Mónica Bayés - Concepedia

Author

Mónica Bayés

Also Known As

Banaschewski, Tobias, Bayes, M., Dorret I. Boomsma, Ewa Ciemniejewska, M Bayes, M Bayés, M G Bayes, M. Bayes, M. Bayés, M. Bayés

109

Publications

14.5K

Citations

H-Index

106

Concepts

All Affiliations

Universitat de Barcelona Centro Nacional de Análisis Genómico Universitat Pompeu Fabra Centre for Genomic Regulation Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública

About

Mónica Bayés is an author at Universitat de Barcelona specializing in medicine, genetics, and psychiatry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	31	38	4.9K
2	Engineering	2	2	149
3	Natural Sciences	2	2	110
4	Public Health	2	2	60
5	Health Sciences	1	1	12

Mónica Bayés

Publications

8.3K

Citations

H-Index

Page 1

	Year	Citations
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia Xosé S. Puente, Magda Pinyol, Vı́ctor Quesada, Nature	2011	1.5K
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia Vı́ctor Quesada, Laura Peña Conde, Neus Villamor, Nature Genetics Somatic VariantChronic Lymphocytic LeukemiaGeneticsIdentifies Recurrent MutationsPathology	2011	988
Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia Marta Kulis, Simon Heath, Marina Bibikova, Nature Genetics ChromatinChronic Lymphocytic LeukemiaChromatin RemodelingEpigenetic ChangeGenetics	2012	585
Differential Association of Circadian Genes with Mood Disorders: CRY1 and NPAS2 are Associated with Unipolar Major Depression and CLOCK and VIP with Bipolar Disorder Virginia Soria, Èrika Martínez‐Amorós, Geòrgia Escaramís, Neuropsychopharmacology GeneticsDifferential AssociationSocial SciencesUnipolar Major DepressionMood Symptom	2010	344
Mutational Mechanisms of Williams-Beuren Syndrome Deletions Mónica Bayés, Luis F. Magano, Nuria Fernández Rivera, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyMolecular Genetics	2003	341
A common variant of the latrophilin 3 gene, LPHN3, confers susceptibility to ADHD and predicts effectiveness of stimulant medication Mauricio Arcos‐Burgos, Mahim Jain, Maria T. Acosta, Molecular Psychiatry AdhdPsychiatryPsychotropic MedicationPsychopharmacologyStimulant Medication	2010	291
Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy Cristina Balbás-Martínez, Ana Sagrera, Enrique Carrillo de Santa Pau, Nature Genetics Tumor BiologyUrologyGenitourinary CancerMedicinePathology	2013	288
Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease Nicholas T. Ventham, Nicholas A. Kennedy, Alex Adams, Nature Communications	2016	264
The Anhidrotic Ectodermal Dysplasia Gene (EDA) Undergoes Alternative Splicing and Encodes Ectodysplasin-A with Deletion Mutations in Collagenous Repeats Mónica Bayés, Andrew J. Hartung, Sini Ezer, Human Molecular Genetics	1998	229
Clinical and genetic distinction between Walker–Warburg syndrome and muscle–eye–brain disease Bru Cormand, Helena Pihko, Mónica Bayés, Neurology	2001	184

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