Nili Avidan
Weizmann Institute of Science(IL)
Publications by Year
Research Areas
Aortic Disease and Treatment Approaches, Connective tissue disorders research, Erythrocyte Function and Pathophysiology, Epigenetics and DNA Methylation, Olfactory and Sensory Function Studies
Most-Cited Works
- → Mutations in smooth muscle α-actin (ACTA2) lead to thoracic aortic aneurysms and dissections(2007)838 cited
- → 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(2001)647 cited
- → Mutations in Smooth Muscle Alpha-Actin (ACTA2) Cause Coronary Artery Disease, Stroke, and Moyamoya Disease, Along with Thoracic Aortic Disease(2009)568 cited
- → The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy(2001)524 cited
- → Identification of the gene causing mucolipidosis type IV(2000)399 cited
- → Exome Sequencing Identifies SMAD3 Mutations as a Cause of Familial Thoracic Aortic Aneurysm and Dissection With Intracranial and Other Arterial Aneurysms(2011)288 cited
- → Mechanisms for Evolving Hypervariability: The Case of Conopeptides(2001)218 cited
- → CATSPER2, a human autosomal nonsyndromic male infertility gene(2003)206 cited
- → USH3A transcripts encode clarin-1, a four-transmembrane-domain protein with a possible role in sensory synapses(2002)172 cited
- → Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1(2002)171 cited