Articles

Search Articles

Advanced search
Help

Catalogue

Articles

Databases

X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (287) 287
Publication (48) 48
Patent (21) 21
Conference Proceeding (6) 6
Book / eBook (2) 2
Book Chapter (1) 1
Compact Disc (1) 1
Data Set (1) 1
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
humans (158) 158
index medicus (134) 134
female (110) 110
male (108) 108
genetics & heredity (95) 95
mutation (77) 77
genetic aspects (55) 55
adult (52) 52
pedigree (52) 52
clinical neurology (42) 42
middle aged (39) 39
research (38) 38
genetic predisposition to disease (37) 37
child (35) 35
genetics (35) 35
article (33) 33
adolescent (32) 32
neurosciences (32) 32
animals (31) 31
genotype (29) 29
polymorphism, single nucleotide (29) 29
risk factors (29) 29
gene (28) 28
mutations (28) 28
phenotype (28) 28
base sequence (26) 26
genes (26) 26
molecular sequence data (26) 26
amino acid sequence (25) 25
biochemistry & molecular biology (25) 25
genome-wide association study (25) 25
gene mutations (24) 24
proteins (24) 24
aged (23) 23
case-control studies (23) 23
chemistry (21) 21
dna mutational analysis (21) 21
metallurgy (21) 21
neurology (21) 21
young adult (21) 21
mice (20) 20
alleles (19) 19
disease (19) 19
expression (19) 19
migraine (19) 19
child, preschool (18) 18
genomes (18) 18
human genetics (18) 18
variants (18) 18
genome-wide association (17) 17
analysis (16) 16
haplotypes (16) 16
consanguinity (15) 15
population (15) 15
risk (15) 15
gene expression (14) 14
genetic disorders (14) 14
genetic variation (14) 14
genomics (14) 14
health aspects (14) 14
homozygote (14) 14
metaanalysis (14) 14
alloys (13) 13
association (13) 13
chromosome mapping (13) 13
deafness (13) 13
exons (13) 13
ferrous or non-ferrous alloys (13) 13
genetic association studies (13) 13
infant (13) 13
polymorphism, single nucleotide - genetics (13) 13
susceptibility loci (13) 13
treatment of alloys or non-ferrous metals (13) 13
biomedicine (12) 12
family (12) 12
migraine disorders - genetics (12) 12
mutation, missense (12) 12
protein (12) 12
abridged index medicus (11) 11
age of onset (11) 11
gene frequency (11) 11
intellectual disability - genetics (11) 11
medical and health sciences (11) 11
medicin och hälsovetenskap (11) 11
molecular medicine (11) 11
mutation - genetics (11) 11
physiological aspects (11) 11
polymerase chain reaction (11) 11
age (10) 10
cancer (10) 10
diagnosis (10) 10
genetic research (10) 10
genetic testing (10) 10
identification (10) 10
medizin (10) 10
migraine with aura - genetics (10) 10
stroke (10) 10
stroke - genetics (10) 10
syndrome (10) 10
aged, 80 and over (9) 9
more...
Library Location Library Location
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


1. 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
Book
Details down arrow
2. 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, ISSN 0036-8075, 1/1998, Volume 279, Issue 5349, pp. 403 - 406
Benign familial neonatal convulsions (BFNC) is an autosomal dominant epilepsy of infancy, with loci mapped to human chromosomes 20q13.3 and 8q24. By positional... 
Complementary DNA | Exons | Epilepsy | Genomics | DNA | Amino acids | Reports | Potassium channels | Genetic mutation | Oocytes | Seizures | GENE | K(V)LQT1 | CLONING | FORM | MULTIDISCIPLINARY SCIENCES | CONVULSIONS | MYOKYMIA | ATAXIA | CHROMOSOME-20 | PROTEINS | SUBUNIT | 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
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
3. 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
  Sarcoidosis is an inflammatory disease characterised by the presence of granulomas that can affect the skin, lungs, heart, brain and nervous system, eyes and... 
