Christopher B. Liebert

947 total citations
11 papers, 711 citations indexed

About

Christopher B. Liebert is a scholar working on Cellular and Molecular Neuroscience, Cell Biology and Neurology. According to data from OpenAlex, Christopher B. Liebert has authored 11 papers receiving a total of 711 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Cellular and Molecular Neuroscience, 7 papers in Cell Biology and 6 papers in Neurology. Recurrent topics in Christopher B. Liebert's work include Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (6 papers) and Endoplasmic Reticulum Stress and Disease (3 papers). Christopher B. Liebert is often cited by papers focused on Hereditary Neurological Disorders (9 papers), Neurological diseases and metabolism (6 papers) and Endoplasmic Reticulum Stress and Disease (3 papers). Christopher B. Liebert collaborates with scholars based in United States, Israel and Germany. Christopher B. Liebert's co-authors include James F. Gusella, Susan A. Slaugenhaupt, Anat Blumenfeld, Channa Maayan, Felicia B. Axelrod, James Mull, Maire Leyne, Maria Idelson, Sandra Gill and Izabela Makałowska and has published in prestigious journals such as Nature Genetics, The American Journal of Human Genetics and Gene.

In The Last Decade

Christopher B. Liebert

10 papers receiving 684 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher B. Liebert United States 7 394 344 135 118 82 11 711
Terry J. Sims United States 20 675 1.7× 276 0.8× 134 1.0× 122 1.0× 66 0.8× 38 980
Christiane Ayer‐LeLievre Sweden 13 537 1.4× 356 1.0× 65 0.5× 94 0.8× 36 0.4× 15 821
Suzanne R. Burstein United States 12 186 0.5× 345 1.0× 92 0.7× 154 1.3× 164 2.0× 17 727
Yuanzheng Gu United States 15 230 0.6× 326 0.9× 104 0.8× 57 0.5× 92 1.1× 21 590
Carol Charniga United States 15 353 0.9× 484 1.4× 66 0.5× 108 0.9× 36 0.4× 17 798
Jijun Wan United States 11 463 1.2× 530 1.5× 80 0.6× 101 0.9× 145 1.8× 15 815
Perrine Gaub Canada 10 362 0.9× 426 1.2× 48 0.4× 39 0.3× 56 0.7× 14 765
Emilio Geijo‐Barrientos Spain 15 298 0.8× 348 1.0× 66 0.5× 36 0.3× 101 1.2× 30 788
А. R. Giniatullin Russia 17 256 0.6× 536 1.6× 207 1.5× 58 0.5× 64 0.8× 31 740
Tine Deconinck Belgium 17 376 1.0× 376 1.1× 89 0.7× 149 1.3× 107 1.3× 28 733

Countries citing papers authored by Christopher B. Liebert

Since Specialization
Citations

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

Fields of papers citing papers by Christopher B. Liebert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher B. Liebert. 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 Christopher B. Liebert. The network helps show where Christopher B. Liebert may publish in the future.

Co-authorship network of co-authors of Christopher B. Liebert

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

All Works

11 of 11 papers shown
1.
Slaugenhaupt, Susan A., Anat Blumenfeld, Sandra Gill, et al.. (2001). Tissue-Specific Expression of a Splicing Mutation in the Gene Causes Familial Dysautonomia. The American Journal of Human Genetics. 68(3). 598–605. 448 indexed citations
2.
Chadwick, Brian P., Maire Leyne, Sandra Gill, et al.. (2000). Cloning, mapping, and expression of a novel brain-specific transcript in the Familial Dysautonomia candidate region on Chromosome 9q31. Mammalian Genome. 11(1). 81–83. 5 indexed citations
3.
Blumenfeld, Anat, Susan A. Slaugenhaupt, Christopher B. Liebert, et al.. (1999). Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31. The American Journal of Human Genetics. 64(4). 1110–1118. 53 indexed citations
4.
Chadwick, Brian P., Sandra Gill, Maire Leyne, et al.. (1999). Cloning, genomic organization and expression of a putative human transmembrane protein related to the Caenorhabditis elegans M01F1.4 gene. Gene. 240(1). 67–73. 3 indexed citations
5.
Slaugenhaupt, Susan A., Anat Blumenfeld, Christopher B. Liebert, et al.. (1995). The human gene for neurotrophic tyrosine kinase receptor type 2 (NTRK2) is located on chromosome 9 but is not the familial dysautonomia gene. Genomics. 25(3). 730–732. 8 indexed citations
6.
Blumenfeld, Anat, Diane Lucente, James A. Trofatter, et al.. (1995). Peripherin gene is linked to keratin 18 gene on human chromosome 12. Somatic Cell and Molecular Genetics. 21(1). 83–88. 7 indexed citations
7.
Slaugenhaupt, Susan A., Alfred L. Roca, Christopher B. Liebert, et al.. (1995). Mapping of the Gene for the Mel1a-Melatonin Receptor to Human Chromosome 4 (MTNR1A) and Mouse Chromosome 8 (Mtnr1a). Genomics. 27(2). 355–357. 72 indexed citations
8.
Slaugenhaupt, Susan, et al.. (1994). Isolation of candidate genes and physical mapping in the Familial Dysautonomia region of chromosome 9q31. The American Journal of Human Genetics. 55(5). 1246–52.
9.
Blumenfeld, Anat, Susan Slaugenhaupt, Diane Lucente, et al.. (1993). The gene for familial dysautonomia is linked to chromosome 9 and shows strong linkage disequilibrium with D9S58. The Society for Neuroscience Abstracts. 19. 1463. 7 indexed citations
10.
Blumenfeld, Anat, Susan A. Slaugenhaupt, Felicia B. Axelrod, et al.. (1993). Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis. Nature Genetics. 4(2). 160–164. 104 indexed citations
11.
Blumenfeld, Anat, Felicia B. Axelrod, James A. Trofatter, et al.. (1993). Exclusion of familial dysautonomia from more than 60% of the genome.. Journal of Medical Genetics. 30(1). 47–52. 4 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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