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"); document.write("
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.*
"); document.write("
Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis.
"); document.write("
Genetics 225:iyad150 (2023)
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Veturi,\ Y.*\ ; de Los Campos,\ G.*\ ; Yi,\ N.*\ ; Huang,\ W.*\ ; Vazquez,\ A.I.*\ ; Kühnel,\ B.
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Modeling heterogeneity in the genetic architecture of ethnically diverse groups using random effect interaction models.
"); document.write("
Genetics 211, 1395–1407 (2019)
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Janevska,\ S.*\ ; Baumann,\ L.*\ ; Sieber,\ C.M.K.*\ ; Münsterkötter,\ M.\ ; Ulrich,\ J.*\ ; Kämper,\ J.*\ ; Güldener,\ U.*\ ; Tudzynski,\ B.*
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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.
"); document.write("
Genetics 208, 153-171 (2018)
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"); document.write("
Schweiger,\ R.*\ ; Weissbrod,\ O.*\ ; Rahmani,\ E.*\ ; Müller-Nurasyid,\ M.\ ; Kunze,\ S.\ ; Gieger,\ C.\ ; Waldenberger,\ M.\ ; Rosset,\ S.*\ ; Halperin,\ E.*
"); document.write("
RL-SKAT: An exact and efficient score Test for heritability and set tests.
"); document.write("
Genetics 207, 1275-1283 (2017)
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"); document.write("
"); document.write("
Budach,\ S.*\ ; Heinig,\ M.\ ; Marsico,\ A.*
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Principles of microRNA regulation revealed through modeling microRNA expression quantitative trait loci.
"); document.write("
Genetics 203, 1629-1640 (2016)
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"); document.write("
Colomé-Tatché,\ M.\ ; Johannes,\ F.*
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Signatures of Dobzhansky-Muller Incompatibilities in the genomes of recombinant inbred lines.
"); document.write("
Genetics 202, 825-841 (2016)
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"); document.write("
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.*
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The genetic basis of composite spike form in barley and \"Miracle-Wheat\".
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Genetics 201, 155-165 (2015)
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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.
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Non-additive effects of genes in human metabolomics.
"); document.write("
Genetics 200, 707-718 (2015)
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Guo,\ H.*\ ; Wang,\ X.*\ ; Gundlach,\ H.\ ; Mayer,\ K.F.X.\ ; Peterson,\ D.G.*\ ; Scheffler,\ B.E.*\ ; Chee,\ P.W.*\ ; Paterson,\ A.H.*
"); document.write("
Extensive and biased intergenomic non-reciprocal DNA exchanges shaped a nascent polyploid genome, \Gossypium\ (cotton).
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Genetics 197, 1153-1163 (2014)
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Panda,\ S.\ ; Wefers,\ B.\ ; Ortiz,\ O.\ ; Floß,\ T.\ ; Schmid,\ B.*\ ; Haass,\ C.*\ ; Wurst,\ W.\ ; Kühn,\ R.
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Highly efficient targeted mutagenesis in mice using TALENs.
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Genetics 195, 703-713 (2013)
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"); document.write("
Johannes,\ F.*\ ; Colomé-Tatché,\ M.
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Quantitative epigenetics through epigenomic perturbation of isogenic lines.
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Genetics 188, 215-227 (2011)
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Roux,\ F.*\ ; Colomé-Tatché,\ M.\ ; Edelist,\ C.*\ ; Wardenaar,\ R.*\ ; Guerche,\ P.*\ ; Hospital,\ F.*\ ; Colot,\ V.*\ ; Jansen,\ R.C.*\ ; Johannes,\ F.*
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Genome-wide epigenetic perturbation jump-starts patterns of heritable variation found in nature.
"); document.write("
Genetics 188, 1015-1017 (2011)
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Eberlein,\ A.*\ ; Takasuga,\ A.*\ ; Setoguchi,\ K.*\ ; Pfuhl,\ R.*\ ; Flisikowski,\ K.*\ ; Fries,\ R.*\ ; Klopp,\ N.\ ; Fürbass,\ R.*\ ; Weikard,\ R.*\ ; Kühn,\ C.*
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Dissection of genetic factors modulating fetal growth in cattle indicates a substantial role of the non-SMC condensin I complex, subunit G (NCAPG) gene.
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Genetics 183, 951-964 (2009)
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Favor,\ J.\ ; Bradley,\ A.*\ ; Conte,\ N.*\ ; Janik,\ D.*\ ; Pretsch,\ W.\ ; Reitmeir,\ P.\ ; Rosemann,\ M.\ ; Schmahl,\ W.*\ ; Wienberg,\ J.*\ ; Zaus,\ I.
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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.
"); document.write("
Genetics 182, 1077-1088 (2009)
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Favor,\ J.\ ; Gloeckner,\ C.J.\ ; Neuhäuser-Klaus,\ A.\ ; Pretsch,\ W.\ ; Sandulache,\ R.\ ; Saule,\ S.*\ ; Zaus,\ I.
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Relationship of Pax6 activity levels to the extent of eye development in the mouse, Mus musculus.
"); document.write("
Genetics 179, 1345-1355 (2008)
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Favor,\ J.\ ; Gloeckner,\ C.J.\ ; Janik,\ D.*\ ; Klempt,\ M.*\ ; Neuhäuser-Klaus,\ A.\ ; Pretsch,\ W.\ ; Schmahl,\ W.*\ ; Quintanilla-Fend,\ L.
