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M. Bayés · SciRah

Researcher profile · Semantic Scholar

M. Bayés

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M. Bayés — researcher profile on SciRah

h-index: 42
Works: 100
Citations: 12K

Most-cited papers

Meta‐analysis of brain‐derived neurotrophic factor p.Val66Met in adult ADHD in four European populations
C. Sánchez-Mora, M. Ribasés, J. A. Ramos-Quiroga, M. Casas +19 more
2010American Journal of Medical Genetics Part B: Neuropsychiatric Genetics12K citations Open access
Semantic Scholar
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. H. S. B. M. S. V. S. M. R. H. B. Lee Ripke Neale Faraone Purcell Perlis Mowry Thapa, Hong S. Lee, S. Ripke, B. Neale +367 more
2013Nature Genetics2,210 citations Open access
Semantic Scholar
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia
X. Puente, M. Pinyol, V. Quesada, Laura Conde +60 more
2011Nature1,658 citations Open access
Semantic Scholar
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia
V. Quesada, Laura Conde, N. Villamor, G. Ordóñez +37 more
2011Nature Genetics1,163 citations Open access
Semantic Scholar
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Colm Lizzy Phil H Laramie Neelroop N Stephen Stephan Be O'Dushlaine Rossin Lee Duncan Parikshak Newhouse R, C. O'Dushlaine, L. Rossin, P. Lee +372 more
2015Nature Neuroscience765 citations Open access
Semantic Scholar
Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia
M. Kulis, S. Heath, M. Bibikova, A. Queirós +37 more
2012Nature Genetics605 citations Open access
Semantic Scholar
Potential Adverse Effects of Amphetamine Treatment on Brain and Behavior: A Review
Mauricio Arcos-Burgos, Mahim Jain, Maria T. Acosta, S. Shively +47 more
2008Molecular Psychiatry423 citations Open access
Semantic Scholar
Differential Association of Circadian Genes with Mood Disorders: CRY1 and NPAS2 are Associated with Unipolar Major Depression and CLOCK and VIP with Bipolar Disorder
V. Soria, E. Martínez-Amorós, G. Escaramís, J. Valero +15 more
2010Neuropsychopharmacology362 citations Open access
Semantic Scholar
Mutational mechanisms of Williams-Beuren syndrome deletions.
M. Bayés, L. Magano, N. Rivera, R. Flores +1 more
2003American Journal of Human Genetics341 citations Open access
Semantic Scholar
Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy
Cristina Balbás-Martínez, A. Sagrera, Enrique Carrillo-de-Santa-Pau, J. Earl +29 more
2013Nature Genetics264 citations Open access
Semantic Scholar
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
R. Maier, G. Moser, Guo-Bo Chen, S. Ripke +373 more
2015American Journal of Human Genetics226 citations Open access
Semantic Scholar
Multicenter Analysis of the SLC6A3/DAT1 VNTR Haplotype in Persistent ADHD Suggests Differential Involvement of the Gene in Childhood and Persistent ADHD
B. Franke, A. Vasquez, S. Johansson, M. Hoogman +29 more
2010Neuropsychopharmacology192 citations Open access
Semantic Scholar
Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB
M. Ribasés, J. Ramos-Quiroga, A. Hervás, R. Bosch +8 more
2009Molecular Psychiatry163 citations Open access
Semantic Scholar
Clinical and genetic distinction between Walker–Warburg syndrome and muscle–eye–brain disease
B. Cormand, H. Pihko, M. Bayés, L. Valanne +10 more
2001Neurology163 citations Open access
Semantic Scholar
Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1.
Jie-Qing Zhou, Marcel Tawk, F. Tiziano, Julien Veillet +13 more
2012American Journal of Human Genetics148 citations Open access
Semantic Scholar
Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study
M. Ribasés, J. Ramos-Quiroga, C. Sánchez-Mora, R. Bosch +10 more
2011Genes, Brain and Behavior135 citations Open access
Semantic Scholar
Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension.
