부산대학교 도서관

Rajcsanyi, L.S.; Peters, T.; Hinney, A.; Schmelting, C.; Kraft, I.; Giuranna, J.; Seitz, J.; Hebebrand, J.; Kesselmeier, M.; Schröder, C.; Beygo, J.; Leitão, E.; Zeschnigk, M.; Horsthemke, B.; Föcker, M.; Herpertz-Dahlmann, B.; de Zwaan, M.; Herzog, W.; Ehrlich, S.; Zipfel, S.; Giel, K.; Egberts, K.; Burghardt, R.; Budeus, B.

In: Scientific Reports. (Scientific Reports, December 2025, 15(1))

Lechner L; Department of Pediatric Endocrinology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany.; Opitz R; Institute for Experimental Pediatric Endocrinology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany.; Silver MJ; Medical Research Council Unit, Gambia at the London School of Hygiene and Tropical Medicine, Fajara, Banjul, PO Box 273, Gambia.; Krabusch PM; Department of Pediatric Endocrinology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany.; Prentice AM; Medical Research Council Unit, Gambia at the London School of Hygiene and Tropical Medicine, Fajara, Banjul, PO Box 273, Gambia.; Field MS; Division of Nutritional Sciences, Cornell University, Ithaca, NY 14850, USA.; Stachelscheid H; Berlin Institute of Health, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, BIH Core Unit Stem Cells and Organoids, 13353 Berlin, Germany.; Leitão E; Institute of Human Genetics, University Hospital Essen, 45147 Essen, Germany.; Schröder C; Institute of Human Genetics, University Hospital Essen, 45147 Essen, Germany.; Fernandez Vallone V; Berlin Institute of Health, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, BIH Core Unit Stem Cells and Organoids, 13353 Berlin, Germany.; Horsthemke B; Institute of Human Genetics, University Hospital Essen, 45147 Essen, Germany.; Jöckel KH; Institute of Medical Informatics, Biometry and Epidemiology, University Hospital Essen, 45147 Essen, Germany.; Schmidt B; Institute of Medical Informatics, Biometry and Epidemiology, University Hospital Essen, 45147 Essen, Germany.; Nöthen MM; Institute of Human Genetics, School of Medicine and University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.; Hoffmann P; Institute of Human Genetics, School of Medicine and University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.; Herms S; Institute of Human Genetics, School of Medicine and University Hospital Bonn, University of Bonn, 53127 Bonn, Germany.; Kleyn PW; Rhythm Pharmaceuticals, Boston, MA 02116, USA.; Megges M; Department of Pediatric Endocrinology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany.; Blume-Peytavi U; Clinical Research Center for Hair and Skin Science, Department of Dermatology and Venerology and Allergology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, and Humboldt-Universität zu Berlin, 10117 Berlin, Germany.; Weiss K; Klinik für Angeborene Herzfehler - Kinderkardiologie, Deutsches Herzzentrum der Charité, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany.; Mai K; Department of Endocrinology, Diabetes, and Nutrition and Charité Center for Cardiovascular Research, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany.; German Center for Diabetes Research, 85764 München-Neuherberg, Germany.; Blankenstein O; Department of Pediatric Endocrinology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany.; Department Endocrinology and Metabolism, Labor Berlin-Charité Vivantes GmbH, 13353 Berlin, Germany.; Obermayer B; Core Unit Bioinformatics (CUBI), Berlin Institute of Health/Charité- Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 10117 Berlin, Germany.; Wiegand S; Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, Center for Social-Pediatric Care/Pediatric Endocrinology and Diabetology, 13353 Berlin, Germany.; Kühnen P; Department of Pediatric Endocrinology, Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, 13353 Berlin, Germany.

Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 101505086 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1946-6242 (Electronic) Linking ISSN: 19466234 NLM ISO Abbreviation: Sci Transl Med Subsets: MEDLINE

Wieczorek D; Newman WG; Wieland T; Berulava T; Kaffe M; Falkenstein D; Beetz C; Graf E; Schwarzmayr T; Douzgou S; Clayton-Smith J; Daly SB; Williams SG; Bhaskar SS; Urquhart JE; Anderson B; O'Sullivan J; Boute O; Gundlach J; Czeschik JC; van Essen AJ; Hazan F; Park S; Hing A; Kuechler A; Lohmann DR; Ludwig KU; Mangold E; Steenpass L; Zeschnigk M; Lemke JR; Lourenco CM; Hehr U; Prott EC; Waldenberger M; Bohmer AC; Horsthemke B; O'Keefe RT; Meitinger T; Burn J; Luedecke HJ; Strom TM

Am. J. Hum. Genet. 95, 698-707 (2014)
Wieczorek, D, Newman, W, Wieland, T, Berulava, T, Kaffe, M, Falkenstein, D, Beetz, C, Graf, E, Schwarzmayr, T, Douzgou, S, Clayton-Smith, J, Daly, S, Williams, S, Bhaskar, S S, Urquhart, J, Anderson, B, O'Sullivan, J, Boute, O, Gundlach, J, Czeschik, J C, van Essen, A J, Hazan, F, Park, S, Hing, A, Kuechler, A, Lohmann, D R, Ludwig, K U, Mangold, E, Steenpaß, L, Zeschnigk, M, Lemke, J R, Lourenco, C M, Hehr, U, Prott, E-C, Waldenberger, M, Böhmer, A C, Horsthemke, B, O'Keefe, R, Meitinger, T, Burn, J, Lüdecke, H-J & Strom, T M 2014, 'Compound Heterozygosity of Low-Frequency Promoter Deletions and Rare Loss-of-Function Mutations in TXNL4A Causes Burn-McKeown Syndrome.', American Journal of Human Genetics, vol. 95, no. 6. https://doi.org/10.1016/j.ajhg.2014.10.014

Farber, C.; Gross, S.; Neesen, J.; Buiting, K.; Horsthemke, B.

