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1. Full Text Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
by van Rheenen, Wouter and Shatunov, Aleksey and Dekker, Annelot M and McLaughlin, Russell L and Diekstra, Frank P and Pulit, Sara L and van der Spek, Rick A. A and Võsa, Urmo and de Jong, Simone and Robinson, Matthew R and Yang, Jian and Fogh, Isabella and van Doormaal, Perry Tc and Tazelaar, Gijs H. P and Koppers, Max and Blokhuis, Anna M and Sproviero, William and Jones, Ashley R and Kenna, Kevin P and van Eijk, Kristel R and Harschnitz, Oliver and Schellevis, Raymond D and Brands, William J and Medic, Jelena and Menelaou, Anoniki and Vajda, Alice and Ticozzi, Nicola and Lin, Kuang and Rogelj, Boris and Vrabec, Katarina and Ravnik-Glavač, Metka and Koritnik, Blaž and Zidar, Janez and Leonardis, Lea and Grošelj, Leja Dolenc and Millecamps, Stéphanie and Salachas, François and Meininger, Vincent and de Carvalho, Mamede and Pinto, Susana and Mora, Jesus S and Rojas-García, Ricardo and Polak, Meraida and Chanan, Siddharthan and Colville, Shuna and Swingler, Robert and Morrison, Karen E and Shaw, Pamela J and Hardy, John and Orrell, Richard W and Pittman, Alan and Sidle, Katie and Fratta, Pietro and Malaspina, Anea and Topp, Simon and Petri, Susanne and Abdulla, Susanne and pper, Carsten and Sendtner, Michael and Meyer, Thomas and Ophoff, Roel A and Staats, Kim A and Wiedau-Pazos, Martina and Lomen-Hoerth, Catherine and van Deerlin, Vivianna M and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Basak, A. Nazli and Tunca, Ceren and Hamzeiy, Hamid and Parman, Yesim and Meitinger, Thomas and Lichtner, Peter and Radivojkov-Blagojevic, Milena and Anes, Christian R and Maurel, Cindy and Bensimon, Gilbert and Landwehrmeyer, Bernhard and Brice, Alexis and Payan, Christine A. M and Saker-Delye, Safaa and Dürr, Alexana and Wood, Nicholas W and Tittmann, Lukas and Lieb, Wolfgang and Franke, Ane and Rietschel, Marcella and Cichon, Sven and Nöthen, Markus M and Amouyel, Philippe and Tzourio, Christophe and Dartigues, Jean-François and Uitterlinden, Ane G and Rivadeneira, Fernando and Estrada, Karol and Hofman, Albert and Curtis, Charles and Blauw, Hylke M and van der Kooi, Anneke J and ... and PARALS Registry and FALS Sequencing Consortium and SLALOM Grp and SLAGEN Consortium and NNIPPS Study Grp and SLAP Registry and SLALOM Group and NNIPPS Study Group and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Klinisk neurovetenskap and Umeå universitet
Nature genetics, ISSN 1061-4036, 2016, Volume 48, Issue 9, pp. 1043 - 1048
To elucidate the genetic architecture of amyotrophic lateral sclerosis (ALS) and find associated loci, we assembled a custom imputation reference panel from... 
PATHWAYS | POPULATION | COMPLEX | FRONTOTEMPORAL DEMENTIA | SUSCEPTIBILITY | SEQUENCE | GENETICS & HEREDITY | ALS | PITFALLS | HEXANUCLEOTIDE REPEAT | EFFICIENT | Proteins - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Munc18 Proteins - genetics | Amyotrophic Lateral Sclerosis - genetics | Humans | Netherlands - epidemiology | Mutation - genetics | Myelin Proteins - genetics | Case-Control Studies | Amyotrophic Lateral Sclerosis - epidemiology | Cohort Studies | Studies | Haplotypes | Consortia | Amyotrophic lateral sclerosis | Genomes | Quality control | Index Medicus | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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2. Predicting Matching Quality of Record Linkage Algorithms on Growing Data Sets
by Schuster, Martin and Tittmann, Lukas and Wolf, Andreas
Studies in health technology and informatics, ISSN 0926-9630, 2018, Volume 253, pp. 70 - 74
A record linkage algorithm tries to identify records which belong to the same individual. We analyze the matching behavior of an approach used in the E-PIX... 
