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Items: 1 to 20 of 106

1.

Linkage and association of febrile seizures to the IMPA2 gene on human chromosome 18.

Nakayama J, Yamamoto N, Hamano K, Iwasaki N, Ohta M, Nakahara S, Matsui A, Noguchi E, Arinami T.

Neurology. 2004 Nov 23;63(10):1803-7.

PMID:
15557493
2.

Turning on the heat: the search for febrile seizure genes.

Winawer M, Hesdorffer D.

Neurology. 2004 Nov 23;63(10):1770-1. No abstract available.

PMID:
15557487
3.

Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder.

Sjøholt G, Ebstein RP, Lie RT, Berle JØ, Mallet J, Deleuze JF, Levinson DF, Laurent C, Mujahed M, Bannoura I, Murad I, Molven A, Steen VM.

Mol Psychiatry. 2004 Jun;9(6):621-9.

PMID:
14699425
4.

Association analysis between polymorphisms in the myo-inositol monophosphatase 2 (IMPA2) gene and bipolar disorder.

Bloch PJ, Weller AE, Doyle GA, Ferraro TN, Berrettini WH, Hodge R, Lohoff FW.

Prog Neuropsychopharmacol Biol Psychiatry. 2010 Dec 1;34(8):1515-9. doi: 10.1016/j.pnpbp.2010.08.015.

PMID:
20800640
6.

A promoter haplotype of the inositol monophosphatase 2 gene (IMPA2) at 18p11.2 confers a possible risk for bipolar disorder by enhancing transcription.

Ohnishi T, Yamada K, Ohba H, Iwayama Y, Toyota T, Hattori E, Inada T, Kunugi H, Tatsumi M, Ozaki N, Iwata N, Sakamoto K, Iijima Y, Iwata Y, Tsuchiya KJ, Sugihara G, Nanko S, Osumi N, Detera-Wadleigh SD, Kato T, Yoshikawa T.

Neuropsychopharmacology. 2007 Aug;32(8):1727-37.

7.

Genetic variants in the IMPA2 gene do not confer increased risk of febrile seizures in Caucasian patients.

Blair MA, Ma S, Abou-Khalil B, Hedera P.

Eur J Neurol. 2007 Apr;14(4):424-7.

PMID:
17388992
8.

Crystal structure of human myo-inositol monophosphatase 2, the product of the putative susceptibility gene for bipolar disorder, schizophrenia, and febrile seizures.

Arai R, Ito K, Ohnishi T, Ohba H, Akasaka R, Bessho Y, Hanawa-Suetsugu K, Yoshikawa T, Shirouzu M, Yokoyama S.

Proteins. 2007 May 15;67(3):732-42.

PMID:
17340635
9.

Significant evidence for linkage of febrile seizures to chromosome 5q14-q15.

Nakayama J, Hamano K, Iwasaki N, Nakahara S, Horigome Y, Saitoh H, Aoki T, Maki T, Kikuchi M, Migita T, Ohto T, Yokouchi Y, Tanaka R, Hasegawa M, Matsui A, Hamaguchi H, Arinami T.

Hum Mol Genet. 2000 Jan 1;9(1):87-91.

10.

Evidence for association of the myo-inositol monophosphatase 2 (IMPA2) gene with schizophrenia in Japanese samples.

Yoshikawa T, Kikuchi M, Saito K, Watanabe A, Yamada K, Shibuya H, Nankai M, Kurumaji A, Hattori E, Ishiguro H, Shimizu H, Okubo Y, Toru M, Detera-Wadleigh SD.

Mol Psychiatry. 2001 Mar;6(2):202-10.

11.

Molecular genetics of febrile seizures.

Iwasaki N, Nakayama J, Hamano K, Matsui A, Arinami T.

Epilepsia. 2002;43 Suppl 9:32-5.

PMID:
12383277
12.

Segregation of a haplotype encompassing FEB1 with genetic epilepsy with febrile seizures plus in a Colombian family.

Caro-Gomez MA, Carrizosa J, Moreno JT, Cabrera D, Bedoya G, Ruiz-Linares A, Franco A, Gomez-Castillo C, Cornejo W, Pineda-Trujillo N.

Epileptic Disord. 2013 Jun;15(2):128-31. doi: 10.1684/epd.2013.0570.

13.

New locus for febrile seizures with absence epilepsy on 3p and a possible modifier gene on 18p.

Nabbout R, Baulac S, Desguerre I, Bahi-Buisson N, Chiron C, Ruberg M, Dulac O, LeGuern E.

Neurology. 2007 Apr 24;68(17):1374-81.

PMID:
17452582
14.

Identification of a novel locus for febrile seizures and epilepsy on chromosome 21q22.

Hedera P, Ma S, Blair MA, Taylor KA, Hamati A, Bradford Y, Abou-Khalil B, Haines JL.

Epilepsia. 2006 Oct;47(10):1622-8.

15.

Genomic structure and novel variants of myo-inositol monophosphatase 2 (IMPA2).

Yoshikawa T, Padigaru M, Karkera JD, Sharma M, Berrettini WH, Esterling LE, Detera-Wadleigh SD.

Mol Psychiatry. 2000 Mar;5(2):165-71.

PMID:
10822344
16.

Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.

Poduri A, Wang Y, Gordon D, Barral-Rodriguez S, Barker-Cummings C, Ulgen A, Chitsazzadeh V, Hill RS, Risch N, Hauser WA, Pedley TA, Walsh CA, Ottman R.

Neurology. 2009 Oct 20;73(16):1264-72. doi: 10.1212/WNL.0b013e3181bd10d3.

17.

Association study of myo-inositol monophosphatase 2 (IMPA2) polymorphisms with bipolar affective disorder and response to lithium treatment.

Dimitrova A, Milanova V, Krastev S, Nikolov I, Toncheva D, Owen MJ, Kirov G.

Pharmacogenomics J. 2005;5(1):35-41.

PMID:
15505643
18.

Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

Br J Dermatol. 2005 Jan;152(1):29-36.

PMID:
15656797
19.

A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33.

Dai XH, Chen WW, Wang X, Zhu QH, Li C, Li L, Liu MG, Wang QK, Liu JY.

Hum Genet. 2008 Nov;124(4):423-9. doi: 10.1007/s00439-008-0566-9.

PMID:
18830713
20.

Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation.

Deprez L, Claes LR, Claeys KG, Audenaert D, Van Dyck T, Goossens D, Van Paesschen W, Del-Favero J, Van Broeckhoven C, De Jonghe P.

Hum Genet. 2006 Jan;118(5):618-25.

PMID:
16273391
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