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Gu, Tingting; Tan, Shengjun; Gou, Xiaoxi; Araki, Hitoshi; Tian, Dacheng (2010). Avoidance of Long Mononucleotide Repeats in Codon Pair Usage. Genetics, 186(3), pp. 1077-1084. Bethesda, Md.: Genetics Society of America 10.1534/genetics.110.121137
Leuenberger, Christoph; Wegmann, Daniel (2010). Bayesian Computation and Model Selection Without Likelihoods. Genetics, 184(1), pp. 243-252. Bethesda, Md.: Genetics Society of America 10.1534/genetics.109.109058
Lindner, Heike; Raissig, Michael T.; Sailer, Christian; Shimosato-Asano, Hiroko; Bruggmann, Rémy; Grossniklaus, Ueli (2012). SNP-Ratio Mapping (SRM): Identifying Lethal Alleles and Mutations in Complex Genetic Backgrounds by Next-Generation Sequencing. Genetics, 191(4), pp. 1381-1386. Bethesda, Md.: Genetics Society of America 10.1534/genetics.112.141341
Slatkin, M.; Excoffier, L. (2012). Serial Founder Effects During Range Expansion: A Spatial Analog of Genetic Drift. Genetics, 191(1), pp. 171-181. Bethesda, Md.: Genetics Society of America 10.1534/genetics.112.139022
Wegmann, Daniel; Currat, Mathias; Excoffier, Laurent (2006). Molecular diversity after a range expansion in heterogeneous environments. Genetics, 174(4), pp. 2009-2020. Bethesda, Md.: Genetics Society of America 10.1534/genetics.106.062851
Claussen, Maike; Koch, Rafael; Jin, Zhao-Yang; Suter, Beat (2006). Functional characterization of Drosophila Translin and Trax. Genetics, 174(3), pp. 1337-1347. Bethesda, Md.: Genetics Society of America 10.1534/genetics.106.063016
Kusterer, Barbara; Piepho, Hans-Peter; Utz, H Friedrich; Schön, Chris C; Muminovic, Jasmina; Meyer, Rhonda C; Altmann, Thomas; Melchinger, Albrecht E (2007). Heterosis for biomass-related traits in Arabidopsis investigated by quantitative trait loci analysis of the triple testcross design with recombinant inbred lines. Genetics, 177(3), pp. 1839-50. Bethesda, Md.: Genetics Society of America 10.1534/genetics.107.077628
Melchinger, A E; Utz, H F; Piepho, H-P; Zeng, Z-B; Schön, C C (2007). The role of epistasis in the manifestation of heterosis: a systems-oriented approach. Genetics, 177(3), pp. 1815-25. Bethesda, Md.: Genetics Society of America 10.1534/genetics.107.077537
Zhuang, Lei; Zhang, Jun; Xiang, Xin (2007). Point mutations in the stem region and the fourth AAA domain of cytoplasmic dynein heavy chain partially suppress the phenotype of NUDF/LIS1 loss in Aspergillus nidulans. Genetics, 175(3), pp. 1185-96. Bethesda, Md.: Genetics Society of America 10.1534/genetics.106.069013
Doll, Eveline; Molnar, Monika; Cuanoud, Gabriella; Octobre, Guillaume; Latypov, Vitaly; Ludin, Katja; Kohli, Jürg (2008). Cohesin and recombination proteins influence the G1-to-S transition in azygotic meiosis in Schizosaccharomyces pombe. Genetics, 180(2), pp. 727-740. Bethesda, Md.: Genetics Society of America 10.1534/genetics.108.092619
