Goh DL - Search Results

1

Strategies for identifying the genetic basis of dyslipidemia: genome-wide association studies vs. the resequencing of extremes.

Khor CC, Goh DL. Khor CC, et al. Among authors: goh dl. Curr Opin Lipidol. 2010 Apr;21(2):123-7. doi: 10.1097/MOL.0b013e328336eae9. Curr Opin Lipidol. 2010. PMID: 20125008 Review.

2

Analysis of clinically relevant variants from ancestrally diverse Asian genomes.

Chan SH, Bylstra Y, Teo JX, Kuan JL, Bertin N, Gonzalez-Porta M, Hebrard M, Tirado-Magallanes R, Tan JHJ, Jeyakani J, Li Z, Chai JF, Chong YS, Davila S, Goh LL, Lee ES, Wong E, Wong TY; SG10K_Health Consortium; Prabhakar S, Liu J, Cheng CY, Eisenhaber B, Karnani N, Leong KP, Sim X, Yeo KK, Chambers JC, Tai ES, Tan P, Jamuar SS, Ngeow J, Lim WK. Chan SH, et al. Nat Commun. 2022 Nov 5;13(1):6694. doi: 10.1038/s41467-022-34116-9. Nat Commun. 2022. PMID: 36335097 Free PMC article.

3

Singapore Undiagnosed Disease Program: Genomic Analysis aids Diagnosis and Clinical Management.

Bhatia NS, Lim JY, Bonnard C, Kuan JL, Brett M, Wei H, Cham B, Chin H, Bosso-Lefevre C, Dharuman P, Escande-Beillard N, Devasia AG, Goh CYJ, Kam S, Liew WK, Liew WK, Lin G, Jain K, Ng AY, Subramanian D, Xie M, Tan YM, Tawari NR, Tiang Z, Ting TW, Tohari S, Tong CK, Lezhava A, Ng SB, Law HY, Venkatesh B, Tomar S, Sethi R, Tan G, Shanmugasundaram A, Goh DL, Lai PS, Lai A, Tan ES, Ng I, Reversades B, Tan EC, Foo R, Jamuar SS; SUREKids Working Group. Bhatia NS, et al. Among authors: goh dl. Arch Dis Child. 2021 Jan;106(1):31-37. doi: 10.1136/archdischild-2020-319180. Epub 2020 Aug 20. Arch Dis Child. 2021. PMID: 32819910

4

Parvalbumin--the major tropical fish allergen.

Lim DL, Neo KH, Yi FC, Chua KY, Goh DL, Shek LP, Giam YC, Van Bever HP, Lee BW. Lim DL, et al. Among authors: goh dl. Pediatr Allergy Immunol. 2008 Aug;19(5):399-407. doi: 10.1111/j.1399-3038.2007.00674.x. Epub 2008 Jan 25. Pediatr Allergy Immunol. 2008. PMID: 18221468

5

Clinical report: a case of Williams Syndrome and Klinefelter Syndrome.

Lee le Y, Quek SC, Chong SS, Tan AS, Lum JM, Goh DL. Lee le Y, et al. Among authors: goh dl. Ann Acad Med Singap. 2006 Dec;35(12):901-4. Ann Acad Med Singap. 2006. PMID: 17219004 Free article.

6

Identification and characterization of novel mouse PDE4D isoforms: molecular cloning, subcellular distribution and detection of isoform-specific intracellular localization signals.

Chandrasekaran A, Toh KY, Low SH, Tay SK, Brenner S, Goh DL. Chandrasekaran A, et al. Among authors: goh dl. Cell Signal. 2008 Jan;20(1):139-53. doi: 10.1016/j.cellsig.2007.10.003. Epub 2007 Oct 12. Cell Signal. 2008. PMID: 18006274

7

Identification and molecular characterization of a novel PDE4D11 cAMP-specific phosphodiesterase isoform.

Lynex CN, Li Z, Chen ML, Toh KY, Low RW, Goh DL, Tay SK. Lynex CN, et al. Among authors: goh dl. Cell Signal. 2008 Dec;20(12):2247-55. doi: 10.1016/j.cellsig.2008.08.020. Epub 2008 Sep 4. Cell Signal. 2008. PMID: 18804162

8

Two consecutive partial liver transplants in a patient with Classic Maple Syrup Urine Disease.

Chin HL, Aw MM, Quak SH, Huang J, Hart CE, Prabhakaran K, Goh DL. Chin HL, et al. Among authors: goh dl. Mol Genet Metab Rep. 2015 Jul 12;4:49-52. doi: 10.1016/j.ymgmr.2015.06.003. eCollection 2015 Sep. Mol Genet Metab Rep. 2015. PMID: 26937410 Free PMC article.

9

A combination of two novel VARS2 variants causes a mitochondrial disorder associated with failure to thrive and pulmonary hypertension.

Chin HL, Goh DL, Wang FS, Tay SKH, Heng CK, Donnini C, Baruffini E, Pines O. Chin HL, et al. Among authors: goh dl. J Mol Med (Berl). 2019 Nov;97(11):1557-1566. doi: 10.1007/s00109-019-01834-5. Epub 2019 Sep 16. J Mol Med (Berl). 2019. PMID: 31529142

10

Reduced resource utilization with early use of next-generation sequencing in rare genetic diseases in an Asian cohort.

Nazeha N, Koh AL, Kam S, Lim JY, Goh DLM, Jamuar SS, Graves N. Nazeha N, et al. Among authors: goh dlm. Am J Med Genet A. 2022 Dec;188(12):3482-3491. doi: 10.1002/ajmg.a.62974. Epub 2022 Sep 25. Am J Med Genet A. 2022. PMID: 36156406

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