F. Nahhas

发表

Outcomes of individuals with profound and partial biotinidase deficiency ascertained by newborn screening in Michigan over 25 years

G. Feldman, B. Wolf, Fatimah A. Nahhas, 2014, Genetics in Medicine.

Novel mutations causing biotinidase deficiency in individuals identified by newborn screening in Michigan including an unique intronic mutation that alters mRNA expression of the biotinidase gene.

G. Feldman, B. Wolf, A. Fribley, 2014, Molecular genetics and metabolism.

Role for Human SIRT2 NAD-Dependent Deacetylase Activity in Control of Mitotic Exit in the Cell Cycle

Michael A. Tainsky, M. Tainsky, A. Goustin, 2003, Molecular and Cellular Biology.

Mutations in SIRT2 deacetylase which regulate enzymatic activity but not its interaction with HDAC6 and tubulin

M. Tainsky, J. Abrams, Fatimah A. Nahhas, 2007, Molecular and Cellular Biochemistry.

Diagnostic markers of ovarian cancer by high-throughput antigen cloning and detection on arrays.

Gerard Tromp, Sorin Draghici, Karen Lu, 2006, Cancer research.

Expression profiling identifies three pathways altered in cellular immortalization: interferon, cell cycle, and cytoskeleton.

A. L. Fridman, B. Ye, P. Roberts, 2006, The journals of gerontology. Series A, Biological sciences and medical sciences.

Evaluation of the human fragile X mental retardation 1 polymerase chain reaction reagents to amplify the FMR1 gene: testing in a clinical diagnostic laboratory.

G. Feldman, T. Prior, P. Snyder, 2012, Genetic testing and molecular biomarkers.

Isochromosome 8q formation is associated with 8p loss of heterozygosity in a prostate cancer cell line

R. K. Bright, W. Sakr, M. Cher, 1999, The Prostate.

Juvenile onset Huntington disease resulting from a very large maternal expansion

G. Feldman, J. Garbern, Fatimah A. Nahhas, 2005, American journal of medical genetics. Part A.

An intergenerational contraction of a fully penetrant Huntington disease allele to a reduced penetrance allele: Interpretation of results and significance for risk assessment and genetic counseling

G. Feldman, S. Feely, J. Garbern, 2009, American journal of medical genetics. Part A.

Extra alleles in FMR1 triple-primed PCR: artifact, aneuploidy, or somatic mosaicism?

G. Feldman, E. Wakeling, F. Nahhas, 2014, The Journal of molecular diagnostics : JMD.