| Year |
Citation |
Score |
| 2024 |
Schmidt A, Casadei N, Brand F, Demidov G, Vojgani E, Abolhassani A, Aldisi R, Butler-Laporte G, Alawathurage TM, Augustin M, Bals R, Bellinghausen C, Berger MM, Bitzer M, Bode C, ... ... Ossowski S, et al. Systematic assessment of COVID-19 host genetics using whole genome sequencing data. Plos Pathogens. 20: e1012786. PMID 39715278 DOI: 10.1371/journal.ppat.1012786 |
0.323 |
|
| 2024 |
Figueroa KP, Gross C, Buena-Atienza E, Paul S, Gandelman M, Kakar N, Sturm M, Casadei N, Admard J, Park J, Zühlke C, Hellenbroich Y, Pozojevic J, Balachandran S, Händler K, ... ... Ossowski S, et al. A GGC-repeat expansion in ZFHX3 encoding polyglycine causes spinocerebellar ataxia type 4 and impairs autophagy. Nature Genetics. PMID 38684900 DOI: 10.1038/s41588-024-01719-5 |
0.325 |
|
| 2023 |
Menzel M, Ossowski S, Kral S, Metzger P, Horak P, Marienfeld R, Boerries M, Wolter S, Ball M, Neumann O, Armeanu-Ebinger S, Schroeder C, Matysiak U, Goldschmid H, Schipperges V, et al. Multicentric pilot study to standardize clinical whole exome sequencing (WES) for cancer patients. Npj Precision Oncology. 7: 106. PMID 37864096 DOI: 10.1038/s41698-023-00457-x |
0.323 |
|
| 2023 |
Weisschuh N, Mazzola P, Zuleger T, Schaeferhoff K, Kühlewein L, Kortüm F, Witt D, Liebmann A, Falb R, Pohl L, Reith M, Stühn LG, Bertrand M, Müller A, Casadei N, ... ... Ossowski S, et al. Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases. Journal of Medical Genetics. PMID 37734845 DOI: 10.1136/jmg-2023-109470 |
0.302 |
|
| 2021 |
Demidov G, Park J, Armeanu-Ebinger S, Roggia C, Faust U, Cordts I, Blandfort M, Haack TB, Schroeder C, Ossowski S. Detection of mobile elements insertions for routine clinical diagnostics in targeted sequencing data. Molecular Genetics & Genomic Medicine. e1807. PMID 34491624 DOI: 10.1002/mgg3.1807 |
0.358 |
|
| 2021 |
Susak H, Serra-Saurina L, Demidov G, Rabionet R, Domènech L, Bosio M, Muyas F, Estivill X, Escaramís G, Ossowski S. Efficient and flexible Integration of variant characteristics in rare variant association studies using integrated nested Laplace approximation. Plos Computational Biology. 17: e1007784. PMID 33606672 DOI: 10.1371/journal.pcbi.1007784 |
0.337 |
|
| 2020 |
Hilke FJ, Sinnberg T, Gschwind A, Niessner H, Demidov G, Amaral T, Ossowski S, Bonzheim I, Röcken M, Riess O, Garbe C, Schroeder C, Forschner A. Distinct Mutation Patterns Reveal Melanoma Subtypes and Influence Immunotherapy Response in Advanced Melanoma Patients. Cancers. 12. PMID 32825510 DOI: 10.3390/Cancers12092359 |
0.352 |
|
| 2020 |
Muyas F, Zapata L, Guigó R, Ossowski S. The rate and spectrum of mosaic mutations during embryogenesis revealed by RNA sequencing of 49 tissues. Genome Medicine. 12: 49. PMID 32460841 DOI: 10.1186/S13073-020-00746-1 |
0.332 |
|
| 2020 |