parameterization | data integration | Record linkage | Algorithms | Medical Record Linkage | Data Accuracy | Information Storage and Retrieval
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3. Full Text Reduced microbiome alpha diversity in young patients with ADHD
by Prehn-Kristensen, Alexander and Zimmermann, Alexandra and Tittmann, Lukas and Lieb, Wolfgang and Schreiber, Stefan and Baving, Lioba and Fischer, Annegret
PLoS ONE, ISSN 1932-6203, 07/2018, Volume 13, Issue 7, pp. e0200728 - e0200728
ADHD is a psychiatric disorder which is characterized by hyperactivity, impulsivity and attention problems. Due to recent findings of microbial involvement in... 
MOLECULAR-GENETICS | ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | GUT-MICROBIOTA | NEUROPSYCHIATRIC DISORDERS | DEFICIT HYPERACTIVITY DISORDER | MULTIDISCIPLINARY SCIENCES | IRON-DEFICIENCY | RATING-SCALE | DOPAMINE TRANSPORTER | BRAIN | CHILDREN | Neisseria - isolation & purification | Attention Deficit Disorder with Hyperactivity - microbiology | Humans | Gastrointestinal Microbiome | Male | Biodiversity | Neisseria - classification | DNA, Bacterial - genetics | Attention Deficit Disorder with Hyperactivity - genetics | Adolescent | RNA, Bacterial - genetics | RNA, Ribosomal, 16S - genetics | Child | Neisseria - genetics | DNA, Ribosomal - genetics | Care and treatment | Research | Microbiota (Symbiotic organisms) | Analysis | Attention-deficit hyperactivity disorder | Biological diversity | Attention deficit disorder | rRNA 16S | Mental disorders | Hyperactivity | Pathogenesis | Microbiomes | Families & family life | Psychotherapy | Alcohol | Systematic review | Mental depression | Microbiota | Microorganisms | Bioindicators | Teenagers | Immune system | Dopamine | Attention deficit hyperactivity disorder | Behavior disorders | Patients | Children & youth | Studies | Autism | Hospitals | Biomarkers | Cocaine | Impulsive behavior | Molecular biology | Child & adolescent psychiatry | Index Medicus
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4. Full Text Phenotypes of organ involvement in sarcoidosis
by Schupp, Jonas Christian and Freitag-Wolf, Sandra and Bargagli, Elena and Mihailović-Vučinić, Violeta and Rottoli, Paola and Grubanovic, Aleksandar and Müller, Annegret and Jochens, Arne and Tittmann, Lukas and Schnerch, Jasmin and Olivieri, Carmela and Fischer, Annegret and Jovanovic, Dragana and Filipovic, Snežana and Videnovic-Ivanovic, Jelica and Bresser, Paul and Jonkers, René and O’Reilly, Kate and Ho, Ling-Pei and Gaede, Karoline I and Zabel, Peter and Dubaniewicz, Anna and Marshall, Ben and Kieszko, Robert and Milanowski, Janusz and Günther, Andreas and Weihrich, Anette and Petrek, Martin and Kolek, Vitezslav and Keane, Michael P and O’Beirne, Sarah and Donnelly, Seamas and Haraldsdottir, Sigridur Olina and Jorundsdottir, Kristin B and Costabel, Ulrich and Bonella, Francesco and Wallaert, Benoît and Grah, Christian and Peroš-Golubičić, Tatjana and Luisetti, Mauritio and Kadija, Zamir and Pabst, Stefan and Grohé, Christian and Strausz, János and Vašáková, Martina and Sterclova, Martina and Millar, Ann and Homolka, Jiří and Slováková, Alena and Kendrick, Yvonne and Crawshaw, Anjali and Wuyts, Wim and Spencer, Lisa and Pfeifer, Michael and Valeyre, Dominique and Poletti, Venerino and Wirtz, Hubertus and Prasse, Antje and Schreiber, Stefan and Krawczak, Michael and Müller-Quernheim, Joachim
European Respiratory Journal, ISSN 0903-1936, 01/2018, Volume 51, Issue 1, pp. 1700991 - 1700991
Sarcoidosis is a highly variable, systemic granulomatous disease of hitherto unknown aetiology. The GenPhenReSa (Genotype-Phenotype Relationship in... 
