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. (71) Beule, Dieter Dr. (1) Blüthgen, Nils (1) Borodina, Tatiana Dr. (1) Braeuning, Caroline (1) 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. (1) Quedenau, Claudia (1) Rajewsky, Nikolaus Prof. Dr. (1) Sai, Somesh (1) Schmitt, Clemens Prof. Dr. (1) Semtner, Marcus Dr. (1) Sunaga-Franze, Daniele Yumi Dr. (1) (-) 2002 (1) 2005 (2) 2013 (10) 2014 (17) (-) 2015 (27) 2016 (31) 2017 (34) 2018 (42) 2019 (35) 2020 (33) (-) 2021 (54) 2022 (47) 2023 (28) 2024 (5) 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 (62) Bioinformatics and Omics Data Science (17) Bioinformatics of RNA Structure and Transcriptome Regulation (8) Biology of Malignant Lymphomas (19) Biomedical Image Analysis (5) Cancer Genetics and Cellular Stress Responses (17) Cardiac MRI (37) Cardiovascular-Hematopoietic Interaction (1) Cell Biology of Immunity (17) Cellular Neurosciences (106) Chromatin (dys)function in disease (2) Clinical Research Unit (7) Clinic of Psychiatry / Modul Psychiatry of Aging (17) Computational methodologies and omic analytics (4) Computational Regulatory Genomics (30) Cryo-Electron Microscopy (4) Developmental Biology / Signal Transduction (44) Developmental Neurobiology (23) Development and Function of Neural Circuits (3) Endocrinology, Diabetes and Nutritional Medicine (9) Epigenetic Modifications in Neuroblastoma (11) Epigenetic Regulation and Chromatin Architecture (21) Experimental Ultrahigh-Field MR (76) 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 (82) 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 Dysregulations in Oncology (16) Immune Mechanisms and Human Antibodies (4) Immune Regulation and Cancer (19) Innate Immunity & Neuroinflammation (14) In Situ Structural Biology (10) Integrative Vascular Biology (29) Interdisciplinary Retina Research (23) Intracellular Proteolysis (34) Kidney Cell Engineering (4) Magnetic Resonance (76) 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 (62) 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 (12) Neuroimmunology Laboratory (11) Neurovascular link in neuroendocrine tumors (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (4) Organoids (3) Out-patient Clinic for Neuroimmunology (113) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (20) Pancreatic Organoid Research and Disease Modeling (29) Pathogenesis of ANCAinduced Glomerulonephritis (23) Pluripotent Stem Cells (11) Protein Production and Characterization (4) Proteome Dynamics (32) Proteomics (19) 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 (29) Spatial Proteomics (3) 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 (41) Systems Biology Imaging (3) Systems biology of cardiovascular and neuronal pathologies (1) Systems Biology of Gene Regulatory Elements (36) Systems Hematology, Stem Cells & Precision Medicine (5) Transgenics (37) Translational Approaches in Heart Failure and Cardiometabolic Disease (22) Translational Bioinformatics (16) 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) 82 Results: Active Filter: Genomics200220152021 Sort: Result score Newest to oldest Oldest to newest June 01, 2015 / Ann Neurol Rare variants in GABA(A) receptor genes in Rolandic epilepsy and related syndromes E.M. Reinthaler B. Dejanovic D. Lal M. Semtner Y. Merkler A. Reinhold D.A. Pittrich C. Hotzy M. Feucht H. Steinboeck U. Gruber-Sedlmayr G. Ronen B. Neophytou J. Geldner E. Haberlandt H. Muhle M.A. Ikram CM. van Duijn A.G. Uitterlinden A. Hofman J. Altmüller A. Kawalia M.R. Toliat P. Nuernberg H. Lerche M. Nothnagel H. Thiele T. Sander J.C. Meier G. Schwarz B.A. Neubauer F. Zimprich July 01, 2015 / Hum Genet Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3 B.S. Budde