Kere J - Search Results

1

Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.

Peyrard-Janvid M, Pegelow M, Koillinen H, Larsson C, Fransson I, Rautio J, Hukki J, Larson O, Karsten AL, Kere J. Peyrard-Janvid M, et al. Among authors: kere j. Eur J Hum Genet. 2005 Dec;13(12):1261-7. doi: 10.1038/sj.ejhg.5201493. Eur J Hum Genet. 2005. PMID: 16160700

2

Genetic heterogeneity and exclusion of a modifying locus at 17p11.2-p11.1 in Finnish families with van der Woude syndrome.

Wong FK, Koillinen H, Rautio J, Teh BT, Ranta R, Karsten A, Larson O, Linder-Aronson S, Huggare J, Larsson C, Kere J. Wong FK, et al. Among authors: kere j. J Med Genet. 2001 Mar;38(3):198-202. doi: 10.1136/jmg.38.3.198. J Med Genet. 2001. PMID: 11303516 Free PMC article. No abstract available.

3

Mapping of the second locus for the Van der Woude syndrome to chromosome 1p34.

Koillinen H, Wong FK, Rautio J, Ollikainen V, Karsten A, Larson O, Teh BT, Huggare J, Lahermo P, Larsson C, Kere J. Koillinen H, et al. Among authors: kere j. Eur J Hum Genet. 2001 Oct;9(10):747-52. doi: 10.1038/sj.ejhg.5200713. Eur J Hum Genet. 2001. PMID: 11781685

4

Collagen XI sequence variations in nonsyndromic cleft palate, Robin sequence and micrognathia.

Melkoniemi M, Koillinen H, Männikkö M, Warman ML, Pihlajamaa T, Kääriäinen H, Rautio J, Hukki J, Stofko JA, Cisneros GJ, Krakow D, Cohn DH, Kere J, Ala-Kokko L. Melkoniemi M, et al. Among authors: kere j. Eur J Hum Genet. 2003 Mar;11(3):265-70. doi: 10.1038/sj.ejhg.5200950. Eur J Hum Genet. 2003. PMID: 12673280

5

Linkage and linkage disequilibrium searched for between non-syndromic cleft palate and four candidate loci.

Koillinen H, Ollikainen V, Rautio J, Hukki J, Kere J. Koillinen H, et al. Among authors: kere j. J Med Genet. 2003 Jun;40(6):464-8. doi: 10.1136/jmg.40.6.464. J Med Genet. 2003. PMID: 12807970 Free PMC article. No abstract available.

6

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.

Peyrard-Janvid M, Anthoni H, Onkamo P, Lahermo P, Zucchelli M, Kaminen N, Hannula-Jouppi K, Nopola-Hemmi J, Voutilainen A, Lyytinen H, Kere J. Peyrard-Janvid M, et al. Among authors: kere j. Hum Genet. 2004 Apr;114(5):510-6. doi: 10.1007/s00439-004-1103-0. Epub 2004 Mar 6. Hum Genet. 2004. PMID: 15007729

7

Family-based association study of DYX1C1 variants in autism.

Ylisaukko-Oja T, Peyrard-Janvid M, Lindgren CM, Rehnström K, Vanhala R, Peltonen L, Järvelä I, Kere J. Ylisaukko-Oja T, et al. Among authors: kere j. Eur J Hum Genet. 2005 Jan;13(1):127-30. doi: 10.1038/sj.ejhg.5201272. Eur J Hum Genet. 2005. PMID: 15470369

8

A genome-wide scan of non-syndromic cleft palate only (CPO) in Finnish multiplex families.

Koillinen H, Lahermo P, Rautio J, Hukki J, Peyrard-Janvid M, Kere J. Koillinen H, et al. Among authors: kere j. J Med Genet. 2005 Feb;42(2):177-84. doi: 10.1136/jmg.2004.019646. J Med Genet. 2005. PMID: 15689458 Free PMC article. No abstract available.

9

Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia.

Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hülsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, Ziegler A, Peyrard-Janvid M, Schulte-Körne G, Nöthen MM, Kere J. Schumacher J, et al. Among authors: kere j. Am J Hum Genet. 2006 Jan;78(1):52-62. doi: 10.1086/498992. Epub 2005 Nov 17. Am J Hum Genet. 2006. PMID: 16385449 Free PMC article.

10

ELMOD2 is a candidate gene for familial idiopathic pulmonary fibrosis.

Hodgson U, Pulkkinen V, Dixon M, Peyrard-Janvid M, Rehn M, Lahermo P, Ollikainen V, Salmenkivi K, Kinnula V, Kere J, Tukiainen P, Laitinen T. Hodgson U, et al. Among authors: kere j. Am J Hum Genet. 2006 Jul;79(1):149-54. doi: 10.1086/504639. Epub 2006 May 9. Am J Hum Genet. 2006. PMID: 16773575 Free PMC article.

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