Oberhettinger P, Schüle L, Marschal M, Bezdan D, Ossowski S, Dörfel D, Vogel W, Rossen JW, Willmann M, Peter S. Description of sp. nov., isolated from human rectal swabs and stool samples. International Journal of Systematic and Evolutionary Microbiology. PMID 32375941 DOI: 10.1099/Ijsem.0.004100 |
0.357 |
|
| 2019 |
Pogoda M, Hilke FJ, Lohmann E, Sturm M, Lenz F, Matthes J, Muyas F, Ossowski S, Hoischen A, Faust U, Sepahi I, Casadei N, Poths S, Riess O, Schroeder C, et al. Single Molecule Molecular Inversion Probes for High Throughput Germline Screenings in Dystonia. Frontiers in Neurology. 10: 1332. PMID 31920950 DOI: 10.3389/Fneur.2019.01332 |
0.393 |
|
| 2019 |
Arcas-García A, Garcia-Prat M, Magallón-Lorenz M, Martin-Nalda A, Drechsel O, Ossowski S, Alonso L, Rivière JG, Soler-Palacín P, Colobran R, Sayós J, Martinez-Gallo M, Franco-Jarava C. The IL2RG R328X nonsense mutation allows partial STAT5 phosphorylation and defines a critical region involved in leaky-SCID phenotype. Clinical and Experimental Immunology. PMID 31799703 DOI: 10.1111/Cei.13405 |
0.326 |
|
| 2019 |
Zwirner K, Hilke FJ, Demidov G, Socarras Fernandez J, Ossowski S, Gani C, Thorwarth D, Riess O, Zips D, Schroeder C, Welz S. Radiogenomics in head and neck cancer: correlation of radiomic heterogeneity and somatic mutations in TP53, FAT1 and KMT2D. Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]. PMID 31123786 DOI: 10.1007/S00066-019-01478-X |
0.303 |
|
| 2019 |
Bosio M, Drechsel O, Rahman R, Muyas F, Rabionet R, Bezdan D, Domenech Salgado L, Hor HG, Schott JJ, Munell F, Colobran R, Macaya A, Estivill X, Ossowski S. eDiVA - Classification and Prioritization of Pathogenic Variants for Clinical Diagnostics. Human Mutation. PMID 31026367 DOI: 10.1002/Humu.23772 |
0.372 |
|
| 2019 |
Rabionet R, Remesal A, Mensa-Vilaró A, Murías S, Alcobendas R, González-Roca E, Ruiz-Ortiz E, Antón J, Iglesias E, Modesto C, Comas D, Puig A, Drechsel O, Ossowski S, Yagüe J, et al. Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic Arthritis. Scientific Reports. 9: 4579. PMID 30872671 DOI: 10.1038/S41598-019-40874-2 |
0.401 |
|
| 2018 |
Soler-Palacín P, Garcia-Prat M, Martín-Nalda A, Franco-Jarava C, Rivière JG, Plaja A, Bezdan D, Bosio M, Martínez-Gallo M, Ossowski S, Colobran R. LRBA Deficiency in a Patient With a Novel Homozygous Mutation Due to Chromosome 4 Segmental Uniparental Isodisomy. Frontiers in Immunology. 9: 2397. PMID 30386343 DOI: 10.3389/Fimmu.2018.02397 |
0.401 |
|
| 2018 |
Muyas F, Bosio M, Puig A, Susak H, Domènech-Salgado L, Escaramis G, Zapata L, Demidov G, Estivill X, Rabionet R, Ossowski S. Allele balance bias identifies systematic genotyping errors and false disease associations. Human Mutation. PMID 30353964 DOI: 10.1002/Humu.23674 |
0.379 |
|
| 2018 |
Zapata L, Pich O, Serrano L, Kondrashov FA, Ossowski S, Schaefer MH. Negative selection in tumor genome evolution acts on essential cellular functions and the immunopeptidome. Genome Biology. 19: 67. PMID 29855388 DOI: 10.1186/S13059-018-1434-0 |
