Maretha Jonge - Concepedia

Author

Maretha Jonge

Also Known As

Bertine Lahuis, Chantal Kemner, Den Hartog, I, Green, Jonathan, Jonge, M. de, M K. D. JONGE, M. V. De Jonge, M. V. de Jonge, M. de Jonge, M.L. de Jonge

144

Publications

8.7K

Citations

H-Index

Concepts

All Affiliations

University Medical Center Utrecht Utrecht University Leiden University University of Oxford Newcastle University

About

Maretha Jonge is an author at University Medical Center Utrecht specializing in autism, social sciences, and psychiatry.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Education	9	9	391
2	Medicine	8	8	569
3	Engineering	1	1	27
4	Language Studies	1	1	10
5	Natural Sciences	1	1	142

Maretha Jonge

Publications

6.5K

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
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
Individual common variants exert weak effects on the risk for autism spectrum disorders Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2012	372
Changes in the Developmental Trajectories of Striatum in Autism Marieke Langen, Hugo G. Schnack, Hilde Nederveen, Biological Psychiatry Neurodevelopmental DisordersCognitive ScienceNeuropsychologyDevelopmental Cognitive NeuroscienceDevelopmental Trajectories	2009	262
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
Gene-Network Analysis Identifies Susceptibility Genes Related to Glycobiology in Autism Bert van der Zwaag, Lude Franke, Martin Poot, PLoS ONE GeneticsMolecular BiologyGene CharacterizationDisease Gene IdentificationGenomics	2009	142
Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia Alistair T. Pagnamenta, Elena Bacchelli, Maretha Jonge, Biological Psychiatry	2010	141
Open-Label Study of Olanzapine in Children with Pervasive Developmental Disorder Chantal Kemner, Sophie H. N. Willemsen‐Swinkels, Maretha Jonge, Journal of Clinical Psychopharmacology Psychotropic MedicationPsychopharmacologyEducationSocial SciencesSocial Communication Disorder	2002	125
A co‐segregating microduplication of chromosome 15q11.2 pinpoints two risk genes for autism spectrum disorder Bert van der Zwaag, Wouter Staal, Ron Hochstenbach, American Journal of Medical Genetics Part B Neuropsychiatric Genetics NeurogenomicsGeneticsRisk GenesMolecular GeneticsDisease Gene Identification	2009	111

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