MacRae CA - Search Results

1

Locus for atrial fibrillation maps to chromosome 6q14-16.

Ellinor PT, Shin JT, Moore RK, Yoerger DM, MacRae CA. Ellinor PT, et al. Among authors: macrae ca. Circulation. 2003 Jun 17;107(23):2880-3. doi: 10.1161/01.CIR.0000077910.80718.49. Epub 2003 Jun 2. Circulation. 2003. PMID: 12782570

2

A disease locus for familial hypertrophic cardiomyopathy maps to chromosome 1q3.

Watkins H, MacRae C, Thierfelder L, Chou YH, Frenneaux M, McKenna W, Seidman JG, Seidman CE. Watkins H, et al. Nat Genet. 1993 Apr;3(4):333-7. doi: 10.1038/ng0493-333. Nat Genet. 1993. PMID: 7981753

3

A familial hypertrophic cardiomyopathy locus maps to chromosome 15q2.

Thierfelder L, MacRae C, Watkins H, Tomfohrde J, Williams M, McKenna W, Bohm K, Noeske G, Schlepper M, Bowcock A, et al. Thierfelder L, et al. Proc Natl Acad Sci U S A. 1993 Jul 1;90(13):6270-4. doi: 10.1073/pnas.90.13.6270. Proc Natl Acad Sci U S A. 1993. PMID: 8327508 Free PMC article.

4

A gene for non-syndromic autosomal dominant progressive postlingual sensorineural hearing loss maps to chromosome 14q12-13.

Manolis EN, Yandavi N, Nadol JB Jr, Eavey RD, McKenna M, Rosenbaum S, Khetarpal U, Halpin C, Merchant SN, Duyk GM, MacRae C, Seidman CE, Seidman JG. Manolis EN, et al. Hum Mol Genet. 1996 Jul;5(7):1047-50. doi: 10.1093/hmg/5.7.1047. Hum Mol Genet. 1996. PMID: 8817345

5

Familial dilated cardiomyopathy locus maps to chromosome 2q31.

Siu BL, Niimura H, Osborne JA, Fatkin D, MacRae C, Solomon S, Benson DW, Seidman JG, Seidman CE. Siu BL, et al. Circulation. 1999 Mar 2;99(8):1022-6. doi: 10.1161/01.cir.99.8.1022. Circulation. 1999. PMID: 10051295

6

Dilated cardiomyopathy and sensorineural hearing loss: a heritable syndrome that maps to 6q23-24.

Schönberger J, Levy H, Grünig E, Sangwatanaroj S, Fatkin D, MacRae C, Stäcker H, Halpin C, Eavey R, Philbin EF, Katus H, Seidman JG, Seidman CE. Schönberger J, et al. Circulation. 2000 Apr 18;101(15):1812-8. doi: 10.1161/01.cir.101.15.1812. Circulation. 2000. PMID: 10769282

7

Mutation in the transcriptional coactivator EYA4 causes dilated cardiomyopathy and sensorineural hearing loss.

Schönberger J, Wang L, Shin JT, Kim SD, Depreux FF, Zhu H, Zon L, Pizard A, Kim JB, Macrae CA, Mungall AJ, Seidman JG, Seidman CE. Schönberger J, et al. Among authors: macrae ca. Nat Genet. 2005 Apr;37(4):418-22. doi: 10.1038/ng1527. Epub 2005 Feb 27. Nat Genet. 2005. PMID: 15735644

8

Human-zebrafish non-coding conserved elements act in vivo to regulate transcription.

Shin JT, Priest JR, Ovcharenko I, Ronco A, Moore RK, Burns CG, MacRae CA. Shin JT, et al. Among authors: macrae ca. Nucleic Acids Res. 2005 Sep 22;33(17):5437-45. doi: 10.1093/nar/gki853. Print 2005. Nucleic Acids Res. 2005. PMID: 16179648 Free PMC article.

9

Cardiac sodium channel gene variants and sudden cardiac death in women.

Albert CM, Nam EG, Rimm EB, Jin HW, Hajjar RJ, Hunter DJ, MacRae CA, Ellinor PT. Albert CM, et al. Among authors: macrae ca. Circulation. 2008 Jan 1;117(1):16-23. doi: 10.1161/CIRCULATIONAHA.107.736330. Epub 2007 Dec 10. Circulation. 2008. PMID: 18071069

10

Cardiac sodium channel mutation in atrial fibrillation.

Ellinor PT, Nam EG, Shea MA, Milan DJ, Ruskin JN, MacRae CA. Ellinor PT, et al. Among authors: macrae ca. Heart Rhythm. 2008 Jan;5(1):99-105. doi: 10.1016/j.hrthm.2007.09.015. Epub 2007 Sep 19. Heart Rhythm. 2008. PMID: 18088563

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