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) Sunaga-Franze, Daniele Yumi Dr. (9) 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) (-) Wyler, Emanuel Dr. (2) 2002 (1) 2005 (2) 2014 (7) 2015 (24) 2016 (29) 2017 (31) 2018 (39) 2019 (30) 2020 (24) 2021 (46) 2022 (36) 2023 (18) 2024 (2) Advanced Light Microscopy (1) Animal Phenotyping (1) Bioinformatics and Omics Data Science (17) Biomedical Image Analysis (1) Cancer Genetics and Cellular Stress Responses (2) Cardiac MRI (4) Cellular Neurosciences (17) Computational methodologies and omic analytics (1) Computational Regulatory Genomics (139) Developmental Biology / Signal Transduction (6) 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 (289) 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 Genetics of Chronic Inflammation and Allergic Disease (2) Myology (1) Non-coding RNAs and Mechanisms of Cytoplasmic Gene Regulation (2) Organoids (1) Out-patient Clinic for Neuroimmunology (1) Out-patient Clinic for Pediatric Allergology and Atopic Dermatitis (2) Pancreatic Organoid Research and Disease Modeling (1) Pluripotent Stem Cells (4) Protein Production and Characterization (1) Proteome Dynamics (13) Proteomics (7) Proteomics and Metabolomics (3) Proteomics and Molecular Mechanisms of Neurodegenerative Diseases (3) Psychoneuroimmunology (4) Quantitative Developmental Biology (3) RNA Biology and Posttranscriptional Regulation (62) Systems Biology Imaging (2) Systems Biology of Gene Regulatory Elements (14) Transgenics (15) Translational Bioinformatics (12) Translational Cardiology and Functional Genomics (2) 289 Results: Active Filter: Altmueller, Janine Dr.med.Harabula, Izabela-CezaraLupianez Garcia, Dario Jesus Dr.Semtner, Marcus Dr.Wyler, Emanuel Dr.Genomics Sort: Result score Newest to oldest Oldest to newest 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 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 January 01, 2018 / Nat Genet Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks F. Demenais P. Margaritte-Jeannin K.C. Barnes W.O.C. Cookson J. Altmüller W. Ang R.G. Barr T.H. Beaty A.B. Becker J. Beilby H. Bisgaard U.S. Bjornsdottir E. Bleecker K. Bonnelykke D.I. Boomsma E. Bouzigon C.E. Brightling M. Brossard G.G. Brusselle E. Burchard K.M. Burkart A. Bush M. Chan-Yeung K.F. Chung A. Couto Alves J.A. Curtin A. Custovic D. Daley J.C. de Jongste B.E. Del-Rio-Navarro K.M. Donohue L. Duijts C. Eng J.G. Eriksson M. Farrall Y. Fedorova B. Feenstra M.A. Ferreira M.B. Freidin Z. Gajdos J. Gauderman U. Gehring F. Geller J. Genuneit S.A Gharib F. Gilliland R. Granell P.E. Graves D.F. Gudbjartsson T. Haahtela S.R. Heckbert D. Heederik J. Heinrich M. Helioevaara J. Henderson B.E. Himes H. Hirose J.N. Hirschhorn A. Hofman P. Holt J. Hottenga T.J. Hudson J. Hui M. Imboden V. Ivanov V.W.V. Jaddoe A. James C. Janson M.R. Jarvelin D. Jarvis G. Jones I. Jonsdottir P. Jousilahti M. Kabesch M. Kähönen D.B. Kantor A.S. Karunas E. Khusnutdinova G.H. Koppelman A.L. Kozyrskyj E. Kreiner M. Kubo R. Kumar A. Kumar M. Kuokkanen L. Lahousse T. Laitinen C. Laprise M. Lathrop S. Lau Y.A. Lee T. Lehtimaeki S. Letort A.M. Levin G. Li L. Liang L.R. Loehr S.J. London D.W. Loth A. Manichaikul I. Marenholz F.J. Martinez M.C. Matheson R.A. Mathias K. Matsumoto H. Mbarek W.L. McArdle