Mullin, B.H.* et al. Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis. Genetics 225:iyad150 (2023)
Veturi, Y.* et al. Modeling heterogeneity in the genetic architecture of ethnically diverse groups using random effect interaction models. Genetics 211, 1395–1407 (2019)
Janevska, S.* et al. Elucidation of the two H3K36me3 histone methyltransferases Set2 and Ash1 in Fusarium fujikuroi unravels their different chromosomal targets and a major impact of Ash1 on genome stability. Genetics 208, 153-171 (2018)
Schweiger, R.* et al. RL-SKAT: An exact and efficient score Test for heritability and set tests. Genetics 207, 1275-1283 (2017)
Budach, S.* ; Heinig, M. & Marsico, A.* Principles of microRNA regulation revealed through modeling microRNA expression quantitative trait loci. Genetics 203, 1629-1640 (2016)
Poursarebani, N.* et al. The genetic basis of composite spike form in barley and "Miracle-Wheat". Genetics 201, 155-165 (2015)
Tsepilov, Y.A. et al. Non-additive effects of genes in human metabolomics. Genetics 200, 707-718 (2015)
Guo, H.* et al. Extensive and biased intergenomic non-reciprocal DNA exchanges shaped a nascent polyploid genome, Gossypium (cotton). Genetics 197, 1153-1163 (2014)
Panda, S. et al. Highly efficient targeted mutagenesis in mice using TALENs. Genetics 195, 703-713 (2013)
Eberlein, A.* et al. Dissection of genetic factors modulating fetal growth in cattle indicates a substantial role of the non-SMC condensin I complex, subunit G (NCAPG) gene. Genetics 183, 951-964 (2009)
Favor, J. et al. Analysis of Pax6 contiguous gene deletions in the mouse, Mus musculus, identifies regions distinct from Pax6 responsible for extreme small-eye and belly-spotting phenotypes. Genetics 182, 1077-1088 (2009)
Favor, J. et al. Relationship of Pax6 activity levels to the extent of eye development in the mouse, Mus musculus. Genetics 179, 1345-1355 (2008)
Favor, J. et al. Type IV procollagen missense mutations associated with defects of the eye, vascular stability, the brain, kidney function and embryonic or postnatal viability in the mouse, Mus musculus: An extension of the Col₄a₁allelic series and the identification of the first twoCol₄a₂ mutant alleles. Genetics 175, 725-736 (2007)
Rubio-Aliaga, I. et al. A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse. Genetics 175, 1451-1463 (2007)
Binladen, J.* et al. Assessing the fidelity of ancient DNA sequences amplified from nuclear genes. Genetics 172, 733-741 (2006)
Noguchi, Y.* et al. Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (tmc1Bth) mouse model of progressive hearing loss DFNA36. Genetics 173, 2111-2119 (2006)
Graw, J. ; Pretsch, W. & Löster, J. Mutation in Intron 6 of the Hamster Mitf Gene Leads to Skipping of the Subsequent Exon and Creates a Novel Animal Model for the Human Waardenburg Syndrome Type II. Genetics 164, 1035-1041 (2003)
Kokubu, C. et al. Undulated short-tail Deletion Mutation in the Mouse Ablates Pax1 and Leads to Ectopic Activation of Neighboring Nkx2-2 in Domains That Normally Express Pax1. Genetics 165, 299-307 (2003)
Santagati, F. et al. Identification of Cis-regulatory elements in the mouse Pax9/Nkx2-9 genomic region: Implication for evolutionary conserved synteny. Genetics 165, 235-242 (2003)
Graw, J. ; Neuhäuser-Klaus, A. ; Löster, J. ; Klopp, N. & Favor, J. Ethylnitrosourea-Induced Base Pair Substitution Affects Splicing of the Mouse gammaE-Crystallin Encoding Gene Leading to the Expression of a Hybrid Protein and to a Cataract. Genetics 161, 1633-1640 (2002)
Favor, J. et al. Molecular characterization of Pax62Neu through Pax610Neu: An extension of the Pax6 allelic series and the identification of two possible hypomorph alleles in the mouse Mus musculus. Genetics 159, 1689-1700 (2001)
Graw, J. et al. Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts. Genetics 157, 1313-1320 (2001)
Pretsch, W. ; Merkle, S. ; Favor, J. & Werner, T. A Mutation Affecting the Lactate Dehydrogenase Locus Ldh-1 in the Mouse. - II. Mechanism of the LDH-A Deficiency Associated with Hemolytic Anemia. Genetics 135, 161-170 (1993)
Pretsch, W. ; Merkle, S. ; Favor, J. & Werner, T. A mutation affecting the lactate dehydrogenase locus Ldh-1 in the mouse. II. Mechanism of the LDH-A deficiency associated with hemolytic anemia. Genetics 135, 161-170 (1993)
Merkle, S. ; Favor, J. ; Graw, J. ; Hornhardt, S.V. & Pretsch, W. Hereditary lactate dehydrogenase A-subunit deficiency as cause of early postimplantation death of homozygotes in Mus musculus. Genetics 131, 413-421 (1992)
Merkle, S. & Pretsch, W. Characterization of triosephosphate isomerase mutants with reduced enzyme activity in Mus musculus. Genetics 123, 837-844 (1989)
Eckardt-Schupp, F. ; Siede, W. & Game, J.C. The RAD24 (= RS1) gene product of Saccharomyces cerevisiae participates in two different pathways of DNA repair. Genetics 115, 83-90 (1987)