PubMed for id: 285600

Year	Number of Results
1998	1
2001	1
2002	1
2003	1
2004	3
2010	1
2011	2
2012	2
2014	1
2016	1
2018	1
2019	2
2020	4
2021	2
2022	2
2023	2
2024	0

1

Prenatal Detection of Novel Compound Heterozygous Splice Site Variants of the KIAA0825 Gene in a Fetus with Postaxial Polydactyly Type A.

Yao Y, Deng S, Zhu F. Yao Y, et al. Genes (Basel). 2022 Jul 11;13(7):1230. doi: 10.3390/genes13071230. Genes (Basel). 2022. PMID: 35886013 Free PMC article.

2

Identification of a novel biallelic missense variant in the KIAA0825 underlies postaxial polydactyly type A.

Hayat A, Umair M, Abbas S, Rauf A, Ahmad F, Ullah S, Ahmad W, Khan B. Hayat A, et al. Genomics. 2020 Jul;112(4):2729-2733. doi: 10.1016/j.ygeno.2020.03.006. Epub 2020 Mar 5. Genomics. 2020. PMID: 32147526 Free article.

3

Variants in KIAA0825 underlie autosomal recessive postaxial polydactyly.

Ullah I, Kakar N, Schrauwen I, Hussain S, Chakchouk I, Liaqat K, Acharya A, Wasif N, Santos-Cortez RLP, Khan S, Aziz A, Lee K, Couthouis J, Horn D, Kragesteen BK, Spielmann M, Thiele H, Nickerson DA, Bamshad MJ, Gitler AD, Ahmad J, Ansar M, Borck G, Ahmad W, Leal SM. Ullah I, et al. Hum Genet. 2019 Jun;138(6):593-600. doi: 10.1007/s00439-019-02000-0. Epub 2019 Apr 13. Hum Genet. 2019. PMID: 30982135 Free PMC article.

4

Identification of GLI1 and KIAA0825 Variants in Two Families with Postaxial Polydactyly.

Ahmad S, Ali MZ, Muzammal M, Khan AU, Ikram M, Muurinen M, Hussain S, Loid P, Khan MA, Mäkitie O. Ahmad S, et al. Genes (Basel). 2023 Apr 5;14(4):869. doi: 10.3390/genes14040869. Genes (Basel). 2023. PMID: 37107627 Free PMC article.

5

Schilit SL, Currall BB, Yao R, Hanscom C, Collins RL, Pillalamarri V, Lee DY, Kammin T, Zepeda-Mendoza CJ, Mononen T, Nolan LS, Gusella JF, Talkowski ME, Shen J, Morton CC. Schilit SL, et al. Eur J Hum Genet. 2016 Nov;24(11):1622-1626. doi: 10.1038/ejhg.2016.64. Epub 2016 Jul 6. Eur J Hum Genet. 2016. PMID: 27381092 Free PMC article.

6

A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population.

Cha PC, Zembutsu H, Takahashi A, Kubo M, Kamatani N, Nakamura Y. Cha PC, et al. J Hum Genet. 2012 Apr;57(4):235-7. doi: 10.1038/jhg.2012.9. Epub 2012 Feb 9. J Hum Genet. 2012. PMID: 22318345

7

Genome-wide association study of diabetic retinopathy in a Taiwanese population.

Huang YC, Lin JM, Lin HJ, Chen CC, Chen SY, Tsai CH, Tsai FJ. Huang YC, et al. Ophthalmology. 2011 Apr;118(4):642-8. doi: 10.1016/j.ophtha.2010.07.020. Epub 2011 Feb 18. Ophthalmology. 2011. PMID: 21310492

8

Genome-wide association study identifies ALLC polymorphisms correlated with FEV₁ change by corticosteroid.

Park TJ, Park JS, Cheong HS, Park BL, Kim LH, Heo JS, Kim YK, Kim KU, Uh ST, Lee HS, Na JO, Seo KH, Choi JS, Kim YH, Kim MS, Park CS, Shin HD. Park TJ, et al. Clin Chim Acta. 2014 Sep 25;436:20-6. doi: 10.1016/j.cca.2014.04.023. Epub 2014 May 2. Clin Chim Acta. 2014. PMID: 24792382 Clinical Trial.

9

Cross-linking mass spectrometry reveals the structural topology of peripheral NuRD subunits relative to the core complex.

Spruijt CG, Gräwe C, Kleinendorst SC, Baltissen MPA, Vermeulen M. Spruijt CG, et al. FEBS J. 2021 May;288(10):3231-3245. doi: 10.1111/febs.15650. Epub 2020 Dec 14. FEBS J. 2021. PMID: 33283408 Free PMC article.

10

The DNA sequence and comparative analysis of human chromosome 5.

Schmutz J, Martin J, Terry A, Couronne O, Grimwood J, Lowry S, Gordon LA, Scott D, Xie G, Huang W, Hellsten U, Tran-Gyamfi M, She X, Prabhakar S, Aerts A, Altherr M, Bajorek E, Black S, Branscomb E, Caoile C, Challacombe JF, Chan YM, Denys M, Detter JC, Escobar J, Flowers D, Fotopulos D, Glavina T, Gomez M, Gonzales E, Goodstein D, Grigoriev I, Groza M, Hammon N, Hawkins T, Haydu L, Israni S, Jett J, Kadner K, Kimball H, Kobayashi A, Lopez F, Lou Y, Martinez D, Medina C, Morgan J, Nandkeshwar R, Noonan JP, Pitluck S, Pollard M, Predki P, Priest J, Ramirez L, Retterer J, Rodriguez A, Rogers S, Salamov A, Salazar A, Thayer N, Tice H, Tsai M, Ustaszewska A, Vo N, Wheeler J, Wu K, Yang J, Dickson M, Cheng JF, Eichler EE, Olsen A, Pennacchio LA, Rokhsar DS, Richardson P, Lucas SM, Myers RM, Rubin EM. Schmutz J, et al. Nature. 2004 Sep 16;431(7006):268-74. doi: 10.1038/nature02919. Nature. 2004. PMID: 15372022

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