Octobre, Guillaume; Lorenz, Alexander; Loidl, Josef; Kohli, Jürg (2008). The Rad52 homologs Rad22 and Rti1 of Schizosaccharomyces pombe are not essential for meiotic interhomolog recombination, but are required for meiotic intrachromosomal recombination and mating-type-related DNA repair. Genetics, 178(4), pp. 2399-2412. Bethesda, Md.: Genetics Society of America 10.1534/genetics.107.085696
Parvanov, Emil; Kohli, Jürg; Ludin, Katja (2008). The Mating-Type-Related Bias of Gene Conversion in Schizosaccharomyces pombe. Genetics, 180(4), pp. 1859-1868. Bethesda, Md.: Genetics Society of America 10.1534/genetics.108.093005
Wegmann, Daniel; Leuenberger, Christoph; Excoffier, Laurent (2009). Efficient Approximate Bayesian Computation Coupled With Markov Chain Monte Carlo Without Likelihood. Genetics, 182(4), pp. 1207-1218. Bethesda, Md.: Genetics Society of America 10.1534/genetics.109.102509
Peischl, Stephan; Kirkpatrick, Mark (2012). Establishment of new mutations in changing environments. Genetics, 191(3), pp. 895-906. Genetics Society of America 10.1534/genetics.112.140756
Steffen, Frank; Bilzer, Thomas; Brands, Jan; Golini, Lorenzo; Jagannathan, Vidhya; Wiedmer, Michaela; Drögemüller, Michaela; Drögemüller, Cord; Leeb, Tosso (2015). A Nonsense Variant in COL6A1 in Landseer Dogs with Muscular Dystrophy. G3 Genes Genomes Genetics, 5(12), pp. 2611-2617. Genetics Society of America 10.1534/g3.115.021923
Wiedmer, Michaela; Oevermann, Anna; Borer, Stephanie; Gorgas, Daniela; Shelton, G. Diane; Drögemüller, Michaela; Jagannathan, Vidhya; Henke, Diana; Leeb, Tosso (2015). A RAB3GAP1 SINE Insertion in Alaskan Huskies with Polyneuropathy, Ocular Abnormalities and Neuronal Vacuolation (POANV) Resembling Human Warburg Micro Syndrome 1 (WARBM1). G3 Genes Genomes Genetics, 6(2), pp. 255-262. Genetics Society of America 10.1534/g3.115.022707
Sayyab, Shumaila; Viluma, Agnese; Bergvall, Kerstin; Brunberg, Emma; Jagannathan, Vidhya; Leeb, Tosso; Andersson, Göran; Bergström, Tomas F (2016). Whole-Genome Sequencing of a Canine Family Trio Reveals a FAM83G Variant Associated with Hereditary Footpad Hyperkeratosis. G3 Genes Genomes Genetics, 6(3), pp. 521-527. Genetics Society of America 10.1534/g3.115.025643
Sadovnick, A Dessa; Traboulsee, Anthony L; Bernales, Cecily Q; Ross, Jay P; Forwell, Amanda L; Yee, Irene M; Guillot-Noel, Lena; Fontaine, Bertrand; Cournu-Rebeix, Isabelle; Alcina, Antonio; Fedetz, Maria; Izquierdo, Guillermo; Matesanz, Fuencisla; Hilven, Kelly; Dubois, Bénédicte; Goris, An; Astobiza, Ianire; Alloza, Iraide; Antigüedad, Alfredo; Vandenbroeck, Koen; ... (2016). Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients. G3 Genes Genomes Genetics, 6(7), pp. 2073-2079. Genetics Society of America 10.1534/g3.116.030841
Waluk, Dominik Pawel; Zur, Gila; Kaufmann, Ronnie; Welle, Monika Maria; Jagannathan, Vidhya; Drögemüller, Cord; Müller, Eliane Jasmine; Leeb, Tosso; Galichet, Arnaud (2016). A Splice Defect in the EDA Gene in Dogs with an X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) Phenotype. G3 Genes Genomes Genetics, 6(9), pp. 2949-2954. Genetics Society of America 10.1534/g3.116.033225