0.406 |
|
| 2018 |
Peter S, Bezdan D, Oberhettinger P, Vogel W, Dörfel D, Dick J, Marschal M, Liese J, Weidenmaier C, Autenrieth I, Ossowski S, Willmann M. Whole-genome sequencing enabling the detection of a colistin-resistant hypermutating Citrobacter werkmanii strain harbouring a novel metallo-β-lactamase VIM-48. International Journal of Antimicrobial Agents. 51: 867-874. PMID 29412174 DOI: 10.1016/J.Ijantimicag.2018.01.015 |
0.413 |
|
| 2018 |
Forschner A, Hilke FJ, Sinnberg T, Niessner H, Eigentler TK, Garbe C, Riess O, Ossowski S, Haack T, Schroeder C. Next-generation-sequencing of advanced melanoma: Which genetic alterations have an impact on systemic therapy response? Journal of Clinical Oncology. 36: e21557-e21557. DOI: 10.1200/Jco.2018.36.15_Suppl.E21557 |
0.356 |
|
| 2017 |
Peter S, Oberhettinger P, Schuele L, Dinkelacker A, Vogel W, Dörfel D, Bezdan D, Ossowski S, Marschal M, Liese J, Willmann M. Genomic characterisation of clinical and environmental Pseudomonas putida group strains and determination of their role in the transfer of antimicrobial resistance genes to Pseudomonas aeruginosa. Bmc Genomics. 18: 859. PMID 29126393 DOI: 10.1186/S12864-017-4216-2 |
0.313 |
|
| 2017 |
Zapata L, Susak H, Drechsel O, Friedländer MR, Estivill X, Ossowski S. Signatures of positive selection reveal a universal role of chromatin modifiers as cancer driver genes. Scientific Reports. 7: 13124. PMID 29030609 DOI: 10.1038/S41598-017-12888-1 |
0.36 |
|
| 2017 |
Urreizti R, Cueto-Gonzalez AM, Franco-Valls H, Mort-Farre S, Roca-Ayats N, Ponomarenko J, Cozzuto L, Company C, Bosio M, Ossowski S, Montfort M, Hecht J, Tizzano EF, Cormand B, Vilageliu L, et al. A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes. Scientific Reports. 7: 44138. PMID 28281571 DOI: 10.1038/Srep44138 |
0.404 |
|
| 2016 |
Zapata L, Ding J, Willing EM, Hartwig B, Bezdan D, Jiao WB, Patel V, Velikkakam James G, Koornneef M, Ossowski S, Schneeberger K. Chromosome-level assembly of Arabidopsis thaliana Ler reveals the extent of translocation and inversion polymorphisms. Proceedings of the National Academy of Sciences of the United States of America. PMID 27354520 DOI: 10.1073/Pnas.1607532113 |
0.488 |
|
| 2016 |
Prasad A, Rabionet R, Espinet B, Zapata L, Puiggros A, Melero C, Puig A, Sarria-Trujillo Y, Ossowski S, Garcia-Muret MP, Estrach T, Servitje O, Lopez-Lerma I, Gallardo F, Pujol RM, et al. Identification of gene mutations and fusion genes in patients with Sézary Syndrome. The Journal of Investigative Dermatology. PMID 27039262 DOI: 10.1016/J.Jid.2016.03.024 |
0.399 |
|
| 2015 |
Hénaff E, Zapata L, Casacuberta JM, Ossowski S. Jitterbug: somatic and germline transposon insertion detection at single-nucleotide resolution. Bmc Genomics. 16: 768. PMID 26459856 DOI: 10.1186/S12864-015-1975-5 |
0.449 |
|
| 2015 |
