Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Adami, Eleonora Dr. (1) Akalin, Altuna Dr. (7) Bader, Michael Prof. Dr. (1) Bähring, Sylvia Dr. (1) Barke, Niclas (1) Bartolomaeus, Theda (1) Beule, Dieter Dr. (5) Birchmeier-Kohler, Carmen Prof. Dr. (1) Blume, Alexander Dr. (1) Blüthgen, Nils (2) Borodina, Tatiana Dr. (4) Braeuning, Caroline (2) Chen, Wei Prof. Dr. (1) Del Giudice, Simone (1) Deter, Aylina (1) Diecke, Sebastian Dr. (2) Escobar Fernandez, Helena Dr. (1) Faxel, Miriam (1) Fischer, Cornelius Dr. (5) Forslund, Sofia Dr. (1) Franke, Vedran Dr. (3) Freimuth, Jonas (1) Fritsche, Raphaela Dr. (1) Ghanbari, Mahsa Dr. (2) Gil, Marine (1) Gotthardt, Michael Prof. Dr. (1) Haghverdi, Laleh Dr. (1) Harabula, Izabela-Cezara (1) Heuser, Arnd Dr. (1) Hinze, Christian Dr. med. Dipl.-Math. (2) Hirsekorn, Antje (5) Hübner, Norbert Prof. Dr. (4) Junker, Jan Philipp Prof. Dr. (1) Kastelic, Nicolai (1) Kempa, Stefan Dr. (1) Klußmann, Enno PD Dr. (1) Kocks, Christine Dr. (2) Kühn, Ralf Dr. (1) Lacadie, Scott Allen Dr. (3) Landthaler, Markus Prof. Dr. (25) Langanki, Reika (1) Leutz, Achim Prof. Dr. (1) Liu, Tiannan (1) Lupianez Garcia, Dario Jesus Dr. (1) Maatz, Henrike Dr. (1) Marko, Lajos Dr. (1) Mastrobuoni, Guido Dr. (1) Merks, Anne Margarete Dr. (1) Minia, Igor Dr. (1) Monti, Remo (1) Müller, Dominik Prof. Dr. (1) Müller, Thomas Dr. (1) Napieczynska, Hanna Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (9) Ohler, Uwe Prof. Dr. (34) Panakova, Daniela Dr. (1) Pombo, Ana Prof. Dr. (1) Popova, Elena Dr. (1) Qadri, Fatimunnisa Dr. (1) Quedenau, Claudia (4) Rajewsky, Nikolaus Prof. Dr. (8) Rautenstrauch, Pia Josefine (2) Ruiz Orera, Jorge Dr. (1) Selbach, Matthias Prof. Dr. (7) Sholokh, Anastasiia (1) Spuler, Simone Prof. (1) Sunaga-Franze, Daniele Yumi Dr. (2) Taube, Martin (1) Teixeira Alves, Luiz Gustavo Dr. (4) Uyar, Bora Dr. (2) Villamil, Gabriel (1) Vucicevic, Dubravka (2) Wendlinger, Sarah (1) Woehler, Andrew Dr. (1) Wurmus, Ricardo (2) Zauber, Henrik Dr. (1) Zimmermann, Karin Dr. (1) Zinzen, Robert Patrick Dr. (1) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (96) (-) Chekulaeva, Marina Dr. (3) (-) Conrad, Thomas Dr. (4) (-) Wyler, Emanuel Dr. (20) 2002 (1) 2005 (2) 2012 (2) 2014 (12) 2015 (27) (-) 2016 (33) (-) 2017 (38) 2018 (42) 2019 (34) 2020 (30) 2021 (60) (-) 2022 (53) 2023 (34) 2024 (7) Bioinformatics and Omics Data Science (3) Biomedical Image Analysis (1) Cardiac MRI (1) Cellular Neurosciences (4) Computational methodologies and omic analytics (1) (-) Computational Regulatory Genomics (8) Developmental Biology / Signal Transduction (1) Epigenetic Regulation and Chromatin Architecture (1) Experimental Ultrahigh-Field MR (7) Genetics and Genomics of Cardiovascular Diseases (3) Genome Engineering & Disease Models (3) (-) Genomics (99) Immune Mechanisms and Human Antibodies (1) Immune Regulation and Cancer (6) Magnetic Resonance (7) Mobile DNA (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (5) Proteome Dynamics (4) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) (-) RNA Biology and Posttranscriptional Regulation (21) Systems Biology Imaging (1) Systems Biology of Gene Regulatory Elements (5) Transgenics (3) Translational Bioinformatics (7) Translational Cardiology and Functional