Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Chen, Wei Prof. Dr. (1) Chu, Van Trung Dr. (4) Fischer, Cornelius Dr. (2) Gerhardt, Holger Prof. Dr. (1) Graf, Robin Dr. (3) Harabula, Izabela-Cezara (1) Kabrani, Eleni Dr. (1) Kempa, Stefan Dr. (1) Kühn, Ralf Dr. (3) Lupianez Garcia, Dario Jesus Dr. (1) Rajewsky, Klaus Prof. Dr. (20) (-) Altmueller, Janine Dr.med. (60) (-) Janz, Martin Dr. (2) (-) Potente, Michael Prof. Dr. (1) (-) Quedenau, Claudia (1) 2002 (1) 2005 (2) (-) 2012 (1) 2014 (8) 2015 (25) (-) 2016 (32) (-) 2017 (32) 2018 (39) 2019 (33) 2020 (27) 2021 (47) 2022 (38) 2023 (21) 2024 (2) Angiogenesis & Metabolism Laboratory (8) Bioinformatics and Omics Data Science (1) Biology of Malignant Lymphomas (6) Cardiac MRI (2) Cellular Neurosciences (4) Computational Regulatory Genomics (2) Epigenetic Regulation and Chromatin Architecture (1) Experimental Ultrahigh-Field MR (9) Genetics and Genomics of Cardiovascular Diseases (3) Genome Engineering & Disease Models (1) (-) Genomics (61) (-) Immune Regulation and Cancer (4) Integrative Vascular Biology (1) Magnetic Resonance (9) Mobile DNA (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) Proteome Dynamics (2) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (1) RNA Biology and Posttranscriptional Regulation (8) Systems Biology of Gene Regulatory Elements (2) Transgenics (1) 65 Results: Active Filter: Altmueller, Janine Dr.med.Janz, Martin Dr.Potente, Michael Prof. Dr.Quedenau, ClaudiaGenomicsImmune Regulation and Cancer201220162017 Sort: Result score Newest to oldest Oldest to newest December 19, 2017 / Cold Spring Harb Mol Case Stud Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia S. Alawbathani A. Kawalia M. Karakaya J. Altmüller P. Nürnberg S. Cirak July 01, 2017 / Clin Genet Genetic heterogeneity in Pakistani microcephaly families revisited I. Ahmad S.M. Baig A.R. Abdulkareem M.S. Hussain I. Sur M.R. Toliat G. Nürnberg N. Dalibor A. Moawia S.S. Waseem M. Asif H. Nagra M. Sher M.M.A. Khan I. Hassan S.U. Rehman H. Thiele J. Altmüller A.A. Noegel P. Nürnberg June 01, 2017 / Immunogenetics Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing J. Altmüller B. Haenisch A. Kawalia M. Menzen M.M. Nöthen H. Fier G.J. Molderings December 01, 2017 / Nat Med A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle M. Awazawa P. Gabel E. Tsaousidou H. Nolte M. Krüger J. Schmitz P.J. Ackermann C. Brandt J. Altmüller S. Motameny F.T. Wunderlich J.W. Kornfeld M. Blüher J.C. Brüning July 01, 2017 / Hum Genet Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability N.C. Bramswig H.J. Lüdecke F.F. Hamdan J. Altmüller F. Beleggia N.H. Elcioglu C. Freyer E.H. Gerkes Y.K. Demirkol K.G. Knupp A. Kuechler Y. Li D.H. Lowenstein J.L. Michaud K. Park A.P.A. Stegmann H.E. Veenstra-Knol T. Wieland B. Wollnik H. Engels T.M. Strom T. Kleefstra D. Wieczorek September 26, 2017 / Mol Ecol Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin S. Dennenmoser F.J. Sedlazeck E. Iwaszkiewicz X.Y. Li J. Altmüller A.W. Nolte November 02, 2017 / Am J Hum Genet De novo mutations in SLC25A24 cause a craniosynostosis syndrome with hypertrichosis, progeroid appearance, and mitochondrial dysfunction N. Ehmke L. Graul-Neumann L. Smorag R. Koenig L. Segebrecht P. Magoulas F. Scaglia E. Kilic A.F. Hennig N. Adolphs N. Saha B. Fauler V.M. Kalscheuer F. Hennig J. Altmüller C. Netzer H. Thiele P. Nürnberg G. Yigit M. Jäger J. Hecht U. Krüger T. Mielke P.M. Krawitz D. Horn M. Schuelke S. Mundlos C.A. Bacino P.E. Bonnen B. Wollnik B. Fischer-Zirnsak U. Kornak October 15, 2017 / Hum Mol Genet A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction W. Fazeli P. Herkenrath B. Stiller A. Neugebauer J. Fricke R. Lang-Roth G. Nürnberg M. Thoenes J. Becker J. Altmüller A.E. Volk C. Kubisch R. Heller December 01, 2017 / Heredity Parallel habitat acclimatization is realized by the expression of different genes in two closely related salamander species (genus Salamandra) D.J. Goedbloed T. Czypionka J. Altmüller A. Rodriguez E. Küpfer O. Segev L. Blaustein