Nili Avidan

Rappaport Family Institute for Research in the Medical Sciences

Publishes on Aortic Disease and Treatment Approaches, Connective tissue disorders research, Erythrocyte Function and Pathophysiology. 75 papers and 5.8k citations.

75Publications

5.8kTotal Citations

Aortic Disease and Treatment Approaches Connective tissue disorders research Erythrocyte Function and Pathophysiology Epigenetics and DNA Methylation Olfactory and Sensory Function Studies

Is this you? Claim your profile.

Add your photo, update your bio, and get notified when your ranking changes.

Top publicationsby citations

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

Dong-Chuan Guo, Hariyadarshi Pannu, Van Tran‐Fadulu et al.|Nature Genetics|2007

Cited by 845

A Missense Mutation in a Highly Conserved Region of CASQ2 Is Associated with Autosomal Recessive Catecholamine-Induced Polymorphic Ventricular Tachycardia in Bedouin Families from Israel

Hadas Lahat, Elon Pras, Tsviya Olender et al.|The American Journal of Human Genetics|2001

Cited by 648Open Access

Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease

Dong-Chuan Guo, Christina L. Papke, Van Tran‐Fadulu et al.|The American Journal of Human Genetics|2009

Cited by 572Open Access

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Iris Eisenberg, Nili Avidan, Tamara Potikha et al.|Nature Genetics|2001

Cited by 528

Identification of the gene causing mucolipidosis type IV

Ruth Bargal, Nili Avidan, Edna Ben‐Asher et al.|Nature Genetics|2000

Cited by 399