Durst R, Sauls K, Peal DS, deVlaming A, Toomer K, Leyne M, Salani M, Talkowski ME, Brand H, Perrocheau M, Simpson C, Jett C, Stone MR, Charles F, Chiang C, ... ... Ossowski S, et al. Mutations in DCHS1 cause mitral valve prolapse. Nature. PMID 26258302 DOI: 10.1038/Nature14670 |
0.326 |
|
| 2015 |
Hor H, Francescatto L, Bartesaghi L, Ortega-Cubero S, Kousi M, Lorenzo-Betancor O, Jiménez-Jiménez FJ, Gironell A, Clarimón J, Drechsel O, Agúndez JA, Kenzelmann Broz D, Chiquet-Ehrismann R, Lleó A, Coria F, ... ... Ossowski S, et al. Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor. Human Molecular Genetics. 24: 5677-86. PMID 26188006 DOI: 10.1093/Hmg/Ddv281 |
0.339 |
|
| 2015 |
Bassaganyas L, Beà S, Escaramís G, Tornador C, Salaverria I, Zapata L, Drechsel O, Ferreira PG, Rodriguez-Santiago B, Tubio JM, Navarro A, Martín-García D, López C, Martínez-Trillos A, López-Guillermo A, ... ... Ossowski S, et al. Sporadic and reversible chromothripsis in chronic lymphocytic leukemia revealed by longitudinal genomic analysis. Leukemia. 29: 758. PMID 25738466 DOI: 10.1038/Leu.2014.309 |
0.366 |
|
| 2015 |
Di Vona C, Bezdan D, Islam AB, Salichs E, López-Bigas N, Ossowski S, de la Luna S. Chromatin-wide profiling of DYRK1A reveals a role as a gene-specific RNA polymerase II CTD kinase. Molecular Cell. 57: 506-20. PMID 25620562 DOI: 10.1016/J.Molcel.2014.12.026 |
0.349 |
|
| 2015 |
Willmann M, Bezdan D, Zapata L, Susak H, Vogel W, Schröppel K, Liese J, Weidenmaier C, Autenrieth IB, Ossowski S, Peter S. Analysis of a long-term outbreak of XDR Pseudomonas aeruginosa: a molecular epidemiological study. The Journal of Antimicrobial Chemotherapy. 70: 1322-30. PMID 25583750 DOI: 10.1093/Jac/Dku546 |
0.394 |
|
| 2015 |
Bullich G, Trujillano D, Santín S, Ossowski S, Mendizábal S, Fraga G, Madrid Á, Ariceta G, Ballarín J, Torra R, Estivill X, Ars E. Targeted next-generation sequencing in steroid-resistant nephrotic syndrome: mutations in multiple glomerular genes may influence disease severity. European Journal of Human Genetics : Ejhg. 23: 1192-9. PMID 25407002 DOI: 10.1038/Ejhg.2014.252 |
0.449 |
|
| 2014 |
Chae E, Bomblies K, Kim ST, Karelina D, Zaidem M, Ossowski S, MartÃn-Pizarro C, Laitinen RA, Rowan BA, Tenenboim H, Lechner S, Demar M, Habring-Müller A, Lanz C, Rätsch G, et al. Species-wide genetic incompatibility analysis identifies immune genes as hot spots of deleterious epistasis. Cell. 159: 1341-51. PMID 25467443 DOI: 10.1016/J.Cell.2014.10.049 |
0.773 |
|
| 2014 |
Trujillano D, Bullich G, Ossowski S, Ballarín J, Torra R, Estivill X, Ars E. Diagnosis of autosomal dominant polycystic kidney disease using efficient PKD1 and PKD2 targeted next-generation sequencing. Molecular Genetics & Genomic Medicine. 2: 412-21. PMID 25333066 DOI: 10.1002/Mgg3.82 |
0.409 |
|
| 2014 |
