Sutcliffe JS - Search Results

1

Functional impact of global rare copy number variation in autism spectrum disorders.

Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, Battaglia A, Berney T, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Bryson SE, Carson AR, Casallo G, Casey J, Chung BH, Cochrane L, Corsello C, Crawford EL, Crossett A, Cytrynbaum C, Dawson G, de Jonge M, Delorme R, Drmic I, Duketis E, Duque F, Estes A, Farrar P, Fernandez BA, Folstein SE, Fombonne E, Freitag CM, Gilbert J, Gillberg C, Glessner JT, Goldberg J, Green A, Green J, Guter SJ, Hakonarson H, Heron EA, Hill M, Holt R, Howe JL, Hughes G, Hus V, Igliozzi R, Kim C, Klauck SM, Kolevzon A, Korvatska O, Kustanovich V, Lajonchere CM, Lamb JA, Laskawiec M, Leboyer M, Le Couteur A, Leventhal BL, Lionel AC, Liu XQ, Lord C, Lotspeich L, Lund SC, Maestrini E, Mahoney W, Mantoulan C, Marshall CR, McConachie H, McDougle CJ, McGrath J, McMahon WM, Merikangas A, Migita O, Minshew NJ, Mirza GK, Munson J, Nelson SF, Noakes C, Noor A, Nygren G, Oliveira G, Papanikolaou K, Parr JR, Parrini B, Paton T, Pickles A, Pilorge M, Piven J, Ponting CP, Posey DJ, Poustka A, Poustka F, Prasad A, Ragoussis J, Renshaw K, Ri… See abstract for full author list ➔ Pinto D, et al. Among authors: sutcliffe js. Nature. 2010 Jul 15;466(7304):368-72. doi: 10.1038/nature09146. Epub 2010 Jun 9. Nature. 2010. PMID: 20531469 Free PMC article.

2

Exploratory subsetting of autism families based on savant skills improves evidence of genetic linkage to 15q11-q13.

Nurmi EL, Dowd M, Tadevosyan-Leyfer O, Haines JL, Folstein SE, Sutcliffe JS. Nurmi EL, et al. Among authors: sutcliffe js. J Am Acad Child Adolesc Psychiatry. 2003 Jul;42(7):856-63. doi: 10.1097/01.CHI.0000046868.56865.0F. J Am Acad Child Adolesc Psychiatry. 2003. PMID: 12819446

3

Autosomal dominant lateral temporal epilepsy: two families with novel mutations in the LGI1 gene.

Hedera P, Abou-Khalil B, Crunk AE, Taylor KA, Haines JL, Sutcliffe JS. Hedera P, et al. Among authors: sutcliffe js. Epilepsia. 2004 Mar;45(3):218-22. doi: 10.1111/j.0013-9580.2004.47203.x. Epilepsia. 2004. PMID: 15009222 Free article.

4

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. Among authors: sutcliffe js. BMC Med Genet. 2004 May 5;5:12. doi: 10.1186/1471-2350-5-12. BMC Med Genet. 2004. PMID: 15128462 Free PMC article.

5

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. Among authors: sutcliffe js. 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

6

Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.

Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Rabionet R, et al. Among authors: sutcliffe js. Neurosci Lett. 2004 Dec 6;372(3):209-14. doi: 10.1016/j.neulet.2004.09.037. Neurosci Lett. 2004. PMID: 15542242

7

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. Among authors: sutcliffe js. BMC Med Genet. 2005 Jan 12;6:1. doi: 10.1186/1471-2350-6-1. BMC Med Genet. 2005. PMID: 15647115 Free PMC article.

8

The GABBR1 locus and the G1465A variant is not associated with temporal lobe epilepsy preceded by febrile seizures.

Ma S, Abou-Khalil B, Sutcliffe JS, Haines JL, Hedera P. Ma S, et al. Among authors: sutcliffe js. BMC Med Genet. 2005 Mar 30;6:13. doi: 10.1186/1471-2350-6-13. BMC Med Genet. 2005. PMID: 15799783 Free PMC article.

9

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD. Sutcliffe JS, et al. Am J Hum Genet. 2005 Aug;77(2):265-79. doi: 10.1086/432648. Epub 2005 Jul 1. Am J Hum Genet. 2005. PMID: 15995945 Free PMC article.

10

Lack of association between autism and SLC25A12.

Rabionet R, McCauley JL, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, DeLong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Rabionet R, et al. Among authors: sutcliffe js. Am J Psychiatry. 2006 May;163(5):929-31. doi: 10.1176/ajp.2006.163.5.929. Am J Psychiatry. 2006. PMID: 16648338

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