INSTRUMENT | INFLAMMATORY-BOWEL-DISEASE | RESPIRATORY SYSTEM | JAPAN | RISK | COHORT | PREVALENCE | EPIDEMIOLOGY | Sarcoidosis - diagnosis | Acute Disease | Europe | Humans | Middle Aged | European Continental Ancestry Group | Genotype | Male | Lung - physiopathology | Tertiary Healthcare | Lymph Nodes - physiopathology | Abdomen | Forced Expiratory Volume | Phenotype | Sarcoidosis - physiopathology | Skin Diseases - physiopathology | Adult | Female | Aged | Lung Diseases - physiopathology | Skin - physiopathology | Eye Diseases - physiopathology | Eye - physiopathology | Joint Diseases - physiopathology | Phenotypes | Sarcoidosis | Central nervous system | Fatigue | Skin | Heart diseases | Genotypes | Lymph nodes | Index Medicus
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5. Full Text The impact of rare variants in FUS in essential tremor
by Hopfner, Franziska and Stevanin, Giovanni and Müller, Stefanie H and Mundwiller, Emeline and Bungeroth, May and Durr, Alexandra and Pendziwiat, Manuela and Anheim, Mathieu and Schneider, Susanne A and Tittmann, Lukas and Klebe, Stephan and Lorenz, Delia and Deuschl, Günther and Brice, Alexis and Kuhlenbäumer, Gregor
Movement Disorders, ISSN 0885-3185, 04/2015, Volume 30, Issue 5, pp. 721 - 724
ObjectiveWe analyzed the coding region of the Fused in Sarcoma (FUS) gene in familial essential tremor (ET) and reviewed previous studies assessing FUS... 
tremor | essential tremor | genetics | meta‐analysis | FUS | Genetics | Tremor | Essential tremor | Meta-analysis | MOVEMENT-DISORDER | GENE | meta-analysis | COMMON | CLINICAL NEUROLOGY | Essential Tremor - genetics | Humans | Middle Aged | RNA-Binding Protein FUS - genetics | Male | Mutation - genetics | Databases, Bibliographic - statistics & numerical data | DNA Mutational Analysis | Aged, 80 and over | Adult | Female | Aged | France | Germany | Index Medicus
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6. Full Text Genome-wide association study of myocardial infarction, atrial fibrillation, acute stroke, acute kidney injury and delirium after cardiac surgery - a sub-analysis of the RIPHeart-Study
by Westphal, Sabine and Westphal, Sabine and Stoppe, Christian and Stoppe, Christian and Gruenewald, Matthias and Gruenewald, Matthias and Bein, Berthold and Bein, Berthold and Renner, Jochen and Renner, Jochen and Cremer, Jochen and Cremer, Jochen and Coburn, Mark and Coburn, Mark and Schaelte, Gereon and Schaelte, Gereon and Boening, Andreas and Boening, Andreas and Niemann, Bernd and Niemann, Bernd and Kletzin, Frank and Kletzin, Frank and Roesner, Jan and Roesner, Jan and Strouhal, Ulrich and Strouhal, Ulrich and Reyher, Christian and Reyher, Christian and Laufenberg-Feldmann, Rita and Laufenberg-Feldmann, Rita and Ferner, Marion and Ferner, Marion and Brandes, Ivo F and Brandes, Ivo F and Bauer, Martin and Bauer, Martin and Kortgen, Andreas and Kortgen, Andreas and Stehr, Sebastian N and Stehr, Sebastian N and Wittmann, Maria and Wittmann, Maria and Baumgarten, Georg and Baumgarten, Georg and Struck, Rafael and Struck, Rafael and Meyer-Treschan, Tanja and Meyer-Treschan, Tanja and Kienbaum, Peter and Kienbaum, Peter and Heringlake, Matthias and Heringlake, Matthias and Schoen, Julika and Schoen, Julika and Sander, Michael and Sander, Michael and Treskatsch, Sascha and Treskatsch, Sascha and Smul, Thorsten and Smul, Thorsten and Wolwender, Ewa and Wolwender, Ewa and Schilling, Thomas and Schilling, Thomas and Degenhardt, Frauke and Degenhardt, Frauke and Franke, Andre and Franke, Andre and Mucha, Soeren and Mucha, Soeren and Tittmann, Lukas and Tittmann, Lukas and Kohlhaas, Madeline and Kohlhaas, Madeline and Fuernau, Georg and Fuernau, Georg and Brosteanu, Oana and Brosteanu, Oana and Hasenclever, Dirk and Hasenclever, Dirk and Zacharowski, Kai and Zacharowski, Kai and Meybohm, Patrick and Stevanovic, Ana and Rossaint, Rolf and Felzen, Marc and Goetzenich, Andreas and Moormann, Tobias and Chalk, Katharina and Knuefermann, Pascal and Boehm, Olaf and Hoeft, Andreas and Winterhalter, Michael and Iken, Sonja and Weber, Christian and Wiedenbeck, Carolin and Schwarzmann, Gerhard and Pense, Karin and Fichtlscherer, Andreas Zierer Stephan and Goerlach, Gerold and ... and RIPHeart-Study Collaborators
BMC cardiovascular disorders, ISSN 1471-2261, 01/2019, Volume 19, Issue 1, pp. 26 - 26
BackgroundThe aim of our study was the identification of genetic variants associated with postoperative complications after cardiac surgery.MethodsWe conducted... 
