Laurie A. Christ

523 total citations
9 papers, 339 citations indexed

About

Laurie A. Christ is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Laurie A. Christ has authored 9 papers receiving a total of 339 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Plant Science and 5 papers in Molecular Biology. Recurrent topics in Laurie A. Christ's work include Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Chromatin Dynamics (4 papers). Laurie A. Christ is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Chromosomal and Genetic Variations (7 papers) and Genomics and Chromatin Dynamics (4 papers). Laurie A. Christ collaborates with scholars based in United States, India and Canada. Laurie A. Christ's co-authors include Stuart Schwartz, Mark A. Micale, Jeffrey M. Conroy, Carol A. Crowe, Evan E. Eichler, Julie E. Horvath, Richard K. Wilson, Xinwei She, Tina Graves and David J. Aughton and has published in prestigious journals such as Nature, The American Journal of Human Genetics and Human Genetics.

In The Last Decade

Laurie A. Christ

9 papers receiving 322 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laurie A. Christ United States 7 248 209 187 69 14 9 339
Elisabeth Ewers Germany 13 381 1.5× 222 1.1× 162 0.9× 175 2.5× 15 1.1× 23 423
M Ferguson-Smith United Kingdom 10 242 1.0× 153 0.7× 168 0.9× 95 1.4× 12 0.9× 15 374
Milly Andrle Austria 7 239 1.0× 195 0.9× 191 1.0× 72 1.0× 8 0.6× 11 358
Ahmed B. Hamid Germany 13 272 1.1× 176 0.8× 136 0.7× 123 1.8× 7 0.5× 24 331
Theresa W. Depinet United States 6 343 1.4× 208 1.0× 281 1.5× 93 1.3× 7 0.5× 7 445
V.K. Maloney United Kingdom 9 263 1.1× 54 0.3× 174 0.9× 46 0.7× 8 0.6× 12 304
Christine A Joyce United Kingdom 8 195 0.8× 68 0.3× 145 0.8× 98 1.4× 12 0.9× 10 255
Reza Saleki United States 4 352 1.4× 138 0.7× 135 0.7× 179 2.6× 12 0.9× 6 382
Carolyn Trunca United States 9 199 0.8× 96 0.5× 98 0.5× 152 2.2× 9 0.6× 14 301
Daniele Caufin Italy 8 181 0.7× 85 0.4× 85 0.5× 83 1.2× 14 1.0× 8 222

Countries citing papers authored by Laurie A. Christ

Since Specialization
Citations

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

Fields of papers citing papers by Laurie A. Christ

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laurie A. Christ. 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 Laurie A. Christ. The network helps show where Laurie A. Christ may publish in the future.

Co-authorship network of co-authors of Laurie A. Christ

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

All Works

9 of 9 papers shown
1.
Izumi, Kosuke, et al.. (2011). Familial 9q22.3 microduplication spanning PTCH1 causes short stature syndrome with mild intellectual disability and dysmorphic features. American Journal of Medical Genetics Part A. 155(6). 1384–1389. 13 indexed citations
2.
Slavin, Thomas P., et al.. (2011). Isolated skeletal malformations in a child with a small mosaic ring microduplication of 18 p11.21q11.2: Genotype–phenotype correlations. American Journal of Medical Genetics Part A. 155(3). 618–621. 3 indexed citations
3.
Kulikowski, Leslie Domenici, et al.. (2005). Breakpoint mapping in a case of mosaicism with partial monosomy 9p23 → pter and partial trisomy 1q41 → qter suggests neo‐telomere formation in stabilizing the deleted chromosome. American Journal of Medical Genetics Part A. 140A(1). 82–87. 13 indexed citations
4.
Christ, Laurie A., et al.. (2005). Characterization of a familial balanced rec(13) in a child with mild MR and his half‐sibling with two structurally rearranged chromosomes 13. American Journal of Medical Genetics Part A. 137A(2). 217–221. 14 indexed citations
5.
Astbury, Caroline, Laurie A. Christ, David J. Aughton, et al.. (2004). Detection of deletions in de novo “balanced” chromosome rearrangements: Further evidence for their role in phenotypic abnormalities. Genetics in Medicine. 6(2). 81–89. 34 indexed citations
6.
Astbury, Caroline, Laurie A. Christ, David J. Aughton, et al.. (2004). Delineation of complex chromosomal rearrangements: evidence for increased complexity. Human Genetics. 114(5). 448–457. 33 indexed citations
7.
She, Xinwei, Julie E. Horvath, Zhaoshi Jiang, et al.. (2004). The structure and evolution of centromeric transition regions within the human genome. Nature. 430(7002). 857–864. 154 indexed citations
8.
Astbury, Caroline, Laurie A. Christ, Anil Kumar, Carol A. Crowe, & Stuart Schwartz. (2001). Elucidation of the mechanisms of chromosome rearrangement: Implications for heightened complexity. ePrints@IISc (Indian Institute of Science). 1 indexed citations
9.
Christ, Laurie A., Carol A. Crowe, Mark A. Micale, Jeffrey M. Conroy, & Stuart Schwartz. (1999). Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9p-Deletion Syndrome. The American Journal of Human Genetics. 65(5). 1387–1395. 74 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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