M. Melbye E. Melen D. Meyers S. Michel H. Mohamdi A.W. Musk R.A. Myers M.A.E. Nieuwenhuis E. Noguchi G.T. O'Connor L.M. Ogorodova C.D. Palmer A. Palotie J.E. Park C.E. Pennell G. Pershagen A. Polonikov D.S. Postma N. Probst-Hensch V.P. Puzyrev B.A. Raby O.T. Raitakari A. Ramasamy S.S. Rich C.F. Robertson I. Romieu M.T. Salam V. Salomaa V. Schluenssen R. Scott P.A. Selivanova T. Sigsgaard A. Simpson V. Siroux L.J. Smith M. Solodilova M. Standl K. Stefansson D.P. Strachan B.H. Stricker A. Takahashi P.J. Thompson G. Thorleifsson U. Thorsteinsdottir C.M.T. Tiesler D.G. Torgerson T. Tsunoda A.G. Uitterlinden R.J.P. van der Valk A. Vaysse S. Vedantam A. von Berg E. von Mutius J.M. Vonk J. Waage N.J. Wareham S.T. Weiss W.B. White M. Wickman E. Widén G. Willemsen L.K. Williams I.M. Wouters J.J. Yang J.H. Zhao M.F. Moffatt C. Ober D.L. Nicolae October 01, 2021 / Genes A homozygous AKNA frameshift variant is associated with microcephaly in a Pakistani family S.S. Waseem A. Moawia B. Budde M. Tariq A. Khan Z. Ali S. Khan M. Iqbal N.A. Malik S.U. Haque J. Altmüller H. Thiele M.S. Hussain S. Cirak S.M. Baig P. Nürnberg February 01, 2022 / Eur J Hum Genet Familial cleft tongue caused by a unique translation initiation codon variant in TP63 J. Schmidt G. Schreiber J. Altmüller H. Thiele P. Nürnberg Y. Li S. Kaulfuß R. Funke B. Wilken G. Yigit B. Wollnik April 01, 2022 / J Am Soc Nephrol Claudin-10a deficiency shifts proximal tubular Cl(-) permeability to cation selectivity via claudin-2 redistribution T. Breiderhoff N. Himmerkus L. Meoli A. Fromm S. Sewerin N. Kriuchkova O. Nagel Y. Ladilov S. Krug C. Quintanova M. Stumpp D. Garbe-Schönberg U. Westernströer C. Merkel M. Brinkhus J. Altmüller M. Schweiger D. Mueller K. Mutig M. Morawski J. Halbritter S. Milatz M. Bleich D. Günzel October 08, 2021 / Med In-depth cell-free DNA sequencing reveals genomic landscape of Hodgkin’s lymphoma and facilitates ultrasensitive residual disease detection S. Sobesky L. Mammadova M. Cirillo E.E.E. Drees J. Mattlener H. Dörr J. Altmüller Z. Shi P.J. Bröckelmann J. Weiss S. Kreissl S. Sasse R.T. Ullrich S. Reinke W. Klapper E. Gerhard-Hartmann A. Rosenwald M.G.M. Roemer P. Nürnberg A. Hagenbeek J.M. Zijlstra D.M. Pegtel A. Engert P. Borchmann B. von Tresckow S. Borchmann March 01, 2022 / Hum Mutat Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex development H.L. Marko N.C. Hornig R.C. Betz P.M. Holterhus J. Altmüller H. Thiele M. Fabiano H.U. Schweikert D. Braun U. Schweizer Pagination Current page 1 Page 2 Page 3 Page 4 … Next page Next › Last page Last »
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 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
January 01, 2018 / Nat Genet Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks F. Demenais P. Margaritte-Jeannin K.C. Barnes W.O.C. Cookson J. Altmüller W. Ang R.G. Barr T.H. Beaty A.B. Becker J. Beilby H. Bisgaard U.S. Bjornsdottir E. Bleecker K. Bonnelykke D.I. Boomsma E. Bouzigon C.E. Brightling M. Brossard G.G. Brusselle E. Burchard K.M. Burkart A. Bush M. Chan-Yeung K.F. Chung A. Couto Alves J.A. Curtin A. Custovic D. Daley J.C. de Jongste B.E. Del-Rio-Navarro K.M. Donohue L. Duijts C. Eng J.G. Eriksson M. Farrall Y. Fedorova B. Feenstra M.A. Ferreira M.B. Freidin Z. Gajdos J. Gauderman U. Gehring