Murgiano, Leonardo; Waluk, Dominik Pawel; Towers, Rachel; Wiedemar, Natalie; Dietrich, Sara Joëlle; Jagannathan, Vidhya; Drögemüller, Michaela; Balmer, Pierre; Druet, Tom; Galichet, Arnaud; Penedo, M Cecilia; Müller, Eliane Jasmine; Roosje, Petra; Welle, Monika Maria; Leeb, Tosso (2016). An Intronic MBTPS2 Variant Results in a Splicing Defect in Horses with Brindle Coat Texture. G3 Genes Genomes Genetics, 6(9), pp. 2963-2970. Genetics Society of America 10.1534/g3.116.032433
Mauri, Nico; Kleiter, Miriam; Leschnik, Michael; Högler, Sandra; Dietschi, Elisabeth; Wiedmer, Michaela; Dietrich, Sara Joëlle; Henke, Diana; Steffen, Frank; Schuller, Simone; Gurtner, Corinne; Stokar-Regenscheit, Nadine; O'Toole, Donal; Bilzer, Thomas; Herden, Christiane; Oevermann, Anna; Jagannathan, Vidhya; Leeb, Tosso (2016). A Missense Variant in KCNJ10 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA1). G3 Genes Genomes Genetics, 7(2), pp. 663-669. Genetics Society of America 10.1534/g3.116.038455
Bauer, Anina Estrella; Hiemesch, Theresa; Jagannathan, Vidhya; Neuditschko, Markus; Bachmann, Iris; Rieder, Stefan; Mikko, Sofia; Penedo, M Cecilia; Tarasova, Nadja; Vitková, Martina; Sirtori, Nicolò; Roccabianca, Paola; Leeb, Tosso; Welle, Monika Maria (2017). A Nonsense Variant in the ST14 Gene in Akhal-Teke Horses with Naked Foal Syndrome. G3 Genes Genomes Genetics, 7(4), pp. 1315-1321. Genetics Society of America 10.1534/g3.117.039511
Yong, Lengxob; Peichel, Catherine; McKinnon, Jeffrey S (2016). Genetic architecture of conspicuous red ornaments in female threespine stickleback. G3 Genes Genomes Genetics, 6(3), pp. 579-588. Genetics Society of America 10.1534/g3.115.024505
Mauri, Nico; Kleiter, Miriam; Dietschi, Elisabeth; Leschnik, Michael; Högler, Sandra; Wiedmer, Michaela; Dietrich, Sara Joëlle; Henke, Diana; Steffen, Frank; Schuller, Simone; Gurtner, Corinne; Stokar von Neuforn, Nadine; O'Toole, Donal; Bilzer, Thomas; Herden, Christiane; Oevermann, Anna; Jagannathan, Vidhya; Leeb, Tosso (2017). A SINE Insertion in ATP1B2 in Belgian Shepherd Dogs Affected by Spongy Degeneration with Cerebellar Ataxia (SDCA2). G3 Genes Genomes Genetics, 7(8), pp. 2729-2737. Genetics Society of America 10.1534/g3.117.043018
Bauer, Anina; De Lucia, Michela; Jagannathan, Vidhya; Mezzalira, Giorgia; Casal, Margaret L; Welle, Monika Maria; Leeb, Tosso (2017). A Large Deletion in the NSDHL Gene in Labrador Retrievers with a Congenital Cornification Disorder. G3 Genes Genomes Genetics, 7(9), pp. 3115-3121. Genetics Society of America 10.1534/g3.117.1124
Feulner, Philine; Schwarzer, Julia; Häsler, Marcel; Meier, Joana; Seehausen, Ole (2018). A Dense Linkage Map of Lake Victoria Cichlids Improved the Pundamilia Genome Assembly and Revealed a Major QTL for Sex-Determination. G3 Genes Genomes Genetics, 8(7), pp. 2411-2420. Genetics Society of America 10.1534/g3.118.200207
Sardell, Jason M; Cheng, Changde; Dagilis, Andrius J; Ishikawa, Asano; Kitano, Jun; Peichel, Catherine L; Kirkpatrick, Mark (2018). Sex Differences in Recombination in Sticklebacks. G3 Genes Genomes Genetics, 8(6), pp. 1971-1983. Genetics Society of America 10.1534/g3.118.200166
