Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Altmueller, Janine Dr.med. (73) Beule, Dieter Dr. (2) Blüthgen, Nils (1) Borodina, Tatiana Dr. (2) Braeuning, Caroline (2) Dechend, Ralf Priv. Doz. (1) Fischer, Cornelius Dr. (1) Geisberger, Sabrina Yasmin Dr. (1) Henssen, Anton Prof. Dr. med. (1) Herse, Florian PD Dr. (1) Hinze, Christian Dr. med. Dipl.-Math. (1) Kocks, Christine Dr. (2) Quedenau, Claudia (1) Rajewsky, Nikolaus Prof. Dr. (2) Sai, Somesh (1) Schmitt, Clemens Prof. Dr. (1) Semtner, Marcus Dr. (1) Sunaga-Franze, Daniele Yumi Dr. (1) (-) 2002 (1) 2005 (2) 2013 (21) 2014 (17) (-) 2015 (28) 2016 (31) 2017 (35) 2018 (42) 2019 (35) 2020 (34) (-) 2021 (57) 2022 (47) 2023 (28) 2024 (12) Advanced Light Microscopy (11) AG Müller/Dechend (ECRC) (85) AG Schreiber [ECRC] (16) Allosteric Proteomics Lab (5) Anchored Signalling (30) Angiogenesis & Metabolism Laboratory (11) Animal Phenotyping (6) Biobank (63) Bioinformatics and Omics Data Science (18) Bioinformatics of RNA Structure and Transcriptome Regulation (9) Biology of Malignant Lymphomas (20) Biomedical Image Analysis (6) Cancer Genetics and Cellular Stress Responses (17) Cardiac MRI (37) Cardiovascular-Hematopoietic Interaction (1) Cell Biology of Immunity (17) Cellular Neurosciences (106) Chemical Biology (198) Chromatin (dys)function in disease (2) Clinical Research Unit (7) Computational and developmental biology (1) Computational methodologies and omic analytics (4) Computational Regulatory Genomics (31) Cryo-Electron Microscopy (4) Developmental Biology / Signal Transduction (45) Developmental Neurobiology (23) Development and Function of Neural Circuits (5) Electron Microscopy (4) Epigenetic Regulation and Chromatin Architecture (21) Experimental Ultrahigh-Field MR (77) Gastrointestinal Barrier, Regeneration and Carcinogenesis (11) Genetics and Genomics of Cardiovascular Diseases (85) Genetics of Congenital Heart Disease (10) Genetics of Metabolic and Reproductive Disorders (7) Genome Diversification & Integrity (6) Genome Engineering & Disease Models (37) Genome instability and somatic mosaicism (5) (-) Genomics (86) Host-microbiome factors in cardiovascular disease (22) Hypertension-caused End-Organ Damage (85) Hypertension-Mediated End-Organ Damage (85) Image Data Analysis (3) immune Cell Function in Health and Disease (10) Immune Mechanisms and Human Antibodies (3) Immune Regulation and Cancer (18) Innate Immunity & Neuroinflammation (14) In Situ Structural Biology (11) Integrative Vascular Biology (29) Interdisciplinary Retina Research (23) Intracellular Proteolysis (34) Kidney Cell Engineering (4) Magnetic Resonance (77) Mathematical Cell Physiology (21) Mathematical Modelling of Cellular Processes (14) Mechanism-based Cancer Therapies (20) Microenvironmental Regulation in Autoimmunity and Cancer (21) Mobile DNA (18) Molecular and cellular basis of behavio (1) Molecular Biology of Peptide Hormones (147) Molecular Cardiovascular Research (44) Molecular Epidemiology (63) Molecular Genetics of Chronic Inflammation and Allergic Disease (20) Molecular Immunology and Gene Therapy (49) Molecular mechanisms of environment sensing (1) Molecular Oncology (7) Molecular Pathways in Cortical Development (9) Molecular Physiology of Somatic Sensation (36) Myology (20) Nephrology and Inflammatory Vascular Diseases (33) Neural Circuits and