Genomics. 65:174-183

Leitão E; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Schröder C; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Parenti I; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Dalle C; Institut du Cerveau et de la Moelle épinière (ICM), Sorbonne Université, UMR S 1127, Inserm U1127, CNRS UMR 7225, F-75013, Paris, France.; Rastetter A; Institut du Cerveau et de la Moelle épinière (ICM), Sorbonne Université, UMR S 1127, Inserm U1127, CNRS UMR 7225, F-75013, Paris, France.; Kühnel T; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Kuechler A; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Kaya S; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Gérard B; Unité de Génétique Moléculaire, IGMA, Hôpitaux Universitaire de Strasbourg, Strasbourg, France.; Schaefer E; Service de Génétique Médicale, IGMA, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.; Nava C; Institut du Cerveau et de la Moelle épinière (ICM), Sorbonne Université, UMR S 1127, Inserm U1127, CNRS UMR 7225, F-75013, Paris, France.; Drouot N; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 67400, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, 67400, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, 67400, France.; Université de Strasbourg, Illkirch, 67400, France.; Engel C; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 67400, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, 67400, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, 67400, France.; Université de Strasbourg, Illkirch, 67400, France.; Piard J; Centre de Génétique Humaine, CHU Besançon, Besançon, France.; INSERM UMR1231, Equipe Génétique des Anomalies du Développement, Université de Bourgogne-Franche-Comté, Dijon, France.; Duban-Bedu B; Centre de génétique chromosomique, Hôpital Saint-Vincent de Paul, Lille, France.; Villard L; Aix-Marseille University, INSERM, MMG, UMR-S 1251, Faculté de médecine, Marseille, France.; Département de Génétique Médicale, APHM, Hôpital d'Enfants de La Timone, Marseille, France.; Stegmann APA; Department of Human Genetics, Radboud University Medical Center, 6500 HB, Nijmegen, The Netherlands.; Department of Clinical Genetics, Maastricht University Medical Center+, Maastricht, The Netherlands.; Vanhoutte EK; Department of Clinical Genetics, Maastricht University Medical Center+, Maastricht, The Netherlands.; Verdonschot JAJ; Department of Clinical Genetics, Maastricht University Medical Center+, Maastricht, The Netherlands.; Cardiovascular Research Institute (CARIM), Departments of Cardiology, Maastricht University Medical Center, Maastricht, The Netherlands.; Kaiser FJ; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Tran Mau-Them F; INSERM UMR1231, Equipe Génétique des Anomalies du Développement, Université de Bourgogne-Franche-Comté, Dijon, France.; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, CHU Dijon Bourgogne, Dijon, France.; Scala M; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16132, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, 16147, Genoa, Italy.; Striano P; Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, 16132, Genoa, Italy.; Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, 16147, Genoa, Italy.; Frints SGM; Department of Clinical Genetics, Maastricht University Medical Center+, Maastricht, The Netherlands.; Department of Genetics and Cell Biology, Faculty of Health Medicine Life Sciences, Maastricht University Medical Center+, Maastricht University, Maastricht, The Netherlands.; Argilli E; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.; Sherr EH; Department of Neurology, University of California, San Francisco, San Francisco, CA, USA.; Institute of Human Genetics and Weill Institute for Neurosciences, University of California, San Francisco, San Francisco, CA, USA.; Elder F; UF de Génomique du Développement, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP-Sorbonne Université, Paris, France.; Buratti J; UF de Génomique du Développement, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP-Sorbonne Université, Paris, France.; Keren B; UF de Génomique du Développement, Département de Génétique, Groupe Hospitalier Pitié-Salpêtrière, APHP-Sorbonne Université, Paris, France.; Mignot C; Institut du Cerveau et de la Moelle épinière (ICM), Sorbonne Université, UMR S 1127, Inserm U1127, CNRS UMR 7225, F-75013, Paris, France.; APHP, Sorbonne Université, Département de Génétique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Groupe Hospitalier Pitié-Salpêtrière and Hôpital Trousseau, Paris, France.; Héron D; APHP, Sorbonne Université, Département de Génétique, Centre de Référence Déficiences Intellectuelles de Causes Rares, Groupe Hospitalier Pitié-Salpêtrière and Hôpital Trousseau, Paris, France.; Mandel JL; Unité de Génétique Moléculaire, IGMA, Hôpitaux Universitaire de Strasbourg, Strasbourg, France.; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 67400, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, 67400, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, 67400, France.; Université de Strasbourg, Illkirch, 67400, France.; Gecz J; School of Medicine, The University of Adelaide, Adelaide, 5005, SA, Australia.; Robinson Research Institute, The University of Adelaide, Adelaide, SA, 5006, Australia.; South Australian Health and Medical Research Institute, The University of Adelaide, Adelaide, 5005, SA, Australia.; Kalscheuer VM; Research Group Development and Disease, Max Planck Institute for Molecular Genetics, Berlin, Germany.; Horsthemke B; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Piton A; Unité de Génétique Moléculaire, IGMA, Hôpitaux Universitaire de Strasbourg, Strasbourg, France.; Institut de Génétique et de Biologie Moléculaire et Cellulaire, Illkirch, 67400, France.; Centre National de la Recherche Scientifique, UMR7104, Illkirch, 67400, France.; Institut National de la Santé et de la Recherche Médicale, U964, Illkirch, 67400, France.; Université de Strasbourg, Illkirch, 67400, France.; Depienne C; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany. christel.depienne@uni-due.de.

Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Holland, A.; Whittington, J.; Cohen, O.; Curfs, L.; Delahaye, F.; Dudley, O.; Horsthemke, B.; Lindgren, A. -C; Nourissier, C.; Sharma, N.; Vogels, A.