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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.
"); document.write("
Genetics 175, 725-736 (2007)
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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.
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A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse.
"); document.write("
Genetics 175, 1451-1463 (2007)
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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.*
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Assessing the fidelity of ancient DNA sequences amplified from nuclear genes.
"); document.write("
Genetics 172, 733-741 (2006)
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Noguchi,\ Y.*\ ; Kurima,\ K.*\ ; Makishima,\ T.*\ ; Hrabě de Angelis,\ M.\ ; Fuchs,\ H.\ ; Frolenkov,\ G.*\ ; Kitamura,\ K.*\ ; Griffith,\ A.J.*
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Multiple quantitative trait loci modify cochlear hair cell degeneration in the Beethoven (tmc1Bth) mouse model of progressive hearing loss DFNA36.
"); document.write("
Genetics 173, 2111-2119 (2006)
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Graw,\ J.\ ; Pretsch,\ W.\ ; Löster,\ J.
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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.
"); document.write("
Genetics 164, 1035-1041 (2003)
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Kokubu,\ C.\ ; Wilm,\ B.\ ; Kokubu,\ T.\ ; Wahl,\ M.\ ; Rodrigo,\ I.\ ; Sakai,\ N.\ ; Santagati,\ F.\ ; Hayashizaki,\ Y.*\ ; Suzuki,\ M.*\ ; Yamamura,\ K.*\ ; Abe,\ K.*\ ; Imai,\ K.
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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.
"); document.write("
Genetics 165, 299-307 (2003)
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"); document.write("
Santagati,\ F.\ ; Abe,\ K.*\ ; Schmidt,\ V.*\ ; Schmitt-John,\ T.*\ ; Suzuki,\ M.*\ ; Yamamura,\ K.*\ ; Imai,\ K.
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Identification of \Cis\-regulatory elements in the mouse \Pax9/Nkx2-9\ genomic region: Implication for evolutionary conserved synteny.
"); document.write("
Genetics 165, 235-242 (2003)
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Graw,\ J.\ ; Neuhäuser-Klaus,\ A.\ ; Löster,\ J.\ ; Klopp,\ N.\ ; Favor,\ J.
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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.
"); document.write("
Genetics 161, 1633-1640 (2002)
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"); document.write("
Favor,\ J.\ ; Peters,\ H.\ ; Hermann,\ T.\ ; Schmahl,\ W.*\ ; Chatterjee,\ B.\ ; Neuhäuser,\ K.A.*\ ; Sandulache,\ R.
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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\.
"); document.write("
Genetics 159, 1689-1700 (2001)
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"); document.write("
Graw,\ J.\ ; Klopp,\ N.\ ; Löster,\ J.\ ; Soewarto,\ D.\ ; Fuchs,\ H.\ ; Becker-Follmann,\ J.*\ ; Reis,\ A.*\ ; Wolf,\ E.*\ ; Balling,\ R.\ ; Hrabě de Angelis,\ M.
"); document.write("
Ethylnitrosourea-induced mutation in mice leads to the expression of a novel protein in the eye and to dominant cataracts.
"); document.write("
Genetics 157, 1313-1320 (2001)
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Wurst,\ W.*\ ; Rossant,\ J.*\ ; Prideaux,\ V.*\ ; Kownacka,\ M.*\ ; Joyner,\ A.*\ ; Hill,\ D.P.*\ ; Guillemot,\ F.*\ ; Gasca,\ S.*\ ; Cado,\ D.*\ ; Auerbach,\ A.*
"); document.write("
A large-scale gene-trap screen for insertional mutations in developmentally regulated genes in mice.
"); document.write("
Genetics 139, 889-899 (1995)
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"); document.write("
Pretsch,\ W.\ ; Merkle,\ S.\ ; Favor,\ J.\ ; Werner,\ T.
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A Mutation Affecting the Lactate Dehydrogenase Locus Ldh-1 in the Mouse. - II. Mechanism of the LDH-A Deficiency Associated with Hemolytic Anemia.
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Genetics 135, 161-170 (1993)
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"); document.write("
Pretsch,\ W.\ ; Merkle,\ S.\ ; Favor,\ J.\ ; Werner,\ T.
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A mutation affecting the lactate dehydrogenase locus Ldh-1 in the mouse. II. Mechanism of the LDH-A deficiency associated with hemolytic anemia.
"); document.write("
Genetics 135, 161-170 (1993)
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"); document.write("
Merkle,\ S.\ ; Favor,\ J.\ ; Graw,\ J.\ ; Hornhardt,\ S.V.\ ; Pretsch,\ W.
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Hereditary lactate dehydrogenase A-subunit deficiency as cause of early postimplantation death of homozygotes in \Mus musculus\.
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Genetics 131, 413-421 (1992)
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"); document.write("
Merkle,\ S.\ ; Pretsch,\ W.
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Characterization of triosephosphate isomerase mutants with reduced enzyme activity in \Mus musculus\.
"); document.write("
Genetics 123, 837-844 (1989)
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"); document.write("
Eckardt-Schupp,\ F.\ ; Siede,\ W.\ ; Game,\ J.C.
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The \RAD24\ (= R\S\\1\) gene product of Saccharomyces cerevisiae participates in two different pathways of DNA repair.
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Genetics 115, 83-90 (1987)
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