Scientific Publications Search Search Author Impact Factor Release Date Research Group Search Sort by RelevanceFrom A-ZAuthored onDate/Time RangeRelease date Order AscDesc Akalin, Altuna Dr. (1) Bader, Michael Prof. Dr. (2) Badillo Lisakowski, Victor Christian Dr. (1) Bähring, Sylvia Dr. (2) Barke, Niclas (1) Bartels-Klein, Eireen (1) Bartolomaeus, Theda (2) Beule, Dieter Dr. (5) Birchmeier, Walter Prof. Dr. (1) Birchmeier-Kohler, Carmen Prof. Dr. (1) Blume, Alexander Dr. (1) Blüthgen, Nils (1) Borodina, Tatiana Dr. (8) Braeuning, Caroline (5) Chen, Wei Prof. Dr. (2) Conrad, Thomas Dr. (15) Dechend, Ralf Priv. Doz. (1) Deter, Aylina (1) Diecke, Sebastian Dr. (4) Escobar Fernandez, Helena Dr. (1) Faxel, Miriam (1) Fischer, Cornelius Dr. (16) Forslund, Sofia Dr. (2) Franke, Vedran Dr. (1) Freimuth, Jonas (1) Geisberger, Sabrina Yasmin Dr. (1) Gerhardt, Holger Prof. Dr. (8) Gotthardt, Michael Prof. Dr. (1) Gouti, Mina Dr. (1) Haas, Simon Dr. rer. nat. (1) Hartl, Kimberly (1) Henssen, Anton Prof. Dr. med. (2) Herse, Florian PD Dr. (1) Heuser, Arnd Dr. (2) Hinze, Christian Dr. med. Dipl.-Math. (1) Hollfinger, Irene (1) Höpken, Uta Elisabeth PD Dr. (1) Hübner, Norbert Prof. Dr. (1) Junker, Jan Philipp Prof. Dr. (1) Kabuss, Loreen-Claudine (1) Kalnytska, Oleksandra (1) Kettenmann, Helmut Prof. Dr. (1) Klaus-Bergmann, Alexandra Dr. (1) Klußmann, Enno PD Dr. (2) Kocks, Christine Dr. (1) Kühn, Ralf Dr. (1) Kunz, Severine Dr. (2) Landthaler, Markus Prof. Dr. (2) Langanki, Reika (2) Lee, Young-Ae Prof. Dr. (2) Leutz, Achim Prof. Dr. (1) Liu, Tiannan (1) Marenholz, Ingo Dr. (1) Marko, Lajos Dr. (2) Müller, Dominik Prof. Dr. (1) Müller, Marion (1) Müllerke, Stefanie (1) Na, Il-Kang Dr. (1) Napieczynska, Hanna Dr. (1) Neuschulz, Anika (1) Obermayer-Wasserscheid, Benedikt Dr. (4) Olivares Chauvet, Pedro Dr. (1) Paul, Friedemann Prof. Dr. med. (1) Plumbom, Izabela (1) Popova, Elena Dr. (1) Potente, Michael Prof. Dr. (58) Qadri, Fatimunnisa Dr. (2) Quedenau, Claudia (7) Rajewsky, Klaus Prof. Dr. (1) Rajewsky, Nikolaus Prof. Dr. (3) Sai, Somesh (1) Schmidt-Krüger, Vanessa Dr. (1) Schmitt, Clemens Prof. Dr. (1) Schwarz, Roland Dr. (1) Secener, Ali Kerim (1) Sholokh, Anastasiia (2) Siffrin, Volker (1) Sigal, Michael Dr. (2) Spuler, Simone Prof. (2) Taube, Martin (1) Teixeira Alves, Luiz Gustavo Dr. (1) Uyar, Bora Dr. (1) Wendlinger, Sarah (1) Willnow, Thomas Prof. Dr. (1) Woehler, Andrew Dr. (1) Wurmus, Ricardo (1) Zimmermann, Karin Dr. (1) Zühlke, Kerstin Dr. (1) (-) Altmueller, Janine Dr.med. (289) (-) Harabula, Izabela-Cezara (2) (-) Lupianez Garcia, Dario Jesus Dr. (1) (-) Semtner, Marcus Dr. (1) (-) Sunaga-Franze, Daniele Yumi Dr. (9) (-) Wyler, Emanuel Dr. (2) 2002 (1) 2005 (2) 2014 (7) 2015 (24) 2016 (29) 2017 (31) 2018 (39) 2019 (31) 2020 (27) 2021 (47) 2022 (38) 2023 (19) 2024 (3) Advanced Light Microscopy (1) AG Müller/Dechend (ECRC) (1) Anchored Signalling (2) Animal Phenotyping (3) Bioinformatics and Omics Data Science (8) Biomedical Image Analysis (1) Cancer Genetics and Cellular Stress Responses (2) Cardiac MRI (4) Cellular Neurosciences (17) Clinical Research Unit (2) Computational methodologies and omic analytics (1) Computational