K. Kronquist

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Pharmacogenetic warfarin dose refinements remain significantly influenced by genetic factors after one week of therapy

Munir Pirmohamed, Robert J Glynn, Stephen E Kimmel, 2011, Thrombosis and Haemostasis.

Isolation of the human peroxisome proliferator activated receptor gamma cDNA: expression in hematopoietic cells and chromosomal mapping.

B. Blumberg, O. Mcbride, G. Greene, 1995, Gene expression.

PCR-based cystic fibrosis (CF) carrier screening in a first-year medical student biochemistry laboratory.

W. Grody, K. Kronquist, E. U. Lee, 1993, American journal of human genetics.

Detection of novel fetal polypeptides in human amniotic fluid using two-dimensional gel electrophoresis.

B. Crandall, K. Kronquist, L. Cosico, 1984, Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine.

Reduced fetal hepatic alpha‐fetoprotein levels in Down' S syndrome

B. Crandall, K. Kronquist, E. Dreazen, 1990, Prenatal diagnosis.

Subpopulations of liver coated vesicles resolved by preparative agarose gel electrophoresis

N. Kedersha, K. Kronquist, D. Hill, 1986, The Journal of cell biology.

Glycoprotein synthesis in the adult rat pancreas. IV. Subcellular distribution of membrane glycoproteins.

D. Lewis, Raymond J MacDonald, K. Kronquist, 1978, Biochimica et biophysica acta.

Evidence for the expression of four myelin basic protein variants in the developing human spinal cord through cDNA cloning

A. Campagnoni, B. Crandall, K. Kronquist, 1987, Journal of neuroscience research.

Isolation and characterization of a cDNA coding for a novel human 17.3k myelin basic protein (MBP) variant

A. Campagnoni, B. Crandall, K. Kronquist, 1986, Journal of neuroscience research.

Enzymatic conversion of proteins to glycoproteins by lipid-linked saccharides: a study of potential exogenous acceptor proteins.

W. Lennarz, K. Kronquist, 1978, Journal of supramolecular structure.

Synthesis and subcellular distribution of heparan sulfate in the rat exocrine pancreas.

K. Kronquist, R. Ronzio, A. Elmahdy, 1977, Archives of biochemistry and biophysics.

Purification and partial characterization of an integral membrane glycoprotein from zymogen granules of dog pancreas

D. Lewis, Raymond J MacDonald, K. Kronquist, 1977, FEBS letters.

Expression of myelin protein genes in the developing brain.

C. Campagnoni, A. Campagnoni, B. Crandall, 1987, Journal de physiologie.

Clinical significance of tri-nucleotide repeats in Fragile X testing: A clarification of American College of Medical Genetics guidelines

E. Spector, S. Sherman, K. Kronquist, 2008, Genetics in Medicine.

d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence.

J. Sass, E. Christensen, J. V. Van Hove, 2017, Molecular genetics and metabolism.

The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: a common epileptic encephalopathy

Hanlin Gao, C. V. van Karnebeek, S. Gospe, 2018, Journal of Inherited Metabolic Disease.

The genotypic spectrum of ALDH7A1 mutations resulting in pyridoxine dependent epilepsy: a common epileptic encephalopathy

Hanlin Gao, C. V. van Karnebeek, S. Gospe, 2018, Journal of Inherited Metabolic Disease.

Laboratory testing for fragile X, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)

E. Lyon, H. Reddi, E. Spector, 2021, Genetics in Medicine.

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.

L. Comanor, C. Sherlock, R. Ziermann, 2003, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

The genetic basis of classic nonketotic hyperglycinemia due to mutations in GLDC and AMT

G. Matthijs, C. Pérez-Cerdá, M. Ugarte, 2016, Genetics in Medicine.

Mechanism of alteration of the functional fraction of lipoprotein lipase in rat heart.

M. Schotz, K. Kronquist, M. Pedersen, 1980, Life sciences.

Biomarkers of oxidative stress, inflammation, and vascular dysfunction in inherited cystathionine β‐synthase deficient homocystinuria and the impact of taurine treatment in a phase 1/2 human clinical trial

U. Christians, K. Moreau, L. Pyle, 2019, Journal of inherited metabolic disease.

Pathogenic variants in GCSH encoding the moonlighting H-protein cause combined nonketotic hyperglycinemia and lipoate deficiency

N. Stence, K. Haldar, M. Ugarte, 2022, Human molecular genetics.

Laboratory and clinical outcomes of pharmacogenetic vs. clinical protocols for warfarin initiation in orthopedic patients

R. Barrack, B. Gage, C. Eby, 2008, Journal of thrombosis and haemostasis : JTH.

Expression of myelin proteins in the developing human spinal cord: Cloning and sequencing of human proteolipid protein cDNA

A. Campagnoni, B. Crandall, W. Macklin, 1987, Journal of neuroscience research.

Laboratory and clinical outcomes of pharmacogenetic vs. clinical protocols for warfarin initiation in orthopedic patients

R. Barrack, B. Gage, C. Eby, 2008, Journal of thrombosis and haemostasis : JTH.