M. Schwalb

发表

Association between gene expression profile and tumor invasion in oral squamous cell carcinoma.

Patricia Soteropoulos, Meera R Hameed, M. Hameed, 2004, Cancer genetics and cytogenetics.

Arvanil and anandamide up-regulate CD36 expression in human peripheral blood mononuclear cells.

E. Vitale, A. Malfitano, L. De Petrocellis, 2007, Immunology letters.

Using the common sense model to understand perceived cancer risk in individuals testing for BRCA1/2 mutations

J. Dermody, D. Toppmeyer, M. Andrykowski, 2005, Psycho-oncology.

Linkage analysis conditional on HLA status in a large North American pedigree supports the presence of a multiple sclerosis susceptibility locus on chromosome 12p12.

M. Rocchi, M. Devoto, C. Specchia, 2002, Human molecular genetics.

Variants of ST8SIA1 Are Associated with Risk of Developing Multiple Sclerosis

M. Devoto, J. Rubio, E. Vitale, 2008, PloS one.

An oligonucleotide based array‐CGH system for detection of genome wide copy number changes including subtelomeric regions for genetic evaluation of mental retardation

J. Dermody, D. Streck, G. Toruner, 2007, American journal of medical genetics. Part A.

Comprehensive genome-wide comparison of DNA and RNA level scan using microarray technology for identification of candidate cancer-related genes in the HL-60 cell line.

J. Kang, P. Tolias, J. Dermody, 2003, Cancer genetics and cytogenetics.

Gene expression after crush injury of human saphenous vein: using microarrays to define the transcriptional profile.

J. Dermody, P. Soteropoulos, M. Schwalb, 2004, Journal of the American College of Surgeons.

Cancer genetics knowledge and beliefs and receipt of results in Ashkenazi Jewish individuals receiving counseling for BRCA1/2 mutations.

D. Toppmeyer, H. Leventhal, M. Marvin, 2004, Cancer control : journal of the Moffitt Cancer Center.

A second Middle Eastern kindred with autosomal recessive non-syndromic hearing loss segregates DFNB9

S. Leal, H. Zenner, E. Vitale, 1998, European Journal of Human Genetics.

High incidence of two methylenetetrahydrofolate reductase mutations (C677T and A1298C) in Hispanics.

D. Chowdary, J. Dermody, D. Streck, 2003, Genetic testing.

Subjective and objective risk of breast cancer in Ashkenazi Jewish individuals at risk for BRCA1/2 mutations.

Kimberly M. Kelly, J. Dermody, D. Toppmeyer, 2004, Genetic testing.

Subjective and Objective Risks of Carrying a BRCA1/2 Mutation in Individuals of Ashkenazi Jewish Descent

J. Dermody, D. Toppmeyer, H. Leventhal, 2003, Journal of Genetic Counseling.

The Decision to Test in Women Receiving Genetic Counseling for BRCA1 and BRCA2 Mutations

J. Dermody, D. Toppmeyer, M. Andrykowski, 2004, Journal of Genetic Counseling.

Novel X-linked mental retardation syndrome with short stature maps to Xq24.

M. Rocchi, M. Devoto, C. Specchia, 2001, American journal of medical genetics.