De-Kayne, Rishi; Feulner, Philine (2018). A European Whitefish Linkage Map and Its Implications for Understanding Genome-Wide Synteny Between Salmonids Following Whole Genome Duplication. G3 Genes Genomes Genetics, 8(12), pp. 3745-3755. Genetics Society of America 10.1534/g3.118.200552
Murgiano, Leonardo; Becker, Doreen; Torjman, Dina; Niggel, Jessica K; Milano, Ausra; Cullen, Cheryl; Feng, Rui; Wang, Fan; Jagannathan, Vidya; Pearce-Kelling, Sue; Katz, Martin L; Leeb, Tosso; Aguirre, Gustavo D (2019). Complex Structural Variant Associated with Non-syndromic Canine Retinal Degeneration. G3 Genes Genomes Genetics, 9(2), pp. 425-437. Genetics Society of America 10.1534/g3.118.200859
Gomez-Saldivar, Georgina; Osuna-Luque, Jaime; Semple, Jennifer I.; Glauser, Dominique A.; Jarriault, Sophie; Meister, Peter (2020). Tissue-Specific Transcription Footprinting Using RNA PoI DamID (RAPID) in Caenorhabditis elegans. Genetics, 216(4), pp. 931-945. Genetics Society of America 10.1534/genetics.120.303774
Kiener, Sarah; Wiener, Dominique J; Hopke, Kaitlin; Diesel, Alison B; Jagannathan, Vidhya; Mauldin, Elizabeth A; Casal, Margret L; Leeb, Tosso (2022). ABHD5 frameshift deletion in Golden Retrievers with ichthyosis. G3 Genes Genomes Genetics, 12(2) Genetics Society of America 10.1093/g3journal/jkab397
Kirkpatrick, Mark; Sardell, Jason M.; Pinto, Brendan J.; Dixon, Groves; Peichel, Catherine L; Schartl, Manfred (2022). Evolution of the canonical sex chromosomes of the guppy and its relatives. G3 Genes Genomes Genetics, 12(2), jkab435. Genetics Society of America 10.1093/g3journal/jkab435
Peona, Valentina; Palacios-Gimenez, Octavio Manuel; Lutgen, Dave; Olsen, Remi André; Alaei Kakhki, Niloofar; Andriopoulos, Pavlos; Bontzorlos, Vasileios; Schweizer, Manuel; Suh, Alexander; Burri, Reto (2023). An annotated chromosome-scale reference genome for Eastern black-eared wheatear (Oenanthe melanoleuca). G3 Genes Genomes Genetics, 13(6) Genetics Society of America 10.1093/g3journal/jkad088
Simon, Rebecca; Kiener, Sarah; Thom, Nina; Schäfer, Laura; Müller, Janina; Schlohsarczyk, Elfi K; Gärtner, Ulrich; Herden, Christiane; Leeb, Tosso; Lühken, Gesine (2023). Identification of an ADAMTS2 frameshift variant in a cat family with Ehlers-Danlos syndrome. G3 Genes Genomes Genetics, 13(9) Genetics Society of America 10.1093/g3journal/jkad152
Rudd Garces, Gabriela; Farke, Daniela; Schmidt, Martin J; Letko, Anna; Schirl, Katja; Abitbol, Marie; Leeb, Tosso; Lyons, Leslie A; Lühken, Gesine (2024). PAX3 haploinsufficiency in Maine Coon cats with dominant blue eyes and hearing loss resembling the human Waardenburg syndrome. G3 Genes Genomes Genetics, 14(9) Genetics Society of America 10.1093/g3journal/jkae131
Stuurman, Jeroen; Hoballah, Maria Elena; Broger, Larissa; Moore, James; Basten, Christopher; Kuhlemeier, Cris (2004). Dissection of floral pollination syndromes in petunia. Genetics, 168(3), pp. 1585-1599. Genetics Society of America 10.1534/genetics.104.031138
