© Pixabay Hübner Lab Genetics and Genomics of Cardiovascular Diseases Profile Team Research Publications News Profile Team Research Publications News Profile Team Group Leader Prof. Dr. Norbert Hübner 87: Timoféeff-Ressovsky-Haus Room: 0.09 nhuebner@mdc-berlin.de +49 30 9406-2530 Scientist Dr. Eleonora Adami Eleonora.Adami@mdc-berlin.de Dr. med. Alena Laschtowitz 87: Timoféeff-Ressovsky-Haus Room: 0.13 Dr. Ning Liang 87: Timoféeff-Ressovsky-Haus Room: 0.10 Ning.Liang@mdc-berlin.de +49 30 9406-4384 Natalia López Anguita 87: Timoféeff-Ressovsky-Haus Room: 0.13 Natalia.LopezAnguita@mdc-berlin.de Dr. Henrike Maatz 87: Timoféeff-Ressovsky-Haus Room: 0.06 h.maatz@mdc-berlin.de +49 30 9406-3037 Dr. Alvaro Perdomo Sabogal Alvaro.Perdomo@mdc-berlin.de Dr. Jorge Ruiz Orera 87: Timoféeff-Ressovsky-Haus Room: 0.17 Jorge.RuizOrera@mdc-berlin.de +49 30 9406-2930 Dr. Kathrin Saar 84: Hermann-von-Helmholtz-Haus Room: 1104 ksaar@mdc-berlin.de +49 30 9406-3534 Secretariat Sabine Meier 87: Timoféeff-Ressovsky-Haus Room: 0.07 Sabine.Meier@mdc-berlin.de +49 30 9406-3512 Technical Assistants Susanne Blachut 87: Timoféeff-Ressovsky-Haus Room: 0.50 s.Blachut@mdc-berlin.de +49 30 9406-3269 Mathias Gerhard 87: Timoféeff-Ressovsky-Haus Room: 0.13 Dr. Giannino Patone 87: Timoféeff-Ressovsky-Haus Room: 0.10 Giannino.Patone@mdc-berlin.de +49 30 9406-3441 Sabine Schmidt 87: Timoféeff-Ressovsky-Haus Room: 0.22 PhD student Nikita Shyam Dewani 87: Timoféeff-Ressovsky-Haus Room: 0.17 Nikita.Dewani@mdc-berlin.de +49 30 9406-3430 Johannes Greiner 87: Timoféeff-Ressovsky-Haus Room: 0.13 Johannes.Greiner@mdc-berlin.de +49 30 9406-2531 Laura Anne Liebig 87: Timoféeff-Ressovsky-Haus Room: 0.13 LauraAnne.Liebig@mdc-berlin.de +49 30 9406-2531 Anna Myronova 87: Timoféeff-Ressovsky-Haus Room: 0.13 Anna.Myronova@mdc-berlin.de +49 30 9406-2531 Nikolay Shvetsov 87: Timoféeff-Ressovsky-Haus Room: 0.13 Nikolay.Shvetsov@mdc-berlin.de +49 30 9406-2531 Research Medical Genomics and Genetics of Cardiovascular and Metabolic Diseases Publications January 01, 2014 / Gut Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α M.A. Brooke H.J. Longhurst V. Plagnol N.S. Kirkby J.A. Mitchell F. Rüschendorf T.D. Warner D.P. Kelsell T.T. MacDonald December 12, 2013 / Cell Rep Quantitative and qualitative proteome characteristics extracted from in-depth integrated genomics and proteomics analysis T.Y. Low S. van Heesch H. van den Toorn P. Giansanti A. Cristobal P. Toonen S. Schaefer N. Hübner B. van Breukelen S. Mohammed E. Cuppen A.J.R. Heck V. Guryev October 01, 2013 / Seizure TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue K. Pernhorst S. Herms P. Hoffmann S. Cichon H. Schulz T. Sander S. Schoch A.J. Becker A. Grote September 03, 2013 / PLoS ONE Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1) A. Pakula J. Schneider J. Janke U. Zacharias H. Schulz N. Hübner A. Mähler A. Spuler S. Spuler P. Carlier M. Boschmann September 01, 2013 / Orthod Fr Defaut primaire d'eruption (DPE) : analyse genetique clinique et moleculaire [Primary failure of eruption (PFE): clinical and molecular genetics analysis] A. Stellzig-Eisenhauer E. Decker P. Meyer-Marcotty C. Rau B.S. Fiebig W. Kress K. Saar F. Rüschendorf N. Hubner T. Grimm E. Witt B.H.F. Weber August 01, 2013 / J Allergy Clin Immunol A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis J. Esparza-Gordillo H. Schaarschmidt L. Liang W. Cookson