Margarita Indelman

3.1k citations

40 papers · 2.0k indexed · h-index 23

Nephrology top 1%
- Parathyroid Disorders and Treatments 6
Cell Biology top 2%
- Skin and Cellular Biology Research 18
Urology top 2%
- Hair Growth and Disorders 8
Genetics top 2%
- Genetic and rare skin diseases. 4
- Genetic Syndromes and Imprinting 3
Rheumatology top 5%
Molecular Biology
- Wnt/β-catenin signaling in development and cancer 7
- Plant Reproductive Biology 4
Physiology
- Erythrocyte Function and Pathophysiology 4

Co-authors: Eli Sprecher Richard N. Bergman Gabriele Richard Orit Topaz Ziad Khamaysi Ilana Chefetz Akemi Ishida‐Yamamoto S. Raimer
Cited by: Nephrology Cell Biology Urology
Journals: Nature Genetics (1 paper)The Journal of Clinical Endocrinology & Metabolism (1 paper)The American Journal of Human Genetics (6 papers)
Partner nations: Israel United States Germany

In The Last Decade

Margarita Indelman

40 papers receiving 2.0k citations

Peers

Countries citing papers authored by Margarita Indelman

Since Specialization

Citations

This map shows the geographic impact of Margarita Indelman's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Margarita Indelman with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Margarita Indelman more than expected).

