Jiao H - Search Results

1

PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants.

Kämpe AJ, Costantini A, Mäkitie RE, Jäntti N, Valta H, Mäyränpää M, Kröger H, Pekkinen M, Taylan F, Jiao H, Mäkitie O. Kämpe AJ, et al. Among authors: jiao h. Osteoporos Int. 2017 Oct;28(10):3023-3032. doi: 10.1007/s00198-017-4150-9. Epub 2017 Jul 26. Osteoporos Int. 2017. PMID: 28748388 Free PMC article.

2

Exome sequencing followed by genotyping suggests SYPL2 as a susceptibility gene for morbid obesity.

Jiao H, Arner P, Gerdhem P, Strawbridge RJ, Näslund E, Thorell A, Hamsten A, Kere J, Dahlman I. Jiao H, et al. Eur J Hum Genet. 2015 Sep;23(9):1216-22. doi: 10.1038/ejhg.2014.255. Epub 2014 Nov 19. Eur J Hum Genet. 2015. PMID: 25406998 Free PMC article.

3

Candidate gene analysis and exome sequencing confirm LBX1 as a susceptibility gene for idiopathic scoliosis.

Grauers A, Wang J, Einarsdottir E, Simony A, Danielsson A, Åkesson K, Ohlin A, Halldin K, Grabowski P, Tenne M, Laivuori H, Dahlman I, Andersen M, Christensen SB, Karlsson MK, Jiao H, Kere J, Gerdhem P. Grauers A, et al. Among authors: jiao h. Spine J. 2015 Oct 1;15(10):2239-46. doi: 10.1016/j.spinee.2015.05.013. Epub 2015 May 15. Spine J. 2015. PMID: 25987191

4

Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants.

Kaartokallio T, Wang J, Heinonen S, Kajantie E, Kivinen K, Pouta A, Gerdhem P, Jiao H, Kere J, Laivuori H. Kaartokallio T, et al. Among authors: jiao h. Sci Rep. 2016 Jul 7;6:29085. doi: 10.1038/srep29085. Sci Rep. 2016. PMID: 27384325 Free PMC article.

5

Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples.

Wang J, Skoog T, Einarsdottir E, Kaartokallio T, Laivuori H, Grauers A, Gerdhem P, Hytönen M, Lohi H, Kere J, Jiao H. Wang J, et al. Among authors: jiao h. Sci Rep. 2016 Sep 16;6:33256. doi: 10.1038/srep33256. Sci Rep. 2016. PMID: 27633116 Free PMC article.

6

CRTAP variants in early-onset osteoporosis and recurrent fractures.

Costantini A, Vuorimies I, Mäkitie R, Mäyränpää MK, Becker J, Pekkinen M, Valta H, Netzer C, Kämpe A, Taylan F, Jiao H, Mäkitie O. Costantini A, et al. Among authors: jiao h. Am J Med Genet A. 2017 Mar;173(3):806-808. doi: 10.1002/ajmg.a.38065. Epub 2016 Nov 30. Am J Med Genet A. 2017. PMID: 27901313 No abstract available.

7

PLS3 Deletions Lead to Severe Spinal Osteoporosis and Disturbed Bone Matrix Mineralization.

Kämpe AJ, Costantini A, Levy-Shraga Y, Zeitlin L, Roschger P, Taylan F, Lindstrand A, Paschalis EP, Gamsjaeger S, Raas-Rothschild A, Hövel M, Jiao H, Klaushofer K, Grasemann C, Mäkitie O. Kämpe AJ, et al. Among authors: jiao h. J Bone Miner Res. 2017 Dec;32(12):2394-2404. doi: 10.1002/jbmr.3233. Epub 2017 Sep 6. J Bone Miner Res. 2017. PMID: 28777485 Free article.

8

Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility.

Costantini A, Skarp S, Kämpe A, Mäkitie RE, Pettersson M, Männikkö M, Jiao H, Taylan F, Lindstrand A, Mäkitie O. Costantini A, et al. Among authors: jiao h. Front Endocrinol (Lausanne). 2018 Jul 10;9:380. doi: 10.3389/fendo.2018.00380. eCollection 2018. Front Endocrinol (Lausanne). 2018. PMID: 30042735 Free PMC article.

9

Impact of estrogen receptor gene polymorphisms and mRNA levels on obesity and lipolysis--a cohort study.

Nilsson M, Dahlman I, Jiao H, Gustafsson JA, Arner P, Dahlman-Wright K. Nilsson M, et al. Among authors: jiao h. BMC Med Genet. 2007 Dec 4;8:73. doi: 10.1186/1471-2350-8-73. BMC Med Genet. 2007. PMID: 18053221 Free PMC article.

10

ROCK2 allelic variants are not associated with pre-eclampsia susceptibility in the Finnish population.

Peterson H, Laivuori H, Kerkelä E, Jiao H, Hiltunen L, Heino S, Tiala I, Knuutila S, Rasi V, Kere J, Kivinen K. Peterson H, et al. Among authors: jiao h. Mol Hum Reprod. 2009 Jul;15(7):443-9. doi: 10.1093/molehr/gap032. Epub 2009 May 12. Mol Hum Reprod. 2009. PMID: 19435756

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