Tiago R. Magalhães - Concepedia

Author

Tiago R. Magalhães

Also Known As

Bailey, A. J., Bolshakova, Nadia, Goldstein, Jacqueline I., Magalhaes, Tiago, Merico, Daniele, T R Magalhães, T. Magalhães, T. R. Magalhaes, Talita Louise Mafra Magalhães, Thiago Martins de Magalhães

Publications

7.5K

Citations

H-Index

Concepts

All Affiliations

University College Dublin Trinity College Dublin Icahn School of Medicine at Mount Sinai Hôpital Robert-Debré Université Paris Cité

About

Tiago R. Magalhães is an author at University College Dublin specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	2.6K
2	Public Health	3	3	2K
3	Biostatistics	3	3	2.1K
4	Social Sciences	1	1	532
5	Neurology	1	1	28

Tiago R. Magalhães

Publications

7.4K

Citations

H-Index

Page 1

	Year	Citations
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Analysis of shared heritability in common disorders of the brain Verneri Anttila, Brendan Bulik‐Sullivan, Hilary K. Finucane, Science Brain FunctionPsychiatric DisordersGeneticsGenetic EpidemiologyNeuropsychiatry	2018	2K
Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders Dalila Pinto, Elsa Delaby, Daniele Merico, The American Journal of Human Genetics	2014	1K
A genome-wide scan for common alleles affecting risk for autism Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2010	585
wishful thinking Encodes a BMP Type II Receptor that Regulates Synaptic Growth in Drosophila Hermann Aberle, A. Pejmun Haghighi, Richard D. Fetter, Neuron Synaptic PlasticitySynaptic GrowthDevelopmental BiologyMolecular NeuroscienceSynaptic Transmission	2002	532
Individual common variants exert weak effects on the risk for autism spectrum disorders Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2012	372
Geospatial Resolution of Human and Bacterial Diversity with City-Scale Metagenomics Ebrahim Afshinnekoo, Cem Meydan, Shanin Chowdhury, Cell Systems	2015	344
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder Jillian P. Casey, Tiago R. Magalhães, Judith Conroy, Human Genetics	2011	200
Unexplained early onset epileptic encephalopathy: Exome screening and phenotype expansion Nicholas M. Allen, Judith Conroy, Amre Shahwan, Epilepsia	2015	176
Association of Genetic Variants with Self-Assessed Color Categories in Brazilians Danielle Fernandes Durso, Sérgio Paulo Bydlowski, Mara Helena Hutz, PLoS ONE EthnicityGenetic TestingGeneticsGenetic EpidemiologyHuman Polymorphism	2014	63

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