S. Mizumoto R. Kogawa C. Becker J. Altmüller H. Thiele F. Rueschendorf M.R. Toliat G. Kaleschke J.M. Haemmerle W. Hoehne K. Sugahara P. Nuernberg I. Kennerknecht January 01, 2002 / Hum Mol Genet STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study G. Duetsch T. Illig S. Loesgen K. Rohde N. Klopp N. Herbon H. Gohlke J. Altmueller M. Wjst June 10, 2021 / Nature Swarm Learning for decentralized and confidential clinical machine learning S. Warnat-Herresthal H. Schultze K.L. Shastry S. Manamohan S. Mukherjee V. Garg R. Sarveswara K. Händler P. Pickkers N.A. Aziz S. Ktena F. Tran M. Bitzer S. Ossowski N. Casadei C. Herr D. Petersheim U. Behrends F. Kern T. Fehlmann P. Schommers C. Lehmann M. Augustin J. Rybniker J. Altmüller N. Mishra J.P. Bernardes B. Krämer L. Bonaguro J. Schulte-Schrepping E. De Domenico C. Siever M. Kraut M. Desai B. Monnet M. Saridaki C.M. Siegel A. Drews M. Nuesch-Germano H. Theis J. Heyckendorf S. Schreiber S. Kim-Hellmuth J. Nattermann D. Skowasch I. Kurth A. Keller R. Bals P. Nürnberg O. Rieß P. Rosenstiel M.G. Netea F. Theis S. Mukherjee M. Backes A.C. Aschenbrenner T. Ulas M.M.B. Breteler E.J. Giamarellos-Bourboulis M. Kox M. Becker S. Cheran M.S. Woodacre E.L. Goh J.L. Schultze November 01, 2021 / Brief Bioinform A comparison of metabolic labeling and statistical methods to infer genome-wide dynamics of RNA turnover E. Boileau J. Altmüller I.S. Naarmann-de Vries C. Dieterich August 01, 2021 / Hum Genet Biallelic mutations in L-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism A.E. Volk A. Hedergott M. Preising S. Rading J. Fricke P. Herkenrath P. Nürnberg J. Altmüller S. von Ameln B. Lorenz A. Neugebauer M. Karsak C. Kubisch December 01, 2021 / Nat Genet Chromothripsis followed by circular recombination drives oncogene amplification in human cancer C. Rosswog C. Bartenhagen A. Welte Y. Kahlert N. Hemstedt W. Lorenz M. Cartolano S. Ackermann S. Perner W. Vogel J. Altmüller P. Nürnberg F. Hertwig G. Göhring E. Lilienweiss A.M. Stütz J.O. Korbel R.K. Thomas M. Peifer M. Fischer October 01, 2021 / Neurogenetics ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants K. Kloth B. Lozic J. Tagoe M.J.V. Hoffer A. Van der Ven H. Thiele J. Altmüller C. Kubisch P.Y.B. Au J. Denecke E.K. Bijlsma D. Lessel November 01, 2021 / Genet Med Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies M. Iqbal R. Maroofian B. Çavdarlı F. Riccardi M. Field S. Banka D.K. Bubshait Y. Li J. Hertecant S.M. Baig D. Dyment S. Efthymiou U. Abdullah E.U.H. Makhdoom Z. Ali T Scherf de Almeida F. Molinari C. Mignon-Ravix B. Chabrol J. Antony L. Ades A.T. Pagnamenta A. Jackson S. Douzgou C. Beetz V. Karageorgou B. Vona A. Rad J.M. Baig T. Sultan J.R. Alvi S. Maqbool F. Rahman M.B. Toosi F. Ashrafzadeh S. Imannezhad E.G. Karimiani Y. Sarwar S. Khan M. Jameel A.A. Noegel B. Budde J. Altmüller S. Motameny W. Höhne H. Houlden P. Nürnberg B. Wollnik L. Villard F.S. Alkuraya M. Osmond M.S. Hussain G. Yigit July 01, 2021 / Nat Cell Biol Niche stiffening compromises hair follicle stem cell potential during ageing by reducing bivalent promoter accessibility J. Koester Y.A. Miroshnikova S. Ghatak C.A. Chacón-Martínez J. Morgner X. Li I. Atanassov J. Altmüller D.E. Birk M. Koch W. Bloch M. Bartusel C.M. Niessen A. Rada-Iglesias S.A. Wickström Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
June 01, 2015 / Ann Neurol Rare variants in GABA(A) receptor genes in Rolandic epilepsy and related syndromes E.M. Reinthaler B. Dejanovic D. Lal M. Semtner Y. Merkler A. Reinhold D.A. Pittrich C. Hotzy M. Feucht H. Steinboeck U. Gruber-Sedlmayr G. Ronen B. Neophytou J. Geldner E. Haberlandt H. Muhle M.A. Ikram CM. van Duijn A.G. Uitterlinden A. Hofman J. Altmüller A. Kawalia M.R. Toliat P. Nuernberg H. Lerche M. Nothnagel H. Thiele T. Sander J.C. Meier G. Schwarz B.A. Neubauer F. Zimprich
