Kaukonen M - Search Results

1

Maternal Inheritance of a Recessive RBP4 Defect in Canine Congenital Eye Disease.

Kaukonen M, Woods S, Ahonen S, Lemberg S, Hellman M, Hytönen MK, Permi P, Glaser T, Lohi H. Kaukonen M, et al. Cell Rep. 2018 May 29;23(9):2643-2652. doi: 10.1016/j.celrep.2018.04.118. Cell Rep. 2018. PMID: 29847795 Free PMC article.

2

A novel missense mutation in ADAMTS10 in Norwegian Elkhound primary glaucoma.

Ahonen SJ, Kaukonen M, Nussdorfer FD, Harman CD, Komáromy AM, Lohi H. Ahonen SJ, et al. Among authors: kaukonen m. PLoS One. 2014 Nov 5;9(11):e111941. doi: 10.1371/journal.pone.0111941. eCollection 2014. PLoS One. 2014. PMID: 25372548 Free PMC article.

3

Increased expression of MERTK is associated with a unique form of canine retinopathy.

Ahonen SJ, Arumilli M, Seppälä E, Hakosalo O, Kaukonen MK, Komáromy AM, Lohi H. Ahonen SJ, et al. Among authors: kaukonen mk. PLoS One. 2014 Dec 17;9(12):e114552. doi: 10.1371/journal.pone.0114552. eCollection 2014. PLoS One. 2014. PMID: 25517981 Free PMC article.

4

Genetic Panel Screening of Nearly 100 Mutations Reveals New Insights into the Breed Distribution of Risk Variants for Canine Hereditary Disorders.

Donner J, Kaukonen M, Anderson H, Möller F, Kyöstilä K, Sankari S, Hytönen M, Giger U, Lohi H. Donner J, et al. Among authors: kaukonen m. PLoS One. 2016 Aug 15;11(8):e0161005. doi: 10.1371/journal.pone.0161005. eCollection 2016. PLoS One. 2016. PMID: 27525650 Free PMC article.

5

A Coding Variant in the Gene Bardet-Biedl Syndrome 4 (BBS4) Is Associated with a Novel Form of Canine Progressive Retinal Atrophy.

Chew T, Haase B, Bathgate R, Willet CE, Kaukonen MK, Mascord LJ, Lohi HT, Wade CM. Chew T, et al. Among authors: kaukonen mk. G3 (Bethesda). 2017 Jul 5;7(7):2327-2335. doi: 10.1534/g3.117.043109. G3 (Bethesda). 2017. PMID: 28533336 Free PMC article.

6

An intronic LINE-1 insertion in MERTK is strongly associated with retinopathy in Swedish Vallhund dogs.

Everson R, Pettitt L, Forman OP, Dower-Tylee O, McLaughlin B, Ahonen S, Kaukonen M, Komáromy AM, Lohi H, Mellersh CS, Sansom J, Ricketts SL. Everson R, et al. Among authors: kaukonen m. PLoS One. 2017 Aug 16;12(8):e0183021. doi: 10.1371/journal.pone.0183021. eCollection 2017. PLoS One. 2017. PMID: 28813472 Free PMC article.

7

Skin microbiota and allergic symptoms associate with exposure to environmental microbes.

Lehtimäki J, Sinkko H, Hielm-Björkman A, Salmela E, Tiira K, Laatikainen T, Mäkeläinen S, Kaukonen M, Uusitalo L, Hanski I, Lohi H, Ruokolainen L. Lehtimäki J, et al. Among authors: kaukonen m. Proc Natl Acad Sci U S A. 2018 May 8;115(19):4897-4902. doi: 10.1073/pnas.1719785115. Epub 2018 Apr 23. Proc Natl Acad Sci U S A. 2018. PMID: 29686089 Free PMC article.

8

Frequency and distribution of 152 genetic disease variants in over 100,000 mixed breed and purebred dogs.

Donner J, Anderson H, Davison S, Hughes AM, Bouirmane J, Lindqvist J, Lytle KM, Ganesan B, Ottka C, Ruotanen P, Kaukonen M, Forman OP, Fretwell N, Cole CA, Lohi H. Donner J, et al. Among authors: kaukonen m. PLoS Genet. 2018 Apr 30;14(4):e1007361. doi: 10.1371/journal.pgen.1007361. eCollection 2018 Apr. PLoS Genet. 2018. PMID: 29708978 Free PMC article.

9

Whole Genome Sequencing of Giant Schnauzer Dogs with Progressive Retinal Atrophy Establishes NECAP1 as a Novel Candidate Gene for Retinal Degeneration.

Hitti RJ, Oliver JAC, Schofield EC, Bauer A, Kaukonen M, Forman OP, Leeb T, Lohi H, Burmeister LM, Sargan D, Mellersh CS. Hitti RJ, et al. Among authors: kaukonen m. Genes (Basel). 2019 May 21;10(5):385. doi: 10.3390/genes10050385. Genes (Basel). 2019. PMID: 31117272 Free PMC article.

10

A putative silencer variant in a spontaneous canine model of retinitis pigmentosa.

Kaukonen M, Quintero IB, Mukarram AK, Hytönen MK, Holopainen S, Wickström K, Kyöstilä K, Arumilli M, Jalomäki S, Daub CO, Kere J, Lohi H; DoGA Consortium. Kaukonen M, et al. PLoS Genet. 2020 Mar 9;16(3):e1008659. doi: 10.1371/journal.pgen.1008659. eCollection 2020 Mar. PLoS Genet. 2020. PMID: 32150541 Free PMC article.

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