Delirium | Myocardial infarction | Stroke | Genome-wide association study | Acute kidney injury | Atrial fibrillation | Cardiac surgery | DEFINITION | PHLPP2 | ACTIVATION | CARDIAC & CARDIOVASCULAR SYSTEMS | KINASE | MECHANISMS | CA2 | DYSFUNCTION | INFLAMMATORY RESPONSE | CEREBRAL ISCHEMIA/REPERFUSION INJURY | Heart | Medical research | Genome-wide association studies | Usage | Complications | Surgery | Medicine, Experimental | Genetic aspects | Research | Heart attack | Risk factors | Oxidative stress | Cardiac arrhythmia | Heart attacks | Heart surgery | Clinical trials | Ryanodine receptors | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Fibrillation | Ischemia | Rodents | Chromosomes | Cerebral infarction | Kidneys | Mortality | Studies | Genetic variance | Coronary vessels | Quality control | Renal failure
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7. Full Text No association between Parkinson disease and autoantibodies against NMDA-type glutamate receptors
by Hopfner, F and Muller, SH and Steppat, D and Miller, J and Schmidt, N and Wandinger, KP and Leypoldt, F and Berg, D and Franke, A and Lieb, W and Tittmann, L and Balzer-Geldsetzer, M and Baudrexel, S and Dodel, R and Hilker-Roggendorf, R and Kalbe, E and Kassubek, J and Klockgether, T and Liepelt-Scarfone, I and Mollenhauer, B and Neuser, P and Reetz, K and Riedel, O and Schulte, C and Schulz, JB and Spottke, A and Storch, A and Trenkwalder, C and Wittchen, HU and Witt, K and Wullner, U and Deuschl, G and Kuhlenbeumer, G
TRANSLATIONAL NEURODEGENERATION, ISSN 2047-9158, 04/2019, Volume 8, Issue 1, pp. 11 - 11
Background: IgG-class autoantibodies to N-Methyl-D-Aspartate (NMDA)-type glutamate receptors define a novel entity of autoimmune encephalitis. Studies... 
Parkinson disease | NMDA IgA/IgM antibodies | DEMENTIA | NMDA antibody | NEUROSCIENCES | Cognitive impairment | Studies | Encephalitis | Medical research | Neurology | Emotional disorders | Memory | Parkinsons disease | Cognitive ability | Standard deviation | Patients | Age | Dementia
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8. Full Text Genome-wide association study in essential tremor identifies three new loci
by Müller, Stefanie H and Girard, Simon L and Hopfner, Franziska and Merner, Nancy D and Bourassa, Cynthia V and Lorenz, Delia and Clark, Lorraine N and Tittmann, Lukas and Soto-Ortolaza, Alexandra I and Klebe, Stephan and Hallett, Mark and Schneider, Susanne A and Hodgkinson, Colin A and Lieb, Wolfgang and Wszolek, Zbigniew K and Pendziwiat, Manuela and Lorenzo-Betancor, Oswaldo and Poewe, Werner and Ortega-Cubero, Sara and Seppi, Klaus and Rajput, Alex and Hussl, Anna and Rajput, Ali H and Berg, Daniela and Dion, Patrick A and Wurster, Isabel and Shulman, Joshua M and Srulijes, Karin and Haubenberger, Dietrich and Pastor, Pau and Vilariño-Güell, Carles and Postuma, Ronald B and Bernard, Geneviève and Ladwig, Karl-Heinz and Dupré, Nicolas and Jankovic, Joseph and Strauch, Konstantin and Panisset, Michel and Winkelmann, Juliane and Testa, Claudia M and Reischl, Eva and Zeuner, Kirsten E and Ross, Owen A and Arzberger, Thomas and Chouinard, Sylvain and Deuschl, Günther and Louis, Elan D and Kuhlenbäumer, Gregor and Rouleau, Guy A
Brain, ISSN 0006-8950, 2016, Volume 139, Issue 12, pp. 3163 - 3169
We conducted a genome-wide association study of essential tremor, a common movement disorder characterized mainly by a postural and kinetic tremor of the upper... 
