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) Chekulaeva, Marina Dr. (1) Chen, Wei Prof. Dr. (2) Gotthardt, Michael Prof. Dr. (1) Harabula, Izabela-Cezara (2) Heinemann, Udo Prof. Dr. (1) Herzog, Margareta (1) Hirsekorn, Antje (2) Hübner, Norbert Prof. Dr. (1) Kempa, Stefan Dr. (1) Kirchner, Marieluise Dr. (1) Lacadie, Scott Allen Dr. (1) Landthaler, Markus Prof. Dr. (12) Lupianez Garcia, Dario Jesus Dr. (1) Maatz, Henrike Dr. (1) Mastrobuoni, Guido Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (13) Radke, Michael Dr. (1) Rybak-Wolf, Agnieszka Dr. (1) Schütz, Anja Dr. (1) Selbach, Matthias Prof. Dr. (3) Vucicevic, Dubravka (1) Wyler, Emanuel Dr. (1) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (45) (-) Fischer, Cornelius Dr. (1) (-) Rajewsky, Nikolaus Prof. Dr. (3) 2002 (1) 2005 (2) 2011 (1) 2012 (1) 2013 (14) (-) 2014 (18) 2015 (27) (-) 2016 (31) 2017 (37) 2018 (42) 2019 (36) 2020 (30) 2021 (52) 2022 (42) 2023 (28) 2024 (6) Cellular Neurosciences (3) Developmental Neurobiology (1) Experimental Ultrahigh-Field MR (6) From Cell States to Function (1) Genetics and Genomics of Cardiovascular Diseases (1) Genetics of Metabolic and Reproductive Disorders (1) Genome Engineering & Disease Models (2) (-) Genomics (46) Immune Regulation and Cancer (3) Magnetic Resonance (6) Proteome Dynamics (3) (-) RNA Biology and Posttranscriptional Regulation (3) Systems Biology of Gene Regulatory Elements (17) Transgenics (2) Translational Cardiology and Functional Genomics (1) 49 Results: Active Filter: Altmueller, Janine Dr.med.Fischer, Cornelius Dr.Rajewsky, Nikolaus Prof. Dr.GenomicsRNA Biology and Posttranscriptional Regulation20142016 Sort: Result score Newest to oldest Oldest to newest December 13, 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 December 04, 2014 / Am J Hum Genet Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome N. Ehmke A. Caliebe R. Koenig S.G. Kant Z. Stark V. Cormier-Daire D. Wieczorek G. Gillessen-Kaesbach K. Hoff A. Kawalia H. Thiele J. Altmüller B. Fischer-Zirnsak A. Knaus N. Zhu V. Heinrich C. Huber I. Harabula M. Spielmann D. Horn U. Kornak J. Hecht P.M. Krawitz P. Nürnberg R. Siebert H. Manzke S. Mundlos December, 2014 / Nat Genet Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy C.A. Martin I. Ahmad A. Klingseisen M.S. Hussain L.S. Bicknell A. Leitch G. Nürnberg M.R. Toliat J.E. Murray D. Hunt F. Khan Z. Ali S. Tinschert J. Ding C. Keith M.E. Harley P. Heyn R. Müller I. Hoffmann V. Cormier-Daire H. Dollfus L. Dupuis A. Bashamboo K. McElreavey A. Kariminejad R. Mendoza-Londono A.T. Moore A. Saggar C. Schlechter R. Weleber H. Thiele J. Altmüller W. Höhne M.E. Hurles A.A. Noegel S.M. Baig P. Nürnberg A.P. Jackson October, 2014 / Hum Mutat Mutation of POC1B in a severe syndromic retinal ciliopathy B.B. Beck J.B. Phillips M.P. Bartram J. Wegner M. Thoenes A. Pannes J. Sampson R. Heller H. Göbel F. Koerber A. Neugebauer A. Hedergott G. Nürnberg P. Nürnberg H. Thiele