MH61009/MH/NIMH NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2001	1
2003	4
2004	3
2005	3
2006	1
2007	1
2008	1
2009	1
2024	0

1

Genome-wide and Ordered-Subset linkage analyses provide support for autism loci on 17q and 19p with evidence of phenotypic and interlocus genetic correlates.

McCauley JL, Li C, Jiang L, Olson LM, Crockett G, Gainer K, Folstein SE, Haines JL, Sutcliffe JS. McCauley JL, et al. BMC Med Genet. 2005 Jan 12;6:1. doi: 10.1186/1471-2350-6-1. BMC Med Genet. 2005. PMID: 15647115 Free PMC article.

2

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.

Hutcheson HB, Olson LM, Bradford Y, Folstein SE, Santangelo SL, Sutcliffe JS, Haines JL. Hutcheson HB, et al. BMC Med Genet. 2004 May 5;5:12. doi: 10.1186/1471-2350-5-12. BMC Med Genet. 2004. PMID: 15128462 Free PMC article.

3

Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures.

Sutcliffe JS, Han MK, Amin T, Kesterson RA, Nurmi EL. Sutcliffe JS, et al. BMC Genomics. 2003 Apr 29;4(1):15. doi: 10.1186/1471-2164-4-15. Epub 2003 Apr 29. BMC Genomics. 2003. PMID: 12720574 Free PMC article.

4

A linkage disequilibrium map of the 1-Mb 15q12 GABA(A) receptor subunit cluster and association to autism.

McCauley JL, Olson LM, Delahanty R, Amin T, Nurmi EL, Organ EL, Jacobs MM, Folstein SE, Haines JL, Sutcliffe JS. McCauley JL, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 Nov 15;131B(1):51-9. doi: 10.1002/ajmg.b.30038. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15389768

5

Linkage and association analysis at the serotonin transporter (SLC6A4) locus in a rigid-compulsive subset of autism.

McCauley JL, Olson LM, Dowd M, Amin T, Steele A, Blakely RD, Folstein SE, Haines JL, Sutcliffe JS. McCauley JL, et al. Am J Med Genet B Neuropsychiatr Genet. 2004 May 15;127B(1):104-12. doi: 10.1002/ajmg.b.20151. Am J Med Genet B Neuropsychiatr Genet. 2004. PMID: 15108191

6

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.

Nurmi EL, Bradford Y, Chen Y, Hall J, Arnone B, Gardiner MB, Hutcheson HB, Gilbert JR, Pericak-Vance MA, Copeland-Yates SA, Michaelis RC, Wassink TH, Santangelo SL, Sheffield VC, Piven J, Folstein SE, Haines JL, Sutcliffe JS. Nurmi EL, et al. Genomics. 2001 Sep;77(1-2):105-13. doi: 10.1006/geno.2001.6617. Genomics. 2001. PMID: 11543639

7

Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism.

Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS. Nurmi EL, et al. Mol Psychiatry. 2003 Jun;8(6):624-34, 570. doi: 10.1038/sj.mp.4001283. Mol Psychiatry. 2003. PMID: 12851639

8

Human serotonin transporter variants display altered sensitivity to protein kinase G and p38 mitogen-activated protein kinase.

Prasad HC, Zhu CB, McCauley JL, Samuvel DJ, Ramamoorthy S, Shelton RC, Hewlett WA, Sutcliffe JS, Blakely RD. Prasad HC, et al. Proc Natl Acad Sci U S A. 2005 Aug 9;102(32):11545-50. doi: 10.1073/pnas.0501432102. Epub 2005 Jul 29. Proc Natl Acad Sci U S A. 2005. PMID: 16055563 Free PMC article.

9

Strong association of de novo copy number mutations with autism.

Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimäki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M. Sebat J, et al. Science. 2007 Apr 20;316(5823):445-9. doi: 10.1126/science.1138659. Epub 2007 Mar 15. Science. 2007. PMID: 17363630 Free PMC article.

10

Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility.

Weiss LA, Kosova G, Delahanty RJ, Jiang L, Cook EH, Ober C, Sutcliffe JS. Weiss LA, et al. Eur J Hum Genet. 2006 Aug;14(8):923-31. doi: 10.1038/sj.ejhg.5201644. Epub 2006 May 17. Eur J Hum Genet. 2006. PMID: 16724005

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