Marianne Stef

864 total citations
25 papers, 665 citations indexed

About

Marianne Stef is a scholar working on Surgery, Molecular Biology and Genetics. According to data from OpenAlex, Marianne Stef has authored 25 papers receiving a total of 665 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Surgery, 12 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Marianne Stef's work include Lipoproteins and Cardiovascular Health (17 papers), Protein Kinase Regulation and GTPase Signaling (6 papers) and Genetic factors in colorectal cancer (4 papers). Marianne Stef is often cited by papers focused on Lipoproteins and Cardiovascular Health (17 papers), Protein Kinase Regulation and GTPase Signaling (6 papers) and Genetic factors in colorectal cancer (4 papers). Marianne Stef collaborates with scholars based in Spain, France and United States. Marianne Stef's co-authors include Lourdes Palacios, Diego Tejedor, Benoı̂t Arveiler, Helena Ostolaza, César Martı́n, Fernando Civeira, Aitor Etxebarria, Estíbaliz Olano-Martin, Asier Benito‐Vicente and Antonio Martı́nez and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Scientific Reports.

In The Last Decade

Marianne Stef

25 papers receiving 649 citations

Peers

Marianne Stef

SURGE

EDM

GENET

W Liu United States

Eleanor Rattenberry United Kingdom

Peter S. Chines United States

Stéphanie Rodriguez United States

Seham Skah France

Timothy R. McPhee Canada

Rosanna Bagnulo Italy

Ashley Cast United States

Mary R. Dusing United States

Keiyan Sy Canada

W Liu United States

Marianne Stef

147 ×0.3

SURGE

235 ×1.4

97 ×0.6

74 ×0.6

EDM

156 ×1.5

GENET

Citations per year, relative to Marianne Stef Marianne Stef (= 1×) peers W Liu

Countries citing papers authored by Marianne Stef

Since Specialization

Citations

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

Fields of papers citing papers by Marianne Stef

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marianne Stef. 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 Marianne Stef. The network helps show where Marianne Stef may publish in the future.

Co-authorship network of co-authors of Marianne Stef

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

All Works

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20 of 20 papers shown

Benito‐Vicente, Asier, Kepa B. Uribe, Asier Larrea‐Sebal, et al.. (2022). Leu22_Leu23 Duplication at the Signal Peptide of PCSK9 Promotes Intracellular Degradation of LDLr and Autosomal Dominant Hypercholesterolemia. Arteriosclerosis Thrombosis and Vascular Biology. 42(7). e203–e216. 4 indexed citations

Stef, Marianne, et al.. (2020). Two new RHD alleles with deletions spanning multiple exons. Transfusion. 61(3). 682–686. 2 indexed citations

Stef, Marianne, et al.. (2020). RH genotyping by nonspecific quantitative next‐generation sequencing. Transfusion. 60(11). 2691–2701. 18 indexed citations

Benito‐Vicente, Asier, Kepa B. Uribe, Shifa Jebari, et al.. (2018). p.(Asp47Asn) and p.(Thr62Met): non deleterious LDL receptor missense variants functionally characterized in vitro. Scientific Reports. 8(1). 16614–16614. 5 indexed citations

Benito‐Vicente, Asier, Kepa B. Uribe, Shifa Jebari, et al.. (2018). Replacement of cysteine at position 46 in the first cysteine-rich repeat of the LDL receptor impairs apolipoprotein recognition. PLoS ONE. 13(10). e0204771–e0204771. 1 indexed citations

Sánchez-Hernández, Rosa M., Fernando Civeira, Marianne Stef, et al.. (2016). Homozygous Familial Hypercholesterolemia in Spain. Circulation Cardiovascular Genetics. 9(6). 504–510. 43 indexed citations

Cenarro, Ana, Aitor Etxebarria, Isabel de Castro-Orós, et al.. (2016). The p.Leu167del Mutation in APOE Gene Causes Autosomal Dominant Hypercholesterolemia by Down-regulation of LDL Receptor Expression in Hepatocytes. The Journal of Clinical Endocrinology & Metabolism. 101(5). 2113–2121. 75 indexed citations

Etxebarria, Aitor, et al.. (2014). Activity-associated effect of LDL receptor missense variants located in the cysteine-rich repeats. Atherosclerosis. 238(2). 304–312. 20 indexed citations

Etxebarria, Aitor, Asier Benito‐Vicente, Lourdes Palacios, et al.. (2014). Functional Characterization and Classification of Frequent Low-Density Lipoprotein Receptor Variants. Human Mutation. 36(1). 129–141. 41 indexed citations

10.

Stef, Marianne, et al.. (2013). A DNA Microarray for the Detection of Point Mutations and Copy Number Variation Causing Familial Hypercholesterolemia in Europe. Journal of Molecular Diagnostics. 15(3). 362–372. 18 indexed citations

11.

Etxebarria, Aitor, Lourdes Palacios, Marianne Stef, et al.. (2011). Functional characterization of splicing and ligand-binding domain variants in the LDL receptor. Human Mutation. 33(1). 232–243. 35 indexed citations

12.

Tejedor, María Teresa, Ana Cenarro, Diego Tejedor, et al.. (2011). New contributions to the study of common double mutants in the human LDL receptor gene. Die Naturwissenschaften. 98(11). 943–949. 5 indexed citations

13.

Palacios, Lourdes, et al.. (2011). Molecular characterization of familial hypercholesterolemia in Spain. Atherosclerosis. 221(1). 137–142. 99 indexed citations

14.

Tejedor, María Teresa, Ana Cenarro, Marianne Stef, et al.. (2010). Haplotype analyses, mechanism and evolution of common double mutants in the human LDL receptor gene. Molecular Genetics and Genomics. 283(6). 565–574. 7 indexed citations

15.

Alonso, Rodrigo, Joep C. Defesche, Diego Tejedor, et al.. (2009). Genetic diagnosis of familial hypercholesterolemia using a DNA-array based platform. Clinical Biochemistry. 42(9). 899–903. 42 indexed citations

16.

Rooryck, Caroline, Marianne Stef, Ingrid Burgelin, et al.. (2009). 2.3 Mb terminal deletion in 12p13.33 associated with oculoauriculovertebral spectrum and evaluation of WNT5B as a candidate gene. European Journal of Medical Genetics. 52(6). 446–449. 30 indexed citations

17.

Stef, Marianne, Delphine Simon, Marie‐Ange Delrue, et al.. (2007). Spectrum of CREBBP gene dosage anomalies in Rubinstein–Taybi Syndrome patients. European Journal of Human Genetics. 15(8). 843–847. 33 indexed citations

18.

Stef, Marianne, Delphine Simon, Ingrid Burgelin, et al.. (2006). Testing and improving experimental parameters for the use of low molecular weight targets in array-CGH experiments. Human Mutation. 27(11). 1143–1150. 2 indexed citations

19.

Costaglioli, Patricia, Jérôme Joubès, Christel Garcia, et al.. (2005). Profiling candidate genes involved in wax biosynthesis in Arabidopsis thaliana by microarray analysis. Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids. 1734(3). 247–258. 67 indexed citations

20.

Dupuy, Denis, Incarnation Aubert, Véronique Guyonnet Dupérat, et al.. (2000). Mapping, Characterization, and Expression Analysis of the SM-20 Human Homologue, C1orf12, and Identification of a Novel Related Gene, SCAND2. Genomics. 69(3). 348–354. 32 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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