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Kathryn Eleanor Kronquist

TitleInstructor
InstitutionUniversity of Colorado Denver - Anschutz Medical Campus
DepartmentSOM-PEDS
Phone720/777-0517

    Collapse Bibliographic 
    Collapse selected publications
    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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    1. Arribas-Carreira L, Dallabona C, Swanson MA, Farris J, ?stergaard E, Tsiakas K, Hempel M, Aquaviva-Bourdain C, Koutsoukos S, Stence NV, Magistrati M, Spector EB, Kronquist K, Christensen M, Karstensen HG, Feichtinger RG, Achleitner MT, Lawrence Merritt Ii J, P?rez B, Ugarte M, Gr?newald S, Riela AR, Julve N, Arnoux JB, Haldar K, Donnini C, Santer R, Lund AM, Mayr JA, Rodriguez-Pombo P, Van Hove JLK. Pathogenic variants in GCSH encoding the moonlighting H-protein cause combined nonketotic hyperglycinemia and lipoate deficiency. Hum Mol Genet. 2023 03 06; 32(6):917-933. PMID: 36190515.
      View in: PubMed
    2. Spector E, Behlmann A, Kronquist K, Rose NC, Lyon E, Reddi HV. Laboratory testing for fragile X, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2021 05; 23(5):799-812. PMID: 33795824.
      View in: PubMed
    3. Van Hove JLK, Freehauf CL, Ficicioglu C, Pena LDM, Moreau KL, Henthorn TK, Christians U, Jiang H, Cowan TM, Young SP, Hite M, Friederich MW, Stabler SP, Spector EB, Kronquist KE, Thomas JA, Emmett P, Harrington MJ, Pyle L, Creadon-Swindell G, Wempe MF, MacLean KN. Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine ?-synthase deficient homocystinuria and the impact of taurine treatment in a phase 1/2 human clinical trial. J Inherit Metab Dis. 2019 05; 42(3):424-437. PMID: 30873612.
      View in: PubMed
    4. Coughlin CR, Swanson MA, Spector E, Meeks NJL, Kronquist KE, Aslamy M, Wempe MF, van Karnebeek CDM, Gospe SM, Aziz VG, Tsai BP, Gao H, Nagy PL, Hyland K, van Dooren SJM, Salomons GS, Van Hove JLK. The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: A common epileptic encephalopathy. J Inherit Metab Dis. 2019 03; 42(2):353-361. PMID: 30043187.
      View in: PubMed
    5. Coughlin CR, Swanson MA, Kronquist K, Acquaviva C, Hutchin T, Rodr?guez-Pombo P, V?is?nen ML, Spector E, Creadon-Swindell G, Br?s-Goldberg AM, Rahikkala E, Moilanen JS, Mahieu V, Matthijs G, Bravo-Alonso I, P?rez-Cerd? C, Ugarte M, Vianey-Saban C, Scharer GH, Van Hove JLK. Correction: The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT. Genet Med. 2018 09; 20(9):1098. PMID: 29300369.
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    6. Coughlin CR, Swanson MA, Spector EB, Kronquist KE, Van Hove JLK. Comment on Late-Onset Nonketotic Hyperglycinemia With a Heterozygous Novel Point Mutation of the GLDC Gene. Pediatr Neurol. 2018 02; 79:e1. PMID: 29239742.
      View in: PubMed
    7. Swanson MA, Garcia SM, Spector E, Kronquist K, Creadon-Swindell G, Walter M, Christensen E, Van Hove JLK, Sass JO. d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence. Mol Genet Metab. 2017 06; 121(2):80-82. PMID: 28462797.
      View in: PubMed
    8. Coughlin CR, Swanson MA, Kronquist K, Acquaviva C, Hutchin T, Rodr?guez-Pombo P, V?is?nen ML, Spector E, Creadon-Swindell G, Br?s-Goldberg AM, Rahikkala E, Moilanen JS, Mahieu V, Matthijs G, Bravo-Alonso I, P?rez-Cerd? C, Ugarte M, Vianey-Saban C, Scharer GH, Van Hove JL. The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT. Genet Med. 2017 01; 19(1):104-111. PMID: 27362913.
      View in: PubMed
    9. Horne BD, Lenzini PA, Wadelius M, Jorgensen AL, Kimmel SE, Ridker PM, Eriksson N, Anderson JL, Pirmohamed M, Limdi NA, Pendleton RC, McMillin GA, Burmester JK, Kurnik D, Stein CM, Caldwell MD, Eby CS, Rane A, Lindh JD, Shin JG, Kim HS, Angchaisuksiri P, Glynn RJ, Kronquist KE, Carlquist JF, Grice GR, Barrack RL, Li J, Gage BF. Pharmacogenetic warfarin dose refinements remain significantly influenced by genetic factors after one week of therapy. Thromb Haemost. 2012 Feb; 107(2):232-40. PMID: 22186998.
      View in: PubMed
    10. Kronquist KE, Sherman SL, Spector EB. Clinical significance of tri-nucleotide repeats in Fragile X testing: a clarification of American College of Medical Genetics guidelines. Genet Med. 2008 Nov; 10(11):845-7. PMID: 18941415.