BTNL2 GENE | RESPIRATORY SYSTEM | SUSCEPTIBILITY | 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
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
4. 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, ISSN 1053-8119, 08/2015, Volume 116, pp. 59 - 67
The brain's serotonergic (5-HT) system has been implicated in controlling impulsive behavior and attentional orienting and linked to impulse control and... 
ADHD | ACUTE TRYPTOPHAN DEPLETION | FRONTAL-CORTEX | HUMANS | POLYMORPHISM | NEUROSCIENCES | NEUROIMAGING | OBSESSIVE-COMPULSIVE DISORDER | GENETIC-VARIATION | 5-HT1A RECEPTOR-BINDING | HEALTHY-VOLUNTEERS | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | MODULATION | 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
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
5. Full Text Editorial
by Kubisch, Christian
Medizinische Genetik, ISSN 0936-5931, 08/2015, Volume 27, Issue 2, pp. 197 - 198
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
6. Full Text Editorial
by Kubisch, Christian
medizinische genetik, ISSN 0936-5931, 8/2015, Volume 27, Issue 2, pp. 197 - 198
Human Genetics | Pediatrics | Medicine & Public Health | Obstetrics/Perinatology | Reproductive Medicine
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
7. Full Text Editorial
by Kubisch, Christian
medizinische genetik, ISSN 0936-5931, 08/2015, Volume 27, Issue 2, p. 197
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
8. Full Text Editorial
by Kubisch, Christian
medizinische genetik, ISSN 0936-5931, 08/2015, Volume 27, Issue 2, pp. 197 - 198
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
9. 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
Unrecognized genome instability syndromes can potentially impede the rational treatment of cancer in rare patients. Identification of cancer patients with a... 
FANCA | myelotoxicity | fanconi anemia | genomic instability | cholangiocarcinoma | CHROMOSOME BREAKAGE | TOXICITY | CANCER | FLUDARABINE | ANDROGEN THERAPY | MALIGNANCY | ONCOLOGY | MUTATIONS | CARCINOMA | REGISTRY | Chemotherapy | Usage | Gemcitabine | Myelosuppression | Dosage and administration | Diagnosis | Research | Cisplatin | Fanconi's anemia | Cancer
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
10. Full Text Analysis of shared heritability in common disorders of the brain
by Anttila, Verneri and Bulik-Sullivan, Brendan and Finucane, Hilary K and Walters, Raymond K and Bras, Jose and Duncan, Laramie and Escott-Price, Valentina and Falcone, Guido J and Gormley, Padhraig and Malik, Rainer and Patsopoulos, Nikolaos A and Ripke, Stephan and Wei, Zhi and Yu, Dongmei and Lee, Phil H and Turley, Patrick and Grenier-Boley, Benjamin and Chouraki, Vincent and Kamatani, Yoichiro and Berr, Claudine and Letenneur, Luc and Hannequin, Didier and Amouyel, Philippe and Boland, Anne and Deleuze, Jean-François and Duron, Emmanuelle and Vardarajan, Badri N and Reitz, Christiane and Goate, Alison M and Huentelman, Matthew J and Ilyas Kamboh, M and Larson, Eric B and Rogaeva, Ekaterina and George-Hyslop, Peter St and Hakonarson, Hakon and Kukull, Walter A and Farrer, Lindsay A and Barnes, Lisa L and Beach, Thomas G and Yesim Demirci, F and Head, Elizabeth and Hulette, Christine M and Jicha, Gregory A and Kauwe, John S.K and Kaye, Jeffrey