Xiaoye Schneider‐Yin

970 total citations
45 papers, 686 citations indexed

About

Xiaoye Schneider‐Yin is a scholar working on Molecular Biology, Rheumatology and Clinical Biochemistry. According to data from OpenAlex, Xiaoye Schneider‐Yin has authored 45 papers receiving a total of 686 indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 22 papers in Rheumatology and 14 papers in Clinical Biochemistry. Recurrent topics in Xiaoye Schneider‐Yin's work include Porphyrin Metabolism and Disorders (39 papers), Folate and B Vitamins Research (22 papers) and Heme Oxygenase-1 and Carbon Monoxide (19 papers). Xiaoye Schneider‐Yin is often cited by papers focused on Porphyrin Metabolism and Disorders (39 papers), Folate and B Vitamins Research (22 papers) and Heme Oxygenase-1 and Carbon Monoxide (19 papers). Xiaoye Schneider‐Yin collaborates with scholars based in Switzerland, France and United States. Xiaoye Schneider‐Yin's co-authors include Elisabeth I. Minder, Jasmin Barman‐Aksözen, Jean‐Charles Deybach, Laurent Gouya, G. Biolcati, Hervé Puy, Glória C. Ferreira, Christoph E. Minder, Daniel Schümperli and Macé M. Schuurmans and has published in prestigious journals such as Nucleic Acids Research, Blood and Gastroenterology.

In The Last Decade

Xiaoye Schneider‐Yin

44 papers receiving 674 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Xiaoye Schneider‐Yin Switzerland 16 580 219 143 142 65 45 686
Joshua D. Bryant United States 8 447 0.8× 118 0.5× 43 0.3× 17 0.1× 65 1.0× 10 612
Peiwei Zhao China 11 160 0.3× 40 0.2× 29 0.2× 79 0.6× 4 0.1× 34 362
Christer Thomsen Sweden 11 260 0.4× 40 0.2× 7 0.0× 61 0.4× 25 0.4× 18 377
Carole Merle France 5 290 0.5× 34 0.2× 16 0.1× 61 0.4× 7 0.1× 5 406
H.C. Janse Netherlands 11 127 0.2× 61 0.3× 35 0.2× 27 0.2× 18 0.3× 17 404
Hans-Jürgen Barrach Germany 8 103 0.2× 129 0.6× 25 0.2× 10 0.1× 13 0.2× 9 422
Rieko Yagi United States 9 533 0.9× 110 0.5× 63 0.4× 14 0.1× 6 0.1× 12 766
Farlyn Z. Hudson United States 11 253 0.4× 27 0.1× 12 0.1× 58 0.4× 9 0.1× 16 443
Rosalind C. Williamson United Kingdom 11 262 0.5× 6 0.0× 46 0.3× 52 0.4× 11 0.2× 17 505
Anjali A. Sarkar United States 11 219 0.4× 25 0.1× 71 0.5× 26 0.2× 4 0.1× 30 408

Countries citing papers authored by Xiaoye Schneider‐Yin

Since Specialization
Citations

This map shows the geographic impact of Xiaoye 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 Xiaoye 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 Xiaoye Schneider‐Yin more than expected).

Fields of papers citing papers by Xiaoye Schneider‐Yin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xiaoye Schneider‐Yin

