Laura Carrel

7.1k total citations · 1 hit paper
46 papers, 4.1k citations indexed

About

Laura Carrel is a scholar working on Genetics, Molecular Biology and Gender Studies. According to data from OpenAlex, Laura Carrel has authored 46 papers receiving a total of 4.1k indexed citations (citations by other indexed papers that have themselves been cited), including 36 papers in Genetics, 25 papers in Molecular Biology and 6 papers in Gender Studies. Recurrent topics in Laura Carrel's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (26 papers), Genomics and Chromatin Dynamics (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Laura Carrel is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (26 papers), Genomics and Chromatin Dynamics (10 papers) and Genetics and Neurodevelopmental Disorders (9 papers). Laura Carrel collaborates with scholars based in United States, Myanmar and United Kingdom. Laura Carrel's co-authors include Huntington F. Willard, Carolyn J. Brown, Jeffrey A. Bailey, Evan E. Eichler, Aravinda Chakravarti, Huntington F. Willard, Karrie Goglin, Christine M. Distèche, Joel B. Berletch and Jun Xu and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

Laura Carrel

45 papers receiving 4.0k citations

Hit Papers

X-inactivation profile reveals extensive variability in X... 2005 2026 2012 2019 2005 500 1000 1.5k

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laura Carrel United States 27 2.6k 2.4k 579 385 238 46 4.1k
Larry J. Shapiro United States 42 2.8k 1.1× 3.5k 1.4× 565 1.0× 204 0.5× 127 0.5× 105 5.6k
Andrew R. Zinn United States 40 2.4k 0.9× 2.1k 0.9× 333 0.6× 140 0.4× 86 0.4× 82 4.3k
Barbara R. Migeon United States 46 3.2k 1.2× 4.2k 1.7× 880 1.5× 304 0.8× 324 1.4× 136 6.3k
Elfride De Baere Belgium 39 1.8k 0.7× 3.1k 1.3× 238 0.4× 478 1.2× 114 0.5× 153 4.4k
Ronald G. Lafrenière Canada 22 2.0k 0.8× 2.9k 1.2× 367 0.6× 168 0.4× 948 4.0× 40 4.1k
Joël Zlotogora Israel 35 2.0k 0.8× 1.9k 0.8× 167 0.3× 234 0.6× 177 0.7× 170 5.0k
Veronica J. Buckle United Kingdom 47 2.1k 0.8× 4.6k 1.9× 1.3k 2.2× 251 0.7× 476 2.0× 91 6.5k
Ulrich Zechner Germany 36 1.6k 0.6× 3.0k 1.2× 367 0.6× 266 0.7× 346 1.5× 121 4.7k
Andy Greenfield United Kingdom 31 1.8k 0.7× 2.7k 1.1× 127 0.2× 268 0.7× 245 1.0× 78 3.7k
Claire Rougeulle France 30 1.8k 0.7× 3.2k 1.3× 301 0.5× 162 0.4× 778 3.3× 60 3.8k

Countries citing papers authored by Laura Carrel

Since Specialization
Citations

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

Fields of papers citing papers by Laura Carrel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Carrel