A and Leverenz, James B and Levey, Allan I and Lieberman, Andrew P and Pankratz, Vernon S and Poon, Wayne W and Quinn, Joseph F and Saykin, Andrew J and Schneider, Lon S and Smith, Amanda G and Sonnen, Joshua A and Stern, Robert A and Van Deerlin, Vivianna M and Van Eldik, Linda J and Harold, Denise and Russo, Giancarlo and Rubinsztein, David C and Bayer, Anthony and Tsolaki, Magda and Proitsi, Petra and Fox, Nick C and Hampel, Harald and Owen, Michael J and Mead, Simon and Passmore, Peter and Morgan, Kevin and Nöthen, Markus M and Rossor, Martin and Lupton, Michelle K and Hoffmann, Per and Kornhuber, Johannes and Lawlor, Brian and McQuillin, Andrew and Al-Chalabi, Ammar and Bis, Joshua C and Ruiz, Agustin and Boada, Mercè and Seshadri, Sudha and Beiser, Alexa and Rice, Kenneth and Van Der Lee, Sven J and De Jager, Philip L and Geschwind, Daniel H and Riemenschneider, Matthias and Riedel-Heller, Steffi and Rotter, Jerome I and Ransmayr, Gerhard and Hyman, Bradley T and Cruchaga, Carlos and Alegret, Montserrat and Winsvold, Bendik and Palta, Priit and Farh, Kai-How and Cuenca-Leon, Ester and Furlotte, Nicholas and Kurth, Tobias and ... and Brainstorm Consortium and The Brainstorm Consortium
Science, ISSN 0036-8075, 06/2018, Volume 360, Issue 6395, pp. 1313 - 1313
Disorders of the brain can exhibit considerable epidemiological comorbidity and often share symptoms, provoking debate about their etiologic overlap. We... 
ANOREXIA-NERVOSA | POPULATION-BASED TWIN | DEFICIT HYPERACTIVITY DISORDER | LONG-TERM SURVIVAL | ALZHEIMERS-DISEASE | MULTIDISCIPLINARY SCIENCES | GENETIC CORRELATIONS | BODY-MASS INDEX | MAJOR DEPRESSIVE DISORDER | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | Genetic Variation | Mental Disorders - genetics | Genome-Wide Association Study | Phenotype | Brain Diseases - classification | Quantitative Trait, Heritable | Brain Diseases - diagnosis | Humans | Mental Disorders - classification | Risk Factors | Brain Diseases - genetics | Mental Disorders - diagnosis | Anorexia | Disorders | Cognitive ability | Bipolar disorder | Posttraumatic stress disorder | Mental depression | Epidemiology | Risk factors | Consortia | Proteins | Ischemia | Etiology | Classification | Gilles de la Tourette syndrome | Alzheimer's disease | Neurological disorders | Neurodegenerative diseases | Comorbidity | Behavior disorders | Anorexia nervosa | Risk analysis | Patients | Neurological diseases | Correlation analysis | Heritability | Attention deficit disorder | Headache | Mental disorders | Medical services | Schizophrenia | Risk sharing | Genomes | Heterogeneity | Biological effects | Risk assessment | Stroke | Phenotypes | Migraine | Attention deficit hyperactivity disorder | Eating disorders | Personality | Genetic diversity | Statistics | Activity patterns | Crohn's Disease | Population (statistical) | Scaffolding | Diagnostic systems | Alzheimers disease | Life Sciences | Human health and pathology | Mental Disorders | Neurons and Cognition | Brain Diseases | Genetics
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
11. 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
Germline mutations in a number of genes involved in the recombinational repair of DNA double-strand breaks are associated with predisposition to breast and... 
