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NeuroImage, ISSN 1053-8119, 04/2018, Volume 169, pp. 374 - 382
Manganese-enhanced magnetic resonance imaging (MEMRI) exploits the biophysical similarity of Ca and Mn to map the brain's activity . However, to what extent... 
Calcium channels | CACNA1C | Activity-dependent | Manganese enhanced MRI | Connectomics | Functional imaging | Index Medicus
Journal Article
Reports of biochemistry & molecular biology, ISSN 2322-3480, 04/2019, Volume 8, Issue 1, pp. 56 - 62
BackgroundAutism spectrum disorders (ASDs) (MIM 209850) are a group of distinct neurodevelopmental disorders characterized by impaired social interactions and... 
Autism Spectrum Disorder | polymorphism | CACNA1C | Channelopathy | Original
Journal Article
Journal of neurochemistry, ISSN 0022-3042, 7/2015, Volume 134, Issue 1, pp. 56 - 65
In neurons, calcium (Ca 2+ ) channels regulate a wide variety of functions ranging from synaptic transmission to gene expression. They also induce neuroplastic... 
calcium channel | CACNA1B | CACNA1C | MYC | Methamphetamine | calcium signaling
Journal Article
Revista Espanola de Cardiologia, ISSN 0300-8932, 2018
Introduction and objectives: A known long QT syndrome-related mutation in Nav1.5 cardiac channels (p.R1644H) was found in 4 members of a Spanish family but... 
Channelopathies | Nav1.5 | Long QT syndrome | CACNA1C | SCN5A | Cav1.2 | Patch-clamp
Journal Article
Lancet, The, ISSN 0140-6736, 2013, Volume 381, Issue 9875, pp. 1371 - 1379
Summary Background Findings from family and twin studies suggest that genetic contributions to psychiatric disorders do not in all cases map to present... 
Internal Medicine | POPULATION | DEPRESSION | MEDICINE, GENERAL & INTERNAL | ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | METAANALYSIS | GENE-EXPRESSION | SCHIZOPHRENIA | CACNA1C | AUTISM SPECTRUM DISORDERS | BIPOLAR DISORDER | ASSOCIATION | Child Development Disorders, Pervasive - epidemiology | Genome-Wide Association Study | Humans | Genetic Loci - genetics | Logistic Models | Bipolar Disorder - genetics | Depressive Disorder, Major - epidemiology | Schizophrenia - epidemiology | Calcium Channels, L-Type - genetics | Schizophrenia - genetics | Attention Deficit Disorder with Hyperactivity - genetics | Child Development Disorders, Pervasive - genetics | Depressive Disorder, Major - genetics | Age of Onset | Polymorphism, Single Nucleotide - genetics | Adult | Child | Bipolar Disorder - epidemiology | Attention Deficit Disorder with Hyperactivity - epidemiology | Physiological aspects | Genetic aspects | Research | Genetic variation | Mental illness | Risk factors | Medical research | Calcium channels | Genes | Depression, Mental | Genomics | Schizophrenia | Bipolar disorder | Child psychopathology | Quantitative genetics | Autism | Medicine, Experimental | Genetic research | Single nucleotide polymorphisms | Studies | Genetics | Children & youth | Attention deficit disorder | Enrichment | Brain | Calcium | Disease | Mental disorders | Hyperactivity | Mental health | Disorders | Genomes | Single-nucleotide polymorphism | Mental depression | Consortia | Datasets | Calcium signalling | Genetic effects | Signal transduction | Regression models | Autopsy | Classification | Psychopathology | Children | Chromosomes | Genotypes | Phenotypes | Channel gating | Attention deficit hyperactivity disorder | Calcium channels (voltage-gated) | Behavior disorders | Regression analysis | Risk analysis | Loci | Quantitative trait loci | Government grants | Calcium channels (L-type) | Diagnostic systems | Polygenic inheritance | Psychiatry | Polymorphism | Index Medicus | Abridged Index Medicus | Neurosciences | Calcium Channels | Pervasive | Attention Deficit Disorder with Hyperactivity | L-Type | Child Development Disorders | Depressive Disorder | Genetic Loci | Single Nucleotide | epidemiology | genetics | Bipolar Disorder | Major | Neurovetenskaper
