Alana C. Cecchi

<i>RNF213</i> Rare Variants in an Ethnically Diverse Population With Moyamoya Disease

Alana C. Cecchi, Dongchuan Guo, Zhao Ren et al. · Stroke · 2014 · 149 citations · Full text

Molecular diagnosis in vascular Ehlers-Danlos syndrome predicts pattern of arterial involvement and outcomes

Sherene Shalhub, James H. Black, Alana C. Cecchi et al. · Journal of Vascular Surgery · 2014 · 127 citations · Full text

Molecular Diagnosis, Vascular Disease, Vasculitis +12

The pleiotropy associated with de novo variants in CHD4, CNOT3, and SETD5 extends to moyamoya angiopathy

Amélie Pinard, Stéphanie Guey, Dongchuan Guo et al. · Genetics in Medicine · 2019 · 55 citations · Full text

Vascular Disease, Genetics, Pathology +3

Missense mutations in <i>FBN1</i> exons 41 and 42 cause Weill–Marchesani syndrome with thoracic aortic disease and Marfan syndrome

Alana C. Cecchi, Naomi Ogawa, Hugo R. Martinez et al. · American Journal of Medical Genetics Part A · 2013 · 44 citations

Association of De Novo <i>RNF213</i> Variants With Childhood Onset Moyamoya Disease and Diffuse Occlusive Vasculopathy

Amélie Pinard, Maximillian D.J. Fiander, Alana C. Cecchi et al. · Neurology · 2021 · 30 citations · Full text