A. Bauerfeind M.A. Lee-Kirsch K. Nemat J. Henderson L. Paternoster J.L. Harper E. Mangold M.M. Nothen F. Rüschendorf T. Kerscher I. Marenholz A. Matanovic S. Lau T. Keil C.P. Bauer M. Kurek A. Ciechanowicz M. Macek A. Franke M. Kabesch N. Hubner G. Abecasis S. Weidinger M. Moffatt Y.A. Lee August 01, 2013 / Cell Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat S.S. Atanur A.G. Diaz K. Maratou A. Sarkis M. Rotival L. Game M.R. Tschannen P.J. Kaisaki G.W. Otto M.C. John Ma T.M. Keane O. Hummel K. Saar W. Chen V. Guryev K. Gopalakrishnan M.R. Garrett B. Joe L. Citterio G. Bianchi M. McBride A. Dominiczak D.J. Adams T. Serikawa P. Flicek E. Cuppen N. Hubner E. Petretto D. Gauguier A. Kwitek H. Jacob T.J. Aitman July 12, 2013 / PLoS ONE Evaluation of 41 candidate gene variants for obesity in the EPIC-Potsdam cohort by multi-locus stepwise regression S. Knueppel K. Rohde K. Meidtner D. Drogan H.G. Holzhuetter H. Boeing E. Fisher July 11, 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen July 09, 2013 / Proc Natl Acad Sci U S A Interfering with Gal-1-mediated angiogenesis contributes to the pathogenesis of preeclampsia N. Freitag I. Tirado-González G. Barrientos F. Herse V.L.J.L. Thijssen S.M. Weedon-Fekjær H. Schulz G. Wallukat B.F. Klapp T. Nevers S. Sharma A.C. Staff R. Dechend S.M. Blois Pagination First page « First Previous page ‹‹ … Page 18 Current page 19 Page 20 Page 21 … Next page ›› Last page Last » News Pagination First page « First Previous page ‹‹ Page 1 Page 2 Page 3 Page 4 Current page 5 Prof. Dr. Norbert Hübner Group Leader Contact nhuebner@mdc-berlin.de Phone: +49 30 9406-2530 Max-Delbrück-Centrum für Molekulare Medizin (MDC) Robert-Rössle-Straße 10 13125 Berlin, Deutschland Building 87, Room 0.09 Norbert Hübner is a DZHK Principal Investigator Internal affiliations Genes, Cells and Cell‑based Medicine (topic 1) Research Topics Genetics & Genomics Gene Expression Regulation & RNA Biology Cardiovascular Research
Team Group Leader Prof. Dr. Norbert Hübner 87: Timoféeff-Ressovsky-Haus Room: 0.09 nhuebner@mdc-berlin.de +49 30 9406-2530 Scientist Dr. Eleonora Adami Eleonora.Adami@mdc-berlin.de Dr. med. Alena Laschtowitz 87: Timoféeff-Ressovsky-Haus Room: 0.13 Dr. Ning Liang 87: Timoféeff-Ressovsky-Haus Room: 0.10 Ning.Liang@mdc-berlin.de +49 30 9406-4384 Natalia López Anguita 87: Timoféeff-Ressovsky-Haus Room: 0.13 Natalia.LopezAnguita@mdc-berlin.de Dr. Henrike Maatz 87: Timoféeff-Ressovsky-Haus Room: 0.06 h.maatz@mdc-berlin.de +49 30 9406-3037 Dr. Alvaro Perdomo Sabogal Alvaro.Perdomo@mdc-berlin.de Dr. Jorge Ruiz Orera 87: Timoféeff-Ressovsky-Haus Room: 0.17 Jorge.RuizOrera@mdc-berlin.de +49 30 9406-2930 Dr. Kathrin Saar 84: Hermann-von-Helmholtz-Haus Room: 1104 ksaar@mdc-berlin.de +49 30 9406-3534 Secretariat Sabine Meier 87: Timoféeff-Ressovsky-Haus Room: 0.07 Sabine.Meier@mdc-berlin.de +49 30 9406-3512 Technical Assistants Susanne Blachut 87: Timoféeff-Ressovsky-Haus Room: 0.50 s.Blachut@mdc-berlin.de +49 30 9406-3269 Mathias Gerhard 87: Timoféeff-Ressovsky-Haus Room: 0.13 Dr. Giannino Patone 87: Timoféeff-Ressovsky-Haus Room: 0.10 Giannino.Patone@mdc-berlin.de +49 30 9406-3441 Sabine Schmidt 87: Timoféeff-Ressovsky-Haus Room: 0.22 PhD student Nikita Shyam Dewani 87: Timoféeff-Ressovsky-Haus Room: 0.17 Nikita.Dewani@mdc-berlin.de +49 30 9406-3430 Johannes Greiner 87: Timoféeff-Ressovsky-Haus Room: 0.13 Johannes.Greiner@mdc-berlin.de +49 30 9406-2531 Laura Anne Liebig 87: Timoféeff-Ressovsky-Haus Room: 0.13 LauraAnne.Liebig@mdc-berlin.de +49 30 9406-2531 Anna Myronova 87: Timoféeff-Ressovsky-Haus Room: 0.13 Anna.Myronova@mdc-berlin.de +49 30 9406-2531 Nikolay Shvetsov 87: Timoféeff-Ressovsky-Haus Room: 0.13 Nikolay.Shvetsov@mdc-berlin.de +49 30 9406-2531
