The prevalence of common BRCA1 and BRCA2 mutations among Ashkenazi Jews.

Por Hartge, P, Struewing, J P, Wacholder, S, Brody, L C, Tucker, M A
Publicado em 1999

Considerations for Designing a Prototype Genetic Test for Use in Translational Research

Por Wade, C.H., McBride, C.M., Kardia, S.L.R., Brody, L.C.
Publicado em 2010

A Response to ‘Why Realistic Test Scenarios in Translational Research Remain Hypothetical’

Por Wade, C.H., McBride, C.M., Kardia, S.L.R., Brody, L.C.
Publicado em 2010

Detection of eight BRCA1 mutations in 10 breast/ovarian cancer families, including 1 family with male breast cancer.

Por Struewing, J P, Brody, L C, Erdos, M R, Kase, R G, Giambarresi, T R, Smith, S A, Collins, F S, Tucker, M A
Publicado em 1995

An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.

Por Mitchell, G A, Brody, L C, Looney, J, Steel, G, Suchanek, M, Dowling, C, Der Kaloustian, V, Kaiser-Kupfer, M, Valle, D
Publicado em 1988

Splice-mediated insertion of an Alu sequence inactivates ornithine delta-aminotransferase: a role for Alu elements in human mutation.

Por Mitchell, G A, Labuda, D, Fontaine, G, Saudubray, J M, Bonnefont, J P, Lyonnet, S, Brody, L C, Steel, G, Obie, C, Valle, D
Publicado em 1991

Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226V.

Por Michaud, J, Thompson, G N, Brody, L C, Steel, G, Obie, C, Fontaine, G, Schappert, K, Keith, C G, Valle, D, Mitchell, G A
Publicado em 1995

Localization of Romano-Ward long QT syndrome gene, LQT1, to the interval between tyrosine hydroxylase (TH) and D11S1349.

Por Russell, M W, Dick, M, Campbell, R M, Hulse, J E, Munroe, D J, Bric, E, Housman, D E, Collins, F S, Brody, L C
Publicado em 1995

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.

Por Mitchell, G A, Brody, L C, Sipila, I, Looney, J E, Wong, C, Engelhardt, J F, Patel, A S, Steel, G, Obie, C, Kaiser-Kupfer, M
Publicado em 1989

Genome-wide studies of von Willebrand Factor Propeptide Identify Loci Contributing to Variation in Propeptide Levels and von Willebrand Factor Clearance

Por Ozel, A.B., McGee, B., Siemieniak, D., Jacobi, P.M., Haberichter, S.L., Brody, L.C., Mills, J.L., Molloy, A.M., Ginsburg, D., Li, J.Z., Desch, K.C.
Publicado no J Thromb Haemost (2016)