(Q84676977)

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9 February 2020

title

Autosomal dominant inheritance of a predisposition to thoracic aortic aneurysms and dissections and intracranial saccular aneurysms (English)

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9 February 2020

10

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9 February 2020

author name string

Ellen Regalado

1

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9 February 2020

Sarah Medrek

2

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9 February 2020

Van Tran-Fadulu

3

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9 February 2020

Dong-Chuan Guo

4

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9 February 2020

Hariyadarshi Pannu

5

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9 February 2020

Hossein Golabbakhsh

6

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9 February 2020

Suzanne Smart

7

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9 February 2020

Julia H Chen

8

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9 February 2020

Sanjay Shete

9

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9 February 2020

Ralph Stern

11

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9 February 2020

Alan C Braverman

12

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9 February 2020

Dianna M Milewicz

13

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9 February 2020

publication date

3 August 2011

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American Journal of Medical Genetics

9 February 2020

published in

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9 February 2020

volume

155A

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9 February 2020

issue

9

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9 February 2020

page(s)

2125-2130

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Familial thoracic aortic dilation and bicommissural aortic valve: A prospective analysis of natural history and inheritance

9 February 2020

cites work

1 reference

12 December 2020

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

1 reference

12 December 2020

Cerebrovascular Involvement in Ehlers-Danlos Syndrome

1 reference

12 December 2020

Subarachnoid hemorrhage and family history. A population-based case-control study

1 reference

12 December 2020

Aneurysm syndromes caused by mutations in the TGF-beta receptor

1 reference

12 December 2020

Prevalence and risk of rupture of intracranial aneurysms: a systematic review

1 reference

12 December 2020

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

1 reference

12 December 2020

A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3.

1 reference

12 December 2020

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

1 reference

12 December 2020

Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study

1 reference

12 December 2020

Mutations in smooth muscle alpha-actin (ACTA2) lead to thoracic aortic aneurysms and dissections.

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutations in myosin heavy chain 11 cause a syndrome associating thoracic aortic aneurysm/aortic dissection and patent ductus arteriosus

1 reference

12 December 2020

MYH11 mutations result in a distinct vascular pathology driven by insulin-like growth factor 1 and angiotensin II

1 reference

12 December 2020

Risk of intracranial aneurysm bleeding in autosomal-dominant polycystic kidney disease.

1 reference

12 December 2020

The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysm

1 reference

12 December 2020

Familial aggregation of both aortic and cerebral aneurysms: evidence for a common genetic basis in a subset of families

1 reference

12 December 2020

Mutations in transforming growth factor-beta receptor type II cause familial thoracic aortic aneurysms and dissections

1 reference

12 December 2020

Subarachnoid hemorrhage: a preventable disease with a heritable component

1 reference

12 December 2020

Reduced penetrance and variable expressivity of familial thoracic aortic aneurysms/dissections

1 reference

12 December 2020

Mutations in smooth muscle alpha-actin (ACTA2) cause coronary artery disease, stroke, and Moyamoya disease, along with thoracic aortic disease

1 reference

12 December 2020

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

1 reference

12 December 2020

A study of inbreeding and kinship in intracranial aneurysms in the Saguenay Lac-Saint-Jean region (Quebec, Canada).

1 reference

12 December 2020

Identifiers

DOI

10.1002/AJMG.A.34050

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9 February 2020

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9 February 2020

PubMed publication ID

21815248

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