M. Del Campo, A. Antonell, L. Magano, F. J. Muñoz +3 more
2006American Journal of Human Genetics121 citations Open access
Semantic Scholar
Whole-exome sequencing in splenic marginal zone lymphoma reveals mutations in genes involved in marginal zone differentiation
N. Martínez, Carmen Almaráz, José P. Vaqué, I. Varela +27 more
2014Leukemia115 citations Open access
Semantic Scholar
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.
A. Laquérriere, J. Maluenda, Adrien Camus, Laura Fontenas +56 more
2014Human Molecular Genetics113 citations
Semantic Scholar
Exome sequencing in multiplex autism families suggests a major role for heterozygous truncating mutations
C. Toma, B. Torrico, A. Hervás, R. Valdés-Mas +8 more
2014Molecular Psychiatry110 citations Open access
Semantic Scholar
Association study of 10 genes encoding neurotrophic factors and their receptors in adult and child attention-deficit/hyperactivity disorder.
M. Ribasés, A. Hervás, J. Ramos-Quiroga, R. Bosch +11 more
2008Biological Psychiatry107 citations
Semantic Scholar
Reversion of a fungal genetic code alteration links proteome instability with genomic and phenotypic diversification
A. R. Bezerra, J. Simões, Wanseon Lee, J. Rung +12 more
2013Proceedings of the National Academy of Sciences of the United States of America98 citations Open access
Semantic Scholar
Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non‐synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment
M. Gratacòs, J. Costas, R. de Cid, M. Bayés +18 more
2009American Journal of Medical Genetics Part B: Neuropsychiatric Genetics98 citations
Semantic Scholar
Altered brain‐derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia
J. Mercader, M. Ribasés, M. Gratacòs, J. R. González +5 more
2007Genes, Brain and Behavior94 citations Open access
Semantic Scholar
A brain-derived neurotrophic factor (BDNF) haplotype is associated with antidepressant treatment outcome in mood disorders
M. Gratacòs, V. Soria, M. Urretavizcaya, J. R. González +6 more
2008The Pharmacogenomics Journal85 citations
Semantic Scholar
Extensive genotyping of the BDNF and NTRK2 genes define protective haplotypes against obsessive-compulsive disorder.
P. Alonso, M. Gratacòs, J. Menchón, J. Saiz-Ruiz +13 more
2008Biological Psychiatry80 citations
Semantic Scholar
Copy number variation at the 7q11.23 segmental duplications is a susceptibility factor for the Williams-Beuren syndrome deletion.
I. Cuscó, R. Corominas, M. Bayés, R. Flores +3 more
2008Genome Research79 citations Open access
Semantic Scholar
Homozygous tandem duplication within the gene encoding the β‐subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa
M. Bayés, Mara Giordano, S. Balcells, D. Grinberg +13 more
199576 citations
Semantic Scholar
Characterization of alternatively spliced products and tissue-specific isoforms of USP28 and USP25
Rebeca Valero, M. Bayés, M. Francisca Sánchez-Font, O. González-Angulo +2 more
2001Genome Biology75 citations Open access
Semantic Scholar
Case-control study of six genes asymmetrically expressed in the two cerebral hemispheres: association of BAIAP2 with attention-deficit/hyperactivity disorder.
M. Ribasés, R. Bosch, A. Hervás, J. Ramos-Quiroga +19 more
2009Biological Psychiatry66 citations
Semantic Scholar
A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13-1p21.
A. Martinez-Mir, M. Bayés, L. Vilageliu, D. Grinberg +7 more
1997Genomics66 citations Open access
Semantic Scholar
Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder
C. Sánchez-Mora, J. Ramos-Quiroga, R. Bosch, M. Corrales +34 more
2015Neuropsychopharmacology65 citations Open access
Semantic Scholar
A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.
M. Bayés, B. Goldaracena, A. Martinez-Mir, M. I. Iragui-Madoz +9 more
1998Journal of Medical Genetics61 citations Open access
