Laura Schultz‐Rogers

1000 total citations
11 papers, 128 citations indexed

About

Laura Schultz‐Rogers is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Laura Schultz‐Rogers has authored 11 papers receiving a total of 128 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 2 papers in Cell Biology. Recurrent topics in Laura Schultz‐Rogers's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and RNA modifications and cancer (2 papers). Laura Schultz‐Rogers is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers) and RNA modifications and cancer (2 papers). Laura Schultz‐Rogers collaborates with scholars based in United States, Netherlands and Germany. Laura Schultz‐Rogers's co-authors include Eric W. Klee, Alejandro Ferrer, Brendan C. Lanpher, Michael T. Zimmermann, Filippo Pinto e Vairo, Tanya L. Schwab, Karl J. Clark, Demetrios T. Braddock, Anupam Kotwal and Ravinder Singh and has published in prestigious journals such as PLoS ONE, Journal of Bone and Mineral Research and eLife.

In The Last Decade

Laura Schultz‐Rogers

11 papers receiving 128 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laura Schultz‐Rogers United States 8 79 60 22 20 11 11 128
Jennifer L. Kemppainen United States 8 56 0.7× 50 0.8× 15 0.7× 7 0.3× 15 1.4× 15 116
Huimin Cai China 7 84 1.1× 17 0.3× 20 0.9× 8 0.4× 10 0.9× 18 157
Alexandra Topa Sweden 7 141 1.8× 117 1.9× 45 2.0× 11 0.6× 5 0.5× 13 239
Alicia B. Byrne Australia 6 46 0.6× 35 0.6× 7 0.3× 19 0.9× 7 0.6× 8 91
Matthias Kettwig Germany 6 75 0.9× 18 0.3× 10 0.5× 19 0.9× 3 0.3× 10 138
Nechama Shalva Israel 5 111 1.4× 64 1.1× 9 0.4× 37 1.9× 5 0.5× 8 190
Mitra Forouhan United Kingdom 4 62 0.8× 36 0.6× 5 0.2× 43 2.1× 4 0.4× 5 111
Edward W. Highsmith United States 8 148 1.9× 35 0.6× 11 0.5× 19 0.9× 8 0.7× 11 248
Simon Whitley United Kingdom 2 108 1.4× 16 0.3× 12 0.5× 50 2.5× 3 0.3× 3 194
Lynn Pais United States 7 96 1.2× 52 0.9× 6 0.3× 11 0.6× 8 0.7× 19 168

Countries citing papers authored by Laura Schultz‐Rogers

Since Specialization
Citations

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

Fields of papers citing papers by Laura Schultz‐Rogers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Schultz‐Rogers

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Schultz‐Rogers. A scholar is included among the top collaborators of Laura Schultz‐Rogers 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 Schultz‐Rogers. Laura Schultz‐Rogers 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.
Fadra, Numrah, Laura Schultz‐Rogers, Pritha Chanana, et al.. (2024). Identification of skewed X chromosome inactivation using exome and transcriptome sequencing in patients with suspected rare genetic disease. BMC Genomics. 25(1). 371–371. 1 indexed citations
2.
Liu, Fang, Sekhar Kambakam, Jordan M. Welker, et al.. (2022). Cre/lox regulated conditional rescue and inactivation with zebrafish UFlip alleles generated by CRISPR-Cas9 targeted integration. eLife. 11. 16 indexed citations
3.
Schultz‐Rogers, Laura, Sekhar Kambakam, Wesley A. Wierson, et al.. (2022). Rbbp4 loss disrupts neural progenitor cell cycle regulation independent of Rb and leads to Tp53 acetylation and apoptosis. Developmental Dynamics. 251(8). 1267–1290. 14 indexed citations
4.
Sweetser, David A., Nina B. Gold, Samantha A. Schrier Vergano, et al.. (2021). Heterozygous variants in PRPF8 are associated with neurodevelopmental disorders. Molecular Genetics and Metabolism. 132. S109–S110. 1 indexed citations
5.
Schultz‐Rogers, Laura, Karthik Muthusamy, Filippo Pinto e Vairo, Eric W. Klee, & Brendan C. Lanpher. (2020). Novel loss-of-function variants in TRIO are associated with neurodevelopmental disorder: case report. BMC Medical Genetics. 21(1). 219–219. 7 indexed citations
6.
Schultz‐Rogers, Laura, Ikuo Masuho, Filippo Pinto e Vairo, et al.. (2020). Haploinsufficiency as a disease mechanism in GNB1‐associated neurodevelopmental disorder. Molecular Genetics & Genomic Medicine. 8(11). e1477–e1477. 13 indexed citations
7.
Gilbert, Melissa A., Laura Schultz‐Rogers, Ramakrishnan Rajagopalan, et al.. (2020). Protein‐elongating mutations inMYH11are implicated in a dominantly inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease. Human Mutation. 41(5). 973–982. 16 indexed citations
8.
Schultz‐Rogers, Laura, Alejandro Ferrer, Michael T. Zimmermann, et al.. (2019). Novel biallelic variants in MSTO1 associated with mitochondrial myopathy. Molecular Case Studies. 5(6). a004309–a004309. 5 indexed citations
9.
Ferrer, Alejandro, Laura Schultz‐Rogers, Charu Kaiwar, et al.. (2019). Three rare disease diagnoses in one patient through exome sequencing. Molecular Case Studies. 5(6). a004390–a004390. 7 indexed citations
10.
Oliver, Gavin R., Xiaojia Tang, Laura Schultz‐Rogers, et al.. (2019). A tailored approach to fusion transcript identification increases diagnosis of rare inherited disease. PLoS ONE. 14(10). e0223337–e0223337. 18 indexed citations
11.
Kotwal, Anupam, Alejandro Ferrer, Rajiv Kumar, et al.. (2019). Clinical and Biochemical Phenotypes in a Family With ENPP1 Mutations. Journal of Bone and Mineral Research. 35(4). 662–670. 30 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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2026