Hegele RA - Search Results

1

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone.

Huang L, Szymanska K, Jensen VL, Janecke AR, Innes AM, Davis EE, Frosk P, Li C, Willer JR, Chodirker BN, Greenberg CR, McLeod DR, Bernier FP, Chudley AE, Müller T, Shboul M, Logan CV, Loucks CM, Beaulieu CL, Bowie RV, Bell SM, Adkins J, Zuniga FI, Ross KD, Wang J, Ban MR, Becker C, Nürnberg P, Douglas S, Craft CM, Akimenko MA, Hegele RA, Ober C, Utermann G, Bolz HJ, Bulman DE, Katsanis N, Blacque OE, Doherty D, Parboosingh JS, Leroux MR, Johnson CA, Boycott KM. Huang L, et al. Among authors: hegele ra. Am J Hum Genet. 2011 Dec 9;89(6):713-30. doi: 10.1016/j.ajhg.2011.11.005. Am J Hum Genet. 2011. PMID: 22152675 Free PMC article.

2

A microdeletion within DAX-1 in X-linked adrenal hypoplasia congenita and hypogonadotrophic hypogonadism.

Wang J, Killinger DW, Hegele RA. Wang J, et al. Among authors: hegele ra. J Investig Med. 1999 May;47(5):232-5. J Investig Med. 1999. PMID: 10361383

3

An approach to ascertain probands with a non-traditional risk factor for carotid atherosclerosis.

Spence JD, Barnett PA, Bulman DE, Hegele RA. Spence JD, et al. Among authors: hegele ra. Atherosclerosis. 1999 Jun;144(2):429-34. doi: 10.1016/s0021-9150(99)00003-9. Atherosclerosis. 1999. PMID: 10407504

4

Lipoprotein-genotype associations in Trinidadian neonates.

Hegele RA, Ban MR, Busch CP, Ramsewak S, Ramdath DD. Hegele RA, et al. Clin Biochem. 1999 Aug;32(6):429-37. doi: 10.1016/s0009-9120(99)00035-1. Clin Biochem. 1999. PMID: 10667478

5

Microsomal triglyceride transfer protein (MTP) gene mutations in Canadian subjects with abetalipoproteinemia.

Wang J, Hegele RA. Wang J, et al. Among authors: hegele ra. Hum Mutat. 2000 Mar;15(3):294-5. doi: 10.1002/(SICI)1098-1004(200003)15:3<294::AID-HUMU14>3.0.CO;2-E. Hum Mutat. 2000. PMID: 10679949

6

Infection-susceptibility alleles of mannose-binding lectin are associated with increased carotid plaque area.

Hegele RA, Ban MR, Anderson CM, Spence JD. Hegele RA, et al. J Investig Med. 2000 May;48(3):198-202. J Investig Med. 2000. PMID: 10822900

7

Polymorphisms in PNLIP, encoding pancreatic lipase, and associations with metabolic traits.

Hegele RA, Ramdath DD, Ban MR, Carruthers MN, Carrington CV, Cao H. Hegele RA, et al. J Hum Genet. 2001;46(6):320-4. doi: 10.1007/s100380170066. J Hum Genet. 2001. PMID: 11393534

8

Single-nucleotide polymorphisms of the nuclear lamina proteome.

Hegele RA, Yuen J, Cao H. Hegele RA, et al. J Hum Genet. 2001;46(6):351-4. doi: 10.1007/s100380170072. J Hum Genet. 2001. PMID: 11393540

9

Single nucleotide polymorphisms of the very low density lipoprotein receptor (VLDLR) gene.

Near SE, Wang J, Hegele RA. Near SE, et al. Among authors: hegele ra. J Hum Genet. 2001;46(8):490-3. doi: 10.1007/s100380170051. J Hum Genet. 2001. PMID: 11501949

10

Allele frequencies for candidate genes in atherosclerosis and diabetes among Trinidadian neonates.

Hegele RA, Ban MR, Carrington CV, Ramdath DD. Hegele RA, et al. Hum Biol. 2001 Aug;73(4):525-31. doi: 10.1353/hub.2001.0052. Hum Biol. 2001. PMID: 11512679

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