Publications January 01, 2014 / Gut Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α M.A. Brooke H.J. Longhurst V. Plagnol N.S. Kirkby J.A. Mitchell F. Rüschendorf T.D. Warner D.P. Kelsell T.T. MacDonald December 12, 2013 / Cell Rep Quantitative and qualitative proteome characteristics extracted from in-depth integrated genomics and proteomics analysis T.Y. Low S. van Heesch H. van den Toorn P. Giansanti A. Cristobal P. Toonen S. Schaefer N. Hübner B. van Breukelen S. Mohammed E. Cuppen A.J.R. Heck V. Guryev October 01, 2013 / Seizure TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue K. Pernhorst S. Herms P. Hoffmann S. Cichon H. Schulz T. Sander S. Schoch A.J. Becker A. Grote September 03, 2013 / PLoS ONE Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1) A. Pakula J. Schneider J. Janke U. Zacharias H. Schulz N. Hübner A. Mähler A. Spuler S. Spuler P. Carlier M. Boschmann September 01, 2013 / Orthod Fr Defaut primaire d'eruption (DPE) : analyse genetique clinique et moleculaire [Primary failure of eruption (PFE): clinical and molecular genetics analysis] A. Stellzig-Eisenhauer E. Decker P. Meyer-Marcotty C. Rau B.S. Fiebig W. Kress K. Saar F. Rüschendorf N. Hubner T. Grimm E. Witt B.H.F. Weber August 01, 2013 / J Allergy Clin Immunol A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis J. Esparza-Gordillo H. Schaarschmidt L. Liang W. Cookson A. Bauerfeind M.A. Lee-Kirsch K. Nemat J. Henderson L. Paternoster J.L. Harper E. Mangold M.M. Nothen F. Rüschendorf T. Kerscher I. Marenholz A. Matanovic S. Lau T. Keil C.P. Bauer M. Kurek A. Ciechanowicz M. Macek A. Franke M. Kabesch N. Hubner G. Abecasis S. Weidinger M. Moffatt Y.A. Lee August 01, 2013 / Cell Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat S.S. Atanur A.G. Diaz K. Maratou A. Sarkis M. Rotival L. Game M.R. Tschannen P.J. Kaisaki G.W. Otto M.C. John Ma T.M. Keane O. Hummel K. Saar W. Chen V. Guryev K. Gopalakrishnan M.R. Garrett B. Joe L. Citterio G. Bianchi M. McBride A. Dominiczak D.J. Adams T. Serikawa P. Flicek E. Cuppen N. Hubner E. Petretto D. Gauguier A. Kwitek H. Jacob T.J. Aitman July 12, 2013 / PLoS ONE Evaluation of 41 candidate gene variants for obesity in the EPIC-Potsdam cohort by multi-locus stepwise regression S. Knueppel K. Rohde K. Meidtner D. Drogan H.G. Holzhuetter H. Boeing E. Fisher July 11, 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen July 09, 2013 / Proc Natl Acad Sci U S A Interfering with Gal-1-mediated angiogenesis contributes to the pathogenesis of preeclampsia N. Freitag I. Tirado-González G. Barrientos F. Herse V.L.J.L. Thijssen S.M. Weedon-Fekjær H. Schulz G. Wallukat B.F. Klapp T. Nevers S. Sharma A.C. Staff R. Dechend S.M. Blois Pagination First page « First Previous page ‹‹ … Page 18 Current page 19 Page 20 Page 21 … Next page ›› Last page Last »
January 01, 2014 / Gut Cryptogenic multifocal ulcerating stenosing enteritis associated with homozygous deletion mutations in cytosolic phospholipase A2-α M.A. Brooke H.J. Longhurst V. Plagnol N.S. Kirkby J.A. Mitchell F. Rüschendorf T.D. Warner D.P. Kelsell T.T. MacDonald