Genetics | Genome-wide association study | Tremor | Essential tremor | Movement disorders | tremor | genetics | genome-wide association study | DISEASE | essential tremor | movement disorders | QUALITY-CONTROL | NEUROSCIENCES | CLINICAL NEUROLOGY | TOOL | Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alpha - genetics | Genome-Wide Association Study | Essential Tremor - genetics | Humans | Protein-Serine-Threonine Kinases - genetics | Polymorphism, Single Nucleotide | alpha Catenin - genetics | Index Medicus | Abridged Index Medicus | 1030 | Original
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9. Full Text The impact of rare variants inFUSin essential tremor
: FUSin ET
by Hopfner, Franziska and Stevanin, Giovanni and Müller, Stefanie H and Mundwiller, Emeline and Bungeroth, May and Durr, Alexandra and Pendziwiat, Manuela and Anheim, Mathieu and Schneider, Susanne A and Tittmann, Lukas and Klebe, Stephan and Lorenz, Delia and Deuschl, Günther and Brice, Alexis and Kuhlenbäumer, Gregor
Movement Disorders, ISSN 0885-3185, 04/2015, Volume 30, Issue 5, pp. 721 - 724
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10. Full Text Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
by McLaughlin, Russell L and Schijven, Dick and van Rheenen, Wouter and van Eijk, Kristel R and O'Brien, Margaret and Kahn, René S and Ophoff, Roel A and Goris, An and Bradley, Daniel G and Al-Chalabi, Ammar and van den Berg, Leonard H and Luykx, Jurjen J and Hardiman, Orla and Veldink, Jan H and Shatunov, Aleksey and Dekker, Annelot M and Diekstra, Frank P and Pulit, Sara L and van der Spek, Rick A. A and van Doormaal, Perry T. C and Sproviero, William and Jones, Ashley R and Nicholson, Garth A and Rowe, Dominic B and Pamphlett, Roger and Kiernan, Matthew C and Bauer, Denis and Kahlke, Tim and Williams, Kelly and Eftimov, Filip and Fogh, Isabella and Ticozzi, Nicola and Lin, Kuang and Millecamps, Stéphanie and Salachas, François and Meininger, Vincent and de Carvalho, Mamede and Pinto, Susana and Mora, Jesus S and Rojas-García, Ricardo and Polak, Meraida and Chanan, Siddharthan and Colville, Shuna and Swingler, Robert and Morrison, Karen E and Shaw, Pamela J and Hardy, John and Orrell, Richard W and Pittman, Alan and Sidle, Katie and Fratta, Pietro and Malaspina, Anea and Petri, Susanne and Abdulla, Susanna and pper, Carsten and Sendtner, Michael and Meyer, Thomas and Wiedau-Pazos, Martina and Lomen-Hoerth, Catherine and van Deerlin, Vivianna M and Trojanowski, John Q and Elman, Lauren and McCluskey, Leo and Basak, Nazli and Meitinger, Thomas and Lichtner, Peter and Blagojevic-Radivojkov, Milena and Anes, Christian R and Maurel, Cindy and Bensimon, Gilbert and Landwehrmeyer, Bernhard and Brice, Alexis and Payan, Christine A. M and Saker-Delye, Safa and Dürr, Alexana and Wood, Nicholas and Tittmann, Lukas and Lieb, Wolfgang and Franke, Ane and Rietschel, Marcella and Cichon, Sven and Nöuthen, Markus M and Amouyel, Philippe and Tzourio, Christophe and Dartigues, Jean-François and Uitterlinden, Ane G and Rivadeneira, Fernando and Estrada, Karol and Hofman, Albert and Curtis, Charles and van der Kooi, Anneke J and de Visser, Marianne and Weber, Markus and Shaw, Christopher E and Smith, Bradley N and Pansarasa, Orietta and Cereda, Cristina and del Bo, Roberto and Comi, Giacomo P and D'alfonso, Sana and ... and Project MinE GWAS Consortium and Schizophrenia Working Grp Psychiat and Schizophrenia Working Group of the Psychiatric Genomics Consortium
Nature communications, ISSN 2041-1723, 2017, Volume 8, Issue 1, pp. 14774 - 14774
We have previously shown higher-than-expected rates of schizophrenia in relatives of patients with amyotrophic lateral sclerosis (ALS), suggesting an... 