A.R. Templeton A.W. Nolte S. Steinfartz October 01, 2017 / JAMA Oncol Germline mutation status, pathological complete response, and disease-free survival in triple-negative breast cancer: secondary analysis of the GeparSixto randomized clinical trial E. Hahnen B. Lederer J. Hauke S. Loibl S. Kröber A. Schneeweiss C. Denkert P.A. Fasching J.U. Blohmer C. Jackisch S. Paepke B. Gerber S. Kümmel C. Schem G. Neidhardt J. Huober K. Rhiem S. Costa J. Altmüller C. Hanusch H. Thiele V. Müller P. Nürnberg T. Karn V. Nekljudova M. Untch G. von Minckwitz R.K. Schmutzler Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
December 19, 2017 / Cold Spring Harb Mol Case Stud Late diagnosis of a truncating WISP3 mutation entails a severe phenotype of progressive pseudorheumatoid dysplasia S. Alawbathani A. Kawalia M. Karakaya J. Altmüller P. Nürnberg S. Cirak
July 01, 2017 / Clin Genet Genetic heterogeneity in Pakistani microcephaly families revisited I. Ahmad S.M. Baig A.R. Abdulkareem M.S. Hussain I. Sur M.R. Toliat G. Nürnberg N. Dalibor A. Moawia S.S. Waseem M. Asif H. Nagra M. Sher M.M.A. Khan I. Hassan S.U. Rehman H. Thiele J. Altmüller A.A. Noegel P. Nürnberg
June 01, 2017 / Immunogenetics Mutational profiling in the peripheral blood leukocytes of patients with systemic mast cell activation syndrome using next-generation sequencing J. Altmüller B. Haenisch A. Kawalia M. Menzen M.M. Nöthen H. Fier G.J. Molderings
December 01, 2017 / Nat Med A microRNA screen reveals that elevated hepatic ectodysplasin A expression contributes to obesity-induced insulin resistance in skeletal muscle M. Awazawa P. Gabel E. Tsaousidou H. Nolte M. Krüger J. Schmitz P.J. Ackermann C. Brandt J. Altmüller S. Motameny F.T. Wunderlich J.W. Kornfeld M. Blüher J.C. Brüning
July 01, 2017 / Hum Genet Heterozygous HNRNPU variants cause early onset epilepsy and severe intellectual disability N.C. Bramswig H.J. Lüdecke F.F. Hamdan J. Altmüller F. Beleggia N.H. Elcioglu C. Freyer E.H. Gerkes Y.K. Demirkol K.G. Knupp A. Kuechler Y. Li D.H. Lowenstein J.L. Michaud K. Park A.P.A. Stegmann H.E. Veenstra-Knol T. Wieland B. Wollnik H. Engels T.M. Strom T. Kleefstra D. Wieczorek
September 26, 2017 / Mol Ecol Copy number increases of transposable elements and protein-coding genes in an invasive fish of hybrid origin S. Dennenmoser F.J. Sedlazeck E. Iwaszkiewicz X.Y. Li J. Altmüller A.W. Nolte
November 02, 2017 / Am J Hum Genet De novo mutations in SLC25A24 cause a craniosynostosis syndrome with hypertrichosis, progeroid appearance, and mitochondrial dysfunction N. Ehmke L. Graul-Neumann L. Smorag R. Koenig L. Segebrecht P. Magoulas F. Scaglia E. Kilic A.F. Hennig N. Adolphs N. Saha B. Fauler V.M. Kalscheuer F. Hennig J. Altmüller C. Netzer H. Thiele P. Nürnberg G. Yigit M. Jäger J. Hecht U. Krüger T. Mielke P.M. Krawitz D. Horn M. Schuelke S. Mundlos C.A. Bacino P.E. Bonnen B. Wollnik B. Fischer-Zirnsak U. Kornak
October 15, 2017 / Hum Mol Genet A TUBB6 mutation is associated with autosomal dominant non-progressive congenital facial palsy, bilateral ptosis and velopharyngeal dysfunction W. Fazeli P. Herkenrath B. Stiller A. Neugebauer J. Fricke R. Lang-Roth G. Nürnberg M. Thoenes J. Becker J. Altmüller A.E. Volk C. Kubisch R. Heller
December 01, 2017 / Heredity Parallel habitat acclimatization is realized by the expression of different genes in two closely related salamander species (genus Salamandra) D.J. Goedbloed T. Czypionka J. Altmüller A. Rodriguez E. Küpfer O. Segev L. Blaustein A.R. Templeton A.W. Nolte S. Steinfartz
October 01, 2017 / JAMA Oncol Germline mutation status, pathological complete response, and disease-free survival in triple-negative breast cancer: secondary analysis of the GeparSixto randomized clinical trial E. Hahnen B. Lederer J. Hauke S. Loibl S. Kröber A. Schneeweiss C. Denkert P.A. Fasching J.U. Blohmer C. Jackisch S. Paepke B. Gerber S. Kümmel C. Schem G. Neidhardt J. Huober K. Rhiem S. Costa J. Altmüller C. Hanusch H. Thiele V. Müller P. Nürnberg T. Karn V. Nekljudova M. Untch G. von Minckwitz R.K. Schmutzler