M. Bayés

M. Gratacós, X. Estivill, J. Leiva-Murillo, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1.

E. Bertini, I. Gut, M. Bayés, 2012, American journal of human genetics.

The anhidrotic ectodermal dysplasia gene (EDA) undergoes alternative splicing and encodes ectodysplasin-A with deletion mutations in collagenous repeats.

J. Kere, M. Bayés, I. Thesleff, 1998, Human molecular genetics.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease

Fredrik Dahl, S. Heath, H. Drummond, 2016, Nature Communications.

Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders.

J. González, M. Gratacós, X. Estivill, 2008, Human molecular genetics.

Mutational mechanisms of Williams-Beuren syndrome deletions.

M. Bayés, Mònica Bayés, R. Flores, 2003, American journal of human genetics.

Differential Association of Circadian Genes with Mood Disorders: CRY1 and NPAS2 are Associated with Unipolar Major Depression and CLOCK and VIP with Bipolar Disorder

M. Gratacós, X. Estivill, G. Escaramís, 2010, Neuropsychopharmacology.

Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia

Alfonso Valencia, Modesto Orozco, Brandy Klotzle, 2012, Nature Genetics.

Genetic susceptibility to obsessive‐compulsive hoarding: the contribution of neurotrophic tyrosine kinase receptor type 3 gene 1

M. Gratacós, X. Estivill, G. Escaramís, 2008, Genes, brain, and behavior.

Clinical and genetic distinction between Walker–Warburg syndrome and muscle–eye–brain disease

M. Bayés, H. Brunner, R. Gershoni-baruch, 2001, Neurology.

Overview of Genotyping

I. Gut, M. Bayés, 2011 .

The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons

Gabriela R. Moura, I. Gut, M. Bayés, 2016, Front. Microbiol..

Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor

Robert Kofler, Lauro Sumoy, Manuela Hummel, 2013, BMC Genomics.

Hemizygosity at the NCF1 gene in patients with Williams-Beuren syndrome decreases their risk of hypertension.

M. Bayés, A. Antonell, M. Del Campo, 2006, American journal of human genetics.

1 Overview of Genotyping

I. Gut, M. Bayés, 2022 .

Genome-wide copy number variation analysis in adult attention-deficit and hyperactivity disorder.

M. Bayés, B. Cormand, C. Sánchez-Mora, 2014, Journal of psychiatric research.

Association between the NMDA glutamate receptor GRIN2B gene and obsessive-compulsive disorder.

M. Gratacós, X. Estivill, G. Escaramís, 2012, Journal of psychiatry & neuroscience : JPN.

Resequencing and association analysis of arylalkylamine N‐acetyltransferase (AANAT) gene and its contribution to major depression susceptibility

M. Gratacós, X. Estivill, G. Escaramís, 2010, Journal of pineal research.

A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication.

C. Freitag, H. Hakonarson, J. Swanson, 2010, Molecular psychiatry.

Ectodysplasin is a collagenous trimeric type II membrane protein with a tumor necrosis factor-like domain and co-localizes with cytoskeletal structures at lateral and apical surfaces of cells.

D. Schlessinger, J. Kere, M. Bayés, 1999, Human molecular genetics.

Candidate system analysis in ADHD: Evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1

C. Freitag, K. Lesch, M. Bayés, 2012, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Exploring DRD4 and its interaction with SLC6A3 as possible risk factors for adult ADHD: A meta‐analysis in four European populations

L. Kiemeney, B. Franke, K. Lesch, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Common variants in the TPH1 and TPH2 regions are not associated with persistent ADHD in a combined sample of 1,636 adult cases and 1,923 controls from four European populations

L. Kiemeney, B. Franke, K. Lesch, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

How to cite this article:

James L. McClelland, B. Franke, K. Lesch, 2011 .

