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Bell*, T.A., de la Casa-Esperon*, E., Doherty*, H.E., Ideraabdullah*, F., Kim, K., Wang, Y., Lange, L.A., Wilhemsen, K., Lange, E.M., Sapienza, C., and Pardo-Manuel de Villena, F. (2006) The paternal gene of the DDK syndrome maps to the Schlafen gene cluster on mouse chromosome 11. Genetics 172, 411-423. *these authors contributed equally to this work

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Ideraabdullah*, F.Y., de la Casa-Esperón*, E., Bell* T.A., Detwiler, D.A., Magnuson, T., Sapienza, C. and Pardo-Manuel de Villena, F. (2004) Genetic and haplotype diversity among wild-derived mouse inbred strains. Genome Research 14, 1880-1887. *these authors contributed equally to this work

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de la Casa-Esperon, E., Loredo-0sti, J C., Pardo-Manuel de Villena, F., Briscoe, T.L., Malette, J.M., Vaughan, J.E., Morgan, K. and Sapienza, C. (2002) X chromosome inactivation effect on maternal recombination and meiotic drive in the mouse. Genetics 161, 1651-1659.

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Pardo-Manuel de Villena, F., de la Casa-Esperon, E., Williams, J., Malette, J.M., Rosa, M. and Sapienza, C. (2000) Heritability of the maternal meiotic drive system linked to Om ad high resolution mapping of the Responder locus. Genetics 155, 283-289.

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Pardo-Manuel de Villena, F., de la Casa-Esperon, E., Briscoe, T.L. and Sapienza, C. (2000) A genetic test to determine the origin of maternal transmission ratio distortion: meiotic drive at the mouse Om locus. Genetics 154, 333-342.

Pardo-Manuel de Villena, F., de la Casa-Esperon, E., Briscoe, T.L., Malette, J.M. and Sapienza, C. (2000). Male offspring-specific, haplotype-dependent, nonrandom cosegregation of alleles at loci on two mouse chromosomes. Genetics 154, 351-356.

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