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1. Full Text Rationale and Design of the Hamburg City Health Study
by Jagodzinski, Annika and Johansen, Christoffer and Koch-Gromus, Uwe and Aarabi, Ghazal and Adam, Gerhard and Anders, Sven and Augustin, Matthias and der Kellen, Ramona B and Beikler, Thomas and Behrendt, Christian-Alexander and Betz, Christian S and Bokemeyer, Carsten and Borof, Katrin and Briken, Peer and Busch, Chia-Jung and Büchel, Christian and Brassen, Stefanie and Debus, Eike S and Eggers, Larissa and Fiehler, Jens and Gallinat, Jürgen and Gellißen, Simone and Gerloff, Christian and Girdauskas, Evaldas and Gosau, Martin and Graefen, Markus and Härter, Martin and Harth, Volker and Heidemann, Christoph and Heydecke, Guido and Huber, Tobias B and Hussein, Yassin and Kampf, Marvin O and von dem Knesebeck, Olaf and Konnopka, Alexander and König, Hans-Helmut and Kromer, Robert and Kubisch, Christian and Kühn, Simone and Loges, Sonja and Löwe, Bernd and Lund, Gunnar and Meyer, Christian and Nagel, Lina and Nienhaus, Albert and Pantel, Klaus and Petersen, Elina and Püschel, Klaus and Reichenspurner, Hermann and Sauter, Guido and Scherer, Martin and Scherschel, Katharina and Schiffner, Ulrich and Schnabel, Renate B and Schulz, Holger and Smeets, Ralf and Sokalskis, Vladislavs and Spitzer, Martin S and Terschüren, Claudia and Thederan, Imke and Thoma, Tom and Thomalla, Götz and Waschki, Benjamin and Wegscheider, Karl and Wenzel, Jan-Per and Wiese, Susanne and Zyriax, Birgit-Christiane and Zeller, Tanja and Blankenberg, Stefan
European journal of epidemiology, ISSN 0393-2990, 02/2020, Volume 35, Issue 2, pp. 169 - 181
Health care | Sexual dysfunction | Hamburg | Brain MRI | Epidemiology | Ocular diseases | Risk factors | Prevention | MRI imaging | Psychiatric and psychosomatic disorders | Vascular diseases | Lifestyle | Health service research | Obesity | Stroke | Nutrition | Cardiac MRI | Survivorship | Coronary heart disease | Resilience | Prospective cohort study | Respiratory diseases | Oral health | Cancer | Dementia | Life Sciences & Biomedicine | Public, Environmental & Occupational Health | Science & Technology | Life Style | Prevalence | Prospective Studies | Humans | Middle Aged | Male | Neoplasms | Incidence | Heart Failure | Female | Surveys and Questionnaires | Atrial Fibrillation | Risk Factors | Chronic Disease - epidemiology | Coronary Artery Disease | Germany - epidemiology | Magnetic Resonance Imaging | Mental Disorders | Proteomics | Quality of Life | Aged | Oral Health | Population Surveillance | Research Design | Cohort Studies | Neuroimaging | Cardiovascular disease | Population studies | Fibrillation | Risk assessment | Dementia disorders | Genetics | Heart diseases | Chronic illnesses | Medical imaging | Coronary artery | Sexual behavior | Uniqueness | Health risks | Risk analysis | Coronary artery disease | Survival | Environmental conditions | Quality of life | Digital media | Magnetic resonance imaging | Diet | Medical prognosis | Biomarkers | Index Medicus
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2. Quia nihil Deo sine pace placet
: Friedensdarstellungen in der Kunst des Mittelalters
by Kubisch, Stephan
1992, Kunstgeschichte, ISBN 9783886605729, Volume Bd. 9, i, 117 p., [37] p. of plates
Peace in art | Peace | Themes, motives | Christian art and symbolism | Religious aspects
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3. Full Text Hereditary Syndromes With Signs of Premature Aging
by Lessel, Davor and Kubisch, Christian
Deutsches Ärzteblatt international, ISSN 1866-0452, 07/2019, Volume 116, Issue 29-30, pp. 489 - 496
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Index Medicus | Review
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4. Full Text The rapid evolution of molecular genetic diagnostics in neuromuscular diseases
by Volk, Alexander E and Kubisch, Christian
Current opinion in neurology, ISSN 1350-7540, 10/2017, Volume 30, Issue 5, pp. 523 - 528