Exploration of 19 serotoninergic candidate genes in adults and children with attention-deficit/hyperactivity disorder identifies association for 5HT2A, DDC and MAOB

X. Estivill, M. Bayés, B. Cormand, 2009, Molecular Psychiatry.

A brain-derived neurotrophic factor (BDNF) haplotype is associated with antidepressant treatment outcome in mood disorders

M. Gratacós, X. Estivill, M. Bayés, 2008, The Pharmacogenomics Journal.

Neurotransmitter systems and neurotrophic factors in autism: association study of 37 genes suggests involvement of DDC

Marta Maristany, Amaia Hervás, M. Bayés, 2013, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

A new locus for autosomal recessive retinitis pigmentosa (RP19) maps to 1p13-1p21.

M. Bayés, M. Baiget, D. Grinberg, 1997, Genomics.

Truncating variant burden in high-functioning autism and pleiotropic effects of LRP1 across psychiatric phenotypes

P. Aloy, J. Fullerton, M. Bayés, 2019, Journal of Psychiatry & Neuroscience.

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

H. Hakonarson, M. Bayés, J. McCracken, 2010, Molecular Psychiatry.

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

J. González, M. Gratacós, X. Estivill, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Case-Control Study of Six Genes Asymmetrically Expressed in the Two Cerebral Hemispheres: Association of BAIAP2 with Attention-Deficit/Hyperactivity Disorder

X. Estivill, K. Lesch, M. Bayés, 2009, Biological Psychiatry.

DIRAS2 is Associated with Adult ADHD, Related Traits, and Co-Morbid Disorders

L. Kiemeney, C. Freitag, H. Völzke, 2012, Neuropsychopharmacology.

An association study of sequence variants in the forkhead box P2 (FOXP2) gene and adulthood attention-deficit/hyperactivity disorder in two European samples

Andreas Reif, K. Lesch, M. Bayés, 2012, Psychiatric genetics.

The involvement of serotonin polymorphisms in autistic spectrum symptomatology

M. Bayés, M. Arranz, B. Cormand, 2014, Psychiatric genetics.

Autosomal recessive retinitis pigmentosa in Spain : Evaluation of 4 genes and 2 loci involved in the disease

M. Bayés, M. Baiget, D. Grinberg, 2012 .

Evidence against involvement of recoverin in autosomal recessive retinitis pigmentosa in 42 Spanish families

M. Bayés, M. Baiget, D. Grinberg, 1995, Human Genetics.

Strategies for the Genetic Analysis of Autosomal Recessive Retinitis Pigmentosa in Spanish Families

M. Bayés, M. Baiget, D. Grinberg, 1997 .

Autosomal recessive retinitis pigmentosa in Spain: evaluation of four genes and two loci involved in the disease

M. Bayés, M. Baiget, D. Grinberg, 1996, Clinical genetics.

Homozygous tandem duplication within the gene encoding the β‐subunit of rod phosphodiesterase as a cause for autosomal recessive retinitis pigmentosa

M. Bayés, S. Amselem, M. Baiget, 1995 .

Contribution of LPHN3 to the genetic susceptibility to ADHD in adulthood: a replication study

M. Bayés, B. Cormand, C. Sánchez-Mora, 2011, Genes, brain, and behavior.

Extensive Genotyping of the BDNF and NTRK2 Genes Define Protective Haplotypes Against Obsessive-Compulsive Disorder

J. González, M. Gratacós, X. Estivill, 2008, Biological Psychiatry.

xtensive Genotyping of the BDNF and NTRK 2 enes Define Protective Haplotypes Against bsessive-Compulsive Disorder

J. González, M. Gratacós, X. Estivill, 2008 .

Variants in estrogen receptor alpha gene are associated with phenotypical expression of obsessive-compulsive disorder

M. Gratacós, X. Estivill, G. Escaramís, 2011, Psychoneuroendocrinology.

Genotipado a gran escala en la investigación del trastorno del espectro autista y el trastorno por déficit de atención con hiperactividad

X. Estivill, M. Bayés, M. Ribasés, 2005 .

Mutation Research/fundamental and Molecular Mechanisms of Mutagenesis Absence of Cytogenetic Effects in Children and Adults with Attention-deficit/hyperactivity Disorder Treated with Methylphenidate

X. Estivill, M. Bayés, B. Cormand, 2022 .

Whole-genome sequencing identifies recurrent mutations in chronic lymphocyticleukaemia

A. Valencia, R. Guigó, X. Estivill, 2011 .

Role of the neurotrophin network in eating disorders' subphenotypes: body mass index and age at onset of the disease.

