Laura Baker

1.5k total citations
17 papers, 405 citations indexed

About

Laura Baker is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Laura Baker has authored 17 papers receiving a total of 405 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Immunology. Recurrent topics in Laura Baker's work include Protein Tyrosine Phosphatases (5 papers), BRCA gene mutations in cancer (3 papers) and Renal and related cancers (3 papers). Laura Baker is often cited by papers focused on Protein Tyrosine Phosphatases (5 papers), BRCA gene mutations in cancer (3 papers) and Renal and related cancers (3 papers). Laura Baker collaborates with scholars based in United States, Canada and Germany. Laura Baker's co-authors include Karen W. Gripp, Deborah L. Stabley, Katia Sol‐Church, Kimberly A. Aldinger, Kristin G. Monaghan, James T. Bennett, Andrew E. Timms, Aida Telegrafi, Nina Powell‐Hamilton and William B. Dobyns and has published in prestigious journals such as The American Journal of Human Genetics, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Laura Baker

16 papers receiving 403 citations

Peers

Laura Baker

GENET

IMMUN

PPCH

ONCOL

Kerra Pearce United Kingdom

Ken C. Lo United States

Vera Uliana Italy

Anna Abramowicz Poland

Nicholas Bockett New Zealand

Suna Önengüt United States

Anikó Újfalusi Hungary

Xike Zhu China

Nienke J.H. van Os Netherlands

Dmitry Penkov Russia

Kerra Pearce United Kingdom

Laura Baker

276 ×1.0

105 ×1.1

GENET

39 ×0.5

IMMUN

22 ×0.5

PPCH

29 ×0.7

ONCOL

Citations per year, relative to Laura Baker Laura Baker (= 1×) peers Kerra Pearce

Countries citing papers authored by Laura Baker

Since Specialization

Citations

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

Fields of papers citing papers by Laura Baker

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Baker

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

All Works

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17 of 17 papers shown

Adeyemi, Adebowale, et al.. (2024). Infant With Beckwith–Wiedemann Requiring Transplant for Hepatic Mesenchymal Hamartoma. Pediatric Transplantation. 29(1). e70015–e70015.

Seligson, Nathan D., Jill Kolesar, Laura Baker, et al.. (2023). Integrating Pharmacogenomic Testing Into Paired Germline and Somatic Genomic Testing in Patients with Cancer. Pharmacogenomics. 24(13). 731–738. 3 indexed citations

Thomas, Morgan, Louise Amlie‐Wolf, Laura Baker, & Karen W. Gripp. (2021). The Genetic Testing Stewardship Program:. Delaware Journal of Public Health. 7(5). 20–23. 3 indexed citations

Amlie‐Wolf, Louise, Laura Baker, Morgan Thomas, et al.. (2021). Novel genetic testing model: A collaboration between genetic counselors and nephrology. American Journal of Medical Genetics Part A. 185(4). 1142–1150. 20 indexed citations

Gripp, Karen W., Laura Baker, Katherine Robbins, et al.. (2020). The novel duplication HRAS c.186_206dup p.(Glu62_Arg68dup): clinical and functional aspects. European Journal of Human Genetics. 28(11). 1548–1554. 3 indexed citations

Bauer, Christiane K., Fanny Kortüm, Janine Altmüller, et al.. (2019). Gain-of-Function Mutations in KCNN3 Encoding the Small-Conductance Ca2+-Activated K+ Channel SK3 Cause Zimmermann-Laband Syndrome. The American Journal of Human Genetics. 104(6). 1139–1157. 40 indexed citations

Shikany, Amy, Laura Baker, Deborah L. Stabley, et al.. (2019). Medically actionable comorbidities in adults with Costello syndrome. American Journal of Medical Genetics Part A. 182(1). 130–136. 8 indexed citations

Lindhurst, Marjorie J., Kim M. Keppler‐Noreuil, Julie C. Sapp, et al.. (2018). Urine cell-free DNA is a biomarker for nephroblastomatosis or Wilms tumor in PIK3CA-related overgrowth spectrum (PROS). Genetics in Medicine. 20(9). 1077–1081. 17 indexed citations

Gripp, Karen W., et al.. (2017). Constitutional LZTR1 mutation presenting with a unilateral vestibular schwannoma in a teenager. Clinical Genetics. 92(5). 540–543. 11 indexed citations

10.

Donkervoort, Sandra, Ellen Knierim, Diana Bharucha‐Goebel, et al.. (2017). Recessive mutation in EXOSC9 disrupts the exosome complex resulting in a novel form of cerebellar hypoplasia/atrophy with early motor neuronopathy. Neuromuscular Disorders. 27. S176–S177. 2 indexed citations

11.

Bertola, Débora Romeo, Deborah L. Stabley, Laura Baker, et al.. (2017). Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp. American Journal of Medical Genetics Part A. 173(5). 1309–1318. 15 indexed citations

12.

Gripp, Karen W., Laura Baker, Vinay Kandula, et al.. (2016). Nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutation. American Journal of Medical Genetics Part A. 170(10). 2559–2569. 48 indexed citations

13.

Gripp, Karen W., Laura Baker, Aida Telegrafi, & Kristin G. Monaghan. (2016). The role of objective facial analysis using FDNA in making diagnoses following whole exome analysis. Report of two patients with mutations in the BAF complex genes. American Journal of Medical Genetics Part A. 170(7). 1754–1762. 34 indexed citations

14.

Gripp, Karen W., Kimberly A. Aldinger, James T. Bennett, et al.. (2016). A novel rasopathy caused by recurrent de novo missense mutations in PPP1CB closely resembles Noonan syndrome with loose anagen hair. American Journal of Medical Genetics Part A. 170(9). 2237–2247. 85 indexed citations

15.

Robbins, Katherine, Deborah L. Stabley, Jennifer Holbrook, et al.. (2016). Paternal uniparental disomy with segmental loss of heterozygosity of chromosome 11 are hallmark characteristics of syndromic and sporadic embryonal rhabdomyosarcoma. American Journal of Medical Genetics Part A. 170(12). 3197–3206. 20 indexed citations

16.

Gripp, Karen W., Katia Sol‐Church, Patroula Smpokou, et al.. (2015). An attenuated phenotype of Costello syndrome in three unrelated individuals with a HRAS c.179G>A (p.Gly60Asp) mutation correlates with uncommon functional consequences. American Journal of Medical Genetics Part A. 167(9). 2085–2097. 18 indexed citations

17.

Aldinger, Kimberly A., Martine Tétreault, Jennifer C. Dempsey, et al.. (2014). Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy. The American Journal of Human Genetics. 95(2). 227–234. 78 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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