Masrouha, Nisrine; Yang, Long; Hijal, Sirine; Larochelle, Stéphane; Suter, Beat (2003). The Drosophila chk2 gene loki is essential for embryonic DNA double-strand-break checkpoints induced in S phase or G2. Genetics, 163(3), pp. 973-982. Genetics Society of America
Kreutzer, Robert; Leeb, Tosso; Müller, Gundi; Moritz, Andreas; Baumgärtner, Wolfgang (2005). A duplication in the canine beta-galactosidase gene GLB1 causes exon skipping and GM1-gangliosidosis in Alaskan huskies. Genetics, 170(4), pp. 1857-1861. Genetics Society of America 10.1534/genetics.105.042580
Greenwood, Anna K; Mills, Margaret G; Wark, Abigail R; Archambeault, Sophie Louise; Peichel, Catherine (2016). Evolution of schooling behavior in threespine sticklebacks is shaped by the Eda gene. Genetics, 203(2), pp. 677-681. Genetics Society of America 10.1534/genetics.116.188342
Peischl, Stephan; Dupanloup, I.; Foucal, A.; Jomphe, M.; Bruat, V.; Grenier, J.-C.; Gouy, A.; Gilbert, K. J.; Gbeha, E.; Bosshard, L.; Hip-Ki, E.; Agbessi, M.; Hodgkinson, A.; Vézina, H.; Awadalla, P.; Excoffier, Laurent (2018). Relaxed Selection During a Recent Human Expansion. Genetics, 208(2), pp. 763-777. Genetics Society of America 10.1534/genetics.117.300551
Lepori, Vincent; Mühlhause, Franziska; Sewell, Adrian C; Jagannathan, Vidhya; Janzen, Nils; Rosati, Marco; Maximiano Alves de Sousa, Filipe Miguel; Tschopp, Aurélie; Schüpbach, Gertraud; Matiasek, Kaspar; Tipold, Andrea; Leeb, Tosso; Kornberg, Marion (2018). A Nonsense Variant in the ACADVL Gene in German Hunting Terriers with Exercise Induced Metabolic Myopathy. G3 Genes Genomes Genetics, 8(5), pp. 1545-1554. Genetics Society of America 10.1534/g3.118.200084
Lucot, Katherine L.; Dickinson, Peter J.; Finno, Carrie J.; Mansour, Tamer A.; Letko, Anna; Minor, Katherine M.; Mickelson, James R.; Drögemüller, Cord; Brown, C. Titus; Bannasch, Danika L. (2018). A Missense Mutation in the Vacuolar Protein Sorting 11 ( VPS11 ) Gene Is Associated with Neuroaxonal Dystrophy in Rottweiler Dogs. G3 Genes Genomes Genetics, 8(8), pp. 2773-2780. Genetics Society of America 10.1534/g3.118.200376
Bosshard, Lars; Dupanloup, Isabelle; Tenaillon, Olivier; Bruggmann, Rémy; Ackermann, Martin; Peischl, Stephan; Excoffier, Laurent (2017). Accumulation of Deleterious Mutations During Bacterial Range Expansions. Genetics, 207(2), pp. 669-684. Genetics Society of America 10.1534/genetics.117.300144
Widmer, Yves F.; Bilican, Adem; Bruggmann, Rémy; Sprecher, Simon G. (2018). Regulators of Long-Term Memory Revealed by Mushroom Body-Specific Gene Expression Profiling in Drosophila melanogaster. Genetics, 209(4), pp. 1167-1181. Genetics Society of America 10.1534/genetics.118.301106
Gilbert, Kimberly J.; Zdraljevic, Stefan; Cook, Daniel E.; Cutter, Asher D.; Andersen, Erik C.; Baer, Charles F. (2022). The distribution of mutational effects on fitness in Caenorhabditis elegans inferred from standing genetic variation. Genetics, 220(1) Genetics Society of America 10.1093/genetics/iyab166
