J. G. A. M. Heister - Concepedia

Author

J. G. A. M. Heister

Radboud University Nijmegen

Also Known As

J G A M Heister, J. G. A. M. Heister, J. Heister, J.G. Heister, J.G.A.M. Angelien Heister, J.G.A.M. Heister

Publications

577

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Leiden University Radboud University Medical Center Karadeniz Technical University

About

J. G. A. M. Heister is an author at Radboud University Nijmegen specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	263
2	Molecular Biology	2	2	238
3	Arts	1	1	25
4	Natural Sciences	1	1	192
5	Biochemistry	1	1	192

J. G. A. M. Heister

Publications

576

Citations

H-Index

Page 1

	Year	Citations
Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency Marieke J. H. Coenen, Hana Antonická, Cristina Ugalde, New England Journal of Medicine MitophagyMitochondrial BiogenesisMitochondrial FunctionBiochemistryMitochondrial Translation	2004	192
Association of the dopamine transporter (<i>SLC6A3/DAT1</i>) gene 9–6 haplotype with adult ADHD Barbara Franke, Martine Hoogman, Alejandro Arias Vásquez, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2008	78
Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family Carolien G. F. de Kovel, Frans A. Hol, J. G. A. M. Heister, Journal of Medical Genetics	2004	74
A novel polyadenylation signal mutation in the α<sub>2</sub>‐globin gene causing α thalassaemia Cornelis L. Harteveld, Monique Losekoot, H. L. Haak, British Journal of Haematology	1994	68
An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD Albert Boonstra, J. J. Sandra Kooij, Jan K. Buitelaar, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2007	46
A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome Ersan Kalay, Arjan P.M. de Brouwer, R Çaylan, Journal of Molecular Medicine Mendelian DisorderNovel D458v MutationGenetic DisorderMedicineGenetics	2005	46
An IVS1–116 (A→G) acceptor splice site mutation in the α<sub>2</sub> globin gene causing α<sup>+</sup> thalassaemia in two Dutch families Cornelis L. Harteveld, J. G. A. M. Heister, Paola Giordano, British Journal of Haematology	1996	27
A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2–q13.4 Ersan Kalay, R Çaylan, Ahmet Faruk Kıroğlu, Journal of Molecular Medicine Developmental BiologyGenetic DisorderGeneticsAudiologyAuditory Physiology	2007	25
Hb Utrecht [α<sub>2</sub> 129(H12)Leu → Pro], a new unstable α2‐chain variant associated with a mild α‐thalassaemic phenotype Cornelis L. Harteveld, Paola Giordano, Monique Losekoot, British Journal of Haematology	1996	20

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