Genomics (1) 124 Results: Active Filter: Altmueller, Janine Dr.med.Chekulaeva, Marina Dr.Conrad, Thomas Dr.Wyler, Emanuel Dr.Computational Regulatory GenomicsGenomicsRNA Biology and Posttranscriptional Regulation201620172022 Sort: Result score Newest to oldest Oldest to newest July 02, 2022 / J Neuroinflammation Spermidine reduces neuroinflammation and soluble amyloid beta in an Alzheimer's disease mouse model K. Freitag N. Sterczyk S. Wendlinger B. Obermayer J. Schulz V. Farztdinov M. Mülleder M. Ralser J. Houtman L. Fleck C. Braeuning R. Sansevrino C. Hoffmann D. Milovanovic S.J. Sigrist T. Conrad D. Beule F.L. Heppner M. Jendrach October 31, 2017 / Genome Biol Widespread activation of antisense transcription of the host genome during herpes simplex virus 1 infection E. Wyler J. Menegatti V. Franke C. Kocks A. Boltengagen T. Hennig K. Theil A. Rutkowski C. Ferrai L. Baer L. Kermas C. Friedel N. Rajewsky A. Akalin L. Dölken F. Grässer M. Landthaler March 01, 2022 / J Med Genet Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883) J. Hauke P. Harter C. Ernst A. Burges S. Schmidt A. Reuss J. Borde N. De Gregorio D. Dietrich A. El-Balat M. Kayali H. Gevensleben F. Hilpert J. Altmüller A. Heimbach W. Meier B. Schoemig-Markiefka H. Thiele R. Kimmig P. Nürnberg K. Kast L. Richters J. Sehouli R.K. Schmutzler E. Hahnen December 19, 2017 / Cold Spring Harb Mol Case Stud Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia S. Alawbathani A. Kawalia M. Karakaya J. Altmüller P. Nürnberg S. Cirak July 01, 2017 / Clin Genet Genetic heterogeneity in Pakistani microcephaly families revisited I. Ahmad S.M. Baig A.R. Abdulkareem M.S. Hussain I. Sur M.R. Toliat G. Nürnberg N. Dalibor A. Moawia S.S. Waseem M. Asif H. Nagra M. Sher M.M.A. Khan I. Hassan S.U. Rehman H. Thiele J. Altmüller A.A. Noegel P. Nürnberg June 01, 2017 / Immunogenetics Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing J. Altmüller B. Haenisch A. Kawalia M. Menzen M.M. Nöthen H. Fier G.J. Molderings December 01, 2017 / Nat Med A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle M. Awazawa P. Gabel E. Tsaousidou H. Nolte M. Krüger J. Schmitz P.J. Ackermann C. Brandt J. Altmüller S. Motameny F.T. Wunderlich J.W. Kornfeld M. Blüher J.C. Brüning July 01, 2017 / Hum Genet Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability N.C. Bramswig H.J. Lüdecke F.F. Hamdan J. Altmüller F. Beleggia N.H. Elcioglu C. Freyer E.H. Gerkes Y.K. Demirkol K.G. Knupp A. Kuechler Y. Li D.H. Lowenstein J.L. Michaud K. Park A.P.A. Stegmann H.E. Veenstra-Knol T. Wieland B. Wollnik H. Engels T.M. Strom T. Kleefstra D. Wieczorek September 26, 2017 / Mol Ecol Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin S. Dennenmoser F.J. Sedlazeck E. Iwaszkiewicz X.Y. Li J. Altmüller A.W. Nolte November 02, 2017 / Am J Hum Genet De novo mutations in SLC25A24 cause a craniosynostosis syndrome with hypertrichosis, progeroid appearance, and mitochondrial dysfunction N. Ehmke L. Graul-Neumann L. Smorag R. Koenig L. Segebrecht P. Magoulas F. Scaglia E. Kilic A.F. Hennig N. Adolphs N. Saha B. Fauler V.M. Kalscheuer F. Hennig J. Altmüller C. Netzer H. Thiele P. Nürnberg G. Yigit M. Jäger J. Hecht U. Krüger T. Mielke P.M. Krawitz D. Horn M. Schuelke S. Mundlos C.A. Bacino P.E. Bonnen B. Wollnik B. Fischer-Zirnsak U. Kornak Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
