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) Fischer, Cornelius Dr. (1) Gotthardt, Michael Prof. Dr. (1) Graf, Robin Dr. (2) Heinemann, Udo Prof. Dr. (1) Herzog, Margareta (1) Hirsekorn, Antje (1) Hübner, Norbert Prof. Dr. (1) Kempa, Stefan Dr. (1) Kirchner, Marieluise Dr. (1) Kühn, Ralf Dr. (10) Landthaler, Markus Prof. Dr. (12) Lupianez Garcia, Dario Jesus Dr. (1) Mastrobuoni, Guido Dr. (1) Obermayer-Wasserscheid, Benedikt Dr. (1) Ohler, Uwe Prof. Dr. (2) Radke, Michael Dr. (1) Rajewsky, Klaus Prof. Dr. (2) Rajewsky, Nikolaus Prof. Dr. (3) Rybak-Wolf, Agnieszka Dr. (1) Schütz, Anja Dr. (1) Selbach, Matthias Prof. Dr. (3) Zauber, Henrik Dr. (1) (-) Altmueller, Janine Dr.med. (36) (-) Chu, Van Trung Dr. (2) (-) Harabula, Izabela-Cezara (2) (-) Maatz, Henrike Dr. (1) (-) Wyler, Emanuel Dr. (1) 2002 (1) 2005 (2) 2012 (2) (-) 2014 (8) 2015 (29) (-) 2016 (32) 2017 (37) 2018 (39) 2019 (37) 2020 (28) 2021 (58) 2022 (48) 2023 (30) 2024 (6) Cellular Neurosciences (3) Computational Regulatory Genomics (1) Developmental Neurobiology (1) Experimental Ultrahigh-Field MR (6) Genetics and Genomics of Cardiovascular Diseases (2) Genetics of Congenital Heart Disease (1) Genetics of Metabolic and Reproductive Disorders (1) (-) Genome Engineering & Disease Models (2) (-) Genomics (36) Immune Regulation and Cancer (3) Magnetic Resonance (6) Proteome Dynamics (2) (-) RNA Biology and Posttranscriptional Regulation (2) Systems Biology of Gene Regulatory Elements (1) Transgenics (2) Translational Cardiology and Functional Genomics (1) 40 Results: Active Filter: Altmueller, Janine Dr.med.Chu, Van Trung Dr.Harabula, Izabela-CezaraMaatz, Henrike Dr.Wyler, Emanuel Dr.Genome Engineering & Disease ModelsGenomicsRNA 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 March 01, 2016 / Am J Med Genet A A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation G. Yigit D. Wieczorek N. Bögershausen F. Beleggia C. Möller-Hartmann J. Altmüller H. Thiele P. Nürnberg B. Wollnik October 01, 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 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 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 December 01, 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 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 August 01, 2014 / J Clin Invest RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing H. Maatz M. Jens M. Liss S. Schafer M. Heinig M. Kirchner E. Adami C. Rintisch V. Dauksaite M.H. Radke M. Selbach P.J.R. Barton S.A. Cook N. Rajewsky M. Gotthardt M. Landthaler N. Hubner Pagination First page « First Previous page ‹ Previous Page 1 Page 2 Page 3 Current page 4
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
March 01, 2016 / Am J Med Genet A A syndrome of microcephaly, short stature, polysyndactyly, and dental anomalies caused by a homozygous KATNB1 mutation G. Yigit D. Wieczorek N. Bögershausen F. Beleggia C. Möller-Hartmann J. Altmüller H. Thiele P. Nürnberg B. Wollnik
October 01, 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
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
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
December 01, 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
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
August 01, 2014 / J Clin Invest RNA-binding protein RBM20 represses splicing to orchestrate cardiac pre-mRNA processing H. Maatz M. Jens M. Liss S. Schafer M. Heinig M. Kirchner E. Adami C. Rintisch V. Dauksaite M.H. Radke M. Selbach P.J.R. Barton S.A. Cook N. Rajewsky M. Gotthardt M. Landthaler N. Hubner