PuSH - Publikationsserver des Helmholtz Zentrums München

Mullin, B.H.* ; Zhu, K.* ; Brown, S.J.* ; Mullin, S.* ; Dudbridge, F.* ; Pavlos, N.J.* ; Richards, J.B.* ; Grundberg, E.* ; Bell, J.T.* ; Zeggini, E. ; Walsh, J.P.* ; Xu, J.* ; Wilson, S.G.*

Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis.

Genetics 225:iyad150 (2023)

Veturi, Y.* ; de Los Campos, G.* ; Yi, N.* ; Huang, W.* ; Vazquez, A.I.* ; Kühnel, B.

Modeling heterogeneity in the genetic architecture of ethnically diverse groups using random effect interaction models.

Genetics 211, 1395–1407 (2019)

Janevska, S.* ; Baumann, L.* ; Sieber, C.M.K.* ; Münsterkötter, M. ; Ulrich, J.* ; Kämper, J.* ; Güldener, U.* ; Tudzynski, B.*

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.* ; Weissbrod, O.* ; Rahmani, E.* ; Müller-Nurasyid, M. ; Kunze, S. ; Gieger, C. ; Waldenberger, M. ; Rosset, S.* ; Halperin, E.*

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)

Colomé-Tatché, M. ; Johannes, F.*

Signatures of Dobzhansky-Muller Incompatibilities in the genomes of recombinant inbred lines.

Genetics 202, 825-841 (2016)

Poursarebani, N.* ; Seidensticker, T.* ; Koppolu, R.* ; Trautewig, C.* ; Gawroński, P.* ; Bini, F.* ; Govind, G.* ; Rutten, T.* ; Sakuma, S.* ; Tagiri, A.* ; Wolde, G.M.* ; Youssef, H.M.* ; Battal, A.* ; Ciannamea, S.* ; Fusca, T.* ; Youssef, H.M.* ; Nussbaumer, T. ; Pozzi, C.* ; Börner, A.* ; Lundqvist, U.* ; Komatsuda, T.* ; Salvi, S.* ; Tuberosa, R.* ; Uauy, C.* ; Sreenivasulu, N.* ; Rossini, L.* ; Schnurbusch, T.*

The genetic basis of composite spike form in barley and "Miracle-Wheat".

Genetics 201, 155-165 (2015)

Tsepilov, Y.A. ; Shin, S.Y.* ; Soranzo, N.* ; Spector, T.D.* ; Prehn, C. ; Adamski, J. ; Kastenmüller, G. ; Wang-Sattler, R. ; Strauch, K. ; Gieger, C. ; Aulchenko, Y.S.* ; Ried, J.S.

Non-additive effects of genes in human metabolomics.

Genetics 200, 707-718 (2015)

Guo, H.* ; Wang, X.* ; Gundlach, H. ; Mayer, K.F.X. ; Peterson, D.G.* ; Scheffler, B.E.* ; Chee, P.W.* ; Paterson, A.H.*

Extensive and biased intergenomic non-reciprocal DNA exchanges shaped a nascent polyploid genome, Gossypium (cotton).

Genetics 197, 1153-1163 (2014)

Panda, S. ; Wefers, B. ; Ortiz, O. ; Floß, T. ; Schmid, B.* ; Haass, C.* ; Wurst, W. ; Kühn, R.

Highly efficient targeted mutagenesis in mice using TALENs.

Genetics 195, 703-713 (2013)

Johannes, F.* ; Colomé-Tatché, M.

Quantitative epigenetics through epigenomic perturbation of isogenic lines.

Genetics 188, 215-227 (2011)

Roux, F.* ; Colomé-Tatché, M. ; Edelist, C.* ; Wardenaar, R.* ; Guerche, P.* ; Hospital, F.* ; Colot, V.* ; Jansen, R.C.* ; Johannes, F.*

Genome-wide epigenetic perturbation jump-starts patterns of heritable variation found in nature.

Genetics 188, 1015-1017 (2011)

Eberlein, A.* ; Takasuga, A.* ; Setoguchi, K.* ; Pfuhl, R.* ; Flisikowski, K.* ; Fries, R.* ; Klopp, N. ; Fürbass, R.* ; Weikard, R.* ; Kühn, C.*

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. ; Bradley, A.* ; Conte, N.* ; Janik, D.* ; Pretsch, W. ; Reitmeir, P. ; Rosemann, M. ; Schmahl, W.* ; Wienberg, J.* ; Zaus, I.

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. ; Gloeckner, C.J. ; Neuhäuser-Klaus, A. ; Pretsch, W. ; Sandulache, R. ; Saule, S.* ; Zaus, I.

Relationship of Pax6 activity levels to the extent of eye development in the mouse, Mus musculus.

Genetics 179, 1345-1355 (2008)

Favor, J. ; Gloeckner, C.J. ; Janik, D.* ; Klempt, M.* ; Neuhäuser-Klaus, A. ; Pretsch, W. ; Schmahl, W.* ; Quintanilla-Fend, L.

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. ; Soewarto, D. ; Wagner, S. ; Klaften, M. ; Fuchs, H. ; Kalaydjiev, S. ; Busch, D.H. ; Klempt, M. ; Rathkolb, B. ; Wolf, E. ; Abe, K. ; Zeiser, S. ; Przemeck, G.K.H. ; Beckers, J. ; Hrabě de Angelis, M.

A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse.

Genetics 175, 1451-1463 (2007)

Binladen, J.* ; Wiuf, C.* ; Gilbert, M.T.P.* ; Bunce, M.* ; Barnett, R.* ; Larson, G.* ; Greenwood, A.D. ; Haile, J.* ; Ho, S.Y.W.* ; Hanson, A.J.* ; Willerslev, E.*

Assessing the fidelity of ancient DNA sequences amplified from nuclear genes.

Genetics 172, 733-741 (2006)

Noguchi, Y.* ; Kurima, K.* ; Makishima, T.* ; Hrabě de Angelis, M. ; Fuchs, H. ; Frolenkov, G.* ; Kitamura, K.* ; Griffith, A.J.*

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. ; Wilm, B. ; Kokubu, T. ; Wahl, M. ; Rodrigo, I. ; Sakai, N. ; Santagati, F. ; Hayashizaki, Y.* ; Suzuki, M.* ; Yamamura, K.* ; Abe, K.* ; Imai, K.

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. ; Abe, K.* ; Schmidt, V.* ; Schmitt-John, T.* ; Suzuki, M.* ; Yamamura, K.* ; Imai, K.

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. ; Peters, H. ; Hermann, T. ; Schmahl, W.* ; Chatterjee, B. ; Neuhäuser, K.A.* ; Sandulache, R.

Molecular characterization of Pax6^2Neu through Pax6^10Neu: 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. ; Klopp, N. ; Löster, J. ; Soewarto, D. ; Fuchs, H. ; Becker-Follmann, J.* ; Reis, A.* ; Wolf, E.* ; Balling, R. ; Hrabě de Angelis, M.