      View in: PubMed
    11. Lenzini PA, Grice GR, Milligan PE, Dowd MB, Subherwal S, Deych E, Eby CS, King CR, Porche-Sorbet RM, Murphy CV, Marchand R, Millican EA, Barrack RL, Clohisy JC, Kronquist K, Gatchel SK, Gage BF. Laboratory and clinical outcomes of pharmacogenetic vs. clinical protocols for warfarin initiation in orthopedic patients. J Thromb Haemost. 2008 Oct; 6(10):1655-62. PMID: 18662264.
      View in: PubMed
    12. Comanor L, Elkin C, Leung K, Krajden M, Kronquist K, Nicolas K, Horansky E, deMedina M, Kittichai P, Sablon E, Ziermann R, Sherlock C. Successful HCV genotyping of previously failed and low viral load specimens using an HCV RNA qualitative assay based on transcription-mediated amplification in conjunction with the line probe assay. J Clin Virol. 2003 Sep; 28(1):14-26. PMID: 12927747.
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    13. Greene ME, Blumberg B, McBride OW, Yi HF, Kronquist K, Kwan K, Hsieh L, Greene G, Nimer SD. Isolation of the human peroxisome proliferator activated receptor gamma cDNA: expression in hematopoietic cells and chromosomal mapping. Gene Expr. 1995; 4(4-5):281-99. PMID: 7787419.
      View in: PubMed
    14. Grody WW, Kronquist KE, Lee EU, Edmond J, Rome LH. PCR-based cystic fibrosis (CF) carrier screening in a first-year medical student biochemistry laboratory. Am J Hum Genet. 1993 Dec; 53(6):1352-5. PMID: 8250051.
      View in: PubMed
    15. Kronquist KE, Dreazen E, Keener SL, Nicholas TW, Crandall BF. Reduced fetal hepatic alpha-fetoprotein levels in Down's syndrome. Prenat Diagn. 1990 Nov; 10(11):739-51. PMID: 1704627.
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    16. Campagnoni AT, Sorg B, Roth HJ, Kronquist K, Newman SL, Kitamura K, Campagnoni C, Crandall B. Expression of myelin protein genes in the developing brain. J Physiol (Paris). 1987; 82(4):229-38. PMID: 2460618.
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    17. Roth HJ, Kronquist KE, Kerlero de Rosbo N, Crandall BF, Campagnoni AT. Evidence for the expression of four myelin basic protein variants in the developing human spinal cord through cDNA cloning. J Neurosci Res. 1987; 17(4):321-8. PMID: 2442403.
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    18. Kronquist KE, Crandall BF, Macklin WB, Campagnoni AT. Expression of myelin proteins in the developing human spinal cord: cloning and sequencing of human proteolipid protein cDNA. J Neurosci Res. 1987; 18(3):395-401. PMID: 2449536.
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    19. Kedersha NL, Hill DF, Kronquist KE, Rome LH. Subpopulations of liver coated vesicles resolved by preparative agarose gel electrophoresis. J Cell Biol. 1986 Jul; 103(1):287-97. PMID: 2941442.
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    20. Roth HJ, Kronquist K, Pretorius PJ, Crandall BF, Campagnoni AT. Isolation and characterization of a cDNA coding for a novel human 17.3K myelin basic protein (MBP) variant. J Neurosci Res. 1986; 16(1):227-38. PMID: 2427738.
      View in: PubMed
    21. Kronquist KE, Crandall BF, Tabsh KM. Characterization of fetal urinary proteins at midgestation and term. Biol Neonate. 1984; 46(6):267-75. PMID: 6518195.
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    22. Kronquist KE, Crandall BF, Cosico LG. Detection of novel fetal polypeptides in human amniotic fluid using two-dimensional gel electrophoresis. Tumour Biol. 1984; 5(1):15-31. PMID: 6208593.
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    23. Kronquist KE, Pedersen ME, Schotz MC. Mechanism of alteration of the functional fraction of lipoprotein lipase in rat heart. Life Sci. 1980 Sep 29; 27(13):1153-8. PMID: 6999273.
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    24. Ronzio RA, Kronquist KE, Lewis DS, MacDonald RJ, Mohrlok SH, O'Donnell JJ. Glycoprotein synthesis in the adult rat pancreas. IV. Subcellular distribution of membrane glycoproteins. Biochim Biophys Acta. 1978 Mar 21; 508(1):65-84. PMID: 629968.
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    25. Kronquist KE, Lennarz WJ. Enzymatic conversion of proteins to glycoproteins by lipid-linked saccharides: a study of potential exogenous acceptor proteins. J Supramol Struct. 1978; 8(1):51-65. PMID: 732307.
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    26. Kronquist KE, Elmahdy A, Ronzio RA. Synthesis and subcellular distribution of heparan sulfate in the rat exocrine pancreas. Arch Biochem Biophys. 1977 Jul; 182(1):188-96. PMID: 142443.
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    27. Lewis DS, MacDonald RJ, Kronquist KE, Ronzio RA. Purification and partial characterization of an integral membrane glycoprotein from zymogen granules of dog pancreas. FEBS Lett. 1977 Apr 01; 76(1):115-20. PMID: 852598.
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