Journal of Intellectual Disability Research. Jun 2009 53(6):538-547.

Beygo J.; Citro V.; Sparago A.; De crescenzo A.; Cerrato F.; Heitmann M.; Rademacher K.; Guala A.; Enklaar T.; Anichini C.; Cirillo silengo M.; Graf N.; Prawitt D.; Cubellis M. V.; Horsthemke B.; Buiting K.; Riccio A.

Hum Mol Genet
Human molecular genetics
22(3) (2013): 544–557. doi:10.1093/hmg/dds465
info:cnr-pdr/source/autori:Beygo J, Citro V, Sparago A, De Crescenzo A, Cerrato F, Heitmann M, Rademacher K, Guala A, Enklaar T, Anichini C, Cirillo Silengo M, Graf N, Prawitt D, Cubellis MV, Horsthemke B, Buiting K, Riccio A./titolo:The molecular function and clinical phenotype of partial deletions of the IGF2%2FH19 imprinting control region depends on the spatial arrangement of the remaining CTCF-binding sites/doi:10.1093%2Fhmg%2Fdds465/rivista:Human molecular genetics (Print)/anno:2013/pagina_da:544/pagina_a:557/intervallo_pagine:544–557/volume:22(3)

Godfrey, L.K.; Liffers, S.-T.; Trajkovic-Arsic, M.; Siveke, J.T.; Forster, J.; Lähnemann, D.; Zeschnigk, M.; Schröder, C.; Köster, J.; Henschel, L.; Ludwig, K.U.; Behrens, D.; Scarpa, A.; Lawlor, R.T.; Witzke, K.E.; Sitek, B.; Johnsen, S.A.; Rahmann, S.; Horsthemke, B.

In: Clinical Epigenetics. (Clinical Epigenetics, December 2024, 16(1))

Lüdecke, H J; Schaper, J; Meinecke, P; Momeni, P; Gross, Stephanie; von Holtum D, D; Hirche, H; Abramowicz, Marc; Albrecht, B; Apacik, C; Christen, H J; Claussen, U; Devriendt, K; Fastnacht, E; Forderer, A; Friedrich, U; Goodship, T H; Greiwe, M; Hamm, H; Hennekam, R C; Hinkel, G K; Hoeltzenbein, M; Kayserili, H; Majewski, F; Mathieu, M; McLeod, R; Midro, A T; Moog, U; Nagai, T; Niikawa, N; Orstavik, K H; Plöchl, Elzbieta; Seitz, C; Schmidtke, J; Tranebjaerg, L; Tsukahara, M; Wittwer, B; Zabel, B; Gillessen-Kaesbach, G.; Horsthemke, B

The American Journal of Human Genetics. 68:81-91

Vollmar, Tobias; Maus, Bärbel; Wurtz, R. P.; Gillessen-Kaesbach, G.; Horsthemke, B.; Wieczorek, D.; Boehringer, S.

European Journal of Medical Genetics. 51:44-53

Rauch, J; Knoch, T A; Solovei, I; Teller, K; Stein, S; Buiting, K; Horsthemke, B; Langowski, J; Cremer, T; Hausmann, M; Cremer, C

Differentiation. 76:66-82

Wieczorek, D.; Ludwig, M.; Boehringer, S.; Jongbloet, P.H.; Gillessen-Kaesbach, G.; Horsthemke, B.

Human Genetics, 121, 3-4, pp. 369-76

Webb, T.; Whittington, J.; Holland, AJ; Soni, S.; Boer, H.; Clarke, D.; Horsthemke, B.

Clinical Genetics. Jan, 2006, Vol. 69 Issue 1, p26, 7 p.

Momeni, P.; Glöckner, G.; Schmidt, O.; von Holtum, D.; Albrecht, B.; Gillessen-Kaesbach, G.; Hennekam, R.; Meinecke, P.; Zabel, B.; Rosenthal, A.; Horsthemke, B.; Lüdecke, H. J.

