Lahiry P[au] - Search Results

Year	Number of Results
2006	1
2007	1
2008	2
2009	2
2010	3
2011	1
2013	2
2014	1
2016	1
2022	1
2023	1
2024	0

1

Joy T, Lahiry P, Pollex RL, Hegele RA. Joy T, et al. Among authors: lahiry p. Curr Diab Rep. 2008 Apr;8(2):141-8. doi: 10.1007/s11892-008-0025-y. Curr Diab Rep. 2008. PMID: 18445357 Review.

2

Kinase mutations in human disease: interpreting genotype-phenotype relationships.

Lahiry P, Torkamani A, Schork NJ, Hegele RA. Lahiry P, et al. Nat Rev Genet. 2010 Jan;11(1):60-74. doi: 10.1038/nrg2707. Nat Rev Genet. 2010. PMID: 20019687 Review.

3

Uncloaking the genetic determinants of metabolic syndrome.

Lahiry P, Pollex RL, Hegele RA. Lahiry P, et al. J Nutrigenet Nutrigenomics. 2008;1(3):118-25. doi: 10.1159/000112459. Epub 2008 Feb 20. J Nutrigenet Nutrigenomics. 2008. PMID: 19776621 Review.

4

Phenomics: expanding the role of clinical evaluation in genomic studies.

Lanktree MB, Hassell RG, Lahiry P, Hegele RA. Lanktree MB, et al. Among authors: lahiry p. J Investig Med. 2010 Jun;58(5):700-6. doi: 10.231/JIM.0b013e3181d844f7. J Investig Med. 2010. PMID: 20216460 Review.

5

Micromethods for the characterization of lipid A-core and O-antigen lipopolysaccharide.

Marolda CL, Lahiry P, Vinés E, Saldías S, Valvano MA. Marolda CL, et al. Among authors: lahiry p. Methods Mol Biol. 2006;347:237-52. doi: 10.1385/1-59745-167-3:237. Methods Mol Biol. 2006. PMID: 17072014 Review.

6

Hemophagocytic Lymphohistiocytosis Gene Variants in Childhood-Onset Systemic Lupus Erythematosus With Macrophage Activation Syndrome.

Lahiry P, Naumenko S, Couse M, Liao F, Dominguez D, Knight A, Levy DM, Misztal M, Ng LWK, Hiraki LT. Lahiry P, et al. J Rheumatol. 2022 Oct;49(10):1146-1151. doi: 10.3899/jrheum.211200. Epub 2022 Jun 1. J Rheumatol. 2022. PMID: 35649546

7

Choosing Wisely: The Canadian Rheumatology Association Pediatric Committee's List of Items Physicians and Patients Should Question.

Lim L, McMillan T, Chédeville G, Lahiry P, Lee JJY, Heale LD, Human AL, McGrath TR, MacQueen SE, Stringer E, Jariwala MP, Neufeld KM, Soon GS, Spiegel LR, Luca NJC. Lim L, et al. Among authors: lahiry p. J Rheumatol. 2023 Aug 1:jrheum.2023-0043. doi: 10.3899/jrheum.2023-0043. Online ahead of print. J Rheumatol. 2023. PMID: 37527858

8

A novel ICK mutation causes ciliary disruption and lethal endocrine-cerebro-osteodysplasia syndrome.

Oud MM, Bonnard C, Mans DA, Altunoglu U, Tohari S, Ng AYJ, Eskin A, Lee H, Rupar CA, de Wagenaar NP, Wu KM, Lahiry P, Pazour GJ, Nelson SF, Hegele RA, Roepman R, Kayserili H, Venkatesh B, Siu VM, Reversade B, Arts HH. Oud MM, et al. Among authors: lahiry p. Cilia. 2016 Apr 11;5:8. doi: 10.1186/s13630-016-0029-1. eCollection 2016. Cilia. 2016. PMID: 27069622 Free PMC article.

9

A mutation in the serine protease TMPRSS4 in a novel pediatric neurodegenerative disorder.

Lahiry P, Racacho L, Wang J, Robinson JF, Gloor GB, Rupar CA, Siu VM, Bulman DE, Hegele RA. Lahiry P, et al. Orphanet J Rare Dis. 2013 Aug 17;8:126. doi: 10.1186/1750-1172-8-126. Orphanet J Rare Dis. 2013. PMID: 23957953 Free PMC article.

10

Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiency.

Farhan SM, Wang J, Robinson JF, Lahiry P, Siu VM, Prasad C, Kronick JB, Ramsay DA, Rupar CA, Hegele RA. Farhan SM, et al. Among authors: lahiry p. Mol Genet Genomic Med. 2014 Jan;2(1):73-80. doi: 10.1002/mgg3.46. Epub 2013 Nov 18. Mol Genet Genomic Med. 2014. PMID: 24498631 Free PMC article.

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