J. Altmüller M.R. Toliat S. Staubach K.M. Boycott E.M. Valente A.R. Janecke T. Eisenberger C. Bergmann L. Tebbe Y. Wang Y. Wu A.M. Fry M. Westerfield U. Wolfrum H.J. Bolz October 27, 2014 / J Cell Biol CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins J. Gao D. Schatton P. Martinelli H. Hansen D. Pla-Martin E. Barth C. Becker J. Altmueller P. Frommolt M. Sardiello E.I. Rugarli November 06, 2014 / Am J Hum Genet Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndrome M.S. Hussain A. Battaglia S. Szczepanski E. Kaygusuz M.R. Toliat S. Sakakibara J. Altmüller H. Thiele G. Nürnberg S. Moosa G. Yigit F. Beleggia S. Tinschert J. Clayton-Smith P. Vasudevan J.E. Urquhart D. Donnai A. Fryer F. Percin F. Brancati A. Dobbie R. Smigiel G. Gillessen-Kaesbach B. Wollnik A.A. Noegel W.G. Newman P. Nürnberg November 15, 2014 / Hum Mol Genet A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family M.A. Khan V.M. Rupp M. Orpinell M.S. Hussain J. Altmüller M.O. Steinmetz C. Enzinger H. Thiele W. Höhne G. Nürnberg S.M. Baig M. Ansar P. Nürnberg J.B. Vincent M.R. Speicher P. Gönczy C. Windpassinger September 09, 2014 / BMC Genomics Deciphering the genetic basis of microcystin tolerance A. Schwarzenberger T. Sadler S. Motameny K. Ben-Khalifa P. Frommolt J. Altmüller K. Konrad E. von Elert July, 2014 / Neurobiol Dis Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy B. Dejanovic D. Lal C.B. Catarino S. Arjune A.A. Belaidi H. Trucks C. Vollmar R. Surges W.S. Kunz S. Motameny J. Altmüller A. Köhler B.A. Neubauer P. Nürnberg S. Noachtar G. Schwarz T. Sander March 27, 2014 / Nat Commun Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids L. Fernandez-Cuesta M. Peifer X. Lu R. Sun L. Ozretić D. Seidal T. Zander F. Leenders J. George C. Müller I. Dahmen B. Pinther G. Bosco K. Konrad J. Altmüller P. Nürnberg V. Achter U. Lang P.M. Schneider M. Bogus A. Soltermann O.T. Brustugun Å. Helland S. Solberg M. Lund-Iversen S. Ansén E. Stoelben G.M. Wright P. Russell Z. Wainer B. Solomon J.K. Field R. Hyde M.P. Davies L.C. Heukamp I. Petersen S. Perner C. Lovly F. Cappuzzo W.D. Travis J. Wolf M. Vingron E. Brambilla S.A. Haas R. Buettner R.K. Thomas Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
December 13, 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
December 04, 2014 / Am J Hum Genet Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome N. Ehmke A. Caliebe R. Koenig S.G. Kant Z. Stark V. Cormier-Daire D. Wieczorek G. Gillessen-Kaesbach K. Hoff A. Kawalia H. Thiele J. Altmüller B. Fischer-Zirnsak A. Knaus N. Zhu V. Heinrich C. Huber I. Harabula M. Spielmann D. Horn U. Kornak J. Hecht P.M. Krawitz P. Nürnberg R. Siebert H. Manzke S. Mundlos