METAANALYSIS | VARIANTS | MULTIDISCIPLINARY SCIENCES | DISEASE | SUSCEPTIBILITY LOCI | ARCHITECTURE | PLEIOTROPY | BIPOLAR DISORDER | GENOME-WIDE ASSOCIATION | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Comorbidity | Amyotrophic Lateral Sclerosis - genetics | Humans | Linear Models | Multifactorial Inheritance | Schizophrenia - epidemiology | Case-Control Studies | Linkage Disequilibrium | Schizophrenia - genetics | Family | Polymorphism, Single Nucleotide | Odds Ratio | Amyotrophic Lateral Sclerosis - epidemiology | Cohort Studies | Index Medicus
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11. Full Text Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
by Schormair, Barbara and Zhao, Chen and Bell, Steven and Tilch, Erik and Salminen, Aaro V and Pütz, Benno and Dauvilliers, Yves and Stefani, Ambra and Högl, Birgit and Poewe, Werner and Kemlink, David and Sonka, Karel and Bachmann, Cornelius G and Paulus, Walter and Trenkwalder, Claudia and Oertel, Wolfgang H and Hornyak, Magdolna and Teder-Laving, Maris and Metspalu, Andres and Hadjigeorgiou, Georgios M and Polo, Olli and Fietze, Ingo and Ross, Owen A and Wszolek, Zbigniew and Butterworth, Adam Stuart and Soranzo, Nicole and Ouwehand, Willem Hendrik and Roberts, David J and Danesh, John and Allen, Richard P and Earley, Christopher J and Ondo, William G and Xiong, Lan and Montplaisir, Jacques and Gan-Or, Ziv and Perola, Markus and Vodicka, Pavel and Dina, Christian and Franke, Andre and Tittmann, Lukas and Stewart, Alexandre FR and Shah, Svati H and Gieger, Christian and Peters, Annette and Rouleau, Guy A and Berger, Klaus and Oexle, Konrad and Di Angelantonio, Emanuele and Hinds, David A and Müller-Myhsok, Bertram and Winkelmann, Juliane and 23andMe Research Team and DESIR study group
ISSN 1474-4422, 2017
BACKGROUND: Restless legs syndrome is a prevalent chronic neurological disorder with potentially severe mental and physical health consequences. Clearer... 
Genetic Predisposition to Disease | Genome-Wide Association Study | Semaphorins | Humans | GPI-Linked Proteins | Restless Legs Syndrome | European Continental Ancestry Group | Nerve Tissue Proteins | Transcription Factors | DNA-Binding Proteins
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12. Full Text Rare variants in ANO3 are not a susceptibility factor in essential tremor
by Hopfner, Franziska and Bungeroth, May and Pendziwiat, Manuela and Tittmann, Lukas and Deuschl, Günther and Schneider, Susanne A and Kuhlenbäumer, Gregor
Parkinsonism and Related Disorders, ISSN 1353-8020, 2013, Volume 20, Issue 1, pp. 134 - 135
Neurology | Genetics | Dystonia | Tremor | Essential tremor | ANO3 | MUTATIONS | CLINICAL NEUROLOGY | Genetic Predisposition to Disease - genetics | Essential Tremor - genetics | Humans | Middle Aged | Female | Male | Aged | Polymorphism, Single Nucleotide | Anoctamins | Chloride Channels - genetics | Reverse Transcriptase Polymerase Chain Reaction | Index Medicus
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