Lisa F. Taft

Characterization of susceptible chiasma configurations that increase the risk for maternal nondisjunction of chromosome 21.

E. Feingold, T. Hassold, G. Karadima, 1997, Human molecular genetics.

Susceptible chiasmate configurations of chromosome 21 predispose to non–disjunction in both maternal meiosis I and meiosis II

Neil E. Lamb, Stephanie L. Sherman, Lisa Taft, 1996, Nature Genetics.

Non-disjunction of chromosome 21 in maternal meiosis I: evidence for a maternal age-dependent mechanism involving reduced recombination.

T. Hassold, M. Petersen, M. Mikkelsen, 1994, Human molecular genetics.

Prevalence of the fragile X syndrome in African-Americans.

D. Crawford, M. Yeargin-Allsopp, C. Boyle, 2002, American journal of medical genetics.

Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population.

D. Crawford, M. Yeargin-Allsopp, C. Boyle, 1999, American journal of human genetics.

Population-based study of congenital heart defects in Down syndrome.

M. Khoury, T. Hassold, S. Freeman, 1998, American journal of medical genetics.

Women’s Attitudes Toward Testing for Fragile X Carrier Status: A Qualitative Analysis

L. Taft, S. Sherman, A. Anido, 2005, Journal of Genetic Counseling.

Elucidating the mechanisms of paternal non-disjunction of chromosome 21 in humans.

M Mikkelsen, T. Hassold, G. Karadima, 1998, Human molecular genetics.