Jugessur A - Search Results

1

Complete mutation screening and haplotype characterization of the BRCA1 gene in 61 familial breast cancer patients from Norway.

Frost P, Jugessur A, Apold J, Heimdal K, Aloysius T, Eliassen AK, Fauske L, Matre G, Eiken HG. Frost P, et al. Among authors: jugessur a. Dis Markers. 2005;21(1):29-36. doi: 10.1155/2005/542928. Dis Markers. 2005. PMID: 15735322 Free PMC article.

2

Enhanced detection of mutations in BRCA1 exon 11 using restriction endonuclease fingerprinting-single-strand conformation polymorphism.

Jugessur A, Frost P, Andersen TI, Steine S, Lindblom A, Børresen-Dale AL, Eiken HG. Jugessur A, et al. J Mol Med (Berl). 2000;78(10):580-7. doi: 10.1007/s001090000147. J Mol Med (Berl). 2000. PMID: 11199332

3

Rapid genotyping of the human renin (REN) gene by the LightCycler® instrument: identification of unexpected nucleotide substitutions within the selected hybridization probe area.

Wee L, Vefring H, Jonsson G, Jugessur A, Lie RT. Wee L, et al. Among authors: jugessur a. Dis Markers. 2010;29(5):243-9. doi: 10.3233/DMA-2010-0754. Dis Markers. 2010. PMID: 21206009 Free PMC article.

4

Genetic variants in IRF6 and the risk of facial clefts: single-marker and haplotype-based analyses in a population-based case-control study of facial clefts in Norway.

Jugessur A, Rahimov F, Lie RT, Wilcox AJ, Gjessing HK, Nilsen RM, Nguyen TT, Murray JC. Jugessur A, et al. Genet Epidemiol. 2008 Jul;32(5):413-24. doi: 10.1002/gepi.20314. Genet Epidemiol. 2008. PMID: 18278815 Free PMC article.

5

Variants of developmental genes (TGFA, TGFB3, and MSX1) and their associations with orofacial clefts: a case-parent triad analysis.

Jugessur A, Lie RT, Wilcox AJ, Murray JC, Taylor JA, Saugstad OD, Vindenes HA, Abyholm F. Jugessur A, et al. Genet Epidemiol. 2003 Apr;24(3):230-9. doi: 10.1002/gepi.10223. Genet Epidemiol. 2003. PMID: 12652527

6

Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads.

Jugessur A, Wilcox AJ, Lie RT, Murray JC, Taylor JA, Ulvik A, Drevon CA, Vindenes HA, Abyholm FE. Jugessur A, et al. Am J Epidemiol. 2003 Jun 15;157(12):1083-91. doi: 10.1093/aje/kwg097. Am J Epidemiol. 2003. PMID: 12796044

7

Haplin power analysis: a software module for power and sample size calculations in genetic association analyses of family triads and unrelated controls.

Gjerdevik M, Jugessur A, Haaland ØA, Romanowska J, Lie RT, Cordell HJ, Gjessing HK. Gjerdevik M, et al. Among authors: jugessur a. BMC Bioinformatics. 2019 Apr 2;20(1):165. doi: 10.1186/s12859-019-2727-3. BMC Bioinformatics. 2019. PMID: 30940094 Free PMC article.

8

Maternal angiotensinogen (AGT) haplotypes, fetal renin (REN) haplotypes and risk of preeclampsia; estimation of gene-gene interaction from family-triad data.

Vefring HK, Wee L, Jugessur A, Gjessing HK, Nilsen ST, Lie RT. Vefring HK, et al. Among authors: jugessur a. BMC Med Genet. 2010 Jun 10;11:90. doi: 10.1186/1471-2350-11-90. BMC Med Genet. 2010. PMID: 20537141 Free PMC article.

9

Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.

Jugessur A, Shi M, Gjessing HK, Lie RT, Wilcox AJ, Weinberg CR, Christensen K, Boyles AL, Daack-Hirsch S, Nguyen TT, Christiansen L, Lidral AC, Murray JC. Jugessur A, et al. PLoS One. 2010 Jul 9;5(7):e11493. doi: 10.1371/journal.pone.0011493. PLoS One. 2010. PMID: 20634891 Free PMC article.

10

X-linked genes and risk of orofacial clefts: evidence from two population-based studies in Scandinavia.

Jugessur A, Skare Ø, Lie RT, Wilcox AJ, Christensen K, Christiansen L, Nguyen TT, Murray JC, Gjessing HK. Jugessur A, et al. PLoS One. 2012;7(6):e39240. doi: 10.1371/journal.pone.0039240. Epub 2012 Jun 19. PLoS One. 2012. PMID: 22723972 Free PMC article.

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