Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 152

1.

Candidate locus analysis of familial ascending aortic aneurysms and dissections confirms the linkage to the chromosome 5q13-14 in Finnish families.

Kakko S, Räisänen T, Tamminen M, Airaksinen J, Groundstroem K, Juvonen T, Ylitalo A, Uusimaa P, Savolainen MJ.

J Thorac Cardiovasc Surg. 2003 Jul;126(1):106-13.

2.

Familial thoracic aortic aneurysms and dissections: genetic heterogeneity with a major locus mapping to 5q13-14.

Guo D, Hasham S, Kuang SQ, Vaughan CJ, Boerwinkle E, Chen H, Abuelo D, Dietz HC, Basson CT, Shete SS, Milewicz DM.

Circulation. 2001 May 22;103(20):2461-8.

3.

Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.

Hasham SN, Willing MC, Guo DC, Muilenburg A, He R, Tran VT, Scherer SE, Shete SS, Milewicz DM.

Circulation. 2003 Jul 1;107(25):3184-90. Epub 2003 Jun 23.

4.

Identification of a chromosome 11q23.2-q24 locus for familial aortic aneurysm disease, a genetically heterogeneous disorder.

Vaughan CJ, Casey M, He J, Veugelers M, Henderson K, Guo D, Campagna R, Roman MJ, Milewicz DM, Devereux RB, Basson CT.

Circulation. 2001 May 22;103(20):2469-75.

5.

Familial thoracic aortic aneurysms and dissections: three families with early-onset ascending and descending aortic dissections in women.

Tran-Fadulu V, Chen JH, Lemuth D, Neichoy BT, Yuan J, Gomes N, Sparks E, Kramer LA, Guo D, Pannu H, Braverman AC, Shete S, Milewicz DM.

Am J Med Genet A. 2006 Jun 1;140(11):1196-202. Erratum in: Am J Med Genet A. 2006 Aug 15;140(16):1796.

PMID:
16646045
6.

Newly mapped gene for thoracic aortic aneurysm and dissection.

Wung SF, Aouizerat BE.

J Cardiovasc Nurs. 2004 Nov-Dec;19(6):409-16. Review.

PMID:
15529063
7.

Familial thoracic aortic aneurysm/dissection with patent ductus arteriosus: genetic arguments for a particular pathophysiological entity.

Khau Van Kien P, Wolf JE, Mathieu F, Zhu L, Salve N, Lalande A, Bonnet C, Lesca G, Plauchu H, Dellinger A, Nivelon-Chevallier A, Brunotte F, Jeunemaitre X.

Eur J Hum Genet. 2004 Mar;12(3):173-80.

8.

Genetic basis of thoracic aortic aneurysms and dissections.

Hasham SN, Guo DC, Milewicz DM.

Curr Opin Cardiol. 2002 Nov;17(6):677-83. Review.

PMID:
12466712
9.

Nonsyndromic genetic predisposition to aortic dissection: a newly recognized, diagnosable, and preventable occurrence in families.

Hasham SN, Lewin MR, Tran VT, Pannu H, Muilenburg A, Willing M, Milewicz DM.

Ann Emerg Med. 2004 Jan;43(1):79-82.

PMID:
14707946
10.

Familial thoracic aortic aneurysms and dissections: identification of a novel locus for stable aneurysms with a low risk for progression to aortic dissection.

Guo DC, Regalado ES, Minn C, Tran-Fadulu V, Coney J, Cao J, Wang M, Yu RK, Estrera AL, Safi HJ, Shete SS, Milewicz DM.

Circ Cardiovasc Genet. 2011 Feb;4(1):36-42. doi: 10.1161/CIRCGENETICS.110.958066. Epub 2010 Dec 16.

11.

Genome-wide linkage in three Dutch families maps a locus for abdominal aortic aneurysms to chromosome 19q13.3.

Van Vlijmen-Van Keulen CJ, Rauwerda JA, Pals G.

Eur J Vasc Endovasc Surg. 2005 Jul;30(1):29-35.

12.

A comparison of genetic chromosomal loci for intracranial, thoracic aortic, and abdominal aortic aneurysms in search of common genetic risk factors.

Ruigrok YM, Elias R, Wijmenga C, Rinkel GJ.

Cardiovasc Pathol. 2008 Jan-Feb;17(1):40-7. Epub 2007 Jul 24. Review.

PMID:
18160059
13.

Familial thoracic aortic aneurysms and dissections--incidence, modes of inheritance, and phenotypic patterns.

Albornoz G, Coady MA, Roberts M, Davies RR, Tranquilli M, Rizzo JA, Elefteriades JA.

Ann Thorac Surg. 2006 Oct;82(4):1400-5.

PMID:
16996941
14.

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.

Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A; French Research Network on FTD/FTD-MND.

Neurology. 2009 May 12;72(19):1669-76. doi: 10.1212/WNL.0b013e3181a55f1c.

PMID:
19433740
15.

Candidate gene regions and genetic heterogeneity in gluten sensitivity.

Holopainen P, Mustalahti K, Uimari P, Collin P, Mäki M, Partanen J.

Gut. 2001 May;48(5):696-701.

16.

Linkage analysis in keratoconus: replication of locus 5q21.2 and identification of other suggestive Loci.

Bisceglia L, De Bonis P, Pizzicoli C, Fischetti L, Laborante A, Di Perna M, Giuliani F, Delle Noci N, Buzzonetti L, Zelante L.

Invest Ophthalmol Vis Sci. 2009 Mar;50(3):1081-6. doi: 10.1167/iovs.08-2382. Epub 2008 Oct 31.

PMID:
18978346
17.

Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.

Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.

Br J Dermatol. 2005 Jan;152(1):29-36.

PMID:
15656797
18.

Analysis of multigenerational families with thoracic aortic aneurysms and dissections due to TGFBR1 or TGFBR2 mutations.

Tran-Fadulu V, Pannu H, Kim DH, Vick GW 3rd, Lonsford CM, Lafont AL, Boccalandro C, Smart S, Peterson KL, Hain JZ, Willing MC, Coselli JS, LeMaire SA, Ahn C, Byers PH, Milewicz DM.

J Med Genet. 2009 Sep;46(9):607-13. doi: 10.1136/jmg.2008.062844. Epub 2009 Jun 18.

PMID:
19542084
19.

Exclusion of 14 candidate loci for primary open angle glaucoma in Finnish families.

Lemmelä S, Ylisaukko-oja T, Forsman E, Järvelä I.

Mol Vis. 2004 Apr 2;10:260-4.

20.

Linkage analysis of SLE susceptibility: confirmation of SLER1 at 5p15.3.

Nath SK, Namjou B, Garriott CP, Frank S, Joslin PA, Kilpatrick J, Kelly JA, Harley JB.

Genes Immun. 2004 May;5(3):209-14.

PMID:
15014430

Supplemental Content

Support Center