Concepedia
Statistics
Publications
7
Citations
489
H-Index
Active since
1998
Affiliations
Triemli Hospital(Current)
Inserm
Délégation Paris 7
Université Paris Cité
Hôpital Louis-Mourier
X. Schneider‐Yin is an author at Triemli Hospital specializing in genetics, human genetics, and life sciences.
Publications per year
1998–2014
Systematic Analysis of Molecular Defects in the Ferrochelatase Gene from Patients with Erythropoietic Protoporphyria
Urszula B. Rüfenacht, Laurent Gouya, X. Schneider‐Yin et al. · The American Journal of Human Genetics · 1998 · 134 citations · Full text
Life Sciences, Genetics, Molecular Genetics +10
Long-term observational study of afamelanotide in 115 patients with erythropoietic protoporphyria
G. Biolcati, Emanuela Marchesini, Fiammetta Sorge et al. · British Journal of Dermatology · 2014 · 103 citations · Full text
Medicine, Dermatology, Pharmacology +14
Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases
Ruwani Katugampola, Michael N. Badminton, A.Y. Finlay et al. · British Journal of Dermatology · 2012 · 95 citations
Medicine, Dermatology, Pediatrics +12
A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases
R. P. Katugampola, A. Anstey, A.Y. Finlay et al. · British Journal of Dermatology · 2012 · 82 citations
Medicine, Hematology, Pediatrics +17
A genotype-phenotype correlation between null-allele mutations in the ferrochelatase gene and liver complication in patients with erythropoietic protoporphyria.
Minder Ei, Laurent Gouya, X. Schneider‐Yin et al. · PubMed · 2002 · 51 citations
Life Sciences, Genetics, Molecular Genetics +17
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