J. Gregg

Predisposition to Thrombosis by a Factor V Mutation Causing Hereditary Resistance to Activated Protein C THROMBOEMBOLIC

J. Gregg, 2022 .

Genotype–Phenotype Association Studies of Chromosome 8p Inverted Duplication Deletion Syndrome

G. Fisch, R. Davis, J. Youngblom, 2011, Behavior genetics.

Linkage-disequilibrium mapping without genotyping

S. Nelson, W. Ewens, T. Shows, 1998, Nature Genetics.

Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray.

D. Geschwind, S. Nelson, J. Ellison, 1998, Developmental genetics.

PUBLISHED VERSION

Huichun Xu, B. Ander, B. Stamova, 2015 .

Detection of differentially expressed genes in primary tumor tissues using representational differences analysis coupled to microarray hybridization.

S. Nelson, S. Welford, J. Gregg, 1998, Nucleic acids research.

Genomic and functional profiling of duplicated chromosome 15 cell lines reveal regulatory alterations in UBE3A-associated ubiquitin-proteasome pathway processes.

J. Gregg, C. Tepper, N. C. Schanen, 2006, Human molecular genetics.

Identifying patterns of copy number variants in case-control studies of human genetic disorders

Ahmed H. Tewfik, Abdullah K. Alqallaf, Scott B. Selleck, 2009, 2009 IEEE International Workshop on Genomic Signal Processing and Statistics.

Prevalence of the factor V-Leiden mutation in four distinct American ethnic populations.

W. Grody, A. Yamane, A. Yamane, 1997, American journal of medical genetics.