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MJ Arranz
MJ Arranz
Fundació Docència i Recerca Mutua Terrassa
Verified email at mutuaterrassa.es
Title
Cited by
Cited by
Year
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
13662018
Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
PH Lee, V Anttila, H Won, YCA Feng, J Rosenthal, Z Zhu, EM Tucker-Drob, ...
Cell 179 (7), 1469-1482. e11, 2019
10332019
A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders.
DA Collier, G Stöber, T Li, A Heils, M Catalano, D Di Bella, MJ Arranz, ...
Molecular psychiatry 1 (6), 453-460, 1996
8911996
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
5032018
Pharmacogenetic prediction of clozapine response
MJ Arranz, J Munro, J Birkett, A Bolonna, D Mancama, M Sodhi, KP Lesch, ...
The Lancet 355 (9215), 1615-1616, 2000
4922000
Pharmacogenetics and pharmacogenomics of schizophrenia: a review of last decade of research
MJ Arranz, J De Leon
Molecular psychiatry 12 (8), 707-747, 2007
4612007
Association between clozapine response and allelic variation in 5-HT2A receptor gene
MJ Arranz, DA Collier, M Sodhi, D Ball, GW Roberts, P Sham, R Kerwin, ...
The Lancet 346 (8970), 281-282, 1995
4441995
Autoantibodies neutralizing type I IFNs are present in~ 4% of uninfected individuals over 70 years old and account for~ 20% of COVID-19 deaths
P Bastard, A Gervais, T Le Voyer, J Rosain, Q Philippot, J Manry, ...
Science immunology 6 (62), eabl4340, 2021
4382021
Meta-analysis of studies on genetic variation in 5-HT2A receptors and clozapine response
MJ Arranz, J Munro, P Sham, G Kirov, RM Murray, DA Collier, RW Kerwin
Schizophrenia research 32 (2), 93-99, 1998
3831998
The–1438A/G polymorphism in the 5-hydroxytryptamine type 2A receptor gene affects promoter activity
MJ Parsons, UM D'Souza, MJ Arranz, RW Kerwin, AJ Makoff
Biological psychiatry 56 (6), 406-410, 2004
3312004
X-linked recessive TLR7 deficiency in~ 1% of men under 60 years old with life-threatening COVID-19
T Asano, B Boisson, F Onodi, D Matuozzo, M Moncada-Velez, ...
Science immunology 6 (62), eabl4348, 2021
3272021
Association between 5-HT2A gene promoter polymorphism and anorexia nervosa
DA Collier, MJ Arranz, T Li, D Mupita, N Brown, J Treasure
The Lancet 350 (9075), 412, 1997
3001997
Evidence for association between polymorphisms in the promoter and coding regions of the 5-HT2A receptor gene and response to clozapine
MJ Arranz, J Munro, MJ Owen, G Spurlock, PC Sham, J Zhao, G Kirov, ...
Molecular psychiatry 3 (1), 61-66, 1998
2821998
Association between clozapine response and allelic variation in the 5-HT2C receptor gene
MS Sodhi, MJ Arranz, D Curtis, DM Ball, P Sham, GW Roberts, J Price, ...
Neuroreport 7 (1), 169-172, 1995
2691995
The serotonin transporter is a potential susceptibility factor for bipolar affective disorder
DA Collier, MJ Arranz, P Sham, S Battersby, H Vallada, P Gill, ...
Neuroreport 7 (10), 1675-1679, 1996
2601996
5-HT2A and 5-HT2C Receptor Polymorphisms and Psychopathology in Late Onset Alzheimer's Disease
C Holmes, MJ Arranz, JF Powell, DA Collier, S Lovestone
Human Molecular Genetics 7 (9), 1507-1509, 1998
2571998
Low activity allele of catechol-O-methyltransferase gene associated with rapid cycling bipolar disorder
G Kirov, KC Murphy, MJ Arranz, I Jones, F McCandles, H Kunugi, ...
Molecular psychiatry 3 (4), 342-345, 1998
2521998
Whole-genome sequencing reveals host factors underlying critical COVID-19
A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ...
Nature 607 (7917), 97-103, 2022
2222022
Paternally inherited cis-regulatory structural variants are associated with autism
WM Brandler, D Antaki, M Gujral, ML Kleiber, J Whitney, MS Maile, ...
Science 360 (6386), 327-331, 2018
2012018
High and low activity alleles of catechol-O-methyltransferase gene: ethnic difference and possible association with Parkinson's disease
H Kunugi, S Nanko, A Ueki, E Otsuka, M Hattori, F Hoda, HP Vallada, ...
Neuroscience Letters 221 (2-3), 202-204, 1997
1861997
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