Bárbara Kremeyer

18.3k total citations
10 papers, 535 citations indexed

About

Bárbara Kremeyer is a scholar working on Genetics, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Bárbara Kremeyer has authored 10 papers receiving a total of 535 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Bárbara Kremeyer's work include Yersinia bacterium, plague, ectoparasites research (3 papers), Genetic Associations and Epidemiology (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Bárbara Kremeyer is often cited by papers focused on Yersinia bacterium, plague, ectoparasites research (3 papers), Genetic Associations and Epidemiology (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Bárbara Kremeyer collaborates with scholars based in United Kingdom, Colombia and United States. Bárbara Kremeyer's co-authors include Susanne Hummel, Andrés Ruiz‐Linares, Bernd Herrmann, Gabriel Bedoya, C. Geoffrey Woods, John N. Wood, Florence R. Fricker, Natalia Acosta‐Baena, Mari‐Wyn Burley and Martin Oppermann and has published in prestigious journals such as Neuron, American Journal of Medical Genetics Part B Neuropsychiatric Genetics and Genes and Immunity.

In The Last Decade

Bárbara Kremeyer

10 papers receiving 522 citations

Peers

Bárbara Kremeyer
S. Komori Japan
Bárbara Kremeyer
Citations per year, relative to Bárbara Kremeyer Bárbara Kremeyer (= 1×) peers S. Komori

Countries citing papers authored by Bárbara Kremeyer

Since Specialization
Citations

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

Fields of papers citing papers by Bárbara Kremeyer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Bárbara Kremeyer

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

All Works

10 of 10 papers shown
1.
Valencia, Jenny García, Ana Valencia, Bárbara Kremeyer, et al.. (2012). Asociación de esquizofrenia y sus dimensiones clínicas con el gen NOS1AP en población colombiana*. Revista Colombiana de Psiquiatría. 41(2). 249–272. 1 indexed citations
2.
Valencia, Ana, Daniel J. White, Heike Müller, et al.. (2010). Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate. Psychiatric Genetics. 20(4). 179–183. 20 indexed citations
3.
Kremeyer, Bárbara, Francisco Lopera, James J. Cox, et al.. (2010). A Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain Syndrome. Neuron. 66(5). 671–680. 333 indexed citations
4.
Kremeyer, Bárbara, Jenny García Valencia, Heike Müller, et al.. (2010). Genome-Wide Linkage Scan of Bipolar Disorder in a Colombian Population Isolate Replicates Loci on Chromosomes 7p21–22, 1p31, 16p12 and 21q21–22 and Identifies a Novel Locus on Chromosome 12q. Human Heredity. 70(4). 255–268. 11 indexed citations
5.
Kremeyer, Bárbara, Jenny García Valencia, Carlos Palacio, et al.. (2008). Evidence for a Role of the <i>NOS1AP (CAPON)</i> Gene in Schizophrenia and Its Clinical Dimensions: An Association Study in a South American Population Isolate. Human Heredity. 67(3). 163–173. 29 indexed citations
6.
Kremeyer, Bárbara, Jenny García Valencia, Emily O. Kerr, et al.. (2006). Transmission distortion of BDNF variants to bipolar disorder type I patients from a south american population isolate,. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 141B(5). 435–439. 20 indexed citations
7.
Kremeyer, Bárbara, Maria Soller, Kristina Lagerstedt‐Robinson, et al.. (2005). The BRCA1 exon 13 duplication in the Swedish population. Familial Cancer. 4(2). 191–194. 14 indexed citations
8.
Hummel, Susanne, Diane Schmidt, Bárbara Kremeyer, Bernd Herrmann, & Martin Oppermann. (2005). Detection of the CCR5-Δ32 HIV resistance gene in Bronze Age skeletons. Genes and Immunity. 6(4). 371–374. 86 indexed citations
9.
Kremeyer, Bárbara, et al.. (2005). Frequency analysis of the ∆32ccr5 HIV resistance allele in a medieval Plague mass grave. Anthropologischer Anzeiger. 63(1). 13–22. 9 indexed citations
10.
Kremeyer, Bárbara, Susanne Hummel, & Bernd Herrmann. (2005). Frequency analysis of the delta32ccr5 HIV resistance allele in a medieval plague mass grave.. PubMed. 63(1). 13–22. 12 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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