July 01, 2015 / Hum Genet Skeletal dysplasia in a consanguineous clan from the island of Nias/Indonesia is caused by a novel mutation in B3GAT3 B.S. Budde S. Mizumoto R. Kogawa C. Becker J. Altmüller H. Thiele F. Rueschendorf M.R. Toliat G. Kaleschke J.M. Haemmerle W. Hoehne K. Sugahara P. Nuernberg I. Kennerknecht
January 01, 2002 / Hum Mol Genet STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study G. Duetsch T. Illig S. Loesgen K. Rohde N. Klopp N. Herbon H. Gohlke J. Altmueller M. Wjst
June 10, 2021 / Nature Swarm Learning for decentralized and confidential clinical machine learning S. Warnat-Herresthal H. Schultze K.L. Shastry S. Manamohan S. Mukherjee V. Garg R. Sarveswara K. Händler P. Pickkers N.A. Aziz S. Ktena F. Tran M. Bitzer S. Ossowski N. Casadei C. Herr D. Petersheim U. Behrends F. Kern T. Fehlmann P. Schommers C. Lehmann M. Augustin J. Rybniker J. Altmüller N. Mishra J.P. Bernardes B. Krämer L. Bonaguro J. Schulte-Schrepping E. De Domenico C. Siever M. Kraut M. Desai B. Monnet M. Saridaki C.M. Siegel A. Drews M. Nuesch-Germano H. Theis J. Heyckendorf S. Schreiber S. Kim-Hellmuth J. Nattermann D. Skowasch I. Kurth A. Keller R. Bals P. Nürnberg O. Rieß P. Rosenstiel M.G. Netea F. Theis S. Mukherjee M. Backes A.C. Aschenbrenner T. Ulas M.M.B. Breteler E.J. Giamarellos-Bourboulis M. Kox M. Becker S. Cheran M.S. Woodacre E.L. Goh J.L. Schultze
November 01, 2021 / Brief Bioinform A comparison of metabolic labeling and statistical methods to infer genome-wide dynamics of RNA turnover E. Boileau J. Altmüller I.S. Naarmann-de Vries C. Dieterich
August 01, 2021 / Hum Genet Biallelic mutations in L-dopachrome tautomerase (DCT) cause infantile nystagmus and oculocutaneous albinism A.E. Volk A. Hedergott M. Preising S. Rading J. Fricke P. Herkenrath P. Nürnberg J. Altmüller S. von Ameln B. Lorenz A. Neugebauer M. Karsak C. Kubisch
December 01, 2021 / Nat Genet Chromothripsis followed by circular recombination drives oncogene amplification in human cancer C. Rosswog C. Bartenhagen A. Welte Y. Kahlert N. Hemstedt W. Lorenz M. Cartolano S. Ackermann S. Perner W. Vogel J. Altmüller P. Nürnberg F. Hertwig G. Göhring E. Lilienweiss A.M. Stütz J.O. Korbel R.K. Thomas M. Peifer M. Fischer
October 01, 2021 / Neurogenetics ANK3 related neurodevelopmental disorders: expanding the spectrum of heterozygous loss-of-function variants K. Kloth B. Lozic J. Tagoe M.J.V. Hoffer A. Van der Ven H. Thiele J. Altmüller C. Kubisch P.Y.B. Au J. Denecke E.K. Bijlsma D. Lessel
November 01, 2021 / Genet Med Biallelic variants in PCDHGC4 cause a novel neurodevelopmental syndrome with progressive microcephaly, seizures, and joint anomalies M. Iqbal R. Maroofian B. Çavdarlı F. Riccardi M. Field S. Banka D.K. Bubshait Y. Li J. Hertecant S.M. Baig D. Dyment S. Efthymiou U. Abdullah E.U.H. Makhdoom Z. Ali T Scherf de Almeida F. Molinari C. Mignon-Ravix B. Chabrol J. Antony L. Ades A.T. Pagnamenta A. Jackson S. Douzgou C. Beetz V. Karageorgou B. Vona A. Rad J.M. Baig T. Sultan J.R. Alvi S. Maqbool F. Rahman M.B. Toosi F. Ashrafzadeh S. Imannezhad E.G. Karimiani Y. Sarwar S. Khan M. Jameel A.A. Noegel B. Budde J. Altmüller S. Motameny W. Höhne H. Houlden P. Nürnberg B. Wollnik L. Villard F.S. Alkuraya M. Osmond M.S. Hussain G. Yigit
July 01, 2021 / Nat Cell Biol Niche stiffening compromises hair follicle stem cell potential during ageing by reducing bivalent promoter accessibility J. Koester Y.A. Miroshnikova S. Ghatak C.A. Chacón-Martínez J. Morgner X. Li I. Atanassov J. Altmüller D.E. Birk M. Koch W. Bloch M. Bartusel C.M. Niessen A. Rada-Iglesias S.A. Wickström