Vered Molho‐Pessach

Author

Vered Molho‐Pessach

Also Known As

Molho-Pessach Vered, V Molcho-Pessach, V Molho-Pessach, V. Molho-Pessach, V. Molho‐Pessach, Vered Molho-Pessach, Vered Molho‐Pessach

100

Publications

2.1K

Citations

H-Index

Concepts

All Affiliations

Hadassah Medical Center Hebrew University of Jerusalem Tel Aviv University Al-Makassed Islamic Charitable Society Hospital Shaare Zedek Medical Center

About

Vered Molho‐Pessach is an author at Hadassah Medical Center specializing in medicine, dermatology, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	20	1.1K
2	Allergy	4	4	134
3	Public Health	2	2	62
4	Cell Biology	2	2	179
5	Natural Sciences	1	1	38

Vered Molho‐Pessach

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
The H Syndrome Is Caused by Mutations in the Nucleoside Transporter hENT3 Vered Molho‐Pessach, Israela Lerer, Dvorah Abeliovich, The American Journal of Human Genetics Molecular PhysiologyDisease MechanismMendelian DisorderGenetic DisorderGenetics	2008	202
H syndrome: The first 79 patients Vered Molho‐Pessach, Yuval Ramot, Frances Camille, Journal of the American Academy of Dermatology Down SyndromeMendelian DisorderAutoimmune DiseaseGenetic DisorderHematology	2013	160
LGR5 expressing skin fibroblasts define a major cellular hub perturbed in scleroderma Chamutal Gur, Shuang-Yin Wang, Fadi Sheban, Cell FibrosisMajor Cellular HubSystemic SclerodermaCutaneous BiologyPathology	2022	141
The H syndrome: A genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations Vered Molho‐Pessach, Ziad Agha, Suhail Aamar, Journal of the American Academy of Dermatology MedicineHistopathologyPathologyClinical DermatologyDermatology	2008	134
Topical phage therapy in a mouse model of Cutibacterium acnes-induced acne-like lesions Amit Rimon, Chani Rakov, Vanda Lerer, Nature Communications	2023	66
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 Eli Sprecher, Vered Molho‐Pessach, Arieh Ingber, Journal of Investigative Dermatology Epidermal Plakophilin 1Signal TransductionGenetic DisorderCutaneous BiologyGenetics	2004	50
Paediatric Erythema Multiforme: Epidemiological, Clinical and Laboratory Characteristics Yael Siedner-Weintraub, Itai Gross, Almog David, Acta Dermato Venereologica DiagnosisPaediatric RadiologyDermatologyRecurrent EmPediatric Epidemiology	2017	50
Mutation in <i>KANK2</i> , encoding a sequestering protein for steroid receptor coactivators, causes keratoderma and woolly hair Yuval Ramot, Vered Molho‐Pessach, Tomer Meir, Journal of Medical Genetics	2014	49
H Syndrome: Recently Defined Genodermatosis With Distinct Histologic Features. A Morphological, Histochemical, Immunohistochemical, and Ultrastructural Study of 10 Cases Victoria Doviner, Alexander Maly, Zvi Neʼeman, American Journal of Dermatopathology	2010	48
Homozygosity mapping identifies a bile acid biosynthetic defect in an adult with cirrhosis of unknown etiology Vered Molho‐Pessach, Jonathan J. Rios, Chao Xing, Hepatology	2011	44

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