Almouzni G, Altucci L, Amati B, Ashley N, Baulcombe D, Beaujean N, Bock C, Bongcam-Rudloff E, Bousquet J, Braun S, Bressac-de Paillerets B, Bussemakers M, Clarke L, Conesa A, Estivill X, ... ... Ossowski S, et al. Relationship between genome and epigenome--challenges and requirements for future research. Bmc Genomics. 15: 487. PMID 24942464 DOI: 10.1186/1471-2164-15-487 |
0.318 |
|
| 2014 |
Zee PC, Mendes-Soares H, Yu YT, Kraemer SA, Keller H, Ossowski S, Schneeberger K, Velicer GJ. A shift from magnitude to sign epistasis during adaptive evolution of a bacterial social trait. Evolution; International Journal of Organic Evolution. 68: 2701-8. PMID 24909926 DOI: 10.1111/Evo.12467 |
0.378 |
|
| 2014 |
Trujillano D, Perez B, González J, Tornador C, Navarrete R, Escaramis G, Ossowski S, Armengol L, Cornejo V, Desviat LR, Ugarte M, Estivill X. Accurate molecular diagnosis of phenylketonuria and tetrahydrobiopterin-deficient hyperphenylalaninemias using high-throughput targeted sequencing. European Journal of Human Genetics : Ejhg. 22: 528-34. PMID 23942198 DOI: 10.1038/Ejhg.2013.175 |
0.475 |
|
| 2014 |
Ramos MD, Trujillano D, Olivar R, Sotillo F, Ossowski S, Manzanares J, Costa J, Gartner S, Oliva C, Quintana E, Gonzalez MI, Vazquez C, Estivill X, Casals T. Extensive sequence analysis of CFTR, SCNN1A, SCNN1B, SCNN1G and SERPINA1 suggests an oligogenic basis for cystic fibrosis-like phenotypes. Clinical Genetics. 86: 91-5. PMID 23837941 DOI: 10.1111/Cge.12234 |
0.374 |
|
| 2013 |
Wijnker E, Velikkakam James G, Ding J, Becker F, Klasen JR, Rawat V, Rowan BA, de Jong DF, de Snoo CB, Zapata L, Huettel B, de Jong H, Ossowski S, Weigel D, Koornneef M, et al. The genomic landscape of meiotic crossovers and gene conversions in Arabidopsis thaliana. Elife. 2: e01426. PMID 24347547 DOI: 10.7554/Elife.01426 |
0.629 |
|
| 2013 |
Hauser F, Chen W, Deinlein U, Chang K, Ossowski S, Fitz J, Hannon GJ, Schroeder JI. A genomic-scale artificial microRNA library as a tool to investigate the functionally redundant gene space in Arabidopsis. The Plant Cell. 25: 2848-63. PMID 23956262 DOI: 10.1105/Tpc.113.112805 |
0.405 |
|
| 2013 |
Koenig D, Jiménez-Gómez JM, Kimura S, Fulop D, Chitwood DH, Headland LR, Kumar R, Covington MF, Devisetty UK, Tat AV, Tohge T, Bolger A, Schneeberger K, Ossowski S, Lanz C, et al. Comparative transcriptomics reveals patterns of selection in domesticated and wild tomato. Proceedings of the National Academy of Sciences of the United States of America. 110: E2655-62. PMID 23803858 DOI: 10.1073/Pnas.1309606110 |
0.776 |
|
| 2013 |
Escaramís G, Tornador C, Bassaganyas L, Rabionet R, Tubio JM, Martínez-Fundichely A, Cáceres M, Gut M, Ossowski S, Estivill X. PeSV-Fisher: identification of somatic and non-somatic structural variants using next generation sequencing data. Plos One. 8: e63377. PMID 23704902 DOI: 10.1371/Journal.Pone.0063377 |
0.414 |
|
| 2013 |
Trujillano D, Ramos MD, González J, Tornador C, Sotillo F, Escaramis G, Ossowski S, Armengol L, Casals T, Estivill X. Next generation diagnostics of cystic fibrosis and CFTR-related disorders by targeted multiplex high-coverage resequencing of CFTR. Journal of Medical Genetics. 50: 455-62. PMID 23687349 DOI: 10.1136/Jmedgenet-2013-101602 |
