MH01375/MH/NIMH NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
1998	1
1999	1
2000	1
2001	5
2003	2
2004	2
2006	1
2007	1
2024	0

1

Why genetic investigation of psychiatric disorders is so difficult.

Bearden CE, Reus VI, Freimer NB. Bearden CE, et al. Curr Opin Genet Dev. 2004 Jun;14(3):280-6. doi: 10.1016/j.gde.2004.04.005. Curr Opin Genet Dev. 2004. PMID: 15172671 Review.

2

Tic symptom profiles in subjects with Tourette Syndrome from two genetically isolated populations.

Mathews CA, Jang KL, Herrera LD, Lowe TL, Budman CL, Erenberg G, Naarden A, Bruun RD, Schork NJ, Freimer NB, Reus VI. Mathews CA, et al. Biol Psychiatry. 2007 Feb 1;61(3):292-300. doi: 10.1016/j.biopsych.2006.02.009. Epub 2006 Apr 11. Biol Psychiatry. 2007. PMID: 16581034

3

Self injurious behaviour in Tourette syndrome: correlates with impulsivity and impulse control.

Mathews CA, Waller J, Glidden D, Lowe TL, Herrera LD, Budman CL, Erenberg G, Naarden A, Bruun RD, Freimer NB, Reus VI. Mathews CA, et al. J Neurol Neurosurg Psychiatry. 2004 Aug;75(8):1149-55. doi: 10.1136/jnnp.2003.020693. J Neurol Neurosurg Psychiatry. 2004. PMID: 15258218 Free PMC article.

4

A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis.

Bull LN, van Eijk MJ, Pawlikowska L, DeYoung JA, Juijn JA, Liao M, Klomp LW, Lomri N, Berger R, Scharschmidt BF, Knisely AS, Houwen RH, Freimer NB. Bull LN, et al. Nat Genet. 1998 Mar;18(3):219-24. doi: 10.1038/ng0398-219. Nat Genet. 1998. PMID: 9500542

5

Fine-resolution mapping by haplotype evaluation: the examples of PFIC1 and BRIC.

Bull LN, Juijn JA, Liao M, van Eijk MJ, Sinke RJ, Stricker NL, DeYoung JA, Carlton VE, Baharloo S, Klomp LW, Abukawa D, Barton DE, Bass NM, Bourke B, Drumm B, Jankowska I, Lovisetto P, McQuaid S, Pawlowska J, Tazawa Y, Villa E, Tygstrup N, Berger R, Knisely AS, Freimer NB, et al. Bull LN, et al. Hum Genet. 1999 Mar;104(3):241-8. doi: 10.1007/pl00008714. Hum Genet. 1999. PMID: 10323248

6

Cultural influences on diagnosis and perception of Tourette syndrome in Costa Rica.

Mathews CA, Herrera Amighetti LD, Lowe TL, van de Wetering BJ, Freimer NB, Reus VI. Mathews CA, et al. J Am Acad Child Adolesc Psychiatry. 2001 Apr;40(4):456-63. doi: 10.1097/00004583-200104000-00015. J Am Acad Child Adolesc Psychiatry. 2001. PMID: 11314572

7

Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes.

Glatt CE, DeYoung JA, Delgado S, Service SK, Giacomini KM, Edwards RH, Risch N, Freimer NB. Glatt CE, et al. Nat Genet. 2001 Apr;27(4):435-8. doi: 10.1038/86948. Nat Genet. 2001. PMID: 11279528

8

Hereditary vascular retinopathy, cerebroretinal vasculopathy, and hereditary endotheliopathy with retinopathy, nephropathy, and stroke map to a single locus on chromosome 3p21.1-p21.3.

Ophoff RA, DeYoung J, Service SK, Joosse M, Caffo NA, Sandkuijl LA, Terwindt GM, Haan J, van den Maagdenberg AM, Jen J, Baloh RW, Barilla-LaBarca ML, Saccone NL, Atkinson JP, Ferrari MD, Freimer NB, Frants RR. Ophoff RA, et al. Am J Hum Genet. 2001 Aug;69(2):447-53. doi: 10.1086/321975. Epub 2001 Jun 28. Am J Hum Genet. 2001. PMID: 11438888 Free PMC article.

9

The genome-wide distribution of background linkage disequilibrium in a population isolate.

Service SK, Ophoff RA, Freimer NB. Service SK, et al. Hum Mol Genet. 2001 Mar 1;10(5):545-51. doi: 10.1093/hmg/10.5.545. Hum Mol Genet. 2001. PMID: 11181579

10

A minimalist approach to gene mapping: locating the gene for acheiropodia, by homozygosity analysis.

Escamilla MA, DeMille MC, Benavides E, Roche E, Almasy L, Pittman S, Hauser J, Lew DF, Freimer NB, Whittle MR. Escamilla MA, et al. Am J Hum Genet. 2000 Jun;66(6):1995-2000. doi: 10.1086/302921. Epub 2000 Apr 25. Am J Hum Genet. 2000. PMID: 10780921 Free PMC article.

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