Salim A - Search Results

1

Neonatal genetics of gene expression reveal potential origins of autoimmune and allergic disease risk.

Huang QQ, Tang HHF, Teo SM, Mok D, Ritchie SC, Nath AP, Brozynska M, Salim A, Bakshi A, Holt BJ, Khor CC, Sly PD, Holt PG, Holt KE, Inouye M. Huang QQ, et al. Among authors: salim a. Nat Commun. 2020 Jul 28;11(1):3761. doi: 10.1038/s41467-020-17477-x. Nat Commun. 2020. PMID: 32724101 Free PMC article.

2

Multi-platform segmentation for joint detection of copy number variants.

Teo SM, Pawitan Y, Kumar V, Thalamuthu A, Seielstad M, Chia KS, Salim A. Teo SM, et al. Among authors: salim a. Bioinformatics. 2011 Jun 1;27(11):1555-61. doi: 10.1093/bioinformatics/btr162. Epub 2011 Apr 5. Bioinformatics. 2011. PMID: 21471018

3

Statistical challenges associated with detecting copy number variations with next-generation sequencing.

Teo SM, Pawitan Y, Ku CS, Chia KS, Salim A. Teo SM, et al. Among authors: salim a. Bioinformatics. 2012 Nov 1;28(21):2711-8. doi: 10.1093/bioinformatics/bts535. Epub 2012 Aug 31. Bioinformatics. 2012. PMID: 22942022 Review.

4

Combined genotype and haplotype tests for region-based association studies.

Zakharov S, Wong TY, Aung T, Vithana EN, Khor CC, Salim A, Thalamuthu A. Zakharov S, et al. Among authors: salim a. BMC Genomics. 2013 Aug 21;14:569. doi: 10.1186/1471-2164-14-569. BMC Genomics. 2013. PMID: 23964661 Free PMC article.

5

Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke.

Abraham G, Malik R, Yonova-Doing E, Salim A, Wang T, Danesh J, Butterworth AS, Howson JMM, Inouye M, Dichgans M. Abraham G, et al. Among authors: salim a. Nat Commun. 2019 Dec 20;10(1):5819. doi: 10.1038/s41467-019-13848-1. Nat Commun. 2019. PMID: 31862893 Free PMC article.

6

Author Correction: Genomic risk score offers predictive performance comparable to clinical risk factors for ischaemic stroke.

Abraham G, Malik R, Yonova-Doing E, Salim A, Wang T, Danesh J, Butterworth AS, Howson JMM, Inouye M, Dichgans M. Abraham G, et al. Among authors: salim a. Nat Commun. 2020 Feb 20;11(1):1036. doi: 10.1038/s41467-020-14717-y. Nat Commun. 2020. PMID: 32080192 Free PMC article.

7

Concordant peripheral lipidome signatures in two large clinical studies of Alzheimer's disease.

Huynh K, Lim WLF, Giles C, Jayawardana KS, Salim A, Mellett NA, Smith AAT, Olshansky G, Drew BG, Chatterjee P, Martins I, Laws SM, Bush AI, Rowe CC, Villemagne VL, Ames D, Masters CL, Arnold M, Nho K, Saykin AJ, Baillie R, Han X, Kaddurah-Daouk R, Martins RN, Meikle PJ. Huynh K, et al. Among authors: salim a. Nat Commun. 2020 Nov 10;11(1):5698. doi: 10.1038/s41467-020-19473-7. Nat Commun. 2020. PMID: 33173055 Free PMC article.

8

Identification of recurrent regions of Copy-Number Variants across multiple individuals.

Mei TS, Salim A, Calza S, Seng KC, Seng CK, Pawitan Y. Mei TS, et al. Among authors: salim a. BMC Bioinformatics. 2010 Mar 22;11:147. doi: 10.1186/1471-2105-11-147. BMC Bioinformatics. 2010. PMID: 20307285 Free PMC article.

9

DECENT: differential expression with capture efficiency adjustmeNT for single-cell RNA-seq data.

Ye C, Speed TP, Salim A. Ye C, et al. Among authors: salim a. Bioinformatics. 2019 Dec 15;35(24):5155-5162. doi: 10.1093/bioinformatics/btz453. Bioinformatics. 2019. PMID: 31197307 Free PMC article.

10

RUV-III-NB: normalization of single cell RNA-seq data.

Salim A, Molania R, Wang J, De Livera A, Thijssen R, Speed TP. Salim A, et al. Nucleic Acids Res. 2022 Sep 9;50(16):e96. doi: 10.1093/nar/gkac486. Nucleic Acids Res. 2022. PMID: 35758618 Free PMC article.

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