Vanessa Bach

518 total citations
12 papers, 260 citations indexed

About

Vanessa Bach is a scholar working on Hematology, Genetics and Nutrition and Dietetics. According to data from OpenAlex, Vanessa Bach has authored 12 papers receiving a total of 260 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Hematology, 6 papers in Genetics and 6 papers in Nutrition and Dietetics. Recurrent topics in Vanessa Bach's work include Iron Metabolism and Disorders (7 papers), Hemoglobinopathies and Related Disorders (6 papers) and Trace Elements in Health (6 papers). Vanessa Bach is often cited by papers focused on Iron Metabolism and Disorders (7 papers), Hemoglobinopathies and Related Disorders (6 papers) and Trace Elements in Health (6 papers). Vanessa Bach collaborates with scholars based in Spain, Palestinian Territory and Peru. Vanessa Bach's co-authors include Ángel F. Remacha, Montserrat Baiget, Paloma Jara, R. Queralt, Ester Margarit, Miquel Bruguera, F Ballesta, Albert Altés, Jordi Félez and Alejandro Moles‐Fernández and has published in prestigious journals such as The Journal of Infectious Diseases, Clinica Chimica Acta and Journal of Medical Genetics.

In The Last Decade

Vanessa Bach

12 papers receiving 259 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Vanessa Bach Spain 9 116 106 74 56 55 12 260
Carole Barin France 10 29 0.3× 142 1.3× 101 1.4× 50 0.9× 14 0.3× 16 302
Matthew J. Ferber United States 6 75 0.6× 29 0.3× 54 0.7× 4 0.1× 50 0.9× 6 175
Rosa Lacerda Portugal 10 227 2.0× 296 2.8× 32 0.4× 229 4.1× 16 0.3× 14 400
Rafael Marino Canada 7 51 0.4× 76 0.7× 54 0.7× 142 2.5× 7 0.1× 11 369
Sankha Subhra Das India 10 19 0.2× 32 0.3× 93 1.3× 46 0.8× 28 0.5× 21 250
Paola Cerani Italy 9 60 0.5× 262 2.5× 89 1.2× 204 3.6× 47 0.9× 13 373
Anne Marie Jouanolle France 7 337 2.9× 453 4.3× 44 0.6× 359 6.4× 36 0.7× 14 526
Shivani Khandwala United Kingdom 6 95 0.8× 214 2.0× 89 1.2× 129 2.3× 21 0.4× 7 372
Shuqian Xu China 10 7 0.1× 189 1.8× 148 2.0× 102 1.8× 28 0.5× 20 381

Countries citing papers authored by Vanessa Bach

Since Specialization
Citations

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

Fields of papers citing papers by Vanessa Bach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Vanessa Bach

This figure shows the co-authorship network connecting the top 25 collaborators of Vanessa Bach. A scholar is included among the top collaborators of Vanessa Bach 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 Vanessa Bach. Vanessa Bach 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.
Montalban, Gemma, Sandra Bonache, Vanessa Bach, et al.. (2021). BRCA1 and BRCA2 whole cDNA analysis in unsolved hereditary breast/ovarian cancer patients. Cancer Genetics. 258-259. 10–17. 5 indexed citations
2.
Bonache, Sandra, Alejandro Moles‐Fernández, Gemma Montalban, et al.. (2018). Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings. Journal of Cancer Research and Clinical Oncology. 144(12). 2495–2513. 49 indexed citations
3.
Montalban, Gemma, Sandra Bonache, Alejandro Moles‐Fernández, et al.. (2018). Screening of BRCA1/2 deep intronic regions by targeted gene sequencing identifies the first germline BRCA1 variant causing pseudoexon activation in a patient with breast/ovarian cancer. Journal of Medical Genetics. 56(2). 63–74. 24 indexed citations
4.
Ruiz‐Riol, Marta, Anuska Llano, Javier Ibarrondo, et al.. (2014). Alternative Effector-Function Profiling Identifies Broad HIV-Specific T-Cell Responses in Highly HIV-Exposed Individuals Who Remain Uninfected. The Journal of Infectious Diseases. 211(6). 936–946. 15 indexed citations
5.
Ballana, Ester, Eva Riveira‐Muñoz, Christian Pou, et al.. (2012). HLA class I protective alleles in an HIV-1-infected subject homozygous for CCR5-Δ32/Δ32. Immunobiology. 218(4). 543–547. 5 indexed citations
6.
Altés, Albert, Vanessa Bach, Anna Esteve‐Codina, et al.. (2009). Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene. Annals of Hematology. 88(10). 951–955. 15 indexed citations
7.
Altés, Albert, Vanessa Bach, Anna Esteve‐Codina, et al.. (2008). Does the SLC40A1 gene modify HFE-related haemochromatosis phenotypes?. Annals of Hematology. 88(4). 341–345. 14 indexed citations
8.
Remacha, Ángel F., Eugenio Berlanga, Assumpta Caixàs, et al.. (2008). Serum soluble transferrin receptor concentrations are increased in central obesity. Results from a screening programme for hereditary hemochromatosis in men with hyperferritinemia. Clinica Chimica Acta. 400(1-2). 111–116. 28 indexed citations
9.
Altés, Albert, et al.. (2007). The relationship between iron overload and clinical characteristics in a Spanish cohort of 100 C282Y homozygous hemochromatosis patients. Annals of Hematology. 86(11). 831–835. 12 indexed citations
10.
Bach, Vanessa, M. J. Barceló, Albert Altés, et al.. (2006). Genotyping the HFE gene by melting point analysis with the LightCycler system: Pros and cons. Blood Cells Molecules and Diseases. 36(2). 288–291. 4 indexed citations
11.
Bach, Vanessa, et al.. (2005). Autosomal dominant hereditary hemochromatosis associated with two novel Ferroportin 1 mutations in Spain. Blood Cells Molecules and Diseases. 36(1). 41–45. 18 indexed citations
12.
Margarit, Ester, Vanessa Bach, Miquel Bruguera, et al.. (2005). Mutation analysis of Wilson disease in the Spanish population - identification of a prevalent substitution and eight novel mutations in the ATP7B gene. Clinical Genetics. 68(1). 61–68. 71 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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