Nature Genetics. 24:71-74

Department of Genetics, Case Western Reserve University School of Medicine, and Center for Human Genetics, University Hospitals of Cleveland, Cleveland; ( host institution ); Ohta, T.; Gray, T.A.; Rogan, P.K.; Buiting, K.; Gabriel, J.M.; Saitoh, S.; Muralidhar, B.; Bilienska, B.; Krajewska-Walasek, M.; Driscoll, D.J.; Horsthemke, B.; Butler, M.G.; Nicholls, R.D.

Biochemistry Publications

Beckmann D; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Römer-Hillmann A; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Krause A; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Hansen U; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Wehmeyer C; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Intemann J; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; de Gorter DJJ; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Dankbar B; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Hillen J; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Heitzmann M; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Begemann I; Institute of Medical Physics and Biophysics, University of Münster, Robert-Koch Straße 31, Münster, Germany.; Galic M; Institute of Medical Physics and Biophysics, University of Münster, Robert-Koch Straße 31, Münster, Germany.; Weinhage T; Department of Pediatric Rheumatology and Immunology, University Children's Hospital Münster, Domagkstraße 3, Münster, Germany.; Foell D; Department of Pediatric Rheumatology and Immunology, University Children's Hospital Münster, Domagkstraße 3, Münster, Germany.; Ai R; Department of Chemistry and Biochemistry, 9500 Gilman Drive, UC San Diego, La Jolla, CA, USA.; Kremerskothen J; Department of Nephrology and Rheumatology, Internal Medicine D, University Hospital Münster, Albert-Schweitzer-Campus 1, Münster, Germany.; Kiener HP; Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Waehringer Guertel 18-20, Vienna, Austria.; Müller S; Institute for Immunology, Jena University Hospital, Friedrich Schiller University, Jena, Leutragraben 3, Jena, Germany.; Kamradt T; Institute for Immunology, Jena University Hospital, Friedrich Schiller University, Jena, Leutragraben 3, Jena, Germany.; Schröder C; Genome Informatics, Institute of Human Genetics, University of Duisburg-Essen, Virchowstraße 183, Essen, Germany.; Leitão E; Institute of Human Genetics, University Hospital of Essen, University of Duisburg-Essen, Hufelandstraße 55, Essen, Germany.; Horsthemke B; Institute of Human Genetics, University Hospital of Essen, University of Duisburg-Essen, Hufelandstraße 55, Essen, Germany.; Rosenstiel P; Institute of Clinical Molecular Biology, University of Kiel, Rosalind-Franklin-Straße 12, Kiel, Germany.; Nordström K; Department of Genetics/Epigenetics, Saarland University, Campus Saarbrücken, Building A2 4, Saarbrücken, Germany.; Gasparoni G; Department of Genetics/Epigenetics, Saarland University, Campus Saarbrücken, Building A2 4, Saarbrücken, Germany.; Gasparoni N; Department of Genetics/Epigenetics, Saarland University, Campus Saarbrücken, Building A2 4, Saarbrücken, Germany.; Walter J; Department of Genetics/Epigenetics, Saarland University, Campus Saarbrücken, Building A2 4, Saarbrücken, Germany.; Li N; Max Planck Institute for Molecular Genetics, Otto-Warburg-Laboratories, Epigenomics, Ihnestraße 63-73, Berlin, Germany.; Yang X; Max Planck Institute for Molecular Genetics, Otto-Warburg-Laboratories, Epigenomics, Ihnestraße 63-73, Berlin, Germany.; Chung HR; Max Planck Institute for Molecular Genetics, Otto-Warburg-Laboratories, Epigenomics, Ihnestraße 63-73, Berlin, Germany.; Institute of Medical Bioinformatics and Biostatistics, Philipps-University Marburg, Bunsenstraße 3, Marburg, Germany.; Pavenstädt H; Department of Nephrology and Rheumatology, Internal Medicine D, University Hospital Münster, Albert-Schweitzer-Campus 1, Münster, Germany.; Lindemann N; Institute of Anatomy and Vascular Biology, University of Münster, Vesaliusweg 2-4, Münster, Germany.; Schnittler HJ; Institute of Anatomy and Vascular Biology, University of Münster, Vesaliusweg 2-4, Münster, Germany.; Wang W; Department of Chemistry and Biochemistry, 9500 Gilman Drive, UC San Diego, La Jolla, CA, USA.; Department of Cellular and Molecular Medicine, 9500 Gilman Drive, UCSD School of Medicine, La Jolla, CA, USA.; Firestein GS; Division of Rheumatology, Allergy and Immunology, 9500 Gilman Drive, UCSD School of Medicine, La Jolla, CA, USA.; Pap T; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany.; Korb-Pap A; Institute of Musculoskeletal Medicine, University Hospital Münster, Albert-Schweitzer-Campus 1, Building D3, Münster, Germany. korba@uni-muenster.de.

Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN: 2041-1723 (Electronic) Linking ISSN: 20411723 NLM ISO Abbreviation: Nat Commun Subsets: MEDLINE

Kaiser, FJ; Möröy, T; Chang Ching Chuan, GTG; Horsthemke, B; Lüdecke, HJ

Journal of Biological Chemistry. 278:38780-38785

Horsthemke, B; Surani, A; James, T; Ohlsson, R

Results Probl Cell Differ. 25:91-118

Department of Genetics, Case Western Reserve University School of Medicine, Universitätsklinikum Essen, Essen, Germany ( host institution ); Ohta, T.; Buiting, K.; Kokkonen, H.; McCandless, S.; Heeger, S.; Leisti, H.; Driscoll, D.J.; Cassidy, S.B.; Horsthemke, B.; Nicholls, R.D.

The American Journal of Human Genetics. 64:385-396

Stunnenberg, HG; Abrignani, S; Adams, D; de Almeida, M; Altucci, L; Amin, V; Amit, I; Antonarakis, SE; Aparicio, S; Arima, T; Arrigoni, L; Arts, R; Asnafi, V; Badosa, ME; Bae, JB; Bassler, K; Beck, S; Berkman, B; Bernstein, BE; Bilenky, M; Bird, A; Bock, C; Boehm, B; Bourque, G; Breeze, CE; Brors, B; Bujold, D; Burren, O; Bussemakers, MJ; Butterworth, A; Campo, E; Carrillo-de-Santa-Pau, E; Chadwick, L; Chan, KM; Chen, W; Cheung, TH; Chiapperino, L; Choi, NH; Chung, HR; Clarke, L; Connors, JM; Cronet, P; Danesh, J; Dermitzakis, M; Drewes, G; Durek, P; Dyke, S; Dylag, T; Eaves, CJ; Ebert, P; Eils, R; Eils, J; Ennis, CA; Enver, T; Feingold, EA; Felder, B; Ferguson-Smith, A; Fitzgibbon, J; Flicek, P; Foo, RSY; Fraser, P; Frontini, M; Furlong, E; Gakkhar, S; Gasparoni, N; Gasparoni, G; Geschwind, DH; Glažar, P; Graf, T; Grosveld, F; Guan, XY; Guigo, R; Gut, IG; Hamann, A; Han, BG; Harris, RA; Heath, S; Helin, K; Hengstler, JG; Heravi-Moussavi, A; Herrup, K; Hill, S; Hilton, JA; Hitz, BC; Horsthemke, B; Hu, M; Hwang, JY; Ip, NY; Ito, T; Javierre, BM; Jenko, S; Jenuwein, T; Joly, Y; Jones, SJM; Kanai, Y; Kang, HG; Karsan, A; Kiemer, AK; Kim, SC