0.32 |
|
| 2013 |
Warthmann N, Ossowski S, Schwab R, Weigel D. Artificial microRNAs for specific gene silencing in rice. Methods in Molecular Biology (Clifton, N.J.). 956: 131-49. PMID 23135850 DOI: 10.1007/978-1-62703-194-3_11 |
0.566 |
|
| 2013 |
Kopischke M, Westphal L, Schneeberger K, Clark R, Ossowski S, Wewer V, Fuchs R, Landtag J, Hause G, Dörmann P, Lipka V, Weigel D, Schulze-Lefert P, Scheel D, Rosahl S. Impaired sterol ester synthesis alters the response of Arabidopsis thaliana to Phytophthora infestans. The Plant Journal : For Cell and Molecular Biology. 73: 456-68. PMID 23072470 DOI: 10.1111/Tpj.12046 |
0.575 |
|
| 2013 |
Wijnker E, James GV, Ding J, Becker F, Klasen JR, Rawat V, Rowan BA, Jong DFd, Snoo CBd, Zapata L, Huettel B, Jong Hd, Ossowski S, Weigel D, Koornneef M, et al. Author response: The genomic landscape of meiotic crossovers and gene conversions in Arabidopsis thaliana Elife. DOI: 10.7554/Elife.01426.020 |
0.596 |
|
| 2012 |
Paschold A, Jia Y, Marcon C, Lund S, Larson NB, Yeh CT, Ossowski S, Lanz C, Nettleton D, Schnable PS, Hochholdinger F. Complementation contributes to transcriptome complexity in maize (Zea mays L.) hybrids relative to their inbred parents. Genome Research. 22: 2445-54. PMID 23086286 DOI: 10.1101/Gr.138461.112 |
0.361 |
|
| 2012 |
Sorge S, Ha N, Polychronidou M, Friedrich J, Bezdan D, Kaspar P, Schaefer MH, Ossowski S, Henz SR, Mundorf J, Rätzer J, Papagiannouli F, Lohmann I. The cis-regulatory code of Hox function in Drosophila. The Embo Journal. 31: 3323-33. PMID 22781127 DOI: 10.1038/Emboj.2012.179 |
0.367 |
|
| 2012 |
Rutter MT, Roles A, Conner JK, Shaw RG, Shaw FH, Schneeberger K, Ossowski S, Weigel D, Fenster CB. Fitness of Arabidopsis thaliana mutation accumulation lines whose spontaneous mutations are known. Evolution; International Journal of Organic Evolution. 66: 2335-9. PMID 22759306 DOI: 10.1111/J.1558-5646.2012.01583.X |
0.553 |
|
| 2012 |
Louis-Dit-Picard H, Barc J, Trujillano D, Miserey-Lenkei S, Bouatia-Naji N, Pylypenko O, Beaurain G, Bonnefond A, Sand O, Simian C, Vidal-Petiot E, Soukaseum C, Mandet C, Broux F, Chabre O, ... ... Ossowski S, et al. KLHL3 mutations cause familial hyperkalemic hypertension by impairing ion transport in the distal nephron. Nature Genetics. 44: 456-60, S1-3. PMID 22406640 DOI: 10.1038/Ng.2218 |
0.342 |
|
| 2011 |
Cao J, Schneeberger K, Ossowski S, Günther T, Bender S, Fitz J, Koenig D, Lanz C, Stegle O, Lippert C, Wang X, Ott F, Müller J, Alonso-Blanco C, Borgwardt K, et al. Whole-genome sequencing of multiple Arabidopsis thaliana populations. Nature Genetics. 43: 956-63. PMID 21874002 DOI: 10.1038/Ng.911 |
0.768 |
|
| 2011 |
Klein JD, Ossowski S, Schneeberger K, Weigel D, Huson DH. LOCAS--a low coverage assembly tool for resequencing projects. Plos One. 6: e23455. PMID 21858125 DOI: 10.1371/Journal.Pone.0023455 |
