L. D. Schroeder

Nonlinear dynamic simulation of a tethered aerostat - A fidelity study

S. P. Jones, L. D. Schroeder, 1999 .

Nonlinear Dynamic Simulation of a Tethered Aerostat: A Fidelity Study

S. P. Jones, L. D. Schroeder, 2001 .

Continuous current capacity of bundled cables for aircraft

L. D. Schroeder, M. Schach, 1954, Transactions of the American Institute of Electrical Engineers, Part II: Applications and Industry.

SMN2 exon 7 splicing is inhibited by binding of hnRNP A1 to a common ESS motif that spans the 3′ splice site

L. D. Schroeder, B. Andresen, N. Gregersen, 2011, Human mutation.

Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency.

L. D. Schroeder, E. R. Baumgartner, L. Bolund, 1999, American journal of human genetics.

Isolated 2-methylbutyrylglycinuria caused by short/branched-chain acyl-CoA dehydrogenase deficiency: identification of a new enzyme defect, resolution of its molecular basis, and evidence for distinct acyl-CoA dehydrogenases in isoleucine and valine metabolism.

L. D. Schroeder, R. Wanders, P. Bross, 2000, American journal of human genetics.

Characterization of mouse Clpp protease cDNA, gene, and protein

L. D. Schroeder, L. Bolund, P. Bross, 2000, Mammalian Genome.

Seemingly neutral polymorphic variants may confer immunity to splicing-inactivating mutations: a synonymous SNP in exon 5 of MCAD protects from deleterious mutations in a flanking exonic splicing enhancer.

L. D. Schroeder, A. Krainer, J. Kjems, 2007, American journal of human genetics.

DNA-based prenatal diagnosis for very-long- chain acyl-CoA dehydrogenase deficiency

L. D. Schroeder, L. Bolund, R. Wanders, 1999, Journal of Inherited Metabolic Disease.

The Deep Intronic c.903+469T>C Mutation in the MTRR Gene Creates an SF2/ASF Binding Exonic Splicing Enhancer, Which Leads to Pseudoexon Activation and Causes the cblE Type of Homocystinuria

L. D. Schroeder, T. K. Doktor, B. Andresen, 2010, Human mutation.