July 02, 2022 / J Neuroinflammation Spermidine reduces neuroinflammation and soluble amyloid beta in an Alzheimer's disease mouse model K. Freitag N. Sterczyk S. Wendlinger B. Obermayer J. Schulz V. Farztdinov M. Mülleder M. Ralser J. Houtman L. Fleck C. Braeuning R. Sansevrino C. Hoffmann D. Milovanovic S.J. Sigrist T. Conrad D. Beule F.L. Heppner M. Jendrach
October 31, 2017 / Genome Biol Widespread activation of antisense transcription of the host genome during herpes simplex virus 1 infection E. Wyler J. Menegatti V. Franke C. Kocks A. Boltengagen T. Hennig K. Theil A. Rutkowski C. Ferrai L. Baer L. Kermas C. Friedel N. Rajewsky A. Akalin L. Dölken F. Grässer M. Landthaler
March 01, 2022 / J Med Genet Sensitivity and specificity of loss of heterozygosity analysis for the classification of rare germline variants in BRCA1/2: results of the observational AGO-TR1 study (NCT02222883) J. Hauke P. Harter C. Ernst A. Burges S. Schmidt A. Reuss J. Borde N. De Gregorio D. Dietrich A. El-Balat M. Kayali H. Gevensleben F. Hilpert J. Altmüller A. Heimbach W. Meier B. Schoemig-Markiefka H. Thiele R. Kimmig P. Nürnberg K. Kast L. Richters J. Sehouli R.K. Schmutzler E. Hahnen
December 19, 2017 / Cold Spring Harb Mol Case Stud Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia S. Alawbathani A. Kawalia M. Karakaya J. Altmüller P. Nürnberg S. Cirak
July 01, 2017 / Clin Genet Genetic heterogeneity in Pakistani microcephaly families revisited I. Ahmad S.M. Baig A.R. Abdulkareem M.S. Hussain I. Sur M.R. Toliat G. Nürnberg N. Dalibor A. Moawia S.S. Waseem M. Asif H. Nagra M. Sher M.M.A. Khan I. Hassan S.U. Rehman H. Thiele J. Altmüller A.A. Noegel P. Nürnberg
June 01, 2017 / Immunogenetics Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing J. Altmüller B. Haenisch A. Kawalia M. Menzen M.M. Nöthen H. Fier G.J. Molderings
December 01, 2017 / Nat Med A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle M. Awazawa P. Gabel E. Tsaousidou H. Nolte M. Krüger J. Schmitz P.J. Ackermann C. Brandt J. Altmüller S. Motameny F.T. Wunderlich J.W. Kornfeld M. Blüher J.C. Brüning
July 01, 2017 / Hum Genet Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability N.C. Bramswig H.J. Lüdecke F.F. Hamdan J. Altmüller F. Beleggia N.H. Elcioglu C. Freyer E.H. Gerkes Y.K. Demirkol K.G. Knupp A. Kuechler Y. Li D.H. Lowenstein J.L. Michaud K. Park A.P.A. Stegmann H.E. Veenstra-Knol T. Wieland B. Wollnik H. Engels T.M. Strom T. Kleefstra D. Wieczorek
September 26, 2017 / Mol Ecol Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin S. Dennenmoser F.J. Sedlazeck E. Iwaszkiewicz X.Y. Li J. Altmüller A.W. Nolte
November 02, 2017 / Am J Hum Genet De novo mutations in SLC25A24 cause a craniosynostosis syndrome with hypertrichosis, progeroid appearance, and mitochondrial dysfunction N. Ehmke L. Graul-Neumann L. Smorag R. Koenig L. Segebrecht P. Magoulas F. Scaglia E. Kilic A.F. Hennig N. Adolphs N. Saha B. Fauler V.M. Kalscheuer F. Hennig J. Altmüller C. Netzer H. Thiele P. Nürnberg G. Yigit M. Jäger J. Hecht U. Krüger T. Mielke P.M. Krawitz D. Horn M. Schuelke S. Mundlos C.A. Bacino P.E. Bonnen B. Wollnik B. Fischer-Zirnsak U. Kornak