U1 SNRNA | KORA | POPULATION | INSTABILITY | GENETICS & HEREDITY | BRCA2 | PROTEINS | FANCONI-ANEMIA | MAMMALIAN-CELLS | PALB2 | FAMILY | 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
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
12. Full Text German or English - that's the question/Deutsch oder Englisch -- das ist hier die Frage
by Kubisch, Christian and Siebert, Reiner
medizinische genetik, ISSN 0936-5931, 03/2018, Volume 30, Issue 1, p. 1
To access, purchase, authenticate, or subscribe to the full-text of this article, please visit this link: http://dx.doi.org/10.1007/s11825-018-0182-6 
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
13. Full Text Erbliche Hörstörungen des Menschen - Die Bedeutung genetischer Ansätze für Medizin und grundlagenwissenschaftliches Verständnis
by Kubisch, Christian
Neuroforum, ISSN 0947-0875, 09/2014, Volume 20, Issue 3, pp. 258 - 263
Deafness | Positional cloning | Hereditary hearing loss | Human genetics | Inner ear physiology
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
14. Full Text Genome-wide association study reveals three susceptibility loci for common migraine in the general population
by Kubisch, Christian and Schürks, Markus and Palotie, Aarno and de Vries, Boukje and Chasman, Daniel I and Buring, Julie E and Ernst, Florian and Völzke, Henry and Griffiths, Lyn R and Launer, Lenore J and Schminke, Ulf and Freilinger, Tobias and van den Maagdenberg, Arn M J M and Ridker, Paul M and Hoffmann, Wolfgang and Ferrari, Michel D and Zee, Robert Y L and Anttila, Verneri and Kurth, Tobias and Fendrich, Konstanze and Terwindt, Gisela M and Kallela, Mikko and IHGC
Nature Genetics, ISSN 1061-4036, 07/2011, Volume 43, Issue 7, pp. 695 - 698
Migraine is a common, heterogeneous and heritable neurological disorder. Its pathophysiology is incompletely understood, and its genetic influences at the... 
NEUROPATHIC PAIN | GENOTYPE IMPUTATION | PACKAGE | GENETICS & HEREDITY | SNPS | RECEPTOR | COHORT | HEALTH | TOOL | United States - epidemiology | Genetic Predisposition to Disease | Genome-Wide Association Study | Prognosis | Humans | Middle Aged | Risk Factors | Male | Genetic Loci | Case-Control Studies | Migraine without Aura - genetics | Chromosomes, Human, Pair 2 - genetics | Migraine without Aura - pathology | Polymorphism, Single Nucleotide - genetics | Female | Chromosomes, Human, Pair 1 - genetics | Migraine without Aura - epidemiology | Chromosomes, Human, Pair 12 - genetics | Cohort Studies | Genetic aspects | Research | Genetic susceptibility | Migraine | Risk factors | Confidence intervals | Genealogy | Womens health | Headaches | Genetics | Genomes | Epidemiology | Meta-analysis
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
15. Full Text Neurofilaments in the diagnosis of motoneuron diseases: A prospective study on 455 patients
by Steinacker, Petra and Feneberg, Emily and Weishaupt, Jochen and Brettschneider, Johannes and Tumani, Hayrettin and Andersen, Peter M and Arnim, Christine A. F. Von and Böhm, Sarah and Kassubek, Jan and Kubisch, Christian and Lulé, Dorothée and Müller, Hans-Peter and Muche, Rainer and Pinkhardt, Elmar and Oeckl, Patrick and Rosenbohm, Angela and Anderl-Straub, Sarah and Volk, Alexander E and Weydt, Patrick and Ludolph, Albert C and Otto, Markus and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk neurovetenskap and Umeå universitet
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 01/2016, Volume 87, Issue 1, pp. 12 - 20
Objectives Biomarkers for the diagnosis of motoneuron diseases (MND) are urgently needed to improve the diagnostic pathway, patient stratification and... 
