John B. Vincent - Concepedia

Author

John B. Vincent

Centre for Addiction and Mental Health ORCID

Also Known As

Arne E. Vaaler, Bergen S, China Scapegoat, Cornelia M van Duijn, Eduard Vieta, Fabian Streit, Gustavo Turecki, Henry Völzke, J B Vincent, J VINCENT

267

Publications

22K

Citations

H-Index

145

Concepts

All Affiliations

Centre for Addiction and Mental Health University of Toronto Hospital for Sick Children University College London King's College London

About

John B. Vincent is an author at Centre for Addiction and Mental Health specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	36	53	8.7K
2	Public Health	8	8	418
3	Natural Sciences	4	4	114
4	Engineering	3	3	377
5	Health Sciences	3	3	363

John B. Vincent

115

Publications

12.2K

Citations

H-Index

Page 1

	Year	Citations
Structural Variation of Chromosomes in Autism Spectrum Disorder Christian R. Marshall, Abdul Noor, John B. Vincent, The American Journal of Human Genetics ChromatinStructural VariationSyndromic AutismGeneticsMolecular Biology	2008	1.8K
Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Pamela Sklar, Stephan Ripke, Laura J. Scott, Nature Genetics Genome-wide Association StudyGenotype-phenotype AssociationPsychiatryGeneticsPsychiatric Genetics	2011	1.4K
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes Douglas M. Ruderfer, Stephan Ripke, Andrew McQuillin, Cell PsychiatryPsychotic DisorderGeneticsSchizophreniaSocial Sciences	2018	797
Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways Liyun Sang, Julie J. Miller, Kevin C. Corbit, Cell Molecular NeuroscienceDisease MechanismGliomaMolecular BiologyComplex Disease	2011	617
Bears Show a Physiological but Limited Behavioral Response to Unmanned Aerial Vehicles Mark A. Ditmer, John B. Vincent, Leland K. Werden, Current Biology Animal BehaviourBehavioral SciencesKinesiologyEngineeringBears Show	2015	336
A role for common fragile site induction in amplification of human oncogenes Asaf Hellman, Eitan Zlotorynski, Stephen W. Scherer, Cancer Cell Knockout MouseGenome InstabilityHuman OncogenesGenetic DisorderGenetics	2002	299
Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder Eli A. Stahl, Gerome Breen, Andreas J. Forstner, NeurogenomicsPsychiatric DisordersGeneticsGenetic EpidemiologyGenomics	2017	255
Incidence, Determinants, and Prognostic Significance of Hyperkalemia and Worsening Renal Function in Patients With Heart Failure Receiving the Mineralocorticoid Receptor Antagonist Eplerenone or Placebo in Addition to Optimal Medical Therapy Patrick Rossignol, Daniela Dobre, John J.V. McMurray, Circulation Heart Failure	2013	250
Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsFragile X Spectrum	2012	228
CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290 Nicholas T. Gorden, Heleen H. Arts, Melissa A. Parisi, The American Journal of Human Genetics Molecular NeuroscienceJoubert SyndromeMedicineGeneticsGenetic Disorder	2008	227

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