Heister JG[au] - Search Results

Year	Number of Results
1994	1
1996	2
2004	3
2005	1
2007	1
2008	2
2024	0

1

A novel locus for autosomal recessive nonsyndromic hearing impairment, DFNB63, maps to chromosome 11q13.2-q13.4.

Kalay E, Caylan R, Kiroglu AF, Yasar T, Collin RW, Heister JG, Oostrik J, Cremers CW, Brunner HG, Karaguzel A, Kremer H. Kalay E, et al. Among authors: heister jg. J Mol Med (Berl). 2007 Apr;85(4):397-404. doi: 10.1007/s00109-006-0136-3. Epub 2007 Jan 9. J Mol Med (Berl). 2007. PMID: 17211611

2

Association of the dopamine transporter (SLC6A3/DAT1) gene 9-6 haplotype with adult ADHD.

Franke B, Hoogman M, Arias Vasquez A, Heister JG, Savelkoul PJ, Naber M, Scheffer H, Kiemeney LA, Kan CC, Kooij JJ, Buitelaar JK. Franke B, et al. Among authors: heister jg. Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1576-9. doi: 10.1002/ajmg.b.30861. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18802924

3

An exploratory study of the relationship between four candidate genes and neurocognitive performance in adult ADHD.

Boonstra AM, Kooij JJ, Buitelaar JK, Oosterlaan J, Sergeant JA, Heister JG, Franke B. Boonstra AM, et al. Among authors: heister jg. Am J Med Genet B Neuropsychiatr Genet. 2008 Apr 5;147(3):397-402. doi: 10.1002/ajmg.b.30595. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 17886261 Free article.

4

Mutant mitochondrial elongation factor G1 and combined oxidative phosphorylation deficiency.

Coenen MJ, Antonicka H, Ugalde C, Sasarman F, Rossi R, Heister JG, Newbold RF, Trijbels FJ, van den Heuvel LP, Shoubridge EA, Smeitink JA. Coenen MJ, et al. Among authors: heister jg. N Engl J Med. 2004 Nov 11;351(20):2080-6. doi: 10.1056/NEJMoa041878. N Engl J Med. 2004. PMID: 15537906 Free article.

5

Hb Kurdistan [alpha 47(CE5)Asp-->Tyr], a new alpha chain variant in combination with beta (0)-thalassemia.

Giordano PC, Harteveld CL, Streng H, Oosterwijk JC, Heister JG, Amons R, Bernini LF. Giordano PC, et al. Among authors: heister jg. Hemoglobin. 1994 Jan;18(1):11-8. doi: 10.3109/03630269409014141. Hemoglobin. 1994. PMID: 8195005

6

Identification of novel locus for autosomal dominant butterfly shaped macular dystrophy on 5q21.2-q33.2.

den Hollander AI, van Lith-Verhoeven JJ, Kersten FF, Heister JG, de Kovel CG, Deutman AF, Hoyng CB, Cremers FP. den Hollander AI, et al. Among authors: heister jg. J Med Genet. 2004 Sep;41(9):699-702. doi: 10.1136/jmg.2004.019562. J Med Genet. 2004. PMID: 15342701 Free PMC article. No abstract available.

7

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.

de Kovel CG, Hol FA, Heister JG, Willemen JJ, Sandkuijl LA, Franke B, Padberg GW. de Kovel CG, et al. Among authors: heister jg. J Med Genet. 2004 Sep;41(9):652-7. doi: 10.1136/jmg.2003.012294. J Med Genet. 2004. PMID: 15342694 Free PMC article.

8

A novel D458V mutation in the SANS PDZ binding motif causes atypical Usher syndrome.

Kalay E, de Brouwer AP, Caylan R, Nabuurs SB, Wollnik B, Karaguzel A, Heister JG, Erdol H, Cremers FP, Cremers CW, Brunner HG, Kremer H. Kalay E, et al. Among authors: heister jg. J Mol Med (Berl). 2005 Dec;83(12):1025-32. doi: 10.1007/s00109-005-0719-4. Epub 2005 Nov 8. J Mol Med (Berl). 2005. PMID: 16283141

9

Hb Utrecht [alpha 2 129(H12)Leu-->Pro], a new unstable alpha 2-chain variant associated with a mild alpha-thalassaemic phenotype.

Harteveld CL, Giordano PC, Losekoot M, Heister JG, Batelaan D, van Delft P, Bruin MC, Bernini LF. Harteveld CL, et al. Among authors: heister jg. Br J Haematol. 1996 Sep;94(3):483-5. doi: 10.1046/j.1365-2141.1996.d01-1828.x. Br J Haematol. 1996. PMID: 8790146

10

An IVS1-116 (A-->G) acceptor splice site mutation in the alpha 2 globin gene causing alpha + thalassaemia in two Dutch families.

Harteveld CL, Heister JG, Giordano PC, Batelaan D, von Delft P, Haak HL, Wijermans PW, Losekoot M, Bernini LF. Harteveld CL, et al. Among authors: heister jg. Br J Haematol. 1996 Dec;95(3):461-6. doi: 10.1046/j.1365-2141.1996.d01-1926.x. Br J Haematol. 1996. PMID: 8943885

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