Wissenschaftliche Publikationen Suche Suche Autor/in Forschungsgruppe Veröffentlichungsdatum Wirkungsfaktor Suchen Sortieren nach RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Reihenfolge AufsteigendAbsteigend Gerhardt, Holger Prof. Dr. (1) Graf, Robin Dr. (2) Harabula, Izabela-Cezara (1) Hirsekorn, Antje (2) Janz, Martin Dr. (1) Kühn, Ralf Dr. (2) Lacadie, Scott Allen Dr. (1) Lupianez Garcia, Dario Jesus Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (7) Potente, Michael Prof. Dr. (1) Rajewsky, Klaus Prof. Dr. (11) Rajewsky, Nikolaus Prof. Dr. (1) Selbach, Matthias Prof. Dr. (2) Vucicevic, Dubravka (1) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (29) (-) Chekulaeva, Marina Dr. (1) (-) Chu, Van Trung Dr. (3) (-) Fischer, Cornelius Dr. (1) (-) Landthaler, Markus Prof. Dr. (4) (-) Wyler, Emanuel Dr. (1) (-) Bioinformatik der Genregulation (4) Experimentelle Ultrahochfeld-MR (4) Genom-Editierung & Krankheitsmodelle (2) (-) Genomics (30) (-) Immunregulation und Krebs (3) Magnetic Resonance (4) Nicht-Kodierende RNAs und Mechanismen der Genregulation im Cytoplasma (1) Proteom Dynamik (2) (-) RNA Biologie und Posttranscriptionale Regulation (5) Systembiologie von Gen-regulatorischen Elementen (1) Transgenics (2) Zelluläre Neurowissenschaften (2) 1999 (1) 2002 (3) 2003 (1) 2004 (5) 2005 (5) 2006 (2) 2007 (2) 2008 (1) 2009 (3) 2010 (3) 2011 (3) 2012 (4) 2013 (6) 2014 (15) 2015 (34) (-) 2016 (40) 2017 (43) 2018 (49) 2019 (45) 2020 (39) 2021 (63) 2022 (58) 2023 (39) 2024 (10) 40 Ergebnisse: Active Filter: Altmueller, Janine Dr.med.Chekulaeva, Marina Dr.Chu, Van Trung Dr.Fischer, Cornelius Dr.Landthaler, Markus Prof. Dr.Wyler, Emanuel Dr.Bioinformatik der GenregulationGenomicsImmunregulation und KrebsRNA Biologie und Posttranscriptionale Regulation2016 Sortieren: Treffgenauigkeit Neueste nach älteste Älteste nach neueste 01. Januar 2016 / PLoS ONE Increased probability of co-occurrence of two rare diseases in consanguineous families and resolution of a complex phenotype by next generation sequencing D. Lal B.A. Neubauer M.R. Toliat J. Altmüller H. Thiele P. Nürnberg C. Kamrath A. Schänzer T. Sander A. Hahn M. Nothnagel 01. September 2016 / Am J Med Genet A A novel homozygous PAM16 mutation in a patient with a milder phenotype and longer survival S. Moosa V. Fano M.G. Obregon J. Altmüller H. Thiele P. Nürnberg G. Nishimura B. Wollnik 04. November 2016 / Sci Rep The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family C. Reiff M. Owczarek-Lipska G. Spital C. Röger H. Hinz C. Jüschke H. Thiele J. Altmüller P. Nürnberg R. Da Costa J. Neidhardt 08. Juli 2016 / PLoS ONE Identification of novel and recurrent disease-causing mutations in retinal dystrophies using whole exome sequencing (WES): Benefits and limitations A. Tiwari J. Lemke J. Altmüller H. Thiele E. Glaus J. Fleischhauer P. Nürnberg J. Neidhardt W. Berger 13. Dezember 2016 / Breast Cancer-Targets Ther Expression and functionality of TRPV1 in breast cancer cells L.V. Weber K. Al-Refae G. Wölk G. Bonatz J. Altmüller C. Becker G. Gisselmann H. Hatt 12. Mai 2016 / N Engl J Med Polyhydramnios, transient antenatal Bartter's syndrome, and MAGED2 mutations K. Laghmani B.B. Beck S.S. Yang E. Seaayfan A. Wenzel B. Reusch H. Vitzthum D. Priem S. Demaretz K. Bergmann L.K. Duin H. Göbel C. Mache H. Thiele M.P. Bartram C. Dombret J. Altmüller P. Nürnberg T. Benzing E. Levtchenko H.W. Seyberth G. Klaus G. Yigit S.H. Lin A. Timmer T.J. de Koning S.A. Scherjon K.P. Schlingmann M.J.M. Bertrand M.M. Rinschen O. de Backer M. Konrad M. Kömhoff 30. August 2016 / Sci Rep Characterization of non-olfactory GPCRs in human