Semantic Scholar
The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases
S. Laurie, D. Piscia, L. Matalonga, A. Corvó +48 more
2022Human Mutation58 citations Open access
Semantic Scholar
Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder.
P. Alonso, M. Gratacòs, C. Segalàs, G. Escaramís +6 more
2012Journal of Psychiatry & Neuroscience57 citations Open access
Semantic Scholar
P0343 - Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders
J. Mercader, E. Saus, Z. Agüera, M. Bayés +22 more
2008European psychiatry57 citations Open access
Semantic Scholar
Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder.
J. Ramos-Quiroga, C. Sánchez-Mora, M. Casas, I. Garcia-Martínez +9 more
2014Journal of Psychiatric Research56 citations
Semantic Scholar
Analysis of two language-related genes in autism: a case–control association study of FOXP2 and CNTNAP2
C. Toma, A. Hervás, B. Torrico, Noemí Balmaña +15 more
2013Psychiatric Genetics56 citations Open access
Semantic Scholar
Variants in estrogen receptor alpha gene are associated with phenotypical expression of obsessive-compulsive disorder.
P. Alonso, M. Gratacòs, C. Segalàs, G. Escaramís +7 more
2011Psychoneuroendocrinology51 citations
Semantic Scholar
Genetic susceptibility to obsessive‐compulsive hoarding: the contribution of neurotrophic tyrosine kinase receptor type 3 gene 1
P. Alonso, M. Gratacòs, J. Menchón, C. Segalàs +9 more
2008Genes, Brain and Behavior49 citations
Semantic Scholar
Novel mutations in the TULP1 gene causing autosomal recessive retinitis pigmentosa.
E. Paloma, L. Hjelmqvist, M. Bayés, B. García-Sandoval +3 more
2000Investigative Ophthalmology and Visual Science49 citations
Semantic Scholar
Resequencing and association analysis of arylalkylamine N‐acetyltransferase (AANAT) gene and its contribution to major depression susceptibility
V. Soria, E. Martínez-Amorós, G. Escaramís, J. Valero +9 more
2010Journal of Pineal Research47 citations
Semantic Scholar
Association study of six candidate genes asymmetrically expressed in the two cerebral hemispheres suggests the involvement of BAIAP2 in autism.
C. Toma, A. Hervás, Noemí Balmaña, E. Vilella +8 more
2011Journal of Psychiatric Research46 citations
Semantic Scholar
Candidate system analysis in ADHD: Evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1
M. Ribasés, J. Ramos-Quiroga, A. Hervás, C. Sánchez-Mora +15 more
2012World Journal of Biological Psychiatry39 citations
Semantic Scholar
Low exchangeability of selenocysteine, the 21st amino acid, in vertebrate proteins.
S. Castellano, Aida M. Andrés, Elena Bosch, M. Bayés +2 more
2009Molecular biology and evolution39 citations Open access
Semantic Scholar
Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease
Margarita Muiños-Gimeno, M. Montfort, M. Bayés, X. Estivill +1 more
2010European Journal of Human Genetics38 citations Open access
Semantic Scholar
Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor
F. Llorens, M. Hummel, L. Pantano, Xavier Pastor +14 more
2013BMC Genomics37 citations Open access
Semantic Scholar
Evaluation of common variants in 16 genes involved in the regulation of neurotransmitter release in ADHD.
C. Sánchez-Mora, B. Cormand, J. Ramos-Quiroga, A. Hervás +13 more
2013European Neuropsychopharmacology37 citations
Semantic Scholar
Adaptive Mistranslation Accelerates the Evolution of Fluconazole Resistance and Induces Major Genomic and Gene Expression Alterations in Candida albicans
Tobias Weil, R. Santamaría, Wanseon Lee, J. Rung +11 more
2017Msphere35 citations Open access
Semantic Scholar
Evolution of Robustness to Protein Mistranslation by Accelerated Protein Turnover
Dorottya Kalapis, A. R. Bezerra, Zoltán Farkas, P. Horváth +7 more
2015PLoS Biology35 citations Open access
Semantic Scholar

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