0.581 |
|
| 2011 |
Guo YL, Fitz J, Schneeberger K, Ossowski S, Cao J, Weigel D. Genome-wide comparison of nucleotide-binding site-leucine-rich repeat-encoding genes in Arabidopsis. Plant Physiology. 157: 757-69. PMID 21810963 DOI: 10.1104/Pp.111.181990 |
0.759 |
|
| 2011 |
Schneeberger K, Ossowski S, Ott F, Klein JD, Wang X, Lanz C, Smith LM, Cao J, Fitz J, Warthmann N, Henz SR, Huson DH, Weigel D. Reference-guided assembly of four diverse Arabidopsis thaliana genomes. Proceedings of the National Academy of Sciences of the United States of America. 108: 10249-54. PMID 21646520 DOI: 10.1073/Pnas.1107739108 |
0.696 |
|
| 2011 |
Hu TT, Pattyn P, Bakker EG, Cao J, Cheng JF, Clark RM, Fahlgren N, Fawcett JA, Grimwood J, Gundlach H, Haberer G, Hollister JD, Ossowski S, Ottilar RP, Salamov AA, et al. The Arabidopsis lyrata genome sequence and the basis of rapid genome size change. Nature Genetics. 43: 476-81. PMID 21478890 DOI: 10.1038/Ng.807 |
0.778 |
|
| 2010 |
Piazza P, Bailey CD, Cartolano M, Krieger J, Cao J, Ossowski S, Schneeberger K, He F, de Meaux J, Hall N, Macleod N, Filatov D, Hay A, Tsiantis M. Arabidopsis thaliana leaf form evolved via loss of KNOX expression in leaves in association with a selective sweep. Current Biology : Cb. 20: 2223-8. PMID 21129970 DOI: 10.1016/J.Cub.2010.11.037 |
0.382 |
|
| 2010 |
Laitinen RA, Schneeberger K, Jelly NS, Ossowski S, Weigel D. Identification of a spontaneous frame shift mutation in a nonreference Arabidopsis accession using whole genome sequencing. Plant Physiology. 153: 652-4. PMID 20388671 DOI: 10.1104/Pp.110.156448 |
0.74 |
|
| 2010 |
Khraiwesh B, Arif MA, Seumel GI, Ossowski S, Weigel D, Reski R, Frank W. Transcriptional control of gene expression by microRNAs. Cell. 140: 111-22. PMID 20085706 DOI: 10.1016/J.Cell.2009.12.023 |
0.509 |
|
| 2010 |
Ossowski S, Schneeberger K, Lucas-Lledó JI, Warthmann N, Clark RM, Shaw RG, Weigel D, Lynch M. The rate and molecular spectrum of spontaneous mutations in Arabidopsis thaliana. Science (New York, N.Y.). 327: 92-4. PMID 20044577 DOI: 10.1126/Science.1180677 |
0.607 |
|
| 2010 |
Schwab R, Ossowski S, Warthmann N, Weigel D. Directed gene silencing with artificial microRNAs. Methods in Molecular Biology (Clifton, N.J.). 592: 71-88. PMID 19802590 DOI: 10.1007/978-1-60327-005-2_6 |
0.586 |
|
| 2009 |
Out AA, van Minderhout IJ, Goeman JJ, Ariyurek Y, Ossowski S, Schneeberger K, Weigel D, van Galen M, Taschner PE, Tops CM, Breuning MH, van Ommen GJ, den Dunnen JT, Devilee P, Hes FJ. Deep sequencing to reveal new variants in pooled DNA samples. Human Mutation. 30: 1703-12. PMID 19842214 DOI: 10.1002/Humu.21122 |
0.555 |
|
| 2009 |
Schneeberger K, Hagmann J, Ossowski S, Warthmann N, Gesing S, Kohlbacher O, Weigel D. Simultaneous alignment of short reads against multiple genomes. Genome Biology. 10: R98. PMID 19761611 DOI: 10.1186/Gb-2009-10-9-R98 |