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

All Works

20 of 20 papers shown
1.
Markus, Havell, Siyuan Chen, Shuang Gao, et al.. (2025). An atlas of single-cell eQTLs dissects autoimmune disease genes and identifies novel drug classes for treatment. Cell Genomics. 5(4). 100820–100820. 2 indexed citations
2.
Gao, Shuang, Siyuan Chen, Havell Markus, et al.. (2025). Integrating axis quantitative trait loci looks beyond cell types and offers insights into brain-related traits. Nature Communications. 16(1). 10606–10606. 1 indexed citations
3.
Wang, Chen, Havell Markus, Avantika R. Diwadkar, et al.. (2025). Integrating electronic health records and GWAS summary statistics to predict the progression of autoimmune diseases from preclinical stages. Nature Communications. 16(1). 180–180. 2 indexed citations
4.
McGuire, Daniel, Havell Markus, Lina Yang, et al.. (2024). Dissecting heritability, environmental risk, and air pollution causal effects using > 50 million individuals in MarketScan. Nature Communications. 15(1). 5357–5357. 3 indexed citations
5.
Khunsriraksakul, Chachrit, Havell Markus, Fang Chen, et al.. (2024). Integrating single cell expression quantitative trait loci summary statistics to understand complex trait risk genes. Nature Communications. 15(1). 4260–4260. 9 indexed citations
6.
Khunsriraksakul, Chachrit, Havell Markus, Matthew T. Patrick, et al.. (2023). Multi-ancestry and multi-trait genome-wide association meta-analyses inform clinical risk prediction for systemic lupus erythematosus. Nature Communications. 14(1). 668–668. 26 indexed citations
7.
Khunsriraksakul, Chachrit, Daniel McGuire, Renan Sauteraud, et al.. (2022). Integrating 3D genomic and epigenomic data to enhance target gene discovery and drug repurposing in transcriptome-wide association studies. Nature Communications. 13(1). 3258–3258. 27 indexed citations
8.
Khunsriraksakul, Chachrit, Havell Markus, Nancy J. Olsen, et al.. (2022). Construction and Application of Polygenic Risk Scores in Autoimmune Diseases. Frontiers in Immunology. 13. 889296–889296. 12 indexed citations
9.
Sauteraud, Renan, et al.. (2021). Inferring genes that escape X-Chromosome inactivation reveals important contribution of variable escape genes to sex-biased diseases. Genome Research. 31(9). 1629–1637. 24 indexed citations
10.
Cheung, Aaron, et al.. (2012). X-Chromosome Inactivation in Rett Syndrome Human Induced Pluripotent Stem Cells. Frontiers in Psychiatry. 3. 24–24. 41 indexed citations
11.
Lopes, Alexandra M., et al.. (2011). Clustered transcripts that escape X inactivation at mouse XqD. Mammalian Genome. 22(9-10). 572–582. 22 indexed citations
12.
Park, Chungoo, Laura Carrel, & Kateryna D. Makova. (2010). Strong Purifying Selection at Genes Escaping X Chromosome Inactivation. Molecular Biology and Evolution. 27(11). 2446–2450. 29 indexed citations
13.
Heard, Édith & Laura Carrel. (2009). Foreword: Coping with sex chromosome imbalance. Chromosome Research. 17(5). 579–583. 1 indexed citations
14.
Carrel, Laura, Chungoo Park, Svitlana Tyekucheva, et al.. (2006). Genomic Environment Predicts Expression Patterns on the Human Inactive X Chromosome. PLoS Genetics. 2(9). e151–e151. 72 indexed citations
15.
Carrel, Laura & Huntington F. Willard. (2005). X-inactivation profile reveals extensive variability in X-linked gene expression in females. Nature. 434(7031). 400–404. 1512 indexed citations breakdown →
16.
Carrel, Laura, et al.. (1999). Germ Cell Development in the XXY Mouse: Evidence That X Chromosome Reactivation Is Independent of Sexual Differentiation. Developmental Biology. 207(1). 229–238. 73 indexed citations
17.
Carrel, Laura & Huntington F. Willard. (1996). An assay for X inactivation based on differential methylation at the fragile X locus,FMR1. American Journal of Medical Genetics. 64(1). 27–30. 62 indexed citations
18.
Carrel, Laura. (1996). X inactivation analysis and DNA methylation studies of the ubiquitin activating enzyme E1 and PCTAIRE-1 genes in human and mouse. Human Molecular Genetics. 5(3). 391–401. 64 indexed citations
19.
Lafrenière, Ronald G., Laura Carrel, & Huntington F. Willard. (1994). A novel transmembrane transporter encoded by the XPCT gene in Xq13.2. Human Molecular Genetics. 3(7). 1133–1139. 93 indexed citations
20.
Willard, H.F., Carolyn J. Brown, Laura Carrel, Brian Hendrich, & Andrew P. Miller. (1993). Epigenetic and Chromosomal Control of Gene Expression: Molecular and Genetic Analysis of X Chromosome Inactivation. Cold Spring Harbor Symposia on Quantitative Biology. 58(0). 315–322. 37 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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