This figure shows the co-authorship network connecting the top 25 collaborators of Xiaoye Schneider‐Yin. A scholar is included among the top collaborators of Xiaoye 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 Xiaoye Schneider‐Yin. Xiaoye Schneider‐Yin is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Halloy, François, Pavithra S. Iyer, Alice Ghidini, et al.. (2020). Delivery of oligonucleotides to bone marrow to modulate ferrochelatase splicing in a mouse model of erythropoietic protoporphyria. Nucleic Acids Research. 48(9). 4658–4671. 22 indexed citations
3.
Barman‐Aksözen, Jasmin, et al.. (2020). Increased phototoxic burn tolerance time and quality of life in patients with erythropoietic protoporphyria treated with afamelanotide – a three years observational study. Orphanet Journal of Rare Diseases. 15(1). 213–213. 23 indexed citations
4.
Vavricka, Stephan R., Henriette Heinrich, Emanuel Burri, et al.. (2018). The Vampire Study: Significant elevation of faecal calprotectin in healthy volunteers after 300 ml blood ingestion mimicking upper gastrointestinal bleeding. United European Gastroenterology Journal. 6(7). 1007–1014. 13 indexed citations
5.
Zhong, Qing, Ulrich Wagner, Francesca Molinari, et al.. (2018). Multi-laboratory proficiency testing of clinical cancer genomic profiling by next-generation sequencing. Pathology - Research and Practice. 214(7). 957–963. 9 indexed citations
6.
Schneider‐Yin, Xiaoye, Philip Went, Jasmin Barman‐Aksözen, et al.. (2014). Biallelic inactivation of protoporphyrinogen oxidase and hydroxymethylbilane synthase is associated with liver cancer in acute porphyrias. Journal of Hepatology. 62(3). 734–738. 19 indexed citations
7.
Barman‐Aksözen, Jasmin, et al.. (2014). In ferrochelatase-deficient protoporphyria patients, ALAS2 expression is enhanced and erythrocytic protoporphyrin concentration correlates with iron availability. Blood Cells Molecules and Diseases. 54(1). 71–77. 33 indexed citations
8.
Ducamp, Sarah, Xiaoye Schneider‐Yin, Felix de Rooij, et al.. (2012). Molecular and functional analysis of the C-terminal region of human erythroid-specific 5-aminolevulinic synthase associated with X-linked dominant protoporphyria (XLDPP). Human Molecular Genetics. 22(7). 1280–1288. 42 indexed citations
9.
Schneider‐Yin, Xiaoye, Rivka Mamet, Vladimı́r Saudek, et al.. (2009). Correlation between biochemical findings, structural and enzymatic abnormalities in mutated HMBS identified in six Israeli families with acute intermittent porphyria. Blood Cells Molecules and Diseases. 42(2). 167–173. 8 indexed citations
10.
Schneider‐Yin, Xiaoye, et al.. (2009). Hypericin and 5-aminolevulinic acid-induced protoporphyrin IX induce enhanced phototoxicity in human endometrial cancer cells with non-coherent white light. Photodiagnosis and Photodynamic Therapy. 6(1). 12–18. 28 indexed citations
11.
Schneider‐Yin, Xiaoye, et al.. (2006). Heterogeneity of mutations in the ferrochelatase gene in Italian patients with erythropoietic protoporphyria. Molecular Genetics and Metabolism. 90(4). 402–407. 15 indexed citations
12.
Gregor, A, et al.. (2002). Molecular study of the hydroxymethlybilane synthase gene (HMBS) among Polish patients with acute intermittent porphyria. Human Mutation. 19(3). 310–310. 14 indexed citations
13.
Hergersberg, Martin, et al.. (2001). Haplotype Analysis in Determination of the Heredity of Erythropoietic Protoporphyria among Swiss Families. Journal of Investigative Dermatology. 117(6). 1521–1525. 10 indexed citations
14.
15.
Schneider‐Yin, Xiaoye, et al.. (2000). New insights into the pathogenesis of erythropoietic protoporphyria and their impact on patient care. European Journal of Pediatrics. 159(10). 719–725. 46 indexed citations
16.
Schneider‐Yin, Xiaoye, Catherine Bogard, Hervé Puy, et al.. (2000). Identification of a Prevalent Nonsense Mutation (W283X) and Two Novel Mutations in the Porphobilinogen Deaminase Gene of Swiss Patients with Acute Intermittent Porphyria. Human Heredity. 50(4). 247–250. 15 indexed citations
17.
Gouya, Laurent, Xiaoye Schneider‐Yin, Carmen Herrero, et al.. (1998). Mutations in the Ferrochelatase Gene of Four Spanish Patients with Erythropoietic Protoporphyria. Journal of Investigative Dermatology. 111(3). 406–409. 12 indexed citations
18.
Minder, Elisabeth I. & Xiaoye Schneider‐Yin. (1996). Age-Dependent Reference Values of Urinary Porphyrins in Children. Clinical Chemistry and Laboratory Medicine (CCLM). 34(5). 439–444. 20 indexed citations
19.
Schneider‐Yin, Xiaoye, et al.. (1995). Human ferrochelatase: a novel mutation in patients with erythropoietic protoporphyria and an isoform caused by alternative splicing. Human Genetics. 95(4). 391–6. 15 indexed citations
20.
Schneider‐Yin, Xiaoye, et al.. (1994). Molecular defects in erythropoietic protoporphyria with terminal liver failure. Human Genetics. 93(6). 711–3. 26 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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