December, 2014 / Nat Genet Mutations in PLK4, encoding a master regulator of centriole biogenesis, cause microcephaly, growth failure and retinopathy C.A. Martin I. Ahmad A. Klingseisen M.S. Hussain L.S. Bicknell A. Leitch G. Nürnberg M.R. Toliat J.E. Murray D. Hunt F. Khan Z. Ali S. Tinschert J. Ding C. Keith M.E. Harley P. Heyn R. Müller I. Hoffmann V. Cormier-Daire H. Dollfus L. Dupuis A. Bashamboo K. McElreavey A. Kariminejad R. Mendoza-Londono A.T. Moore A. Saggar C. Schlechter R. Weleber H. Thiele J. Altmüller W. Höhne M.E. Hurles A.A. Noegel S.M. Baig P. Nürnberg A.P. Jackson
October, 2014 / Hum Mutat Mutation of POC1B in a severe syndromic retinal ciliopathy B.B. Beck J.B. Phillips M.P. Bartram J. Wegner M. Thoenes A. Pannes J. Sampson R. Heller H. Göbel F. Koerber A. Neugebauer A. Hedergott G. Nürnberg P. Nürnberg H. Thiele J. Altmüller M.R. Toliat S. Staubach K.M. Boycott E.M. Valente A.R. Janecke T. Eisenberger C. Bergmann L. Tebbe Y. Wang Y. Wu A.M. Fry M. Westerfield U. Wolfrum H.J. Bolz
October 27, 2014 / J Cell Biol CLUH regulates mitochondrial biogenesis by binding mRNAs of nuclear-encoded mitochondrial proteins J. Gao D. Schatton P. Martinelli H. Hansen D. Pla-Martin E. Barth C. Becker J. Altmueller P. Frommolt M. Sardiello E.I. Rugarli
November 06, 2014 / Am J Hum Genet Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndrome M.S. Hussain A. Battaglia S. Szczepanski E. Kaygusuz M.R. Toliat S. Sakakibara J. Altmüller H. Thiele G. Nürnberg S. Moosa G. Yigit F. Beleggia S. Tinschert J. Clayton-Smith P. Vasudevan J.E. Urquhart D. Donnai A. Fryer F. Percin F. Brancati A. Dobbie R. Smigiel G. Gillessen-Kaesbach B. Wollnik A.A. Noegel W.G. Newman P. Nürnberg
November 15, 2014 / Hum Mol Genet A missense mutation in the PISA domain of HsSAS-6 causes autosomal recessive primary microcephaly in a large consanguineous Pakistani family M.A. Khan V.M. Rupp M. Orpinell M.S. Hussain J. Altmüller M.O. Steinmetz C. Enzinger H. Thiele W. Höhne G. Nürnberg S.M. Baig M. Ansar P. Nürnberg J.B. Vincent M.R. Speicher P. Gönczy C. Windpassinger
September 09, 2014 / BMC Genomics Deciphering the genetic basis of microcystin tolerance A. Schwarzenberger T. Sadler S. Motameny K. Ben-Khalifa P. Frommolt J. Altmüller K. Konrad E. von Elert
July, 2014 / Neurobiol Dis Exonic microdeletions of the gephyrin gene impair GABAergic synaptic inhibition in patients with idiopathic generalized epilepsy B. Dejanovic D. Lal C.B. Catarino S. Arjune A.A. Belaidi H. Trucks C. Vollmar R. Surges W.S. Kunz S. Motameny J. Altmüller A. Köhler B.A. Neubauer P. Nürnberg S. Noachtar G. Schwarz T. Sander
March 27, 2014 / Nat Commun Frequent mutations in chromatin-remodelling genes in pulmonary carcinoids L. Fernandez-Cuesta M. Peifer X. Lu R. Sun L. Ozretić D. Seidal T. Zander F. Leenders J. George C. Müller I. Dahmen B. Pinther G. Bosco K. Konrad J. Altmüller P. Nürnberg V. Achter U. Lang P.M. Schneider M. Bogus A. Soltermann O.T. Brustugun Å. Helland S. Solberg M. Lund-Iversen S. Ansén E. Stoelben G.M. Wright P. Russell Z. Wainer B. Solomon J.K. Field R. Hyde M.P. Davies L.C. Heukamp I. Petersen S. Perner C. Lovly F. Cappuzzo W.D. Travis J. Wolf M. Vingron E. Brambilla S.A. Haas R. Buettner R.K. Thomas