Leal SM - Search Results

1

Whole genome sequencing identifies candidate genes for familial essential tremor and reveals biological pathways implicated in essential tremor aetiology.

Clark LN, Gao Y, Wang GT, Hernandez N, Ashley-Koch A, Jankovic J, Ottman R, Leal SM, Rodriguez SMB, Louis ED. Clark LN, et al. Among authors: leal sm. EBioMedicine. 2022 Nov;85:104290. doi: 10.1016/j.ebiom.2022.104290. Epub 2022 Sep 29. EBioMedicine. 2022. PMID: 36183486 Free PMC article.

2

A fast and noise-resilient approach to detect rare-variant associations with deep sequencing data for complex disorders.

Cheung YH, Wang G, Leal SM, Wang S. Cheung YH, et al. Among authors: leal sm. Genet Epidemiol. 2012 Nov;36(7):675-85. doi: 10.1002/gepi.21662. Epub 2012 Aug 3. Genet Epidemiol. 2012. PMID: 22865616 Free PMC article.

3

SimRare: a program to generate and analyze sequence-based data for association studies of quantitative and qualitative traits.

Li B, Wang G, Leal SM. Li B, et al. Among authors: leal sm. Bioinformatics. 2012 Oct 15;28(20):2703-4. doi: 10.1093/bioinformatics/bts499. Epub 2012 Aug 22. Bioinformatics. 2012. PMID: 22914216 Free PMC article.

4

Testing for rare variant associations in the presence of missing data.

Auer PL, Wang G, Leal SM. Auer PL, et al. Among authors: leal sm. Genet Epidemiol. 2013 Sep;37(6):529-38. doi: 10.1002/gepi.21736. Epub 2013 Jun 11. Genet Epidemiol. 2013. PMID: 23757187 Free PMC article.

5

PhenoMan: phenotypic data exploration, selection, management and quality control for association studies of rare and common variants.

Li B, Wang G, Leal SM. Li B, et al. Among authors: leal sm. Bioinformatics. 2014 Feb 1;30(3):442-4. doi: 10.1093/bioinformatics/btt682. Epub 2013 Dec 12. Bioinformatics. 2014. PMID: 24336645 Free PMC article.

6

Power analysis and sample size estimation for sequence-based association studies.

Wang GT, Li B, Santos-Cortez RP, Peng B, Leal SM. Wang GT, et al. Among authors: leal sm. Bioinformatics. 2014 Aug 15;30(16):2377-8. doi: 10.1093/bioinformatics/btu296. Epub 2014 Apr 28. Bioinformatics. 2014. PMID: 24778108 Free PMC article.

7

Variant association tools for quality control and analysis of large-scale sequence and genotyping array data.

Wang GT, Peng B, Leal SM. Wang GT, et al. Among authors: leal sm. Am J Hum Genet. 2014 May 1;94(5):770-83. doi: 10.1016/j.ajhg.2014.04.004. Am J Hum Genet. 2014. PMID: 24791902 Free PMC article.

8

RNF213 rare variants in an ethnically diverse population with Moyamoya disease.

Cecchi AC, Guo D, Ren Z, Flynn K, Santos-Cortez RL, Leal SM, Wang GT, Regalado ES, Steinberg GK, Shendure J, Bamshad MJ; University of Washington Center for Mendelian Genomics; Grotta JC, Nickerson DA, Pannu H, Milewicz DM. Cecchi AC, et al. Among authors: leal sm. Stroke. 2014 Nov;45(11):3200-7. doi: 10.1161/STROKEAHA.114.006244. Epub 2014 Oct 2. Stroke. 2014. PMID: 25278557 Free PMC article.

9

Collapsed haplotype pattern method for linkage analysis of next-generation sequence data.

Wang GT, Zhang D, Li B, Dai H, Leal SM. Wang GT, et al. Among authors: leal sm. Eur J Hum Genet. 2015 Dec;23(12):1739-43. doi: 10.1038/ejhg.2015.64. Epub 2015 Apr 15. Eur J Hum Genet. 2015. PMID: 25873013 Free PMC article.

10

Generation of sequence-based data for pedigree-segregating Mendelian or Complex traits.

Li B, Wang GT, Leal SM. Li B, et al. Among authors: leal sm. Bioinformatics. 2015 Nov 15;31(22):3706-8. doi: 10.1093/bioinformatics/btv412. Epub 2015 Jul 14. Bioinformatics. 2015. PMID: 26177964 Free PMC article.

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