Regulatory Genomics (6) Developmental Biology / Signal Transduction (5) Developmental Neurobiology (1) Epigenetic Regulation and Chromatin Architecture (7) Experimental Ultrahigh-Field MR (20) Genetics and Genomics of Cardiovascular Diseases (9) Genetics of Metabolic and Reproductive Disorders (19) Genome Diversification & Integrity (1) Genome Engineering & Disease Models (15) (-) Genomics (298) Host-microbiome factors in cardiovascular disease (2) Hypertension-caused End-Organ Damage (1) Hypertension-Mediated End-Organ Damage (1) Immune Mechanisms and Human Antibodies (3) Immune Regulation and Cancer (23) Magnetic Resonance (20) Mathematical Modelling of Cellular Processes (1) Microenvironmental Regulation in Autoimmunity and Cancer (1) Mobile DNA (1) Molecular Biology of Peptide Hormones (2) Molecular Cardiovascular Research (1) Molecular Genetics of Chronic Inflammation and Allergic Disease (2) Myology (2) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (1) Organoids (1) Out-patient Clinic for Neuroimmunology (1) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (2) Pluripotent Stem Cells (6) Protein Production and Characterization (1) Proteome Dynamics (8) Proteomics (8) Proteomics and Metabolomics (3) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (3) Psychoneuroimmunology (4) Quantitative Developmental Biology (1) RNA Biology and Posttranscriptional Regulation (55) Systems Biology Imaging (1) Systems Biology of Gene Regulatory Elements (11) Transgenics (15) Translational Bioinformatics (11) 298 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Semtner, Marcus Dr.Sunaga-Franze, Daniele Yumi Dr.Wyler, Emanuel Dr.Genomics Sort: Result score Newest to oldest Oldest to newest June 04, 2020 / Nutrition Intestinal expression of TLR gene changes early after gastric bypass and association with type 2 diabetes remission P. Sala R.S.M.M. Torrinhas D.C. Fonseca N.M. Machado J. Singer P. Singer G.R. Ravacci G. Belarmino B.A.M. Ferreira M. Marques R. K. Ishida I.F.M.S. Guarda E.G.H. de Moura P. Sakai M.A. Santo D.Y. Sunaga S.B. Heymsfield D.P.S. Bezerra M.L. Corrêa-Giannella D.L. Waitzberg January 05, 2005 / BMC Pulm Med Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families J. Altmüller C. Seidel Y.A. Lee S. Loesgen D. Bulle F. Friedrichs H. Jellouschek J. Kelber A. Keller A. Schuster M. Silbermann W. Wahlen P. Wolff F. Rueschendorf G. Schlenvoigt P. Nuernberg M. Wjst January 01, 2005 / Allergy A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3 T. Kurz J. Altmueller K. Strauch F. Rueschendorf A. Heinzmann M.F. Moffatt W.O.C.M. Cookson F. Inacio P. Nuernberg H.H. Stassen K.A. Deichmann 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 February 05, 2024 / Eur J Hum Genet Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy M. Koko M.A. Elseed I.N. Mohammed A.A. Hamed A.S.I. Abd Allah A. Yahia R.A. Siddig J. Altmüller M.R. Toliat E.O. Elmahdi M. Amin E. A. Ahmed I.Z.M. Eltazi F.A. Elmugadam W.A. Abdelgadir E. Eltaraifee M.O.M. Ibrahim N.M.H. Ali H.M. Malik A.M. Babai Y.H. Bakhit P. Nürnberg M.E. Ibrahim M.A. Salih J. Schubert L.E.O. Elsayed H. Lerche February 19, 2024 / Front Genet The role