sperm with a focus on GPR18 C. Flegel F. Vogel A. Hofreuter S. Wojcik C. Schoeder K. Kieć-Kononowicz N.H. Brockmeyer C.E. Müller C. Becker J. Altmüller H. Hatt G. Gisselmann 15. Juli 2016 / eLife Tumor suppression in basal keratinocytes via dual non-cell-autonomous functions of a Na,K-ATPase beta subunit J. Hatzold F. Beleggia H. Herzig J. Altmüller P. Nürnberg W. Bloch B. Wollnik M. Hammerschmidt 01. Juni 2016 / PLoS Pathog The WOPR protein Ros1 is a master regulator of sporogenesis and late effector gene expression in the maize pathogen Ustilago maydis M. Tollot D. Assmann C. Becker J. Altmüller J.Y. Dutheil C.E. Wegner R. Kahmann 01. August 2016 / Biol Chem A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of product J. Altmüller S. Motameny C. Becker H. Thiele S. Chatterjee B. Wollnik P. Nürnberg Seitennummerierung Aktuelle Seite 1 Seite 2 Seite 3 Seite 4 Nächste Seite Next › Letzte Seite Last »
01. Januar 2016 / PLoS ONE Increased probability of co-occurrence of two rare diseases in consanguineous families and resolution of a complex phenotype by next generation sequencing D. Lal B.A. Neubauer M.R. Toliat J. Altmüller H. Thiele P. Nürnberg C. Kamrath A. Schänzer T. Sander A. Hahn M. Nothnagel
01. September 2016 / Am J Med Genet A A novel homozygous PAM16 mutation in a patient with a milder phenotype and longer survival S. Moosa V. Fano M.G. Obregon J. Altmüller H. Thiele P. Nürnberg G. Nishimura B. Wollnik
04. November 2016 / Sci Rep The mutation p.E113K in the Schiff base counterion of rhodopsin is associated with two distinct retinal phenotypes within the same family C. Reiff M. Owczarek-Lipska G. Spital C. Röger H. Hinz C. Jüschke H. Thiele J. Altmüller P. Nürnberg R. Da Costa J. Neidhardt
08. Juli 2016 / PLoS ONE Identification of novel and recurrent disease-causing mutations in retinal dystrophies using whole exome sequencing (WES): Benefits and limitations A. Tiwari J. Lemke J. Altmüller H. Thiele E. Glaus J. Fleischhauer P. Nürnberg J. Neidhardt W. Berger
13. Dezember 2016 / Breast Cancer-Targets Ther Expression and functionality of TRPV1 in breast cancer cells L.V. Weber K. Al-Refae G. Wölk G. Bonatz J. Altmüller C. Becker G. Gisselmann H. Hatt
12. Mai 2016 / N Engl J Med Polyhydramnios, transient antenatal Bartter's syndrome, and MAGED2 mutations K. Laghmani B.B. Beck S.S. Yang E. Seaayfan A. Wenzel B. Reusch H. Vitzthum D. Priem S. Demaretz K. Bergmann L.K. Duin H. Göbel C. Mache H. Thiele M.P. Bartram C. Dombret J. Altmüller P. Nürnberg T. Benzing E. Levtchenko H.W. Seyberth G. Klaus G. Yigit S.H. Lin A. Timmer T.J. de Koning S.A. Scherjon K.P. Schlingmann M.J.M. Bertrand M.M. Rinschen O. de Backer M. Konrad M. Kömhoff
30. August 2016 / Sci Rep Characterization of non-olfactory GPCRs in human sperm with a focus on GPR18 C. Flegel F. Vogel A. Hofreuter S. Wojcik C. Schoeder K. Kieć-Kononowicz N.H. Brockmeyer C.E. Müller C. Becker J. Altmüller H. Hatt G. Gisselmann
15. Juli 2016 / eLife Tumor suppression in basal keratinocytes via dual non-cell-autonomous functions of a Na,K-ATPase beta subunit J. Hatzold F. Beleggia H. Herzig J. Altmüller P. Nürnberg W. Bloch B. Wollnik M. Hammerschmidt
01. Juni 2016 / PLoS Pathog The WOPR protein Ros1 is a master regulator of sporogenesis and late effector gene expression in the maize pathogen Ustilago maydis M. Tollot D. Assmann C. Becker J. Altmüller J.Y. Dutheil C.E. Wegner R. Kahmann
01. August 2016 / Biol Chem A systematic comparison of two new releases of exome sequencing products: the aim of use determines the choice of product J. Altmüller S. Motameny C. Becker H. Thiele S. Chatterjee B. Wollnik P. Nürnberg