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1. Full Text A pharmacogenetic intervention for the improvement of the safety profile of antipsychotic treatments
by Arranz, MJ and Gonzalez-Rodriguez, A and Perez-Blanco, J and Penades, R and Gutierrez, B and Ibanez, L and Arias, B and Brunet, M and Cervilla, J and Salazar, J and Catalan, R
TRANSLATIONAL PSYCHIATRY, ISSN 2158-3188, 07/2019, Volume 9, Issue 1, pp. 177 - 8
Antipsychotic drugs fail to achieve adequate response in 30-50% of treated patients and about 50% of them develop severe and lasting side effects. Treatment... 
CYTOCHROME-P450 | ANTIDEPRESSANT | COSTS | METABOLISM | CYP2D6 | GENETICS | PSYCHIATRY | SCHIZOPHRENIA | GUIDANCE | Intervention | Psychotropic drugs | Index Medicus
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2. Tailoring psychiatric treatment using genetic information
: pharmacogenetic prediction of treatment response
by Arranz, Maria J
2007, Psychopharmacogenetics : genetic factors influencing the kinetics and dynamics of psychotropic drugs
Pharmacogenetics | Psychopharmacology | Psychotropic Drugs
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3. Tailoring psychiatric treatment using genetic information
: pharmacogenetic prediction of treatment response
by Arranz, Maria J
2007, Psychopharmacogenetics : genetic factors influencing the kinetics and dynamics of psychotropic drugs
Pharmacogenetics | Psychopharmacology | Psychotropic Drugs
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4. Influence of neurotransmitter receptor variants on interactions with psychotropic drugs
by Arranz, Maria J
2007, Psychopharmacogenetics : genetic factors influencing the kinetics and dynamics of psychotropic drugs
Pharmacogenetics | Psychopharmacology | Psychotropic Drugs
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5. Influence of neurotransmitter receptor variants on interactions with psychotropic drugs
by Arranz, Maria J
2007, Psychopharmacogenetics : genetic factors influencing the kinetics and dynamics of psychotropic drugs
Pharmacogenetics | Psychopharmacology | Psychotropic Drugs
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6. Full Text Positive parenting in Spain: introduction to the special issue
by Arranz Freijo, Enrique B and Rodrigo López, Maria J
Early Child Development and Care, ISSN 0300-4430, 11/2018, Volume 188, Issue 11, pp. 1503 - 1513
This introduction presents a general overview of the regulations, policies, programmes and actions which currently exist in Spain within the field of positive... 
Positive parenting | family policy | EDUCATION & EDUCATIONAL RESEARCH | IMPLEMENTATION | PROGRAMS | PSYCHOLOGY, DEVELOPMENTAL | Leisure Time | Parenting Styles | Public Policy | Program Descriptions | Foreign Countries | Family Relationship | Program Design | Family Programs | Young Children | Parent Child Relationship | Nongovernmental Organizations | Perinatal Influences | Child Development | Toddlers | Children | Foster Care | Parent Education | Health promotion | Reunification | Antenatal | Perinatal | Foster care | Childbirth & labor | Temporary foster care | Parents & parenting | Parenting skills | Family support | Child development | Leisure | Childhood | Nongovernmental organizations | Regulation
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7. Full Text Tu1293 Soluble TNF Serum Levels During the Induction Phase in Crohn's Disease Patients With Anti-TNF Treatment
by Chaparro, Maria and Guerra, Iván and Iborra, Marisa and Nuño, Jose Luis Cabriada and Bujanda, Luis and Taxonera, Carlos and García-Sánchez, Valle and Marin-Jimenez, Ignacio and Barreiro-de Acosta, Manuel and Vera, Isabel and Arranz, María Dolores Martín and Hernandez-Breijo, Borja and Mesonero, Francisco and Sempere, Laura and Arroyo, María Teresa and Hinojosa, Joaquin and Ramas, Mercedes and Algaba, Alicia and Beltran, Belen and Pescador, Ainhoa Rodriguez and Perugorría, Maria J and Olivares, David and Cantero, Jose Manuel Benitez and Tardío, Lidia and Ferreiro, Rocio and Royo, Virginia Matallana and Senent, Silvia Gomez and Guijarro, Luis and Gisbert, Javier P
Gastroenterology, ISSN 0016-5085, 2015, Volume 148, Issue 4, pp. S-850 - S-850
Gastroenterology and Hepatology | Tumor necrosis factor
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8. Full Text Long-term effectiveness of a smartphone app for improving healthy lifestyles in general population in primary care: Randomized controlled trial (evident II study)
by Garcia-Ortiz, Luis and Recio-Rodriguez, Jose Ignacio and Agudo-Conde, Cristina and Patino-Alonso, María Carmen and Maderuelo-Fernandez, Jose-Angel and Gento, Irene Repiso and Puig, Elisa Puigdomenech and Gonzalez-Viejo, Natividad and Arietaleanizbeaskoa, Maria Soledad and Schmolling-Guinovart, Yolanda and Gomez-Marcos, Manuel Angel and Rodriguez-Sanchez, Emiliano and Mobilizing Minds Research Group and EVIDENT Investigators Group
Journal of Medical Internet Research, ISSN 2291-5222, 04/2018, Volume 20, Issue 4, pp. e107 - e107
Information and communication technologies are currently among the supporting elements that may contribute to improving health and changing lifestyles. The aim... 