December 12, 2013 / Cell Rep Quantitative and qualitative proteome characteristics extracted from in-depth integrated genomics and proteomics analysis T.Y. Low S. van Heesch H. van den Toorn P. Giansanti A. Cristobal P. Toonen S. Schaefer N. Hübner B. van Breukelen S. Mohammed E. Cuppen A.J.R. Heck V. Guryev
October 01, 2013 / Seizure TLR4, ATF-3 and IL8 inflammation mediator expression correlates with seizure frequency in human epileptic brain tissue K. Pernhorst S. Herms P. Hoffmann S. Cichon H. Schulz T. Sander S. Schoch A.J. Becker A. Grote
September 03, 2013 / PLoS ONE Altered expression of cyclin A 1 in muscle of patients with facioscapulohumeral muscle dystrophy (FSHD-1) A. Pakula J. Schneider J. Janke U. Zacharias H. Schulz N. Hübner A. Mähler A. Spuler S. Spuler P. Carlier M. Boschmann
September 01, 2013 / Orthod Fr Defaut primaire d'eruption (DPE) : analyse genetique clinique et moleculaire [Primary failure of eruption (PFE): clinical and molecular genetics analysis] A. Stellzig-Eisenhauer E. Decker P. Meyer-Marcotty C. Rau B.S. Fiebig W. Kress K. Saar F. Rüschendorf N. Hubner T. Grimm E. Witt B.H.F. Weber
August 01, 2013 / J Allergy Clin Immunol A functional IL-6 receptor (IL6R) variant is a risk factor for persistent atopic dermatitis J. Esparza-Gordillo H. Schaarschmidt L. Liang W. Cookson A. Bauerfeind M.A. Lee-Kirsch K. Nemat J. Henderson L. Paternoster J.L. Harper E. Mangold M.M. Nothen F. Rüschendorf T. Kerscher I. Marenholz A. Matanovic S. Lau T. Keil C.P. Bauer M. Kurek A. Ciechanowicz M. Macek A. Franke M. Kabesch N. Hubner G. Abecasis S. Weidinger M. Moffatt Y.A. Lee
August 01, 2013 / Cell Genome sequencing reveals loci under artificial selection that underlie disease phenotypes in the laboratory rat S.S. Atanur A.G. Diaz K. Maratou A. Sarkis M. Rotival L. Game M.R. Tschannen P.J. Kaisaki G.W. Otto M.C. John Ma T.M. Keane O. Hummel K. Saar W. Chen V. Guryev K. Gopalakrishnan M.R. Garrett B. Joe L. Citterio G. Bianchi M. McBride A. Dominiczak D.J. Adams T. Serikawa P. Flicek E. Cuppen N. Hubner E. Petretto D. Gauguier A. Kwitek H. Jacob T.J. Aitman
July 12, 2013 / PLoS ONE Evaluation of 41 candidate gene variants for obesity in the EPIC-Potsdam cohort by multi-locus stepwise regression S. Knueppel K. Rohde K. Meidtner D. Drogan H.G. Holzhuetter H. Boeing E. Fisher
July 11, 2013 / Am J Hum Genet Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathy A.K. Arndt S. Schaefer J.D. Drenckhahn M.K. Sabeh E.R. Plovie A. Caliebe E. Klopocki G. Musso A.A. Werdich H. Kalwa M. Heinig R.F. Padera K. Wassilew J. Bluhm C. Harnack J. Martitz P.J. Barton M. Greutmann F. Berger N. Huebner R. Siebert H.H. Kramer S.A. Cook C.A. Macrae S. Klaassen
July 09, 2013 / Proc Natl Acad Sci U S A Interfering with Gal-1-mediated angiogenesis contributes to the pathogenesis of preeclampsia N. Freitag I. Tirado-González G. Barrientos F. Herse V.L.J.L. Thijssen S.M. Weedon-Fekjær H. Schulz G. Wallukat B.F. Klapp T. Nevers S. Sharma A.C. Staff R. Dechend S.M. Blois
Prof. Dr. Norbert Hübner Group Leader Contact nhuebner@mdc-berlin.de Phone: +49 30 9406-2530 Max-Delbrück-Centrum für Molekulare Medizin (MDC) Robert-Rössle-Straße 10 13125 Berlin, Deutschland Building 87, Room 0.09 Norbert Hübner is a DZHK Principal Investigator Internal affiliations Genes, Cells and Cell‑based Medicine (topic 1)