Bourgain C - Search Results

1

Searching for secondary findings: considering actionability and preserving the right not to know.

Isidor B, Julia S, Saugier-Veber P, Weil-Dubuc PL, Bézieau S, Bieth E, Bonnefont JP, Munnich A, Bourdeaut F, Bourgain C, Chassaing N, Corradini N, Haye D, Plaisancie J, Dupin-Deguine D, Calvas P, Mignot C, Cogné B, Manouvrier S, Pasquier L, Héron D, Boycott KM, Turrini M, Vears DF, Nizon M, Vincent M. Isidor B, et al. Among authors: bourgain c. Eur J Hum Genet. 2019 Oct;27(10):1481-1484. doi: 10.1038/s41431-019-0438-x. Epub 2019 Jun 11. Eur J Hum Genet. 2019. PMID: 31186543 Free PMC article. No abstract available.

2

[Susceptibility genetics of common conditions in clinical practice].

Turrini M, Connault J, Bourgain C. Turrini M, et al. Among authors: bourgain c. Med Sci (Paris). 2020 May;36(5):515-520. doi: 10.1051/medsci/2020083. Epub 2020 May 26. Med Sci (Paris). 2020. PMID: 32452374 Free article. French.

3

Genomic susceptibility in practice: The regulatory trajectory of non-rare thrombophilia (NRT) genetic tests in the clinical management of venous thrombo-embolism (VTE).

Turrini M, Bourgain C. Turrini M, et al. Among authors: bourgain c. Soc Sci Med. 2022 Jul;304:112903. doi: 10.1016/j.socscimed.2020.112903. Epub 2020 Mar 3. Soc Sci Med. 2022. PMID: 32156430

4

Appraising screening, making risk in/visible. The medical debate over Non-Rare Thrombophilia (NRT) testing before prescribing the pill.

Turrini M, Bourgain C. Turrini M, et al. Among authors: bourgain c. Sociol Health Illn. 2021 Aug;43(7):1627-1642. doi: 10.1111/1467-9566.13348. Epub 2021 Jul 22. Sociol Health Illn. 2021. PMID: 34293180 Review.

5

Are genome-wide association studies all that we need to dissect the genetic component of complex human diseases?

Bourgain C, Génin E, Cox N, Clerget-Darpoux F. Bourgain C, et al. Eur J Hum Genet. 2007 Mar;15(3):260-3. doi: 10.1038/sj.ejhg.5201753. Epub 2006 Dec 13. Eur J Hum Genet. 2007. PMID: 17164797

6

The ethics of genomic medicine: redefining values and norms in the UK and France.

Gaille M, Horn R; UK-FR GENE (Genetics and Ethics Network) Consortia. Gaille M, et al. Eur J Hum Genet. 2021 May;29(5):780-788. doi: 10.1038/s41431-020-00798-2. Epub 2021 Jan 17. Eur J Hum Genet. 2021. PMID: 33456054 Free PMC article.

7

Complex trait mapping in isolated populations: Are specific statistical methods required?

Bourgain C, Génin E. Bourgain C, et al. Eur J Hum Genet. 2005 Jun;13(6):698-706. doi: 10.1038/sj.ejhg.5201400. Eur J Hum Genet. 2005. PMID: 15785775 Review.

8

Comparison of family based haplotype methods using intragenic SNPs in candidate genes.

Bourgain C, Genin E, Clerget-Darpoux F. Bourgain C, et al. Eur J Hum Genet. 2002 May;10(5):313-9. doi: 10.1038/sj.ejhg.5200808. Eur J Hum Genet. 2002. PMID: 12082506

9

Are common disease susceptibility alleles the same in outbred and founder populations?

Newman DL, Hoffjan S, Bourgain C, Abney M, Nicolae RI, Profits ET, Grow MA, Walker K, Steiner L, Parry R, Reynolds R, McPeek MS, Cheng S, Ober C. Newman DL, et al. Among authors: bourgain c. Eur J Hum Genet. 2004 Jul;12(7):584-90. doi: 10.1038/sj.ejhg.5201191. Eur J Hum Genet. 2004. PMID: 15100713

10

Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus.

Bourgain C, Hoffjan S, Nicolae R, Newman D, Steiner L, Walker K, Reynolds R, Ober C, McPeek MS. Bourgain C, et al. Am J Hum Genet. 2003 Sep;73(3):612-26. doi: 10.1086/378208. Epub 2003 Aug 15. Am J Hum Genet. 2003. PMID: 12929084 Free PMC article.

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