Behaviour (13) Neuroimmunology Laboratory (11) Neurovascular link in neuroendocrine tumors (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (4) Organoids (4) Out-patient Clinic for Neuroimmunology (114) Pancreatic Organoid Research and Disease Modeling (29) Pathogenesis of ANCAinduced Glomerulonephritis (23) Pluripotent Stem Cells (11) Protein Production and Characterization (4) Proteome Dynamics (34) Proteomics (20) Proteomics and Metabolomics (19) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (82) Psychoneuroimmunology (10) Quantitative Developmental Biology (11) Quantitative Stem Cell Biology (3) RNA Biology and Posttranscriptional Regulation (34) Screening Unit (198) Spatial Proteomics (4) Stem Cell Dynamics and Mitochondrial Genomics (10) Stem Cell Modeling of Development and Disease (3) Structural Biology of Membrane-Associated Processes (17) Synaptic Transmission and Plasticity (43) Systems Biology Imaging (4) Systems biology of cardiovascular and neuronal pathologies (1) Systems Biology of Gene Regulatory Elements (39) Systems Hematology, Stem Cells & Precision Medicine (5) Transgenics (37) Translational Approaches in Heart Failure and Cardiometabolic Disease (21) Translational Bioinformatics (17) Translational Cardiology and Functional Genomics (22) Translational Neuroimmunology (11) Translational Oncology of Solid Tumors (303) Translational Organ Models (17) Translational Tumorimmunology (6) Tumor heterogeneity and treatment resistance in pediatric cancer (1) 86 Results: Active Filter: Genomics200220152021 Sort: Result score Newest to oldest Oldest to newest November, 2015 / Plant Physiol Floral induction in Arabidopsis by FLOWERING LOCUS T requires direct repression of BLADE-ON-PETIOLE genes by the homeodomain protein PENNYWISE F. Andrés M. Romera-Branchat R. Martínez-Gallegos V. Patel K. Schneeberger S. Jang J. Altmüller P. Nürnberg G. Coupland September 22, 2015 / Proc Biol Sci Ectodysplasin signalling genes and phenotypic evolution in sculpins (Cottus) J. Cheng F. Sedlazek J. Altmüller A.W. Nolte November, 2015 / Am J Med Genet A Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes B. Gollasch F.B. Basmanav A. Nanda G. Fritz H. Mahmoudi H. Thiele M. Wehner S. Wolf J. Altmüller P. Nürnberg J. Frank R.C. Betz November, 2015 / Neurobiol Aging De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients A. Hübers W. Just A. Rosenbohm K. Müller N. Marroquin I. Goebel J. Högel H. Thiele J. Altmüller P. Nürnberg J.H. Weishaupt C. Kubisch A.C. Ludolph A.E. Volk October, 2015 / Mol Cell Probes Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome A. Kuechler J. Altmüller P. Nürnberg S. Kotthoff C. Kubisch G. Borck October 01, 2015 / Am J Hum Genet Loss-of-function GAS8 mutations cause primary ciliary dyskinesia and disrupt the nexin-dynein regulatory complex H. Olbrich C. Cremers N.T. Loges C. Werner K.G. Nielsen J.K. Marthin M. Philipsen J. Wallmeier P. Pennekamp T. Menchen C. Edelbusch G.W. Dougherty O. Schwartz H. Thiele J. Altmüller F. Rommelmann H. Omran July 15, 2015 / Int J Cancer Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas I. Spier S. Holzapfel J. Altmüller B. Zhao S. Horpaopan S. Vogt S. Chen M. Morak S. Raeder K. Kayser D. Stienen R. Adam P. Nürnberg G. Plotz E. Holinski-Feder R.P. Lifton H. Thiele P. Hoffmann V. Steinke S. Aretz July 01, 2015 / Hum Mol