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Items: 1 to 20 of 166

1.

Trait components provide tools to dissect the genetic susceptibility of migraine.

Anttila V, Kallela M, Oswell G, Kaunisto MA, Nyholt DR, Hamalainen E, Havanka H, Ilmavirta M, Terwilliger J, Sobel E, Peltonen L, Kaprio J, Farkkila M, Wessman M, Palotie A.

Am J Hum Genet. 2006 Jul;79(1):85-99.

2.

Consistently replicating locus linked to migraine on 10q22-q23.

Anttila V, Nyholt DR, Kallela M, Artto V, Vepsäläinen S, Jakkula E, Wennerström A, Tikka-Kleemola P, Kaunisto MA, Hämäläinen E, Widén E, Terwilliger J, Merikangas K, Montgomery GW, Martin NG, Daly M, Kaprio J, Peltonen L, Färkkilä M, Wessman M, Palotie A.

Am J Hum Genet. 2008 May;82(5):1051-63. doi: 10.1016/j.ajhg.2008.03.003.

3.

A genome-wide linkage study of bipolar disorder and co-morbid migraine: replication of migraine linkage on chromosome 4q24, and suggestion of an overlapping susceptibility region for both disorders on chromosome 20p11.

Oedegaard KJ, Greenwood TA, Lunde A, Fasmer OB, Akiskal HS, Kelsoe JR; NIMH Genetics Initiative Bipolar Disorder Consortium..

J Affect Disord. 2010 Apr;122(1-2):14-26. doi: 10.1016/j.jad.2009.06.014.

PMID:
19819557
4.

A susceptibility locus for migraine with aura, on chromosome 4q24.

Wessman M, Kallela M, Kaunisto MA, Marttila P, Sobel E, Hartiala J, Oswell G, Leal SM, Papp JC, Hämäläinen E, Broas P, Joslyn G, Hovatta I, Hiekkalinna T, Kaprio J, Ott J, Cantor RM, Zwart JA, Ilmavirta M, Havanka H, Färkkilä M, Peltonen L, Palotie A.

Am J Hum Genet. 2002 Mar;70(3):652-62.

5.

Genomewide significant linkage to migrainous headache on chromosome 5q21.

Nyholt DR, Morley KI, Ferreira MA, Medland SE, Boomsma DI, Heath AC, Merikangas KR, Montgomery GW, Martin NG.

Am J Hum Genet. 2005 Sep;77(3):500-12.

6.

A genome-wide linkage scan provides evidence for both new and previously reported loci influencing common migraine.

Ligthart L, Nyholt DR, Hottenga JJ, Distel MA, Willemsen G, Boomsma DI.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1186-95. doi: 10.1002/ajmg.b.30749.

PMID:
18361423
7.

Genomewide linkage scan for nicotine dependence: identification of a chromosome 5 risk locus.

Gelernter J, Panhuysen C, Weiss R, Brady K, Poling J, Krauthammer M, Farrer L, Kranzler HR.

Biol Psychiatry. 2007 Jan 1;61(1):119-26.

PMID:
17081504
8.

Further evidence for a susceptibility locus contributing to reading disability on chromosome 15q15-q21.

Schumacher J, König IR, Schröder T, Duell M, Plume E, Propping P, Warnke A, Libertus C, Ziegler A, Müller-Myhsok B, Schulte-Körne G, Nöthen MM.

Psychiatr Genet. 2008 Jun;18(3):137-42. doi: 10.1097/YPG.0b013e3282fb7fc6.

PMID:
18496212
9.

Linkage analysis of high myopia susceptibility locus in 26 families.

Paget S, Julia S, Vitezica ZG, Soler V, Malecaze F, Calvas P.

Mol Vis. 2008;14:2566-74.

10.

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.

Alkelai A, Kohn Y, Olender T, Sarner-Kanyas K, Rigbi A, Hamdan A, Ben-Asher E, Lancet D, Lerer B.

Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):914-25. doi: 10.1002/ajmg.b.30918.

PMID:
19152384
11.

Resting metabolic rate and respiratory quotient: results from a genome-wide scan in the Quebec Family Study.

Jacobson P, Rankinen T, Tremblay A, Pérusse L, Chagnon YC, Bouchard C.

Am J Clin Nutr. 2006 Dec;84(6):1527-33.

12.

A new susceptibility locus for migraine with aura in the 15q11-q13 genomic region containing three GABA-A receptor genes.

Russo L, Mariotti P, Sangiorgi E, Giordano T, Ricci I, Lupi F, Chiera R, Guzzetta F, Neri G, Gurrieri F.

Am J Hum Genet. 2005 Feb;76(2):327-33.

13.

A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity.

Lee H, Jen JC, Wang H, Chen Z, Mamsa H, Sabatti C, Baloh RW, Nelson SF.

Hum Mol Genet. 2006 Jan 15;15(2):251-8.

PMID:
16330481
14.

A visual migraine aura locus maps to 9q21-q22.

Tikka-Kleemola P, Artto V, Vepsäläinen S, Sobel EM, Räty S, Kaunisto MA, Anttila V, Hämäläinen E, Sumelahti ML, Ilmavirta M, Färkkilä M, Kallela M, Palotie A, Wessman M.

Neurology. 2010 Apr 13;74(15):1171-7. doi: 10.1212/WNL.0b013e3181d8ffcb.

15.

Molecular genetics of migraine.

de Vries B, Frants RR, Ferrari MD, van den Maagdenberg AM.

Hum Genet. 2009 Jul;126(1):115-32. doi: 10.1007/s00439-009-0684-z. Review.

PMID:
19455354
16.

Familial hemiplegic migraine in the west of Scotland: a clinical and genetic study of seven families.

Ahmed MA, Reid E, Cooke A, Arngrímsson R, Tolmie JL, Stephenson JB.

J Neurol Neurosurg Psychiatry. 1996 Dec;61(6):616-20.

17.

Migraine with aura susceptibility locus on chromosome 19p13 is distinct from the familial hemiplegic migraine locus.

Jones KW, Ehm MG, Pericak-Vance MA, Haines JL, Boyd PR, Peroutka SJ.

Genomics. 2001 Dec;78(3):150-4.

PMID:
11735221
18.

Follow-up analysis of 180 Chinese Han families: identification of a novel locus for psoriasis at 2p22.3-11.2.

Sun LD, Yang S, Liu JJ, Ren YQ, Fan X, Xu SX, Zhou L, Yang CJ, Xiao FL, Gao M, Cui Y, Du WH, Huang W, Zhang XJ.

Br J Dermatol. 2008 Mar;158(3):512-7. doi: 10.1111/j.1365-2133.2007.08417.x.

PMID:
18241272
19.

Genome-wide linkage analysis of lipids in nondiabetic Chinese and Japanese from the SAPPHIRe family study.

Hsiao CF, Chiu YF, Chiang FT, Ho LT, Lee WJ, Hung YJ, Chen YD, Donlon TA, Jorgenson E, Curb D, Risch N, Hsiung CA; SAPPHIRe Study Group..

Am J Hypertens. 2006 Dec;19(12):1270-7.

PMID:
17161774
20.

Suggestive genetic linkage to chromosome 11p11.2-q12.2 in hereditary prostate cancer families with primary kidney cancer.

Johanneson B, Deutsch K, McIntosh L, Friedrichsen-Karyadi DM, Janer M, Kwon EM, Iwasaki L, Hood L, Ostrander EA, Stanford JL.

Prostate. 2007 May 15;67(7):732-42.

PMID:
17372923

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