Exercise | Mediterranean diet | Smartphone | Vascular stiffness
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9. Full Text Genome-wide association analysis identifies 13 new risk loci for schizophrenia
by Ripke, Stephan and O'Dushlaine, Colm and Chambert, Kimberly and Moran, Jennifer L and Kähler, Anna K and Akterin, Susanne and Bergen, Sarah E and Collins, Ann L and Crowley, James J and Fromer, Menachem and Kim, Yunjung and Lee, Sang Hong and Magnusson, Patrik K. E and Sanchez, Nick and Stahl, Eli A and Williams, Stephanie and Wray, Naomi R and Xia, Kai and Bettella, Francesco and Borglum, Anders D and Bulik-Sullivan, Brendan K and Cormican, Paul and Craddock, Nick and de Leeuw, Christiaan and Durmishi, Naser and Gill, Michael and Golimbet, Vera and Hamshere, Marian L and Holmans, Peter and Hougaard, David M and Kendler, Kenneth S and Lin, Kuang and Morris, Derek W and Mors, Ole and Mortensen, Preben B and Neale, Benjamin M and O'Neill, Francis A and Owen, Michael J and Milovancevic, Milica Pejovic and Posthuma, Danielle and Powell, John and Richards, Alexander L and Riley, Brien P and Ruderfer, Douglas and Rujescu, Dan and Sigurdsson, Engilbert and Silagadze, Teimuraz and Smit, August B and Stefansson, Hreinn and Steinberg, Stacy and Suvisaari, Jaana and Tosato, Sarah and Verhage, Matthijs and Walters, James T and Levinson, Douglas F and Gejman, Pablo V and Laurent, Claudine and Mowry, Bryan J and O'Donovan, Michael C and Pulver, Ann E and Schwab, Sibylle G and Wildenauer, Dieter B and Dudbridge, Frank and Shi, Jianxin and Albus, Margot and Alexander, Madeline and Campion, Dominique and Cohen, David and Dikeos, Dimitris and Duan, Jubao and Eichhammer, Peter and Godard, Stephanie and Hansen, Mark and Lerer, F. Bernard and Liang, Kung-Yee and Maier, Wolfgang and Mallet, Jacques and Nertney, Deborah A and Nestadt, Gerald and Norton, Nadine and Papadimitriou, George N and Ribble, Robert and Sanders, Alan R and Silverman, Jeremy M and Walsh, Dermot and Williams, Nigel M and Wormley, Brandon and Arranz, Maria J and Bakker, Steven and Bender, Stephan and Bramon, Elvira and Collier, David and Crespo-Facorro, Benedicto and Hall, Jeremy and Iyegbe, Conrad and Jablensky, Assen and Kahn, Rene S and Kalaydjieva, Luba and Lawrie, Stephen and Lewis, Cathryn M and ... and Multictr Genetic Studies Schizophr and Wellcome Trust Case Control Consor and Psychosis Endophenotypes Int Conso and Wellcome Trust Case Control Consortium 2 and Multicenter Genetic Studies of Schizophrenia Consortium and Psychosis Endophenotypes International Consortium
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 10, pp. 1150 - 1159
Schizophrenia is an idiopathic mental disorder with a heritable component and a substantial public health impact. We conducted a multi-stage genome-wide... 
