Kere J - Search Results

1

FUT2 Variants Confer Susceptibility to Familial Otitis Media.

Santos-Cortez RLP, Chiong CM, Frank DN, Ryan AF, Giese APJ, Bootpetch Roberts T, Daly KA, Steritz MJ, Szeremeta W, Pedro M, Pine H, Yarza TKL, Scholes MA, Llanes EGDV, Yousaf S, Friedman N, Tantoco MLC, Wine TM, Labra PJ, Benoit J, Ruiz AG, de la Cruz RAR, Greenlee C, Yousaf A, Cardwell J, Nonato RMA, Ray D, Ong KMC, So E, Robertson CE, Dinwiddie J, Lagrana-Villagracia SM; University of Washington Center for Mendelian Genomics (UWCMG); Gubbels SP, Shaikh RS, Cass SP, Einarsdottir E, Lee NR, Schwartz DA, Gloria-Cruz TLI, Bamshad MJ, Yang IV, Kere J, Abes GT, Prager JD, Riazuddin S, Chan AL, Yoon PJ, Nickerson DA, Cutiongco-de la Paz EM, Streubel SO, Reyes-Quintos MRT, Jenkins HA, Mattila P, Chan KH, Mohlke KL, Leal SM, Hafrén L, Chonmaitree T, Sale MM, Ahmed ZM. Santos-Cortez RLP, et al. Among authors: kere j. Am J Hum Genet. 2018 Nov 1;103(5):679-690. doi: 10.1016/j.ajhg.2018.09.010. Epub 2018 Oct 25. Am J Hum Genet. 2018. PMID: 30401457 Free PMC article.

2

Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.

Höglund P, Sistonen P, Norio R, Holmberg C, Dimberg A, Gustavson KH, de la Chapelle A, Kere J. Höglund P, et al. Among authors: kere j. Am J Hum Genet. 1995 Jul;57(1):95-102. Am J Hum Genet. 1995. PMID: 7611301 Free PMC article.

3

Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.

Höglund P, Holmberg C, de la Chapelle A, Kere J. Höglund P, et al. Among authors: kere j. Am J Hum Genet. 1994 Oct;55(4):747-52. Am J Hum Genet. 1994. PMID: 7942853 Free PMC article.

4

A rare reciprocal translocation (12;21) segregating for nine generations.

Koskinen S, Onnelainen T, de la Chapelle A, Kere J. Koskinen S, et al. Among authors: kere j. Hum Genet. 1993 Nov;92(5):509-12. doi: 10.1007/BF00216460. Hum Genet. 1993. PMID: 8244343 Review.

5

Microsatellite diversity and the demographic history of modern humans.

Jorde LB, Rogers AR, Bamshad M, Watkins WS, Krakowiak P, Sung S, Kere J, Harpending HC. Jorde LB, et al. Among authors: kere j. Proc Natl Acad Sci U S A. 1997 Apr 1;94(7):3100-3. doi: 10.1073/pnas.94.7.3100. Proc Natl Acad Sci U S A. 1997. PMID: 9096352 Free PMC article.

6

Anhidrotic ectodermal dysplasia (EDA) protein expressed in MCF-7 cells associates with cell membrane and induces rounding.

Ezer S, Schlessinger D, Srivastava A, Kere J. Ezer S, et al. Among authors: kere j. Hum Mol Genet. 1997 Sep;6(9):1581-7. doi: 10.1093/hmg/6.9.1581. Hum Mol Genet. 1997. PMID: 9285797

7

Transglutaminase 1 mutations in autosomal recessive congenital ichthyosis: private and recurrent mutations in an isolated population.

Laiho E, Ignatius J, Mikkola H, Yee VC, Teller DC, Niemi KM, Saarialho-Kere U, Kere J, Palotie A. Laiho E, et al. Among authors: kere j. Am J Hum Genet. 1997 Sep;61(3):529-38. doi: 10.1086/515498. Am J Hum Genet. 1997. PMID: 9326318 Free PMC article.

8

Genetic background of congenital chloride diarrhea in high-incidence populations: Finland, Poland, and Saudi Arabia and Kuwait.

Höglund P, Auranen M, Socha J, Popinska K, Nazer H, Rajaram U, Al Sanie A, Al-Ghanim M, Holmberg C, de la Chapelle A, Kere J. Höglund P, et al. Among authors: kere j. Am J Hum Genet. 1998 Sep;63(3):760-8. doi: 10.1086/301998. Am J Hum Genet. 1998. PMID: 9718329 Free PMC article.

9

Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.

Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Virolainen E, et al. Among authors: kere j. Am J Hum Genet. 2000 Mar;66(3):1132-7. doi: 10.1086/302813. Am J Hum Genet. 2000. PMID: 10712223 Free PMC article.

10

A candidate gene for psoriasis near HLA-C, HCR (Pg8), is highly polymorphic with a disease-associated susceptibility allele.

Asumalahti K, Laitinen T, Itkonen-Vatjus R, Lokki ML, Suomela S, Snellman E, Saarialho-Kere U, Kere J. Asumalahti K, et al. Among authors: kere j. Hum Mol Genet. 2000 Jun 12;9(10):1533-42. doi: 10.1093/hmg/9.10.1533. Hum Mol Genet. 2000. PMID: 10888604

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