Praphanphoj V - Search Results

1

The Thai reference exome (T-REx) variant database.

Shotelersuk V, Wichadakul D, Ngamphiw C, Srichomthong C, Phokaew C, Wilantho A, Pakchuen S, Nakhonsri V, Shaw PJ, Wasitthankasem R, Piriyapongsa J, Wangkumhang P, Assawapitaksakul A, Chetruengchai W, Lapphra K, Khuninthong A, Makarawate P, Suphapeetiporn K, Mahasirimongkol S, Satproedprai N, Porntaveetus T, Pisitkun P, Praphanphoj V, Kantaputra P, Tassaneeyakul W, Tongsima S. Shotelersuk V, et al. Among authors: praphanphoj v. Clin Genet. 2021 Dec;100(6):703-712. doi: 10.1111/cge.14060. Epub 2021 Sep 22. Clin Genet. 2021. PMID: 34496037

2

Insight into the peopling of Mainland Southeast Asia from Thai population genetic structure.

Wangkumhang P, Shaw PJ, Chaichoompu K, Ngamphiw C, Assawamakin A, Nuinoon M, Sripichai O, Svasti S, Fucharoen S, Praphanphoj V, Tongsima S. Wangkumhang P, et al. Among authors: praphanphoj v. PLoS One. 2013 Nov 4;8(11):e79522. doi: 10.1371/journal.pone.0079522. eCollection 2013. PLoS One. 2013. PMID: 24223962 Free PMC article.

3

PTPRF is disrupted in a patient with syndromic amastia.

Ausavarat S, Tongkobpetch S, Praphanphoj V, Mahatumarat C, Rojvachiranonda N, Snabboon T, Markello TC, Gahl WA, Suphapeetiporn K, Shotelersuk V. Ausavarat S, et al. Among authors: praphanphoj v. BMC Med Genet. 2011 Mar 31;12:46. doi: 10.1186/1471-2350-12-46. BMC Med Genet. 2011. PMID: 21453473 Free PMC article.

4

Microcephalic osteodysplastic primordial dwarfism with severe microdontia and skin anomalies: confirmation of a new syndrome.

Kantaputra PN, Tanpaiboon P, Unachak K, Praphanphoj V. Kantaputra PN, et al. Among authors: praphanphoj v. Am J Med Genet A. 2004 Oct 1;130A(2):181-90. doi: 10.1002/ajmg.a.30079. Am J Med Genet A. 2004. PMID: 15372530 Review.

5

Mesomelic dysplasia Kantaputra type is associated with duplications of the HOXD locus on chromosome 2q.

Kantaputra PN, Klopocki E, Hennig BP, Praphanphoj V, Le Caignec C, Isidor B, Kwee ML, Shears DJ, Mundlos S. Kantaputra PN, et al. Among authors: praphanphoj v. Eur J Hum Genet. 2010 Dec;18(12):1310-4. doi: 10.1038/ejhg.2010.116. Epub 2010 Jul 21. Eur J Hum Genet. 2010. PMID: 20648051 Free PMC article.

6

Contiguous gene syndrome of holoprosencephaly and hypotrichosis simplex: association with an 18p11.3 deletion.

Kantaputra PN, Limwongse C, Tochareontanaphol C, Mutirangura A, Mevatee U, Praphanphoj V. Kantaputra PN, et al. Among authors: praphanphoj v. Am J Med Genet A. 2006 Dec 1;140(23):2598-602. doi: 10.1002/ajmg.a.31386. Am J Med Genet A. 2006. PMID: 17001671

7

Prenatal exclusion of subtelomeric deletion 1p by fluorescent in situ hybridization.

Phupong V, Praphanphoj V, Shotelersuk V. Phupong V, et al. Among authors: praphanphoj v. Arch Gynecol Obstet. 2007 Apr;275(4):237-40. doi: 10.1007/s00404-006-0246-8. Epub 2006 Sep 16. Arch Gynecol Obstet. 2007. PMID: 16983561

8

Tetralogy of Fallot with absent pulmonary valve in a de novo derivative chromosome 9 with duplication of 9p13 --> 9pter and deletion of 9q34.3.

Tansatit M, Kongruttanachok N, Kongnak W, Arunpan S, Maneeshote P, Buasorn V, Praphanphoj V, Shotelersuk V. Tansatit M, et al. Among authors: praphanphoj v. Am J Med Genet A. 2006 Sep 15;140(18):1981-7. doi: 10.1002/ajmg.a.31424. Am J Med Genet A. 2006. PMID: 16906562 No abstract available.

9

Glucocorticoid receptor gene (NR3C1) promoter is hypermethylated in Thai females with major depressive disorder.

Nantharat M, Wanitchanon T, Amesbutr M, Tammachote R, Praphanphoj V. Nantharat M, et al. Among authors: praphanphoj v. Genet Mol Res. 2015 Dec 29;14(4):19071-9. doi: 10.4238/2015.December.29.15. Genet Mol Res. 2015. PMID: 26782558 Free article.

10

Tricho-rhino-phalangeal syndrome with supernumerary teeth.

Kantaputra P, Miletich I, Lüdecke HJ, Suzuki EY, Praphanphoj V, Shivdasani R, Wuelling M, Vortkamp A, Napierala D, Sharpe PT. Kantaputra P, et al. Among authors: praphanphoj v. J Dent Res. 2008 Nov;87(11):1027-31. doi: 10.1177/154405910808701102. J Dent Res. 2008. PMID: 18946009

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