J. G. A. M. Heister

Mutant Mitochondrial Elongation Factor G1 and Combined Oxidative Phosphorylation Deficiency

Marieke J. H. Coenen, Hana Antonická, Cristina Ugalde et al. · New England Journal of Medicine · 2004 · 195 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Association of the dopamine transporter (<i>SLC6A3/DAT1</i>) gene 9–6 haplotype with adult ADHD

Barbara Franke, Martine Hoogman, Alejandro Arias Vásquez et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2008 · 78 citations · Full text

Medicine, Genetics, Molecular Genetics +17

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 et al. · Journal of Medical Genetics · 2004 · 74 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

A novel polyadenylation signal mutation in the α₂‐globin gene causing α thalassaemia

Cornelis L. Harteveld, Monique Losekoot, H. L. Haak et al. · British Journal of Haematology · 1994 · 68 citations

Life Sciences, Genetics, Molecular Genetics +15

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 et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2007 · 46 citations · Full text

Medicine, Genetics, Molecular Genetics +17