Fields of papers citing papers by Margarita Indelman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Margarita Indelman. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Margarita Indelman. The network helps show where Margarita Indelman may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Margarita Indelman, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Margarita Indelman Line = papers co-authored together Margarita Indelman links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Clinico-pathological manifestations of variant late infantile neuronal ceroid lipofuscinosis (vLINCL) caused by a novel mutation in MFSD8 gene European Journal of Medical Genetics ·Hanna Mandel,Ksenya Cohen Katsanelson,Morad Khayat,Ilana Chervinsky,Eugene Vladovski,Theodor C. Iancu,Margarita Indelman,Yoseph Horovitz,Eli Sprecher,Stavit A. Shalev,Ronen Spiegel	2014	19
2	Postzygotic HRAS Mutation Causing Both Keratinocytic Epidermal Nevus and Thymoma and Associated With Bone Dysplasia and Hypophosphatemia Due to Elevated FGF23 The Journal of Clinical Endocrinology & Metabolism ·Emily Avitan‐Hersh,Sameh Tatur,Margarita Indelman,Vardit Gepstein,Roni Shreter,Dov Hershkovitz,Riva Brick,Richard N. Bergman,Dov Tiosano	2013	23
3	Acrokeratosis Verruciformis of Hopf Showing P602L Mutation in ATP2A2 and Overlapping Histopathological Features With Darier Disease American Journal of Dermatopathology ·Richard N. Bergman,Tanya Sezin,Margarita Indelman,Wissam Helou,Emily Avitan‐Hersh	2012	8
4	ADULT Syndrome Caused by a Mutation Previously Associated with EEC Syndrome Pediatric Dermatology ·Emily Avitan‐Hersh,Margarita Indelman,Richard N. Bergman,Eli Sprecher	2010	19
5	Insulin-Like Growth Factor-Binding Protein 7 Regulates Keratinocyte Proliferation, Differentiation and Apoptosis Journal of Investigative Dermatology ·Janna Nousbeck,Ofer Sarig,Nili Avidan,Margarita Indelman,Richard N. Bergman,Michal Ramon,Claes D. Enk,Eli Sprecher	2009	34
6	Disadhesion of epidermal keratinocytes: A histologic clue to palmoplantar keratodermas caused by DSG1 mutations Journal of the American Academy of Dermatology ·Richard N. Bergman,Dov Hershkovitz,Dana Fuchs,Margarita Indelman,Yael Ben-David Gadot,Eli Sprecher	2009	19
7	Alopecia, Neurological Defects, and Endocrinopathy Syndrome Caused by Decreased Expression of RBM28, a Nucleolar Protein Associated with Ribosome Biogenesis The American Journal of Human Genetics ·Janna Nousbeck,Ronen Spiegel,Akemi Ishida‐Yamamoto,Margarita Indelman,Ayelet Shani‐Adir,Noam Adir,E. Lipkin,Sivan Bercovici,Dan Geiger,Maurice A. M. Van Steensel,Peter M. Steijlen,Richard N. Bergman,Albrecht Bindereif,Mordechai Choder,Stavit A. Shalev,Eli Sprecher	2008	55
8	Defective Lamellar Granule Secretion in Arthrogryposis, Renal Dysfunction, and Cholestasis Syndrome Caused by a Mutation in VPS33B Archives of Dermatology ·Dov Hershkovitz,Hannah Mandel,Akemi Ishida‐Yamamoto,Ilana Chefetz,B. Hino,Anthony Luder,Margarita Indelman,Richard N. Bergman,Eli Sprecher	2008	33
9	Autosomal Recessive Ichthyosis with Hypotrichosis Caused by a Mutation in ST14, Encoding Type II Transmembrane Serine Protease Matriptase The American Journal of Human Genetics ·Lina Basel‐Vanagaite,Revital Attia,Akemi Ishida‐Yamamoto,Limor Rainshtein,Dan Ben Amitai,Raziel Lurie,Metsada Pasmanik‐Chor,Margarita Indelman,Alex Zvulunov,Shirley Saban,Nurit Magal,Eli Sprecher,Mordechai Shohat	2007	137
10	Molecular Epidemiology of Hereditary Epidermolysis Bullosa in a Middle Eastern Population Journal of Investigative Dermatology ·Judeh Abu Sa'd,Margarita Indelman,Ellen G Pfendner,Tzipora C. Falik‐Zaccai,Mordechai Mizrachi-Koren,Stavit A. Shalev,Dani Ben Amitai,Annick Raas-Rothshild,Ayelet Adir-Shani,Z Borochowitz,Ruth Gershoni‐Baruch,Morad Khayat,Daniela Landau,Gabriele Richard,Richard N. Bergman,Jouni Uitto,Moien Kanaan,Eli Sprecher	2006	42
11	Naegeli-Franceschetti-Jadassohn Syndrome and Dermatopathia Pigmentosa Reticularis: Two Allelic Ectodermal Dysplasias Caused by Dominant Mutations in KRT14 The American Journal of Human Genetics ·Jennie Lugassy,Peter Itin,Akemi Ishida‐Yamamoto,Kristen E. Holland,Susan Huson,Dan Geiger,Hans Christian Hennies,Margarita Indelman,Dani Bercovich,Jouni Uitto,Richard N. Bergman,John A. McGrath,Gabriele Richard,Eli Sprecher	2006	76
12	Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations Journal of the American Academy of Dermatology ·Mordechai Mizrachi-Koren,Saar Shemer,M.C. Morgan,Margarita Indelman,Ziad Khamaysi,Danny Petronius,Ora Bitterman‐Deutsch,Hans Christian Hennies,Richard N. Bergman,Eli Sprecher	2006	22
13	Hyperphosphatemic familial tumoral calcinosis caused by a mutation in GALNT3 in a European kindred Journal of Human Genetics ·Polina Specktor,John Graham Cooper,Margarita Indelman,Eli Sprecher	2006	57
14	A Deleterious Mutation in SAMD9 Causes Normophosphatemic Familial Tumoral Calcinosis The American Journal of Human Genetics ·Orit Topaz,Margarita Indelman,Ilana Chefetz,Dan Geiger,Aryeh Metzker,Yoram Altschuler,Mordechai Choder,Dani Bercovich,Jouni Uitto,Richard N. Bergman,Gabriele Richard,Eli Sprecher	2006	96
15	Identification of a Novel Locus Associated with Congenital Recessive Ichthyosis on 12p11.2–q13 Journal of Investigative Dermatology ·Mordechai Mizrachi-Koren,Dan Geiger,Margarita Indelman,Ora Bitterman‐Deutsch,Richard N. Bergman,Eli Sprecher	2005	19
16	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 The American Journal of Human Genetics ·Eli Sprecher,Akemi Ishida‐Yamamoto,Mordechai Mizrahi-Koren,Debora Rapaport,Dorit Goldsher,Margarita Indelman,Orit Topaz,Ilana Chefetz,Hanna Keren,Timothy J. O’Brien,Dani Bercovich,Stavit A. Shalev,Dan Geiger,Richard N. Bergman,Mia Horowitz,Hanna Mandel	2005	131
17	Mutations in GALNT3, encoding a protein involved in O-linked glycosylation, cause familial tumoral calcinosis Nature Genetics ·Orit Topaz,Daniel L. Shurman,Richard N. Bergman,Margarita Indelman,Paulina Ratajczak,Mordechai Mizrachi,Ziad Khamaysi,Doron M. Behar,Dan Petronius,Vered Friedman,Israel Zelikovic,S. Raimer,Arieh Metzker,Gabriele Richard,Eli Sprecher	2004	424
18	Homozygous Splice Site Mutations in PKP1 Result in Loss of Epidermal Plakophilin 1 Expression and Underlie Ectodermal Dysplasia/Skin Fragility Syndrome in Two Consanguineous Families Journal of Investigative Dermatology ·Eli Sprecher,Vered Molho‐Pessach,Arieh Ingber,Efraim Sagi,Margarita Indelman,Richard N. Bergman	2004	38
19	Epidermolytic Hyperkeratosis and Epidermolysis Bullosa Simplex Caused by Frameshift Mutations Altering the V2 Tail Domains of Keratin 1 and Keratin 5 Journal of Investigative Dermatology ·Eli Sprecher,Gil Yosipovitch,Richard N. Bergman,Dan Ciubutaro,Margarita Indelman,Ellen G Pfendner,Leok Goh,Christopher J. Miller,Jouni Uitto,Gabriele Richard	2003	34
20	A Missense Mutation in CDH3, Encoding P-Cadherin, Causes Hypotrichosis with Juvenile Macular Dystrophy Journal of Investigative Dermatology ·Margarita Indelman,Richard N. Bergman,Danny Petronius,Dan Ciubutaro,Eli Sprecher,Raziel Lurie,Gabriele Richard,Benjamin T. Miller,Rina Leibu	2002	47

About Margarita Indelman

Margarita Indelman is a scholar working on Cell Biology, Urology and Nephrology, having authored 40 papers that have together received 2.0k indexed citations. Recurring topics across this work include Skin and Cellular Biology Research (18 papers), Hair Growth and Disorders (8 papers), Wnt/β-catenin signaling in development and cancer (7 papers), Parathyroid Disorders and Treatments (6 papers), Erythrocyte Function and Pathophysiology (4 papers), Genetic and rare skin diseases. (4 papers), Plant Reproductive Biology (4 papers) and Genetic Syndromes and Imprinting (3 papers). The work is most often cited by research in Nephrology (472 citations), Cell Biology (576 citations) and Urology (192 citations). Margarita Indelman has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Eli Sprecher, Richard N. Bergman, Gabriele Richard, Orit Topaz, Ziad Khamaysi, Ilana Chefetz, Akemi Ishida‐Yamamoto, S. Raimer, Paulina Ratajczak and Doron M. Behar. Their work appears in journals such as Nature Genetics, The Journal of Clinical Endocrinology & Metabolism and The American Journal of Human Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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