TAU-PROTEIN | SURGERY | DIFFERENTIAL-DIAGNOSIS | PSYCHIATRY | ALZHEIMERS-DISEASE | MARKERS | CSF BIOMARKERS | AMYOTROPHIC-LATERAL-SCLEROSIS | CEREBROSPINAL-FLUID | CLINICAL NEUROLOGY | HEAVY-CHAIN | PROGNOSTIC BIOMARKER | LIGHT LEVELS | Predictive Value of Tests | Intermediate Filaments - pathology | Prognosis | Prospective Studies | Humans | Middle Aged | Amyotrophic Lateral Sclerosis - diagnosis | Male | Neurofilament Proteins - cerebrospinal fluid | Young Adult | Amyotrophic Lateral Sclerosis - cerebrospinal fluid | Aged, 80 and over | Adult | Female | Diagnosis, Differential | Reproducibility of Results | tau Proteins - cerebrospinal fluid | Motor Neuron Disease - cerebrospinal fluid | Disease Progression | DNA - genetics | Neurologic Examination | Adolescent | Aged | Biomarkers - cerebrospinal fluid | Motor Neuron Disease - diagnosis | Cytoplasmic filaments | Research | Cerebrospinal fluid | Biological markers | Analysis | Clinical Medicine | Neurology | Neurologi | Medical and Health Sciences | Medicin och hälsovetenskap | Motor Neurons | Neurofilament Proteins | Klinisk medicin
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
16. Full Text Erbliche Hörstörungen des Menschen – die Bedeutung genetischer Ansätze für Medizin und grundlagenwissenschaftliches Verständnis
by Kubisch, Christian
e-Neuroforum, ISSN 1868-856X, 09/2014, Volume 20, Issue 3, pp. 258 - 263
Hereditary hearing loss in humans - the importance of genetic approaches for clinical medicine and basic science Hereditary hearing loss belongs to the most... 
human genetics | in­ner ear physiology | positional cloning | deafness | hereditary hearing loss
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
17. Full Text The Discovery of a LEMD2-Associated Nuclear Envelopathy with Early Progeroid Appearance Suggests Advanced Applications for AI-Driven Facial Phenotyping
by Marbach, Felix and Rustad, Cecilie F and Riess, Angelika and Đukić, Dejan and Hsieh, Tzung-Chien and Jobani, Itamar and Prescott, Trine and Bevot, Andrea and Erger, Florian and Houge, Gunnar and Redfors, Maria and Altmueller, Janine and Stokowy, Tomasz and Gilissen, Christian and Kubisch, Christian and Scarano, Emanuela and Mazzanti, Laura and Fiskerstrand, Torunn and Krawitz, Peter M and Lessel, Davor and Netzer, Christian
The American Journal of Human Genetics, ISSN 0002-9297, 04/2019, Volume 104, Issue 4, pp. 749 - 757
Over a relatively short period of time, the clinical geneticist’s “toolbox” has been expanded by machine-learning algorithms for image analysis, which can be... 
deep neuronal network” and “intra-syndromal similarity | next-generation phenotyping | LEM domain-containing protein 2 | nuclear envelopathy | progeria-like | LOCALIZATION | MUTATIONS | MEMBRANE PROTEIN LEM2 | GENETICS & HEREDITY | Genetic disorders | Gene mutations | Analysis | Machine learning | Genetic aspects | Research | Growth disorders | Report
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights
18. 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 Hamalainen, Eija 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 ... and Int Headache Genetics Consortium and International Headache Genetics Consortium
Nature Genetics, ISSN 1061-4036, 08/2016, Volume 48, Issue 8, pp. 856 - 866
textabstractMigraine is a debilitating neurological disorder affecting around one in seven people worldwide, but its molecular mechanisms remain poorly... 
SYSTEMATIC ANALYSIS | MYOCARDIAL-INFARCTION | GENOTYPE IMPUTATION | GENETICS & HEREDITY | GENE-EXPRESSION | SMOOTH-MUSCLE-CELLS | FAMILIAL HEMIPLEGIC MIGRAINE | RECEPTOR-RELATED PROTEIN-1 | SINGLE-NUCLEOTIDE POLYMORPHISMS | SPREADING DEPRESSION | GENOME-WIDE ASSOCIATION | 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
Journal Article
Details down arrow
Digital rights down arrow
loading Loading Rights