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Margarita Indelman | Researchclopedia

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Margarita Indelman

Rambam Health Care Campus

48

Works

3,145

Citations

27

h-index

39

i10-index

Research Topics

Skin and Cellular Biology Research Hair Growth and Disorders Wnt/β-catenin signaling in development and cancer

Affiliations

Thomas Jefferson University2003–2003

Bethlehem University2003–2003

Technion – Israel Institute of Technology2003–2016

Sheba Medical Center2016–2016

Rabin Medical Center2003–2003

Top Works

Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis

Orit Topaz,Daniel L. Shurman,et al.

2004591 citations

Parathyroid Disorders and Treatments

Plant Reproductive Biology

SERKAL Syndrome: An Autosomal-Recessive Disorder Caused by a Loss-of-Function Mutation in WNT4

Hannah Mandel,Revital Shemer,et al.

2008278 citations

A Mutation in SNAP29, Coding for a SNARE Protein Involved in Intracellular Trafficking, Causes a Novel Neurocutaneous Syndrome Characterized by Cerebral Dysgenesis, Neuropathy, Ichthyosis, and Palmoplantar Keratoderma

Eli Sprecher,Akemi Ishida‐Yamamoto,et al.

2005197 citations

Autosomal Recessive Ichthyosis with Hypotrichosis Caused by a Mutation in ST14, Encoding Type II Transmembrane Serine Protease Matriptase

Lina Basel‐Vanagaite,Revital Attia,et al.

2007189 citations

Detection of a chromosomal region with two quantitative trait loci, affecting cold tolerance and fish size, in an F2 tilapia hybrid

Avner Cnaani,Eric M. Hallerman,et al.

2003146 citations

Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14

Jennie Lugassy,Peter Itin,et al.

2006137 citations

A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification

Ilana Chefetz,Raoul Heller,et al.

2005137 citations

A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis

Orit Topaz,Margarita Indelman,et al.

2006136 citations

Population-Specific Association between a Polymorphic Variant in ST18, Encoding a Pro-Apoptotic Molecule, and Pemphigus Vulgaris

Ofer Sarig,Sivan Bercovici,et al.

201297 citations