Journal Article
by Sklar, Pamela and Ripke, Stephan and Scott, Laura J and Andreassen, Ole A and Cichon, Sven and Craddock, Nick and Edenberg, Howard J and Nurnberger Jr, John I and Rietschel, Marcella and Blackwood, Douglas and Corvin, Aiden and Flickinger, Matthew and Guan, Weihua and Mattingsdal, Morten and McQuillin, Andrew and Kwan, Phoenix and Wienker, Thomas F and Daly, Mark and Dudbridge, Frank and Holmans, Peter A and Lin, Danyu and Burmeister, Margit and Greenwood, Tiffany A and Hamshere, Marian L and Muglia, Pierandrea and Smith, Erin N and Zandi, Peter P and Nievergelt, Caroline M and McKinney, Rebecca and Shilling, Paul D and Schork, Nicholas J and Bloss, Cinnamon S and Foroud, Tatiana and Koller, Daniel L and Gershon, Elliot S and Liu, Chunyu and Badner, Judith A and Scheftner, William A and Lawson, William B and Nwulia, Evaristus A and Hipolito, Maria and Coryell, William and Rice, John and Byerley, William and McMahon, Francis J and Schulze, Thomas G and Berrettini, Wade and Lohoff, Falk W and Potash, James B and Mahon, Pamela B and McInnis, Melvin G and Zöllner, Sebastian and Zhang, Peng and Craig, David W and Szelinger, Szabocls and Barrett, Thomas B and Breuer, René and Meier, Sandra and Strohmaier, Jana and Witt, Stephanie H and Tozzi, Federica and Farmer, Anne and McGuffin, Peter and Strauss, John and Xu, Wei and Kennedy, James L and Vincent, John B and Matthews, Keith and Day, Richard and Ferreira, Manuel A and O'Dushlaine, Colm and Perlis, Roy and Raychaudhuri, Soumya and Ruderfer, Douglas and Lee, Phil H and Smoller, Jordan W and Li, Jun and Absher, Devin and Bunney, William E and Barchas, Jack D and Schatzberg, Alan F and Jones, Edward G and Meng, Fan and Thompson, Robert C and Watson, Stanley J and Myers, Richard M and Akil, Huda and Boehnke, Michael and Chambert, Kim and Moran, Jennifer and Scolnick, Ed and Djurovic, Srdjan and Melle, Ingrid and Morken, Gunnar and Gill, Michael and Morris, Derek and Quinn, Emma and Mühleisen, Thomas W and Degenhardt, Franziska A and Mattheisen, Manuel and ... and Psychiat GWAS Consortium Bipolar D and Psychiatric GWAS Consortium Bipolar Disorder Working Group and Sahlgrenska akademin and Institutionen för neurovetenskap och fysiologi, sektionen för psykiatri och neurokemi and Göteborgs universitet and Gothenburg University and Institute of Neuroscience and Physiology, Department of Psychiatry and Neurochemistry and Sahlgrenska Academy
Nature Genetics, ISSN 1061-4036, 10/2011, Volume 43, Issue 10, pp. 977 - 985
Journal Article
PROGRESS IN NEUROBIOLOGY, ISSN 0301-0082, 10/2012, Volume 99, Issue 1, pp. 1 - 14
Journal Article
Nature Communications, ISSN 2041-1723, 01/2016, Volume 7, Issue 1, p. 10370
Timothy Syndrome (TS) is a multisystem disorder, prominently featuring cardiac action potential prolongation with paroxysms of life-threatening arrhythmias.... 
VOLTAGE-DEPENDENT-INACTIVATION | CALMODULIN | MULTIDISCIPLINARY SCIENCES | CA2+ CHANNELS | SUDDEN CARDIAC DEATH | LONG QT SYNDROME | OF-FUNCTION MUTATIONS | CACNA1C | RAT VENTRICULAR MYOCYTES | SELECTIVITY | CALCIUM-CHANNEL
Journal Article