부산대학교 도서관

Claussnitzer, M; Dankel, SN; Klocke, B; Grallert, H; Glunk, V; Berulava, T; Lee, H; Oskolkov, N; Fadista, J; Ehlers, K; Wahl, S; Hoffmann, C; Qian, K; Ronn, T; Riess, H; Muller-Nurasyid, M; Bretschneider, N; Schroeder, T; Skurk, T; Horsthemke, B; Spieler, D; Klingenspor, M; Seifert, M; Kern, MJ; Mejhert, N; Dahlman, I; Hansson, O; Hauck, SM; Bluher, M; Arner, P; Groop, L; Illig, T; Suhre, K; Hsu, YH; Mellgren, G; Hauner, H; Laumen, H

Cell. 156(1-2):343-358

Horsthemke B; University Hospital Essen Institute for Human Genetics Hufelandstr. 55 45147 Essen Germany.

Publisher: De Gruyter Country of Publication: Germany NLM ID: 9440651 Publication Model: eCollection Cited Medium: Internet ISSN: 1863-5490 (Electronic) Linking ISSN: 09365931 NLM ISO Abbreviation: Med Genet Subsets: PubMed not MEDLINE

Godfrey LK; Bridge Institute of Experimental Tumor Therapy (BIT) and Division of Solid Tumor Translational Oncology (DKTK), West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.; German Cancer Consortium (DKTK), partner site Essen, a partnership between German Cancer Research Center (DKFZ) and University Hospital Essen, Heidelberg, Germany.; Forster J; German Cancer Consortium (DKTK), partner site Essen, a partnership between German Cancer Research Center (DKFZ) and University Hospital Essen, Heidelberg, Germany.; Genome Informatics, Institute of Human Genetics, University Duisburg-Essen, Essen, Germany.; Liffers ST; Bridge Institute of Experimental Tumor Therapy (BIT) and Division of Solid Tumor Translational Oncology (DKTK), West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.; German Cancer Consortium (DKTK), partner site Essen, a partnership between German Cancer Research Center (DKFZ) and University Hospital Essen, Heidelberg, Germany.; Schröder C; Genome Informatics, Institute of Human Genetics, University Duisburg-Essen, Essen, Germany.; Köster J; Bioinformatics and Computational Oncology, Institute for Artificial Intelligence in Medicine, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Henschel L; Institute of Human Genetics, School of Medicine & University Hospital Bonn, University of Bonn, Bonn, Germany.; Ludwig KU; Institute of Human Genetics, School of Medicine & University Hospital Bonn, University of Bonn, Bonn, Germany.; Lähnemann D; German Cancer Consortium (DKTK), partner site Essen, a partnership between German Cancer Research Center (DKFZ) and University Hospital Essen, Heidelberg, Germany.; Trajkovic-Arsic M; Bridge Institute of Experimental Tumor Therapy (BIT) and Division of Solid Tumor Translational Oncology (DKTK), West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.; German Cancer Consortium (DKTK), partner site Essen, a partnership between German Cancer Research Center (DKFZ) and University Hospital Essen, Heidelberg, Germany.; Behrens D; EPO Experimental Pharmacology and Oncology GmbH, Berlin-Buch, Germany.; Scarpa A; Department of Diagnostics and Public Health, Pathological Anatomy Section, University and Hospital Trust of Verona, Verona, Italy.; ARC-Net Cancer Research Centre, University and Hospital Trust of Verona, Verona, Italy.; Lawlor RT; ARC-Net Cancer Research Centre, University and Hospital Trust of Verona, Verona, Italy.; Witzke KE; Medizinisches Proteom-Center/Zentrum Für Protein-Diagnostik, Ruhr-Universität Bochum, Bochum, Germany.; Sitek B; Medizinisches Proteom-Center/Zentrum Für Protein-Diagnostik, Ruhr-Universität Bochum, Bochum, Germany.; Klinik für Anästhesiologie, Intensivmedizin und Schmerztherapie, Universitätsklinikum Knappschaftskrankenhaus Bochum, Bochum, Germany.; Johnsen SA; Department of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Göttingen, Germany.; Robert Bosch Center for Tumor Diseases, Stuttgart, Germany.; Rahmann S; Algorithmic Bioinformatics, Center for Bioinformatics Saar and Saarland University, Saarland Informatics Campus, Saarbrücken, Germany.; Horsthemke B; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Zeschnigk M; German Cancer Consortium (DKTK), partner site Essen, a partnership between German Cancer Research Center (DKFZ) and University Hospital Essen, Heidelberg, Germany.; Institute of Human Genetics, University Hospital Essen, University Duisburg-Essen, Essen, Germany.; Siveke JT; Bridge Institute of Experimental Tumor Therapy (BIT) and Division of Solid Tumor Translational Oncology (DKTK), West German Cancer Center, University Hospital Essen, University of Duisburg-Essen, Essen, Germany. jens.siveke@uk-essen.de.; German Cancer Consortium (DKTK), partner site Essen, a partnership between German Cancer Research Center (DKFZ) and University Hospital Essen, Heidelberg, Germany. jens.siveke@uk-essen.de.; National Center for Tumor Diseases (NCT) West, Campus Essen, Essen, Germany. jens.siveke@uk-essen.de.

Publisher: BiomedCentral Country of Publication: Germany NLM ID: 101516977 Publication Model: Electronic Cited Medium: Internet ISSN: 1868-7083 (Electronic) Linking ISSN: 18687075 NLM ISO Abbreviation: Clin Epigenetics Subsets: MEDLINE

American Journal of Medical Genetics. Part C, Seminars in Medical Genetics; August 2010, Vol. 154 Issue: 3 p321-328, 8p

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

Horsthemke B; Institut Für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, 45122, Essen, Germany. bernhard.horsthemke@uni-due.de.; Bird A; Wellcome Centre for Cell Biology, University of Edinburgh, Edinburgh, EH9 3BF, UK.

Publisher: BioMed Central Country of Publication: England NLM ID: 101471619 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-8935 (Electronic) Linking ISSN: 17568935 NLM ISO Abbreviation: Epigenetics Chromatin 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.

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

Journal of intellectual disability research : JIDR. 53(6):538-547

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

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.