untargeted Metabolomics for Autism Spectrum Disorders: Current Status and Future Directions. Front Psychiatry. 2019; 10:647. PMID: 31551836.
      Citations:    
    6. Rossetti LZ, Glinton K, Yuan B, Liu P, Pillai N, Mizerik E, Magoulas P, Rosenfeld JA, Karaviti L, Sutton VR, Lalani SR, Scott DA. Review of the phenotypic spectrum associated with haploinsufficiency of MYRF. . 2019 07; 179(7):1376-1382. PMID: 31069960.
      Citations:    
    7. Glinton KE, Levy HL, Kennedy AD, Pappan KL, Elsea SH. Untargeted metabolomics identifies unique though benign biochemical changes in patients with pathogenic variants in UROC1. Mol Genet Metab Rep. 2019 Mar; 18:14-18. PMID: 30619714.
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    8. Glinton KE, Sharp EA, Mendelsohn MJ. An 8-Year-Old Male With Fever of Unknown Origin. Clin Pediatr (Phila). 2018 09; 57(10):1239-1242. PMID: 29557188.
      Citations:    Fields:    Translation:HumansCells
    9. Glinton KE, Benke PJ, Lines MA, Geraghty MT, Chakraborty P, Al-Dirbashi OY, Jiang Y, Kennedy AD, Grotewiel MS, Sutton VR, Elsea SH, El-Hattab AW. Disturbed phospholipid metabolism in serine biosynthesis defects revealed by metabolomic profiling. Mol Genet Metab. 2018 03; 123(3):309-316. PMID: 29269105.
      Citations: 8     Fields:    Translation:HumansCells
    10. Pratt LM, Mogali S, Glinton K. Solvent effects on the aggregation state of lithium dialkylaminoborohydrides. J Org Chem. 2003 Aug 22; 68(17):6484-8. PMID: 12919007.
      Citations: 1     Fields:    
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