diagnostic RNA sequencing | exome sequencing | neuromuscular disorders | Neurosciences | Clinical Neurology | Neurosciences & Neurology | Life Sciences & Biomedicine | Science & Technology | Exome | Pathology, Molecular - trends | Genetic Testing | Humans | Neuromuscular Diseases - diagnosis | Sequence Analysis, DNA | Neuromuscular Diseases - genetics | Index Medicus
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5. Full Text A Potassium Channel Mutation in Neonatal Human Epilepsy
by Christian Biervert and Björn C. Schroeder and Christian Kubisch and Samuel F. Berkovic and Peter Propping and Thomas J. Jentsch and Ortrud K. Steinlein
Science (American Association for the Advancement of Science), ISSN 0036-8075, 1/1998, Volume 279, Issue 5349, pp. 403 - 406
Complementary DNA | Exons | Epilepsy | Genomics | DNA | Amino acids | Reports | Potassium channels | Genetic mutation | Oocytes | Seizures | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy | Neurology | Biological and medical sciences | Medical sciences | Nervous system (semeiology, syndromes) | Potassium - metabolism | Potassium Channels, Voltage-Gated | Frameshift Mutation | Humans | Open Reading Frames | Molecular Sequence Data | Epilepsy - metabolism | Male | Action Potentials | Brain - metabolism | Potassium Channels - metabolism | KCNQ2 Potassium Channel | Cloning, Molecular | Epilepsy - genetics | Female | Chromosomes, Human, Pair 20 | Infant, Newborn | Amino Acid Sequence | Oocytes - metabolism | Xenopus laevis | Chromosome Mapping | Potassium Channels - genetics | Animals | Pedigree | Potassium Channels - chemistry | Mutagenesis, Insertional | Physiological aspects | Genetic aspects | Spasms, Infantile | Epilepsy in children | Brain | Cloning | Genes | Potassium | Reptiles & amphibians | Age | Index Medicus
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6. Full Text First independent replication study confirms the strong genetic association of ANXA11 with sarcoidosis
by Li, Yun and Pabst, Stefan and Kubisch, Christian and Grohé, Christian and Wollnik, Bernd
Thorax, ISSN 0040-6376, 10/2010, Volume 65, Issue 10, pp. 939 - 940
Life Sciences & Biomedicine | Respiratory System | Science & Technology | Genetic Predisposition to Disease | Humans | Middle Aged | Sarcoidosis - genetics | Polymorphism, Single Nucleotide | Annexins - genetics | Case-Control Studies | Sarcoidosis | Gene mutations | Analysis | Development and progression | Reports | Genetic aspects | Annexins | Cell division | Genes | Index Medicus
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7. Full Text Fatal myelotoxicity following palliative chemotherapy with cisplatin and gemcitabine in a patient with Stage IV cholangiocarcinoma linked to post mortem diagnosis of fanconi anemia
by Engel, Nils W and Schliffke, Simon and Schüller, Ulrich and Frenzel, Christian and Bokemeyer, Carsten and Kubisch, Christian and Lessel, Davor
Frontiers in oncology, ISSN 2234-943X, 2019, Volume 9, Issue MAY, p. 420
FANCA | myelotoxicity | fanconi anemia | genomic instability | cholangiocarcinoma | Life Sciences & Biomedicine | Oncology | Science & Technology | Chemotherapy | Usage | Gemcitabine | Myelosuppression | Dosage and administration | Diagnosis | Research | Cisplatin | Fanconi's anemia | Cancer
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8. Full Text Interactive effects of citalopram and serotonin transporter genotype on neural correlates of response inhibition and attentional orienting
by Fischer, Adrian G and Endrass, Tanja and Goebel, Ingrid and Reuter, Martin and Montag, Christian and Kubisch, Christian and Ullsperger, Markus
NeuroImage (Orlando, Fla.), ISSN 1053-8119, 08/2015, Volume 116, pp. 59 - 67
Neuroimaging | Neurosciences | Neurosciences & Neurology | Life Sciences & Biomedicine | Radiology, Nuclear Medicine & Medical Imaging | Science & Technology | Humans | Male | Electroencephalography | Young Adult | Attention - physiology | Serotonin Plasma Membrane Transport Proteins - genetics | Citalopram - administration & dosage | Serotonin Uptake Inhibitors - administration & dosage | Attention - drug effects | Adult | Cerebral Cortex - physiology | Female | Cerebral Cortex - drug effects | Inhibition (Psychology) | Serotonin | Analysis | Phenols | Hallucinogenic drugs | Serotonin uptake inhibitors | Genetic aspects | Gene expression | Neurophysiology | Studies | Genotype & phenotype | Antidepressants | Index Medicus