0.576 |
|
| 2009 |
Mirouze M, Reinders J, Bucher E, Nishimura T, Schneeberger K, Ossowski S, Cao J, Weigel D, Paszkowski J, Mathieu O. Selective epigenetic control of retrotransposition in Arabidopsis. Nature. 461: 427-30. PMID 19734882 DOI: 10.1038/Nature08328 |
0.513 |
|
| 2009 |
Schneeberger K, Ossowski S, Lanz C, Juul T, Petersen AH, Nielsen KL, Jørgensen JE, Weigel D, Andersen SU. SHOREmap: simultaneous mapping and mutation identification by deep sequencing. Nature Methods. 6: 550-1. PMID 19644454 DOI: 10.1038/Nmeth0809-550 |
0.631 |
|
| 2009 |
Molnar A, Bassett A, Thuenemann E, Schwach F, Karkare S, Ossowski S, Weigel D, Baulcombe D. Highly specific gene silencing by artificial microRNAs in the unicellular alga Chlamydomonas reinhardtii. The Plant Journal : For Cell and Molecular Biology. 58: 165-74. PMID 19054357 DOI: 10.1111/J.1365-313X.2008.03767.X |
0.481 |
|
| 2008 |
Ossowski S, Schneeberger K, Clark RM, Lanz C, Warthmann N, Weigel D. Sequencing of natural strains of Arabidopsis thaliana with short reads. Genome Research. 18: 2024-33. PMID 18818371 DOI: 10.1101/Gr.080200.108 |
0.676 |
|
| 2008 |
Khraiwesh B, Ossowski S, Weigel D, Reski R, Frank W. Specific gene silencing by artificial MicroRNAs in Physcomitrella patens: an alternative to targeted gene knockouts. Plant Physiology. 148: 684-93. PMID 18753280 DOI: 10.1104/Pp.108.128025 |
0.554 |
|
| 2008 |
De Bona F, Ossowski S, Schneeberger K, Rätsch G. Optimal spliced alignments of short sequence reads. Bioinformatics (Oxford, England). 24: i174-80. PMID 18689821 DOI: 10.1186/1471-2105-9-S10-O7 |
0.413 |
|
| 2008 |
Warthmann N, Chen H, Ossowski S, Weigel D, Hervé P. Highly specific gene silencing by artificial miRNAs in rice. Plos One. 3: e1829. PMID 18350165 DOI: 10.1371/Journal.Pone.0001829 |
0.515 |
|
| 2008 |
Ossowski S, Schwab R, Weigel D. Gene silencing in plants using artificial microRNAs and other small RNAs. The Plant Journal : For Cell and Molecular Biology. 53: 674-90. PMID 18269576 DOI: 10.1111/J.1365-313X.2007.03328.X |
0.602 |
|
| 2007 |
Kim S, Plagnol V, Hu TT, Toomajian C, Clark RM, Ossowski S, Ecker JR, Weigel D, Nordborg M. Recombination and linkage disequilibrium in Arabidopsis thaliana. Nature Genetics. 39: 1151-5. PMID 17676040 DOI: 10.1038/Ng2115 |
0.616 |
|
| 2007 |
Clark RM, Schweikert G, Toomajian C, Ossowski S, Zeller G, Shinn P, Warthmann N, Hu TT, Fu G, Hinds DA, Chen H, Frazer KA, Huson DH, Schölkopf B, Nordborg M, et al. Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana. Science (New York, N.Y.). 317: 338-42. PMID 17641193 DOI: 10.1126/Science.1138632 |
0.683 |
|
| 2006 |
Schwab R, Ossowski S, Riester M, Warthmann N, Weigel D. Highly specific gene silencing by artificial microRNAs in Arabidopsis. The Plant Cell. 18: 1121-33. PMID 16531494 DOI: 10.1105/Tpc.105.039834 |
0.504 |
|
| Show low-probability matches. |