DEPENDENT CALCIUM-CHANNELS | INDIVIDUALS | COMMON VARIANTS | DE-NOVO | METAANALYSIS | SUSCEPTIBILITY | GENETICS & HEREDITY | GENE-EXPRESSION | BIPOLAR DISORDER | PARTICIPATION | MICRORNA | Genetic Predisposition to Disease | Genome-Wide Association Study | Sweden | Schizophrenia - genetics | Humans | Female | Male | Polymorphism, Single Nucleotide | Case-Control Studies | Schizophrenia | Genetic aspects | Single nucleotide polymorphisms | Research | Risk factors | Studies | Councils | Sample size | Genomics | Genomes | Chromosomes | Index Medicus | Medicinsk genetik | Hälsovetenskap | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Psykiatri | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Klinisk medicin
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10. Full Text Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
by Ruderfer, Douglas M and Ripke, Stephan and McQuillin, Andrew and Boocock, James and Stahl, Eli A and Pavlides, Jennifer M. Whitehead and Mullins, Niamh and Charney, Alexander W and Ori, Anil P.S and Loohuis, Loes M. Olde and Domenici, Enrico and Di Florio, Arianna and Papiol, Sergi and Kalman, Janos L and Trubetskoy, Vassily and Adolfsson, Rolf and Agartz, Ingrid and Agerbo, Esben and Akil, Huda and Albani, Diego and Albus, Margot and Alda, Martin and Alexander, Madeline and Alliey-Rodriguez, Ney and Als, Thomas D and Amin, Farooq and Anjorin, Adebayo and Arranz, Maria J and Awasthi, Swapnil and Bacanu, Silviu A and Badner, Judith A and Baekvad-Hansen, Marie and Bakker, Steven and Band, Gavin and Barchas, Jack D and Barroso, Ines and Bass, Nicholas and Bauer, Michael and Baune, Bernhard T and Begemann, Martin and Bellenguez, Celine and Belliveau, Richard A and Bellivier, Frank and Bender, Stephan and Bene, Judit and Bergen, Sarah E and Berrettini, Wade H and Bevilacqua, Elizabeth and Biernacka, Joanna M and Bigdeli, Tim B and Black, Donald W and Blackburn, Hannah and Blackwell, Jenefer M and Blackwood, Douglas H.R and Pedersen, Marianne Giortz and Pedersen, Carsten Bocker and Boehnke, Michael and Boks, Marco and Borglum, Anders D and Bramon, Elvira and Breen, Gerome and Brown, Matthew A and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Budde, Monika and Bulik-Sullivan, Brendan and Bumpstead, Suzannah J and Bunney, William and Burmeister, Margit and Buxbaum, Joseph D and Bybjerg-Grauholm, Jonas and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Cairns, Murray J and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Casas, Miquel and Casas, Juan P and Catts, Stanley V and Cervantes, Pablo and Chambert, Kimberley D and Chan, Raymond C.K and Chen, Eric Y.H and Chen, Ronald Y.L and Cheng, Wei and Cheung, Eric F.C and Chong, Siow Ann and Clarke, Toni-Kim and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Coleman, Jonathan R.I and Collier, David A and Cormican, Paul and Coryell, William and Craddock, Nicholas and ... and Psychosis Endophenotypes Inter and Psychiat Genomics Consortium and Wellcome Trust Case-Control and Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium. Electronic address: douglas.ruderfer@vanderbilt.edu
Cell, ISSN 0092-8674, 06/2018, Volume 173, Issue 7, pp. 1705 - 1715.e16
Schizophrenia and bipolar disorder are two distinct diagnoses that share symptomology. Understanding the genetic factors contributing to the shared and... 
bipolar disorder | schizophrenia | subphenotypes | psychosis | polygenic risk | GWAS | GENE | DETERMINANTS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE ASSOCIATIONS | PSYCHIATRIC-DISORDERS | RISK | WIDE ASSOCIATION | COPY NUMBER VARIATION | TRAITS | IDENTIFICATION | CELL BIOLOGY | Index Medicus
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11. Full Text Association between 5-HT(2A) gene promoter polymorphism and anorexia nervosa [5]
by Collier, David A and Arranz, Maria J and Li, Tao and Mupita, Dennis and Brown, Nigel and Treasure, Janet
Lancet, ISSN 0140-6736, 08/1997, Volume 350, Issue 9075, p. 412
  Collier et al found that the rise in estrogen at puberty in the context of stress might destabilize the serotonin-hypothalamic pituitary-adrenal body... 
