X. Schneider‐Yin

637 total citations
12 papers, 374 citations indexed

About

X. Schneider‐Yin is a scholar working on Molecular Biology, Rheumatology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, X. Schneider‐Yin has authored 12 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Rheumatology and 5 papers in Pulmonary and Respiratory Medicine. Recurrent topics in X. Schneider‐Yin's work include Porphyrin Metabolism and Disorders (12 papers), Folate and B Vitamins Research (7 papers) and Methemoglobinemia and Tumor Lysis Syndrome (4 papers). X. Schneider‐Yin is often cited by papers focused on Porphyrin Metabolism and Disorders (12 papers), Folate and B Vitamins Research (7 papers) and Methemoglobinemia and Tumor Lysis Syndrome (4 papers). X. Schneider‐Yin collaborates with scholars based in Switzerland, France and Israel. X. Schneider‐Yin's co-authors include Elisabeth I. Minder, Hervé Puy, Laurent Gouya, Jean‐Charles Deybach, Johann Steurer, Emanuela Marchesini, R Aquaron, G. Biolcati, Y Nordmann and Beat W. Schäfer and has published in prestigious journals such as The American Journal of Human Genetics, British Journal of Dermatology and Journal of the European Academy of Dermatology and Venereology.

In The Last Decade

X. Schneider‐Yin

12 papers receiving 363 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
X. Schneider‐Yin Switzerland 8 337 116 116 103 27 12 374
Jacqueline Woolf United Kingdom 6 247 0.7× 99 0.9× 75 0.6× 65 0.6× 4 0.1× 8 264
Doreen Meissner South Africa 7 285 0.8× 87 0.8× 67 0.6× 84 0.8× 12 0.4× 9 314
Felix de Rooij France 9 361 1.1× 110 0.9× 29 0.3× 184 1.8× 11 0.4× 9 385
Eliane Sardh Sweden 13 467 1.4× 217 1.9× 90 0.8× 94 0.9× 4 0.1× 30 486
MH Steinberg United States 9 66 0.2× 89 0.8× 13 0.1× 19 0.2× 17 0.6× 10 411
Oğuz Çilingir Türkiye 8 87 0.3× 22 0.2× 10 0.1× 12 0.1× 9 0.3× 39 166
Markus Rasmussen Sweden 5 189 0.6× 29 0.3× 26 0.2× 7 0.1× 7 0.3× 6 357
Maria Letícia Ribeiro Portugal 9 35 0.1× 36 0.3× 15 0.1× 38 0.4× 8 0.3× 18 234
Dan Glass United Kingdom 5 106 0.3× 5 0.0× 7 0.1× 20 0.2× 17 0.6× 6 228
Tracey Bishop United States 5 53 0.2× 22 0.2× 132 1.1× 30 0.3× 3 0.1× 10 231

Countries citing papers authored by X. Schneider‐Yin

Since Specialization
Citations

This map shows the geographic impact of X. Schneider‐Yin'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 X. Schneider‐Yin with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites X. Schneider‐Yin more than expected).

Fields of papers citing papers by X. Schneider‐Yin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by X. Schneider‐Yin. 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 X. Schneider‐Yin. The network helps show where X. Schneider‐Yin may publish in the future.

Co-authorship network of co-authors of X. Schneider‐Yin

This figure shows the co-authorship network connecting the top 25 collaborators of X. Schneider‐Yin. A scholar is included among the top collaborators of X. Schneider‐Yin based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with X. Schneider‐Yin. X. Schneider‐Yin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

12 of 12 papers shown
1.
Biolcati, G., et al.. (2014). Long-term observational study of afamelanotide in 115 patients with erythropoietic protoporphyria. British Journal of Dermatology. 172(6). 1601–1612. 65 indexed citations
2.
Katugampola, Ruwani, Michael N. Badminton, A.Y. Finlay, et al.. (2012). Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases. British Journal of Dermatology. 167(4). 901–913. 47 indexed citations
3.
Anstey, A., A.Y. Finlay, Sharon D. Whatley, et al.. (2012). A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases. British Journal of Dermatology. 167(4). 888–900. 37 indexed citations
4.
Schneider‐Yin, X., Rivka Mamet, Liran Horev, et al.. (2010). A homoallelic FECH mutation in a patient with both erythropoietic protoporphyria and palmar keratoderma. Journal of the European Academy of Dermatology and Venereology. 24(11). 1349–1353. 11 indexed citations
5.
Schneider‐Yin, X., Reno S. Bladergroen, Pamela Poblete‐Gutiérrez, et al.. (2009). Identification of a recurrent mutation in the protoporphyrinogen oxidase gene in Swiss patients with variegate porphyria: clinical and genetic implications.. PubMed. 55(2). 96–101. 3 indexed citations
6.
Schneider‐Yin, X., et al.. (2009). Variations in the length of poly-C and poly-T tracts in intron 3 of the human ferrochelatase gene.. PubMed. 55(2). 102–10. 4 indexed citations
7.
Schneider‐Yin, X., et al.. (2009). A systematic review of treatment options for dermal photosensitivity in erythropoietic protoporphyria.. PubMed. 55(1). 84–97. 64 indexed citations
8.
Schneider‐Yin, X., Rivka Mamet, Elisabeth I. Minder, & N. Schoenfeld. (2008). Biochemical and molecular diagnosis of erythropoietic protoporphyria in an Ashkenazi Jewish family. Journal of Inherited Metabolic Disease. 31(S2). 363–367. 11 indexed citations
9.
Schneider‐Yin, X., Martin Hergersberg, Macé M. Schuurmans, A Gregor, & Elisabeth I. Minder. (2004). Mutation hotspots in the human porphobilinogen deaminase gene: Recurrent mutations G111R and R173Q occurring at CpG motifs. Journal of Inherited Metabolic Disease. 27(5). 625–631. 6 indexed citations
10.
Gouya, Laurent, et al.. (2002). A genotype-phenotype correlation between null-allele mutations in the ferrochelatase gene and liver complication in patients with erythropoietic protoporphyria.. PubMed. 48(1). 91–6. 28 indexed citations
11.
Gouya, Laurent, X. Schneider‐Yin, Hervé Puy, et al.. (1998). Systematic Analysis of Molecular Defects in the Ferrochelatase Gene from Patients with Erythropoietic Protoporphyria. The American Journal of Human Genetics. 62(6). 1341–1352. 97 indexed citations
12.
Schneider‐Yin, X., et al.. (1993). [Often unrecognized: erythropoietic protoporphyria].. PubMed. 123(6). 229–33. 1 indexed citations

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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