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9. Full Text Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine
by Gormley, A.M and Stefansson, Hreinn and Winsvold, Bendik and Palta, Priit and Esko, Tõnu and Pers, Tune and Farh, Kai-How and Cuenca-Leon, E and Muona, M and Furlotte, N.A and Kurth, Karl and Ingason, Anes and Mcmahon, George and Ligthart, Lannie and Terwindt, Gisela and Todt, Unda and Müller-Myhsok, Bertram and Ran, C and Gordon, S.G and Stam, Anine and Steinberg, Stacy and Göbel, Hartmut and Koiranen, Markku and Quaye, Lydia and Adams, H.H.H and Lehtimäki, Terho and Sarin, A.-P and Wedenoja, J and Hinds, David A and Buring, J.E and Schürks, Markus and Ridker, Paul and Hrafnsdottir, M.G and Ring, Susan and Hottenga, Jouke Jan and Penninx, Brenda and Färkkilä, Markus and Artto, Ville and Hämäläinen, Eija and Lucae, Susanne and Malik, Rainer and Heath, Anew C and Madden, Pamela and Martin, Nicholas and Montgomery, Grant and Kurki, M.I and Kals, Mart and Mägi, Reedik and Pärn, K and Huang, H and Byrnes, A.E and Franke, Lude and Huang, Jian and Stergiakouli, Evangelia and Lee, Phil and Sandor, C and Webber, C and Cader, Z and Müller-Myhsok, B and Schreiber, Stefan and Meitinger, Thomas and Hagen, Knut and Salomaa, Veikko and Heikkilä, Kauko and Loehrer, Elizabeth and Uitterlinden, Ané and Hofman, A and Duijn, Cornelia and Cherkas, Lynn and Pedersen, L.M and Stubhaug, A and Nielsen, C.S and Männikkö, M and Mihailov, Evelin and Milani, Lili and Esserlind, A.-L and Christensen, A.F and Hansen, T.F and Werge, Thomas and Kaprio, Jaakko and Aromaa, Arpo and Raitakari, Olli and Ikram, Arfan and Ikram, Kamran and Jarvelin, Marjo-Riitta and Metspalu, Anes and Kubisch, Christian and Strachan, David and Ferrari, Michel and Belin, A.C and Wessman, Maija and Maagdenberg, Arn and Zwart, John-Anker and Boomsma, Dorret and Smith, G.D and Stefansson, K and Eriksson, Nicholas and Daly, Mark and Neale, Benjamin and Olesen, Jes and ... and Int Headache Genetics Consortium and International Headache Genetics Consortium
Nature genetics, ISSN 1061-4036, 08/2016, Volume 48, Issue 8, pp. 856 - 866
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Genome-Wide Association Study | Migraine Disorders - genetics | Genetic Markers - genetics | Genomics | Humans | Genetic Loci - genetics | Polymorphism, Single Nucleotide - genetics | Vascular Diseases - genetics | Muscle, Smooth - metabolism | Case-Control Studies | Quantitative trait loci | Genome-wide association studies | Migraine | Genetic aspects | Gene expression | Identification and classification | Health aspects | Risk factors | Methods | Studies | Confidence intervals | Consortia | Headaches | Gene loci | Genomes | Meta-analysis | Index Medicus | Medicin och hälsovetenskap
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10. Full Text Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene
by Meindl, Alfons and Wichmann, Hans E and Niederacher, Dieter and Hartmann, Linda and Schmutzler, Rita K and Kubisch, Christian and Neveling, Kornelia and Deißler, Helmut and Kiechle, Marion and Hellebrand, Heide and Hanenberg, Helmut and Lichtner, Peter and Engel, Christoph and Mathew, Christopher G and Wappenschmidt, Barbara and Erven, Verena and Honisch, Ellen and Schindler, Detlev and Freund, Marcel and Müller-Myhsok, Bertram and Wiek, Constanze and Ramser, Juliane and Kast, Karin and Schaal, Heiner
Nature genetics, ISSN 1061-4036, 05/2010, Volume 42, Issue 5, pp. 410 - 414
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Female genital diseases | Tumors | Genetic Predisposition to Disease | Humans | DNA-Binding Proteins - genetics | Case-Control Studies | Ovarian Neoplasms - genetics | Phenotype | Breast Neoplasms - genetics | Pedigree | Alleles | Germ-Line Mutation | Female | Fanconi Anemia - genetics | Models, Genetic | Mutation | Germany | Genetic susceptibility | Gene mutations | Genetic aspects | Breast cancer | Research | Health aspects | Risk factors | Ovarian cancer | Proteins | Genetics | Genes | Index Medicus
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