Genetics | Anorexia | Biochemistry | Estrogen
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12. Full Text Paternally inherited cis-regulatory structural variants are associated with autism
by Brandler, William M and Antaki, Danny and Gujral, Madhusudan and Kleiber, Morgan L and Whitney, Joe and Maile, Michelle S and Hong, Oanh and Chapman, Timothy R and Tan, Shirley and Tandon, Prateek and Pang, Timothy and Tang, Shih C and Vaux, Keith K and Yang, Yan and Harrington, Eoghan and Juul, Sissel and Turner, Daniel J and Thiruvahindrapuram, Bhooma and Kaur, Gaganjot and Wang, Zhuozhi and Kingsmore, Stephen F and Gleeson, Joseph G and Bisson, Denis and Kakaradov, Boyko and Telenti, Amalio and Venter, J. Craig and Corominas, Roser and Toma, Claudio and Cormand, Bru and Rueda, Isabel and Guijarro, Silvina and Messer, Karen S and Nievergelt, Caroline M and Arranz, Maria J and Courchesne, Eric and Pierce, Karen and Muotri, Alysson R and Iakoucheva, Lilia M and Hervas, Amaia and Scherer, Stephen W and Corsello, Christina and Sebat, Jonathan
Science, ISSN 0036-8075, 04/2018, Volume 360, Issue 6386, pp. 327 - 331
The genetic basis of autism spectrum disorder (ASD) is known to consist of contributions from de novo mutations in variant-intolerant genes. We hypothesize... 
DE-NOVO | RARE | SPECTRUM DISORDER | MULTIDISCIPLINARY SCIENCES | GENES | TRANSCRIPTION | ARCHITECTURE | PATTERNS | RISK | MUTATIONS | GENOME | Autism Spectrum Disorder - genetics | Sequence Deletion | Genetic Predisposition to Disease | Exons | Humans | Gene Expression Regulation | Selection, Genetic | Transcription Factors - genetics | Promoter Regions, Genetic - genetics | RNA, Untranslated - genetics | Genetic Variation | Pedigree | Mutation | Genome, Human | Paternal Inheritance | Autism | Genetic aspects | Genetic variation | Health aspects | Genetic variance | Offspring | Genes | Genomes | Regulatory sequences | Children | Natural selection | Gene sequencing | Index Medicus
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13. Full Text 5-HT(2A) and 5-HT(2C) receptor polymorphisms and psychopathology in late onset Alzheimer's disease
by Holmes, Clive and Arranz, Maria J and Powell, John F and Collier, David A and Lovestone, Simon
Human Molecular Genetics, ISSN 0964-6906, 09/1998, Volume 7, Issue 9, pp. 1507 - 1509
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14. Full Text Neurophysiological mechanism of possibly confounding peripheral activation of the facial nerve during corticobulbar tract monitoring
by Téllez, Maria J and Ulkatan, Sedat and Urriza, Javier and Arranz-Arranz, Beatriz and Deletis, Vedran
Clinical Neurophysiology, ISSN 1388-2457, 2015, Volume 127, Issue 2, pp. 1710 - 1716
Highlights • Our results revealed a potential pitfall in the current methodology of facial corticobulbar tract monitoring due to possibly confounding facial... 
Neurology | Cranial nerve | Near-threshold | Intraoperative monitoring | Motor-evoked potential | Hyperexcitability | Corticobulbar tract | AXONS | MOTOR EVOKED-POTENTIALS | HUMAN MEDIAN NERVE | NEUROSCIENCES | CLINICAL NEUROLOGY | RECOVERY | EXCITABILITY | ELECTRICAL-STIMULATION | ANESTHETIZED HUMANS | Humans | Middle Aged | Child, Preschool | Male | Facial Nerve - physiology | Action Potentials - physiology | Young Adult | Peripheral Nerves - physiology | Adolescent | Adult | Female | Transcranial Direct Current Stimulation - methods | Child | Pyramidal Tracts - physiology | Neurophysiology | Index Medicus
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15. Full Text Impaired development of neocortical circuits contributes to the neurological alterations in DYRK1A haploinsufficiency syndrome
by Arranz, Juan and Balducci, Elisa and Arató, Krisztina and Sánchez-Elexpuru, Gentzane and Najas, Sònia and Parras, Alberto and Rebollo, Elena and Pijuan, Isabel and Erb, Ionas and Verde, Gaetano and Sahun, Ignasi and Barallobre, Maria J and Lucas, José J and Sánchez, Marina P and de la Luna, Susana and Arbonés, Maria L
Neurobiology of Disease, ISSN 0969-9961, 07/2019, Volume 127, pp. 210 - 222
Autism spectrum disorders are early onset neurodevelopmental disorders characterized by deficits in social communication and restricted repetitive behaviors,... 
Neurodevelopment | Cerebral cortex | DYRK1A mutations | Epilepsy | Autism spectrum disorder | Transcriptome | AUTISM | SPECIFICITY | PHOSPHORYLATION | KINASE | NEUROSCIENCES | INTELLECTUAL DISABILITY | GENE | DOWN-SYNDROME | NEUROGENESIS | MUTATIONS | AUTOPHOSPHORYLATION | Autism | Brain | Development and progression | Neurosciences | Down syndrome
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