of microRNAs in defining LSECs cellular identity and in regulating F8 gene expression M. A. Jamil R. Al-Rifai N. Nuesgen J. Altmüller J. Oldenburg O. El-Maarri 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 February 01, 2016 / Genome Res Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice M. Spielmann N. Kakar N. Tayebi C. Leettola G. Nürnberg N. Sowada D.G. Lupiáñez I. Harabula R. Flöttmann D. Horn W.L. Chan L. Wittler R. Yilmaz J. Altmüller H. Thiele H. van Bokhoven C.E. Schwartz P. Nürnberg J.U. Bowie J. Ahmad C. Kubisch S. Mundlos G. Borck February 01, 2022 / Am J Med Genet A Genomic basis of syndromic short stature in an Algerian patient cohort S. Moosa F. Chentli J. Altmüller N. Bögershausen P. Nürnberg G. Yigit Y. Li B. Wollnik Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
June 04, 2020 / Nutrition Intestinal expression of TLR gene changes early after gastric bypass and association with type 2 diabetes remission P. Sala R.S.M.M. Torrinhas D.C. Fonseca N.M. Machado J. Singer P. Singer G.R. Ravacci G. Belarmino B.A.M. Ferreira M. Marques R. K. Ishida I.F.M.S. Guarda E.G.H. de Moura P. Sakai M.A. Santo D.Y. Sunaga S.B. Heymsfield D.P.S. Bezerra M.L. Corrêa-Giannella D.L. Waitzberg
January 05, 2005 / BMC Pulm Med Phenotypic and genetic heterogeneity in a genome-wide linkage study of asthma families J. Altmüller C. Seidel Y.A. Lee S. Loesgen D. Bulle F. Friedrichs H. Jellouschek J. Kelber A. Keller A. Schuster M. Silbermann W. Wahlen P. Wolff F. Rueschendorf G. Schlenvoigt P. Nuernberg M. Wjst
January 01, 2005 / Allergy A genome-wide screen on the genetics of atopy in a multiethnic European population reveals a major atopy locus on chromosome 3q21.3 T. Kurz J. Altmueller K. Strauch F. Rueschendorf A. Heinzmann M.F. Moffatt W.O.C.M. Cookson F. Inacio P. Nuernberg H.H. Stassen K.A. Deichmann
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
February 05, 2024 / Eur J Hum Genet Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy M. Koko M.A. Elseed I.N. Mohammed A.A. Hamed A.S.I. Abd Allah A. Yahia R.A. Siddig J. Altmüller M.R. Toliat E.O. Elmahdi M. Amin E. A. Ahmed I.Z.M. Eltazi F.A. Elmugadam W.A. Abdelgadir E. Eltaraifee M.O.M. Ibrahim N.M.H. Ali H.M. Malik A.M. Babai Y.H. Bakhit P. Nürnberg M.E. Ibrahim M.A. Salih J. Schubert L.E.O. Elsayed H. Lerche
February 19, 2024 / Front Genet The role of microRNAs in defining LSECs cellular identity and in regulating F8 gene expression M. A. Jamil R. Al-Rifai N. Nuesgen J. Altmüller J. Oldenburg O. El-Maarri
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
February 01, 2016 / Genome Res Exome sequencing and CRISPR/Cas genome editing identify mutations of ZAK as a cause of limb defects in humans and mice M. Spielmann N. Kakar N. Tayebi C. Leettola G. Nürnberg N. Sowada D.G. Lupiáñez I. Harabula R. Flöttmann D. Horn W.L. Chan L. Wittler R. Yilmaz J. Altmüller H. Thiele H. van Bokhoven C.E. Schwartz P. Nürnberg J.U. Bowie J. Ahmad C. Kubisch S. Mundlos G. Borck
February 01, 2022 / Am J Med Genet A Genomic basis of syndromic short stature in an Algerian patient cohort S. Moosa F. Chentli J. Altmüller N. Bögershausen P. Nürnberg G. Yigit Y. Li B. Wollnik