Anne H. Child

Biochemistry, Genetics and Molecular Biology · Life Sciences

50h-index9.6kcitations193works14.02yr avg
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Research Topics

Connective tissue disorders research(96), Aortic Disease and Treatment Approaches(53), Cardiac Valve Diseases and Treatments(47), Glaucoma and retinal disorders(34), Aortic aneurysm repair treatments(17)

Publications193 total

The pectus care guidelines: best practice consensus guidelines from the joint specialist societies SCTS/MF/CWIG/BOA/BAPS for the treatment of patients with pectus abnormalities
European Journal of Cardio-Thoracic Surgery·2024· 14 cited
Exaggerated elastin turnover in young individuals with Marfan syndrome: new insights from the AIMS trial
European Heart Journal Open·2023· 11 citedOpen Access
A phenotypic screen of Marfan syndrome iPSC-derived vascular smooth muscle cells uncovers GSK3β as a new target
Stem Cell Reports·2023· 13 citedOpen Access
We must build a supportive and safe structure for primary care pharmacy teams
Pharmaceutical journal/˜The œpharmaceutical journal·2023Open Access
Angiotensin receptor blockers and β blockers in Marfan syndrome: an individual patient data meta-analysis of randomised trials
The Lancet·2022· 104 citedOpen Access
Determining the genetic contribution in patients with non-syndromic ascending thoracic aortic aneurysms: Correlation with findings from computational pathology
International Journal of Cardiology·2022· 3 cited
Variants in ciliary genes POC5 and TTLL11 lead to scoliosis
Brain and Spine·2022Open Access
Exaggerated elastin turnover in childhood and adolescence in Marfan syndrome – correlation with age – new insights from the AIMS trial
European Heart Journal·2021· 1 citedOpen Access
Prevalence of POC5 Coding Variants in French-Canadian and British AIS Cohort
Genes·2021· 7 citedOpen Access
5 Exaggerated elastin turnover in childhood and adolescence in marfan syndrome - correlation with age - new insights from the aims trial
2021· 2 citedOpen Access
Genetic variant of TTLL11 gene and subsequent ciliary defects are associated with idiopathic scoliosis in a 5-generation UK family
Scientific Reports·2021· 29 citedOpen Access
Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial
The Lancet·2019· 128 citedOpen Access
Prevalence and progression of aortic root dilatation in highly trained young athletes
Heart·2019· 65 citedOpen Access
Fate of the Aortic Arch Following Surgery on the Aortic Root and Ascending Aorta in Bicuspid Aortic Valve
The Annals of Thoracic Surgery·2018· 23 citedOpen Access
Clinical history and management recommendations of the smooth muscle dysfunction syndrome due to ACTA2 arginine 179 alterations
Genetics in Medicine·2018· 80 citedOpen Access
Pectus Updates and Special Considerations in Marfan Syndrome
Pediatric Reports·2018· 24 citedOpen Access
Non-cardiac manifestations of Marfan syndrome
ASVIDE·2017· 1 cited
Non-cardiac manifestations of Marfan syndrome
Annals of Cardiothoracic Surgery·2017· 22 citedOpen Access
The role of advanced echocardiography and cardiovascular magnetic resonance in the assessment of myocardial function in Marfan syndrome—An update
Echocardiography·2017· 5 cited
Marfan Syndrome and Aortopathies
2016
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Frequent Co-authors

Glen Brice(15), Cathérine Boileau(11), Lesley C. Adès(10), Gwenaëlle Collod‐Béroud(9), Guillaume Jondeau(9), Mansoor Sarfarazi(8), Julie De Backer(8), Laurence Faivre(7), Eloisa Arbustini(7), Anatoli Kiotsekoglou(7), Christophe Béroud(7), Peter N. Robinson(7), K G Burnand(7), Bart Loeys(6), Christine Binquet(6), Élodie Gautier(6), Karin Mayer(6), Mine Arslan‐Kirchner(6), Paolo Comeglio(6), Claire Bonithon‐Kopp(6)