Genet Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability N. Rosin N.H. Elcioglu F. Beleggia P. Isgüven J. Altmüller H. Thiele K. Steindl P. Joset A. Rauch P. Nürnberg B. Wollnik G. Yigit January 04, 2021 / J Biol Chem Ion transporter NKCC1, modulator of neurogenesis in murine olfactory neurons C. Haering N. Kanageswaran P. Bouvain P. Scholz J. Altmüller C. Becker G. Gisselmann J. Wäring-Bischof H. Hatt January, 2015 / Hum Genet STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly N. Kakar J. Ahmad D.J. Morris-Rosendahl J. Altmüller K. Friedrich G. Barbi P. Nürnberg C. Kubisch W.B. Dobyns G. Borck Pagination First page « First Previous page ‹ Previous … Page 3 Current page 4 Page 5 Page 6 … Next page Next › Last page Last »
November, 2015 / Plant Physiol Floral induction in Arabidopsis by FLOWERING LOCUS T requires direct repression of BLADE-ON-PETIOLE genes by the homeodomain protein PENNYWISE F. Andrés M. Romera-Branchat R. Martínez-Gallegos V. Patel K. Schneeberger S. Jang J. Altmüller P. Nürnberg G. Coupland
September 22, 2015 / Proc Biol Sci Ectodysplasin signalling genes and phenotypic evolution in sculpins (Cottus) J. Cheng F. Sedlazek J. Altmüller A.W. Nolte
November, 2015 / Am J Med Genet A Identification of a novel mutation in RIPK4 in a kindred with phenotypic features of Bartsocas-Papas and CHAND syndromes B. Gollasch F.B. Basmanav A. Nanda G. Fritz H. Mahmoudi H. Thiele M. Wehner S. Wolf J. Altmüller P. Nürnberg J. Frank R.C. Betz
November, 2015 / Neurobiol Aging De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients A. Hübers W. Just A. Rosenbohm K. Müller N. Marroquin I. Goebel J. Högel H. Thiele J. Altmüller P. Nürnberg J.H. Weishaupt C. Kubisch A.C. Ludolph A.E. Volk
October, 2015 / Mol Cell Probes Exome sequencing identifies a novel heterozygous TGFB3 mutation in a disorder overlapping with Marfan and Loeys-Dietz syndrome A. Kuechler J. Altmüller P. Nürnberg S. Kotthoff C. Kubisch G. Borck
October 01, 2015 / Am J Hum Genet Loss-of-function GAS8 mutations cause primary ciliary dyskinesia and disrupt the nexin-dynein regulatory complex H. Olbrich C. Cremers N.T. Loges C. Werner K.G. Nielsen J.K. Marthin M. Philipsen J. Wallmeier P. Pennekamp T. Menchen C. Edelbusch G.W. Dougherty O. Schwartz H. Thiele J. Altmüller F. Rommelmann H. Omran
July 15, 2015 / Int J Cancer Frequency and phenotypic spectrum of germline mutations in POLE and seven other polymerase genes in 266 patients with colorectal adenomas and carcinomas I. Spier S. Holzapfel J. Altmüller B. Zhao S. Horpaopan S. Vogt S. Chen M. Morak S. Raeder K. Kayser D. Stienen R. Adam P. Nürnberg G. Plotz E. Holinski-Feder R.P. Lifton H. Thiele P. Hoffmann V. Steinke S. Aretz
July 01, 2015 / Hum Mol Genet Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability N. Rosin N.H. Elcioglu F. Beleggia P. Isgüven J. Altmüller H. Thiele K. Steindl P. Joset A. Rauch P. Nürnberg B. Wollnik G. Yigit
January 04, 2021 / J Biol Chem Ion transporter NKCC1, modulator of neurogenesis in murine olfactory neurons C. Haering N. Kanageswaran P. Bouvain P. Scholz J. Altmüller C. Becker G. Gisselmann J. Wäring-Bischof H. Hatt
January, 2015 / Hum Genet STIL mutation causes autosomal recessive microcephalic lobar holoprosencephaly N. Kakar J. Ahmad D.J. Morris-Rosendahl J. Altmüller K. Friedrich G. Barbi P. Nürnberg C. Kubisch W.B. Dobyns G. Borck