Similar articles for PMID: 16467216

Year	Number of Results
1996	1
2000	2
2001	1
2002	2
2003	4
2004	3
2005	7
2006	9
2007	2
2008	1
2009	1
2010	1
2011	2
2012	2
2014	1
2015	1
2019	1
2020	1
2024	0

1

Independent replication and initial fine mapping of 3p21-24 in Asperger syndrome.

Rehnström K, Ylisaukko-oja T, Nieminen-von Wendt T, Sarenius S, Källman T, Kempas E, von Wendt L, Peltonen L, Järvelä I. Rehnström K, et al. J Med Genet. 2006 Feb;43(2):e6. doi: 10.1136/jmg.2005.033621. J Med Genet. 2006. PMID: 16467216 Free PMC article.

2

Genome-wide scan for loci of Asperger syndrome.

Ylisaukko-oja T, Nieminen-von Wendt T, Kempas E, Sarenius S, Varilo T, von Wendt L, Peltonen L, Järvelä I. Ylisaukko-oja T, et al. Mol Psychiatry. 2004 Feb;9(2):161-8. doi: 10.1038/sj.mp.4001385. Mol Psychiatry. 2004. PMID: 14966474

3

Fine mapping of Xq11.1-q21.33 and mutation screening of RPS6KA6, ZNF711, ACSL4, DLG3, and IL1RAPL2 for autism spectrum disorders (ASD).

Kantojärvi K, Kotala I, Rehnström K, Ylisaukko-Oja T, Vanhala R, von Wendt TN, von Wendt L, Järvelä I. Kantojärvi K, et al. Autism Res. 2011 Jun;4(3):228-33. doi: 10.1002/aur.187. Epub 2011 Feb 22. Autism Res. 2011. PMID: 21384559

4

Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.

EPICURE Consortium; Leu C, de Kovel CG, Zara F, Striano P, Pezzella M, Robbiano A, Bianchi A, Bisulli F, Coppola A, Giallonardo AT, Beccaria F, Trenité DK, Lindhout D, Gaus V, Schmitz B, Janz D, Weber YG, Becker F, Lerche H, Kleefuss-Lie AA, Hallman K, Kunz WS, Elger CE, Muhle H, Stephani U, Møller RS, Hjalgrim H, Mullen S, Scheffer IE, Berkovic SF, Everett KV, Gardiner MR, Marini C, Guerrini R, Lehesjoki AE, Siren A, Nabbout R, Baulac S, Leguern E, Serratosa JM, Rosenow F, Feucht M, Unterberger I, Covanis A, Suls A, Weckhuysen S, Kaneva R, Caglayan H, Turkdogan D, Baykan B, Bebek N, Ozbek U, Hempelmann A, Schulz H, Rüschendorf F, Trucks H, Nürnberg P, Avanzini G, Koeleman BP, Sander T. EPICURE Consortium, et al. Epilepsia. 2012 Feb;53(2):308-18. doi: 10.1111/j.1528-1167.2011.03379.x. Epub 2012 Jan 13. Epilepsia. 2012. PMID: 22242659 Free article.

5

Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping.

Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li TK, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, Begleiter H, Reich T. Foroud T, et al. Alcohol Clin Exp Res. 2000 Jul;24(7):933-45. Alcohol Clin Exp Res. 2000. PMID: 10923994 Clinical Trial.

6

Genome-wide linkage analysis for celiac disease in North American families.

Neuhausen SL, Feolo M, Camp NJ, Farnham J, Book L, Zone JJ. Neuhausen SL, et al. Am J Med Genet. 2002 Jul 22;111(1):1-9. doi: 10.1002/ajmg.10527. Am J Med Genet. 2002. PMID: 12124726

7

[Genetic factors in Asperger syndrome].

Sasaki T. Sasaki T. Nihon Rinsho. 2007 Mar;65(3):443-8. Nihon Rinsho. 2007. PMID: 17354555 Review. Japanese.

8

Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21.

Paavola P, Heliö T, Kiuru M, Halme L, Turunen U, Terwilliger J, Karvonen AL, Julkunen R, Niemelä S, Nurmi H, Färkkilä M, Kontula K. Paavola P, et al. Eur J Hum Genet. 2001 May;9(5):328-34. doi: 10.1038/sj.ejhg.5200626. Eur J Hum Genet. 2001. PMID: 11378820

9

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. Lin MW, et al. Br J Dermatol. 2005 Jan;152(1):29-36. doi: 10.1111/j.1365-2133.2004.06254.x. Br J Dermatol. 2005. PMID: 15656797

10

Evidence for linkage to and association with type 1 diabetes at the 3q21 region in the Finnish population.

Laine AP, Turpeinen H, Veijola R, Hermann R, Simell O, Knip M, Ilonen J. Laine AP, et al. Genes Immun. 2006 Jan;7(1):69-72. doi: 10.1038/sj.gene.6364269. Genes Immun. 2006. PMID: 16292340

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