J. González, M. Gratacós, X. Estivill, 2010, Journal of psychiatric research.

Altered brain‐derived neurotrophic factor blood levels and gene variability are associated with anorexia and bulimia

M. Gratacós, X. Estivill, M. Bayés, 2007, Genes, brain, and behavior.

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.

I. Gut, M. Bayés, J. Melki, 2014, Human molecular genetics.

Association Study of 10 Genes Encoding Neurotrophic Factors and Their Receptors in Adult and Child Attention-Deficit/Hyperactivity Disorder

M. Gratacós, X. Estivill, M. Bayés, 2008, Biological Psychiatry.

Familial hemiplegic migraine: linkage to chromosome 14q32 in a Spanish kindred

M. Bayés, R. Corominas, B. Cormand, 2009, neurogenetics.

Design and evaluation of a panel of single-nucleotide polymorphisms in microRNA genomic regions for association studies in human disease

X. Estivill, M. Bayés, Y. Espinosa-Parrilla, 2010, European Journal of Human Genetics.

A new autosomal recessive retinitis pigmentosa locus maps on chromosome 2q31-q33.

M. Bayés, M. Baiget, D. Grinberg, 1998, Journal of medical genetics.

A novel mutation in exon 17 of the β-subunit of rod phosphodiesterase in two RP sisters of a consanguineous family

M. Bayés, M. Baiget, D. Grinberg, 2004, Human Genetics.

A Brain-Derived Neurotrophic Factor Haplotype Is Associated with Therapeutic Response in Obsessive-Compulsive Disorder

M. Gratacós, X. Estivill, G. Escaramís, 2009, Biological Psychiatry.

Reversion of a fungal genetic code alteration links proteome instability with genomic and phenotypic diversification

Manuel A. S. Santos, Gabriela R. Moura, M. Gut, 2013, Proceedings of the National Academy of Sciences.

Frequency of the arylsulphatase A pseudodeficiency allele in the Spanish population

M. Bayés, G. Marfany, W. Lissens, 1993, Clinical genetics.

Colorectal Adenomas Contain Multiple Somatic Mutations That Do Not Coincide with Synchronous Adenocarcinoma Specimens

I. Varela, I. Gut, M. Piris, 2015, PloS one.

The prevalence and transcriptional activity of the mucosal microbiota of ulcerative colitis patients

S. Heath, H. Drummond, C. Lees, 2018, Scientific Reports.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

D. Ledbetter, J. Sutcliffe, D. Rujescu, 2014 .

Putative association of a mutant ROM1 allele with retinitis pigmentosa

M. Bayés, M. Baiget, D. Grinberg, 1997, Human Genetics.

P0343 - Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders

M. Gratacós, X. Estivill, M. Bayés, 2008, European psychiatry.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

D. Ledbetter, J. Sutcliffe, D. Rujescu, 2014 .

Low exchangeability of selenocysteine, the 21st amino acid, in vertebrate proteins.

R. Guigó, S. Castellano, A. Andrés, 2009, Molecular biology and evolution.

Case–Control Genome-Wide Association Study of Persistent Attention-Deficit Hyperactivity Disorder Identifies FBXO33 as a Novel Susceptibility Gene for the Disorder

L. Kiemeney, B. Franke, K. Lesch, 2015, Neuropsychopharmacology.

Candidate system analysis in ADHD: Evaluation of nine genes involved in dopaminergic neurotransmission identifies association with DRD1

C. Freitag, K. Lesch, M. Bayés, 2012, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

P0343 - Association of NTRK3 and its interaction with NGF suggest an altered cross-regulation of the neurotrophin signaling pathway in eating disorders

J. González, M. Gratacós, X. Estivill, 2008, European Psychiatry.