Detalhe da pesquisa
1.
Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21.
Am J Med Genet B Neuropsychiatr Genet
; 156B(1): 36-43, 2011 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-21184582
2.
Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.
Am J Med Genet B Neuropsychiatr Genet
; 153B(2): 503-511, 2010 Mar 05.
Artigo
Inglês
| MEDLINE | ID: mdl-19591125
3.
Polymorphisms in GRIK4, HTR2A, and FKBP5 show interactive effects in predicting remission to antidepressant treatment.
Neuropsychopharmacology
; 35(3): 727-40, 2010 Feb.
Artigo
Inglês
| MEDLINE | ID: mdl-19924111
4.
Gender-specific association of galanin polymorphisms with HPA-axis dysregulation, symptom severity, and antidepressant treatment response.
Neuropsychopharmacology
; 35(7): 1583-92, 2010 Jun.
Artigo
Inglês
| MEDLINE | ID: mdl-20237460
5.
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis.
J Neuroimmunol
; 227(1-2): 162-6, 2010 Oct 08.
Artigo
Inglês
| MEDLINE | ID: mdl-20598377
6.
Evidence for STAT4 as a common autoimmune gene: rs7574865 is associated with colonic Crohn's disease and early disease onset.
PLoS One
; 5(4): e10373, 2010 Apr 29.
Artigo
Inglês
| MEDLINE | ID: mdl-20454450
7.
Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression.
Biol Psychiatry
; 68(6): 578-85, 2010 Sep 15.
Artigo
Inglês
| MEDLINE | ID: mdl-20673876
8.
Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample.
J Neural Transm (Vienna)
; 115(11): 1587-9, 2008 Nov.
Artigo
Inglês
| MEDLINE | ID: mdl-18810304
9.
The ATG16L1 gene variants rs2241879 and rs2241880 (T300A) are strongly associated with susceptibility to Crohn's disease in the German population.
Am J Gastroenterol
; 103(3): 682-91, 2008 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-18162085
10.
PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome.
Nat Genet
; 40(8): 946-8, 2008 Aug.
Artigo
Inglês
| MEDLINE | ID: mdl-18660810
11.
Role of PPARG gene variants in inflammatory bowel disease.
Inflamm Bowel Dis
; 17(4): 1057-8, 2011 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-20722066