Slaheddine Marrakchi

Author

Hopital Universitaire Hedi Chaker ORCID

Also Known As

S Marrakchi, S. Marrakchi, Samira Marrakchi, Slaheddine Marrakchi

112

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Hopital Universitaire Hedi Chaker Hôpital Saint-Louis Assistance Publique – Hôpitaux de Paris Nagoya City University University of Glasgow

About

Slaheddine Marrakchi is an author at Hopital Universitaire Hedi Chaker specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	509
2	Molecular Genetics	4	4	103
3	Public Health	2	2	28
4	Cell Biology	1	1	31
5	Immunology	1	1	44

Slaheddine Marrakchi

Publications

2.4K

Citations

H-Index

Page 1

	Year	Citations
Interleukin-36–Receptor Antagonist Deficiency and Generalized Pustular Psoriasis Slaheddine Marrakchi, Philippe Guigue, Blair R. Renshaw, New England Journal of Medicine	2011	965
Trial of Spesolimab for Generalized Pustular Psoriasis H. Bachelez, Siew Eng Choon, Slaheddine Marrakchi, New England Journal of Medicine	2021	317
Biophysical parameters of skin: map of human face, regional, and age‐related differences Slaheddine Marrakchi, Howard I. Maïbach Contact Dermatitis	2007	186
Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans Franz P.W. Radner, Slaheddine Marrakchi, Peter Kirchmeier, PLoS Genetics Developmental AnomalyMendelian DisorderSplice Site MutationGenetic DisorderGenetics	2013	154
Efficacy and safety of subcutaneous spesolimab for the prevention of generalised pustular psoriasis flares (Effisayil 2): an international, multicentre, randomised, placebo-controlled trial Akimichi Morita, Bruce Strober, A. David Burden, The Lancet Effisayil 2MedicineClinical DermatologyPlacebo-controlled TrialSubcutaneous Spesolimab	2023	100
Sodium Lauryl Sulfate-Induced Irritation in the Human Face: Regional and Age-Related Differences Slaheddine Marrakchi, Howard I. Maïbach Skin Pharmacology and Physiology	2006	86
Mutations in SULT2B1 Cause Autosomal-Recessive Congenital Ichthyosis in Humans Lisa Heinz, Gwang-Jin Kim, Slaheddine Marrakchi, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyPathology	2017	82
Study protocol of the global Effisayil 1 Phase II, multicentre, randomised, double-blind, placebo-controlled trial of spesolimab in patients with generalized pustular psoriasis presenting with an acute flare Siew Eng Choon, Mark Lebwohl, Slaheddine Marrakchi, BMJ Open	2021	73
Identification of <i>Malassezia</i> species from Tunisian patients with pityriasis versicolor and normal subjects S. Ben Salah, F. Makni, Slaheddine Marrakchi, Mycoses	2005	51
Correction: Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans Franz P.W. Radner, Slaheddine Marrakchi, Peter Kirchmeier, PLoS Genetics	2013	46

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