F. Geller J. Genuneit S.A Gharib F. Gilliland R. Granell P.E. Graves D.F. Gudbjartsson T. Haahtela S.R. Heckbert D. Heederik J. Heinrich M. Helioevaara J. Henderson B.E. Himes H. Hirose J.N. Hirschhorn A. Hofman P. Holt J. Hottenga T.J. Hudson J. Hui M. Imboden V. Ivanov V.W.V. Jaddoe A. James C. Janson M.R. Jarvelin D. Jarvis G. Jones I. Jonsdottir P. Jousilahti M. Kabesch M. Kähönen D.B. Kantor A.S. Karunas E. Khusnutdinova G.H. Koppelman A.L. Kozyrskyj E. Kreiner M. Kubo R. Kumar A. Kumar M. Kuokkanen L. Lahousse T. Laitinen C. Laprise M. Lathrop S. Lau Y.A. Lee T. Lehtimaeki S. Letort A.M. Levin G. Li L. Liang L.R. Loehr S.J. London D.W. Loth A. Manichaikul I. Marenholz F.J. Martinez M.C. Matheson R.A. Mathias K. Matsumoto H. Mbarek W.L. McArdle M. Melbye E. Melen D. Meyers S. Michel H. Mohamdi A.W. Musk R.A. Myers M.A.E. Nieuwenhuis E. Noguchi G.T. O'Connor L.M. Ogorodova C.D. Palmer A. Palotie J.E. Park C.E. Pennell G. Pershagen A. Polonikov D.S. Postma N. Probst-Hensch V.P. Puzyrev B.A. Raby O.T. Raitakari A. Ramasamy S.S. Rich C.F. Robertson I. Romieu M.T. Salam V. Salomaa V. Schluenssen R. Scott P.A. Selivanova T. Sigsgaard A. Simpson V. Siroux L.J. Smith M. Solodilova M. Standl K. Stefansson D.P. Strachan B.H. Stricker A. Takahashi P.J. Thompson G. Thorleifsson U. Thorsteinsdottir C.M.T. Tiesler D.G. Torgerson T. Tsunoda A.G. Uitterlinden R.J.P. van der Valk A. Vaysse S. Vedantam A. von Berg E. von Mutius J.M. Vonk J. Waage N.J. Wareham S.T. Weiss W.B. White M. Wickman E. Widén G. Willemsen L.K. Williams I.M. Wouters J.J. Yang J.H. Zhao M.F. Moffatt C. Ober D.L. Nicolae
October 01, 2021 / Genes A homozygous AKNA frameshift variant is associated with microcephaly in a Pakistani family S.S. Waseem A. Moawia B. Budde M. Tariq A. Khan Z. Ali S. Khan M. Iqbal N.A. Malik S.U. Haque J. Altmüller H. Thiele M.S. Hussain S. Cirak S.M. Baig P. Nürnberg
February 01, 2022 / Eur J Hum Genet Familial cleft tongue caused by a unique translation initiation codon variant in TP63 J. Schmidt G. Schreiber J. Altmüller H. Thiele P. Nürnberg Y. Li S. Kaulfuß R. Funke B. Wilken G. Yigit B. Wollnik
April 01, 2022 / J Am Soc Nephrol Claudin-10a deficiency shifts proximal tubular Cl(-) permeability to cation selectivity via claudin-2 redistribution T. Breiderhoff N. Himmerkus L. Meoli A. Fromm S. Sewerin N. Kriuchkova O. Nagel Y. Ladilov S. Krug C. Quintanova M. Stumpp D. Garbe-Schönberg U. Westernströer C. Merkel M. Brinkhus J. Altmüller M. Schweiger D. Mueller K. Mutig M. Morawski J. Halbritter S. Milatz M. Bleich D. Günzel
October 08, 2021 / Med In-depth cell-free DNA sequencing reveals genomic landscape of Hodgkin’s lymphoma and facilitates ultrasensitive residual disease detection S. Sobesky L. Mammadova M. Cirillo E.E.E. Drees J. Mattlener H. Dörr J. Altmüller Z. Shi P.J. Bröckelmann J. Weiss S. Kreissl S. Sasse R.T. Ullrich S. Reinke W. Klapper E. Gerhard-Hartmann A. Rosenwald M.G.M. Roemer P. Nürnberg A. Hagenbeek J.M. Zijlstra D.M. Pegtel A. Engert P. Borchmann B. von Tresckow S. Borchmann
March 01, 2022 / Hum Mutat Genomic variants reducing expression of two endocytic receptors in 46,XY differences of sex development H.L. Marko N.C. Hornig R.C. Betz P.M. Holterhus J. Altmüller H. Thiele M. Fabiano H.U. Schweikert D. Braun U. Schweizer